Trend in Opinion on Medicare Part D Among Seniors
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The latest Kaiser Health Tracking Poll finds the public’s views souring on the Affordable Care Act (ACA) in November, with about half having an unfavorable view of the law and a third having a favorable view, a gap that was seen only once before, during the Republican presidential primaries in 2011. This negative shift in opinion comes amid heavy news coverage of the website problems plaguing the law’s online health insurance exchanges and stories about individuals being dropped from their insurance coverage because their plans don’t meet minimum requirements set by the ACA, stories that were followed closely by more than half the American public this month. The partisan divide on the law continues, but support among Democrats dropped sharply this month after rallying in September and October. Views among women also shifted this month, and for the first time in Kaiser tracking, the share of women with an unfavorable view outnumbered those with a favorable view by a large margin (48 percent versus 32 percent). Visibility of the health insurance exchanges increased among the public overall in November, but reaching the uninsured with information remains a challenge – about four in ten uninsured say they’ve heard nothing at all about the new marketplaces to date, and two-thirds say they still don’t have enough information about the law to know how it will impact them. Still, nearly six in ten of those who currently lack coverage say they plan to get insurance in 2014.
Amid heavy news coverage of HealthCare.gov’s website problems and stories about individuals being dropped from their insurance plans, the American public’s overall views of the ACA took a negative turn in November. This month, roughly half (49 percent) say they have an unfavorable view of the law and a third (33 percent) have a favorable view. In nearly four years of Kaiser tracking on the law, the gap between negative and positive views (currently 16 percentage points) has been this large only once before, in October 2011 (17 percentage points) when the ACA was getting lots of negative attention in the Republican presidential primaries and the country was focused on the upcoming election and the Occupy Wall Street movement.

Views of the law shifted more negative this month among most demographic groups, but the drop was sharpest among Democrats. After rebounding in September and October, the share of Democrats viewing the law favorably stands at 55 percent in November, closer to where it had been earlier in 2013.

Women, who have historically been evenly divided on the law, registered their most negative views on the law to date, with 48 percent saying they have an unfavorable view of the law and 32 percent favorable. The gap between unfavorable and favorable views among women is up 15 percentage points since last month.

This negative shift in views of the law may be driven more by concern about the law’s impact on the country overall than on one’s personal situation. While a plurality says they don’t think the law will make much difference for their own families (a share that hasn’t changed much over the past year), the share saying the country will be worse off under the law reached a new high in Kaiser polling this month. Forty-three percent now say the law will leave the country worse off (up from 38 percent last month), compared with 34 percent who think the country will be better off and 15 percent who say it won’t make much difference.


This negative shift in views comes at a time when the public reports paying close attention to news stories related to the ACA. Over half (55 percent) say they have followed news about website problems with the health law’s online insurance marketplaces “very” or “fairly” closely (roughly equal to the share who reported following these stories in October). The same share reports paying close attention to news stories about people being dropped from their health insurance. Attention to both of these news stories trails behind attention to reports about U.S. economic conditions.

The public’s evaluation of the news coverage they’ve seen is somewhat mixed. More than half say news coverage of the law has been mostly about politics and controversies, while fewer than one in ten say it’s been mostly about how the law will impact people and three in ten say it’s been a mix of the two. While four in ten say the news coverage they’ve seen has been mostly balanced, almost twice as many believe coverage is biased against the law as say it is biased in favor (33 percent versus 17 percent).

Just over a month into open enrollment in the ACA’s health insurance exchanges, visibility of the new marketplaces has increased. This month, 42 percent of the public say they have heard “a lot” or “some” about the health insurance marketplace, twice the share who reported hearing as much in September. Among the uninsured, a key target group for outreach, visibility of the exchanges has also increased since September (from 15 percent to 29 percent), though it remains lower than among the general public.
| FIGURE 8: Visibility of ACA’s Health Insurance Marketplaces Increases in November | ||||
| As you may know, the health care law creates health insurance exchanges or marketplaces where people who don’t get coverage through their employers can shop for insurance and compare prices and benefits. How much, if anything, have you heard about this new health insurance marketplace, also known as (STATE EXCHANGE NAME)] in your state? | ||||
| Total public | Uninsured (age<65) | |||
| Nov-2013 | Sept-2013 | Nov-2013 | Sept-2013 | |
| A lot | 22 | 5 | 15 | 4 |
| Some | 20 | 14 | 14 | 11 |
| Only a little | 31 | 32 | 33 | 32 |
| Nothing at all | 25 | 48 | 38 | 52 |
Reaching the uninsured with information remains a challenge – 38 percent of those without insurance say they have heard “nothing at all” about the health insurance marketplace, and two-thirds (65 percent) still feel they do not have enough information about the law to understand how it will impact them and their family. Advertising is one way the uninsured may learn about the law, and this month, 35 percent of the uninsured say they saw at least one ad providing information about how to get coverage.
Despite the information challenge, nearly six in ten (58 percent) of the uninsured say they plan to get health insurance in 2014, while a third (34 percent) say they won’t get coverage and 8 percent are unsure.
Since October 1, many journalists and others have drawn parallels between the ACA’s troubled rollout and the Medicare “Part D” prescription drug benefit, which some say had a similarly rocky launch in 2006. Among seniors, the program was unpopular at first; 50 percent had an unfavorable view of the program and 28 percent a favorable view in December 2005, just before enrollment began. In November 2006, when the first year enrollment was complete and most of those who enrolled had some experience using their new plans, views were more positive, with 42 percent of seniors expressing a favorable view of the program and 34 percent an unfavorable one.
The latest Kaiser Health Tracking poll finds that seven years later, the Medicare Part D benefit is quite popular: 63 percent of seniors view it favorably and just 14 percent view it unfavorably. Among those who are enrolled in a prescription drug plan, 85 percent say their experiences using the benefit have been positive, including six in ten (59 percent) who say they’ve been “very” positive.
Of course, it is far too early to tell what will happen to public opinion on the ACA as it moves through the next phase of implementation, but the Medicare Part D experience suggests that it is not unusual for a new law of this sort to be poorly perceived at the outset.

This Kaiser Health Tracking Poll was designed and analyzed by public opinion researchers at the Kaiser Family Foundation (KFF) led by Mollyann Brodie, Ph.D., including Liz Hamel, Bianca DiJulio, and Jamie Firth. The survey was conducted November 13-18, 2013, among a nationally representative random digit dial telephone sample of 1,204 adults ages 18 and older, living in the United States, including Alaska and Hawaii (note: persons without a telephone could not be included in the random selection process). Computer-assisted telephone interviews conducted by landline (602) and cell phone (602, including 342 who had no landline telephone) were carried out in English and Spanish by Princeton Data Source under the direction of Princeton Survey Research Associates International (PSRAI). Both the random digit dial landline and cell phone samples were provided by Survey Sampling International, LLC. For the landline sample, respondents were selected by asking for the youngest adult male or female currently at home based on a random rotation. If no one of that gender was available, interviewers asked to speak with the youngest adult of the opposite gender. For the cell phone sample, interviews were conducted with the person who answered the phone. KFF paid for all costs associated with the survey.
The combined landline and cell phone sample was weighted to balance the sample demographics to match estimates for the national population using data from the Census Bureau’s 2011 American Community Survey (ACS) on sex, age, education, race, Hispanic origin, nativity (for Hispanics only), and region along with data from the 2010 Census on population density. The sample was also weighted to match current patterns of telephone use using data from the July-December 2012 National Health Interview Survey. The weight takes into account the fact that respondents with both a landline and cell phone have a higher probability of selection in the combined sample and also adjusts for the household size for the landline sample. All statistical tests of significance account for the effect of weighting.
The margin of sampling error including the design effect for the full sample is plus or minus 3 percentage points. Numbers of respondents and margin of sampling error for key subgroups are shown in the table below. For results based on other subgroups, the margin of sampling error may be higher. Sample sizes and margin of sampling errors for other subgroups are available by request. Note that sampling error is only one of many potential sources of error in this or any other public opinion poll.
| Group | N (unweighted) | M.O.S.E. |
| Total | 1204 | ±3 percentage points |
| Uninsured, under age 65 | 151 | ±8 percentage points |
| Age 65 or older | 356 | ±6 percentage points |
| Democrats | 346 | ±6 percentage points |
| Republicans | 295 | ±7 percentage points |
| Independents | 388 | ±6 percentage points |
| Men | 578 | ±5 percentage points |
| Women | 626 | ±5 percentage points |
October 1, 2013 was a landmark date for the Affordable Care Act (ACA), with the start of open enrollment in the law’s Health Insurance Marketplaces and the growth of Medicaid enrollment in some states. Several weeks into open enrollment, many people – including journalists, policymakers, and the public at large – are eager for early data indicating how the law is working from the perspective of potential enrollees. In particular, given the problems with Healthcare.Gov and some of the state exchange websites, many people want quantitative data about people’s experiences attempting to purchase or enroll in some sort of health insurance coverage using these mechanisms. In the long run, data from large federal surveys will be available to help answer questions about the enrollment experience, but in the short term, some may turn to national public opinion polls to see what can be learned.
In this Data Note, we raise a note of caution about the possible pitfalls of using standard national public opinion polls to make judgments about Americans’ early experiences with health plan enrollment under the ACA.
The primary issue with trying to assess the early impact of the ACA through national, random sample surveys that use a standard methodology and sample size comes down to raw numbers. There generally just aren’t enough people to look at.
Let’s start with the broadest group that stands to be impacted by the ACA’s coverage expansions: the roughly 40 million adults who are currently uninsured, comprising roughly 21 percent of the nonelderly adult population. While a substantial share by most measures, this amounts to relatively few interviews when translated to a nationally representative, random sample survey.
To make it more concrete, a typical national public opinion poll with a total sample size of 1,200 adults yields between 140 to 175 interviews with uninsured individuals.1 The margin of sampling error (MOSE) around survey estimates based on this group is in the range of plus or minus 8 to 10 percentage points. While it’s possible to use a poll of this type to report broadly on the views and experiences of the uninsured, the sample size constrains pollsters’ ability to detect changes over time. For example, in a typical national public opinion poll with a MOSE of plus or minus 3 percentage points, if the survey finds 35 percent of people overall report a certain behavior, the chances are very high (95 out of 100) that if you interviewed the whole population, the “real” answer would lie between 32 percent and 38 percent. For a subgroup the size of the uninsured, with a MOSE of plus or minus 10 percentage points, the likely range of answers widens from 25 percent to 45 percent. One of the key questions people will want to answer about ACA enrollment is whether the share of the uninsured who are attempting to sign up for coverage is increasing or decreasing. With such a wide MOSE range around each point estimate, it will be difficult for pollsters to answer this type of question by detecting changes over time. Further, starting with a group of this size makes it difficult (and sometimes impossible) to analyze subgroups of interest within the uninsured (for example, young adults).
Another group that the media has focused on recently amid reports of cancelled insurance policies is those who purchase insurance on the individual market. This group amounts to about 8.5 million adults, or roughly 5 percent of the nonelderly adult population, and represents fewer than 100 interviews out of a typical 1,200 person survey. In this case, the MOSE is so large that most researchers consider estimates based on this population to be too unreliable to report.2
Further complicating matters is the fact that looking at all the uninsured as one undifferentiated group misses some of the important complexities of the law. In fact, there are many individual characteristics that will impact people’s eligibility for various coverage options under the ACA. For example, subsidies to help people purchase coverage are available for those within a certain income range based on the federal poverty level (FPL), which is calculated using a formula that includes household size and income.3 Asking the right questions to determine where an individual falls on the FPL scale is complicated, and survey respondents are often hesitant to divulge all of the information necessary to make the calculation. While researchers often ask these questions on surveys that focus on poverty and income, these questions take up valuable time on a survey, and are outside the scope of most national opinion polls.
Determining eligibility for the Medicaid expansion is also complicated. Prior to the ACA, each state had its own set of rules to determine eligibility. The law was initially intended to expand Medicaid to cover all individuals with incomes of 138 percent of the FPL or less, but the 2012 Supreme Court ruling made the Medicaid expansion optional for states. As a result, determining whether an individual is eligible for Medicaid depends not only on where they fall on the FPL scale, but also on the state in which they reside. The bottom line for national public opinion polls with traditional sample sizes in the range of 1,000 to 1,200 is that it will be impossible to break out the experiences of these various groups with any specificity.
It is also worth noting that some people will think they are eligible for coverage under the ACA when in fact they are not. For example, undocumented immigrants are not eligible to enroll in Medicaid or participate in the exchanges, but in some parts of the country they make up a significant share of the uninsured. A recent Kaiser survey of the uninsured in California found that about a fifth of the state’s uninsured self-identified as being undocumented,4 and that nearly half this group thought they may be eligible for coverage through Medicaid or the California exchange. Ideally, the undocumented should be excluded from survey estimates of enrollment experiences. However, like income, immigration status is a sensitive topic, and while it is possible to tackle this issue in more targeted projects like the Kaiser California Uninsured Survey, this is another topic that is outside the scope of most national surveys.
When it comes to quantifying the experiences of those who have enrolled so far, the case for using national surveys is even bleaker. The Obama Administration reported that as of the start of November, 106,185 people had enrolled using the exchanges and 396,261 were deemed eligible for Medicaid or the Children’s Health Insurance Program.5 This represents a tiny fraction of the overall adult population, and would be impossible to identify in a typical national random sample survey.
Even by the end of 2014, when CBO projects that roughly 7 million people will enroll in health insurance through the exchanges and 9 million will gain coverage through Medicaid or the Children’s Health Insurance Program,6 this only represents roughly 2 to 3 percent of the total nonelderly population (including children) and is still too few to expect to reliably break out in a national survey with a typical sample size.
| FIGURE 1: Numbers And Percentages Of Some Key Groups Of Interest In Measuring ACA Impact | |||||
| Estimated number of nonelderly adults (millions) | Percent of nonelderly adult population | Ease of identifying via survey | Number of interviews in a typical national random sample survey (N=1200) | MOSE range (plus or minus X percentage points) | |
| Currently uninsured7 | 40.2 | 21% | Easy | 140-175 | 8 to 10 |
| Currently purchase own insurance in individual market8 | 8.5 | 5% | Easy | 75-90 | 12 to 13 |
| Eligible for subsidies to purchase insurance in the exchanges (includes currently insured)9 | 16.3 | 9% | Difficult (requires FPL calculation) | 65-80 | 13 to 14 |
| Uninsured and eligible for Medicaid as of January 2014 (includes newly eligible + previously eligible)10 | 8.7 | 5% | Very difficult (requires FPL calculation and varies by state) | 30-40 | >15 |
| Uninsured and undocumented11 | 5.7 | 3% | Difficult (sensitive questions) | 15-30 | >15 |
| Currently uninsured, not tax credit eligible, and would have been eligible for Medicaid but live in a state not expanding (the “gap” group)12 | 4.8 | 3% | Very difficult (requires FPL calculation and varies by state) | 15-30 | >15 |
Another complicating factor in using standard national public opinion polls to measure early ACA impact is that some of the groups most likely to have early experiences with the law, including those with lower incomes and those who speak a language other than English, are populations that are often under-represented in surveys. Weighting survey data to national demographic benchmarks helps account for this under-representation and ensures that the overall survey results are nationally representative, but the fact remains that this phenomenon exacerbates the issue of having too few interviews with individuals in these groups to reliably describe their experiences with the law.
This is even the case with the Kaiser Health Tracking Poll, despite the fact that we take special measures and make extra efforts to maximize inclusion of these groups, such as completing half the survey interviews via cell phones (which younger people and racial and ethnic minorities use in disproportionate numbers) and offering respondents the option of being interviewed in Spanish or English. The tracking poll has a minimum overall sample size of 1,200 and in some months is increased to 1,500. These extra measures all increase the cost of conducting a survey, which does not fit within many polling organizations’ budgets. As a result, many polls reported in the news are based on surveys with smaller overall sample sizes, fewer cell phone interviews, and English-only interviewing. While these methodological details may not have a significant impact on a survey’s ability to represent the overall views of adults nationally, they can make a big difference when it comes to measuring the experiences of some of the groups described above. Surveys conducted via the Internet can be particularly problematic, given the lower level of Internet access and online experience among this population.
Another major challenge is designing survey questions that will correctly identify those who actually tried to sign up for coverage through the ACA and what their experiences were. While it might be tempting to just ask Americans whether they had tried to sign up for health insurance at Healthcare.Gov, this would certainly provide a misleading result. While much of the news coverage has focused on enrollment through the federal website, there are actually many different ways people can start the enrollment process, many different pathways through the process, and many different potential outcomes. Individuals attempting to sign up online may start not at Healthcare.Gov but at their own state’s exchange website (if they live in a state that is administering its own exchange). Alternatively, they may go to a state Medicaid office, meet with an ACA Navigator or Assister, or call either a national or state-based telephone help line. Some may start the process at the health insurance exchange but end up enrolling in Medicaid. Others may find that they’re eligible to purchase coverage through the exchange but not to receive federal subsidies to help pay for their coverage. Some may go to the website or seek in-person help with the intention of signing up for coverage right away, and others may go to gather information and plan to sign up for coverage later. Many will have no idea that their experience was brought to them by the ACA at all. These are just a few of the factors that complicate any effort to quantify a single “enrollment experience.”
While not a good vehicle for measuring early enrollment experiences, national public opinion polls can provide other types of useful information for those trying to gauge how ACA implementation is going. For example, polls can measure the public’s perceptions (how well do people think the rollout is going?), understanding and awareness (are they learning more about the law over time?), media exposure (what are they hearing on the news and what is their reaction to the news?), and opinions (does all of this change how they feel about the law overall, or not?). National polls can also be used to gauge the types of discussions people are having with their family and friends about their experiences, giving a sense of what the national dialogue is like. These are the types of questions we have asked over time in the Kaiser Health Tracking Poll, and we’ll continue to do so going forward.
With the Kaiser Health Tracking poll, we’ll also continue to report broadly on the views of the uninsured. While we can’t use this survey to break them down into the Medicaid eligible or the exchange shoppers, or to quantify their enrollment experiences, we can measure things like the extent to which they feel they understand the law, the extent to which they feel the law is helping or hurting them, their awareness of the individual mandate, and whether they intend to seek coverage over the next year or plan to remain uninsured.
For more in-depth data on enrollment experiences, we’ll rely on specially designed projects, like the Foundation’s panel survey of 2,000 randomly selected uninsured Californians.13 The baseline survey was conducted last summer, before the ACA open enrollment period, and the next wave will follow up with the same respondents in March, exploring who signed up for coverage, what choices they made, and how they evaluate their experience and the coverage they obtained. Projects like this take a longer time to field than a typical national opinion poll, but allow us to address some of the methodological concerns raised above to provide reliable data describing the experiences of key groups targeted by coverage expansion under the ACA.
This last of three case studies examining key operational aspects of coordinated care initiatives in Medicaid focuses on Rhode Island’s Chronic Care Sustainability Initiative (CSI), a multi-payer patient-centered medical home program in which the one Medicaid health plan and all commercial health plans in the state participate. Hallmarks of the initiative are the engaged leadership of the health insurance commissioner and key stakeholders; mandatory participation by commercial insurers, but participatory governance; a common developmental contract used by all payers; and investments in health information technology and other support for practice transformation. Medicaid’s large role as a payer makes it a key source of leverage in multi-payer initiatives, and Medicaid plan and provider experience serving populations with complex needs can also benefit such endeavors. Alignment of goals, performance metrics, practice transformation resources, and incentives across payers sends practices and providers coherent policy and financial signals regarding desired models and outcomes of health care delivery, and increases their potential impact.
This last of three case studies examining key operational aspects of coordinated care initiatives in Medicaid focuses on Rhode Island’s Chronic Care Sustainability Initiative (CSI). This multi-payer, patient-centered medical home (PCMH) initiative includes the one Medicaid health plan in the state and the commercial health plans, one of the largest of which has many Medicaid as well as commercial enrollees. These payers provide practices that participate in the CSI with financial incentives and practice transformation resources to develop a sustainable model of patient-centered chronic care for adults. The payers use a common contract with the practices that specifies uniform requirements and performance metrics, and they pay practices a uniform monthly per capita care management fee to support nurse care managers, who are integral to Rhode Island’s model. These fees and other investments in practice transformation also help finance data infrastructure at the practice level that is necessary to support a PCMH. CSI policy development and practices are guided by a multi-stakeholder group in a governance structure shaped by the consensus-oriented style and leadership of Rhode Island’s health insurance commissioner. The Office of the Health Insurance Commissioner (OHIC) and the Executive Office of Health and Human Services (EOHHS), where the Medicaid program resides, convene the project jointly.
The common contract is central to the multi-payer system. When multiple payers use a common contract, practices face uniform metrics, requirements, and incentives, and can invest in practice improvements that benefit all patients. In the CSI, common contract specifications were developed through a consensus process that included plans and providers. Because an OHIC representative was present at the meetings, antitrust restrictions that would otherwise have barred this process could be waived.
Medicaid participation in a multi-payer initiative presents opportunities and challenges. Because Medicaid is a large purchaser, leveraging its impact matters. Medicaid plan and provider experience in serving high-need populations has benefited the initiative. At the same time, plans and practices with sizeable Medicaid patient panels face challenges, as performance metrics are not risk-adjusted. However, the CSI rewards safety-net practices if they get “half-way to the goal.”
Combining a collaborative model with a mandate is useful. Multi-payer initiatives require buy-in. Even beginning as a voluntary pilot, the CSI might have been hard to launch without the health insurance commissioner’s leadership. Plans acknowledged that the subsequent mandate to participate probably helped move the PCMH effort forward statewide, but, importantly, consensus-style governance has lent acceptability to the mandate. Because the mandate operates through the OHIC, it covers commercial insurers, but it does not extend to self-insured employers or public purchasers. However, the Medicaid plan has always participated, and commercial plans must now pay practices care management fees for their Medicaid as well as their commercial members.
Collaboration requires time, effort, and leadership. The operation of a multi-payer initiative requires plans, practices, and purchasers to make significant commitments of time, focus, and effort on an ongoing basis. Active stakeholder leadership and engagement are necessary to build trust among parties and confidence that aligned action can advance shared goals for patient care and delivery system performance.
Multi-payer initiatives and practice transformation require infrastructure and entail new costs. Convening meetings, collecting data centrally to aggregate across payers, and other activities required to manage a multi-payer initiative all cost money. In addition to the overhead and infrastructure costs to manage the system are significant costs for developing infrastructure at the practice level for data collection and analytics, and for other changes, such as integration of nurse care managers. Care management payments to practices provide critical financing to support such transformation. With the expiration of federal grant funds to support health information technology, maintaining adequate funding is challenging.
Maintaining payer support may require evidence of savings. Health plans’ willingness to provide practices with additional support may ultimately depend on a demonstrated return on investment – evidence that investing in primary care is not only improving patient care, but also generating savings somewhere in the system. Some payers wondered whether payment to practices should be more strongly tied to their performance on clinical process and outcome metrics.
Practice transformation is the beginning, not the end, of system change. The CSI has focused mainly on what goes on in primary care practices, but, ultimately, performance should be measured not just at the practice level, but at the system level, using metrics like aggregate rates of hospitalization and emergency department use. At this writing, hospitals were not yet at the CSI table, but, more recently, the state has been engaging hospitals and has added performance measures on hospital use that are tied to payment.
Rhode Island has been successful in engaging plans, providers, and purchasers in a broad medical home initiative. A multi-payer system, including Medicaid in this case and several others nationwide, translates into important advantages for practices and providers, giving them a common, aligned set of goals, performance metrics, practice transformation resources, and incentives. Rhode Island’s ability to implement the CSI was enhanced by engaged leadership, a mixed regulatory-collaborative approach, the state’s small size, and the small number of major payers. Even under these conducive conditions, the organizational commitment, investment, and resources required to develop and implement a multi-payer PCMH initiative have been extensive, and mustering the necessary financing is a formidable, ongoing challenge. While the CSI model may not be feasible in other states, or may need adaptation, it illustrates the potential to leverage Medicaid’s role as a payer to transform health care delivery. Ultimately, to succeed most fully in improving care and reducing costs, multi-payer initiatives will need to extend beyond the sphere of primary care to engage specialists, hospitals, and others in the medical neighborhood. As the ACA expansion of coverage takes effect, and states and other entities seek to improve care delivery and orient payment toward performance, both the scale and momentum of multi-payer initiatives like the CSI can be expected to grow.
In recent years, a growing number of states have undertaken major delivery system reforms in Medicaid, seeking to improve care coordination and health outcomes for Medicaid beneficiaries, and to reduce spending growth in the program. To help inform the development of such initiatives in other places, the Kaiser Commission on Medicaid and the Uninsured worked with Mathematica Policy Research to examine key operational features of coordinated care initiatives in Medicaid in three states – Colorado, North Carolina, and Rhode Island. This issue brief focuses on Rhode Island’s Chronic Care Sustainability Initiative (CSI), a multi-payer, statewide patient-centered medical home (PCMH) initiative. Because Medicaid is the largest health care purchaser in the state, the program’s participation in Rhode Island’s initiative is one crucial source of its leverage.
The information and perspectives presented here are based on a review of CSI program documents and on telephone interviews with the program managers, two large participating health plans, and two participating practices with Medicaid patients — a community health center, and an office-based practice with both commercially-insured and Medicaid patients.
The CSI, which launched in 2008, had its origins in Rhode Island’s participation in a 2006 foundation-funded initiative that aimed to align public purchasers, private purchasers, and health plans in regional partnerships to more effectively leverage improvements in care for people with chronic conditions.1 Rhode Island has used this multi-payer strategy to support the PCMH model statewide.2 With strong leadership from the state’s health insurance commissioner, a multi-stakeholder group determined that the pilot program should align quality improvement and financial incentives among purchasers, health plans, and providers; improve chronic care in primary care settings; and make primary care a more attractive and viable specialty in Rhode Island.3 The idea was to use the leverage of the state’s large capitated health plans and Medicaid’s major role as a purchaser to drive the desired improvements.
Since the beginning, the CSI has included the two largest commercial health plans in the state – Blue Cross & Blue Shield of Rhode Island (BCBS) and UnitedHealth Care (UHC) – and the state’s one Medicaid health plan, Neighborhood Health Plan of Rhode Island (NHP). (UHC has many Medicaid as well as commercial members.) These payers provide practices that participate in the CSI with financial incentives and practice transformation resources to develop a sustainable model of patient-centered chronic care for adults.
Originally a voluntary pilot, the CSI was formalized in 2011 by state legislation, sponsored by the health insurance commissioner, mandating that all state-regulated (i.e., commercial) health plans participate. In 2012, Rhode Island required all commercial plans with Medicaid contracts to participate in the CSI. As a result, these plans are now required to pay supplemental care management fees to participating practices not just for their commercial enrollees, but also for their Medicaid enrollees if the practice serves at least 200 of them. Medicare began to participate in the initiative when CMS selected Rhode Island for the Multi-Payer Advanced Primary Care Practice (MAPCP) demonstration in July 2011. Therefore, participating practices now receive supplemental payments for Medicare beneficiaries, Medicaid beneficiaries in managed care (about 60% of the total Medicaid population), and privately insured patients. Because the CSI does not include Medicaid patients who are enrolled in the state’s fee-for-service primary care case management (PCCM) program, the PCCM program was outside the scope of this study. However, we were told that, like CSI practices, primary care providers in the PCCM program receive supplemental fees to support nurse care managers, and that the state uses the same performance metrics in both programs. In addition, the Executive Office of Health and Human Services (EOHHS), where the Medicaid program resides organizationally, is a co-convener of the project with the Office of the Health Insurance Commissioner (OHIC) and has taken a more active role in the initiative in recent years. State Medicaid officials attend CSI meetings and the program provides non-financial support for the initiative.
Practices must be selected for the CSI in order to receive supplemental payments from plans. Initially, in 2008, five primary care practices identified as “champions” were selected to participate. Eight more practices were added in 2010, three were added in 2012, and consistent with the state’s strategic plan, 20 practices were added in 2013, including several multi-site practices. The initiative now includes 36 practices, 48 practice sites, and 297 physicians serving an estimated 250,000 Rhode Islanders, approximately 25% of the state’s total population. Under the strategic plan, another 20 practices will be added in each of the next four years and the initiative is slated to serve more than 500,000 patients. At the end of 2012, Medicaid managed care enrollees accounted for about 25% of patients in CSI practices, commercial enrollees constituted 51%, Medicare Advantage enrollees made up 9%, and Medicare fee-for-service beneficiaries made up 15%.4
The following elements are central to the multi-payer medical home initiative:
A common developmental contract, which all health plans use with participating practices.5 Appendix 1 outlines key elements of the developmental contract: supplemental payments, required practice improvements, performance metrics, and staging of the contract provisions as practices come on line.
A uniform per member per month (PMPM) fee for care coordination, which all plans pay participating practices, and which help finance the practice infrastructure needed to support a PCMH. Practices can also earn additional performance incentive payments.
Practice transformation investments, to support the addition of a nurse care manager, in particular. These investments also support the development and use of electronic health record (EHR)-based performance metrics, and participation in learning collaboratives.
A multi-stakeholder leadership group, which guides CSI policy development and practice transformation.
The health insurance commissioner’s leadership and Rhode Island’s small size and long history of collaboration among major stakeholders have had a defining influence on the CSI’s development and structure. All those interviewed considered the health insurance commissioner’s leadership to have been instrumental in engaging commercial insurers in the initiative and enabling them to develop a common contract. The fact that many of the key actors in the CSI go back years together has also been helpful. The medical directors from several health plans trained together, the health insurance commissioner was formerly the director of NHP, and the current Medicaid medical director was the original CSI project staff person.
Governance. Governance of the CSI was structured to be collaborative and participatory.6 A large Steering Committee and a smaller Executive Committee set strategic direction for the CSI and are responsible for its overall governance; they include representation from the three major stakeholder groups – providers, payers, and purchasers (i.e., employers and Medicaid). The Steering Committee develops consensus on major issues, such as chronic conditions to be targeted, metrics, and payment strategies. While not required to do so, the Executive Committee also operates by consensus. Appendix 2 shows the governance structure, which, besides the Steering Committee and an Executive Committee, includes Working Committees on data and evaluation; practice training support and transformation; practice reporting; payment reform/contracting; and service expansion and integration. The purpose and scope of these Working Committees are outlined in Appendix 3.
The governance structure has remained largely unchanged, although it is now being refined and more formally constituted. In 2013, a Patient Advisory Subcommittee is being introduced to serve as the voice of patients and families and provide advice and input to the Steering and Executive Committees.7 In addition, a new Marketing and Communications Subcommittee is charged with increasing awareness of PCMH among employers and labor unions, increasing patient participation in PCMH practices; supporting the Patient Advisory Subcommittee, and conducting liaison with other community agencies.
Authority. A broader goal of the health insurance commissioner’s is to increase the role of primary care in health care delivery. Operationally, his strategy is to shift Rhode Island’s “primary care spend” from 8% of total health care spending currently, to 30%. To move in this direction, he has required state-regulated insurers to increase the share of their premiums spent on primary care by 1 percentage point per year over the period 2010-2014. Insurer investments in the CSI (e.g., their supplemental payments to participating practices) count toward this required annual increase. The health insurance commissioner has also interpreted his authority to allow him to require plans to contribute to the overhead costs of the data and related infrastructure for the CSI; these costs have grown recently because the federal Beacon Community Program, which provided grants for health information technology and other infrastructure, has ended. Insurer expenditures on these costs also count toward the primary care spend goal.
Operational management. The OHIC, with the support of a staff person then at the state’s Quality Improvement Organization (and now the state’s Medicaid medical director), was responsible for appointing the original Steering Committee and managing CSI’s day-to-day operations. At that time, staffing for the initiative was minimal— just two full-time staff funded by a foundation grant and the health plans. The Rhode Island Foundation, the state’s only community foundation, later served as a vehicle for accepting and handling external funding support for the CSI, and also provided office space for the program. When the original staff left in 2011, the state issued a competitive solicitation for project direction and project management support, and the contract was awarded to Commonwealth Medicine, the medical school at the University of Massachusetts.
Infrastructure. Substantial infrastructure is needed for the CSI to work. Essential components include:
For part of the CSI’s history, the Beacon grant provided crucial financing to the Rhode Island Quality Institute (RIQI) for some of these infrastructure costs (except for the first item).8 9 With Beacon’s expiration, the costs are now being transferred to the CSI itself and payers are being asked to cover more of them. (The RIQI will continue to do portions of the work related to data collection and analysis, but practice transformation services are no longer procured through the RIQI.) As the CSI expands to include more practices, the needs for infrastructure development and funding will grow. In 2013, the annual cost of administering CSI will be $2.2 million, up from about $0.5 million for its first contract, which started in December 2011.10 About half of the total budget will go to organizations providing support to the RIQI for work previously funded under the Beacon grant.11 In early 2013, Rhode Island received a federal grant for up to $1.6 million under the Center for Medicare and Medicaid Innovation (CMMI) State Innovation Models (SIM) initiative, which is designed to foster state-based models for multi-payer payment and health care delivery system transformation.12 Interviewees expressed hope that the award will allow the CSI to develop a more permanent operating model suitable to a broad-based permanent program.
The common contract is central to the multi-payer model. The common developmental contract was not easily developed, but its use is central to the CSI. The consistency across all payers of a core set of required metrics, and fixed supplemental payments to practices tied to performance expectations, align the incentives and goals that practices face, and encourage practices to pool the supplemental revenues from all their payers to invest in improvements that benefit all their patients. Interviewees representing practices favored having common metrics over different metrics for four or five different payers, and they pointed out that common metrics also reduce overhead costs for practices.
The common requirements were developed through a consensus process involving participating stakeholders (largely plans and providers). Plans had to be willing to modify their existing contract requirements, at least to some extent. For example, a plan might have to give up “home-grown” requirements of its own in favor of the common contract’s emphasis on NCQA accreditation. Similarly, national firms with common requirements across their health plans had to be willing to make exceptions for a plan operating in Rhode Island if the firm’s and the CSI’s requirements differed. Because of anti-trust laws that limit health plans’ ability to discuss pricing with each other, the deliberations that produced consensus on certain requirements of the common contract would not have been feasible except for the health insurance commissioner’s central convening authority. Specifically, the common developmental contract requires health plans to make a uniform contribution to practices to finance infrastructure-building. Such payments are legally considered to be pricing-related, but the discussion could take place as long as it was convened by OHIC.
Leverage and experience. Because Medicaid is such a large purchaser in Rhode Island – it accounts for a substantial share of health care costs in the state – the ability to leverage the program is integral to the CSI’s impact. Although the majority of adults in Rhode Island are commercially insured, Medicaid is the dominant source of coverage in some CSI practices and covers a substantial share of patients in others. As Medicaid plan officials see it, an important gain from the CSI is that, with all payers at the table, Medicaid and commercial plans can learn from each another. Small plans get what one interviewee described as “a brain trust of medical directors committed to improving quality and re-engineering change in office-based care.” CSI principals say that the initiative has benefited significantly from the experience of plans and safety-net providers serving Medicaid patients, as they have been leaders in quality improvement and have a greater understanding of what it takes to coordinate care, often among many providers, for populations with complex needs for health services and other supports. The CSI provides a framework and environment for consultation and sharing of knowledge and ideas, and helps to avoid the problem of “reengineering a system that works for only one-third of [a] health plan’s members.”
Patient mix differences and fair payment. CSI plans and practices with a sizeable share of Medicaid patients face some unique challenges. Performance metrics are not currently risk-adjusted, possibly because of delays in data acquisition and a lack of resources and expertise to develop a methodology. The RIQI is now taking on the methodological work for risk-adjustment through a subcontract with Research Triangle Institute. Compared with the privately insured, Medicaid patients are more likely to have mental health co-morbidities as well as socioeconomic hardships that contribute to poorer health outcomes. In addition, a substantial share of the patients served by community health centers participating in the CSI are uninsured, making management of their care more challenging and performance benchmarks harder to achieve. (Health centers generally include the uninsured in their performance metrics because they operate on a philosophy that all patients are treated the same and that performance metrics need to be practice-wide, not payer-specific.) Recognizing the potentially higher risk profile of Medicaid and uninsured patients, and seeking to be fair to practices, the CSI established a “half-way to the goal line” approach that rewards practices with incentive payments if they get half-way to the performance benchmark relative to where they started. Stakeholders speaking from a Medicaid perspective praised this measure as a constructive compromise that rewards practices and providers in the safety-net space for their progress toward CSI goals. They expressed concern that plans not view the practices to which this policy applies as “slackers,” but highlighted that the consensus-oriented governance of the CSI provides a structure for discussing and resolving issues that have different implications for different stakeholders.
Consensus helps legitimate authority. Getting multiple payers to work together on a unified strategy requires a lot of buy-in. Having the CSI pilot begin on a voluntary basis almost certainly helped foster willingness to participate. But even the voluntary initiative might well have been harder to achieve without Rhode Island’s long history of collaboration and what stakeholders describe as the talented leadership of the health insurance commissioner. The health plan representatives who were interviewed do not like the requirement to participate, but acknowledged that the mandate was probably valuable to the effort to extend the chronic care initiative to all adults statewide. By pairing a mandate for commercial insurer participation with a consensus-oriented approach to governance, the state is able to exert leverage that is needed to direct health plans to do some things differently and to spend money in ways that, except for the primary care spend requirement, they would not. It is likely that one reason private insurers have accepted the mandate is that, while their participation is required, they are also part of the consensus process that determines the specific requirements of the initiative.
The locus of authority determines its reach. Because the mandate to participate in the CSI operates through the OHIC, it does not reach all plans or purchasers in the state. The OHIC’s authority covers commercial insurers, but does not extend to self-insured employers or to public purchasers. Although the legislative mandate does not apply to the Medicaid plan, this plan has participated voluntarily in the CSI from the beginning, and, since 2012, the state has required all health plans with Medicaid contracts to pay the supplemental care management fees to practices on behalf of their Medicaid as well as their commercial enrollees, if the practice serves at least 200 of their Medicaid members. The CSI mandate does not apply to the Medicare program, but Medicare participates under the aegis of the Multi-payer Advanced Primary Care Practice (MAPCP) demonstration.
Stakeholder commitment. The development and operation of a governance process that is based on consensus decision-making require heavy investments of time by many parties, and a strong commitment to work together to hammer out common goals and objectives and implement the initiative. Ongoing operation of the CSI succeeds because its key stakeholders — plans, practices, and purchasers — continually commit significant time, focus, and effort to the enterprise. To illustrate, the administrator of one participating family medicine practice with eight providers reported that she routinely attends five different CSI-related meetings monthly, as well as ad hoc meetings. Collectively, two or three other individuals in the practice attend another five to six meetings each month on data, reporting, care management, and other topics.
Engaged leadership. Leadership from all the stakeholder groups has been critical to the CSI’s success. Even in a state with a collaborative tradition, there exist competing interests, gaps in trust, and other sources of tension between parties that must be addressed. Individual stakeholders with different perspectives must, through dialogue and other interaction, gain confidence in the other participants and the fairness of the project to perceive an alignment between their own goals and interests and the initiative’s aims. The CSI management team highlighted plan and provider engagement in the initiative as a key to building increased trust between these two groups. Conversations facilitated by the learning collaboratives helped to give plans confidence in providers’ commitment to practice transformation and the use of metrics to drive change, and to give providers confidence that plans are paying them fairly and giving them the data they need to improve care management.
Overhead costs. Convening meetings, collecting and reporting data centrally for aggregation across payers, and providing assistance to help practices change, are all overhead costs that require funding. Perhaps because the CSI started out as a small pilot, such costs were underestimated initially. Also, because administrative and staff support for the initiative was limited early on, development of a formal organizational structure (e.g., by-laws) was delayed. Funding constraints also led the CSI to rely on different financing approaches for learning collaboratives at different times, rather than on an established and stable means of support.
The timing of the Beacon grant to Rhode Island was fortunate. The overlap between the needs of the CSI and the purposes of the grant – to link development of EHRs to clinical practice improvement and enhanced outcomes – gave the state access early on to substantial support to build infrastructure. However, such grants are not routine and they are typically time-limited. With the Beacon grant’s termination, the CSI health plans are providing additional funding for infrastructure (over and above their care management payments to practices) for at least one year, but there is concern about their ability and willingness to maintain this support over time, particularly if the amount required of them grows. Some expressed the view that, because more work on the data infrastructure was not accomplished earlier, progress was delayed and opportunities were lost, adding to health plans’ and practices’ current costs. For example, if the infrastructure for the exchange of clinical data had been more developed, CSI would not have to invest as much now in claims-based “work-arounds” to analyze costs across all payers.
Costs of practice-level infrastructure-building. Like other efforts to develop patient-centered models of primary care, the CSI generates new needs for spending – to manage the multi-payer effort, collect data, create metrics and reporting processes, and support practice transformation. Primary care practices need to set up systems to track data relevant to the metrics they must report and integrate these metrics into their performance improvement programs. The supplemental payments to participating practices provide critical additional funding to support other required practice changes as well, such as expanded use of nurse care managers who can spend more clinical time with patients. One practice manager reported that the supplemental payments have allowed her to fund a nurse care manager, hire a full-time quality assistant who can do “deeper dives” into the data (e.g., to understand outliers), and keep the practice open longer hours. Some practices had already made some of the needed investments before the supplemental payments became available, but even for these practices that are farther along, the care management fees help finance intensified efforts and additional staff time to participate in learning collaboratives with other practices.
At least some of the CSI practices are finding the supplemental payments insufficient to cover all the costs involved in participating. They explained that they continue to participate for the good of their patients, whom they see getting better care because of the practice changes spurred by the initiative. Consensus is lacking on what level of support participating practices require. Sponsors of similar initiatives elsewhere can also anticipate debate about the appropriate levels of payment to support the practice-level infrastructure needed to support patient-centered care.
Those we interviewed noted that the health care environment is very fluid in Rhode Island, as it is elsewhere in the nation. The practices that participated in the CSI from the outset were early adopters of change who were philosophically committed to its success; the practices joining now may not be as committed to doing what is necessary internally to develop clinical data and use them to improve performance, although they should be able to benefit from the experience of the established practices. Health plans say that their willingness to provide practices with additional support ultimately depends on a demonstrated return on investment. In today’s payment reform environment, they say, they need evidence that investing in primary care is not only improving patient care and patient experience, but also generating savings somewhere in the system. Some payers wondered aloud whether practices should have more “skin in the game” – that is, whether their payment should be more strongly tied to their performance on clinical process and outcome metrics. It could be that the ability to maintain support for these kinds of initiatives will require settling the return-on-investment question, challenging though that may be.
There was agreement that, ultimately, performance should be measured not just at the level of individual practices, but also at the system level, using metrics like aggregate ED, hospitalization, and readmission rates. Clearly, hospitals are integral to true systemic change. At this writing, hospitals were not yet at the CSI table, and stakeholders reported that they were still relatively traditional, with a primary focus on filling beds; they added that ACO development and hospital acquisition of practices remained limited in the state. As a consequence, the CSI has been focused mainly on what goes on in primary care practices. More recently, however, the state says it has been engaging hospitals, and has added performance measures on hospitalization and ED use that are tied to payment. One interviewee placed the CSI in the broader context of system transformation this way: “I think we’re working towards a system that is more integrated and will address the whole triple aim. Has that been proved yet? I don’t know. I think we’re still walking down the road. We certainly can’t continue in this [current] system. I think this (medical home model) has more optimism around it than other types of approaches. But…we’re not there yet. This is new territory.”
Rhode Island has been successful in engaging health plans, providers, and purchasers in a multi-payer collaboration to support PCMHs, with the goal of improving chronic care for all Rhode Island adults. The leverage exerted by a multi-payer strategy, including Medicaid in this case and several others nationwide, translates into important advantages for practices, giving them a common, aligned set of goals, metrics and performance benchmarks, practice transformation resources, and incentives, across payers and purchasers, to support practice changes that will benefit all their patients.
Rhode Island’s ability to implement the CSI was enhanced by a number of factors. The distinctive leadership of the health insurance commissioner, and his preference for collaboration around policy goals rather than a purely regulatory approach, were crucial. In a different state context, mandating payer participation and the “primary care spend” could be more challenging. The small number of major payers in the state also helped, and the fact that many stakeholders knew each other and understood each other’s goals made it easier for them to “get on same page.” In addition, many Rhode Island practices and providers serve patients with a mix of health insurance, and may be receptive to participating in an initiative that standardizes the requirements and incentives they face from different payers.
But while Rhode Island has some distinctive attributes, the state has confronted some challenges and issues that are likely to be common to states pursuing multi-payer initiatives. Rhode Island’s need to identify new resources for implementation, and the finding that buy-in is important to maintain support for the initiative, are lessons useful to states broadly. The kinds of tensions between plans, practices, and providers that have required negotiation in Rhode Island are pretty universal; other states may wish to consider whether the inclusive and consensus-oriented approach to development and governance that Rhode Island adopted might help bridge differences and build trust among the stakeholders in their environments.
The reality that system-level health improvements and cost savings require change beyond the sphere of primary care is also not unique to Rhode Island, and states generally can benefit from CSI leadership’s observation that specialists, hospitals, and others in the medical neighborhood must also be engaged for multi-payer medical home initiatives to succeed most fully. While the CSI model may not be feasible in other states, or may warrant adaptation, it demonstrates how Medicaid’s role as a major payer can be leveraged to transform health care delivery and payment. As the ACA expansion of coverage brings more Americans into the health care system, and states and other entities seek to improve care delivery and orient payment toward performance, both the scale and momentum of multi-payer efforts like the CSI can be expected to grow.
This Kaiser Commission on Medicaid and the Uninsured (KCMU) issue brief was prepared by Marsha Gold and Winnie Wang of Mathematica Policy Research and Julia Paradise of the Kaiser Family Foundation.
The authors express their appreciation to David Bourassa, Renee Bromley, Deidre Gifford, Debra Hurwitz, Mack Johnston, David Keller, and Renee Rulin, whose expertise and insights were invaluable to this project.
Performance Targets
Target 1: Structural Improvements (Practice Metric): Hire a nurse care manager; establish a compact with four specialists including a hospitalist; establish a plan/policy for after-hours care; have an electronic medical record and achieve Level 1 meaningful use; comply with the Quality Partners of Rhode Island Hospital and community physician best practices; demonstrate best practices for outpatient transitions of care; demonstrate use of evidence-based care; submit quality data
Target 2: Clinical Process Measures (Provider Metric): Achieve benchmark goals on specified CAHPS survey items; meet benchmark goal or achieve 50 percent improvement on at least four of seven metrics: Diabetes HbA1C <8, Diabetes BP<140/90,Diabetes LDL <100,Hypertension <140/90,Tobacco Cessation, Adult BMI (18-64), Adult BMI (65+)
Target 3: Outcome Measures (Provider Metric): CSI practices, in aggregate, to reduce emergency department and all-cause inpatient hospital admission rates by 7.5% and 5% respectively, relative to a comparison group
Staging

Source: CSI-RI: Strategic Planning, Final Plan, February 21, 2013. http://www.pcmhri.org/files/uploads/CSI_Strategic_Plan_Summary%20March%202013.pdf
Source: CSI-RI: Strategic Planning, Final Plan, February 21, 2013. http://www.pcmhri.org/files/uploads/CSI_Strategic_Plan_Summary%20March%202013.pdf
On January 1, 2014, many key provisions of the Affordable Care Act (ACA) will start to go into effect, including the expansion of Medicaid to low-income adults and the launch of new Medicaid eligibility and enrollment processes, which are designed to move toward a coordinated enrollment system across health coverage programs, including Medicaid, CHIP, and the new Health Insurance Marketplaces. Over the past year, states have made steady and significant progress preparing for these changes, but readiness varies considerably as 2014 nears, and implementation work and ongoing process improvements will continue into the foreseeable future. To provide greater insight into the status of implementation, this report provides an overview of key state Medicaid eligibility and enrollment policies slated to go into effect, based on data released by the Centers for Medicare and Medicaid Services (CMS). The data provide insight into who will be eligible for Medicaid and CHIP across states and how individuals will enroll in coverage.
On January 1, 2014, many key provisions of the Affordable Care Act (ACA) will start to go into effect, including the expansion of Medicaid to low-income adults and the launch of new Medicaid eligibility and enrollment processes, which are designed to move toward a coordinated enrollment system across health coverage programs, including Medicaid, CHIP, and the new Health Insurance Marketplaces. Over the past year, states have made steady and significant progress preparing for these changes, but readiness varies considerably as 2014 nears, and implementation work and ongoing process improvements will continue into the foreseeable future. To provide greater insight into the status of implementation, this report provides an overview of key state Medicaid eligibility and enrollment policies slated to go into effect based on data released by the Centers for Medicare and Medicaid Services (CMS). (See the Appendix Tables for state-specific data.)
The ACA, as enacted, expands Medicaid to nearly all adults at or below 138 percent of the federal poverty level (FPL) as of January 1, 2014. This expansion, however, was effectively made a state option as a result of the Supreme Court ruling on the constitutionality of the ACA, and as of October 24, 2013, 26 states, including DC, are moving forward with the expansion, while the remaining 25 states are not moving forward at this time (Figure ES-1). There is no deadline for states to adopt the expansion, and several states are still actively considering it.

Eligibility levels for parents and other adults will significantly increase in states implementing the Medicaid expansion, while large coverage gaps will remain in states not expanding at this time. In the 26 states expanding Medicaid, the median eligibility threshold for parents will increase from 106 to 138 percent of the FPL and the median limit for adults without dependent children will significantly rise from 0 to 138 percent of the FPL (Figure ES-2). However, many poor parents and other adults will remain ineligible in the 25 states not expanding at this time. In 21 states, parent eligibility levels will remain below 100 percent of the FPL, with eligibility levels below half of poverty in 14 states. Overall, the median eligibility level for parents in these states will be just 47 percent of the FPL and only Wisconsin will provide full Medicaid coverage to adults without dependent children. Parents and other adults with incomes above these limited Medicaid eligibility levels but below 100 percent of the FPL will fall into a coverage gap, since they will earn too much to qualify for Medicaid but too little to qualify for premium tax credits in the Marketplaces, which begin at 100 percent of the FPL. This gap will leave nearly five million uninsured adults without a new coverage option.

Coverage for children and pregnant women through Medicaid and CHIP will remain strong in 2014. More than half of the states (30, including DC) will cover children in families with incomes at or above 250 percent of the FPL and 20, including DC, will cover children in families with incomes at or above 300 percent of the FPL. Moreover, despite some eligibility reductions for pregnant women, as of January 1, 2014, 32 states, including DC, will cover pregnant women at or above 200 percent of the FPL. As such, while coverage for parents and childless adults will markedly improve in states implementing the Medicaid expansion, their median eligibility level will still remain lower than that of children and pregnant women (Figure ES-3). These disparities in eligibility across groups will be even starker in states that are not expanding Medicaid.

The ACA envisions seamless and timely access to the continuum of health coverage options regardless of where or how someone applies. To achieve these objectives, the ACA establishes new expectations for simplifying the application process, coordinating enrollment, and moving toward paperless verification of eligibility. These include state adoption of a single streamlined application that screens for all health coverage options, electronic transfers of accounts between agencies to facilitate transitions across health coverage programs, and reliance on trusted sources of electronic data rather than requesting paper documentation to verify eligibility criteria.
As of October 1, 2013, 43 of 50 reporting states have deployed a single, streamlined application through their Medicaid agency. The seven remaining reporting states are in the process of developing their single, streamlined application, and nearly all anticipate having it in place by January 2014. In the interim, these states are utilizing their existing Medicaid applications and individuals who may be eligible for premium tax credits are being directed to apply through the federal Marketplace. Among the 43 Medicaid agencies that have a single streamlined application as of October 1, 2013, all had a paper version available while 36 had an online version. Looking ahead, states will continue work to make the application available through multiple modes, including online, phone, in-person, or mail. Moreover, in 32 states, further revisions will be made to their single streamlined application to meet the ACA standards, for example, by removing questions that are not relevant to eligibility.
The ability to electronically transfer individual accounts between state Medicaid/CHIP agencies and Marketplaces to coordinate enrollment is in various stages of development. Among the 17 states with State-based Marketplaces (SBMs), all but two (2) have an integrated or linked technology system that determines eligibility for all insurance affordability options and facilitates the next steps for enrollment. However, in states using the Federally-Facilitated Marketplace (FFM), electronic transfers of individual accounts between the FFM and Medicaid/CHIP agencies are essential for coordinating enrollment. Due to ongoing technological challenges with the FFM, these transfers have been delayed and alternative strategies have been put into place. For example, until the FFM can begin transferring electronic accounts to state Medicaid and CHIP agencies, it is sending batches of basic data on individuals the FFM has determined or assessed as potentially eligible for Medicaid/CHIP. Similarly, if a state Medicaid/CHIP agency is unable to transfer an account to the FFM, it can direct individuals to apply directly through the FFM. Moving forward, implementing electronic account transfers will be key to minimizing burdens on consumers and ensuring they are successfully enrolled in the coverage for which they are eligible regardless of where they apply, providing “no wrong door” access to coverage envisioned by the ACA.
States are submitting verification plans to CMS that outline the electronic data sources and procedures they will use to verify eligibility criteria. As of November 15, 2013, 35 verification plans have been approved by CMS and made publicly available. States continue to have the option to accept self-attestation without additional verification for non-financial eligibility criteria except for Social Security Numbers, citizenship, and immigration status, which states are required to verify under law. The majority of reporting states will rely on self-attestation of state residency (28 of 35), and household composition (33 of 35), while fewer will do so for age and date of birth (13 of 35). The remaining states will either verify these criteria to determine eligibility or post-enrollment. For income, states must verify financial information from an electronic data source; however, this can be done post-enrollment after the state determines eligibility based on the individual’s attestation. All 35 reporting states will verify income through electronic sources, with 30 states doing so to determine eligibility and five (5) states verifying income post-enrollment. In addition, 23 states will conduct routine ongoing post-enrollment checks of financial information, although consumers also are required to report changes that may affect eligibility.
CMS has offered states five strategies to facilitate processing applications for large numbers of people who become newly eligible for Medicaid on January 1 and the transition to new enrollment processes. All of the approaches are intended to promote enrollment and retention, while minimizing administrative burdens for states. They include early adoption of MAGI-based eligibility standards, extending renewal periods for existing enrollees, enrolling eligible Supplemental Nutrition Assistance Program participants in Medicaid based on available data, enrolling parents in Medicaid based on their children’s eligibility information, and providing 12-month continuous eligibility for parents and other adults. A state may adopt any of these facilitated enrollment approaches regardless of whether it plans to implement the Medicaid expansion. Nearly half (25) of states have taken up the option to extend renewals, 15 have adopted MAGI early, five (5) are enrolling individuals based on SNAP data, and three (3) are using eligibility data for children to enroll their parents (Figure ES- 4). Overall, 30 states have adopted at least one of the strategies, and 11 have adopted two or more of these approaches. Three (3) states (NJ, OR, and WV) have adopted four of the five.

Looking ahead to 2014, coverage for parents and other adults will significantly improve in the 26 states implementing the Medicaid expansion and eligibility levels for children and pregnant women will remain strong across states. As such, as the ACA is fully implemented, Medicaid offers the potential to significantly reduce the number of uninsured. Outreach and enrollment efforts will be key for increasing coverage and it will be important for these efforts to be ongoing throughout the year since Medicaid enrollment is not limited to the Marketplace’s open enrollment period. In contrast to gains in states expanding Medicaid, large coverage gaps will remain in the states that do not expand, leaving millions of poor uninsured adults without access to a new coverage option.
To date, states have made meaningful progress in implementing key provisions of the ACA to provide streamlined Medicaid eligibility and enrollment processes, but readiness varies considerably. Moreover, the technology problems that have hampered the launch of open enrollment through the new Marketplaces, particularly the federal Marketplace (HealthCare.gov), have led to delays in coordination across Medicaid, CHIP, and Marketplace coverage. However, even with these early implementation challenges, some states have been successfully enrolling people in Medicaid and several have gotten a significant jump-start through the facilitated enrollment strategies offered by CMS. In the coming months, work will continue to deploy new processes and systems to move toward the ACA’s vision of a simplified, consumer-friendly experience. As such, January 2014 will represent the first step toward a modernized, streamlined system to connect individuals to expanded coverage options as established through the ACA, but fully achieving that vision will require time, persistence, and a commitment to continual program improvement.
As the first day of coverage under the Affordable Care Act (ACA) approaches, states are continuing work to modernize their procedures and systems to implement key provisions of the law to simplify enrollment in Medicaid and CHIP and coordinate with the new Health Insurance Marketplaces, which opened their doors on October 1, 2013. Beginning January 1, 2014, low-income adults will become newly eligible for Medicaid in the 26 states that have chosen to implement the ACA’s Medicaid expansion. Additionally, all states will transform their processes to align eligibility requirements for Medicaid, CHIP, and premium tax credits in the Marketplaces, streamline and modernize the application experience, and move toward a coordinated enrollment system across health coverage programs. Over the past year, states have made steady and significant progress preparing for these changes, but readiness varies considerably as 2014 nears, and work on implementation and process improvements will continue into the foreseeable future. This report provides an overview of key state Medicaid eligibility and enrollment policies that will be in effect as of January 1, 2014, based on data released by the Centers for Medicare and Medicaid Services (CMS). The data provide insight into who will be eligible for Medicaid and CHIP across states and how individuals will enroll in coverage. (See Appendix Tables 1 through 9 for state-specific data on policies.)
Throughout the last year, political divides continued over the ACA, but the law remains in place. With open enrollment for coverage through the new Marketplaces beginning on October 1st, the country is turning its attention to how the ACA is implemented, including a number of key provisions that impact Medicaid and CHIP eligibility and enrollment.
As enacted, the ACA extends Medicaid to nearly all adults at or below 138 percent of the federal poverty level (FPL) as of January 1, 2014. However, as a result of the Supreme Court ruling on the ACA, implementation of the Medicaid expansion is now effectively a state option. As of October 24, 2013, 26 states, including DC, are moving forward with the expansion (Figure 1). In some cases, CMS is working with states to develop expansion approaches under Section 1115 waiver authority (Box 1). There is no deadline for states to adopt the expansion, and several states are still actively considering the option. However, states delaying the expansion will miss out on the opportunity to receive the 100 percent federal funding for newly eligible individuals available in calendar years 2014 through 2016.

Regardless of state decisions to expand Medicaid, all states must implement new streamlined enrollment processes under the ACA. These procedures are designed to align eligibility determinations for Medicaid, CHIP, and premium tax credits in the Marketplaces. They also aim to establish a faster, more consumer-friendly enrollment experience, provide individuals multiple avenues to apply, and rely on electronic data instead of paper documentation to verify information where possible. To implement these new processes, almost all states are building new Medicaid eligibility and enrollment systems or conducting major upgrades of their existing systems. The federal government has provided time-limited 90 percent federal funding to support this system development work. CMS issued a final set of rules for these eligibility and enrollment changes in July 2013, providing guidelines for states as they were rewriting policies, revamping business processes, and developing their systems.
Box 1: Section 1115 Waivers and the Medicaid ExpansionTo date, of the states moving forward with the Medicaid expansion, three (AR, IA, and MI) are pursuing approaches that require Section 1115 waiver demonstration authority. As of November 15, 2013, Arkansas is the only state to have received approval. The state will use Medicaid funds to subsidize the purchase of coverage for Medicaid-eligible individuals through qualified health plans (QHP) in the Marketplace, with supplemental benefits and cost-sharing protections to meet minimum Medicaid standards. Iowa and Michigan await federal action their proposals. Additionally, there are a number of states with waivers that currently provide more limited coverage to parents and/or adults without dependent children. Most of these waivers are set to expire December 31, 2013, when this coverage could transition to the Medicaid expansion as it goes into effect. Some of these waivers were “bridge” waivers that were specifically designed to help states get an early start on the expansion. While most states with these expiring waivers are implementing the full Medicaid expansion, two states (Indiana and Oklahoma) not moving forward at this time. These states received approval to extend their waivers for one year, preserving their existing limited waiver coverage. However, many poor adults in these states who would have gained full Medicaid coverage under the expansion will not obtain access to a new coverage option in its absence and will likely remain uninsured.
For more details, see: Kaiser Commission on Medicaid and the Uninsured, “A Look at Section 1115 Medicaid Demonstration Waivers Under the ACA: A Focus on Childless Adults.” October 2013.
To further assist states in implementing the Medicaid provisions of the ACA, CMS offered new opportunities to facilitate enrollment. In May, the administration provided states five (5) new targeted enrollment and renewal strategies. These options are designed to help states accommodate application and enrollment increases as they transition to the new eligibility rules, with the hope of easing the administrative burden for states and simplifying the process for consumers.
To date, states have made significant progress in implementing these Medicaid and CHIP provisions but readiness varies considerably. Moreover, the technology problems that have hampered the launch of open enrollment through the new Marketplaces, particularly the federal Marketplace (HealthCare.gov), have led to challenges and delays with new processes designed to coordinate enrollment for Medicaid, CHIP, and Marketplace coverage. With 2014 quickly approaching, state implementation work remains in high gear and the coming weeks are important for states to meet specific milestones. States that will not be able to implement all of the new processes within the timeline established by the law are working with CMS to develop mitigation plans designed to help ensure individuals can still connect to coverage. Even with these early implementation challenges, some states have been successfully enrolling people into Medicaid as they have addressed technological glitches with their state Marketplace websites. Moreover, several states have gotten a significant jump-start through the facilitated enrollment strategies offered by CMS.
The ACA changes how financial eligibility will be determined for many Medicaid beneficiaries, standardizing the approach across states as well as health insurance affordability programs. Beginning January 2014, financial eligibility for parents, pregnant women, children, and the expansion adults will be based on Modified Adjusted Gross Income (MAGI), as defined in the Internal Revenue Code. The move to MAGI for these non-elderly, non-disabled groups will result in some changes from current Medicaid rules related to calculating family size and income and will largely align Medicaid financial eligibility determinations with the standards used to determine eligibility for premium tax credits and cost-sharing reductions in the new Marketplaces.1 Aligning the determination requirements across all insurance affordability programs is intended to promote seamless coordination and avoid gaps or overlaps in eligibility.2
To carry out the transition to MAGI, states must convert their existing Medicaid and CHIP eligibility levels for these groups to MAGI-equivalent levels. Today there is significant variation across states and eligibility categories in how income disregards and deductions are applied to determine if an individual meets the financial eligibility requirements for Medicaid or CHIP. For example, a state often disregards certain income from an individual’s gross income (e.g., $90 for a working parent), deducts certain expenses (e.g., childcare), and then compares the result to a net income standard.3 When states transition to MAGI, they will discontinue the use of these disregards and deductions; instead, they will use the MAGI-equivalent income threshold that takes into account states’ previous use of disregards and deductions and apply a standard disregard of five percentage points of the federal poverty level in certain circumstances (Box 2). States worked with CMS to develop their converted MAGI levels using one of three available methods.4
Box 2: Use of the Five Percentage Point of the Federal Poverty Level Disregard Under MAGI
Under the new MAGI rules, a standard income disregard of five percentage points of the federal poverty level will be applied, but only if it affects an individual’s eligibility. For example, the Medicaid expansion for adults extends eligibility to 133 percent of the FPL. However, a parent with income at 138 percent of the FPL in a state implementing the expansion would be determined eligible because after the five percentage point disregard, he or she would meet the income standard of 133 percent FPL. Upper income levels reported in this brief take into account this standard disregard.
The MAGI converted thresholds are intended to approximate states’ existing eligibility levels in the aggregate to prevent individuals from losing coverage due to the transition to MAGI. While MAGI converted thresholds differ from existing levels, they are designed to result in roughly the same number of people being eligible under the new standard as would have been eligible under the old standard (Box 3). In some cases, the converted thresholds will be the income eligibility limits in place as of January 1, 2014. For example, in most of the states not implementing the Medicaid expansion, the income limit for parents will be the MAGI conversion of their existing parent eligibility level. The MAGI converted thresholds will also be used for a number of other purposes, including 1) maintaining Medicaid and CHIP eligibility levels for children through October 1, 2019, as required by the ACA; 2) establishing minimum eligibility thresholds for parents, pregnant women, and other adults;5 3) determining the income levels at which premiums will apply; and 4) calculating the availability of the enhanced matching rate for newly-eligible adults.
Box 3: Understanding Differences Between January 2013 and January 2014 Eligibility Levels
Appendix Tables 1-3 show income eligibility levels for children, pregnant women, parents and other adults as of January 2013 and January 2014.
States that had previously aligned children’s coverage levels across the different age groups merged the groups for conversion purposes in order to preserve the alignment. Otherwise, states were required to convert each eligibility category separately, including their Medicaid thresholds for infants, children ages one to five, and children ages six to eighteen. If the amount of the average disregards and/or the original threshold differed between the groups, disparate converted levels across the ages could result, as is seen in 18 states (Appendix Table 1). States have an opportunity to standardize their eligibility thresholds by adjusting the level for the older group to match that of the younger group, but only until December 31, 2013.6
Beginning in 2014, as part of the continuum of coverage, the ACA expands Medicaid to nearly all adults with incomes at or below 138 percent of the FPL. Moreover, the ACA requires states to maintain eligibility thresholds for children that are at least equal to those they had in place at the time the law was enacted through September 30, 2019. To help preserve the base of coverage upon which the ACA expansions build, states were also required to maintain eligibility levels for other groups, but this requisite will end on January 1, 2014.
Eligibility levels for parents and childless adults will significantly increase in the 26 states, including DC, that are expanding Medicaid to adults. Fifteen (15) of the 26 states moving forward with the Medicaid expansion already cover parents at or above the poverty level through Medicaid, but adults without dependent children are eligible for full Medicaid coverage in just nine (9) of these states (AZ, CO, CT, DE, DC, HI, MN, NY, and VT), of which only six (6) cover them at or above poverty (Appendix Table 2). In the expansion states, eligibility levels will increase for parents in 16 states and for childless adults in 24 states. Overall, the median eligibility threshold for parents in these states will increase from 106 to 138 percent of the FPL, while the median threshold for adults without dependent children will increase from 0 to 138 percent of the FPL. Three (3) states (CT, DC, and MN) will cover parents above the new expansion level of 138 percent of the FPL (Figure 2) and the District of Columbia and Minnesota will cover adults without dependent children above this level (Figure 3), although Minnesota will reduce eligibility levels for parents relative to its 2013 levels. In addition, four (4) other states (NJ, NY, RI, and VT) that previously extended Medicaid eligibility to parents with incomes above 138 percent of the FPL are reducing eligibility to 138 percent of the FPL as of January 2014; many of these parents will be eligible for tax credits to purchase coverage through the new Marketplaces.


In the 25 states not expanding Medicaid at this time, many poor parents and other adults will remain ineligible for coverage. In 21 of the states, eligibility levels for parents will be below 100 percent of the FPL, with eligibility levels remaining below half of poverty in 14 states. In addition, Maine and Wisconsin will reduce eligibility for parents from 133 to 105 percent of the FPL and 200 to 100 percent of the FPL, respectively, as the requirement to maintain coverage ends on January 1, 2014. Adults without dependent children generally will remain ineligible for full Medicaid coverage in non-expansion states. Overall, in these 25 states, the median eligibility level for parents will be just 47 percent of the FPL, with only four (4) states (AK, ME, TN, and WI) covering parents with incomes at or above poverty; only Wisconsin will provide full Medicaid coverage to adults without dependent children. Parents and other adults with incomes above these limited Medicaid eligibility levels but below 100 percent of the FPL will fall into a coverage gap, which will leave nearly five million uninsured adults without access to a new coverage option (Box 4).
Box 4: The Coverage Gap Could Leave Nearly 5 Million Poor Adults Uninsured
Nationally, nearly five million poor uninsured adults will fall into the “coverage gap” because they live in states that are not expanding Medicaid to adults at this time. Those in the gap earn too much to qualify under their state’s Medicaid eligibility guidelines and too little to qualify for premium tax credits to purchase coverage through the new Marketplaces. More than one-third of those falling in the gap reside in just two states – Texas (22 percent) and Florida (16 percent) (Figure 4).
See: Kaiser Commission on Medicaid and the Uninsured, “The Coverage Gap: Uninsured Poor Adults in States that Do Not Expand Medicaid.” October 2013.

Coverage for children through Medicaid and CHIP will remain strong in 2014, with the median eligibility level at 255 percent of the FPL. More than half of the states (30, including DC) will cover children in families with incomes at or above 250 percent of the FPL and 20, including DC, will cover children in families with incomes at or above 300 percent of the FPL (Figure 5 and Appendix Table 1). Moreover, 18 states currently covering older children up to 133 percent of the FPL in separate CHIP programs will shift coverage for these children to Medicaid, as the ACA establishes a minimum Medicaid eligibility level of 138 percent of the FPL for all children up to age 19.7 Prior to the ACA, states were required to cover children up to age 6 with incomes up to 133 percent of the FPL through Medicaid, but the minimum eligibility level for older children was 100 percent of the FPL. This shift from CHIP to Medicaid must occur regardless of whether the state is expanding Medicaid to adults; states will continue to receive the enhanced CHIP matching rate for uninsured children in this income group. CMS has been assisting states with this shift and, in some cases, may permit an alternative transition approach, such as at a child’s next regularly scheduled renewal rather than by January 1, 2014.

Despite two (2) states reducing eligibility, most will continue to cover pregnant women above the federal minimum standards. As of January 1, 2014, the median eligibility level for pregnant women will be 203 percent of the FPL, with 31 states, including DC, covering pregnant women at or above 200 percent of the FPL (Figure 6 and Appendix Table 3). Two states, Oklahoma and Virginia, will reduce eligibility for pregnant women from 185 to 133 percent of the FPL and 200 to 143 percent of the FPL, respectively, as the requirement to maintain coverage ends on January 1, 2014. Louisiana has also indicated plans to reduce eligibility for pregnant women as of January 1, 2014, but this change was not reflected in the data from CMS as of November 15, 2013.8

Eligibility for parents and other adults will continue to lag behind that of children and pregnant women. While coverage for parents and childless adults will markedly improve in states implementing the Medicaid expansion, their median eligibility levels will still remain significantly lower than that of children and pregnant women. These disparities in eligibility across groups will be even starker in states that are not expanding Medicaid (Figure 7).

The ACA envisions seamless and timely access to the continuum of coverage options regardless of where or how someone applies. To achieve these objectives, the ACA establishes new expectations for simplifying the application process, coordinating enrollment, and moving toward paperless verification of eligibility. Many of these changes accelerate successful state strategies in harnessing technology to make the process work better for both individuals and state agencies.
The ACA requires Medicaid, CHIP, and the new health insurance Marketplaces to adopt a single, streamlined application that screens eligibility for all coverage options. To this end, HHS created a consumer-tested model application, which states can customize to better fit their programs. For example, states can substitute state agency names, logos, and phone numbers. States can also eliminate questions that aren’t applicable, such as how long a child has been uninsured in a state that does not impose a waiting period in CHIP. Alternatively, states may develop their own single, streamlined application, subject to HHS approval. However, alternative applications may only include questions relevant to the eligibility and administration of all of the insurance affordability programs, and only for individuals who are applying for coverage.
Most states (43) will use a state alternative online application, while seven (7) will adopt the HHS model online application. Fewer states (30) are using or plan to use a state alternative for their paper application (Figure 8). In 32 of the states using an alternative application, the version that is initially available will need further revisions to fully comply with the ACA standards, for example, by removing questions that are not relevant to eligibility. Notably, in 15 states, multi-benefit applications are available that allow individuals to simultaneously apply for health coverage and other benefits such as food or childcare assistance. Like the alternative application, a multi-benefit application must ask the relevant questions for all health insurance affordability programs. It must also clearly indicate which questions are optional for determining eligibility for health insurance coverage only.

State Medicaid agencies are required to make the single streamlined application available through multiple modes, including online, by phone, and on paper by January 1, 2014. As of October 1, 2013, 43 of 50 reporting states have deployed a single, streamlined application through their Medicaid agency, with 43 state Medicaid agencies having a paper version in place and 36 having launched an online version. The seven (7) remaining reporting states are in the process of developing their single, streamlined applications with nearly all anticipating completion by January 1, 2014 (Appendix Table 4). In the interim, these states are continuing to utilize their existing Medicaid applications and individuals who may be eligible for premium tax credits are being directed to apply through the federal Marketplace.9 Looking ahead states will continue work to make the single streamlined application available through all required modes, although some state agencies may not have all of these avenues available until later in 2014. In these cases, CMS is working with states to develop mitigation plans to help ensure consumers can connect to coverage.
Coordination between Medicaid, CHIP, and the Marketplace will be key for achieving the ACA’s no wrong door approach to coverage. States have the option to decide whether the Marketplace (State-based (SBM) or Federally-facilitated (FFM)) will determine eligibility for Medicaid and CHIP or assess potential eligibility and send the case to the Medicaid and CHIP agency for a final determination.10 To facilitate coordination across programs and prevent individuals from having to provide information more than once, state agencies and Marketplaces are expected to electronically transfer an account with all of the individual’s information promptly and without undue delay and are not allowed to request any information or documentation that the individual has already provided.
Coordination processes will vary based on whether the Marketplace has the authority to assess or determine Medicaid eligibility. For example, if an individual applies through a Marketplace that determines Medicaid/CHIP eligibility, the Marketplace will make a final eligibility determination and transfer the account of any eligible individual to the Medicaid/CHIP agency for enrollment, without a second review of eligibility. In contrast, if an individual applies through a Marketplace that assesses Medicaid/CHIP eligibility, it will transfer the account for any individual assessed as potentially eligible for Medicaid/CHIP for a final determination by the Medicaid/CHIP agency. If determined eligible for Medicaid/CHIP, the individual will be enrolled. If determined ineligible for Medicaid/CHIP, the agency will transfer the individual’s account back to the Marketplace for a review of eligibility for premium tax credits. As a result, some individuals may be transferred back and forth between coverage programs before they are determined eligible. Among the 34 federal or partnership Marketplace states, as well as Idaho and New Mexico (which are initially relying on the FFM to handle Marketplace eligibility and enrollment), the FFM will assess Medicaid/CHIP eligibility in 24 states and make final Medicaid/CHIP eligibility determinations in 12 states. In seven (7) of these 12 states, the FFM will make determinations temporarily until the state’s Medicaid/CHIP eligibility system is able to meet the ACA requirements (Appendix Table 5).
The ability to electronically transfer individual accounts between state Medicaid/CHIP agencies and the Marketplaces is in various stages of development. All but two (2) of the 17 states with SBMs share an integrated or linked technology system that determines eligibility for all insurance affordability options and facilitates the next steps for enrollment. However, in states using the FFM, electronic transfers of individual accounts between the Marketplace and Medicaid/CHIP agencies are essential for coordinating enrollment. Due to ongoing technological challenges with the FFM, these transfers have been delayed. As such, alternative strategies have been put into place. For example, until the FFM can begin transferring electronic accounts to state Medicaid and CHIP agencies, it is sending batches with basic data on individuals the FFM has assessed as potentially eligible for Medicaid/CHIP. Similarly, if a state Medicaid/CHIP agency is unable to screen for premium tax credits and transfer the account to the FFM it can advise potentially-eligible individuals to apply directly through the FFM. Moving forward, implementing electronic account transfers will be key to minimizing burdens on consumers and ensuring that they only need to submit a single application, as envisioned by the ACA’s no wrong door approach to coverage.
Beginning in January 2014, states are expected to rely on trusted electronic data sources rather than paper documentation to verify eligibility. Only when information cannot be obtained through an electronic data source or is not ‘‘reasonably compatible’’ with information provided by the consumer can additional information, including paper documentation, be requested. To facilitate electronic verification, states are expected to establish data linkages with federal and state data sources. A federal data hub provides access to information from multiple federal agencies including the Internal Revenue Service (IRS), the Social Security Administration (SSA), and the Department of Homeland Security (DHS). In addition, states are commonly accessing databases that collect state wage information, unemployment compensation information, vital statistics, and eligibility data for other public programs. Ultimately the goal is for these data interfaces to provide real-time or immediate access to data, however, in some cases, data may continue to be exchanged in a process that “batches” requests for information for multiple people on a daily or other periodic basis. In these instances, data is also returned in batches, which may result in a lag before the requested data is available and can be used to verify eligibility. When this is the case, states may pend or hold the application until the data is received and reviewed. Alternatively, some states may use the data to verify eligibility after they have enrolled the individual based on his/her self-attestation.
States are submitting verification plans to CMS, which outline the electronic data sources and procedures they will use to verify eligibility criteria. For the majority of states, the heightened reliance on electronic verification requires a redesign of business practices to implement a real-time, data-driven approach to verification. Each state must file a plan with CMS describing the agency’s verification policies and procedures including the data sources used at application and renewal, the frequency of data checks, and how the state determined the usefulness of electronic data sources.11 While there is no formal process for federal approval, the verification plans are used to confirm state implementation of the new standards established by the ACA, and will be used for quality and audit purposes going forward.12 As of November 15, 35 verification plans have been approved and made publicly available.
States continue to have the option to accept self-attestation for all non-financial eligibility criteria except where otherwise required by statute. Under law, states must verify Social Security Numbers (SSNs), citizenship, and immigration status. For other non-financial aspects of eligibility (e.g., state residency, age/date of birth, and household composition), states have more flexibility and may choose 1) to rely on self-attestation without additional verification, 2) rely on self-attestation to make the eligibility determination and verify post-enrollment, or 3) verify data to determine eligibility. For pregnancy, states must accept self-attestation, although they may request verification if multiple babies are expected. If states verify non-financial eligibility criteria, they are expected to use electronic data and eliminate or minimize requirements for paper documentation at both application and renewal. Even in states accepting self-attestation without further verification, the state may have access to electronic data for some people (for example, if the consumer is also enrolled in SNAP), which may be used to confirm eligibility.13 Moreover, states always have the option to verify any data that it considers questionable. All 35 reporting states will verify SSNs, citizenship, and immigration status through federal data sources as required by law. Most states plan to rely on self-attestation of state residency (28 of 35) and household composition (33 of 35). In contrast, the majority of the reporting states (22 of 35) plan to verify age and date of birth, with 18 verifying data to make the eligibility determination and 4 doing so post-enrollment (Figure 9 and Appendix Table 6).

For income, states must verify financial information from an electronic data source; however, this can be done post-enrollment after the state determines eligibility based on the individual’s attestation.14 States also may accept self-attestation for certain types of income that cannot be verified through an electronic source. All 35 reporting states will verify income through electronic sources, with 30 states doing so to determine eligibility and five (5) states verifying income post-enrollment (Figure 9 and Appendix Table 7). In addition, 23 states will be conducting routine ongoing post-enrollment checks of financial information to identify changes in income over time, although the frequency of these checks varies. Consumers are still required to report changes that may impact their eligibility.
States are relying on a variety of data sources to verify eligibility criteria. States have latitude to determine if a particular income data source is “useful” but neither the age nor cost of obtaining the data can be used as a reason to continue requiring paper documentation. SSNs and citizenship will be verified via an electronic match with the SSA, while immigration status will be verified through the DHS Systematic Alien Verification for Entitlements (SAVE) database. Frequently-used data sources for other non-financial eligibility criteria include the SSA, the Public Assistance Reporting Information System (PARIS), and state databases, such as the Department of Motor Vehicles (DMV), vital statistics, and public assistance records for Temporary Assistance to Needy Families (TANF) and SNAP. The most common data sources that states will use to verify income at application, renewal and post-enrollment include the IRS, SSA, state wage data, state unemployment data and commercial databases that provide payroll information for some employers, such as TALX (also known as the Work Number) (Appendix Table 8).
States may set “reasonable compatibility” standards to address situations in which self-attested income and electronic sources are inconsistent. In Medicaid and CHIP, data are always considered reasonably compatible if the individual’s self-attested income and the electronic data source are both at, below, or above the income standard—in these cases, the difference does not impact eligibility. In cases where self-attested income is above the standard and electronic data are below, or vice versa, states have flexibility to define when inconsistencies between the two sources are considered reasonably compatible. If the difference between the electronic data and the consumer’s self-attestation is within the reasonable compatibility standard, the self-attestation is used. If the data are not reasonably compatible under this standard, the state may accept a reasonable explanation of the difference and/or request paper documentation of income
| Table 1: Reasonable Compatibility Approaches Used by Medicaid Agencies at Application | |
| Total Number of States Reporting | 35 |
| If attestation and data are both | |
| Below the income limit, determined eligible for Medicaid | 35 (required) |
| Abovethe income limit, determined ineligible for Medicaid and screen for advance premium tax credits | 35 (required) |
| If attestation is below and data are above the income limit: | |
| Determine eligible for Medicaid if within reasonable compatibility standard | 27 |
| If not within the reasonable compatibility standard: | |
| Ask for reasonable explanation from individual | 26 |
| Require paper documentation of income | 9 |
| If attestation is above and data are below the income limit: | |
| Determine ineligible for Medicaid, screen for advance premium tax credits | 30 |
| Ask for a reasonable explanation of the difference from the individual* | 3 |
| Require paper documentation of income | 2 |
| *Note if the reasonable explanation is not sufficient, states may ask for paper documentation.Source: Based on analysis of Centers for Medicare and Medicaid Services State Medicaid & CHIP Policies for 2014: Medicaid/CHIP Verification Plans conducted by the Kaiser Commission on Medicaid and the Uninsured with the Georgetown Center for Children and Families. Data are available at: http://www.medicaid.gov/Medicaid-CHIP-Program-Information/By-State/By-State.html | |
To facilitate processing applications for large numbers of people who become newly eligible for Medicaid on January 1, CMS has offered states five strategies to help manage the transition. Highlighted in a May 17, 2013 letter to state officials,15 these approaches are intended to promote enrollment and retention, while smoothing the administrative burden as states shift to new eligibility processes. A state may adopt any of these facilitated enrollment approaches regardless of whether it plans to implement the Medicaid expansion, and as of October 1, a number of states have taken up at least one of these options (Figure 10 and Appendix Table 9).

Overall, 30 states have adopted at least one of the strategies, and 11 have adopted two or more of these approaches. Three (3) states (NJ, OR, and WV) have adopted four of the five. These strategies include:
Two of these strategies, enrolling eligible SNAP participants and enrolling parents based on their children’s eligibility data, allow states to get a jump-start on their Medicaid expansions by significantly streamlining the process and utilizing data already available to states. Experiences in the four states that have already launched these strategies indicate they can be highly successful in connecting people to coverage, reaching a significant share of adults eligible for the Medicaid expansion while minimizing burdens for both eligibility staff and individuals and reducing traffic through enrollment systems. Overall, in these four states, over 223,000 individuals have been enrolled through these strategies as of November 15, 2013.19
Looking ahead to 2014, coverage for parents and other adults will significantly improve in the 26 states implementing the Medicaid expansion and eligibility levels for children and pregnant women will remain strong across states. As such, as the ACA is fully implemented, Medicaid offers the potential to significantly reduce the number of uninsured. Outreach and enrollment efforts will be key for increasing coverage and it will be important for these efforts to be ongoing throughout the year since Medicaid enrollment is not limited to the Marketplace’s open enrollment period. In contrast to gains in states expanding Medicaid, large coverage gaps will remain in the states that do not expand, leaving millions of poor uninsured adults without access to a new coverage option.
To date, states have made meaningful progress in implementing key provisions of the ACA to provide streamlined Medicaid eligibility and enrollment processes, but readiness varies considerably. Moreover, the technology problems that have hampered the launch of open enrollment through the new Marketplaces, particularly the federal Marketplace (HealthCare.gov), have led to delays in coordination across Medicaid, CHIP, and Marketplace coverage. However, even with these early implementation challenges, some states have been successfully enrolling people in Medicaid and several have gotten a significant jump-start through the facilitated enrollment strategies offered by CMS. In the coming months, work will continue to deploy new processes and systems to move toward the ACA’s vision of a simplified, consumer-friendly experience. As such, January 2014 will represent the first step toward a modernized, streamlined system to connect individuals to expanded coverage options as established through the ACA, but fully achieving that vision will require time, persistence, and a commitment to continual program improvement.
Beginning January 1, 2014, millions of low-income parents and other adults will become newly eligible for coverage in states implementing the Affordable Care Act’s (ACA’s) expansion of Medicaid to adults with incomes at or below 138% of the federal poverty level (FPL). To help states launch the expansion and efficiently enroll eligible individuals, CMS has offered states a series of facilitated enrollment options. These options include strategies, referred to as “fast track enrollment” in this issue brief, that allow states to enroll eligible individuals into coverage using data already available from their Supplemental Nutrition Assistance programs (SNAP) and/or their Medicaid or Children’s Health Insurance Program (CHIP) programs for children. This issue brief provides an overview of the new “fast track” enrollment options, including how they have been implemented, their impacts, and key lessons learned. It is based on a series of interviews with state officials in Arkansas, Illinois, Oregon and West Virginia.
Beginning January 1, 2014, millions of low-income parents and other adults will become newly eligible for coverage in states implementing the Affordable Care Act’s (ACA’s) expansion of Medicaid to adults with incomes at or below 138% of the federal poverty level (FPL).1 To help states launch the expansion and efficiently enroll eligible individuals, CMS has offered states a series of facilitated enrollment options. These options include strategies, referred to as “fast track enrollment” in this issue brief, that allow states to enroll eligible individuals into coverage using data already available from their Supplemental Nutrition Assistance programs (SNAP) and/or their Medicaid or Children’s Health Insurance Program (CHIP) programs for children. These strategies complement the array of other pathways currently in place to connect Medicaid-eligible individuals to coverage, which include applying directly through state Medicaid agencies or through the new Marketplaces established by the ACA. To date, these fast track enrollment strategies have been implemented in four states: Arkansas,2 Illinois, Oregon, and West Virginia. New Jersey also recently secured approval to implement fast track enrollment and is scheduled to begin implementation in November.
This issue brief provides an overview of the new “fast track” enrollment options, including how they have been implemented, their impacts, and key lessons learned. It is based on a series of interviews with state officials in Arkansas, Illinois, Oregon, and West Virginia conducted by Manatt Health Solutions and the Kaiser Commission on Medicaid and the Uninsured. In sum it finds that
On May 17, 2013, the U.S. Department of Health and Human Services (HHS) sent a letter to State Medicaid Directors and State Health Officials advising them of options available to facilitate the enrollment of eligible individuals into Medicaid.3 Two of the options, referred to as “fast track” enrollment in this brief, allow states to use data that they already have on hand to identify and enroll eligible people into Medicaid.4 The fast track options draw on earlier experiences with Express Lane Eligibility and share many key elements with the deemed enrollment of Medicaid beneficiaries into the low-income subsidy for Medicare Part D.5 They provide states with an efficient way to make progress toward their Medicaid enrollment goals at a time when they are busy implementing the Medicaid expansion; establishing or coordinating with new Marketplaces; and launching new eligibility and enrollment systems. States can apply for approval to use either of these options at any time prior to the end of calendar year 2015. Specifically, under the new “fast-track” enrollment options states may:
Under both of these fast track enrollment options, the existing data sources jump-start the enrollment process by helping states identify income-eligible individuals. However, the options stop short of allowing states to automatically enroll SNAP beneficiaries or parents of Medicaid or CHIP children into Medicaid. States must take additional steps to ensure that individuals want to be enrolled in coverage and that the state has all of the necessary information to verify eligibility. For example, states must secure an application signature from eligible individuals; provide them with information on their rights and responsibilities; and verify their non-financial eligibility for coverage in accordance with Medicaid standards. In addition, within a year of their initial enrollment (or earlier if they report a change in circumstances), states must evaluate fast track enrollees using the new Medicaid income and household composition rules.
As of November 15, 2013, five states with Medicaid expansions have received approval to use the fast track enrollment options, as shown in Table 1 below. (In Arkansas, the state is implementing a premium assistance model that allows Medicaid funds to be used to purchase Qualified Health Plans (QHPs) through the Marketplace for newly eligible adults.) All five use SNAP data to identify Medicaid-eligible individuals, and three (New Jersey, Oregon, and West Virginia) have also adopted the strategy to use Medicaid enrollment data for children to reach eligible parents. As of early November, four of the five states have implemented fast-track enrollment. New Jersey plans to begin implementation in mid-November. As noted, states may apply for approval to use either of these options at any time prior to the end of calendar year 2015, so additional states may take up the strategies moving forward.
| Table 1: State Adoption of Fast Track Enrollment Options, November 15, 2013 | |||
| State | Using SNAP Data | Parents of Medicaid/CHIP Children | Implemented? |
| Arkansas | Y | Y | |
| Illinois | Y | Y | |
| New Jersey | Y | Y | Nov. 15, 2013 |
| Oregon | Y | Y | Y |
| West Virginia | Y | Y | Y |
While there are a number of variations in how the four states implemented the fast track enrollment options, they all followed several basic steps, which include the following:
1. Identify eligible individuals within existing, approved data sources. All four states examined their SNAP enrollment data to identify individuals eligible for Medicaid. Two states (Oregon and West Virginia) also used their existing data on families with children enrolled in Medicaid to identify eligible parents (Table 2). Using these data sources, all four states selected individuals with incomes at or below the Medicaid expansion income limit who were not already enrolled in Medicaid. Arkansas, Oregon, and West Virginia included both parents and adults without dependent children (or “childless adults”) below the income eligibility limit. In contrast, Illinois solely focused on identifying eligible childless adults. The states used the fast track enrollment strategies primarily to reach adults eligible for the Medicaid expansion as of January 2014. However, Arkansas and West Virginia also elected to use fast-track to reach already eligible children who were not yet enrolled in Medicaid, who could begin receiving coverage immediately. Similarly, in some cases, these strategies also connected currently eligible parents to coverage.
2. Send eligible individuals a streamlined enrollment form. After identifying eligible individuals, the states sent them a letter and a simple one- or two-page enrollment form (see Box 1). Individuals were required to answer a handful of questions about non-financial eligibility for coverage as needed to allow the states to verify their citizenship or immigration status, sign the form to indicate they wanted coverage and that they were aware of their rights and responsibilities, and then return it to the state.9 In some instances, the enrollment form asks for a few additional pieces of information, such as whether an individual has coverage through an alternative source (to facilitate third party liability recovery efforts) or if a person is of American Indian descent (to assess whether he or she can be enrolled in managed care). People can return the form through the mail and, in Oregon and West Virginia, they also have the option to call a toll-free number and provide the necessary information and a telephonic signature over the phone.
| Table 2: Key Features of State Fast Track Enrollment Strategies | |||||
| State | Target SNAP Population | Modes to Return Enrollment Form | |||
| Parents | Childless Adults | Children | Phone | ||
| Arkansas | Y | Y | Y | Y | |
| Illinois | Y | Y | Y | ||
| Oregon | Y | Y | Y | Y | |
| West Virginia | Y | Y | Y | Y | |
All four states sought to make their fast-track enrollment forms and notices easy to read and use. For example, Oregon’s fast track notices were written in simple language, included significant white space, and were signed by the state’s Medicaid director, to highlight that there was a “real person” within the state agency behind the communication. The state also provided people with a self-addressed, stamped envelope to return their enrollment form. In some instances, states faced technological barriers that limited the options they had available to design their notices and enrollment forms. In Oregon and West Virginia, for example, because of technological limitations, the states sent a separate enrollment form to each individual in a household who was identified as eligible for Medicaid rather than a single household form. But, states developed ways to compensate for limitations. For example, Illinois was limited in its ability adopt a consumer-friendly designs for its notices within its legacy computer system, so it accompanied the enrollment notice and form with a very easy-to-read one-page brochure.
Officials noted that while many consumers appreciated the short, easy-to-read forms and streamlined enrollment process, some contacted call centers or eligibility workers seeking confirmation that the forms were legitimate because they were surprised and skeptical about the ease of the enrollment process. To help address these issues, states included their official seal on fast track correspondence and a phone number that people could call for further information or clarification.
3. Verify non-financial eligibility for coverage. After receiving the forms back, states verify the citizenship status of the individuals in accordance with Medicaid standards. In general, these standards require states to electronically verify the person’s status using the federal data services hub and, if citizenship cannot be established through this means, to rely on a paper verification process.10 Similarly, for non-citizens, if immigration has not yet been verified, the state will seek to verify status through available electronic data sources, or paper documentation when electronic data are not available. If citizenship or immigration information cannot be verified, the person is found ineligible for Medicaid. States used a variety of strategies to streamline the processing of the returned enrollment forms. For example, West Virginia and Arkansas included bar codes on the forms so that eligibility workers could easily scan them into the state’s eligibility system when they were returned. Arkansas, Illinois and Oregon used their central processing units or set up a special team to verify and confirm eligibility. Illinois officials noted that having a handful of key people working on the initiative enabled them to quickly identify and resolve issues and allowed their other eligibility workers to focus on broader ACA implementation efforts.
4. Confirm eligibility. After states complete the verification process, they send eligible people a notice confirming their eligibility and advising them that their coverage becomes effective starting January 1, 2014. Illinois and Oregon also included enrollment cards in this mailing. Officials noted that although individuals were advised that coverage would not begin until January 1, some consumers thought their coverage was immediately effective and tried to use it upon receiving their eligibility confirmation. To minimize this problem, the states highlighted the January 1, 2014 effective date of coverage whenever possible, often mentioning it multiple times in the same letter to consumers. West Virginia is attempting to avoid this confusion among consumers by waiting until closer to the effective coverage date to send eligibility confirmations and enrollment cards. In the interim, it is notifying consumers that it has received their enrollment form and that they will receive their determination in December 2013.
5. Facilitate enrollment into health plan. In Illinois and West Virginia, Medicaid beneficiaries generally are provided with services through a fee-for-service delivery system. In Oregon, however, adults enrolled in the Medicaid expansion select a coordinated care organization from which to receive services while in Arkansas they select a QHP offered through the Marketplace. As such, both of these states also provide individuals information on how to select a plan with their enrollment confirmation. If new enrollees do not select a plan within the state’s required timeframe, they are automatically enrolled in a plan by the state. All four states view fast track enrollment primarily as a time-limited strategy for facilitating early enrollment into their new Medicaid expansion. In the weeks and months remaining in 2013, Arkansas, Oregon and West Virginia are conducting “second round” mailings and/or calling people who did not respond to the first mailing to ensure the correspondence was not overlooked or misplaced. They also are developing procedures to address changes in circumstances prior to January 1, 2014 and planning to re-verify that fast track enrollees are not already enrolled in Medicaid shortly before their coverage goes into effect on January 1, 2014. At this point, none of the four states are planning to use fast track on an ongoing basis.
To date, approximately 223,000 people in these four states have been enrolled in Medicaid through these fast-track enrollment efforts. Enrollment numbers range from 35,500 in Illinois to 63,465 in Arkansas (Table 3). These numbers in Arkansas and West Virginia include some currently eligible children who were immediately connected to coverage through these initiatives. The states are continuing to process all returned enrollment forms, so these enrollment numbers will likely continue to increase as the states finalize verification and processing of all returned forms. Through these enrollment gains, the fast track enrollment strategies have enabled all four states to make significant progress in reaching and enrolling individuals eligible under the Medicaid expansion. For example, the number of people determined eligible for Medicaid through fast track in less than two months represents 18% of Illinois’ first-year Medicaid enrollment goal of 200,000 and one-quarter of the total coverage goal of 250,000 in Arkansas. In Oregon, state officials report that fast track enrollment has reduced the number of uninsured people in the state by 10% in less than one month.
All four states had robust response rates among individuals who received the fast track enrollment letters. Response rates to the initial letters and enrollment forms varied from 27% in Oregon to 46% in West Virginia. State officials noted that they were surprised and encouraged by these high levels of response. Moreover, since Arkansas, Oregon, and West Virginia sent or plan to send a follow-up letter or communication to individuals that did not respond to the initial letter, these response rates may continue to increase. For example, eligibility workers in Arkansas and West Virginia are calling people at home if they did not respond to the initial letter. In Arkansas, eligibility workers reported having a hard time reaching people by phone but, when they did, roughly 90% indicated they wanted the coverage. Since the state accepts telephonic signatures for the fast track enrollment form, eligibility workers are able to promptly enroll people over the phone. Other factors may also impact the response rate in these states including the level of unmet need for health care services and the states’ Medicaid eligibility levels prior to the Medicaid expansion.
| Table 3: Fast Track Enrollment Outcomes Reported November 15, 2013 | ||||
| State | Date Enrollment Form Sent | Number Receiving Enrollment Form | Percent of Forms Returned to State | Number of People Verified as Eligible and Enrolled |
| Arkansas | September 3, 2013 | 154,000 | 41% | 63,465 |
| Illinois | August 23, 2013 | 123,000 | 33% | 35,500 |
| Oregon | September 30, 2013 | 260,000 | 27% | 70,000 |
| West Virginia | Early September 2013 | 118,000 | 46% | 54,100 |
| Total | 655,000 | 223,065 | ||
| Notes: The number of individuals receiving the enrollment form includes 9,000 children in Arkansas, 30,000 parents of children enrolled in Medicaid in Oregon, and 28,046 parents of children enrolled in Medicaid in West Virginia. Illinois has 2,300 returned forms remaining that need to be processed. In Arkansas and West Virginia the number of people verified and enrolled includes children currently eligible for coverage. Additionally, in the three states that targeted parents using SNAP data, some parents may be eligible under current rules. | ||||
Each state took some steps to tailor its fast track initiative to its unique circumstances, including the structure of its eligibility rules and enrollment system and its overall ACA communication and outreach efforts. However, some common “lessons learned” can be drawn from the four states’ experiences.
It was quick and easy, gave us the biggest bang for the buck, and it was easy for staff to manage.
We were looking for a way to not create duplicative work for the eligible clients and to meet guiding principles to reduce waste and inefficiency in the health care system. So requiring someone to reapply when we know their income and situation would be a waste.
While implementing these fast track initiatives required upfront investments of time and effort, they paid off with substantial coverage gains while minimizing the burden on individuals, staff, and enrollment systems. As noted, implementing the fast track enrollment strategies did require upfront investments of time and effort to identify the target populations and send out and process enrollment forms. However, state officials unequivocally indicated that these investments were worth it. From the state perspective, they generated substantial gains in coverage in a short time frame while minimizing burdens on individuals, eligibility workers, and enrollment assisters and reducing traffic to the new Marketplace enrollment systems.
The fast track initiative has been a positive experience for both consumers and state enrollment staff. As indicated by the high response rate to the fast track enrollment letters, consumers were highly motivated to enroll through this streamlined approach. State officials reported that consumers expressed gratitude for both the availability of coverage under the expansion and the ease of the fast track enrollment process, sometimes by attaching thank you notes to their enrollment forms. Enrollment staff also welcomed the streamlined enrollment approach, and state officials indicated that eligibility workers felt positive about being able to quickly confirm eligibility for many consumers who they would have denied in the past under eligibility rules prior to the Medicaid expansion. Finally, state officials highlighted that fast track enrollment has helped to acclimate their eligibility workers to the new, data-driven approach to evaluating Medicaid eligibility required by the Affordable Care Act.
Make it simple and seamless and any way you want to apply without having to sit and produce all of this documentation. It has been a real cultural shift for our county workers. This is the changing face of Medicaid. Things aren’t working the way they used to work.
…for years they’ve had to say “no” to people…and now they just get to say “yes” you can have coverage.
The fast track enrollment initiative can be integrated into broader ACA outreach and enrollment initiatives. To varying degrees, the four states sought to integrate their fast track enrollment initiatives into broader ACA outreach and enrollment efforts. For example, Oregon adopted a marketing-based approach to implementing its fast track initiative — it developed a special section on its web site to share information, trained Navigators and other assisters on fast track, designed consumer-friendly forms, and included a marketing brochure along with the enrollment form it sent to consumers.11 Arkansas used its state Marketplace logo, “Get In,” on its enrollment form to help ensure that consumers would connect fast track enrollment with the state’s larger initiatives to enroll people into Medicaid and Marketplace coverage. It also included a note on its enrollment form alerting consumers that other uninsured family members who were not being enrolled under the fast track initiative can still apply for new coverage options online.
In conclusion, the experience of these four states demonstrates that fast track strategies represent a highly effective enrollment option for states. By using data already available to them and drawing on their expertise with eligibility and enrollment systems, these four states have been able to jump-start enrollment into their Medicaid expansions, enrolling more than 221,000 people in just two months. As result, they have made substantial progress toward their Medicaid enrollment goals while minimizing burdens on individuals, staff, and enrollment systems.
This brief was prepared by Jocelyn Guyer and Tanya Schwartz with Manatt Health Solutions and Samantha Artiga with the Kaiser Family Foundation’s Commission on Medicaid and the Uninsured. The authors extend their deep appreciation to the state officials who shared their time and expertise to inform this work, as well as to Donna Cohen Ross and Deborah Bachrach for their careful review of and comments on this issue brief.
Based on the assumption of increased coverage and therefore reduced uncompensated care costs under the Affordable Care Act (ACA), the law calls for a reduction in federal Medicaid Disproportionate Share Hospital (DSH) allotments. The statute requires annual aggregate reductions in federal DSH funding from FY 2014 through FY 2020. To implement these annual reductions, the statute requires the Secretary of HHS to develop a methodology to allocate the reductions that must take into account 5 factors: impose a smaller percentage reduction on low DSH states; impose larger percentage reductions on states that have the lowest percentages of uninsured individuals; impose larger percentage reductions on states that do not target their DSH payments on hospitals with high volumes of Medicaid inpatients or with high levels of uncompensated care, and the methodology must take into account whether the DSH allotment for a state was included in the budget neutrality calculation for a coverage expansion approved under section 1115 as of July 31, 2009. The Centers for Medicare and Medicaid Services (CMS) released a final rule to allocate the reduction in the DSH allotments for FY 2014 and FY 2015 in September 2013. This brief provides some background in DSH payments, how DSH payments are affected by the ACA, the methodology for the DSH reductions across states for FY 2014 and FY 2015 and a look at the implications of the DSH reductions.
A Data Note based on the Kaiser Family Foundation California Uninsured Baseline Survey
In California, as across the United States, the young uninsured are a key piece of the new Affordable Care Act (ACA) marketplace puzzle. Having a good-sized component of young people, with their generally more robust health and less frequent need for medical care and prescription drugs, in the newly created insurance pools would provide an important counterbalance to the incoming group of Americans who had previously been locked out of coverage because of preexisting health conditions.
In this data note, we take a closer look at a broadly defined ‘young invincible’ population using a recently released baseline survey of California’s uninsured population by the Kaiser Family Foundation (KFF). The representative, probability-based sample survey is the first of what is expected to be a series of four surveys that will track the views and experiences of the same group of people over the next two years.1 For the purposes of this analysis, we are defining the young uninsured as those Californians aged 19 to 34 that have not had insurance for at least two months and by their income and status as citizens or permanent residents should be eligible to participate in the ongoing insurance expansion under the 2010 health law. Overall, these young uninsured Californians make up nearly half (47 percent) of the state’s adult, eligible uninsured population.2
The majority of the Golden State’s young uninsured are men – 59 percent are male, 41 percent are female – a distribution not significantly different than California’s eligible uninsured as a group, which tends to be disproportionately male due to Medi-Cal’s previous rules regarding eligibility. Roughly half are Latino, much like the state’s uninsured population as a whole. Compared to the state’s older uninsured population, the young uninsured are more likely to report being American born citizens: 78 percent say so, compared to about six in ten of those age 35 and over. Like the rest of the eligible uninsured, a large share live in very low-income households, with roughly half (48 percent) saying their household’s annual income is 138% or less of the Federal Poverty Level (FPL) Medi-Cal eligibility ceiling.3
| Figure 1 | 19-34 | 35-49 | 50-64 |
| Race/Ethnicity | |||
| White | 29% | 29% | 42% |
| Black | 7 | 6 | 7 |
| Asian | 13 | 5 | 5 |
| Other | 3 | 11 | 7 |
| Hispanic | 48 | 49 | 39 |
| Were you born in the United States or in another country? | |||
| U.S. | 78% | 58% | 62% |
| Another country | 22 | 41 | 37 |
| Eligibility Level | |||
| Medicaid target group (138% FPL or below) | 48% | 49% | 42% |
| Exchanges subsidy target group (139% – 400% FPL) | 41 | 37 | 43 |
| More than 400% FPL | 5 | 11 | 11 |
The 19 to 34 year olds are also different in predictable ways in terms of their stage of life: more than six in ten (63 percent) have yet to marry, compared to fewer than two in ten among older uninsured; roughly one in four (28 percent) have a dependent child at home, compared to more than half (55 percent) of those in the middle age group; and roughly one in eight (12 percent) are students.
| Figure 2 | 19-34 | 35-49 | 50-64 |
| Marital status | |||
| Married | 21% | 47% | 45% |
| Living with partner | 10 | 15 | 9 |
| Previously married | 6 | 20 | 29 |
| Never married | 63 | 17 | 18 |
| Are you a parent of a child under age 19 living in your household? | |||
| Yes | 28% | 55% | 18% |
| No | 72 | 45 | 82 |
| Employment status | |||
| Employed | 64% | 59% | 49% |
| Unemployed, looking | 17 | 22 | 22 |
| Unemployed, not looking | 3 | 4 | 7 |
| Student | 12 | 1 | <1 |
| Other | 5 | 14 | 21 |
| Education | |||
| Less than high school | 13% | 31% | 27% |
| High school | 34 | 26 | 21 |
| Some college | 37 | 30 | 38 |
| College or more | 15 | 13 | 14 |
Though these Californians are relatively young, most of those aged 19 to 34 report that they have been uninsured for a significant length of time. Overall, six in ten among the young uninsured say they have been uninsured for at least two years. Four in ten have lost insurance within the past two years, compared to roughly three in ten among the older groups. As is true for the rest of the state’s uninsured, the main reason this group remains uninsured is cost-related: half (48 percent) say the main reason they don’t have health insurance is that it’s too expensive.
| Figure 3 | 19-34 | 35-49 | 50-64 |
| And how long have you been uninsured? | |||
| Less than two years (NET) | 40% | 27% | 29% |
| 2 months to less than a year | 19 | 14 | 15 |
| 1 year to less than 2 years | 21 | 13 | 14 |
| Two years or more | 60 | 72 | 71 |
This group does stand out as having a different past relationship with health insurance coverage compared to those 35 and older. While a majority of those aged 50 to 64, and nearly half of the middle-aged group, say that their previous source of health coverage was through an employer, only 22 percent of those under age 35 say the same. Newer to the workforce, their experience with employer-sponsored coverage is obviously more limited. Instead, one in four say that before they were uninsured they were on their parents’ health plan, and nearly as many (22 percent) say they were covered by Medi-Cal or another state’s Medicaid program (programs that have been required to cover low-income youth until they turn 19). Four in ten among this group have been on Medi-Cal at some point in the past. Note they are also the group least likely to have shopped for health insurance in the individual market: 20 percent have done so, roughly half as many as among older uninsured Californians. In this respect, the exchange experience will be even newer for this group than for other uninsured Californians.
| Figure 4 | 19-34 | 35-49 | 50-64 |
| Before you were uninsured, what was your main source of health insurance coverage? | |||
| Plan through your/your spouse’s employer | 22% | 47% | 59% |
| Coverage under your parents’ plan | 26 | 4 | 1 |
| Medicaid/Medi-Cal | 22 | 21 | 9 |
| Never had insurance | 23 | 21 | 17 |
| Have you, yourself, ever received health insurance through Medi-Cal, or not? | |||
| Yes | 40% | 39% | 27% |
| No | 58 | 60 | 73 |
| Have you ever tried to buy health insurance on your own, either for yourself or for your family, or not? | |||
| Yes | 20% | 37% | 44% |
| No | 80 | 63 | 56 |
This group of uninsured report experiencing at least two of the benefits of youth: They are less likely to report feeling financial stress than their older peers, and they are more likely to say they are in good health.
Across several fronts, the young uninsured report feeling less financial insecurity than those in the thick of child-rearing or in the pre-retirement years. Overall, half say they feel secure when it comes to their financial position, compared to roughly a third of those aged 35 and over. They report less worry about their income keeping up with rising prices and about having enough money for what must seem a far-distant retirement horizon.
Despite this comparatively optimistic picture, it’s important to keep in mind that this still leaves half among this group saying they do not feel financially secure at this point, an important consideration when it comes to evaluating any costs that might come with new insurance coverage.
| Figure 5 | 19-34 | 35-49 | 50-64 |
| All in all, how financially secure do you feel? | |||
| Secure | 51% | 38% | 32% |
| Insecure | 49 | 61 | 67 |
| “Very worried” about not having enough money for retirement | 51% | 68% | 68% |
| “Very worried” about income not keeping up with rising prices | 50% | 67% | 68% |
Those under age 35 are also more likely than older Californians without coverage to say they are in good health, with three in four saying so. They are also less likely to report having a disability, handicap or chronic disease. But while just over half in this group – 54 percent – say that their health needs are basically being adequately met at this point, the rest – 45 percent – say they are not getting the care they need.
| Figure 6 | 19-34 | 35-49 | 50-64 |
| In general, would you say your health is… | |||
| Excellent/very good/good | 74% | 63% | 51% |
| Fair/poor | 25 | 36 | 49 |
| Does any disability, handicap, or chronic disease keep you from participating fully in work, school, housework, or other activities? | |||
| Yes | 8% | 15% | 25% |
| No | 91 | 85 | 75 |
| Overall, how well would you say your health needs are being met today? | |||
| Very/somewhat well | 54% | 46% | 48% |
| Not too/not at all well | 45 | 54 | 51 |
Their overall good health, however, does not protect this group from incurring medical bills on occasion and then having trouble paying them.
Young people are just as likely as any other uninsured state resident to say they have had trouble paying medical bills over the past year. Overall, four in ten (39 percent) say so – and they report just as much worry about paying for health care going forward. Just over seven in ten of those aged 19 to 34 years say they are “very worried” about how they would pay for health care in the case of a serious accident or illness, putting their concern about a catastrophic medical event well within range of uninsured Californians of any age. They are somewhat less worried about not being able to cover the cost of routine health care services: 44 percent are very worried about this, compared to about 55 percent of older uninsured.
| Figure 7 | 19-34 | 35-49 | 50-64 |
| In the past 12 months, did you have any problems paying medical bills, or not? | |||
| Yes | 39% | 43% | 42% |
| Used up all or most of your savings because of medical bills | 18 | 18 | 24 |
| Been contacted by a collection agency because of medical bills | 20 | 20 | 18 |
| Spent less on food because of medical bills | 18 | 20 | 26 |
| No | 61 | 56 | 58 |
| How worried are you about not being able to pay medical bills in the event of a serious illness or accident? | |||
| Very worried | 73% | 78% | 77% |
| Somewhat worried | 20 | 16 | 16 |
| Not too worried | 5 | 2 | 5 |
| Not at all worried | 2 | 4 | 3 |
| How worried are you about not being able to pay medical bills for routine health care services? | |||
| Very worried | 44% | 56% | 55% |
| Somewhat worried | 32 | 25 | 26 |
| Not too worried | 19 | 14 | 13 |
| Not at all worried | 6 | 5 | 6 |
One way this generation deals with the problem of hard to pay medical bills is, like the rest of the uninsured population, by skipping health care, even when they feel they need it. Roughly six in ten (59 percent) in this population say that they’ve gone without needed health care since they’ve been uninsured because of the cost. This is somewhat lower than their older compatriots, but still a majority among a supposedly “invincible” population.
The large majority of young people – about eight in ten – say it is difficult for their family to afford health care, though they don’t express quite as much intensity on the issue as older uninsured Californians. For example, 42 percent of those aged 19 to 34 say their family finds it “very difficult” to afford health care, compared to 63 percent of those aged 50 to 64.
| Figure 8 | 19-34 | 35-49 | 50-64 |
| Percent who say they have done each of the following during the time that they’ve been uninsured because of the cost… | |||
| …gone without health care you thought you needed | 59% | 66% | 72% |
| …put off or postponed preventive health services, such as a yearly check-up or routine test | 65 | 68 | 75 |
| …skipped dental care or checkups | 68 | 72 | 75 |
| In general, how easy or difficult is it for you and your family to afford health care? | |||
| Very easy | 2% | 4% | 2% |
| Somewhat easy | 16 | 8 | 4 |
| Somewhat difficult | 37 | 32 | 27 |
| Very difficult | 42 | 52 | 63 |
Perhaps because of these worries and negative financial experiences involving medical bills, about three in four of California’s young uninsured say they feel the need to have health insurance. On the other hand, one in four say they feel healthy enough that they don’t really need coverage.
And the majority of young people – six in ten – say that health insurance is worth the cost.
| Figure 9 | 19-34 | 35-49 | 50-64 |
| Which of the following comes closer to your view? | |||
| Health insurance is something I need | 74% | 84% | 85% |
| I’m healthy enough that I don’t really need health insurance | 25 | 14 | 14 |
| Would you say that health insurance IS or IS NOT worth the money it costs? | |||
| Health insurance is worth the money | 61% | 53% | 53% |
| Health insurance is not worth the money | 32 | 40 | 38 |
The uninsured 19 to 34 year olds look roughly the same as the rest of the state’s eligible uninsured population when it comes to general views of the health law: somewhat more positive toward the law than the American public nationwide,4 but even more likely to feel they don’t have enough information to understand how it will impact them personally. Overall, half of those under 35 have a favorable view of the ACA, 27 percent an unfavorable view and 21 percent don’t have any opinion. Though many have a sense of whether or not they like the law as a whole, at least at the end of the summer far fewer felt confident they understood how the law’s changes would affect their own lives. Overall, seven in ten (69 percent) said they don’t know what to expect in terms of personal impact. And as of the end of August, most had heard little or nothing about the Medi-Cal expansion (77 percent) or the creation of the Covered California insurance marketplace (88 percent), similar to their older peers.
| Figure 10 | 19-34 | 35-49 | 50-64 |
| As you may know, a health reform bill – sometimes called Obamacare – was signed into law in 2010. Given what you know about the health reform law, do you have a generally favorable or generally unfavorable opinion of it? | |||
| Favorable | 51% | 44% | 49% |
| Unfavorable | 27 | 30 | 35 |
| Don’t know | 21 | 26 | 17 |
| Do you feel you have enough information about the health reform law to understand how it will impact you and your family, or not? | |||
| Yes | 30% | 26% | 30% |
| No | 69 | 73 | 69 |
Because of this limited exposure to recent information about the rollout of the insurance coverage expansions under the ACA, it is perhaps not surprising that as of late August, many young people in California were not aware of their potential eligibility for either subsidy assistance on the exchanges or inclusion in the expanded Medi-Cal program. Awareness of the availability of tax credit help when purchasing through Covered California was particularly limited at this early point. Overall, roughly seven in ten young people identified as in the appropriate income group either thought they would not be eligible for financial assistance (43 percent) or weren’t sure (26 percent).
| Figure 11: AMONG THOSE IN EXCHANGE TARGET GROUP (>138% – 400% FPL) | 19-34 | 35-49 | 50-64 |
| As far as you know, will you personally be eligible to get financial assistance from the government to help pay for health insurance as a result of the health care law, or not? | |||
| Yes | 32% | 15% | 28% |
| No | 43 | 47 | 39 |
| Don’t know | 26 | 38 | 33 |
Uninsured Californians of all ages, including younger folks, were more likely to recognize their potential eligibility for the Medi-Cal program, a program they may be more familiar through previous exposure or family and friend networks. Still, roughly four in ten of the 19 to 34 year olds expected to be eligible for Medi-Cal were not aware of this eligibility as of August (25 percent in the target group thought they would not be eligible, and another 17 percent had no idea either way).
| Figure 12: AMONG THOSE IN MEDI-CAL TARGET GROUP (≤138% FPL) | 19-34 | 35-49 | 50-64 |
| As far as you know, will you personally be eligible to get insurance through Medi-Cal as a result of the health care law, or not? | |||
| Yes | 57% | 54% | 44% |
| No | 25 | 26 | 28 |
| Don’t know | 17 | 20 | 29 |
When told or reminded that “nearly all Americans [will be required] to have health insurance by 2014 or else pay a fine,” a clear majority of the youngest group of uninsured Californians – 58 percent – said they planned to get coverage next year. At least as of late summer, roughly a third thought they would remain uninsured.
| Figure 13 | 19-34 | 35-49 | 50-64 |
| As you may know, the health care law requires nearly all Americans to have health insurance by 2014 or else pay a fine. Do you think you will obtain health insurance in 2014, or do you think you will remain uninsured? | |||
| Will obtain health insurance in 2014 | 58% | 48% | 52% |
| Will remain uninsured | 33 | 33 | 27 |
| Depends on the cost | 4 | 11 | 12 |
As is true in other age groups, a large majority of young people said that if they were told they were eligible for Medi-Cal, they would sign up.
| Figure 14 | 19-34 | 35-49 | 50-64 |
| If you were told you were eligible for Medi-Cal, would you want to enroll, or not? | |||
| Yes | 82% | 88% | 84% |
| No | 13 | 8 | 11 |
Though there are many avenues for Californians to learn about the new insurance options, including in-person and phone opportunities, much of the shopping and learning is structured around the web. This is an advantage for younger state residents, as compared to the older uninsured population, the 19 to 34 year olds are more likely to have access to the internet overall, more likely to have internet access in their own home, and more likely to have at least occasionally bought things online. Still, it’s worth noting that just under half (44 percent) have rarely or never made an online purchase.
| Figure 15 | 19-34 | 35-49 | 50-64 |
| Percent who say they do NOT have internet access… | |||
| …at home | 20% | 31% | 34% |
| …anywhere | 5 | 18 | 24 |
| How often do you use the Internet to buy a product online, such as books, music, toys or clothing, or not? | |||
| Very/somewhat often | 28% | 19% | 14% |
| Just occasionally | 27 | 20 | 20 |
| Rarely/never | 44 | 62 | 66 |
Most of California’s youngest uninsured residents report that they are healthy, but like the rest of the uninsured, most say they have skipped needed medical care because of cost during their period of uninsurance and they report a high degree of worry about what would happen if they were to become severely ill or be injured. Many have struggled to pay the health bills they have incurred. And perhaps because of all these reasons, most say that they feel the need for health insurance.
At the same time, in the months before open enrollment in California, this generation of the uninsured was just as likely as any other to feel they didn’t understand the health reform changes coming down the pike and to have heard little about the state marketplace or Medi-Cal expansions. And as a consequence, there likely remains a fair bit of eligibility confusion to sort out. Add to this the fact that half of this younger group feel financially insecure and only one in five have shopped for insurance before on their own, and it becomes clear that the open enrollment period will be a learning experience on all sides.
Over the next several months many of these young Californians will be learning more about the health coverage available to them via various ACA channels, and many will take steps to understand the costs and benefits such coverage will offer them. Beginning next spring, KFF will be back in the field revisiting these young people and asking them to reflect on their experiences – or lack of experience – with Medi-Cal and the exchanges.
The survey of California’s uninsured population was designed and analyzed by public opinion researchers at the Kaiser Family Foundation. Fieldwork was conducted in English and Spanish via telephone by SSRS, an independent research company, from July 11 through August 29, 2013, among a representative sample of 2,001 adults ages 19 to 64 living in California, who reported having been without health insurance for at least two months at the time of the interview. Of the 2,001 respondents, 990 were interviewed via landline, and 1,011 via cell phone. The current data note is based on the 515 respondents that were between the ages of 19 and 34 at the time of the interview, and that qualified as being part of the ‘eligible uninsured’ (those who reported being U.S. citizens or permanent residents, and thus eligible for the health insurance expansion under the Affordable Care Act). The margin of sampling error including the design effect for the sample of eligible uninsured 19 to 34 year olds, on which most findings in this Data Note are based, is plus or minus 6 percentage points. Numbers of respondents and margin of sampling error for other age groups are show in the table below. To access a more detailed methodology, please see the online report.
| Group | N | MOSE |
| Total Eligible Uninsured | 1,584 | +/- 4 percentage points |
| Eligible uninsured by Age | ||
| Eligible uninsured, 19-34 | 515 | +/- 6 percentage points |
| Eligible uninsured, 35-49 | 433 | +/- 6 percentage points |
| Eligible uninsured, 50-64 | 636 | +/- 5 percentage points |

Final update made on November 13, 2013 (no further updates will be made)
On April 12, 2011, Governor Martin O’Malley (D) signed SB 182/HB 166 into law establishing the Maryland Health Benefit Exchange (MBHE).1 In May of the following year, Governor O’Malley signed additional Marketplace legislation (SB 372/HB 433) which addressed multiple Marketplace implementation and operational issues and was based on recommendations by the Board of Directors and advisory groups from 2011.2 In August 2012, the state announced that the name for the new insurance Marketplace would be Maryland Health Connection.
Structure: The legislation defines the MBHE as a quasi-governmental organization, specifically a “public corporation and independent unit of state government.”
Governance: The MHBE is governed by a nine-member board, including the Executive Director of Maryland’s Health Care Commission as the Chair, Secretary of Health and Mental Hygiene, Commissioner of Insurance, and six members appointed by the Governor and with consent from the Senate. Half of these members represent employers and individuals using the Maryland Health Connection and half provide specific knowledge and expertise. Board members cannot be affiliated with a carrier, insurance producer, third-party administrator, managed care organization, person contracting or in position to contract with the Marketplace, or any trade associations for these entities.
Current appointed Board members are:Darrell Gaskin (Vice Chair) Johns Hopkins Bloomberg School of Public HealthKenneth Apfel, University of Maryland, School of Public PolicyGeorges Benjamin, American Public Health AssociationJennifer Goldberg, Maryland Legal Aid BureauEnrique Martinez-Vidal, AcademyHealth and Robert Wood Johnson FoundationThomas Saquella, Maryland Retailers Association
The Board hired an Executive Director in mid-September 2011.
The MBHE is required by statute to maintain at least two standing advisory committees, though the subjects may change to support the decision-making for that particular year. Currently, the Board has five advisory committees to study particular topics: implementation, the Navigator program, continuity of care, plan management, and web-based entities.3 Staff from the MBHE and other state agencies will look to the Advisory Committees to make recommendations on policy options, not to vote on policy decisions.
Contracting with Plans: In the first two years of operation, Maryland Health Connection will act as a clearinghouse with any qualified health plan (QHP) in the state eligible to participate. Beginning in 2016, Maryland Health Connection will have the authority to employ an alternative contracting option or active purchaser strategy, such as competitive bidding or negotiations with carriers.
Each carrier must offer at least one QHP in each of the bronze, silver, and gold metal levels. Carriers may submit a single zero cost-sharing plan at the bronze level that is available to Native Americans. Carriers may only offer four benefit plan designs per metal level in the individual and SHOP Marketplaces. This count excludes benefit plan designs that carriers are required by legislation to offer (e.g. catastrophic plans). Carriers in Maryland Health Connection will be allowed to rate by age, geography (the state is divided into four rating regions), and tobacco use.4
Carriers participating in the individual Marketplace must offer at least one silver and one gold level plan in the individual market outside of the Marketplace (if the carrier offers any plans outside of the Marketplace). The same applies for the small group market. Carriers must offer at least one catastrophic plan on the Marketplace if the carrier offers catastrophic plans outside the Marketplace. Carriers must also offer a child-only plan that is rated for child-only coverage in Individual markets inside and outside of the Marketplace.5
Carriers with state market share above a certain threshold must sell QHPs in Maryland Health Connection. The minimum participation threshold for carriers is $20 million in the small group market and $10 million in the individual market.
The MBHE board approved plan certification policies related to: service area designation; licensure and solvency; benefit design standards and review; marketing standards; review of rate changes; transparency and quality data; and access to essential community providers. The Marketplace will perform annual reviews of all participating carriers and provide performance reviews that highlight areas for improvement.6 Carriers will be required to complete corrective action plans based on the issues in the annual review, and recertification will occur biennially.7
In the first year, insurers will “self-define” network adequacy standards and submit provider data to the CRISP (Chesapeake Regional Information System for our Patients) Provider Information Management System. Insurance carriers will be required to participate in the Maryland Health Care Commission’s existing quality and performance evaluation system. In addition, carriers will be required to provide the MBHE with data each quarter regarding the number and type of providers available, the ability of enrollees to access services, and utilization and complaint data. The MBHE will accept Medicaid or Commercial accreditation and allow a one year grace period for non-accredited insurers to become accredited. In the second year of operation, the MBHE will reassess accreditation requirements, appropriate standardized network adequacy requirements, and other possible changes to plan management policies.
The Maryland Insurance Administration has approved premium rates for the individual market in 2014. Six carriers are participating in Maryland Health Connection’s individual market statewide,8 and all are offering coverage in the state’s largest rating area.9 Consumers will have a choice of 45 medical QHPs.10 Maryland’s Insurance Commissioner reduced the proposed premium rates by every insurance carrier in the individual market in Maryland, including reducing proposed increases for a majority of carriers by more than 50%. An analysis conducted by the Marketplace estimated that three out of four individuals and families expected to enroll for coverage through Maryland Health Connection will qualify for tax credits to reduce their health insurance rates.11
On September 17, 2013, the Maryland Insurance Administration approved health insurance policies and premium rates for plans to be sold through the Small Business Health Options Program (SHOP) for small employers.12 Thirteen carriers filed to sell health benefit plans in the small group market. The opening of the SHOP Marketplace has been delayed until April 2013 due to problems with the website. Small businesses with one to 50 full-time equivalent employees are eligible may enroll. Coverage begins on or after March 1, 2014. 13
Dental and Vision Plans: In December 2012, the Board revised the interim plan management policies and procedures for adult and pediatric dental and vision plans.14 The MBHE anticipates requiring that all adult vision and dental coverage be offered through stand-alone plans with price disclosure to allow consumers to compare options. Pediatric vision coverage cannot be offered through stand-alone plans and must always be offered as part of the health benefit plan or as an additional benefit that can be purchased along with the health benefit plan. Pediatric dental coverage can be offered as part of the health benefit plan, as an additional benefit that can be purchased separately, or through a stand-alone plan.
Thirty-six of the 45 medical plans available on the individual Marketplace will include embedded pediatric dental benefits. Four carriers will be offering a stand-alone dental benefit. All stand-alone dental plans will be offered statewide.15 Stand-alone pediatric dental plans in Maryland Health Connection are required to use the same out-of-pocket maximums as those required on the Federally Facilitated Marketplace, set at $1,000 for one child and $2,000 for two or more children.16
Risk Adjustment, Reinsurance, and Risk Corridors: Maryland intends to use federal services to administer the state’s risk adjustment program but the MBHE will administer the state’s reinsurance program.
Consumer Assistance and Outreach: In April 2013, Maryland Health Connection launched its consumer assistance program. The Marketplace awarded $24 million in grant funds to six regional organizations to serve as Connector Entities. An estimated 300 new jobs will be created by the establishment of these Connectors, which will employ Navigators and In-person Assisters to help individuals and small employers through outreach and education, eligibility determinations, and enrollment into Medicaid and QHPs.
In addition to the six Connector entities, nearly 50 subcontractors will support the outreach, education, and enrollment efforts of Navigators and Assisters throughout the state. These organizations include health departments, hospitals, health clinics, community-based organizations, homeless shelters, workforce development centers and faith-based organizations. The intent of the regional approach is to ensure that all populations are reached including those with Limited English Proficiency, disabilities or those that may be in underserved communities.
Navigators must be trained and certified by Connector Entities, and will help counsel and enroll residents into QHPs and Medicaid through the Marketplace. In-person Assisters are not certified, but will be trained to provide information, assistance, and enrollment into Medicaid. Both Navigators and Assisters will provide information about eligibility requirements for federal premium subsidies and cost-sharing assistance, and assess eligibility requirements for Medicaid and CHIP. Navigators and Assisters will provide referrals to appropriate agencies, including the Attorney General’s Health Education and Advocacy Unit (HEAU) and the Maryland Insurance Administration (MIA) for applicants and enrollees with grievances, complaints, questions or the need for other social services through the Department of Health and Mental Hygiene and the Department of Human Resources (Social Services).17
There are separate Navigator programs for the small group and individual markets. SHOP Navigators are required to obtain a special license from the Insurance Commissioner and training/authorization from the MBHE. Outreach Entities are encouraged, but not required, to provide SHOP Marketplace Navigator services through direct employment or engagement with SHOP Navigators. Staff can be trained to serve as Navigators to both the individual and SHOP Marketplaces, but the funding for the two Marketplaces will be tracked separately.
Maryland will also have Certified Application Counselors (CACs), certified individuals who are employed by or volunteer with a sponsoring entity (which may be a community-based organization, health care provider, unit of state or local government, or other entities). CACs are subject to the same requirements, restrictions, conflict of interest rules, and oversight applicable to Navigators; are not compensated by the Marketplace, carriers, producers, or third-party administrators for consumer assistance services; do not impose fees for consumer assistance services; must disclose conflicts-of-interest; and must act in the best interest of the consumer. CACs may provide information to, and help consumers apply for and enroll in qualified health plans (QHPs) and qualified dental plans. They may also provide information on insurance affordability programs and help consumers determine eligibility for, and access, tax credits. They may provide uniform, factual, unbiased information approved by the state’s Medicaid program about all participating MCOs and providers, but may not express an assessment about, select, or counsel an applicant about an MCO.18
Licensed insurance producers can sell plans both inside and outside Maryland Health Connection, after receiving training and authorization by MHBE. Producers will receive instruction on the Marketplace, insurance plans, federal tax credits and cost-sharing reductions, and will be paid directly by carriers. MBHE will require carriers to retain information about policies and procedures used to determine producer compensation both inside and outside the Connection. The Maryland Insurance Administration and the MBHE will use this information to assess whether additional action is necessary beginning in the second year of operations. Maryland Health Connection estimates that 2,000 brokers will become authorized to sell plans through the Marketplace.19
As of September 27, 2013, 164 Navigators, 170 Assisters, and 1,236 caseworkers have been trained. As of October 3, 1,827 producers have been trained. More training sessions are scheduled.20
The Consolidated Service Center is the main entry point for questions related to Maryland Health Connection, Medicaid eligibility and enrollment, and any other question related to health insurance.21 The Center manages calls from individuals, employees, employers, Navigators, Assisters, and others.
The consumer portal for Maryland Health Connection, with the new branding strategy, first went live in August 2012. On October 1, 2013, it began accepting applications online. Maryland Health Connection offers a variety of resources on its website in Spanish, including fact sheets, FAQs, and videos. It is working to the make the full website available in Spanish. It also offers a Spanish version of its application for health coverage and financial assistance, and bi-lingual staff in call centers and Connector Entities.22
On September 3, 2013, Maryland Health Connection launched its advertising and outreach campaign. The integrated campaign includes advertising, social media and partnership strategies developed to provide consumers with the information they require to shop, compare and select health insurance through Maryland Health Connection. The statewide campaign includes television, radio, print advertising, out of-home and digital media. Central to the campaign is custom music that reinforces the key benefits of health coverage, including peace of mind, convenience, financial security and access to health care. The custom music has been produced in four musical genres: contemporary, Latin, country and urban.23
During the open enrollment period, Maryland Health Connection will partner with the Baltimore Ravens to help raise awareness of the importance of health insurance and the availability of coverage options. Research shows that 71 percent of the uninsured population in Maryland have watched, attended or listened to a Ravens game in the past 12 months. Maryland Health Connection will also partner with Giant Food and CVS Pharmacy throughout the state to provide information and literature on health insurance for consumers.24
Small Business Health Options Program (SHOP) Marketplace: In 2014 and 2015, the size of small employers in the SHOP Marketplace will be limited to an average of 50 or fewer employees. In addition, the individual and SHOP Marketplaces plan to be merged in 2016. The SHOP will offer two coverage models for employers: an employer choice model in which the employer can select an insurer and allow employees to choose among all plans offered by that insurer; and an employee choice model in which the employer selects a metal tier and allows employees to select among all QHPs available within that tier. In order for an employer to purchase through the SHOP, current rules require 75% of employees to participate. Employees covered under other group health plans, enrolled in public programs, or for whom the coverage does not meet the federal definition of “affordable,” will not be included in the minimum participation calculation employers must have a minimum participation.25 However, the Policy and Government Relations Department is still working on regulations covering SHOP minimum participation, in addition to SHOP eligibility appeals and individual eligibility.26
Currently, third party administrators and brokers play a key role in the selection, purchase, and administration of insurance for small businesses.27 For this reason, Maryland Health Connectionis certifying entities to service the small group market on behalf of the Health Connection if they
In August 2013, Maryland Health Connection announced the opportunity for third-party administrators (TPAs) to become certified to participate in the administration of the SHOP Marketplace. Nearly 70 percent of small businesses in Maryland utilize TPAs to enroll in health benefits, and small employers rely on their services. TPAs will be able to help employers and employees compare and select qualified health plans (QHPs), administer enrollment and eligibility changes, and perform premium billing and collections. TPAs will be allowed to use Maryland Health Connections or the TPA’s systems to present and administer QHP information. Organizations that wish to become TPAs business partners must complete a certification process.28 They must also meet the criteria of the ACA and state requirements, adhere to a rigorous set of performance measure and service levels, and be subject to oversight by the Marketplace. These certified entities will receive compensation on a per-employee-per-month basis commensurate with what the market pays for services today, currently estimated at 0.5% to 1.0% of premiums. The Marketplace selected six organizations to be SHOP third-party administrator (TPA) partners for January 1, 2014.29
Financing: Once Maryland Health Connection is operational, it is authorized to collect fees or assessments from participating plans, though not to the extent that the fees create a competitive disadvantage with plans offered outside the Health Connection.
In September 2012, a subcontractor providing analytic support to the Joint Committee recommended a financing model that blends multiple approaches rather than relying on a single revenue source.30 An example hybrid financing approach might include a combination of revenue collected from the non-group, small group, and large group markets, providers, and cigarette sales. In December 2012, the Joint Committee submitted a report to the Governor and General Assembly which included the following recommendations: the state should use a combination of at least two revenue streams; a transaction-based assessment on the whole non-group and small group market is preferable to an assessment applied only to plans inside Maryland Health Connection; and a broad-based assessment on the larger group market and/or an increase in the tobacco tax should be considered, while an assessment on hospitals should not be considered.
Basic Health Program (BHP): Maryland is considering establishing an optional coverage program available through the Affordable Care Act (ACA) which allows states to use federal funding to offer subsidized health insurance to adults with incomes between 139 and 200% of the federal poverty level (FPL) who would otherwise be eligible to purchase subsidized coverage through a Marketplace. The DHMH, together with a subcontractor, completed an analysis of the effect of a BHP in Maryland and found that it may redirect funds away from Maryland Health Connection. In addition, the state would have to bear expenses related to program administration and quality monitoring. In February 2012, the MBHE Board agreed with the Department’s recommendation that a decision on the BHP be deferred pending availability of additional federal guidance and information about rates and fiscal risks to the state.31
Essential Health Benefits (EHB): The Affordable Care Act requires that all individual and small-group plans sold in a state, including those offered through the Marketplace, cover certain defined health benefits. The Maryland Health Care Reform Coordinating Council formed an advisory committee to assist in selecting the state’s EHB benchmark plan. On December 17, 2012, the Council reevaluated possible benchmark plans in light of new federal guidance and selected the state’s largest small group plan, CareFirst of Maryland (Blue Cross Blue Shield)-HMO HSA Open Access plan. The Council also designated the GEHA Standard Option federal employee plan for the Maryland’s behavioral health benefit. Finally, the council designated the state’s current mandated habilitative services for individuals up age 19 and adopted the small group rehabilitative benefit for as the habilitative benefit for individuals over age 19.32
The DHMH has received three federal grants: an Exchange Planning grant of $1 million; an Early Innovator grant of $6.2 million to develop a Marketplace IT infrastructure that could be replicated by other states; a Level One Establishment grant of $27 million to conduct data and policy analysis that will inform the technical and operational infrastructure of Maryland Health Connection and enable rapid implementation of the IT platform; and a Level Two Establishment Grant of $123 million to support continued policy development and consumer outreach, assistance, and education.33
In addition, Maryland, along with nine other states, is receiving technical assistance from the Robert Wood Johnson Foundation through the State Health Reform Assistance Network; this assistance includes help with setting up health insurance Marketplaces, expanding Medicaid to newly eligible populations, streamlining eligibility and enrollment systems, instituting insurance market reforms and using data to drive decisions.34
On December 7, 2012, Maryland received conditional approval from the U.S. Department of Health and Human Services (HHS) to establish a state-based Marketplace.35 The Maryland Health Connection Marketplace portal opened on October 1, 2013 and has begun enrolling qualified individuals and families into coverage. However, the opening of the SHOP has been delayed until April 2014.
Additional information about the Maryland Health Connection can be found at the state’s back office Marketplace website (Maryland Health Benefit Exchange) and its customer portal (Maryland Health Connection). You can also obtain information from Maryland Health Connection’s Facebook page, Twitter feed, or You Tube page.
As stakeholders gather for the 2013 International Conference on Family Planning in Ethiopia, a new Kaiser Family Foundation analysis finds donor governments provided about US$900 million in bilateral funding for family planning programs in 2012, and an additional US$432 million in core contributions to the United Nations Population Fund (UNFPA). The first of its kind, this report establishes a baseline level of donor government funding for family planning activities in 2012 that can be used to track total international assistance funding levels for family planning over time as well as commitments donor governments made at last year’s London Summit on Family Planning. Family planning services were defined to include counseling; information, education and communication activities; delivery of contraceptives; capacity building and training. The analysis finds the U.S. provided more than half of bilateral funding for family planning programs in 2012, providing US$485 million. It was followed by the U.K. (US$99.4 million), the Netherlands (US$65.5 million) France (US$49.6 million) and Germany (US$47.6 million).
In July 2012, the U.K. Government and the Bill & Melinda Gates Foundation – in partnership with the United Nations Population Fund (UNFPA), civil society organizations, developing countries, donor governments, the private sector, and multilateral organizations – co-sponsored the London Summit on Family Planning, an effort to provide voluntary family planning services to an additional 120 million women and girls in developing countries by 2020 through new commitments. A key step in assessing progress towards these commitments is tracking expenditures for family planning. While all financing sources are critical to helping to scale-up the response, donor governments provide a significant share of global funding for family planning services.1
This analysis establishes a baseline level of funding in 2012 that can be used to track total international assistance funding levels for family planning over time as well as specific donor government progress in meeting London Summit on Family Planning commitments. It examines funding for family planning provided by the 24 governments who were members of the Organisation for Economic Co-operation and Development (OECD), Development Assistance Committee (DAC) in 2012. Of these, eleven made specific commitments at the Summit to increase funding for family planning including: Australia, Denmark, the European Commission, France, Germany, Japan, Korea, the Netherlands, Norway, Sweden, and the U.K.2 In addition, there are several other donor governments, particularly the United States and Canada, which, while not making specific commitments at the Summit, also provide funding for family planning activities. In general, family planning services are defined to include the following activities: counseling; information, education and communication activities; delivery of contraceptives; capacity building and training. In addition, family-planning-related activities funded in the context of other official development assistance sectors (e.g. education, civil society) are reflected in this analysis. Key findings include (also, see Table):
In the wake of the commitments made during the London Summit, timely and accurate tracking of donor financing for family planning takes on new urgency. The data presented in this analysis should be considered a work in progress as donor governments refine existing methodologies to track funding for family planning activities. As we continue to track donor government funding for family planning in future years, we will aim to provide additional detail and trend analyses.
| Table: Donor Government Family Planning Disbursements, 2012 | |||
| Country | Bilateral Disbursements(US$ millions) | UNFPA – Core Contributions(US$ millions) | Total (US$ millions) |
| Australia | $42.7 | $14.9 | $57.5 |
| Canada | $41.5 | $17.4 | $58.9 |
| Denmark | $13.0 | $44.0 | $57.0 |
| France | $49.6 | $0.5 | $50.1 |
| Germany | $47.6 | $20.7 | $68.3 |
| Netherlands | $65.5 | $49.0 | $114.5 |
| Norway | $3.3 | $59.4 | $62.7 |
| Sweden | $41.2 | $66.3 | $107.5 |
| U.K. | $99.4 | $31.8 | $131.2 |
| U.S. | $485.0 | $30.2 | $515.2 |
| Other DAC Countries | $11.0 | $98.0 | $109.1 |
| Total | $899.8 | $432.3 | $1332.1 |
Access to family planning (FP) services has a significant impact on the health and wellbeing of women and girls, and on global health and development more broadly. Family planning – the ability of individuals and couples to determine their desired number of children as well as the timing of and spacing between births – can help prevent pregnancy-related health risks, reduce infant mortality, and help in the prevention of sexually transmitted diseases such as HIV/AIDS.3 Currently, it is estimated that more than 200 million women worldwide would like to delay or stop childbearing, but they do not have access to contraceptives.4 The international community has long recognized the importance of improving access to family planning services. In 1994, at the International Conference on Population and Development (ICPD), 179 governments committed to a 20-year plan of action aimed at providing, among other things, universal access to family planning and sexual and reproductive health services and reproductive rights. Additionally, in 2005, a specific target on reproductive health was added to Millennium Development Goal (MDG) 5, four years after the MDGs were first adopted by Member States of the United Nations. More recently, in July 2012, the U.K. Government and the Bill & Melinda Gates Foundation, in partnership with UNFPA, civil society organizations, developing countries, donor governments, the private sector, and multilateral organizations met at the London Summit on Family Planning and made commitments aimed at providing voluntary family planning services to an additional 120 million women and girls in developing countries by 2020 (see Box 1).
Box 1: International Conference on Population and Development (ICPD), Millennium Development Goals (MDGs), & the London Summit on Family PlanningInternational Conference on Population and Development (ICPD), 1994:
Millennium Development Goal (MDG) 5, 2000:
London Summit on Family Planning, 2012: “By 2020, the goal is to deliver contraceptives, information, and services to a total of 380 million women and girls in developing countries so they can plan their families.”
Box 2: Other Sources of Funding for FP in Low- & Middle-Income Countries
While this report focuses on donor governments, there are three other major funding streams for FP assistance: multilateral organizations, the private sector, and domestic resources.
Multilateral Organizations: Provide assistance for FP using pooled funds from member contributions and other means. The primary multilateral organization addressing FP is the United Nations Population Fund (UNFPA). Contributions to multilateral organizations are usually made by governments, but can be provided by private organizations and individuals, as in the case of UNFPA. Some multilateral organizations are designed to address specific issues (such as UNFPA, which also finances reproductive health and other population related activities); donor government contributions to UNFPA are highlighted as part of the donor government’s financing effort in this analysis. Donor government contributions to multilateral organizations that are not specifically designed to address population activities, but may include such activities within their broader portfolio (such as the World Bank), are not included in this analysis.
Private Sector: Foundations (charitable and corporate philanthropic organizations), corporations, faith-based organizations, and international non-governmental organizations (NGOs) provide support for FP activities in low- and middle-income countries not only in terms of funding, but through in-kind support; commodity donations; and co-investment strategies with government and other sectors.
Domestic Resources: Including both spending by country governments that also receive international assistance for FP and by households/individuals within these countries, represent a significant and critical part of the response.
This analysis establishes a baseline level of funding in 2012 that can be used to track total international assistance funding levels for family planning over time as well as specific donor government progress in meeting London Summit on Family Planning commitments. It includes an analysis of funding provided by the 24 governments who were members of the Organization for Economic Co-operation and Development (OECD), Development Assistance Committee (DAC) in 2012.6 Of these, eleven made specific commitments at the Summit to increase funding for family planning.[endnote 91389-1] In addition, there are several other donor governments, particularly the United States and Canada, which, while not making specific commitments at the Summit, also provide funding for family planning activities.
Data for this analysis were collected directly from donor governments and supplemented by the OECD Creditor Reporting System (CRS). For purposes of this analysis, family planning services were defined to include the following activities as specified in the CRS: counseling; information, education and communication (IEC) activities; delivery of contraceptives; capacity building and training.7 Where bilateral family planning funding was included as part of broader reproductive and maternal health activities or other non-health-sector activities, we worked directly with donor governments to identify family planning specific amounts to the extent possible (see Methodology for more information).
Donor government bilateral assistance for family planning includes both actual funding amounts provided (e.g., cash transfers) as well as other types of transactions and activities (e.g., technical assistance) and products (e.g., commodities). In 2012, donor governments are estimated to have disbursed8 US$899.8 million in bilateral funding for family planning activities (see Table & Annex).
The United States (US$485.0 million) was the largest bilateral donor in 2012 accounting for more than half (54%) of total bilateral assistance (see Figure 1). The U.K. (US$99.4 million, 11%) was the second largest bilateral donor followed by the Netherlands (US$65.5 million, 7%), France (US$49.6 million, 6%), and Germany (US$47.6 million, 5%).
The eleven donor governments that made commitments at the London Summit on Family Planning (Australia, Denmark, the European Commission, France, Germany, Japan, Korea, the Netherlands, Norway, Sweden, and the U.K.) accounted for US$371.8 million (41%) of total donor government disbursements for family planning in 2012.

While the majority of donor government assistance for family planning is provided bilaterally, donors also provide support for family planning activities through multilateral organizations, such as the United Nations Population Fund (UNFPA). Created in 1969, UNFPA supports sexual and reproductive health activities in many low- and middle-income countries and was a key partner in the London Summit on Family Planning (see Box 3).
Box 3: United Nations Population Fund (UNFPA) Mission, Goals, & London Summit on Family Planning Commitment
UNFPA Mission: Deliver a world where every pregnancy is wanted, every birth is safe, every young person’s potential is fulfilled.
UNFPA Goals:
UNFPA London Summit on Family Planning Commitment: “UNFPA will double the proportion of its resources focused on family planning from 25% to 40 % based on current funding levels, bringing new funding of at least US $174 million per year from core and noncore funds. This will include a minimum of US $54 million per year, from 2013-2019, in increased funding for family planning from UNFPA’s core resources.”
In 2012, donor governments provided US$432.3 million in core contributions to UNFPA.9 Sweden was the largest donor (US$66.3 million, 15%) followed by Norway (US$59.4 million, 14%), the Netherlands (US$49.0 million, 11%), Denmark (US$44.0 million, 10%), the U.K. (US$31.8 million, 7%), and the U.S. (US$30.2 million, 7%) (see Figure 2).

While it was not possible to calculate an adjusted “family planning share” of UNFPA’s 2012 budget and attribute a portion of a donor government’s UNFPA contribution to family planning specific activities,10 it is important to note the relative balance between a donor’s core-contributions to UNFPA and its bilateral funding for family planning. For instance, three of the ten donor governments profiled provided a larger contribution to UNFPA than their bilateral disbursement: Denmark, Norway, & Sweden.
The eleven donor governments that made commitments at the London Summit on Family Planning (Australia, Denmark, the European Commission, France, Germany, Japan, Korea, the Netherlands, Norway, Sweden, and the U.K.) accounted for US$311.7 million (71%) of total core-contributions to UNFPA in 2012.
The data provided in this analysis provide a baseline level of donor government funding for FP activities in low- and middle-income countries. At the London Summit on Family Planning donors made commitments totaling $2.6 billion in additional funding for family planning.11 While most donor governments have yet to finalize 2013 funding levels, preliminary data indicate two donor governments (the U.K. and Norway) have increased funding for family planning in 2013: U.K. family-planning-specific funding is estimated to be approximately US$105 million, a 5% increase over 2012 levels, and Norway has budgeted approximately $25 million in new family planning-specific funding. In addition, while family-planning-specific funding is not yet available, the Netherlands increased funding in 2013 for “Sexual and Reproductive Health & Rights, including HIV/AIDS” to US$504.1 million. The increases by the U.K. and the Netherlands fulfill their London Summit commitments. As donor governments conclude the 2013 fiscal year, it will be important to track funding for family planning activities in order to determine whether the London Summit commitments are being met.
Bilateral and multilateral data on donor government assistance for FP in low- and middle-income countries were collected from multiple sources. The research team collected bilateral assistance data directly for 10 governments: Australia, Canada, Denmark, Germany, France, the Netherlands, Norway, Sweden, the United Kingdom, and the United States during the first half of 2013. Data represent the fiscal year 2012 period for all governments except for Denmark and Germany (data are from FY/CY 2011). Direct data collection from these donors was desirable because they represent the preponderance of donor government assistance for family planning and the latest official statistics – from the Organisation for Economic Co-operation and Development (OECD) Creditor Reporting System (CRS) (see: http://www.oecd.org/dac/stats/data – are from 2011 and do not include all forms of international assistance (e.g., funding to countries such as Russia and the Baltic States that are no longer included in the CRS database). In addition, the CRS data may not include certain funding streams provided by donors, such as FP components of mixed-purpose grants to non-governmental organizations. Where donor governments were members of the European Union (EU), the research team ensured that no double-counting of funds occurred between EU Member State reported amounts and EC reported amounts for international FP assistance. Data for all other OECD DAC member governments – Austria, Belgium, the European Union, Finland, Greece, Ireland, Italy, Japan, Korea, Luxembourg, New Zealand, Portugal, Spain, and Switzerland – who collectively accounted for less than 2 percent of bilateral family planning disbursements, were obtained from the OECD CRS and are from calendar year 2011.
For purposes of this analysis, funding was counted as family planning if it met the OECD CRS purpose code definition: “Family planning services including counselling; information, education and communication (IEC) activities; delivery of contraceptives; capacity building and training.” In addition, family-planning-related activities funded in the context of other official development assistance sectors (e.g. education, civil society) are reflected in this analysis. Project-level data were reviewed for Canada, Denmark, France, Germany, the Netherlands, Norway, Sweden, and the United Kingdom to determine whether all or a portion of the funding could be counted as family planning. Family-planning-specific funding totals for Australia and the United States were obtained through direct communications with government representatives. Funding attributed to the United Kingdom represents budgeted disbursements. Funding totals presented in this analysis should be considered preliminary estimates approved by representatives of the 10 donor governments who were contacted directly.
It was difficult in some cases to disaggregate bilateral family planning funding from broader reproductive and maternal health totals, as the two are sometimes represented as integrated totals. In addition, family-planning-related activities funded in the context of other official development assistance sectors (e.g. education, civil society) have in the past remained largely unidentified. For purposes of this analysis, we worked closely with the largest donors to family planning to identify such family-planning-specific funding where possible (see Annex for detailed data table).
Bilateral funding is defined as any earmarked (FP-designated) amount. U.S. bilateral “enacted” data, or “commitments”, correspond to amounts appropriated for the 2012 fiscal year. UNFPA contributions from all governments correspond to amounts received during the 2012 calendar year, regardless of which contributor’s fiscal year such disbursements pertain to.
With some exceptions, bilateral assistance data were collected for disbursements. A disbursement is the actual release of funds to, or the purchase of goods or services for, a recipient. Disbursements in any given year may include disbursements of funds committed in prior years and in some cases, not all funds committed during a government fiscal year are disbursed in that year. In addition, a disbursement by a government does not necessarily mean that the funds were provided to a country or other intended end-user. Enacted amounts represent budgetary decisions that funding will be provided, regardless of the time at which actual outlays, or disbursements, occur. In recent years, most governments have converted to cash accounting frameworks, and present budgets for legislative approval accordingly; in such cases, disbursements were used as a proxy for enacted amounts. In the U.S. case, both enacted and disbursement data were available for analysis.
UNFPA core contributions were obtained from United Nations Executive Board documents; however, we were unable to determine what share of these core contributions are attributable to family planning specifically (since such funding is also used to support broader reproductive health and related efforts). To date, UNFPA family planning activities have often been reported as part of broader categories, including reproductive health and maternal and child health, as well as part of larger multisectoral efforts, including those in education, human rights, and capacity building. It is expected that such disaggregation will be available in the future and UNFPA reports that it is currently working to develop such a methodology for doing so. Other than contributions provided by governments to UNFPA, un-earmarked general contributions to United Nations entities, most of which are membership contributions set by treaty or other formal agreement (e.g., the World Bank’s International Development Association or United Nations country membership assessments), are not identified as part of a donor government’s FP assistance even if the multilateral organization in turn directs some of these funds to FP. Rather, these would be considered as FP funding provided by the multilateral organization, as in the case of the World Bank’s efforts, and are not considered for purposes of this report.
The fiscal year period varies by country. The U.S. fiscal year runs from October 1-September 30. The Australian fiscal year runs from July 1-June 30. The fiscal years for Canada and the U.K. are April 1-March 31. Denmark, France, Germany, the Netherlands, Norway, and Sweden use the calendar year. The OECD uses the calendar year, so data collected from the CRS for other donor governments reflect January 1-December 31. Most UN agencies use the calendar year and their budgets are biennial.
All data are expressed in US dollars (USD). Where data were provided by governments in their currencies, they were adjusted by average daily exchange rates to obtain a USD equivalent, based on foreign exchange rate historical data available from the U.S. Federal Reserve (see: http://www.federalreserve.gov/). Data obtained from UNFPA were already adjusted by UNFPA to represent a USD equivalent based on date of receipts.
| Donor Government Family Planning Disbursements, 2012* | |||||
| Country | London Summit on Family Planning Commitments | Bilateral(US$ millions) | Multilateral – UNFPA Core Contributions(US$ millions)** | Total(US$ millions) | Notes |
| Australia | “plans to spend an additional AUD58 million over 5 years on family planning, doubling annual contributions to AUD53 million by 2016. This commitment will form a part of Australia’s broader investments in maternal, reproductive and child health (at least AUD1.6 billion over five years to 2015).” | $42.7 | $14.9 | $57.5 | Australia identified US$44.6 in FY11/12 using the FP2020-agreed methodology, which includes a percentage of a donor’s core contribution to UNFPA. Australian bilateral funding was determined by adjusting its total funding level to take into account its UNFPA contribution. |
| Canada | (none) | $41.5 | $17.4 | $58.9 | Bilateral funding is for family planning and reproductive health activities (including life skills education) in FY12. |
| Denmark | “an additional $13 million over eight years,” | $13.0 | $44.0 | $57.0 | Bilateral funding is family planning specific in FY11, the most recent year available, and includes a specific contribution (in addition to its core contribution) to UNFPA’s “Reproductive Health Commodities Fund.” |
| France | “an additional €100m on Family Planning within the context of reproductive health through to 2015, in nine countries in francophone Africa.” | $49.6 | $0.5 | $50.1 | Bilateral funding is for a mix of family planning, reproductive health and maternal/child health activities in FY12. |
| Germany | “€400m … to Reproductive Health and Family Planning over 4 years, of which 25% (€100m …) are likely to be dedicated directly to Family Planning, depending on partner countries priorities..” | $47.6 | $20.7 | $68.3 | Bilateral funding is family planning specific in FY11, the most recent year available. |
| Netherlands | “€370 million in 2012 for sexual and reproductive health and rights, including HIV and health, and [plans] to extend this amount from €381 million in 2013 to €413 million in 2015.” | $65.5 | $49.0 | $114.5 | The Netherlands provided a total of US$484.8 million in FY12 for “Sexual and Reproductive Health & Rights, including HIV/AIDS” of which an estimated US$65.5 million was for family planning specific activities. In FY13, the Netherlands increased funding for “Sexual and Reproductive Health & Rights, including HIV/AIDS” to US$504.1 million. |
| Norway | “doubling its investment from US $25 million to US $50 million over eight years.” | $3.3 | $59.4 | $62.7 | Bilateral funding is family planning specific in FY12. For FY13, the Norwegian budget provides an estimated US$25 million in “new” (additional) family planning funding as well as a slight increase in its UNFPA contribution. |
| Sweden | … increasing “spending on contraceptives from its 2010 level of US $32 million per year to US $40 million per year, totaling an additional US $40 million between 2011 and 2015.” | $41.2 | $66.3 | $107.5 | Bilateral funding is for family planning and reproductive health in FY12. |
| U.K.*** | “. . . committing £516 million (US $800 million) over eight years . . .” | $99.4 | $31.8 | $131.2 | Bilateral funding is family planning specific in FY12/13. Family planning specific funding is estimated to increase to US$103 million in FY13/14. |
| U.S. | (none) | $485.0 | $30.2 | $515.2 | USAID stipulates that specified bilateral subtotal is family planning specific in FY12. |
| Other DAC Countries**** | – | $11.0 | $98.0 | $109.1 | Bilateral funding was obtained from the Organisation for Economic Co-operation and Development (OECD) Credit Reporting System (CRS) database and represents funding provided in 2011, the most recent year available. |
| Total | $899.8 | $432.3 | $1332.1 | ||
| *A disbursement is the actual release of funds to, or the purchase of goods or services for, a recipient. Disbursements in any given year may include disbursements of funds committed in prior years and in some cases, not all funds committed during a government fiscal year are disbursed in that year.**All UNFPA core contributions are for FY 2012.***U.K. funding totals are budgeted disbursements.****Austria, Belgium, European Union, Finland, Greece, Ireland, Italy, Japan, Korea, Luxembourg, New Zealand, Portugal, Spain, and Switzerland. The Czech Republic, Iceland, and the Slovak Republic became members of the DAC in 2013 and therefore, were not included in the analysis. | |||||