Understanding the Impact of New Treatments on HIV Testing: Summary of a Forum

Published: Jan 1, 1998

Recognizing this as a critical time in the HIV epidemic, the Kaiser Family Foundation convened a meeting on January 28 – 30, 1998 to re-examine HIV testing. Participants from community agencies, advocacy groups, national associations, and all levels of government, as well as researchers and legal experts, were brought together. This document summarizes their discussions on current understanding of and new research on HIV testing, identifying key concerns, and discussions on how to enhance HIV testing programs and policies. The primary principle which emerged during the meeting was that knowledge of HIV status is desirable because it allows individuals to make informed treatment and prevention decisions.

Kaiser Family Foundation/Harvard University National Survey of Americans’ Views on Consumer Protection in Managed Care – News Release

Published: Jan 1, 1998

Kaiser/Harvard National Survey of Americans’ Views On Consumer Protection In Managed Care

Public Supports Broad Range Of Proposals For Federal Consumer Protection In Managed Care, But Potential Consequences Raised By Critics Also Hit Home

Embargoed for release until: 9:30 a.m. ET, Wednesday, January 21, 1998

For further information contact: Matt James or Tina Hoff

Access to Specialists Public’s Number One Consumer Protection Priority

Washington, DC — As the debate over regulation of the health care market takes shape, a new survey by the Kaiser Family Foundation and Harvard University finds that significant majorities of Americans favor the key measures intended to protect consumers in the President’s “Consumer Bill of Rights” and in legislative proposals before the Congress. Close to half of Americans — 48 percent — report that they personally, or someone they know, have experienced at least one of the problems addressed by the proposed regulations, including needing more information about health plans (29%), difficulty getting permission to see a medical specialist (24%), problems getting a plan to pay an emergency room bill (19%), and being unable to file an appeal to an independent agency for a denied claim (17%).

However, some of the arguments already being voiced against Federal regulation by its critics — that it will result in higher insurance premiums, too much government involvement in health care, and will cause employers to drop coverage — worry many people and weaken support.

“The consumer protection measures being proposed are modest steps that address some of the problems people are having in managed care,” said Drew E. Altman, Ph.D., President, Kaiser Family Foundation. “But, support may fall if the public comes to see them as part of a larger government health reform plan that could result in employers dropping coverage or higher health insurance premiums.”

Among the arguments against regulation made by critics, Americans respond most strongly to the possibility of some employers dropping health care coverage. Hearing that a measure might increase the cost of health insurance or might get the government “too involved” in health care also results in a drop in support, although majorities still support legislation on four out of six of the proposed requirements for health plans: providing more information, allowing direct access to gynecologists, paying for emergency room visits, and allowing independent appeals.

Public Favors Consumer Protections, But Consequences Raised By Critics Register

Would you favor a law requiring health plans to … Would you still favor such a law if you heard it might result in … An increase in insurance premiums Government too involved Employers dropping coverage Provide more informationabout how health plans operate 92% 58% 55% 54% Allow denied claims to be appealedto independent reviewer 88% 63% 51% 49% Allow a woman to see a gynecologist without pre-approval 82% 63% 51% 48% Provide greater access to medical specialists 81% 58% 47% 46% Pay for emergency room visits 79% 62% 52% 48% Allow patients to sue for malpractice 64% 48% 38% 36%

When asked which among six consumer protection proposals they would give the greatest priority, requiring health plans to provide greater access to medical specialists, including gynecologists, was the public’s top priority. It is named by 37 percent of Americans, followed by, laws mandating that plans pay for emergency room visits (18%) and provide more information about benefits and policy (18%). The right to sue health plans directly for malpractice ranked last among these proposals with just 8 percent of Americans naming this as the most important one.

The “Bill of Rights”

Three quarters of the public (72%) support passing into law the “Consumer Bill of Rights,” proposed by a Presidential advisory commission at the end of last year and endorsed by the President; 17 percent oppose. After hearing of the potential consequences raised by critics, support for the “Bill of Rights”declines. The support declines the most when the effect is believed to have a greater magnitude. When presented with the possibility of premium increases: 43 percent would still favor it if their premium increase were small, $1-5 per month (43% would oppose), but drops to 28 percent if their increase were larger, $15-20 per month (57% would oppose). About half (48%) would still favor the “Bill of Rights” if it meant the government were “somewhat more” involved (38% would oppose), and 45 percent if the government were involved “a lot more” (40% would oppose). Support declines markedly if people believe employers would drop coverage: 20 percent would favor if passing it if it meant only a “small number of employers” dropped coverage (65% would oppose), and 13 percent if a “large number of employers” dropped coverage (73% would oppose).

“If the public sees the debate as being about an abstract consumer bill of rights, support will not be sustained in the face of possible negative consequences,” said Robert J. Blendon, Sc.D., Professor of Health Policy and Political Analysis, Harvard University. “But, if it is framed around the specific concerns people have the public will stay on board.”

Yet, as the debate over the new “Bill of Rights” starts, many Americans are confused about what it is actually proposed to do. Just 15 percent are aware that its primary purpose is to recommend practices health insurance plans should follow to ensure patients are treated fairly and get the care they need. Close to a quarter (22%) wrongly believe it calls for universal health coverage, and 9 percent think it would tell doctors how to treat certain medical conditions. Twenty-one percent (21%) think it does all three. A third (33%) are simply unsure what it is about. Most Americans do not think the “Bill of Rights” is the same as President Clinton’s previous health reform plan. Just 7 percent believe it is very similar to the Clinton plan, 27 percent consider it a “scaled-down version,” and 24 percent say it is a different proposal that calls for more modest changes. But, many — 42 percent — can’t say how it compares, if at all.

Regulation: Who Should Do It?

As compared to how effective Americans perceive regulation to be in protecting consumers in other areas — including, automobile safety, food safety, airline safety, and protections against environmental hazards — current government action in the area of health insurance ranks last. A majority (53%) say the government has not been effective in protecting the interests of health care consumers (34% say “somewhat effective” and 7% say “very effective”). By comparison, 82 percent say auto safety regulation has been effective (53% say “somewhat effective” and 29% say “very effective”).

When asked who should protect managed care consumers, a majority (57%) of Americans think the primary responsibility should rest with a non-government independent organization; a quarter (23%) think the government should serve this function, and 15 percent say it is the managed care industry itself. However, when specific agencies such as the Securities and Exchange Commission or the Federal Aviation Administration are given as examples, half (51%) would favor establishing a new independent regulatory agency to oversee the health insurance industry; 43 percent say creating such an agency would expand government’s role too much and increase health care costs.

A question about a telephone hotline for health care consumers to call to get help with problems underscores Americans’ skepticism about the government. While 70 percent of Americans say it is “very important” to have such a service, just 43 percent say it is “very important” if the government were responsible for setting up the hotline.


Methodology

The Kaiser/Harvard National Survey of Americans’ Views on Consumer Protections in Managed Care is a product of the Kaiser-Harvard Program on the Public and Health/Social Policy. It was designed and analyzed by researchers at the Kaiser Family Foundation and Harvard University. The survey was conducted by telephone by Princeton Survey Research Associates with 1,204 adults (age 18 or older) nationwide between December 12-30, 1997. Additional questions were asked as part of a national omnibus telephone survey of 1,012 adults (age 18 or older) conducted January 8-12, 1998. The margin of sampling error for both national samples are plus or minus 3 percent. The margin of sampling error may be higher for some of the sub-sets in this analysis.

The Kaiser Family Foundation, based in Menlo Park, California, is a non-profit, independentnational health care philanthropy and is not associated with Kaiser Permanente or KaiserIndustries. The Foundation’s work is focused on four main areas: health policy, reproductive health, and HIV in the United States, and health and development in South Africa.

Copies of the questionnaire and top line data for the findings reported in this release available by calling the Kaiser Family Foundation’s publication request line at 1-800-656-4533 (Ask for #1356). Also available is the top line data from the Kaiser Family Foundation/Harvard 1997 National Survey of Americans on Managed Care (Ask for #1328). These documents are also available on the Kaiser Family Foundation website at http://www.kff.org.

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Kaiser/Harvard National Survey of Americans’ Views On Consumer Protection In Managed CarePress Release Survey Chart Pack

National Survey of Small Business Executives on Health Care

Published: Dec 31, 1997

A survey of 800 small business executives on their views on health care and the coverage they offer their employees. The survey also asked small employers how they feel about current proposals to protect consumers and regulate managed care.

The Dynamics of Current Medicaid Enrollment Changes – Report

Published: Dec 31, 1997

The Dynamics of Current Medicaid Enrollment Changes

Report available in PDF format.Return to top

The Dynamics of Current Medicaid Enrollment ChangesReport

Poll Finding

Kaiser Family Foundation/Princeton Survey Research Associates Study of Media Coverage of Managed Care: January 1990 – June 1997

Published: Dec 31, 1997

An analysis of media coverage (both print and broadcast) of managed care, from January 1 1990 to June 30, 1997. The study found that early coverage focused on managed care as a business story, and later years focused more on patient care and concerns about backlash. Overall, the media was found to be neutral in its coverage of managed care, although network TV and special series in newspapers were mostly critical.

The Dynamics of Current Medicaid Enrollment Changes

Published: Dec 31, 1997

Insights three focus groups consisting mainly of state officials with everyday involvement in welfare and Medicaid eligibility issues. The groups were asked to identify and discuss the important forces and factors behind the overall changes in enrollment.

Native Americans and Medicaid: Coverage and Financing Issues – Report

Published: Dec 30, 1997

Native Americans and Medicaid:Coverage and Financing Issues

Prepared by Andy Schneider and JoAnn Martinez, The Center on Budget and Policy Priorities for The Kaiser Commission on the Future of Medicaid

December 1997

Table Of ContentsHighlights ii I: Background On Native American Health Care 1 II: Medicaid’s Role For Native Americans 4 1. Medicaid as a Source of Health Coverage 4 2. Medicaid as a Source of Revenue for Hospitals and Clinics 6 3. Medicaid and Managed Care 10 4. Medicaid as Medicare Premium Assistance 14 5. Medicaid as a Source of Long-Term Care Coverage 15 III: Policy Issues For Native Ameircans In Managed Care 16 1. Policy Issues 16 2. Conclusion 18 Endnotes 20 Tables 22 Highlights

There are an estimated 2.3 million Native Americans — American Indians and Alaska Natives — in the U.S. About half of the Native American population lives on or near reservations; the other half resides in other rural areas and in urban areas. The Native American population includes 554 tribes recognized by the federal government as well as other tribes, largely in California, that do not have federal recognition.

Medicaid plays several significant roles for Native Americans. The Medicaid program acts as:

  • An insurance program covering physician, hospital, and other basic health care services for eligible Native Americans, especially families with children;
  • A source of revenue for Indian Health Services (IHS) and tribally-operated clinics and hospitals;
  • A purchaser of managed care products;
  • A source of financial assistance for low-income elderly and disabled Native Americans to meet Medicare premium and cost-sharing obligations; and
  • A source of coverage for nursing home care and other long-term care services for frail elderly and disabled Native Americans.

All Native Americans that are members of federally recognized tribes are eligible to receive services from the IHS. Because of high rates of poverty among Native Americans, Medicaid is an important publicly funded health program for Native Americans. In 1996, it is estimated that Medicaid covered nearly 40 percent of the Native American population.

Medicaid as a Source of Revenue

Medicaid is an important source of revenue for Native American health facilities. In fiscal year 1997, IHS and tribally operated facilities were projected to receive $184.3 million in Medicaid reimbursements. This amount is equal to about 10 percent of the $1.8 billion appropriated for IHS and tribally-provided health services that year. Medicaid is an open-ended entitlement program. In contrast, the IHS receives funding through the domestic appropriations which are subject to broad caps over the next five years. As a result, Medicaid payments will become an increasingly important source of funding for many IHS, tribal, and urban programs.

The structure of the Medicaid program provides financial incentives for states to encourage beneficiaries to use tribal health facilities. Medicaid is a matching program under which the federal government contributes money to the states to pay for covered services on behalf of Medicaid beneficiaries. The federal government’s share of these costs ranges from 50 percent in wealthier states to nearly 80 percent in the poorest states. On average, the federal government pays 57 percent of a state’s Medicaid costs. In contrast, the cost of services provided to Medicaid beneficiaries by a hospital, clinic, or other facility of the IHS or by a tribe or tribal organization is matched by the federal government at a 100 percent rate in a Memorandum of Agreement (MOA) between IHS, the Health Care Financing Administration (HCFA), December 19th 1996. Thus, the state is fully reimbursed by the federal government and is not required to contribute any of its own funds toward the cost of care. This provision does not apply to urban Indian programs.

Medicaid and Managed Care

Over the past few years, Medicaid in many states has been shifting from a predominantly fee-for-service program to a program that purchases services from managed care organizations (MCOs) or primary care case management organizations (PCCMs). This shift presents critical policy issues for the IHS, tribal health programs, and urban Indian health programs. Provisions in the Balanced Budget Act of 1997 will accelerate these changes.

  • Mandatory Beneficiary Enrollment in Managed Care. Under the Balanced Budget Act, states have the authority to require most Medicaid beneficiaries to enroll in MCOs or PCCMs. States can only require Native Americans in Medicaid to receive services through an MCO or PCCM if the MCO or PCCM is the IHS, a tribally operated program, or an urban Indian health program. States do not have authority to require Medicaid-eligible Native Americans to enroll in MCOs that are not operated by the IHS, a tribe, or an urban Indian organization. States do have the authority to require such enrollment under “section 1115” demonstration waivers or under “section 1915(b)” program waivers. Native Americans, who are eligible for Medicaid, have the choice of enrolling in any participating, Medicaid MCO operating in their area.
  • Capitation Payments under Medicaid Managed Care. The December 1996 MOA does not expressly address payments to MCOs. Presumably, the 100 percent federal matching rate is payable to MCOs or PCCMs operated by the IHS or tribes. This interpretation would be consistent with the clear policy for fee-for-service arrangements.
  • Strategic Choices for Native American Health Facilities. Managed care dramatically affects the strategic choices available to Native American health facilities.
    • IHS facilities can establish their own MCO or PCCM and seek to contract with the state to enroll Indian and non-Indian Medicaid beneficiaries; subcontract with a private MCO or PCCM and provide services to the Indian and non-Indian enrollees of that MCO or PCCM; or continue to be reimbursed by Medicaid on a fee-for-service basis and remain unaffiliated with any Medicaid MCO or PCCM.
    • Tribally owned and operated services face similar choices with two important differences. If they are also a Federally Qualified Health Center (FQHC), then they have additional financial protections until 2003. Second, they may be able to assume financial risk, allowing them the option of becoming an MCO.
    • Because urban Indian facilities are historically underfunded and do not benefit from the 100 percent matching rate, they face considerably greater challenges in adapting to the managed care environment. Their most viable option is to attempt to subcontract with an MCO or PCCM although there are no guarantees that this approach will be successful.

Native Americans and Medicaid: Coverage And Financing Issues

Traditionally, Native Americans have relied upon the facilities and programs of the Indian Health Service (IHS) for access to health care. Although the IHS remains the primary source of health care delivery and financing for most Indian tribes, public programs such as Medicare and Medicaid are playing a larger and larger role in the financing of care for Native Americans living on or near reservations as well as those in urban areas. Because of the high incidence of poverty among American Indians and Alaska Natives, Medicaid – the federal-state health care program for low-income people – is of particular importance.

Medicaid plays several different roles of significance to Native Americans. Medicaid is an insurance program, offering coverage for physician, hospital, and other basic health care services to eligible Indians, especially families with children. It is a source of revenue for IHS and tribally-operated clinics and hospitals that deliver those basic services. Through its purchase of managed care products, Medicaid is reshaping the health care delivery system for many Native Americans and other underserved low-income populations. Medicaid also assists low-income elderly and disabled Indians who are eligible for Medicare in meeting their premium and cost-sharing obligations. Finally, Medicaid offers coverage for nursing home care and other long-term care services needed by frail elderly and disabled Native Americans.

This Policy Brief provides an overview of Medicaid from the standpoint of Native Americans with an emphasis on Medicaid as an insurance program and a purchaser of managed care. This Brief supplements other Policy Briefs and background materials on Medicaid issued by the Commission.1 It incorporates the changes to Medicaid made by the Balanced Budget Act of 1997.2 This Policy Brief focuses on those federal policies common to all state Medicaid programs and does not review the details of any particular state program. Because Medicaid is administered by states within broad federal guidelines, Medicaid programs vary significantly from state to state with respect to benefits, eligibility, provider payment, and administration. However, the information contained in this Policy Brief is the starting point for understanding the Medicaid program in any particular state.

I: Background On Native American Health Care

There are an estimated 2.3 million Native Americans – American Indians and Alaska Natives – in the U.S. About half of the Native American population lives on or near reservations; the other half resides in other rural areas and in urban areas. The Native American population includes 554 tribes recognized by the federal government as well as other tribes, largely in California, that for various reasons do not have federal recognition. The federally recognized tribes vary in size from less than 100 to more than 100,000 members. The economic status of these tribes varies substantially; some are wealthy, but many face conditions of high unemployment and high rates of poverty. Indians in urban areas, who are frequently not enrolled members of federally-recognized tribes, are often unemployed.

The driving force for many of the health status and health coverage problems facing Native Americans as a whole is poverty. Not all Indians are poor, but a very large proportion of them are. U.S. Census data indicate that in 1996, 30.9% of Native Americans as a whole had family incomes below the poverty line, in comparison with 13.8% for the U.S. population as a whole.

The health status of Native Americans is significantly lower than that of the rest of the U.S. population. 3 According to the Indian Health Service (IHS) of the Department of Health and Human Services, the age-adjusted mortality rate for American Indians and Alaska Natives residing in the areas served by the IHS was 594.1 (per 100,000 population) for calendar years 1991-1993, compared to a rate of 504.2 for the entire U.S. population in 1992. ,4 In some IHS areas, the rate is double that of the total U.S. population. For instance, in the South Dakota, North Dakota, Nebraska and Iowa area the rate for calendar years 1991-1993 was 1,045.9.

Although there are significant variations from area to area, Native Americans as a whole have higher rates of death and injury caused by accidents and violence (including suicide and homicide) than the U.S. population generally. For the same 1991-1993 period, the IHS service area population had an accident mortality rate of 83.4 (per 100,000 population), compared with a rate of 29.4 for the entire U.S. population in 1992. Many of these deaths are related to the high incidence of alcohol abuse in a number Indian communities. Native Americans have higher rates of mortality from alcoholism than the U.S. population generally. The alcoholism mortality rate for the IHS service area population was 38.4 (per 100,000 population) over the 1991-1993 period compared to a rate of 6.8 among the entire U.S. population in 1992. Finally, the incidence of diabetes among Native Americans is significantly higher than that among the U.S. population generally. The diabetes mellitus mortality rate for the IHS service area population was 31.7 (per 100,000 population) over the 1991-1993 period, in comparison with the rate of 11.9 among the entire U.S. population in 1992.

The agency responsible for providing or paying for the provision of health services to most American Indians and Alaska Natives is the Indian Health Service (IHS). The IHS estimates its 1996 patient population – i.e., those eligible for health care services provided through or paid by the IHS – at 1.4 million Native Americans, most of whom live on reservations. This represents about three-fifths of the 2.3 million Native Americans in the U.S. Eligibility for IHS care is determined under federal statute and regulation and depends largely (but not exclusively) upon membership in a federally-recognized tribe and residence on or near a reservation. Federal recognition of a tribe is generally predicated on treaty or federal statute or both.

The IHS delivers care directly to Indians who meet IHS eligibility criteria through 40 hospitals, 64 health centers, 5 school health centers, and 50 smaller health stations located in 17 states. The IHS also makes arrangements, through contracts or “compacts,” directly with Indian tribes to deliver care to their own members. Currently tribes operate 9 hospitals, 116 outpatient health centers, 5 school health centers, 56 smaller health stations, and 171 Alaska village clinics under these arrangements. Finally the IHS funds 34 urban Indian programs ranging from outreach and referral programs to outpatient health clinics. Specialized and/or expensive diagnostic and treatment services that the IHS (or tribes) cannot offer directly through their own facilities in a particular area may, subject to the availability of funds, be purchased from non-IHS (or non-tribal) providers on a fee-for-service basis through the “contract health services” (CHS) program. Urban Indian programs do not have access to CHS funds.

In 1997, 57.2 percent of the $1.8 billion appropriated to IHS for services was spent on IHS direct operations, 41.5 percent was spent on tribally-operated hospitals and clinics, and 1.4 percent was spent on urban Indian programs. Of the $1.1 billion appropriated to IHS for direct services, $235 million, or 22 percent, took the form of contract health services purchased from non-IHS providers. The comparable CHS figure for tribal providers was $133.4 million, or 18 percent of the total $750 million in fiscal year 1997 appropriations allocated to tribal providers.

II: Medicaid’s Role For Native Americans

Medicaid as a Source of Health Coverage

In part because of high rates of poverty and unemployment, Native Americans are less likely than other Americans to have employer-sponsored or other types of private health insurance coverage. In addition, Native Americans are less likely to be enrolled in public health insurance programs like Medicare and Medicaid. According to U.S. Census data for 1996, 18.1 percent of Native Americans had no health insurance while 47.7 percent had private insurance, 39 percent were enrolled in Medicaid, 10.1 percent were enrolled in Medicare, and 4.1 percent were covered through the Civilian Health and Medical Programs of the Uniformed Services (CHAMPUS).5 The IHS data base indicates that, as of August 12, 1997, of the 1,784,000 individuals registered as IHS patients, 466,000, or 26 percent, were eligible for Medicaid.6

Nationally, Medicaid is the second largest health insurance program after Medicare. The Congressional Budget Office estimates that in 1998 Medicaid will cover 44 million individuals, half of whom are children. Each of these individuals is entitled to have payment made on his or her behalf for covered services received from participating hospitals, physicians, and other providers. Medicaid benefit packages vary from state to state, but they all include physician services; laboratory and x-ray services; inpatient and outpatient hospital services; early and periodic screening, diagnostic, and treatment (EPSDT) services for children; and services provided by federally qualified health centers (FQHCs).

Individual Entitlement

Individuals who meet Medicaid eligibility standards are entitled to coverage. This applies to Native Americans as it does to other American citizens. Historically, some state and local officials viewed the health coverage of American Indians and Alaska Natives as exclusively a federal responsibility and sought to exclude Native Americans from Medicaid coverage.7 Although Medicaid is administered and financed in part by the states, Native Americans who meet the Medicaid eligibility requirements of the state in which they reside are, as a matter of law,8 entitled to Medicaid coverage.9 This is true whether a Native American lives on or near a reservation or in an urban area, and whether or not a Native American is eligible for IHS services.10

Eligibility Requirements

To qualify for Medicaid in any particular state, an individual must be a resident of that state. In addition, regardless of the state in which an individual resides, an individual must meet both categorical eligibility requirements and financial eligibility requirements. Categorical eligibility requirements relate to the age or characteristics of an individual: children, pregnant women, elderly, and disabled are among the categories of individuals that may qualify for Medicaid. Financial eligibility requirements relate to the amount of income or assets an individual is permitted to have (standards), and how those amounts are calculated (methodologies). Individuals who do not meet the categorical requirements – for example, non-elderly adults who are not disabled and do not have children – may not qualify for Medicaid no matter how poor they are. There are exceptions to this general rule. Some states cover poor single adults under “section 1115” demonstration waivers granted by the Secretary of Health and Human Services. 11

States have flexibility within broad federal guidelines to establish eligibility rules for their Medicaid programs, but there are certain groups of individuals that any state receiving federal Medicaid matching funds must cover. For example:

  • with respect to children, states must at a minimum cover all infants up to age one (and pregnant women) with family incomes at or below 133 percent of the poverty level ($17,729 per year for a family of three in 1997), all children under age six with family income at or below 133 percent of the federal poverty line, and all children under age 14 with family income below 100 percent of the federal poverty line ($13,330 per year for a family of three in 1997). Many states have elected to set higher Medicaid eligibility thresholds for children under regular Medicaid law or under demonstration waivers.
  • with respect to elderly and disabled individuals, states must at a minimum cover those individuals receiving benefits under the Supplemental Security Income (SSI) program. The exception to this rule is that states may use eligibility standards that were in effect in 1972 in determining eligibility for elderly or disabled individuals; 11 states have opted to do so.

Table 1 shows the Medicaid income eligibility thresholds in effect in each state as of October, 1997, for pregnant women, children, and aged and disabled individuals. These data, which were made available by the National Governors’ Association, describe the thresholds as a percentage of the federal poverty level.

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Native Americans and Medicaid: Coverage and Financing IssuesReport Part One Report Two Report Three Report Four

Covering Mental Health: A Resource Guide for Reporters and Editors

Published: Dec 30, 1997
  • Resource List: Covering Mental Health: A Resource Guide for Reporters and Editors

The Medicare Program: Servicios De Salud Administrados Por Medicare

Published: Dec 30, 1997

Panorama General: Medicare proporciona servicios de salud a casi 39 millones de norteamericanos, incluyendo aproximadamente a 34 millones de ancianos y a 5 millones de discapacitados. La gran mayoria de estas personas cubren sus gastos medicos directamente mediante el programa tradicional de “pago por servicio,” mientras que el 15 porciento restante (mas de 5 millone de beneficiarios) estan cubiertos bajo algun plan de servicio medico contratado con Medicare, principalmente las organizaciones de administracion de la salud (HMO por sus siglas en ingles).

  • Fact Sheet: Servicios De Salud Administrados Por Medicare