Thursday, February 2, 2012
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This free, monthly update synthesizes news coverage from hundreds of print and broadcast news sources related to health and health care issues affecting underserved and racial and ethnic communities.
The update also summarizes recent journal articles and other research developments in the field and features a data slide from a relevant Kaiser Family Foundation publication.
DISPARITIES IN THE NEWS
1. In Maryland, A Prescription for Better Health Care
2. More Docs No Help for Racial Colonoscopy Gap
3. Programs Improve Diabetes Care in Low-Income Areas
4. Asian-Americans More Apt to Die in Hospital After Heart Attacks
5. Lower Risk of Death Linked With Access to Key Attributes of
Primary Care, UC Davis Study Shows
6. Blacks’ Health Care: ‘Looking for Ways to Close The Gap’ in
Maryland
7. The Income Penalty For Diabetes: $160,000
8. New Clues Revealed in Studies of Stillbirth
9. Black Health Care Coalition Advocates for Health Choices
10. Healthcare Plan for Low-Income Adults Includes Mental Health
Benefit
11. NAMI Program Offers Life Coaching to Those with Mental
Illnesses
12. Family Support Motivates Mexican-Americans to Adopt Healthy Habits
13. Cancer Deaths Drop, But Incidence Rises
14. In Extreme Old Age, Blacks Outlive Whites on Average
15. Diagnosis, Treatment of Depression Among Elderly Depend On
Racial, Cultural Factors
DISPARITIES IN RESEARCH
16. Trends in Melanoma Mortality Among Non-Hispanic Whites by
Educational Attainment, 1993 – 2007
17. Lower Socioeconomic Status and Disability Among US Adults With
Chronic Kidney Disease, 1999 – 2008
18. Hispanic Lesbians and Bisexual Women at Heightened Risk or
Health Disparities
19. Characteristics Associated with the Initiation of Radiation
Therapy After Breast-Conserving Surgery among African American and
White Women Diagnosed with Early-Stage Breast Cancer in Maryland,
2000 – 2006
20. Medical Expenditures Among Immigrant and Nonimmigrant Groups in
the United States
21. Impact of Electronic Health Records on Racial and Ethnic
Disparities in Blood Pressure Control at US Primary Care Visits
22. The Impact of Socioeconomic Inequalities and Lack of Health
Insurance on Physical Functioning Among Middle-Aged and Older
Adults in the United States
23. Children With Cerebral Palsy: Racial Disparities in Functional
Limitations
24. Disability Among Lesbian, Gay, and Bisexual Adults:
Disparities in Prevalence and Risk
25. Racial and Ethnic Disparities in Obesity During the Transition
to Adulthood: The Contingent and Nonlinear Impact of Neighborhood
Disadvantage
DISPARITIES DATA SPOTLIGHT
Financial and Educational Worries by Race
DISPARITIES IN THE NEWS
1. In Maryland, A Prescription for Better Health Care
A recent article in the Washington Post discussed some of the geographic health disparities that exist in Maryland and what Lt. Gov. Anthony G. Brown and others are doing to improve the situation.
Areas with a high population of people of color are more likely to experience higher rates of chronic disease, low-birthweight babies and limited access to care. One such area is Prince George County, Maryland, which includes a high population of blacks, in addition to high rates of asthma, HIV infection, diabetes, and a limited number of primary care medical facilities according to the article. Furthermore, a 2007 Rand report estimated that 80,000 adults in Prince George County, MD were uninsured. This rate was more than double the rate in Howard County, and nearly 33 percent higher than the rate in Montgomery County. The article noted out that most uninsured residents wait until the last minute to seek care, and the care they do receive tends to be more expensive. Lt. Gov. Anthony G. Brown unveiled a proposal to reduce health disparities within the state. This proposal was created by a group headed by E. Albert Reece, dean of the University of Maryland medical school. The group recommended that the Maryland legislatures create health-care zones, which would give local governments the authority to office incentives to providers to encouragement them to practice in underserved areas. The idea is similar to economic-enterprise zones. “There is, I think, both a moral imperative and, quite frankly, an economic imperative and a case to be made that health disparities need to be eliminated,” Brown said.
Brown hopes to roll out a pilot program in the fall, which he hopes will bring down the cost associated with health disparities in the state. The pilot program is also expected to be funded through governor’s budget when it is released according to the article (Spivack, 1/17).
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2. More Docs No Help for Racial Colonoscopy Gap
A recent article in Medpage Today
reported on a study that examined the relationship between the
physician supply and disparities in colon cancer screening among
Medicare beneficiaries in Texas, and surprisingly found greater
disparities in areas with more physicians.
Prior research has demonstrated persistent racial and ethnic
disparities in colorectal cancer screening rates. The authors of
this study hypothesized that disparities would be smaller in areas
where providers are plentiful. Using claims data from almost
975,000 Medicare beneficiaries in Texas who were white, black, or
Hispanic and between the ages 66 to 79 years in 2007, the
researchers compared colonoscopy rates by provider availability.
Physician availability was measured using the number of doctors per
10,000 people who are 65 or older in a given Hospital Service Area.
After adjusting for age, sex, comorbidities, income, and risk
factors for colon cancer, the authors found blacks and Hispanics
were less likely to have a colonoscopy than whites. Even after
controlling for those who live in areas with the highest odds of
receiving a colorectal screening, racial and ethnic disparities
remained. The results indicate that the odds of receiving a
colonoscopy for people of color increased when physicians who
perform colorectal screenings were more available.
The authors noted that “Our data imply that increasing
colonoscopist capacity alone may not improve colonoscopy use and
may be associated with increased racial/ethnic disparities”
(Ullman, 1/17).
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3. Programs Improve Diabetes Care in Low-Income Areas
According to a recent article published by MedPage Today, two new
initiatives have been successful in improving diabetes management
in underserved populations.
Previous research indicates that many factors contribute to racial
and ethnic disparities in diabetes and many efforts are underway to
bridge the gap. In one study, Dr.
Peter Huckfeldt investigated the impact of diabetes management
interventions in Los Angeles, CA. The study found health
improvements for patients enrolled in community interventions
featuring targeted diabetes care as well as integrated primary
care. In the second study, Dr.
Monica Peek also found promising results for a diabetes management
program in Chicago. This program aimed to reduce disparities
through community partnerships as well as culturally competent
patient education and provider trainings.
Both studies concluded that the health care safety net can be
strengthened to better address the needs of high risk diabetes
patients (Neale, 1/13).
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4. Asian-Americans More Apt to Die in Hospital After Heart Attacks
Health Day reported on a five-year study that found improvement in the number
of heart attack mortalities among Asian-Americans; however, they
were still more likely than whites to die in a hospital.
The study included over 107,000 Asian-American and white heart
attack patients from 2003 to 2008. The authors explored what
certain measures of care, (e.g. whether a patient received an
aspirin or ACE inhibitors, counseling on how to quit smoking, were
made available to a patient after discharge. The results found
Asian-Americans were less likely to receive such care and twice as
likely to die in a hospital after a heart attack. “Health
disparities are a serious public health concern in the United
States and we’ve seen that different racial and ethnic groups often
receive unequal treatment for the same diagnosis,” said Dr. Feng
Qian, a research assistant professor in the anesthesiology
department at the University of Rochester Medical Center in New
York. Possible factors for the disparity included Asian-Americans
being much older, and other health issues such as diabetes,
hypertension, and smoking. The researchers did find as the quality
of care improved, the health disparity decreased. “This improved
care is more significant and sustainable the longer hospitals
participate in the program,” said Qian.
These results prompted the lead author, Dr. Qian, to say “Future
studies should look more specifically at differences in care among
racial subgroups as well as at more long-term outcomes,” (Dallas,
1/10).
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5. Lower Risk of Death Linked With Access to Key Attributes of
Primary Care, UC Davis Study Shows
In a recent article published by Health Canal, new research has linked three primary care
characteristics with reduced morality risk.
Previous studies have found reduced mortality risk for individuals
living in regions with high concentrations of primary care
practitioners. In a new study, Anthony Jerant sought to determine
if three primary care practice characteristics were associated with
increased life expectancy. Using data from the Medical Expenditure
Panel Surveys, the study analyzed patient descriptions of their
main doctor’s office. The researchers found that respondents whose
primary doctor’s office provided: patient-centered care,
comprehensive health care services, and extended office hours fared
the best over a six year period.
The study concluded that these three characteristics are key
features of high quality primary care. Jerant noted that due to
reduced health care access among uninsured and low-income
populations, targeted interventions would be needed to ensure
equitable access to quality primary care (Health Canal, 01/10).
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6. Blacks’ Health Care: ‘Looking for Ways to Close The Gap’ in
Maryland
A recent article published in the Gazette discussed what some are doing to reduce health disparities among the black population in Prince George County, Maryland.
According to the article, blacks disproportionally experience higher rates of infant mortality, hypertension, diabetes, and strokes than whites. Michael Chiaramonte, CEO of Southern Maryland Hospital, is part of a 10-member committee that is responsible for exploring health disparities among Maryland’s population. This committee will be rolling out a number of new initiatives that will help reduce health disparities according to the article. One of the initiatives includes increasing the number of primary care visits among the black population. According to the article, increasing primary care visits will be one way to dramatically reduce disparities in health outcomes for blacks.
Some of the other areas leaders in Prince George County have been concerned about include bringing down costs of care. The cost of care, according to the article, is tied with increasing the number of primary care visits. “The key to reducing health costs has to do with getting the patient the right level of care at the right time,” said Chiaramonte (Robins, 1/09).
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7. The Income Penalty for Diabetes: $160,000
A recent article published by Kaiser Health News discussed a recent study
published in Health Affairs, which found that a young person with
diabetes can expect to make $160,000 less in their lifetime and
experience 0.25 fewer years of school than their peers.
The study’s findings showed young diabetic adults are more likely
to drop out of high school and make less money in their lifetime
than their peers who do not have diabetes. “High school is
relatively young to have such large effects,” said Jesse M.
Fletcher, lead author and associate professor of health policy at
the Yale School of Public Health. He continued by noting that this
can potentially have a significant impact on society because a they
are more likely to use food stamps and welfare, in addition to
serve time in jail. Currently, the United States spends more than
$200 billion each year for the cost of people with diabetes.
Fletcher adds that this is concerning because the number of
Americans with diabetes (23 million) is expected to increase as
more Americans are becoming obese. The explanation for the loss of
income and dropping out of high school varies according to the
article. An employer being reluctant to hire a diabetic worker or
an employee missing work due to poor health conditions Fletcher
explains as potentially income loss factors. He also explained that
a child missing school more often than their peers or costs are too
high for families due to illness are potential factors associated
with less education. Fletcher suggest future research will have to
explore diabetic children at the elementary and junior high level
to determine if early screening and intervention would be
beneficial.
The study used data from the 1994 and 2008 data files by the
National Longitudinal Study of Adolescent Health. Although the
study controlled for a number of different factors, a possible
limitation included that the study did not distinguish between Type
I or Type II diabetes (Gold, 1/09).
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8. New Clues Revealed in Studies of Stillbirth
According to a recent article published in The New York Times, two new
studies have identified the most common risk factors and causes of
stillbirths.
Stillbirths occur in the United States at a higher rate than in
many other developed nations. One team of researchers set out to
identify risk factors that could predict stillbirths early in a
pregnancy. A second team focused on identifying probable cause of
death in 512 stillbirth cases. Both studies found significant and
unexplained racial and ethnic variations. Black women were twice as
likely to have a stillbirth, with the largest disparities occurring
early in pregnancy. While black women were more likely to lose a
child due to an infection, white and Hispanic women were more
likely to lose a child due to umbilical cord abnormalities.
The research teams concluded that additional research is needed to
identify the causes of racial disparities. While some risk factors
cannot be modified (such as a mother’s age or ethnicity), future
studies may find additional risk factors that can be managed
(Bakalar, 01/09).
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9. Black Health Care Coalition Advocates for Health Choices
A recent article published in the Kansas City Star discussed what a non-profit organization
and its former chairman has done to improve the health of local
black residents in the Greater Kansas City area.
The Black Health Care Coalition, an organization that has launched
a number of education and outreach campaigns targeted to local
black residents of the Greater Kansas City area, which provided
health screenings and lifestyle education seminars. The
organization has spread its message and mission to local churches,
community centers, and elsewhere according to the article. Although
this organization targets the black population, Melissa Robinson,
president and CEO of the Black Health Care Coalition, said no one
is turned away and the goal is to improve the health of everyone.
“By improving the population of the black community, it will
improve the populations as a whole,” said Jasper Fullard, Jr.,
founder and now vital advisor to Black Health Care Coalition. Other
initiatives included teaching residents to cook better and choose
healthier foods, and have frequent health screenings. Certain
challenges were highlighted in the article however. For example,
local residents have limited accessible walking trails and grocery
stores that offer fresh and affordable fruits and vegetables.
Additionally, some retailers are staying away from operating in the
urban areas of Kansas City, which many city leaders are frustrated
about. “We will be fighting this for years and years to come. It’s
an ongoing problem. It’s not a reason to grow weary or give up,”
said Fullard.
The Southern Christian Leadership Conference of Greater Kansas City
will honor Fullard for his work to fight health disparities.
Fullard founded the organization 26 years ago and the organization
will continue to work on improving the health of local residents in
the area (Bormann, 1/08).
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10. Healthcare Plan for Low-Income Adults Includes Mental Health
Benefit
A recent article published in HealthyCal discussed a program that
will help provide treatment to the millions of adults in California
suffering from a mental illness before some of health reform’s
mandates go into effect in 2014.
A study by the UCLA Center for Health Policy Research found that
roughly 2 million Californians need some sort of treatment for a
mental illness. Additionally, no legislation in the state mandates
coverage for mental health treatment according to the article. The
study also found 87 percent of the uninsured adults with a mental
illness go without treatment. “The need, we know, for many is
enormous,” said Rusty Selix, executive director of the Mental
Health Association in California. A state and federal program will
now bring relief and needed services to the millions of individuals
before the 2014 mandates are set to go into effect. Some of the
health benefits include up to 10 days of acute inpatient treatment
per year and a total of 12 days per year of outpatient treatments.
According to the article, this program is designed for low-income
individuals suffering from a mental illness. However, a mental
illness, e.g. schizophrenia, runs through all the populations of
different income levels. So the program does permit eligibility
those with a slightly higher income.
Despite the benefits, the
program does face some potential challenges, e.g. providing enough
mental health, substance abuse care, and bi-lingual providers. “The
compensation is so low. Services are usually provided by
community-based groups, non-profits, and their funding has been
reduced,” said Louise Rogers, deputy chief of San Mateo County’s
health system.
Despite the challenges, Rogers estimates that 3,300 people who are
in need of mental health and substance abuse care in San Mateo, CA
will now receive the care they need. Additionally, many mental
health officials around the state are happy that this will give
California a head start before the 2014 mandates are set to go into
effect according to the article (Moran, 1/08).
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11. NAMI Program Offers Life Coaching to Those with Mental
Illnesses
Be Well, a program similar to Weight Watchers, provides peer-
support and health education to those struggling with a mental
illness in Wisconsin, the Appleton Post Crescent reports.
People living with a mental illness live 25 years or less than
those who do not have a mental illness. Additionally, a mental
illness is often linked to low socioeconomic and social status
according to the article. Be Well, a program started by the Fox
Valley chapter of National Alliance on Mental Illness (NAMI), is
attempting to address these health issues. The program primarily
provides education and support to those who are most vulnerable. Be
Well, which functions similar to Weight Watchers, is a support
system of peers who all are struggling with a mental illness and
each participant learns about nutrition, sleep, medication side
effects and tobacco use. “It’s a wonderful pairing; it’s very
motivating. Lots of people learned things they never knew about how
to eat well, how medications worked and why they were so
unmotivated to work or get out,” said Beth Clay, executive director
of NAMI Fox Valley. Volunteers are also a component of the program
according to the article. For example, Rebecca Arrowood, a student
from the University of Wisconsin-Green Bay, is responsible for
lining up speakers for the 12 week program. Jen Parsons, a personal
trainer and NAMI Fox Valley volunteer for nearly eight years, plays
a role in the Be Well wellness program.
Overall, the program was a huge success and is benefitting so many
individuals on so many levels,” said Parsons. The 12 week program
begins again January 18th (Anderson, 1/08).
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12. Family Support Motivates Mexican-Americans to Adopt Healthy
Habits
A recent article published in Health Behavior News Service discussed a study which found that encouragement
from family members helped Mexican-Americans improve their diet and
fitness behaviors.
Obesity is more prevalent in Mexican-Americans populations than
among their non-Hispanic white peers. In a new study, researchers
from the University of Memphis investigated the health behaviors of
161 multi-generational Mexican-American families. Participants
received personalized information regarding family history, risk of
chronic disease, and information about healthy lifestyle changes.
The study followed up with participants over time to learn more
about ongoing dietary and fitness choices, motivation levels, and
the potential influence of encouragement from family and friends.
The study concluded that that having at least one supportive friend
or family member motivated participants to live healthier lives.
According to lead study researcher Dr. Sato Ashida, these findings
demonstrate that “influence from [social] network members provides
a potentially culturally appropriate strategy to motivate
individual behavior change.” Participants who received
encouragement from loved ones were more likely to engage in regular
exercise and eat more fruits and vegetables (Kennedy, 01/05).
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13. Cancer Deaths Drop, But Incidence Rises
A recent article published in Medscape Medical News discussed a new report
highlighting recent reductions in cancer related deaths and rising
incidence rates for seven types of cancer.
Overall, cancer mortality rates have declined in recent years.
However, considerable geographic, racial, and ethnic variation in
cancer incidence and mortality continues to exist. Notably, due to
regional smoking behaviors, lung cancer is four times more
prevalent in Kentucky than in Utah. Cancer incidence and death
rates are also consistently higher for blacks than for whites, with
some variation across gender and cancerous condition. For example,
black men are 15% more likely to be diagnosed with cancer and 33%
more likely to die from cancer than to white men. Compared to
blacks and whites, all other minority groups had lower rates of
cancer incidence and mortality.
In the last decade, incidence rates of cancers of the pancreas,
liver, thyroid, kidney, and melanoma have all increased. In
addition, esophageal adenocarcinoma and oropharyngeal cancer rates
have also increased. Further research is needed to better
understand these trends and determine if more diagnoses are being
made due to better technology or if incidence rates are truly on
the rise (Nelson, 01/05).
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14. In Extreme Old Age, Blacks Outlive Whites on Average
According to a recent article from Newsworks, elderly
blacks live longer than elderly whites.
Despite reduced life expectancies from birth through adulthood,
there is a reversal of trends for blacks who live beyond 80 years
of age. According to Duke University researcher Keith Whitfield,
African Americans who live to extreme old age “are actually a very,
very select group of people who have resilient factors.” Many of
these African Americans, who have lived to extreme old age, did so
despite the many chronic diseases that disproportionately affect
and reduce life expectancy for blacks including: high blood
pressure, stroke, diabetes.
According to Whitfield, the exceptional resilience of this group is
likely attributable to a combination of genetic and behavioral
factors. Effective stress management skills may have provided
protective health benefits for elderly African Americans, many of
whom lived through times of heightened violence and discrimination
(English, 01/02).
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15. Diagnosis, Treatment of Depression Among Elderly Depend On
Racial, Cultural Factors
A recent article published by Medical News Today, highlights
racial and ethnic disparities in depression care among the elderly.
Depression can significantly diminish quality of life and
complicate coexisting medical conditions. For this reason,
depression is a significant public health issue for elderly
populations. A new study from Rutgers University found that elderly
African Americans are significantly less likely to be appropriately
diagnosed or treated for depression. Lead study researcher Ayse
Akincigil noted that “help-seeking patterns differ by
race/ethnicity, contributing to the gap in depression diagnosis
rates.” The study also indicated that shame, denial, and insurance
status may also be significant obstacles for black patients
struggling with depression.
The study concludes that additional measures must be taken to
“reduce the burden of undetected and untreated depression and to
identify the barriers that generate disparities.” According to the
researchers, universal depression screening and increases in
treatment reimbursement rates may be effective in increasing access
to appropriate care for low-income and minority patients (Medical
News Today, 01/02).
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DISPARITIES IN RESEARCH
16. Trends in Melanoma Mortality Among Non-Hispanic Whites by
Educational Attainment, 1993 – 2007
A recent study published in Archives of Dermatology found educational
attainment and death from melanoma to be strongly associated with
non-Hispanic whites.
According to the study, research has found an association between
socioeconomic status (SES) and survival among melanoma patients. In
this study, the researchers used data from the National Vital
Statistics System for the years of 1993 through 2007 to examine the
relationship between education and melanoma mortality in young and
middle-aged non-Hispanic white adults. The researchers analyzed
data from the 26 states that were collecting information on
education in 1993. Education as categorized into three levels: less
than 12 years (did not complete high school), 12 years (high school
graduate or equivalent), or 13 years or more (some college or
college graduate). Several years of data were combined to create
three categories: 1993-1997, 1998-2002, and 2003-2007. A total of
21,230 deaths were reported from 1993 through 2007. The results
indicated there was an overall decrease in mortality rates for both
white men and women decreased from 1993 to 2007. These declines,
however, were only statistically significant among those who had
some college or higher. Mortality rates among the least educated
remain statistically unchanged between 1993 and 2007. The study
also found higher melanoma mortality rates among the least
educated. This change created a significant SES disparity in
melanoma mortality in 2003 – 2007 relative to 1993 – 1997. This
disparity increased roughly 51 percent for men and 35 percent in
women.
The authors concluded that persistent disparity of melanoma
mortality rates among low SES individuals and the widening gap by
educational attainment calls for more targeted programs. For
example, educational programs that target high-risk subgroups of
low SES.
(Cokkinides VE, Geller AC, Jemal A. Trends in melanoma mortality
among non-Hispanic whites by educational attainment, 1993 – 2007.
Archives of Dermatology. 2012 Jan;
doi:10.1001/archdermatol.2011.2779).
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17. Lower Socioeconomic Status and Disability Among US Adults With
Chronic Kidney Disease, 1999 – 2008
A recent study published by the Centers for Disease Control and
Prevention: Preventing Chronic Disease found people
living in a lower socioeconomic status (SES) with chronic kidney
disease (CKD) have a greater risk of developing a disability.
Prior research has demonstrated a relationship between disability
and chronic kidney disease, a relationship between SES and the
development and progression of CKD, and a relationship between SES
and disability, but few studies have determined whether there is a
relationship between SES and disability in patients with CKD. The
study used data from a nine-year merged file of the National Health
and Nutrition Examination Survey (NHANES), 1999 – 2008. The sample
size for analysis was 4,257. Inclusion requirements included a
participant whose serum creatinine, urinary creatinine, and urinary
albumin measurements indicated CKD and were 20 years of age or
older. The participants were asked if any of the following
disabilities were caused by CKD: difficulty performing activities
of daily living (ADL) instrumental ADL, lower-extremity mobility
(LEM), and leisure and social activities (LSA). The majority of
participants reported some type of disability caused by CKD
according to the findings. For example, after adjusting for age and
sex, 1 in 5 persons reported ADL limitations. The most prevalent
type of disability among participants was LEM (50%). The ADL
prevalence rate for blacks and Mexican Americans was higher than
whites. However, race and ethnicity was not a factor for developing
a disability due to CKD—except for ADL—after adjusting for
sociodemographic factors, health care access, and other clinical
variables. Furthermore, a lower prevalence of a disability was
associated with participants with higher levels of education and
income. The linear association between socioeconomic status (SES)
and developing a disability dude to CKD reinforces the notion that
health outcomes and health status tend to be worse for those in a
lower SES according to the authors. One explanation for this
disparity is the cost barriers associated with care and management
for CKD.
The authors indicate that this study was important because it
highlighted how health outcomes for people with CKD in a lower SES
are worse. Further research will have to explore this association
and discover possible mechanisms that are targeted towards lower
education or income levels earlier in order to prevent further loss
of income due to worse health outcomes.
(Plantinga CL, Johansen KL, Schillinger D, et al. Lower
socioeconomic status and disability among US adults with chronic
kidney disease, 1999 – 2008. Centers for Disease Control and
Prevention: Preventing Chronic Disease. 2012 Jan; 9(ISSN: 1545-
1151).
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18. Hispanic Lesbians and Bisexual Women at Heightened Risk or
Health Disparities
A recent study published in the American Journal of Public Health
found Hispanic lesbian and bisexual women tend to be at a greater
risk of worse health outcomes than Hispanic heterosexual as well as
white lesbian and bisexual women.
Little background literature covers health disparities among sexual
minorities of color, especially Hispanics, according to the
authors. This study aims to explore how Hispanic sexual minorities
fare in health care access, health outcomes, health status, and
health risk behaviors. The study used the weighted-data from a 7-
year merged file of the Washington State Behavioral Risk Factor
Surveillance System (BRFSS), 2003 – 2009. The sample size for the
analysis was 6,338. Only Hispanic and white women who self-
identified as lesbian, bisexual, or heterosexual were included in
the study. Within the sample, 1.1% were Hispanic lesbian and 1.6%
were Hispanic bisexual. Data were collected for health status,
health risk behaviors, health outcomes, and health care access.
Hispanic lesbian and bisexual women did not differ from white
lesbian and bisexual women for many health and demographic
indicators, but some differences were observed. For example,
Hispanic lesbian women tended to have a higher prevalence of
lifetime asthma than all the other groups. Furthermore, Hispanic
lesbian women also reported higher smoking rates and lower exercise
rates than Hispanic heterosexual women. Hispanic bisexual women
tended to have higher rates of mental distress and worse general
health than both white and Hispanic heterosexual women as well as
white lesbian and bisexual women. This study is one of the first
studies to assess disparities among Hispanic lesbian and bisexual
women according to the authors.
The authors suggest that further research is needed in order to
develop culturally appropriate programs that meet the needs of
these subgroups. This in turn, as the authors argue, will achieve
the goals laid out Healthy People 2020.
(Kim HJ, Fredriksen-Goldsen K. Hispanic lesbians and bisexual women
at heightened risk or health disparities. American Journal of
Public Health. 2012 Jan; 102(1): 9 – 15).
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19. Characteristics Associated with the Initiation of Radiation
Therapy After Breast-Conserving Surgery among African American and
White Women Diagnosed with Early-Stage Breast Cancer in Maryland,
2000 – 2006
A recent study published in Annals of Epidemiology found that between 2000 and 2006, black women of a lower
socioeconomic status (SES) in Maryland were less likely to use
radiation therapy (RT) after breast-conserving surgery (BCS) than
white women.
Prior research has found RT after BCS improves the quality of life.
However, the proportion of patients not undergoing RT after BCS has
almost doubled in the years between 1989 to 1995 (10% to 19%)
according to the authors. This study aims to explore what factors
are associated with receiving an RT after BCS in Maryland. This
study concentrated only on black and white women with early-stage
breast cancer who received a BCS from 2000 to 2006 in Maryland. The
data used for the study was retrieved from the Maryland Cancer
Registry (MCR), which releases quarterly reports about all human
cancer cases that occur in the state. The primary interest was if a
patient was considered low income. The study’s standard for low
income was if 1) the patient was insured through Medicaid, 2)
resided in a zip code with a median family income lower than the
250% of the federal poverty level (FPL) in 1999 (less than an
annual income of $42,575.50 for a family of four), or 3) the
patient received services from the Maryland Breast and Cervical
Cancer Screening Program or the Maryland Breast and Cervical Cancer
Diagnosis and Treatment Program (BCCDTP). The outcome of interest
was whether the patient did have an RT after a BCS. Of the total
14,971 breast cancer patients, 23% were black while 77% were white.
Women who had private insurance and/or had a tumor size less than
or equal to 2 cm were more likely to use RT after BCS according to
the findings. Patients who were less likely to use radiation tended
to be 80 years of age or older, low income, and black. According to
the authors, this study confirming racial and socioeconomic
disparities among women with breast cancer was consistent with the
literature.
Although black women were 17% less likely to use RT, this disparity
decreased after 2003 according to the findings. The authors argue
future research will need to explore the uptake of RT and other
prescribed treatments after BCS.
(Royak-Schaler R, Pelser C, Langenberg P, et al. Characteristics
associated with the initiation of radiation therapy after breast-
conserving surgery among African American and white women diagnosed
with early-stage breast cancer in Maryland, 2000 – 2006. Annals of
Epidemiology. 2012 Jan; 22(1): 29 – 36).
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20. Medical Expenditures Among Immigrant and Nonimmigrant Groups in
the United States
A recent study published in Medical Care found medical expenditures among immigrants
(non-citizens and foreign born) were disproportionally lower than
non-immigrants (US citizens) and were more likely to not have a
usual source of care.
Not much has contributed to the literature about expenditures and
cost of care among immigrants in the United States. This study
investigated the medical expenditures and costs incurred between
non-citizens, foreign-born, and US-born citizens. They used data
from a nine year merged file of the Medical Expenditures Panel
Survey (MEPS). The MEPS combined data file was linked with the data
from the National Health Interview Survey (NHIS), which was created
by the Agency for health care Research Quality staff. These two
data files were linked in order to identify the immigration status
of a respondent. A total of 190,965 non-institutionalized US
adults, older than 18 years of age, were included in the study’s
sample. The outcome of interest was whether immigration status had
an influence on the amount of self-reported health care
expenditures. The independent factors included race and ethnicity,
age, gender, education. The “enabling” factors included household
income, insurance status, and availability of a usual source of
care. The results varied, especially in the total amount of
expenditures between groups and what was the primary source for
their medical expenditures. For example, non-citizens largely used
out-of-pocket sources, while US born citizens relied largely on
private coverage. Public sources had the most variation throughout
the study period. Consistently, foreign born citizens largely used
public coverage; however, non-citizens relied more on public aid
than US born citizens in the earlier years of the study. This
dissipated by 2002 and non-citizens rarely used public aid. Despite
non-citizens relying heavily on using out-of-pocket methods, non-
citizens spent far less on medical costs than any other group
according to the findings. This study is consistent with literature
according to the authors.
The low expenditure among non-citizens can be an explanatory factor
for why they tend to experience worse health outcomes.
Additionally, these results suggest that extending health insurance
coverage, increasing awareness about centralized health care, and
usual source of care access could potentially provide an equitable
health care system for all the authors argue.
(Tarraf W, Miranda PY, Gonzŕlez HM. Medical expenditures among
immigrant and nonimmigrant groups in the United States: findings
from the Medical Expenditures Panel Survey (2000 – 2008). Medical
Care. 2012 Jan; doi: 10.1097/MLR.0b013e318241e5c2).
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21. Impact of Electronic Health Records on Racial and Ethnic
Disparities in Blood Pressure Control at US Primary Care Visits
A recent study published in Archives of Internal Medicine found that
black and white patients experience similar levels of blood
pressure if they visit a doctor who uses electronic health records
(EHR) with clinical decision support (CDS).
Prior research has indicated improved blood pressure among patients
whose doctor used both electronic health records (EHR) and clinical
decision support (CDS). For this study, the researchers sought to
determine whether the benefits achieved are shared equally among
patients of different racial and ethnic backgrounds. Using data
from the National Ambulatory Medical Care Survey (NAMCS, which is a
nationally representative survey of primary care visits by the
National Center for Health Statistics (NCHS), the primary outcome
of interest was whether a patient’s blood pressure improved.
Visits were grouped by race and ethnicity and whether the patient
visited a doctor who used EHR and/or CDS. Analyses controlled for
age, sex, diabetes, practice ownership, and insurance type of
insurance. Patients who visited a doctor that used both EHRs and
CDS experienced improved levels of blood pressure, and Hispanic
patients experienced significant improvement. The results also
showed that there was no disparity between the black and white
patients whose providers used HER and/or CDS. However, racial
disparities persisted for the black patients who visited a doctor
that did not use EHR and CDS.
The authors suggested these findings highlighted primary care may
reduce morbidity and mortality from cardiovascular disease and
reduce blood pressure control disparities by implementing EHRs with
CDS.
(Dal Pan GJ, Temple R. Impact of electronic health records on
racial and ethnic disparities in blood pressure control at US
primary care visits. Archives of Internal Medicine. 2012 Jan; 172
(1): 75 – 76).
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22. The Impact of Socioeconomic Inequalities and Lack of Health
Insurance on Physical Functioning Among Middle-Aged and Older
Adults in the United States
A recent study published in Health and Social Care in the Community found that having more financial
resources and private health insurance predicted better physical
functioning over time.
Prior research has shown that individuals with lower socioeconomic
status have higher rates of mortality and morbidity. This study
sought to determine how socioeconomic status and lack of private
health insurance influence physical functioning later in life. The
study used 1994 – 2006 data from the Health and Retirement Study
(HRS), a national longitudinal panel study of adults over 50 years
of age and their spouses. The researchers selected a sample of
6,519 adults who provided complete information regarding their
health, socioeconomic, financial, and health insurance status. Due
to small sample sizes for other racial groups, only white and black
adults were included in the sample. In the HRS dataset, respondents
provided information on gender, race, household income, household
assets, educational attainment, and enrollment in private health
insurance. Physical function was the primary outcome variable of
this study. This variable was defined as level of difficulty with
any of five basic activities of daily living (ADL): walking across
a room, bathing, eating, dressing, and getting into and out of bed.
The researchers included several control variables including age at
baseline, marital status, employment status, and birth cohorts to
control for any historical effects. The study found that having
more financial resources and private insurance were significant
predictors of better physical functioning across racial groups.
After controlling for socioeconomic status, declines in physical
function were similar across racial groups. However, changes in
socioeconomic status resulted in greater improvements in physical
functioning for women than for men. As the socioeconomic gap
narrowed with age, the researchers also found that the impact of
educational attainment, gender, and race on physical functioning
diminished over time. These findings were consistent with previous
research findings indicating that the economically disadvantaged
are more likely to experience more rapid declines in physical
functioning.
In light of these findings, the researchers indicate that policy
interventions are needed to reduce the negative impact of
socioeconomic inequalities on physical functioning. Future research
is also needed to consider how education may contribute to racial
disparities in physical functioning.
(Kim J, Richardson V. The impact of socioeconomic inequalities and
lack of health insurance on physical functioning among middle-aged
and older adults in the United States. Health and Social Care in
the Community. 2012 Jan; 20(1): 42 – 51).
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23. Children With Cerebral Palsy: Racial Disparities in Functional
Limitations
A recent study published in Epidemiology found that cerebral
palsy is generally more prevalent among black children compared to
white children, with the most striking disparities occurring among
those with severe functional limitations.
Cerebral palsy is a developmental disability that impairs motor
function. While prior research has demonstrated that cerebral palsy
ranges in severity, it is unclear if racial and ethnic disparities
exist in the prevalence of this disease. This study sought to
understand if cerebral palsy is more prevalent among black
children, considering the full spectrum of functional limitations.
The study used 2006 surveillance data from Centers for Disease
Control’s Autism and Developmental Disabilities Network (ADDM) to
identify 8-year-old children with cerebral palsy residing in
Alabama, Georgia, Missouri, and Wisconsin. The researchers included
a sample of 476 children with mild, moderate, severe, and unknown
motor skill limitations due to cerebral palsy. To better understand
potential racial disparities across levels of functional
limitation, the researchers used multiple imputation models to
stratify cases by severity and better understand the health status
of children missing motor limit classifications. The imputation
models revealed that children missing motor limit classifications
were more likely to have milder symptoms. Using this adjusted
analysis, researchers found that racial disparities only existed
among children with severe motor limitations. Black children were
70% more likely to have severe cerebral palsy than white children.
These findings were consistent with previous research highlighting
the prevalence and severity of cerebral palsy among non-Hispanic
black children.
The authors indicate that there is a complex relationship between
race and the prevalence and severity of cerebral palsy. It is not
yet clear if there is differential ascertainment of the disease or
if access to care plays a larger role creating racial disparities.
Further research is also needed to generalize these studies to
children of other racial and ethnic backgrounds.
(Maenner MJ, Benedict RE, Arneson CK, et al. Children with cerebral
palsy: racial disparities in functional limitations. Epidemiology.
2012 Jan; 23(1): 35 – 43).
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24. Disability Among Lesbian, Gay, and Bisexual Adults:
Disparities in Prevalence and Risk
A recent study published in the American Journal of Public Health found higher rates of disability among lesbian,
gay, and bisexual (LGB) adults in Washington state.
Almost 50 million American adults have disabilities and many
require specialized care on a daily basis. This study sought to
examine patterns of disability by sexual orientation to understand
if LGB populations are especially vulnerable. The researchers
analyzed four years of Behavioral Risk Factor Surveillance System
(BRFSS) data to examine the health status of 82,531 adults living
in Washington State. The study was limited to English or Spanish
speaking adults who self-identified as: heterosexual, lesbian, gay,
or bisexual. The primary outcome was self-reported disability
status, defined as any physical, mental, or emotions problems
limiting daily life. The researchers captured several
sociodemographic variables including: racial identity (white or
non-white); age; relationship status (married, partnered, or
other); household income; and educational attainment. The study
also captured several covariates of disability including: chronic
health conditions, health risk behaviors, and physical and mental
health status. The study found that sexual orientation was
predictive of disability and that higher rates of disability occur
among LGB populations, especially among lesbians and bisexual
adults. These findings are consistent with prior research
indicating that non-heterosexual populations experience disparities
in physical and mental health.
The authors indicated that disability rates among gay men may be
decreased by addressing specific high risk behaviors (such as
smoking) and mental distress. However, researchers believe this
strategy would be less effective in reducing disability among
bisexuals and lesbians. Additional research is needed to understand
the role stress and stigma may play in increasing the prevalence of
disability among LGB populations.
(Fredriksen-Goldsen KI, Kim HJ, Barkan SE. Disability among
lesbian, gay, and bisexual adults: disparities in prevalence and
risk. American Journal of Public Health. 2012 Jan; 102(1): 16 –
21).
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25. Racial and Ethnic Disparities in Obesity During the Transition
to Adulthood: The Contingent and Nonlinear Impact of Neighborhood
Disadvantage
A recent study published in the Journal of Youth and Adolescence found that
neighborhood disadvantage increases the risk of obesity and
partially explains racial and ethnic disparities in obesity among
young women.
Children who are obese during adolescence are at risk of developing
additional health complications as they enter adulthood. This study
sought to determine the influence of neighborhood economic
disadvantaged on the onset of obesity in young adults across racial
and ethnic groups. Using 1994 data from the National Longitudinal
Study of Adolescent Health (Add Health), the study analyzed the
health status of 5,759 teenagers. The key variables included in the
study were obesity (obese or not obese); gender; race and ethnicity
(black, white, or Hispanic); and neighborhood disadvantage (a
measure of economic insecurity at the census tract level). The
authors found that black and Hispanic teenage girls were nearly
twice as likely to become obese compared to white girls. Black boys
were slightly more likely to become obese compared to white boys.
The study also found neighborhood disadvantage to be significant
predictor of obesity among teenage girls. While this variable
explained much of the disparity between black and white girls, it
minimally explained the disparity between Hispanic and white girls.
The authors concluded that policy interventions improving public
safety and access to nutritious food in disadvantage neighborhoods
will help reduce childhood obesity. However, additional research is
needed to better understanding the factors contributing to obesity
among Hispanic girls.
(Nicholson LM, Browning CR. Racial and ethnic disparities in
obesity during the transition to adulthood: the contingent and
nonlinear impact of neighborhood disadvantage. Journal of Youth and
Adolescence. 2012 Jan; 41(1): 53 – 66).
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DISPARITIES DATA SPOTLIGHT
Financial and Educational Worries by Race

The results of a new poll by the Kaiser Family Foundation and the
Washington Post found fewer black women said they frequently
experienced stress than white women, but more black women than
white women are worried about certain aspects of their life.
Nearly 2 in 5 black women and 1 in 4 white women with children are
very worried about being able to provide a good education their
children, and almost 2 in 5 black women and 3 in 10 white women are
very worried about having enough money to pay their bills. These
are some of the findings highlighted in a new poll from the
Washington Post and the Kaiser Family Foundation. The poll was
conducted by telephone, and included nearly 2,000 adults. It asked
covered a variety of topics from self-esteem and stress to
perceptions of Michelle Obama.
To learn more about the poll,
please visit the
Washington Post.
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