Are doctors biased?
Satel, Sally ; Klick, Jonathan
Two 50-YEAR-OLD men arrive at an emergency room with acute chest
pain. One is white and the other black Will they get the same quality of
treatment and have the same chance of recovery? We would hope so, but
many experts today insist that their race will profoundly affect how the
medical-care system deals with them and that the black patient will get
much inferior care. Is this really true? And if so, why? Are differences
in treatment due to deliberate discrimination or other (less invidious)
factors?
Interest in the determinants of minority health has grown
considerably since the publication of the Report of the Secretary's
Task Force on Black and Minority Health by the U.S. Department of
Health, Education, and Welfare in 1985. The academic literature falls
into two categories. One line of inquiry emphasizes overt or subtle
racial discrimination by physicians. Research reports in this category
assert that many physicians treat their white patients better than their
minority patients on the basis of race alone. We call this the
"biased-doctor model" of treatment disparities.
The other line of research focuses on the influence of so-called
third factors that are correlated with race. These factors can influence
care at the level of the health system, the physician, or both. They
include, for example, variations in insurance coverage (insured versus
uninsured versus underinsured; public versus private health plans;
profit versus not-for-profit health plans), quality of physicians,
regional variations in medical practices, and patient characteristics
(such as clinical features of disease or health literacy).
Of course, it is possible that both of these
mechanisms--"biased doctors" and "third
factors"--could operate simultaneously. Yet it is the biased-doctor
model that has acquired considerable weight in both academic literature
and the popular press. It enjoyed a great boost in visibility from a
2002 report from the Institute of Medicine (IOM), part of the National
Academy of Sciences. The IOM provides lawmakers with advice on matters
of biomedical science, medicine, and health and issues high-profile
reports written by panels of outside experts. Unequal Treatment:
Confronting Racial and Ethnic Disparities in Health Care was widely
hailed as the authoritative study on health disparities. It concluded
that the dynamics of the doctor-patient relationship--"bias,"
"prejudice," and "discrimination"--were a
significant cause of the treatment differential and, by extension, of
the poorer health of minorities. Much media fanfare greeted the IOM
report, and virtually every story ran the triumphant remark of Dr.
Lucille Perez, then president of the National Medical Association, which
represents black physicians: "It validates what many of us have
been saying for so long--that racism is a major culprit in the mix of
health disparities and has had a devastating impact on
African-Americans."
In this essay, we evaluate some of the studies routinely put forth
as evidence of harmful discrimination. We report evidence not considered
by the IOM panel. These additional findings indicate that race-related
variables, such as geography and socioeconomic status, shine important
explanatory light into the recesses of the treatment gap. Without
adequate controls for just such variables, it is simply not possible to
distinguish care patterns that correlate with race from those that are
due directly to race. Indeed, as we will see, when researchers employ
designs that control for more third factors, the magnitude of any race
effect shrinks considerably, if it does not disappear altogether.
Public health as civil rights
FIRST, A BRIEF SKETCH of how we got here. Just before Christmas
2003, the Agency for Health Care Research and Quality of the U.S.
Department of Health and Human Services (HHS) released the National
Healthcare Disparities Report. It documented an all-too-familiar
problem: the poorer health status of individuals on the lower rungs of
the socioeconomic ladder and the fact that they often receive inadequate
treatment compared to people with more resources and education.
The report sparked a heated controversy over whether HHS had
downplayed the charge of racial bias in the health-care system. At issue
were revisions made in a prepublication draft shortly before its
release. Those consisted, among other things, of using the more neutral
word difference instead of disparity to describe discrepancies between
the health of whites and minorities. This might seem like an innocuous
substitution, but it was not. In public health circles, the word
"disparity" has come to connote unfair difference due to a
patient's race or ethnicity. It "has begun to take on the
implication of injustice," observed epidemiologist Olivia
Carter-Pokras at the University of Maryland. (1) Architects of the
agency report, however, argued that the more neutral term difference
more accurately describes the findings of the report.
The switching of difference and disparity prompted Henry Waxman,
ranking minority member of the House Government Reform Committee, to
send a harsh letter to then-HHS secretary Tommy Thompson. The word
substitution, Waxman wrote, " alter[ed] the report's meaning
... and fit a pattern of the manipulation of science by the Bush
Administration." (2) The revision also set alarm bells ringing
among a range of constituencies. "By tampering with the conclusions
of its own scientists, HHS is placing politics before social
justice," wrote members of the Congressional Black Caucus,
Congressional Asian Pacific American Caucus, and Congressional Hispanic
Caucus in a joint press release. (3) The National Medical Association
pronounced itself "appalled." (4) Physicians for Human Rights
bemoaned "remov[al] from the text [of] any inference of prejudice
on the part of providers, and [its] focus on individual responsibility
for disparities." (5)
The critics who scolded HHS for its revised executive summary cited
the 2002 IOM report as proof that bias was common among physicians. To
be fair, the IOM report acknowledged the roles of other factors in
minority health, but it put heavy emphasis on the failure of the medical
profession to purge its ranks of prejudice--a shortcoming that was, as
the report put it, "rooted in historic and contemporary
inequities."
Although the IOM report is now the most widely cited source for
this claim, it was hardly the first to make the argument. A decade
earlier in the Journal of the American Medical Association, Secretary of
Health and Human Services Louis Sullivan cast minority health as a civil
rights issue, writing, "There is clear, demonstrable, undeniable
evidence of discrimination and racism in our health care system."
The Reverend Al Sharpton warned in 1998 that "health will be
the new civil rights battlefront"; that same year, President
Clinton remarked in a radio address delivered during Black History Month
that "nowhere are the divisions of race and ethnicity more sharply
drawn than in the health of our people" and speculated that one of
the causes might be "discrimination in the delivery of health
services." In the March/April, 2005 issue of Health Affairs,
Senator Ted Kennedy urged that "greater resources should be given
to the HHS Office for Civil Rights." And, in an especially alarmist tone, Marian Wright Edelman of the Children's Defense Fund told the
2005 graduating class of Colgate University that "the new racism
that is seeping across our country is wrapped up ... in racial
disparities in health."
This social justice perspective continues to frame the issue of
minority health. For example, introducing the Health Care Equity and
Accountability Act in 2003, Senator Tom Daschle cited the need to
correct doctors' "bias," "stereotyping," and
"discrimination." The American Medical Association felt moved
to reaffirm its "long-standing policy of zero tolerance [against]
racially or culturally biased health care." (6) The American Public
Health Association "call[ed] on the President and the Congress of
the United States to recognize and promote legal redress for
discrimination in health and health care." (7) On the research
front, the National Institutes of Health are funding research on
"the effect of racial and ethnic discrimination on health care
delivery." (8) In some medical schools, "racial
sensitivity" training is now required. And in 2005, New Jersey was
the first state to pass a law requiring doctors to receive
"cultural competency" training as a condition of obtaining or
renewing their licenses to practice medicine. Unfortunately, these
institutional mandates and practices legitimate the "biased-doctor
model" of health disparities at the expense of other factors.
Limits of the IOM report
THE MOST RIGOROUS studies reviewed by the IOM sought to control for
confounding clinical or economic variables, such as concurrent illness,
supplemental insurance, or patients' refusal to undergo procedures.
But because most of the studies were retrospective and relied upon chart
review or large Medicare administrative databases, many such variables
could not be captured.
Some of these are generally recorded, such as comorbid conditions
and severity of disease at the time care is sought. Others are often
missing from administrative databases--for instance, EKG subtleties,
position of occlusion in carotid and coronary vessels, coronary ejection
fraction, and pulmonary function test performance--even though they
figure importantly in physician decision making. Moreover--and this is
key--these unrecorded variables do vary by race and ethnicity. Note, for
example, the well-documented frequency with which coronary angiograms of
black patients show less anatomical suitability for intervention--either
lesions in the vessels are too diffuse for angioplasty, or the patients
have a higher incidence of normal-appearing vessels, despite the
clinical appearance of having suffered acute myocardial infarction. An
examination of records, therefore, could suggest a racial bias in
treatment simply because coronary angiograms are less often given to
black patients, and the records themselves do not indicate the reasons
for those treatment decisions.
Consequently, the panel concluded that treatment differences occur
everywhere and that they are manifest for all kinds of care. (9) But
this conclusion was in error, as other studies indicate. Baicker and
colleagues at Dartmouth College, for example, have shown important
regional inconsistencies in treatment. One region might display wide
race disparities in some procedures, such as hip replacement or back
surgery, smaller discrepancies in bypass, and almost no gap in
mammograms. (10) Does that mean that doctors in the region who perform
hip replacements are biased, but cardiac-care doctors are not? Or is it
possible that there are other, benign reasons for those statistical
disparities?
Missing variables are not the entire story, however. Other kinds of
evidence are necessary to bestow a fuller picture of the dynamics
involved in treatment differences and permit more confidence in the
IOM's claims about bias on the part of providers. For example, we
need many more prospective studies that ask doctors and patients about
how they make decisions to offer and to accept, respectively, particular
treatments.
Researchers at the Philadelphia Veterans Affairs Medical Center
found that more blacks than whites (61 percent versus 29 percent)
maintained the folk belief that the spread of lung cancer was
accelerated when the tumor was exposed to air during surgery and would
oppose surgery because of this. (11) A related study conducted at
Detroit's Henry Ford Health System found that black patients with
operable lung cancer refused surgery over three times more often than
whites (19 percent versus 5 percent), though both whites and blacks were
offered the surgery at similar rates. (12)
But tests and procedures are not always offered at the same rate.
Asking doctors why they did not order a particular test could yield
explanations such as the one offered by Dr. Gary Curhan, writing in the
Journal of the American Medical Association (JAMA) in 2005 about
work-ups for first-time kidney stones: "If the patient is
uninterested in making long-term lifestyle changes or taking medication,
then I do not proceed with an evaluation [for a first stone.]" In
other words, the physician decides to undertake an expensive work-up
only if a patient is invested in cooperating with the diet and other
lifestyle changes needed to improve his condition--otherwise, he treats
the patient's symptoms without looking for a specific cause.
These are just two of countless examples showing how a
patient's characteristics can influence the care he receives. In a
sweeping book, The Status Syndrome: How Social Standing Affects Our
Health and Longevity (Bloomsbury Publishing, 2005), epidemiologist and
physician Sir Michael Marmot documents the importance of factors that
are not readily measured by disparity researchers--in part because their
accounting requires time-consuming, face-to-face interviewing. For
example, Marmot emphasizes the importance of personal autonomy and
control over one's life circumstances. With respect to treatment
per se, it is not surprising that patients with chaotic lifestyles--an
often inevitable aspect of living in or near poverty irrespective of
race--are not going to be good candidates for ongoing care requiring
complex regimens.
A third kind of study valuable for understanding race-related
factors in treatment compares care provided by white and black doctors
to white and black patients. For example, evidence that doctors of both
races treat black patients similarly, say, in terms of rate of referral
for catheterization--even if both refer black patients less often than
they do white patients--would cause us to question a charge of bias. We
are aware of only one study that has analyzed data with this question in
mind. Jersey Chen and colleagues at Yale University analyzed data from
the Cooperative Cardiovascular Project. (13) They evaluated 40,000
Medicare beneficiaries hospitalized for acute myocardial infarction in
1994 and 1995 to determine whether differences between black patients
and white patients in the use of cardiac catheterization within sixty
days after acute myocardial infarction varied according to the race of
their attending physicians. Black patients had significantly lower rates
of cardiac catheterization than white patients, regardless of whether
their attending physician was white (38.4 percent rate of
catheterization for black patients versus 45.7 percent for whites) or
black (38.2 percent versus 49.6 percent).
There was no significant interaction between the race of the
patients and the race of the physicians in the use of cardiac
catheterization, strongly suggesting that racial bias was not at issue.
Critics of the Chen study, however, have suggested that the
predominantly white cardiologists to whom the black internists referred
their patients exhibited racial bias by undertreating the black
patients. (14) To this Chen and colleagues reply by noting this would
mean that black attending physicians concurred with and supported
racially biased decisions--a scenario they believe unlikely. (15)
Moreover, the adjusted mortality rate among black patients was lower
than or similar to that among white patients for up to three years after
the infarction, suggesting that the care received by the patients, even
if it was different, was equally effective.
Is geography destiny?
WITH MOST HEALTH care delivered locally--and with racial and ethnic
groups not evenly scattered about the country--it is imperative that
researchers account for geography in evaluations of health disparities.
When they do, they discover that geographic residence often explains
race-related differences in treatment better than even income or
education. One of the most striking limitations of the IOM report is the
absence of such an analysis.
Consider the concept of the "hospital referral region,"
or HRR. The Dartmouth Atlas of Health Care defines an HRR as a
geographic area served by a major hospital equipped with comprehensive
surgical capacity, also known as a tertiary care hospital. In the United
States there are 306 HRRs, yet only 3 6 of them have a nationally
representative mix of residents. Among the rest, a number have black
population rates that are three to six times the national average of 13
percent. Because health care varies a great deal depending on where
people live, and because blacks are overrepresented in regions of the
United States that are burdened with poorer health facilities,
disparities are destined to be, at least in part, a function of
residence.
Medicare datasets do not include geographic identifiers, so
geographic data are often lost to researchers who rely on these sources.
Consequently, as Amitabh Chandra and Jon Skinner of Dartmouth College
have observed, many disparity evaluations do not sufficiently control
for geographic variation among patients. (16) This can produce
misleading findings.
For example, assume black patients from city x and city Y receive
exactly the same care as white patients from the same places. In city x,
all patients receive suboptimal care; in city y, all patients receive
excellent care.
Now compare the care of all black residents of cities x and Y with
the care of whites from both cities. If the proportion of black
residents in the two cities is not identical, there will appear to be
racial differences in treatment even though blacks and whites living in
the same place receive the same care. Thus, if minority patients are not
randomly distributed throughout locations--only 6 percent of poor whites
live in high-poverty neighborhoods, whereas 22 percent of Hispanics and
34 percent of blacks do--geographic differences in utilization and
health outcomes are going to appear, analytically, as racial
disparities. And researchers who fail to control for location effects
will interpret geographic health disparities as racial disparities.
As a rule, the quality of care received by blacks is inversely
related to the concentration of black residents in the local population.
For example, Baicker, Chandra, and Skinner found that the frequency of
annual eye exams in black diabetic patients covered by Medicare declined
as the number of blacks in the local population increased. (17) Along
these lines, blacks who lived in predominantly white HRRs received the
same or slightly better eye care than whites. Angus Deaton of Princeton
University and Darren Lubotsky of the University of Illinois have found
that at both the regional and the metropolitan statistical area levels,
white and black mortality rates are higher in areas where blacks make up
a larger portion of the total population. Similarly, the Dartmouth group
found significantly higher risk-adjusted mortality following acute
myocardial infarction in U.S. hospitals that disproportionately serve
black patients. (18) In her study, Amber Barnato and colleagues found
that 1,000 of 4,690 hospitals nationwide accounted for treating 8 5
percent of the black Medicare patients in 1994-95. (19)
The effects of location on health disparities have also been
studied using infant mortality rates. Jeannette Rogowski and colleagues
at RAND used the rich Vermont-Oxford network dataset to examine the
effects of hospital quality on the mortality rates of very
low-birthweight babies, controlling for condition of the baby at birth
(via Apgar scores) as well as other characteristics such as gestational
age, race, method of delivery, birth defects, and prenatal care. (20)
The authors found that black babies were more likely to be born in
hospitals that primarily served minority areas (57 percent for black
births as compared with 18 percent for white births).
Thus, at a minimum, black and white babies are not being delivered
at the same kinds of hospitals. The characteristics of the hospitals
serving these two populations also varied systematically. Black babies
were significantly more likely to be born in government-run hospitals
that served a relatively high proportion of Medicaid patients and where
doctors spent less time with patients due to high patient volume (and
for other reasons as well). Further, the hospitals where black babies
were born were significantly less likely to have neonatal intensive care
units or to perform neonatal cardiac surgery.
In the Rogowski analysis of 28-day infant mortality rates, these
hospital characteristics proved to be a significant source of variation
in the survival chances between white and black babies. Babies born in
minority-serving hospitals were 30 percent more likely to die in the
first 28 days than those born in hospitals that served few minorities
(less than 15 percent of patients), and this effect was quantitatively
similar for both white and black babies.
Although not nearly as important as the minority-serving versus
majority-serving distinction, many other hospital characteristics that
differed by race also proved significant in determining mortality. For
instance, having a neonatal intensive care unit that performed cardiac
surgery reduced infant mortality by 14 percent, and being born in a
government-run hospital raised mortality rates by 7 percent relative to
a private, not-for-profit hospital and by 24 percent relative to a
for-profit hospital. Again, these results included controls for
condition at birth, prenatal care, maternal income and education levels,
and gestational age.
Thus, by focusing on race we miss a very important cause of
health-care difference: geography. Where a person lives, irrespective of
race, has a much larger effect on how the medical system treats him.
Variation among hospitals is another factor for which disparity
studies often do not control. Indeed, the studies below describe a
pervasive trend: Hospitals that treat greater numbers of minority
patients generally offer poorer-quality service than those that treat
fewer minorities.
In general, hospitals that perform a low volume of surgical
procedures such as coronary bypass, gall bladder removal, or valve
replacement have higher mortality rates for the given procedures than
those that perform more. A 2002 study by John Birkmeyer and others in
the New England Journal of Medicine showed that black patients were more
likely to be treated at low-volume hospitals and more likely to die for
that reason. The crucial importance of volume has been underscored by
the Leapfrog Group (a coalition of more than 80 large public and private
insurance purchasers), which urges both patients and payers to select
hospitals that perform a certain minimum threshold number of procedures
per year.
Elizabeth Bradley of Yale and colleagues found that
hospital-to-hospital differences made a considerable impact on treatment
differentials in the case of suspected heart attack. The cohorts
included 37,143 patients receiving angioplasty at 4 3 4 hospitals and
73,032 patients receiving fibrinolytic therapy (medicine to dissolve
blood clots in coronary arteries) in 1,052 hospitals. Their findings,
published in 2004 in JAMA: "A substantial portion of the racial and
ethnic disparity in time to treatment is accounted for by the hospital
to which a patient is admitted, in contrast to differential treatment by
race and ethnicity inside the hospital."
A nationwide study of all Medicare patients treated in 4,690
hospitals between 1994 and 1995 for acute myocardial infarction revealed
a similar finding. On average, black patients went to hospitals that
used evidence-based medical treatments (that is, state-of-the-art
practices) less frequently and had worse mortality rates (but higher
rates of cardiac procedures, suggesting better-quality surgical than
medical care). "Incorporating the hospital effect altered the
finding of racial disparity analyses and explained more of the
disparities than race," wrote Amber Barnato of the University of
Pittsburgh and her coauthors.
Once again, we find that minority patients receive different
treatments than whites primarily because they attend lower-quality
hospitals--a pattern that helps exonerate physicians from the charge of
systematic bias in their treatment of patients. Most likely, this is a
function of minorities' disproportionate poverty or near-poverty
status. Studies comparing similarly disadvantaged blacks and groups of
whites (such as those clustered in poverty in Appalachia and rural
Maine) would underscore the primacy of social capital.
Debunking the "biased-doctor" model
A CENTRAL ASSUMPTION THAT underlies the biased-doctor model is that
black patients are treated worse than white patients I when served by
the same (white) doctor. But research published in 2004 in the New
England Journal of Medicine by Peter Bach and colleagues at
Manhattan's Memorial Sloan-Kettering Cancer Center and the Center
for the Study of Health Care Change in Washington has produced findings
that cast doubt on that assumption. The authors showed that white and
black patients, on average, do not even visit the same population of
physicians--making the idea of preferential treatment by individual
doctors a far less compelling explanation for disparities in health.
They showed, too, that a higher proportion of the doctors that black
patients tend to see may not be in a position to provide optimal care.
The research team examined more than 150,000 visits by black and
white Medicare recipients to 4,355 primary-care physicians nationwide in
2001. It found that the vast majority of visits by black patients--80
percent--were made to a small group of physicians--22 percent of all
those in the study. Is it possible, the researchers asked, that doctors
who disproportionately treat black patients are different from other
doctors? Do their clinical qualifications and their resources differ?
The answer is yes. Physicians of any race in the study who
disproportionately treated black patients were less likely to have
passed a demanding certification exam in their specialty than the
physicians treating white patients. More important, they were more
likely to answer "not always" when asked whether they had
access to high-quality colleague-specialists, such as cardiologists or
gastroenterologists, to whom they could refer their patients or to
nonemergency hospital services, diagnostic imaging, and ancillary
services, such as home health aid.
These patterns reflect geographic distribution. Primary-care
physicians who lack board certification and who encounter obstacles to
specialized services are more likely to practice in areas where blacks
receive their care--namely, poorer neighborhoods, as measured by the
median income. Bach and his colleagues suggest that these differences
play a considerable role in racial disparities in health care and health
status. They make a connection between well-established facts: that
physicians who are not board-certified are less likely to follow
screening recommendations and more likely to manage symptoms rather than
pursue diagnosis. Thus, rates of screening for breast and cervical
cancer or high blood pressure are lower among black patients than white,
and black patients are more likely to receive a diagnosis when their
diseases are at an advanced stage.
Limited access to specialty services similarly puts black patients
at a disadvantage. The Bach study is the first to examine
physicians' access to specialty care and nonemergency hospital
admissions in light of the race of the patients they treat. That
capacities of doctors who treat black patients may account for some part
of the health gap was considered in a 2002 study by researchers at the
Harvard School of Public Health. The study found that physicians working
for Medicare managed-care plans in which black patients were heavily
enrolled provided lower-quality care to all patients. Specifically,
their patients were less likely to receive the four clinical services
the authors measured--mammography, eye exam for diabetics, beta-blocker
after myocardial infarction, and follow-up after hospitalization for
mental illness. (21)
A report in the American Journal of Public Health in 2000 found
that blacks in a sample of almost 30,000 patients in New York State
undergoing cardiovascular surgery in 1996 had poorer access to
high-quality surgeons than did whites. Even among patients at the same
hospital, whites were treated by better-performing surgeons, a
phenomenon that may reflect some selection of patients by surgeons based
on insurance coverage. (22) Donald Gemson of the Columbia University
School of Public Health and colleagues showed that foreign-trained
physicians and doctors not board-certified were more likely to treat
black patients in New York City than to treat whites. They also found
that practitioners whose caseload was more than 50 percent black or
Hispanic were less likely to follow nationally recognized treatment
guidelines, such as recommending mammograms or flu vaccinations for the
elderly. (23) Kevin Heslin of Charles R. Drew University and his team
showed a correlation between physicians' experience in treating HIV and the race of their HIV patients, with HIV-positive black patients
more likely to be treated by physicians less experienced with the
disease. (24)
At the Center for Studying Health System Change in Washington,
D.C., J. Lee Hargraves and colleagues used the Community Tracking Study
Physician Survey, a nationally representative study of American
physicians, to assess their abilities to obtain medically necessary
services for their patients. (25) Physicians were asked how often they
could arrange referrals to specialists and inpatient admissions for
their patients. According to the survey, black physicians were more
likely to report difficulties admitting patients to hospitals than white
physicians, and Hispanic physicians were more likely to report having a
poor specialty-referral network than white physicians.
It is important to recognize that many of the physicians working in
black communities are hardworking, committed individuals who earn
considerably less than other doctors. As Bach's team notes, they
deliver more charity care than doctors who mostly treat white patients
and derive a higher volume of their practice revenue from Medicaid, a
program whose fees are notoriously low. They are often solo
practitioners who scramble to make good referrals for their patients but
are stymied by a dearth of well-trained colleagues and by limited access
to professional networks with advanced diagnostic techniques.
Class trumps race
TO RETURN TO the question we posed at the beginning--would a white
patient and a black patient arriving at the emergency room receive the
same care?--we see that the question itself (at least as it is commonly
understood) is flawed. The question presumes that black and white
patients frequent the same health-care services, carry the same
insurance coverage, and have identical health conditions--yet the data
reveal that often they do not.
The most obvious and influential causes of these disparities reside
in the differing health resources available to blacks and whites,
including the quality of the physicians who treat them. These features
place the emphasis on aspects of the health-care system in generating
race-related differentials in treatment and far less so on clinically
unjustifiable differences in treatment of white and minority patients by
a given physician.
Meanwhile, true physician "bias" is very difficult to
measure and define (since rational inferences are not the same as
genuine prejudice). The Institute of Medicine panel might well have come
to that conclusion itself had Congress directed it to evaluate the
relative contributions of geographic, demographic, social, and economic
factors in explaining discrepancies in care and outcomes. With that
charge, the panel might well have come to a similar conclusion about the
contribution of bias and the dubious value of emphasizing its role in
maintaining the care gap and trying to combat it.
But if physicians cannot fairly be accused of bias, does this not
just shift the charge of bias to the health-care system? In other words,
do black patients receive poorer care because they are black or because
they have disproportionately lower incomes and social capital (for
example, less capacity for negotiating complex systems) than whites--and
are thus disproportionately mired in systems that are underfinanced?
The most recent report from the Agency for Healthcare Research and
Quality suggests this is so. It examines, separately, quality by race
and quality by income. (26) It says that "remote rural
populations" receive poor care, and "many racial and ethnic
minorities and persons of lower socioeconomic positions" receive
suboptimal care.
A better test of the class-trumps-race hypothesis would be to
compare the quality of care received by poor whites clustered in a
particular geographic area (for example, Appalachian populations) to
that received by poor blacks who are clustered for example, in southeast
Washington, D.C. If, after accounting for regional differences in
practice or in health-care financing, comparable (and suboptimal) care
were demonstrated, this would provide powerful support for the idea that
systems serving poor people, irrespective of race, provide lower-quality
care. Until such data are published--surprisingly we could find no
reports on care of low-income whites versus low-income minorities--the
allegation of racial bias in the system is unsupported. (27)
Fortunately, policymakers are attuned to the quality problem and
are grappling with it on several fronts, including the promotion and
spread of information technology, performance enhancement of medical
systems, outcome-based reimbursement to providers, and provider
incentives (including malpractice reform, tax breaks, and assertion of
market mechanisms that, among other things, reward physicians for the
time they spend with patients). They also recognize that low-income
patients benefit from a strong safety net provided by the federally
funded community health-care system (guaranteeing a usual source of
care); grassroots outreach through black churches, social clubs, and
worksites; patient "navigators" to help negotiate the system;
language services; and efforts to get more good doctors into distressed
neighborhoods. Seemingly simple innovations, such as clinic night hours,
could be a great boon to patients with hourly-wage employment who risk a
loss of income, or even their jobs, by taking time off from work for
doctors' appointments.
Much has been made of the need for greater sensitivity in the
doctor-patient relationship. Common sense dictates that patients benefit
when they trust their physicians and interact with them productively.
But the remedies for unsatisfactory doctor-patient relationships do not
reside in racial sensitivity training for health-care professionals or
the specter of Title VI litigation--all of which have been advocated.
Ultimately, improvement in the quality of care and self-care would
elevate the status of minority health appreciably. But the greater
public-health good would be served by applying these goals to all
underserved people rather than focusing on minorities. By focusing on
those with the worst health, the targets of intervention will still turn
out to be poor minority groups, but they will include lower-class whites
as well. For example, establishing screening (for cancer, diabetes, or
hypertension) or wellness-education programs in benighted areas such as
southeast Washington, D.C., or the Watts neighborhood of Los Angeles
would benefit all residents and shrink overall racial differentials in
health outcome because they would disproportionately target minorities.
Perhaps one of the most important factors in health
disparities--self-care--does not depend much on health systems, except,
perhaps, as vehicles for education. It is behaviors such as smoking,
excessive alcohol use, unhealthy dietary patterns, and lack of exercise
that figure so prominently in the development and course of chronic
disease. In this arena, too, the influence of class outstrips race.
Words such as "prejudice," "bias" and
"discrimination" are charged and divisive. Nonetheless, many
medical schools, health philanthropies, policymakers, and politicians
are proceeding as if physician "bias" were an established
fact.
Civil rights advocates talk about the lingering shadow cast by
troubled race relations on the health-care system. Yet, paradoxically,
health campaigns that seek to educate about the alleged bias of
physicians will only inflame the mistrust that some minority patients
already harbor. Concentrating on improving the health of all underserved
Americans is the fairest and most efficient public health agenda.
Sally Satel is a resident scholar at the American Enterprise
Institute and the staff psychiatrist at the Oasis Clinic in Washington,
D.C. She is coauthor, with Christina Hoff Sommers, of One Nation Under
Therapy (St. Martin's Press, 2005). Jonathan Klick is the Jeffrey
A. Stoops Professor of Law at the Florida State University and an
adjunct scholar at the American Enterprise Institute.
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(2) Consortium of Social Science Associations, "COSSA:
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(February 12, 2004).
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(5) Leonard S. Rubenstein and Gretchen Borchelt,
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(8) U.S. Department of Health and Human Services, "The Effect
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(9) Paul D. Stein et al., "Venous Thromboembolic Disease:
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discharge survey found no difference by race in terms of venous
ultrasound, contrast venography, radioisotope lung scan, or duration of
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thrombosis (DVT) and pulmonary embolus (PE) were the same in blacks and
whites.
(10) Katherine Baicker et al., "Who You Are and Where You
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(11) Mitchell L. Margolis et al., "Racial Differences
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(12) Jennifer McCann et al., "Evaluation of the Causes for
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(19) Amber Barnato et al., "Hospital-Level Racial Disparities
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(20) Leo Morales et al., "Mortality Among Very Low Birthweight
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(23) Donald Gemson, Jack Elinson, and Peter Messeri,
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and Minority Patients," Journal of Community Health 13:1 (1988).
(24) Kevin C. Heslin et al., "Racial and Ethnic Differences in
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