Ali
S, Osberg JS.
Differences in follow-up visits between African-American and white Medicaid
children hospitalized with asthma.
J Health Care Poor Underserved. 1997;8(1):83-98.
This well-designed study sought to examine whether racial disparities
persist in primary care for children with asthma, a chronic yet highly
treatable condition, across a clinically and demographically comparable
population with the same health insurance coverage. It also sought to
determine if the guidelines set by the NIH to assist clinicians with the
diagnosis and treatment of asthma were adhered to in the delivery of care,
specifically, the recommended guidelines for follow-up visits subsequent
to hospitalizations.
The authors identified a sample of 500 Medicaid-enrolled children (207
African American, 293 white) who had been hospitalized for asthma. All
lived in an urban area of Massachusetts and thus shared similar socioeconomic
status and environmental barriers to care. Using this study sample, the
investigators were able to control for the commonly stated risk factors
for asthma hospitalization and death – i.e. poverty, urban residence,
and health insurance coverage. Claims data for the six-month period after
hospitalization were analyzed to determine the number of asthma-related
and non-asthma-related primary care visits, emergency room visits and
hospitalizations. The number of visits was examined at two weeks, four
weeks, and six months after hospitalization.
There were no statistically significant differences in the socio-demographic
characteristics of African-Americans and whites at the 0.05 level. Regarding
the NIH recommended guidelines for follow-up visits within two weeks of
hospitalization, the study found that, in that time period, 90 percent
of the 500 Medicaid children had not seen a physician for asthma. “Asthma
management guidelines also recommend that children have regular contact
with a clinician to monitor their condition.” However, “in
the Medicaid sample, by six months post-discharge, 81 percent of the children
still had not received a follow up visit for asthma; about one in five
children (21 percent) had not seen a physician at all.”
When results were stratified by race, there were significant differences
in rates of post-hospital care. In the two weeks after hospitalization,
94 percent of African American children versus 87 percent of white children
had not seen a physician for asthma. “African American children
were half as likely to have received follow-up care for asthma compared
with their white counterparts (6 and 13 percent, respectively).”
After four weeks, 85 percent of white children and 93 percent of African
American children had not see a physician for asthma. At six months, “the
racial disparity in asthma-related physician visits persisted; 87 percent
of African American children and 77 percent of white children still had
not seen a physician for asthma.” These differences were all statistically
significant at the 0.05 level. Emergency room visits and hospitalizations
did not differ significantly by race; however, the use of emergency services
for both groups suggests “that asthma is a persistent and serious
problem for this population.” Furthermore, the lack of significant
differences in hospital readmission and ER visit rates between African
American and white children indicate that African American children “were
not making up for [the] utilization deficit by having more urgent care.”
The authors conclude “that the vast majority of the 500 children
studied experienced follow-up care well below the recommended level.”
More disturbing is the finding that “within this population of children
generally receiving suboptimal care, African American children fared even
worse.”
Given the makeup of this study population, the authors were able to dismiss
“underlying racial differences in poverty and other environmental
or social conditions” as possible explanations for these disparities.
A possible explanation proposed is African Americans’ “deep-seated
distrust of the health care system.” As a potential solution, the
investigators suggest that “culturally sensitive providers are needed
to offer appropriate medical advice but also to understand the day to
day difficulties associated with living in the patient’s home, school,
and work environments.” They state, “the inability of providers
to relate to minority patients on a more personal level may act as a barrier
to appropriate care-seeking behavior” and contend that the “impact
of racism on patterns of health services utilization deserves further
consideration.”