The Morehouse Faculty Development Program: Methods
and 3-year Outcomes
George Rust, MD, MPH; Vera Taylor, MSTC; René
Morrow, MBA; James Everett, MD, PhD
Background and Objectives: Faculty development
is an established method for increasing the number and effectiveness
of faculty in family medicine. However, few published studies
focus specifically on the use of faculty development to increase
minority representation among faculty. Underrepresented minorities
comprise 20% of the nation’s population but only 3% of medical
school faculty. In the entire nation, only 52 full-time teachers
of family medicine are African-Americans. Morehouse School
of Medicine has developed an effective model for training
large numbers of underrepresented minority physicians to become
academic family physicians. From 1993–1996, we trained 23
community-based physicians, three new faculty, six existing
faculty, and three full-time fellows as teachers of family
medicine. Of 35 participants, 33 were underrepresented minorities.
Cultural issues in teaching and communication are an integral
part of the curriculum. Seventy-three percent of graduates
now teach medical students or residents either full-time or
part-time. Further studies are needed to test the replicability
of this model in non-minority institutions, as well as to
achieve greater cost-effectiveness and improve academic outcomes
such as publications and research. Significant faculty diversity
is necessary and achievable, if institutions are willing to
commit significant resources and network with minority health
professionals and institutions.
Medical
Education and Minority Health
(Fam Med 1998;30(3):162-7.)
Training Family
Medicine Faculty
to Teach in Underserved Settings
Joshua Freeman, MD; Ronald Loewe, PhD;
Janice Benson, MD
Background and Objectives: Because minority
physicians are more likely to practice in minority or medically
underserved communities, meeting the health care needs of
underserved populations requires that programs not only train
such physicians but train minority faculty to act as teachers
and role models. The Faculty Development Center in Family
Medicine at Cook County Hospital has had more than 120 graduates,
most of whom are teaching and practicing in underserved settings.
Nearly half have been minorities, the result of the priority
given to recruitment of minority fellows. The curriculum is
specifically geared to prepare faculty to work in underserved
settings and nurture future physicians for these settings.
Workforce diversity can be achieved only by major changes
in the institutional culture of medical education, which federal
policy can encourage by setting high standards for grant funding
preferences and supporting centers of excellence for training
minority physicians and faculty.
Medical Education and Minority
Health
(Fam Med 1998;30(3):168-72.)
Knowledge and Care
of Chronic Illness in Three Ethnic Minority Groups
Gay Becker, PhD; Yewoubdar
Beyene, PhD; Edwina M. Newsom; Denise V. Rodgers, MD
Background and Objectives: Despite advances
in medical approaches to the management of chronic illnesses,
relatively little is known about how older members of ethnic
minority groups view their chronic illnesses or how they manage
them in daily life.
Methods: We recruited 35 African-Americans,
61 Latinos, and 55 Filipino-Americans, all over age 50. Criteria
for entry into the study was the presence of one or more chronic
illnesses. Findings are based on structured and semi-structured
questions in one in-depth interview. Qualitative data on transcribed
interviews with 151 respondents was analyzed.
Results: Comparison of the three groups
revealed social and cultural differences and similarities
that affected the management of chronic illness. The extent
to which respondents demonstrated an understanding of their
illnesses as chronic varied considerably, with discernible
differences among groups about knowledge of illness and self-care
practices.
Conclusions: Our findings showed that although
major chronic illnesses were, for the most part, the same
for all three groups, each group differed in its response
to and management of its illnesses. These findings have implications
for the education of physicians in training.
Cultural Competence
(Fam Med 1998;30(3):173-8.)
Hmong/Medicine Interactions:
Improving Cross-cultural Health Care
Bruce Barrett, MD, PhD; Kathleen Shadick,
RN, MSN; Rae Schilling, PhD, PsyD; Liz Spencer RD, MS; Salvador
del Rosario; Ka Moua; May Vang
Background and Objectives: There are now
more than 100,000 Hmong (Southeast Asian) refugees in the
United States. This study examined interactions between Hmong
patients and their health care providers and identified specific
factors that either enable or obstruct health care delivery.
Methods: We used semistructured
interview techniques to investigate patients’ and providers’
experiences, looking for attitudes, ideas, or behaviors that
could be modified to improve health care delivery. Interviews
with 23 Hmong patients, 18 health care providers, and six
translators were audiotaped, transcribed, and analyzed by
a multidisciplinary team. Methods included text analysis,
theme identification, rank ordering, participant observation,
immersion-crystallization, and open-ended discussion.
Results: Hmong patients and
their US-trained health care providers have different health
belief systems. Both linguistic and cultural translation were
seen as problematic. Additionally, an overwhelming number
of patients identified kindness, caring, and a positive attitude
as important provider characteristics. Providers noted difficulties
in understanding Hmong conceptions of acute versus chronic
diseases, illness prevention, and pain, both physical and
psychological. Many respondents gave suggestions for improvement:
1) learn more about each other’s cultures, 2) be patient,
kind, and positive, 3) avoid negative statements or predictions,
4) improve translation quality, 5) explain medical terms using
visual aids, 6) respect Hmong family-centered decision making,
7) increase the time allotted for translated clinical encounters,
and 8) train Hmong health care providers.
Conclusions: Many
basic issues in relations between clinicians and Hmong patients
must be addressed to improve health care communication.
Cultural Competence
(Fam Med 1998;30(3):179-84.)
Sudanese Refugees
in a Minnesota Family Practice Clinic
David V. Power, MD, MPH; Dianna J. Shandy,
MA
Background and Objectives:
During the 1990s, African refugees from
the southern Sudan were resettled in Minnesota. This research
characterizes the health care utilization of a small sample
of these recently arrived refugees and describes their health
histories. Methods: Data were abstracted from the medical
charts of all identified Sudanese patients in an urban, Midwestern
family practice residency unit.
Methods: Data were abstracted
from the medical charts of all identified Sudanese patients
in an urban, Midwestern family practice residency unit.
Results: A small sample of
Sudanese refugees were found to have high rates of prior infectious
illness and experienced communication difficulties in accessing
health care.
Conclusions: Information
about this sample’s demographic variables, health behavior,
health histories, and communication difficulties are documented.
Some descriptors of the Nuer ethnic group are provided, and
issues are raised that may help health care workers provide
more culturally competent care to this Sudanese refugee population.
Cultural Competence
(Fam Med 1998;30(3):185-9.)
Health Status of
American Indians/Alaska Natives: General Patterns of Mortality
Martin C. Mahoney, MD, PhD; Arthur M.
Michalek, PhD
Background and Objectives:
Investigations of American Indian and
Alaska Native (AI/AN) populations suggest patterns of mortality
that differ from the general population. Mortality data reveal
excess overall mortality among AI/ANs, as well as excesses
for specific causes of death, including accidents, diabetes,
liver disease, pneumonia/influenza, suicide, homicide, and
tuberculosis. A relative deficit of deaths has been noted
for heart disease, cancer, and HIV infections. It is important
that physicians demonstrate cultural competence so they may
provide quality medical care for the populations they serve.
Activities such as provider education, risk assessment, and
emphasis on preventive services are offered to facilitate
integration into teaching curricula. Knowledge of distinctive
mortality patterns among AI/ANs will help clinicians recognize
the unique needs of these patients.
Clinical Issues in Minority Health
(Fam Med 1998;30(3):190-5.)
Barriers to Health
Care Access
for Latino Children: A Review
Glenn Flores, MD; Luis R. Vega
Background and Objectives:
More than 9 million Latino children
currently live in the United States. Latinos will soon be
the largest minority group in the country, but little is known
about access barriers to health care faced by Latino children.
We reviewed the literature to define specific barriers to
care for Latino children, identify methodologic problems,
and highlight the clinical and research implications of the
identified barriers.
Methods: We did a MEDLINE search,
using combinations of the key words Hispanic, children, and
access. Study exclusion criteria included “not an original
research article,” “enrolled only adult subjects,” “no separate
data analysis for children,” and “dental care focus.”
Results: The search yielded
497 citations, of which 27 met the inclusion criteria. Of
the 32 potential barriers identified, 21 had good supportive
evidence. Lack of health insurance was a consistent barrier;
recent data revealed that 26% of Latino children are uninsured,
compared with 10% of white children and 14% of African-American
children. Latino children also are at greater risk for episodic
insurance coverage, low rates of private insurance, and loss
of employee-based coverage. Parent beliefs about the etiology
and treatment of their child’s illness, use of home remedies,
choice of sources of advice, and folk medicine practices may
also influence how health care is obtained. Few data are available
on differences in access among major Latino subpopulations,
and no studies focused primarily on barriers as perceived
by Latino parents. Evidence is equivocal or lacking that the
following are barriers for Latino children: immigration status,
duration of parent residency in the United States, and acculturation.
Several barriers were identified that originate with practices
and behaviors of health care providers, including reduced
screening, missed vaccination opportunities, decreased likelihood
of receiving prescriptions, and poor communication.
Conclusions: Lack
of health insurance and lack of a regular source of care are
major access barriers for Latino children, but many other
barriers were identified that also can have a substantial
effect on health care. In addition, the behaviors and practices
of both health care providers and parents can affect access
to care. Too little is known about what parents perceive to
be the major barriers, access differences among Latino subpopulations,
the roles of language and culture, and the causes of obstacles
resulting from the actions of providers.
Clinical Issues in Minority Health
(Fam Med 1998;30(3):196-205.)
Filling the Gap:
Equity and Access to Oral Health Services for Minorities and
the Underserved
M. Ann Drum, DDS, MPH; D.W. Chen, MD,
MPH; Rosemary E. Duffy, DDS, MPH
Background and Objectives:
Family physicians and other primary
care providers play a pivotal role in preventing oral disease,
especially among minority and underserved populations who
have limited access to dental services and poorer oral health
status. Oral diseases/conditions, such as caries, baby bottle
tooth decay, gingivitis, periodontitis, oral pharyngeal malignancies,
and orofacial trauma, are prevalent and costly, yet largely
preventable. Given their role in promoting and protecting
overall health and their historical role in serving minority
and underserved families, family physicians occupy a unique
position to assure equity, access, and improvement in oral
health for all Americans.
Clinical Issues in Minority Health
(Fam Med 1998;30(3):206-9.)
Panic Disorder in Hispanic
Patients
David A. Katerndahl, MD, MA; Janet P.
Realini, MD, MPH
Background and Objectives:
This study determined the proportion
of community-dwelling Hispanics who present for medical care
for their panic attacks and identified factors associated
with seeking care. We also compared characteristics of Hispanic
subjects with those of non-Hispanic white panic sufferers.
Methods: In this community-based
study, subjects with panic attacks completed a structured
interview concerning health care utilization, panic characteristics,
coexisting psychiatric problems, and illness attitudes. Hispanics
were self-identified and completed the Cuellar acculturation
scale for Mexican-Americans.
Results: Twenty-nine (53.7%)
of 54 Hispanic subjects had sought medical care for their
panic attacks. Care seeking in non-Hispanic whites was not
dependent on these factors.
Conclusions: Half
of the Hispanics with panic attacks seek no medical care for
their attacks. Predictors of seeking care among Hispanics
in San Antonio included coping style, symptom perceptions,
and access to transportation.
Clinical Issues in Minority Health
(Fam Med 1998;30(3):210-4.)
Patient Ethnicity
and Diagnosis of Emotional Disorders in Women
Shae Graham Kosch, PhD; Mary Ann Burg,
MSW, PhD;
Shifa Podikuju
Background and Objectives:
Ethnic background and family resources
have not been sufficiently examined in relation to emotional
disorders and their treatment in primary care settings. This
study examined the diagnosis and management of psychological
disorders in family practice patients to explore how ethnicity
may affect the diagnosis and treatment of emotional disorders.
Methods: A random sample of
family practice patients was selected from 1 year of office
visits. The charts of 100 African-American and 100 Caucasian
women were audited for primary and secondary diagnoses, presenting
symptoms, prescriptions, psychotherapy referrals, history
of domestic violence and substance use, and family and demographic
characteristics. Chi-square tests of association and multiple
regression were used to analyze the data.
Results: Ethnic background
was significantly associated with a diagnosis of a psychiatric
disorder; 44% of Caucasian patients were diagnosed with an
emotional disorder, compared with 24% of African-Americans.
Proportionately more Caucasian patients with psychiatric diagnoses
were treated with psychotropic medications. Patient race,
marital status, and insurance status explained 15% of the
variance in psychiatric diagnoses.
Conclusions: Women’s
ethnicity is significantly associated with the diagnosis of
emotional disorders and their treatment.
Clinical Issues in Minority Health
(Fam Med 1998;30(3):215-9.)
Supplemental Fitness
Activities and Fitness in Urban Elementary School Classrooms
Mark B. Stephens, MD, MS; Susan W. Wentz,
MD, MS
Background and Objectives:
The physical activity levels of US children
are declining. Opportunities for physical activity within
city schools are constrained by time and space limits. This
study determined whether a supplemental program of physical
activity would significantly alter the fitness levels of low-income,
minority, urban elementary schoolchildren.
Methods: Ninety-nine students
from two Cleveland Public Schools served as subjects. One
school received a 15-week intervention program where teams
of two medical students met with urban elementary schoolchildren
three times a week for physical activity sessions. The other
school served as a control and received no supplemental activity
other than a regularly scheduled physical education class
held once a week. We obtained field measurements of skinfold
thickness, heart rate response to submaximal exercise, and
sit and reach flexibility.
Results: The supplemental activity
group showed significant improvements in flexibility, body
composition, and heart rate response to submaximal exercise.
Conclusions: This
investigation indicates that a program of fitness activities
conducted within the classroom can significantly improve levels
of fitness in urban elementary schoolchildren.
Clinical Issues in Minority Health
(Fam Med 1998;30(3):220-3.)
Race and Ethnicity
in Research
on Infant Mortality
Matthew R. Anderson, MD; Susan Moscou,
FNP, MPH
Background and Objectives:
Race and ethnicity are variables frequently
used in medical research. However, researchers employ race
and ethnicity in different ways and with differing intent.
This leads to confusion over the interpretation of racial
or ethnic differences. This study sought to determine how
race and ethnicity are used in research on infant mortality.
Methods: We did a structured
literature review of original research related to infant mortality
published between January 1995 and June 1996 and indexed in
the Core Contents section of MEDLINE.
Results: The supplemental activity
group showed significant improvements in flexibility, body
composition, and heart rate response to submaximal exercise.
Conclusions: There
are several problems and ambiguities in the use of race and
ethnicity in clinical research. Researchers who use racial
or ethnic categories should do so for specified reasons and
adopt clear definitions of the categories used.
Methodologic Issues in Minority Health Research
(Fam Med 1998;30(3):224-7.)
Disaggregating the
Effects of Race
on Breast Cancer Survival
Daniel L. Howard, PhD; Roy Penchansky,
DBA;
Morton B. Brown, PhD
Background and Objectives:
This study examines differences in breast
cancer survival between African-American and white women to
determine whether there is a racial difference in survival
after accounting for established influences on outcome, such
as stage of cancer, health status, health behavior, utilization
patterns, access to care, quality of care, and the doctor-patient
relationship.
Methods: This study is a retrospective
review of clinical records. The sample consists of 246 patients
of three staff model HMOs who had mastectomies at stage II
or above. Data on patient demographics, stage of cancer, health
status, and health behavior and utilization, including preventive
care, were extracted from patient records. Multivariate logistic
regression was used to predict the determinants of advanced
stage of cancer. Cox survival analysis was used to predict
the determinants of survival.
Results: Missed appointments
and stage of cancer were the key determinants of survival.
The effect of race on survival was marginal after adjusting
for these factors. Race, patients who missed appointments,
and patients who delayed in reporting breast cancer symptoms
were determinants of advanced stage. African-Americans were
overrepresented among patients who missed appointments.
Conclusions: Missed
appointments was a determinant of both advanced stage and
shorter survival. This measure is an important component of
how race affects survival. Compliance with appointment keeping
and alleviating reasons for noncompliance must be considered
as factors in breast cancer survival.
Methodologic Issues in Minority Health Research
(Fam Med 1998;30(3):228-35.)
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