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Our Mission:
To improve communication between health care
providers and their patients with limited English proficiency.
Our Goal:
Develop affordable models that will help doctors,
hospitals and their staff care for a changing patient population
by funding ten demonstration sites in regions with established
or emerging fast-growing Latino populations.
A growing body of research on health disparities
between ethnic groups is making increasingly clear that being a
member of a minority group in the United States, in and of itself,
can be a barrier to health care. And though socioeconomic status
and ethnicity are only two elements in the larger picture of access
to care, statistically they have shown themselves to be critically
important. The inability to speak English, in particular, has been
empirically associated with less care-seeking and diminished access.
Most health care professionals enter
their careers with the desire to cure or heal. For this reason,
we can assume that non-financial barriers to care are erected unconsciously
and unintentionally. It is the hope of this initiative that with
adequate research, training and resources, the tide of U.S. health
care can be turned to work more effectively with Limited-English-Proficient
(LEP) populations.
Language barriers create problems
for both patients and providers. For patients, language and communication
influence how and if LEP patients access and experience health
care. Because of language barriers, LEP patients often encounter
the following basic types of problems:
- Lack of awareness of existing services and how to access them.
- Difficulty in making appointments and accessing basic information
about the visit, when they do seek care.
- Inability to communicate adequately with health care support
staff, providers, and ancillary staff at all points within the
healthcare delivery system.
- Low patient satisfaction with cross-language encounters, which
may lead to reluctance to return to the health care setting.
Furthermore, research shows that
even when LEP patients are able to access health care, health care
quality may be diminished and health outcomes may be poorer for
them than for other patients. Specifically:
- LEP patients receive less detailed information about rehabilitation
therapy, and understand less of the instructions related to medication.1
- After cross-language encounters, patients are less likely to
keep subsequent appointments and are more likely to make emergency
room visits than are patients in same-language encounters. 2
- Non-English speakers are less likely to receive preventive
services. 3
- Latino parents, in one study, cited language barriers as the
cause of misdiagnoses, poor medical care and inappropriate medications
and/or hospitalizations of their children. 4
Language barriers often cause health care providers challenges in the following tasks:
- In making an accurate diagnosis.
- In meeting informed consent responsibilities.
- While explaining care options to NEP/LEP patients. (This may
lead to more limited options for caring for the patient).
- During health education efforts.
- In convincing NEP/LEP patients to comply with a treatment regimen
they may not understand.
Though language barriers have long
been a concern for health professionals and patients in this country,
the debate over what qualifies as adequate supplementary language
services for LEP patients and how to pay for these services has
been especially heated in the last year. This debate gathered steam
after the release of the Office of Civil Right's policy guidance
on Aug. 30, 2000, which clarified the existing policies of the
Department of Health and Human Services for LEP populations. The
guidance makes clear requirements5 to
which health care providers (and others) who receive federal funds
must adhere in order to continue receiving federal funding such
as payments from Medicaid and Medicare.
The Civil Rights Act of 1964 states
that "No person in the United States shall on the ground of
race, color or national origin, be excluded from participation
in, be denied the benefits of, or be subjected to discrimination
under any program or activity receiving Federal financial assistance."6 Culture
and language have typically been considered an essential part of "national
origin."7 As such,
some key players in the health care environment have sought to
address this issue, though few have done so as thoroughly as the
recent OCR guidance. State and Federal laws require healthcare
providers and managed care organizations to have medical interpreters
for LEP patients but typically do not define what constitutes adequate
training or proficiency for interpreters.
The OCR guidelines are distilled
into four key mandates:
- Assessment. The organizations serving beneficiaries
of federal programs must develop and implement a comprehensive
written policy that will ensure meaningful communication.
- Development of Comprehensive Written Policy on Language
Access. The organizations serving beneficiaries of federal
programs must develop and implement a comprehensive written
policy that will ensure meaningful communication.
- Training of Staff. The organizations serving beneficiaries
of federal programs must take steps to ensure that staff understands
the policy and is capable of carrying it out.
- Vigilant Monitoring. The organizations serving beneficiaries
of federal programs conducts regular oversight of the language
assistance program to ensure that LEP persons meaningfully access
the program. 8
The central issue of the debate
following the OCR guidance has been that, despite a fairly broad
sense in the health care community that LEP populations indeed
have a right to the services of a medical interpreter, these services
can add significant cost to care; a cost that is not currently
specifically addressed by federal funding.
Furthermore, there is little consensus
around what constitutes adequate training for a medical interpreter,
what constitutes quality translation of materials and not much
is known empirically about the effectiveness of interpreter services.
Health care providers currently
face the overwhelming challenge of meeting the cultural and language
needs of wide array of subpopulations. This project chose to concentrate
research on Latinos because of their growing numerical significance
in the United States. Over the last ten years, the Latino population
in the United States has grown to reach over 37 million, with Latinos
representing 13% of all Americans. 9 The
potential language barriers faced by Latino populations are also
significant. The Census 2000 Supplementary Survey estimates that
over 44 million Americans over the age of 5 speak a language other
than English at home, and that for 62% of those 44 million, that
language spoken in the home is Spanish.
In addition to their high growth
and relative need of language services, working with Latinos-because
of the wide variety of their countries of origin-offers a unique
opportunity for insights into the interplay of culture and language
in the health care setting. By specifically addressing language,
we hope to learn more about what is needed for providers to effectively
ensure equal access to health services for NEP and LEP populations.
Population
According to the 2000 Census, the Hispanic population
in the United States is 37 million. This number can be broken down
into subgroups as follows:
Mexican: 20.6 million
Puerto Rican (living in the domestic U.S.): 3.4 million
Puerto Rican (living in Puerto Rico): 3.8 million
Cuban: 1.2 million
Dominican: 765,000
Other: 10 million
Spaniard: 100,000
Central American: 1.7 million
Salvadoran: 655,000
Guatemalan: 372,000
Honduran: 218,000
Nicaraguan: 178, 000
Panamanian: 92, 000
Costa Rican: 69,000
Other: 104,000
South American: 1.4 million
Colombian: 471,000
Ecuadorian: 261,000
Peruvian: 234,000
Argentinean: 101,000
Venezuelan: 92,000
Chilean: 69,000
Bolivian: 42,000
Uruguayan: 19,000
Paraguayan: 9,000
Other: 58,000
Though the Latino population
resides throughout the United States, knowing where its largest
concentrations and most significant areas of growth are can help
us understand where the language barriers issue may be most pressing.
Some statistics:
- 43.5% of Hispanics live in the West
- 32.8% of Hispanics live in the South
- 14.9% of Hispanics live in the Northeast
- 8.9% of Hispanics live in the Midwest
- 4.2 million Hispanics live in Los Angeles County
- 42.1% of the total state population of New Mexico is Hispanic
(the highest proportion for any state). 10
Health Status
The health status of Latinos in the United States
is complex, comprised by a population that experiences a variety
of both health risks and unique protective factors.
According to a report published
by the President's Initiative on Race in 1998 11,
the following are some facts about Latino health status:
- Health status of younger groups of Hispanics may be declining.
- Hispanics (along with American Indians) face higher than average
homicide rates.
- HIV kills black and Hispanic young adults at significantly
higher rates than non-Hispanic whites, Asians or American Indians.
- Blacks and Hispanics are more likely to have disabilities and
chronic disease than white elderly persons, but to some extent
these differences are explained by differences in socioeconomic
status.
- Hispanics are less likely to have health insurance than non-Hispanic
whites.
- Hispanic infant mortality rates are equivalent to those of
non-Hispanic whites, despite lower socioeconomic status of Hispanics.
- Hispanics have lower death rates than non-Hispanic whites for
cancer and heart disease.
Given the demographic complexity
of the Latino population in the United States, data has also been
collected about the health status of Hispanic origin subgroups.
According to a report published by the National Center for Health
Statistics in February of 2000: 12
- Cubans report better health than other Hispanic origin subgroups
(which included Puerto Rican, Mexican, and Other Hispanic).
- A larger percent of Puerto Ricans as compared with other Hispanic
subgroups reported seeing a physician within the past year.
- Cuban individuals reported fewer days lost from school and/or
work than the other three Hispanic origin subgroups.
- A higher percentage of Puerto Ricans had one or more hospital
stay in the past year than other Hispanic origin subgroups.
- A greater percentage of Puerto Rican women considered themselves "current
smokers" at the time of the study, than did members of other
Hispanic origin subgroups.
- Cuban individuals reported having a higher level of knowledge
about AIDS than members of other subgroups.
1-Shapiro J and Saltzer
E (1981). Cross-cultural aspects of physician-patient communication
patterns. Urban Health. Vol 10, 10-15.
2-Manson A. (1988). Language concordance
as a determinant of patient compliance and emergency
room visits in patients with asthma. Medical Care.
Vol. 26. 1119-1128.
3-Woloshin S, Schwartz LM, Katz SJ, and Welch
HG. (1997). Is language a barrier to the use of preventive services?
Journal of General Internal Medicine. Vol. 12, 472-477.
4-Flores G, Abreau M, Olivar M, and Kastner
B. (1998). Access barriers to health care for Latino children.
Archives of Pediatric and Adolescent Medicine. Vol. 152,
119-1125.
5- http://www.hhs.gov/ocr/lep/guide.html
6-Section 601 of Title VI of the Civil Rights Act of
1964, 42 U.S.C. Section 2000d et. seq.
7-Woloshin S, Bickell NA, Schwartz
LM, Gany F and Welch HG. (1995). Language Barriers in Medicine
in the United States. Journal of the American Medical Association.
Vol. 273 (9), 724-728.
8- http://www.hhs.gov/ocr/lep/guide.html
9-LA
Times, 1/21/03, Latinos Now Largest Minority.
10-The Hispanic Population. Census 2000 Brief.
11-Council of Economic Advisors for the President's
Initiative on Race. "Changing America: Indicators of Social and
Economic Well-Being by Race and Hispanic Origin." 1998 http://w3.access.gpo.gov/eop/ca
12-Hajat A, Luca JB, Kington R. Health outcomes among
Hispanic subgroups: United States, 1992-95. Advance data from vital
and health statistics; no. 310. Hyattsville, Maryland: National Center
for Health Statistics, 2000.
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