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Language is the means by which a physician and a patient exchange illness-related information, share beliefs about health and illness, and engage in shared decision making. When language barriers exist in provider–patient interactions, patients are likely to incur more cost. For example, patients with limited-English-proficiency (LEP) have higher use, longer stay, and more resource utilization (e.g., diagnostic testing) of emergency visits, and reduced use of preventive care and primary care services. Patients with LEP are significantly disadvantaged when interacting with providers, experiencing problematic care. They are less likely to receive follow-up appointments after an emergency visit, less likely to understand a health care provider's instructions, less likely to receive emotional support from their provider, and less satisfied with the quality of care (even in areas unrelated to language). Compared to English-speaking counterparts, patients with LEP make fewer comments during a medical encounter, and the ones they do make are more likely to be ignored by their providers. The literature is replete with studies showing how language barriers can negatively affect access to and quality of care and can lead to undesirable health consequences.

Parents' LEP status is also a major predictor of their children's health disparities. Children of parents with LEP (compared to those with English-proficient parents) have delayed illness care, reduced routine care, higher resource utilization for diagnostic testing, and longer visits in the emergency department. Parents with LEP have a higher risk of problematic medication dosing. They also have odds that are three times as high of a child having fair/poor health status, double the odds of a child spending at least one day in bed for illness in the past year, and significantly greater odds of a child not being brought in for needed medical care for six of nine access barriers to care. When aiming to improve health disparities for minority and immigrant children, it is important to recognize their parents' LEP status as a critical factor in their illness experiences and management.

The Solution?

Interpreters often are viewed as the standard solution to language barriers between providers and patients by health care communities and policy makers. In the United States, since the late 1970s, there have been federal and state legislative efforts to require physicians to provide interpreters for patients with LEP. The most recent action at the federal level is an Executive Order, Improving Access to Services for Persons with Limited English Proficiency, issued by former president Bill Clinton on August 11, 2000, which resulted in U.S. Department of Health and Human Services' guidelines in 2003 to require health care providers to offer language assistance for persons with LEP. As of 2012, many national and regional interpreter associations in the United States have advocated for a national certification for medical interpreters, although a standardized process is still a work in progress.

The assumption that interpreters are the solution to language barriers is largely based on the conceptualization that interpreters can act as cultural brokers and patient advocates in cross-cultural encounters, improving patients' access to and quality of care. However, providers often are concerned about interpreters' involvement and power, fearing their influence over the provider–patient relationship as well as the content and process of provider–patient communication. As a result, the codes of ethics for medical interpreters traditionally view interpreters as a conduit, requiring them to adopt a passive, noninterfering role that provides neutral and faithful relay of information. Many researchers, however, have demonstrated that such an expectation is unrealistic and impractical due to the complexity and dynamics of cross-cultural medical encounters. Rather than prescribing a limited role to interpreters to ensure high quality care, researchers have recommended that providers receive training on working with (different types of) interpreters, be adaptive to the communicative needs and contexts in interpreter-mediated interactions, and nurture institutional cultures and practices that promote interpreters' (appropriate) involvement in the delivery of care.

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