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| April
12, 2006
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| Phillips,
Patterson Encourage State to Collect Complete Health Data |
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| Ethnicity, Language Data Help Target Health Disparities | |||
| Metropolitan
King County Councilmembers Larry
Phillips and Julia
Patterson are encouraging the Washington State Department of
Health to require hospitals to gather additional information that can assist
health officials in identifying health disparities in their communities.
“Health professionals told us at our February Town Hall meeting that information is a critical tool in combating the health disparities that continue to affect low-income communities and communities of color,” said Phillips, chair of the County Council. “If they know about medical problems that are prevalent in a specific community or ethnic group, they can plan a course of action to combat those problems. The information we’re asking hospitals to collect can literally save lives—but only if it’s available.” “King County struggles to accurately gauge the degree of health disparities, mainly because data regarding patient demographics does not exist. When we know, from hospital statistics, who is suffering at high rates from chronic, transmissible and preventable diseases, we can best target our public health resources to provide the greatest benefit to the communities that need it most,” said Patterson, chair of the King County Board of Health. “Ultimately, the goal is to ensure that patients who are poor, minorities, or limited English speakers receive the same quality of care as those who are affluent.” Both Phillips and Patterson have sent letters to Secretary of Health Mary Selecky, asking that the State Department of Health require hospitals to include Race/Ethnicity and primary language in the data collected as part of the Comprehensive Hospital Abstract Reporting System (CHARS). CHARS was originally developed to monitor hospital charges
and set billing rates, but has developed into a health assessment tool
representing data on hundreds of thousands of hospitalizations and billions
of dollars of charges each year. CHARS data is now an essential part of
local planning and disease monitoring efforts. A recent decision by the
CHARS Recommendation Committee to have hospitals asked for patient race/ethnicity
information, prompted the Councilmembers to ask that hospitals also collect
data on the patient’s primary language needed for communicating
health information between the patient and provider. “Health
disparities are a reality—the challenge for us is where to place
the resources needed to end those disparities,” said Phillips. “The
information we’re asking for can act as a road map of communities
that need help. We need to start collecting it as soon as possible.”
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Phone: (206) 296-1000 | Fax: (206) 296-0198 | TTY/TDD:
(206) 296-1024 | Toll Free: (800) 325-6165 |
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