You are not currently logged in.
Access JSTOR through your library or other institution:
Quality Enhancement Research Initiative for Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome: Framework and Plan
Samuel A. Bozzette, Barbara Phillips, Steven Asch, Allen L. Gifford, Leslie Lenert, Terri Menke, Eduardo Ortiz, Douglas Owens and Lawrence Deyton
Vol. 38, No. 6, VA QUERI Supplement: VA's Quality Enhancement Research Initiative (Jun., 2000), pp. I60-I69
Published by: Lippincott Williams & Wilkins
Stable URL: http://www.jstor.org/stable/3767346
Page Count: 10
You can always find the topics here!Topics: HIV, AIDS, Viral diseases, Antiretrovirals, Health outcomes, Databases, Disease risk, Quality of life, Epidemiology, Infections
Were these topics helpful?See something inaccurate? Let us know!
Select the topics that are inaccurate.
Preview not available
The Veterans Health Administration (VHA) sees ≈17,000 human immunodeficiency virus (HIV)-infected patients each year, which makes it the largest provider of HIV care in the United States. HIV causes chronic progressive disease that leads to early death. Newer combination antiretroviral treatments are effective but expensive and difficult to use. The HIV Quality Enhancement Research Initiative (HIV-QUERI) uses the QUERI process to identify high-risk and high-volume populations (step 1), which includes those already under VHA care for HIV, those who do not know of their infection, and those at risk for HIV. In identifying best practices (step 2), the HIV-QUERI will benefit greatly from existing guidelines for the care of established HIV infection, but gaps in knowledge regarding adherence to medication regimens and cost-effective screening are large. To identify existing practice patterns (step 3), the HIV-QUERI will develop a clean analytic data set based on Immunology Case Registry files and expand it through a survey of veterans. Interventions to improve care (step 4) will include national, regional, and site-specific feedback on performance relative to quality standards, as well as patient-level and provider-level interventions to improve adherence and support medical decision-making. To document that best practices improve outcomes and quality of life (steps 5 and 6), HIV-QUERI will track indicators on an ongoing basis by use of the Immunology Case Registry database and possible future waves of the survey. In addition, we will require that these issues be addressed in evaluations of HIV-QUERI interventions. In the present article, we present these steps within a framework and plan.
Medical Care © 2000 Lippincott Williams & Wilkins