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First published February 24, 2006 as JAMIA PrePrint; doi:10.1197/jamia.M2005
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J Am Med Inform Assoc. 2006;13:253-260. DOI 10.1197/jamia.M2005.
© 2006 American Medical Informatics Association


Viewpoint Paper

Viewpoint: A Pragmatic Approach to Constructing a Minimum Data Set for Care of Patients with HIV in Developing Countries

William M. Tierney, MD, Eduard J. Beck, MBBS, PhD, Reed M. Gardner, PhD, Beverly Musick, MS, Mark Shields, MD, MPH, MS, Naomi M. Shiyonga and Mark H. Spohr, MD

Affiliations of the authors: Indiana University School of Medicine, Indianapolis, IN (WMT, BM); Regenstrief Institute, Inc., Indianapolis, IN (WMT); World Health Organization, Geneva, Switzerland (EJB); McGill University, Montreal, Quebec, Canada (EJB); Department of Medical Informatics, University of Utah School of Medicine, Salt Lake City, UT (RMG); Oak Ridge Institute of Science and Education, Oak Ridge, TN (MS); Centers for Disease Control and Prevention, Global AIDS Program, Lusaka, Zambia (MS); National AIDS, TB, and Leprosy Control Programme, Ministry of Health, Nairobi, Kenya (NMS); USAID MEASURE Evaluation, John Snow, Inc., Arlington, VA (MHS).

Correspondence and reprints: William M. Tierney, MD, Room M200-OPW, Wishard Memorial Hospital, 1001 West Tenth Street, Indianapolis, IN 46202; e-mail: <wtierney{at}iupui.edu>.

Received for publication: 10/11/05; accepted for publication: 02/13/06.

Providing quality health care requires access to continuous patient data that developing countries often lack. A panel of medical informatics specialists, clinical human immunodeficiency virus (HIV) specialists, and program managers suggests a minimum data set for supporting the management and monitoring of patients with HIV and their care programs in developing countries. The proposed minimum data set consists of data for registration and scheduling, monitoring and improving practice management, and describing clinical encounters and clinical care. Data should be numeric or coded using standard definitions and minimal free text. To enhance accuracy, efficiency, and availability, data should be recorded electronically by those generating them. Data elements must be sufficiently detailed to support clinical algorithms/guidelines and aggregation into broader categories for consumption by higher level users (e.g., national and international health care agencies). The proposed minimum data set will evolve over time as funding increases, care protocols change, and additional tests and treatments become available for HIV-infected patients in developing countries.







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Copyright © 2006 by the American Medical Informatics Association.