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Projecting the cost-effectiveness of adherence interventions in persons with human immunodeficiency virus infection - 28/08/11

Doi : 10.1016/j.amjmed.2003.07.007 
Sue J. Goldie, MD, MPH a, , A.David Paltiel, PhD c, Milton C. Weinstein, PhD a, Elena Losina, PhD d, e, George R. Seage, ScD, MPH b, April D. Kimmel e, Rochelle P. Walensky, MD, MPH e, f, Paul E. Sax, MD f, Kenneth A. Freedberg, MD, MSc a, d
a Center for Risk Analysis (SJG, MCW, KAF), Harvard School of Public Health, Boston, Massachusetts, USA 
b Department of Health Policy and Management, and Department of Epidemiology (GRS), Harvard School of Public Health, Boston, Massachusetts, USA 
c Department of Epidemiology and Public Health (ADP), Yale University School of Medicine, New Haven, Connecticut, USA 
d Departments of Epidemiology and Biostatistics (EL, KAF), Boston University School of Public Health, Boston, Massachusetts, USA 
e Divisions of General Medicine and Infectious Diseases and the Partners AIDS Research Center (EL, ADK, RPW, KAF), Massachusetts General Hospital, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA 
f Division of Infectious Diseases (RPW, PES), Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA 

*Requests for reprints should be addressed to Sue J. Goldie, MD, MPH, Department of Health Policy and Management, Harvard School of Public Health, 718 Huntington Avenue, 2nd Floor, Boston, Massachusetts 02115-5924, USA

Abstract

Purpose

To explore the cost-effectiveness of interventions to improve adherence to combination antiretroviral therapy in patients with human immunodeficiency virus (HIV) infection.

Methods

A simulation model of HIV infection, incorporating CD4 cell count and HIV ribonucleic acid levels as predictors of disease progression, was used to estimate the lifetime costs and quality-adjusted life expectancy associated with clinical interventions to improve adherence to antiretroviral therapy (e.g., directly observed therapy, automatic medication dispensers, beepers, portable alarms) in a clinical trial cohort with early disease (mean CD4 count, 350 cells/μL), a clinical trial cohort with advanced disease (mean CD4 count, 87 cells/μL), and an urban cohort (mean CD4 count, 217 cells/μL). Data were from clinical trials, national databases, and published literature.

Results

For relatively healthy patients with early disease, interventions that reduced virologic failure rates by 10% increased quality-adjusted life expectancy by 3.2 months, whereas those that reduced failure by 80% increased quality-adjusted life expectancy by 34.8 months, as compared with standard care. The cost-effectiveness ratio was below $50,000 per quality-adjusted life-year (QALY) for interventions costing $100 per month provided that failure rates were reduced by at least 10%, and for those costing $500 per month provided that failure rates were reduced by more than 50%. For both patients with advanced disease and those from an urban cohort, adherence interventions costing about $500 per month (e.g., directly observed therapy) had to reduce failure by about 25% to have cost-effectiveness ratios below $50,000 per QALY.

Conclusion

In patients with lower baseline levels of adherence or advanced disease, even very expensive, moderately effective adherence interventions are likely to confer cost-effectiveness benefits that compare favorably with other interventions.

Le texte complet de cet article est disponible en PDF.

Plan


 Supported in part by the Society of General Internal Medicine, 1998 Lawrence S. Linn Award, and by the Centers for Disease Control and Prevention (Cooperative Agreements 114927, 119525), the National Institute of Allergy and Infectious Diseases (AI42006, AI01794, U0138838, P30AI42851), and the Health Resources and Services Administration (award number HA 00176).


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Vol 115 - N° 8

P. 632-641 - décembre 2003 Retour au numéro
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