Analysis of life-long strategies to prevent Pneumocystis carinii pneumonia in patients with variable HIV progression rates. NLM AIDSLINE Important note: Information in this article was accurate in 1999. The state of the art may have changed since the publication date.

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Analysis of life-long strategies to prevent Pneumocystis carinii pneumonia in patients with variable HIV progression rates.

AIDS. 1998 Jul 30;12(11):1317-25. Unique Identifier : AIDSLINE MED/98372116
Wynia MK; Ioannidis JP; Lau J; Division of Clinical Care Research, New England Medical Center; Hospitals, Boston, Massachusetts, USA.


Abstract: OBJECTIVE: To compare strategies for life-long prophylaxis of Pneumocystis carinii pneumonia (PCP) in a group of AIDS patients with a wide range of disease progression rates. DESIGN: Markov decision models. METHODS: Prophylaxis strategies using high and low doses of trimethoprim-sulfamethoxazole (TS), dapsone, and/or aerosolized pentamidine in sequence, were compared. Efficacy and toxicity rates for prophylaxis regimens were taken from a meta-analysis of pertinent randomized controlled trials. Outcomes measured included lifetime episodes of PCP and drug toxicity per 100 patients treated, average life expectancy, and cost. RESULTS: For patients with an expected survival of 3 years after commencement of prophylaxis, the use of standard or low dose TS as the first choice agent was comparable, and both were superior to the other strategies for preventing PCP (between nine and 26 fewer episodes of PCP per 100 patients treated) though they were more toxic (11-44 more episodes of toxicity per 100 patients treated). Life expectancy was similar for all of the treatment strategies. With slower rates of disease progression (expected survival > 3.8 years), as seen with current antiretroviral regimens, the use of low dose TS as the first choice agent dominated the use of standard dose TS; when the expected survival time was 7 years, initial use of low dose TS led to 2.8 fewer episodes of PCP per 100 patients treated, 32 fewer episodes of toxicity per 100 patients treated, and US$1381 per patient lower cost, compared with prophylaxis with standard dose TS. CONCLUSION: For patients with AIDS and expected survival > 3.8 years, low dose TS is better than standard dose TS as the first choice agent for preventing PCP. As patients with AIDS live longer, the routine use of low dose TS will be more than adequate for patients at risk for PCP.
Keywords: JOURNAL ARTICLE Antifungal Agents/ADVERSE EFFECTS/ECONOMICS/*THERAPEUTIC USE AIDS-Related Opportunistic Infections/ECONOMICS/*PREVENTION & CONTROL/PHYSIOPATHOLOGY Disease Progression Drug Costs Health Care Costs Human Life Expectancy Markov Chains Pneumonia, Pneumocystis carinii/ECONOMICS/*PREVENTION & CONTROL/ PHYSIOPATHOLOGY Support, U.S. Gov't, P.H.S. Time Factors Trimethoprim-Sulfamethoxazole Combination/ADVERSE EFFECTS/ ECONOMICS/*THERAPEUTIC USEKWDjournalarticleantifungalagents/adverseeffects/economics/KWDtherapeuticuseaids-relatedopportunisticinfections/economics/KWDprevention&control/physiopathologydiseaseprogressiondrugcostshealthcarecostshumanlifeexpectancymarkovchainspneumonia,pneumocystiscarinii/economics/KWDprevention&control/physiopathologysupport,uKWDsKWDgov't,pKWDhKWDsKWDtimefactorstrimethoprim-sulfamethoxazolecombination/adverseeffects/economics/KWDtherapeuticuse
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Copyright © 1999 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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