AIDSWEEKLY Plus; June 10, 2002
Michael Greer, Senior Medical Writer
"Human immunodeficiency virus (HIV)-infected patients receiving highly active antiretroviral therapy (HAART) have experienced a dramatic decrease in Pneumocystis carinii pneumonia (PCP), necessitating reassessment of clinical guidelines for prophylaxis," explained Dr. Sue J. Goldie and colleagues at Harvard University, Boston University, and Massachusetts General Hospital in Boston, the U.S. Centers for Disease Control and Prevention in Atlanta, Yale University in New Haven, Connecticut, and the Community Research Initiative New England in Brookline, Massachusetts.
Goldie and coauthors were able to determine the most cost-effective points to halt PCP prophylaxis, as well as the most cost-effective prophylactic agents, according to their report.
The researchers used a simulation model to find the quality-adjusted life expectancy (QALE) and cost per quality-adjusted life year (QALY) for a number of prophylaxis end points in patients whose CD4 cell counts rose during highly active antiretroviral therapy (HAART). The cost-effectiveness of alternative agents for patients unable to tolerate standard trimethoprim-sulfamethoxazole (TMP/SMX) prophylaxis were also examined, they said.
Delaying the end of prophylaxis until CD4 cell counts rose to at least 300 cells/µL saved US$9400/QALY compared with prophylactic regimens ending at a CD4 cell count of only 200 cells/µL, study data showed. Moreover, the decision to wait until CD4 cell counts hit at least 300 cells/µL prevented 9 PCP infections per 1000 patients treated.
Dapsone provided efficacy similar to that of atovaquone in TMP/SMX-intolerant patients and cost only US$4500/QALY, in contrast to atovaquone's price tag of more than US$1.5 million/QALY (Prophylaxis for human immunodeficiency virus-related Pneumocystis carinii pneumonia - Using simulation modeling to inform clinical guidelines, Arch Intern Med 2002 Apr 22;162(8):921-8.
"Delaying discontinuation of PCP prophylaxis until the first observed CD4 cell count greater than 300/µL is cost-effective and provides an explicit 'PCP prophylaxis stopping criterion,'" Goldie and colleagues concluded. "In TMP/SMX-intolerant patients, dapsone is more cost effective than atovaquone."
The corresponding author for this report is Sue J. Goldie, MD, MPH, Center for Risk Analysis, Department of Health Policy and Management, Harvard School of Public Health, 718 Huntington Ave, Second Floor, Boston, MA 02115, USA.
A search at www.NewsRx.net using the search term "AIDS and HIV therapy" yielded 1101 articles in 27 specialized reports.
Key points reported in this study include:
This article was prepared by AIDS Weekly editors from staff and other reports.
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