JAIDS Journal of Acquired Immune Deficiency Syndromes · 2001 · 24 citations · 15 references
PharmacotherapyPilot StudyDrug ResistancePreventive MedicineClinical EpidemiologyClinical TrialsPublic HealthMatching PlaceboTherapeutic Drug MonitoringPrimary PreventionCotrimoxazole GroupHivPharmacologyCd4 Cell CountHiv-1–infected AdultsSexual HealthTreatment And PreventionGlobal HealthAntiviral TherapyMedicinePharmacoepidemiology
Objectives: To assess the efficacy and tolerance of chemoprophylaxis with cotrimoxazole compared with placebo among HIV-1-infected adults. Design: Randomized, double-blind, placebo-controlled clinical trial in the urban community of Dakar, Senegal. Methods: Eligibility criteria were age greater than 15 years, HIV-1 or HIV-1 and HIV-2 dual seropositivity, CD4 cell count lower than 400 copies/mm3, no progressive infection, no previous history of intolerance to sulphonamide, lack of severe anemia or neutropenia, and renal or hepatic failure. Written informed consent was obtained. Recruited patients received 80 mg of trimethoprim and 400 mg of sulphamethoxazole daily or a matching placebo. The main outcomes were survival and the occurrence of clinical events defined as Pneumocystis carinii pneumonia, cerebral toxoplasmosis, bacterial pneumonia, infectious enteritis, bacterial meningitis, urinary tract infection, bacterial otitis and sinusitis, and pyomyositis. Results: Between September 1996 and March 1998, 297 patients were screened, and 100 were randomized in the study. Demographic, clinical, and biological characteristics of the two groups were similar as was the mean length of follow-up (7.7 months for the cotrimoxazole group vs. 8.0 months for the placebo group). There was no significant difference between the two groups in survival (hazard ratio = 0.84; 95% confidence interval [CI]: 0.36-1.94) in the probability of severe event occurrence, defined as death or hospital admission (hazard ratio = 1.10; 95% CI: 0.57-2.13), or in the probability of clinical event occurrence (hazard ratio = 1.19; 95% CI: 0.55-2.59). Adjustment for initial CD4 cell count did not change these results. A low dose of cotrimoxazole was tolerated well clinically as well as biologically; only one treatment interruption occurred as the result of a moderate cutaneous eruption (grade 2). Conclusion: Our study does not show a beneficial effect of chemoprophylaxis with low-dose cotrimoxazole on survival or occurrence of opportunistic or nonopportunistic infections for HIV-1-infected patients in Dakar, Senegal.
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The mortality and pathology of HIV infection in a West African city
Sebastian Lucas, A. Hounnou, Christopher S. Peacock et al. · AIDS · 1993 · 564 citations
Stefan Z. Wiktor, Madeleine Sassan‐Morokro, Alison D. Grant et al. · The Lancet · 1999 · 425 citations
Pulmonary Tuberculosis, Treatment And Prevention, Tuberculosis Prevention +7
M. M. E. Schneider, Andy I. M. Hoepelman, Jan Karel M. Eeftinck Schattenkerk et al. · New England Journal of Medicine · 1992 · 278 citations · Full text