Document 0804 DOCN M9590804 TI Efficacy and toxicity of two doses of trimethoprim-sulfamethoxazole as primary prophylaxis against Pneumocystis carinii pneumonia in patients with human immunodeficiency virus. Dutch AIDS Treatment Group. DT 9509 AU Schneider MM; Nielsen TL; Nelsing S; Hoepelman AI; Eeftinck Schattenkerk JK; van der Graaf Y; Kolsters AF; Borleffs JC; Department of Internal Medicine (Section of Immunology and; Infectious Diseases), University Hospital Utrecht, Netherlands. SO J Infect Dis. 1995 Jun;171(6):1632-6. Unique Identifier : AIDSLINE MED/95287064 AB The efficacy and toxicity of trimethoprim-sulfamethoxazole (TMP-SMZ) as primary prophylaxis against Pneumocystis carinii pneumonia (PCP) for patients with human immunodeficiency virus (HIV) infection was assessed by comparing the effects of two dosages (480 or 960 mg once a day) of the drug. The multicenter trial involved 260 HIV-infected patients with CD4 cell counts < 0.2 x 10(9)/L and no history of PCP. Patients were randomly assigned to the treatment groups. After a median follow-up of 376 days (range, 1-1219), none of the patients developed PCP. Most adverse reactions that required discontinuation were seen within the first month of TMP-SMZ use and were seen more frequently and earlier in the 960-mg group (hazard ratio, 1.4; 95% confidence interval, 0.95-2.02; P = .007). For patients with HIV infection, 480 mg of TMP-SMZ is as efficacious as but less toxic than 960 mg of the drug for primary prophylaxis against PCP. DE Acquired Immunodeficiency Syndrome/*DRUG THERAPY Adult Aged Dose-Response Relationship, Drug Human Middle Age Pneumonia, Pneumocystis carinii/*PREVENTION & CONTROL Sulfamethoxazole/*ADMINISTRATION & DOSAGE Support, Non-U.S. Gov't Survival Analysis Toxoplasmosis/COMPLICATIONS Trimethoprim/*ADMINISTRATION & DOSAGE CLINICAL TRIAL JOURNAL ARTICLE MULTICENTER STUDY RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).