TY - JOUR
T1 - Primary prophylaxis with pyrimethamine for toxoplasmic encephalitis in patients with advanced human immunodeficiency virus disease
T2 - Results of a randomized trial
AU - Terry Beirn Community Programs for Clinical on AIDS
AU - Mark A, Jacobson
AU - Besch, C. Lynn
AU - Child, Carroll
AU - Hafner, Richard
AU - Matts, John P.
AU - Muth, Katherine
AU - Wentworth, Deborah N
AU - Neaton, Jim
AU - Abrams, Donald
AU - Rimland, David
AU - Perez, George
AU - Grant, Irene H.
AU - Saravolatz, Louis D.
AU - Brown, Lawrence S.
AU - Deyton, Lawrence
N1 - Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 1994/2
Y1 - 1994/2
N2 - Pyrimethamine, 25 mg thrice weekly, was evaluated as primary prophylaxis for toxoplasmic encephalitis (TE) in a double-blind, randomized clinical trial in patients with human immunodeficiency virus (HIV) disease, absolute CD4 lymphocyte count of <200/μL (or prior AIDS-defining opportunistic infection), and the presence of serum IgG to Toxoplasma gondii. Leucovorin was coadministered only for hematologic toxicity. There was a significantly higher death rate among patients receiving pyrimethamine (relative risk [RR], 2.5; 95% confidence interval [CI], 1.3-4.8; P =.006), even after adjusting for factors predictive of survival. The TE event rate was low in both treatment groups (not significant). Only 1 of 218 patients taking trimethoprim-sulfamethoxazole but 7 of 117 taking aerosolized pentamidine for prophylaxis against Pneumocystis carinii pneumonia developed TE (adjusted RR for the trimethoprim-sulfamethoxazole group, 0.16; 95% CI, 0.01-1.79; P =.14). Thus, for HIV-infected patients receiving trimethoprim-sulfamethoxazole, additional prophylaxis for TE appears unnecessary.
AB - Pyrimethamine, 25 mg thrice weekly, was evaluated as primary prophylaxis for toxoplasmic encephalitis (TE) in a double-blind, randomized clinical trial in patients with human immunodeficiency virus (HIV) disease, absolute CD4 lymphocyte count of <200/μL (or prior AIDS-defining opportunistic infection), and the presence of serum IgG to Toxoplasma gondii. Leucovorin was coadministered only for hematologic toxicity. There was a significantly higher death rate among patients receiving pyrimethamine (relative risk [RR], 2.5; 95% confidence interval [CI], 1.3-4.8; P =.006), even after adjusting for factors predictive of survival. The TE event rate was low in both treatment groups (not significant). Only 1 of 218 patients taking trimethoprim-sulfamethoxazole but 7 of 117 taking aerosolized pentamidine for prophylaxis against Pneumocystis carinii pneumonia developed TE (adjusted RR for the trimethoprim-sulfamethoxazole group, 0.16; 95% CI, 0.01-1.79; P =.14). Thus, for HIV-infected patients receiving trimethoprim-sulfamethoxazole, additional prophylaxis for TE appears unnecessary.
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U2 - 10.1093/infdis/169.2.384
DO - 10.1093/infdis/169.2.384
M3 - Article
C2 - 8106772
AN - SCOPUS:0028012422
SN - 0022-1899
VL - 169
SP - 384
EP - 394
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 2
ER -