Source:http://linkedlifedata.com/resource/pubmed/id/11015150
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2000-10-16
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pubmed:abstractText |
Trimethoprim-sulfamethoxazole (TMP/SMX) is recognized as the superior agent for Pneumocystis carinii pneumonia (PCP) prophylaxis but a high incidence of adverse drug reactions, which may be due to toxic drug metabolites, limits its use. AIDS Clinical Trials Group protocol 268 was a randomized, double-blind, controlled two-arm trial designed to determine whether gradual initiation of TMP/SMX suspension reduced the incidence of treatment-limiting adverse drug reactions compared with routine initiation of double-strength (DS; 160 mg/800 mg) tablets. In all, 372 HIV-1-infected study subjects with a CD4+ cell count <250 x 10 cells/mm3 who had not previously received TMP/SMX for PCP prophylaxis were randomized to receive either daily TMP/SMX DS tablets or a gradually increasing dose of TMP/SMX suspension. The suspension dose was increased to reach the equivalent of a DS tablet by study day 13. During the first 2 weeks, study subjects also received a matching placebo tablet/suspension. After week 2, all study subjects received TMP/SMX tablets for the next 10 weeks. There were significantly fewer study subjects who discontinued prophylaxis during the first 12 weeks when TMP/SMX therapy was initiated gradually (17%) than when initiated in DS tablet formulation (33%) (p =.0002). Gradual initiation was also associated with significantly fewer adverse drug reactions. Gradual initiation of TMP/SMX for primary PCP prophylaxis reduces the incidence of its treatment-limiting adverse effects.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1525-4135
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
337-43
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11015150-AIDS-Related Opportunistic Infections,
pubmed-meshheading:11015150-Adult,
pubmed-meshheading:11015150-Anti-Infective Agents,
pubmed-meshheading:11015150-CD4 Lymphocyte Count,
pubmed-meshheading:11015150-Double-Blind Method,
pubmed-meshheading:11015150-Drug Eruptions,
pubmed-meshheading:11015150-Female,
pubmed-meshheading:11015150-Fever,
pubmed-meshheading:11015150-HIV Infections,
pubmed-meshheading:11015150-HIV-1,
pubmed-meshheading:11015150-Humans,
pubmed-meshheading:11015150-Male,
pubmed-meshheading:11015150-Nausea,
pubmed-meshheading:11015150-Pneumonia, Pneumocystis,
pubmed-meshheading:11015150-Pruritus,
pubmed-meshheading:11015150-Trimethoprim-Sulfamethoxazole Combination
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pubmed:year |
2000
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pubmed:articleTitle |
Reduced toxicity with gradual initiation of trimethoprim-sulfamethoxazole as primary prophylaxis for Pneumocystis carinii pneumonia: AIDS Clinical Trials Group 268.
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pubmed:affiliation |
Division of Infectious Disease, The Ohio State University, Columbus, Ohio, USA. para.1.osu.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Randomized Controlled Trial
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