Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/60489
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dc.contributor.authorSubsai Kongsaengdaoen_US
dc.contributor.authorKanoksri Samintarapanyaen_US
dc.contributor.authorKanokporn Oranratnachaien_US
dc.contributor.authorWantana Prapakarnen_US
dc.contributor.authorChatchawann Apichartpiyakulen_US
dc.date.accessioned2018-09-10T03:43:37Z-
dc.date.available2018-09-10T03:43:37Z-
dc.date.issued2008-01-01en_US
dc.identifier.issn15570886en_US
dc.identifier.issn15451097en_US
dc.identifier.other2-s2.0-77955660977en_US
dc.identifier.other10.1177/1545109707301244en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955660977&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60489-
dc.description.abstractBackground: Toxoplasmic encephalitis (TE), caused by Toxoplasma gondii, is common in AIDS patients. TE can result in tissue destruction via massive inflammation and brain abscess formation. Methods: Randomized controlled trials were performed in AIDS patients to assess which drug regimen was optimally effective for the treatment of TE. AIDS patients with TE were randomly divided into 3 groups that received a 6-week course of either pyrimethamine (50 mg/ day or 100 mg/day) plus sulfadiazine (4 g/day) and folinic acid (25 mg/day) or trimethoprim (10 mg/kg/day) plus sulfamethoxazole (50 mg/kg/day) (TMP-SMX), and results were evaluated with respect to clinical response, mortality, morbidity, and serious adverse events. The primary outcome was defined as death in the first 6-week period. The secondary outcome was successful treatment within 6 weeks without severe adverse events, bone marrow suppression, drug-induced rash, or any other event that caused a change in the treatment regimen. Results: The results from this study showed that in AIDS patients, TE was most successfully treated with the combination of pyrimethamine (50 mg/day) plus sulfadiazidine (4 g/day) and folinic acid (25 mg/day); failure rates were not significantly different among the 3 treatment groups. Conclusions: Available data suggest that of the currently available options, treatment of TE with pyrimethamine at 50 mg/day plus sulfadiazidine at 4 g/day provides the best primary outcome for AIDS patients with TE; however, because this study was terminated prematurely, we suggest that treatment with intravenous TMP-SMX be further evaluated to determine its efficacy. © 2008 Sage Publications.en_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleRandomized controlled trial of pyrimethamine plus sulfadiazine versus trimethoprim plus sulfamethoxazole for treatment of toxoplasmic encephalitis in AIDS patientsen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of the International Association of Physicians in AIDS Careen_US
article.volume7en_US
article.stream.affiliationsRajavithi Hospitalen_US
article.stream.affiliationsLumpang Hospitalen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsRangsit Universityen_US
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