Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59827
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dc.contributor.authorPeter G. Pappasen_US
dc.contributor.authorPloenchan Chetchotisakden_US
dc.contributor.authorRobert A. Larsenen_US
dc.contributor.authorWeerawat Manosuthien_US
dc.contributor.authorMichele I. Morrisen_US
dc.contributor.authorThomansak Anekthananonen_US
dc.contributor.authorSomnuek Sungkanuparphen_US
dc.contributor.authorKhauncahi Supparatpinyoen_US
dc.contributor.authorTracy L. Nolenen_US
dc.contributor.authorLouise O. Zimmeren_US
dc.contributor.authorAmy S. Kendricken_US
dc.contributor.authorPhillip Johnsonen_US
dc.contributor.authorJack D. Sobelen_US
dc.contributor.authorScott G. Filleren_US
dc.date.accessioned2018-09-10T03:22:06Z-
dc.date.available2018-09-10T03:22:06Z-
dc.date.issued2009-06-15en_US
dc.identifier.issn10584838en_US
dc.identifier.other2-s2.0-66949179737en_US
dc.identifier.other10.1086/599112en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=66949179737&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59827-
dc.description.abstractBackground. Cryptococcosis is a life-threatening infection among patients with human immunodeficientcy virus (HIV) infection. Therapeutic options for the treatment of central nervous system cryptococcosis are limited, especially in resource-limited settings. Methods. We conducted a randomized, open-label, phase II trial in Thailand and the United States that compared the safety and efficacy of intravenous amphotericin B deoxycholate (AmB) 0.7 mg/kg (the standard therapy) with that of AmB 0.7 mg/kg plus fluconazole 400 mg (the low-dosage combination) or AmB 0.7 mg/kg plus fluconazole 800 mg (the high-dosage combination) administered daily for 14 days, followed by fluconazole alone at the randomized dosage (400 or 800 mg per day) for 56 days. The primary safety end point was the number of severe or life-threatening treatment-related toxicities; the primary efficacy end point was a composite of survival, neurologic stability, and negative cerebrospinal fluid culture results after 14 days of therapy. Results. A total of 143 patients were enrolled. There were no differences in treatment-related toxicities among the 3 arms. Toxicity was predictable and was most often related to AmB, and it included electrolyte abnormalities, anemia, nephrotoxicity, and infusion-related events. At day 14, 41%, 27%, and 54% of patients in the standard therapy, low-dosage combination, and high-dosage combination therapy arms, respectively, demonstrated successful outcomes. A trend towards better outcomes in the combination therapy arms was seen at days 42 and 70. Conclusions. AmB plus fluconazole administered at a dosage of 800 mg for 14 days, followed by fluconazole administered at a dosage of 800 mg daily for 56 days, is well-tolerated and efficacious among HIV-positive patients with central nervous system cryptococcosis. These results have significant treatment implications and should be validated in a randomized phase III trial. Clinical trials registration. This clinical trial is registered in the National Library of Medicine's registry (http: //www.clinicaltrials.gov) under the registration number NCT00145249. © 2009 by the Infectious Diseases Society of America. All rights reserved.en_US
dc.subjectMedicineen_US
dc.titleA phase II randomized trial of amphotericin B alone or combined with fluconazole in the treatment of HIV-associated cryptococcal meningitisen_US
dc.typeJournalen_US
article.title.sourcetitleClinical Infectious Diseasesen_US
article.volume48en_US
article.stream.affiliationsUniversity of Alabamaen_US
article.stream.affiliationsUniversity of Southern Californiaen_US
article.stream.affiliationsHarbor-UCLA Medical Centeren_US
article.stream.affiliationsUniversity of Miamien_US
article.stream.affiliationsRho Federal Systems Division, Inc.en_US
article.stream.affiliationsUniversity of Texas Systemen_US
article.stream.affiliationsWayne State Universityen_US
article.stream.affiliationsKhon Kaen Universityen_US
article.stream.affiliationsBamrasnaradura Infectious Diseases Instituteen_US
article.stream.affiliationsFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Alabama at Birminghamen_US
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