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DC Field | Value | Language |
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dc.contributor.author | W. Manosuthi | en_US |
dc.contributor.author | P. Chetchotisakd | en_US |
dc.contributor.author | T. L. Nolen | en_US |
dc.contributor.author | D. Wallace | en_US |
dc.contributor.author | S. Sungkanuparph | en_US |
dc.contributor.author | T. Anekthananon | en_US |
dc.contributor.author | K. Supparatpinyo | en_US |
dc.contributor.author | P. G. Pappas | en_US |
dc.contributor.author | R. A. Larsen | en_US |
dc.contributor.author | S. G. Filler | en_US |
dc.contributor.author | D. Andes | en_US |
dc.date.accessioned | 2018-09-04T04:51:28Z | - |
dc.date.available | 2018-09-04T04:51:28Z | - |
dc.date.issued | 2010-04-01 | en_US |
dc.identifier.issn | 14681293 | en_US |
dc.identifier.issn | 14642662 | en_US |
dc.identifier.other | 2-s2.0-77950813660 | en_US |
dc.identifier.other | 10.1111/j.1468-1293.2009.00778.x | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77950813660&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/51091 | - |
dc.description.abstract | Objectives:The aim of the present study was to assess fluconazole pharmacokinetic measures in serum and cerebrospinal fluid (CSF); and the correlation of these measures with clinical outcomes of invasive fungal infections. Methods:A randomized trial was conducted in HIV-infected patients receiving three different regimens of fluconazole plus amphotericin B (AmB) for the treatment of cryptococcal meningitis. Regimens included fluconazole 400 mg/day+AmB (AmB+Fluc400) or fluconazole 800 mg/day+AmB (AmB+Fluc800) (14 days followed by fluconazole alone at the randomized dose for 56 days); or AmB alone for 14 days followed by fluconazole 400 mg/day for 56 days. Serum (at 24 h after dosing) and CSF samples were taken at baseline and days 14 and 70 (serum only) for fluconazole measurement, using gas-liquid chromatography. Results: Sixty-four treated patients had fluconazole measurements: 11 in the AmB group, 12 in the AmB+Fluc400 group and 41 in the AmB+Fluc800 group. Day 14 serum concentration geometric means were 24.7 mg/L for AmB+Fluc400 and 37.0 mg/L for AmB+Fluc800. Correspondingly, CSF concentration geometric means were 25.1 mg/L and 32.7 mg/L. Day 14 Serum and CSF concentrations were highly correlated with AmB+Fluc800 (P<0.001, r=0.873) and AmB+Fluc400 (P=0.005, r=0.943). Increased serum area under the curve (AUC) appears to be associated with decreased mortality at day 70 (P=0.061, odds ratio=2.19) as well as with increased study composite endpoint success at days 42 and 70 (P=0.081, odds ratio=2.25 and 0.058, 2.89, respectively). Conclusion:High fluconazole dosage (800 mg/day) for the treatment of HIV-associated cryptococcal meningitis was associated with high serum and CSF fluconazole concentration. Overall, high serum and CSF concentration appear to be associated with increased survival and primary composite endpoint success. © 2009 British HIV Association. | en_US |
dc.subject | Medicine | en_US |
dc.title | Monitoring and impact of fluconazole serum and cerebrospinal fluid concentration in HIV-associated cryptococcal meningitis-infected patients | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | HIV Medicine | en_US |
article.volume | 11 | en_US |
article.stream.affiliations | Bamrasnaradura Infectious Diseases Institute | en_US |
article.stream.affiliations | Khon Kaen University | en_US |
article.stream.affiliations | Rho Federal Systems Division, Inc. | en_US |
article.stream.affiliations | RTI International | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | Faculty of Medicine, Chiang Mai University | en_US |
article.stream.affiliations | University of Alabama School of Medicine | en_US |
article.stream.affiliations | Keck School of Medicine of USC | en_US |
article.stream.affiliations | David Geffen School of Medicine at UCLA | en_US |
article.stream.affiliations | University of Wisconsin Madison | en_US |
Appears in Collections: | CMUL: Journal Articles |
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