Publication:
Nevirapine plasma concentrations and concomitant use of rifampin in patients coinfected with HIV-1 and tuberculosis

dc.contributor.authorReshma S. Autaren_US
dc.contributor.authorFerdinand W.N.M. Witen_US
dc.contributor.authorJongkol Sankoteen_US
dc.contributor.authorApicha Mahanonthariten_US
dc.contributor.authorThanomsak Anekthananonen_US
dc.contributor.authorPiroon Mootsikapunen_US
dc.contributor.authorKhanjtta Sujaikaewen_US
dc.contributor.authorDavid A. Cooperen_US
dc.contributor.authorJoep M.A. Langeen_US
dc.contributor.authorPraphan Phanuphaken_US
dc.contributor.authorKiat Ruxrungthamen_US
dc.contributor.authorDavid M. Burgeren_US
dc.contributor.otherThe HIV Netherlands Australia Thailand Research Collaborationen_US
dc.contributor.otherUniversity of Amsterdamen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherKirby Instituteen_US
dc.contributor.otherUniversity of New South Wales (UNSW) Australiaen_US
dc.contributor.otherPharmAccess Foundationen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherRadboud University Nijmegen Medical Centreen_US
dc.date.accessioned2018-06-21T08:20:33Z
dc.date.available2018-06-21T08:20:33Z
dc.date.issued2005-12-01en_US
dc.description.abstractObjectives: In countries with high numbers of HIV/tuberculosis coinfection nevirapine and rifampin are used extensively. However, limited data are available about whether or not nevirapine and rifampin can be safely co-administered without the plasma concentration of nevirapine falling below therapeutic levels. Methods: Blood samples for determination of nevirapine plasma concentrations were collected from patients using nevirapine 200 mg twice daily with or without concomitant rifampin. Bivariate and multivariate linear regression models were used to investigate factors possibly related to nevirapine concentrations. Results: We received 74 blood samples from patients using nevirapine plus rifampin, and collected blood samples from an equal number of controls using nevirapine only. Groups were similar for age, gender, weight, height and body mass index (BMI). In the rifampin group the mean nevirapine concentration was 5.47 ± 2.66mg/l, whereas in the control group the mean nevirapine concentration was 8.72 ± 3.98 mg/l. In the rifampin group seven nevirapine trough concentrations were low (<3.1 mg/l), while in the control group two patients had low nevirapine trough concentrations (P=0.164). In the multivariate linear regression analysis, corrected for time after drug intake, the use of rifampin was significantly (P<0.001) associated with lower nevirapine plasma concentrations, whereas higher BMI reached borderline significance (P=0.065). Conclusion: Although nevirapine plasma concentrations were 3.3 mg/l lower when co-administered with rifampin, still more than 86% of these patients had nevirapine plasma concentrations >3.1 mg/l. Our results suggest that from a pharmacological point of view the majority of Thai coinfected patients, who have low BMIs, reach nevirapine plasma concentrations that are adequate for treatment of HIV. However this can only be undertaken if nevirapine plasma concentration monitoring is available and can be closely followed. © 2005 International Medical Press.en_US
dc.identifier.citationAntiviral Therapy. Vol.10, No.8 (2005), 937-943en_US
dc.identifier.issn13596535en_US
dc.identifier.other2-s2.0-30444444706en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16730
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=30444444706&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleNevirapine plasma concentrations and concomitant use of rifampin in patients coinfected with HIV-1 and tuberculosisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=30444444706&origin=inwarden_US

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