Nevirapine Levels after Discontinuation of Rifampicin Therapy and 60‐Week Efficacy of Nevirapine‐Based Antiretroviral Therapy in HIV‐Infected Patients with Tuberculosis
1Bamrasnaradura Infectious Diseases Institute, Ministry of Public Health, Nonthaburi, and 2The HIV Netherlands‐Australia‐Thailand Research Collaboration, Thai Red Cross AIDS Research Centre and Chulalongkorn University, and 3Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
Seventy patients with human immunodeficiency virus (HIV) and tuberculosis coinfection who initiated nevirapine‐based antiretroviral therapy and had trough nevirapine levels determined while receiving rifampicin were enrolled in a study. After discontinuation of rifampicin therapy, mean nevirapine levels (± standard deviation) increased from
mg/L to
mg/L (
), but no nevirapine‐related adverse events occurred. There was no statistically significant difference in 60‐week antiviral efficacy between these patients and patients receiving nevirapine‐based antiretroviral therapy alone (
).
Received 21 July 2006; accepted 1 September 2006; electronically published 21 November 2006.
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