Hepatitis associated with prothionamide for treatment of multidrug-resistant tuberculosis

Han Lin Hsu, Kuan Jen Bai, Yi Chun Chiang, Shian Jiun Lin, Ming Chih Yu

研究成果: 雜誌貢獻文章

4 引文 斯高帕斯(Scopus)

摘要

Timely and intensive monitoring for, and management of, adverse effects caused by anti-tuberculosis drugs are essential components of control programs for multidrug-resistant tuberculosis (MDR-TB). This retrospective case series was conducted in northern Taiwan from January 2007 to December 2008 at Taipei Medical University-Wan Fang Hospital, a 750-bed tertiary-care center and MDR-TB referral center. Hepatitis associated with prothionamide was defined as the recurrence of hepatitis after a second prothionamide treatment re-challenge. In total, 47 patients with MDR-TB enrolled in the Directly Observed Therapy, Short Course-Plus Program were identified during the study period, and 44 (93.6%) were treated with prothionamide. Seven of these 44 patients (15.9%) developed hepatitis after being treated with prothionamide concurrent with other anti-tuberculosis agents. Hepatitis associated with prothionamide occurred in three of these seven patients (6.8%). In these three patients, hepatitis developed following treatment with prothionamide for 28 days, 39 days or 45 days. Hepatitis developed rapidly after re-challenge with prothionamide at 4 days, 4 days and 3 days, respectively. Liver function returned to the normal range after cessation of prothionamide treatment for 19 days, 27 days or 28 days. Close monitoring of liver function was necessary in MDR-TB patients who received prothionamide treatment.
原文英語
頁(從 - 到)923-927
頁數5
期刊Journal of the Formosan Medical Association = Taiwan yi zhi
109
發行號12
DOIs
出版狀態已發佈 - 十二月 2010

ASJC Scopus subject areas

  • Medicine(all)

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