In 1996 a six-month short-course chemotherapy was adopted as a standard chemotherapy for pulmonary tuberculosis in Japan. The frequency of implementation of short course chemotherapy for smear positive new case was only sixty percent in 2003, although a short course chemotherapy was recommended all over the world for avoidance of acquiring a new resistance among new drug resistant tuberculosis. The reasons for the low adaptation of short course chemotherapy were speculated that high rate of elderly patients, and high frequency of drug-induced hepatitis. From our 14-year experience, the frequency of drug-induced hepatitis was 7.8% for all patients with standard 6-month or 9-month regimen, 7.2% in the patients with normal liver function tests at the start of chemotherapy, and 11.8% in the patients with any kinds of abnormality. The death rate was 0.04% among treated patients, and fatality was 0.49% among the patients with drug-induced hepatitis. Positive HCV antibody and less than 1,000 cells/μL of peripheral lymphocyte count at the beginning of treatment were independent risk factors for druginduced hepatitis. The management of hepatitis during antituberculosis treatment was also referred.
CITATION STYLE
Wada, M. (2005). Anti-tuberculosis drug-induced hepatitis. In Kekkaku (Vol. 80, pp. 607–611). https://doi.org/10.3329/bjch.v46i1.70010
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