H. Turktas et al., HEPATOTOXICITY OF ANTITUBERCULOSIS THERAPY (RIFAMPICIN, ISONIAZID ANDPYRAZINAMIDE) OR VIRAL-HEPATITIS, Tubercle and lung disease, 75(1), 1994, pp. 58-60
Setting: Department of Chest Diseases, Gazi University Faculty of Medi
cine and Ataturk Chest Diseases Hospital. Ankara, Turkey. Objective: T
he primary purpose of this study was to assess the contributory role o
f viral hepatitis in antituberculosis drug hepatotoxicity. Design: Ser
ologic markers for viral hepatitis were studied in 57 patients who dev
eloped acute hepatitis during antituberculosis therapy with rifampicin
and isoniazid. Results: Among 705 adult tuberculous patients, 57 (8.1
%) developed acute hepatitis during therapy with rifampicin and isonia
zid. Serologic markers confirmed the presence of hepatitis B in 6 (10.
5%) and hepatitis C in 4 (7%) of the 57 patients. Acute hepatitis A wa
s not diagnosed in any of the patients. Conclusion: Hepatitis occurrin
g during antituberculosis therapy may not be drug-induced in all patie
nts. Apart from the other factors mentioned above the endemicity of vi
ral hepatitis in developing countries could be responsible for the hig
her incidence of antituberculosis-drug hepatitis.