There is little published information regarding treatment completion, safety, and efficacy of
rifampin administered daily for 4 months-a recommended alternative to 9 months of
isoniazid for
therapy of
latent tuberculosis infection. In an open-label randomized trial at a university-affiliated respiratory hospital, consenting patients whose treating physician had recommended
therapy for
latent tuberculosis infection were randomized to daily self-administered
rifampin for 4 months or daily self-administered
isoniazid for 9 months. Of 58 patients randomized to
rifampin, 53 (91%) took 80% of doses, and 50 (86%) took more than 90% of doses within 20 weeks compared with 44 (76%) and 36 (62%) who took 80 and 90%, respectively, of doses of
isoniazid within 43 weeks (relative risks: 80% of doses, 1.2 [95% confidence interval: 1.02, 1.4]; 90% of doses, 1.4 [1.1, 1.7]). Adverse events resulted in permanent discontinuation of
therapy for two (3%) patients taking
rifampin, and for eight (14%) patients taking
isoniazid. Three patients developed
drug-induced hepatitis--all were taking
isoniazid. Total costs of
therapy were significantly higher for
isoniazid. In conclusion, completion of
therapy was significantly better with 4 months of
rifampin and major side effects were somewhat lower. Further studies are needed to assess the safety and efficacy of the 4-month
rifampin regimen.