Schechter Mauro, Zajdenverg Roberto, Falco Gisely, Barnes Grace Link, Faulhaber José Cláudio, Coberly Jacqueline S, Moore Richard D, Chaisson Richard E
Infectious Diseases Service, Hospital Universitário Clementino Fraga Filho, Rio de Janeiro, Brazil.
Am J Respir Crit Care Med. 2006 Apr 15;173(8):922-6. doi: 10.1164/rccm.200512-1953OC. Epub 2006 Feb 10.
Treatment of latent tuberculosis (TB) infection with weekly rifapentine and isoniazid is a potentially effective alternative to current therapies.
To compare the efficacy of weekly rifapentine/isoniazid to daily rifampin/pyrazinamide in preventing TB in household contacts of patients with pulmonary TB in Brazil.
Contacts of patients with TB were randomized to rifapentine 900 mg/isoniazid 900 mg once weekly for 12 wk or rifampin 450-600 mg/pyrazinamide 750-1,500 mg daily for 8 wk and followed for at least 2 yr.
TB rates, adverse events, and adherence to therapy.
A total of 399 household contacts were enrolled, 206 in the rifapentine/isoniazid arm and 193 in the rifampin/pyrazinamide arm. The median age was 34 yr, median weight was 63 kg, 60% of participants were female, and only one patient was HIV infected. Rifapentine/isoniazid was well tolerated, but the trial was halted by the investigators before completion because of unanticipated hepatotoxicity in the rifampin/pyrazinamide arm. Twenty of 193 participants (10%) receiving rifampin/pyrazinamide experienced grade 3 or 4 hepatotoxicity, compared with 2 of 206 participants (1%) on rifapentine/isoniazid (p<0.001). There were no hospitalizations or deaths due to hepatotoxicity, and all participants' liver enzyme levels returned to normal during follow-up. During follow-up, four cases of active TB developed, three in the rifapentine/isoniazid group and one in the rifampin/pyrazinamide group (1.46 vs. 0.52%; difference, 0.94%; 95% confidence interval, -1.6 to 3.7%).
Rifapentine/isoniazid was better tolerated than rifampin/pyrazinamide and was associated with good protection against TB. Rifapentine/isoniazid weekly for 12 wk is likely a promising therapy for latent TB infection.
每周使用利福喷汀和异烟肼治疗潜伏性结核感染是当前疗法的一种潜在有效替代方案。
比较每周使用利福喷汀/异烟肼与每日使用利福平/吡嗪酰胺预防巴西肺结核患者家庭接触者发生结核病的疗效。
将结核病患者的接触者随机分为两组,一组每周一次服用利福喷汀900毫克/异烟肼900毫克,共12周;另一组每日服用利福平450 - 600毫克/吡嗪酰胺750 - 1500毫克,共8周,并随访至少2年。
结核病发病率、不良事件及治疗依从性。
共纳入399名家庭接触者,利福喷汀/异烟肼组206人,利福平/吡嗪酰胺组193人。中位年龄为34岁,中位体重为63千克,60%的参与者为女性,仅1名患者感染艾滋病毒。利福喷汀/异烟肼耐受性良好,但由于利福平/吡嗪酰胺组出现意外的肝毒性,研究人员在试验完成前终止了试验。193名接受利福平/吡嗪酰胺治疗的参与者中有20人(10%)发生3级或4级肝毒性,而利福喷汀/异烟肼组206名参与者中有2人(1%)出现肝毒性(p<0.001)。没有因肝毒性导致的住院或死亡情况,所有参与者的肝酶水平在随访期间均恢复正常。随访期间,出现4例活动性结核病例,利福喷汀/异烟肼组3例,利福平/吡嗪酰胺组1例(1.46%对0.52%;差异为0.94%;95%置信区间为 - 1.6至3.7%)。
利福喷汀/异烟肼比利福平/吡嗪酰胺耐受性更好,且对结核病有良好的预防作用。每周一次使用利福喷汀/异烟肼治疗12周可能是治疗潜伏性结核感染的一种有前景的疗法。