首页> 外文期刊>The Lancet >Rifapentine and isoniazid once a week versus rifampicin and isoniazid twice a week for treatment of drug-susceptible pulmonary tuberculosis in HIV-negative patients: a randomised clinical trial.
【24h】

Rifapentine and isoniazid once a week versus rifampicin and isoniazid twice a week for treatment of drug-susceptible pulmonary tuberculosis in HIV-negative patients: a randomised clinical trial.

机译:利福喷丁和异烟肼每周一次与利福平和异烟肼每周两次用于治疗HIV阴性患者的药物敏感性肺结核:一项随机临床试验。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Rifapentine has a long half-life in serum, which suggests a possible treatment once a week for tuberculosis. We aimed to compare rifapentine and isoniazid once a week with rifampicin and isoniazid twice a week. METHODS: We did a randomised, multicentre, open-label trial in the USA and Canada of HIV-negative people with drug-susceptible pulmonary tuberculosis who had completed 2 months of a 6-month treatment regimen. We randomly allocated patients directly observed treatment with either 600 mg rifapentine plus 900 mg isoniazid once a week or 600 mg rifampicin plus 900 mg isoniazid twice a week. Primary outcome was failure/relapse. Analysis was by intention to treat. FINDINGS: 1004 patients were enrolled (502 per treatment group). 928 successfully completed treatment, and 803 completed the 2-year 4-month study. Crude rates of failure/relapse were 46/502 (9.2%) in those on rifapentine once a week, and 28/502 (5.6%) in those given rifampicin twice a week (relative risk 1.64, 95% CI 1.04-2.58, p=0.04). By proportional hazards regression, five characteristics were independently associated with increased risk of failure/relapse: sputum culture positive at 2 months (hazard ratio 2.8, 95% CI 1.7-4.6); cavitation on chest radiography (3.0, 1.6-5.9); being underweight (3.0, 1.8-4.9); bilateral pulmonary involvement (1.8, 1.0-3.1); and being a non-Hispanic white person (1.8, 1.1-3.0). Adjustment for imbalances in 2-month culture and cavitation diminished the association of treatment group with outcome (1.34; 0.83-2.18; p=0.23). Of participants without cavitation, rates of failure/relapse were 6/210 (2.9%) in the once a week group and 6/241 (2.5%) in the twice a week group (relative risk 1.15; 95% CI 0.38-3.50; p=0.81). Rates of adverse events and death were similar in the two treatment groups. INTERPRETATION: Rifapentine once a week is safe and effective for treatment of pulmonary tuberculosis in HIV-negative people without cavitation on chest radiography. Clinical, radiographic, and microbiological data help to identify patients with tuberculosis who are at increased risk of failure or relapse when treated with either regimen.
机译:背景:利福喷丁在血清中具有较长的半衰期,这表明可能每周进行一次结核病治疗。我们旨在每周比较一次利福喷丁和异烟肼与每周两次利福平和异烟肼的比较。方法:我们在美国和加拿大对艾滋病毒阴性的药物敏感型肺结核患者进行了一项随机,多中心,开放标签的试验,这些患者已完成6个月治疗方案的2个月。我们随机分配直接观察的患者,每周一次600毫克利福喷汀加900毫克异烟肼,或每周两次两次600毫克利福平加900毫克异烟肼治疗。主要结果是失败/复发。分析是按意向进行的。结果:纳入了1004例患者(每个治疗组502例)。 928人成功完成了治疗,803人完成了为期2年4个月的研究。每周一次使用利福喷汀的患者失败/复发的粗略率分别为46/502(9.2%),每周两次接受利福平的患者的失效率/复发率分别为28/502(5.6%)(相对风险1.64,95%CI 1.04-2.58,p = 0.04)。通过比例风险回归,五个特征独立于失败/复发风险的增加:2个月时痰培养阳性(风险比2.8,95%CI 1.7-4.6);胸部X线照相上的空化(3.0,1.6-5.9);体重不足(3.0,1.8-4.9);双侧肺部受累(1.8,1.0-3.1);并且是非西班牙裔白人(1.8,1.1-3.0)。调整2个月培养和空化的失衡可减少治疗组与结局的关联(1.34; 0.83-2.18; p = 0.23)。在没有气蚀的参与者中,每周一次的组失败/复发率是6/210(2.9%),每周两次的组是6/241(2.5%)(相对危险度1.15; 95%CI 0.38-3.50;相对危险度)。 p = 0.81)。两组的不良事件和死亡发生率相似。解释:利福喷丁每周一次可安全有效地治疗HIV阴性人群的肺结核,而无需在胸部X光片上进行气穴治疗。临床,影像学和微生物学数据可帮助确定在接受任何一种疗法治疗后失败或复发风险增加的结核病患者。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号