利福喷丁联合异烟肼治疗印度儿童结核感染的疗效观察

R. Singh, Umesh Kumar
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引用次数: 0

摘要

背景:结核病(TB)感染的治疗可以有效地预防其发展并治愈它。12岁及以上的人可以安全有效地服用利福喷丁和异烟肼三个月来治疗潜伏性结核感染。已发表的儿童数据有限。印度儿童每周使用利福喷丁加异烟肼(3 HP) 3个月的数据目前尚无。目的:比较9H和3HP方案治疗结核儿童的治疗完成率和药物不良反应发生率。方法:这是一项前瞻性、开放标签、多中心随机试验,涉及新诊断结核病的儿童。263名参与者随机分为两组,3HP组131名患者,9H组132名患者。主要终点是在12个月内完成270天的治疗。分析两组患者的药物不良反应。结果:9H组与3HP组比较,退出9H组的人停止参与的频率更高。退出的原因是同意撤回。3HP组肝毒性发生率低于9H组。3HP组2级和3级不良反应较多。结论:与9H方案相比,3HP方案完成率更高,并且对不良反应的耐受性更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Rifapentine plus isoniazid in the treatment of tuberculosis infection in children in India
Background: Treatment of tuberculosis (TB) infection effectively prevents its progression and cures it. Persons aged 12 and older can safely and effectively take rifapentine and isoniazid for three months to treat latent tuberculosis infection. Published data for children is limited. Data on the 3-month weekly rifapentine plus isoniazid (3 HP) in children in India are currently unavailable.Objective: To compare the treatment completion rates and incidence rates of adverse drug reactions among childrens with TB undergoing the 9H and 3HP regimens. Methods: This was a prospective, open-label, multicentre randomised trial involving children with newly diagnosed TB. 263 participants were randomised into two groups to have 131 patients in the 3HP group and 132 to the 9H group. Primary endpoint was completion of the 270-day treatment within 12 months. Adverse drug reaction were analysed in both the groups. Results: Comparing the 9H group with the 3HP group, those who dropped out of the 9H group stopped participating more often. Reason for dropping out was consent withdrawal. Incidence of hepatotoxicity was lower in the 3HP group than in the 9H group. However, grade 2 and 3 ADR were more in the 3HP group. Conclusion: An increased completion rate was seen with the 3HP regimen compared with the 9H regimen, as well as better tolerance to adverse effects.
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