Bose Anuradha, Kalita Soumik, Rose Winsley, Tharyan Prathap
Department of Community Health, Christian Medical College, Vellore, India, 632002.
Cochrane Database Syst Rev. 2014 Jan 28;2014(1):CD007953. doi: 10.1002/14651858.CD007953.pub2.
Childhood tuberculosis (TB) is a neglected global public health problem. Short treatment courses with rifampicin-containing anti-TB drugs given daily for six-months cure over 90% of infected children, but poor adherence reduces treatment success. Intermittent, short-course anti-TB regimens, given two or three times a week under direct observation, are associated with higher adherence in observational studies; but how they compare with daily treatment in relation to cure is unclear. Current international and national recommendations differ on use of intermittent regimens to treat TB in children.
To compare the efficacy and safety of intermittent, short-course anti-TB regimens (twice- or thrice-weekly) with daily short-course anti-TB regimens in treating childhood TB.
We searched the Cochrane Infectious Disease Group Specialized Register, Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, LILACS, clinical trials registries, regional databases, conference proceedings, and references without language restrictions up to 30 May 2013; and contacted experts for relevant published, unpublished, and on-going trials.
Randomized controlled trials (RCTs) and quasi-RCTs of children aged 15 years or younger, diagnosed with TB (according to the World Health Organization diagnostic categories 1, 2, or 3), who were treated with intermittent twice-weekly or thrice-weekly, short-course anti-TB regimens compared to daily short-course anti-TB treatment regimens. All regimens had to contain rifampicin for at least the first two months.
The review authors independently screened and selected trials, assessed risk of bias, and extracted data. We sought clarifications from trial authors. We pooled relative risks with their 95% confidence intervals and used a random-effects model where there was significant heterogeneity. We assessed overall evidence-quality using the GRADE approach.
We included four trials published between 1996 to 2000 that randomized 563 children (465 evaluable) aged five months to 15 years to intermittent twice-weekly versus daily anti-TB treatment. Two trials were from India, one from South Africa, and one from Turkey. All trials used rifampicin and isoniazid, three trials used pyrazinamide, and one trial used streptomycin. The drug combination, and the duration of intermittent and daily treatments differed between trials, and no trials used drug combinations and schedules currently recommended for childhood TB. No trial reported if any child was HIV-positive.In comparisons of twice-weekly versus daily anti-TB treatment regimens, the trials did not detect differences in the number of patients cured, but trials were small, and the comparator regimens were not standard (four trials, 465 children; very low quality evidence). Trials were underpowered to provide estimates for death (two trials, 213 participants, very low quality evidence), relapse (one trial, 214 participants,very low quality evidence), and treatment limiting adverse events (four trials, 441 participants, very low quality evidence)Reported adherence to treatment was similar (87% versus 84%; four trials, 458 children, very low quality evidence)We did not find trials comparing the commonly used thrice-weekly anti-TB short-course regimen with the daily treatment regimen.
AUTHORS' CONCLUSIONS: Trials conducted to date are insufficient to support or refute the use of intermittent twice- or thrice-weekly, short-course treatment regimens over daily short-course treatment in children with TB. Further randomized trials conducted in high TB-transmission settings will help inform policy and practice.
儿童结核病是一个被忽视的全球公共卫生问题。使用含利福平的抗结核药物进行为期六个月的每日短程治疗可治愈90%以上的受感染儿童,但依从性差会降低治疗成功率。在直接观察下每周进行两到三次的间歇性短程抗结核治疗方案,在观察性研究中显示出更高的依从性;但在治愈率方面,它们与每日治疗相比情况如何尚不清楚。目前国际和国家在儿童结核病治疗中使用间歇性治疗方案的建议存在差异。
比较间歇性短程抗结核治疗方案(每周两次或三次)与每日短程抗结核治疗方案治疗儿童结核病的疗效和安全性。
我们检索了Cochrane传染病组专业注册库、Cochrane对照试验中央注册库(CENTRAL)、MEDLINE、EMBASE、LILACS、临床试验注册库、区域数据库、会议论文集,并检索了截至2013年5月30日无语言限制的参考文献;并联系专家获取相关已发表、未发表和正在进行的试验。
对15岁及以下、被诊断为结核病(根据世界卫生组织诊断类别1、2或3)的儿童进行的随机对照试验(RCT)和半随机对照试验,将间歇性每周两次或三次的短程抗结核治疗方案与每日短程抗结核治疗方案进行比较。所有方案在前两个月至少都要含有利福平。
综述作者独立筛选和选择试验、评估偏倚风险并提取数据。我们向试验作者寻求澄清。我们汇总相对风险及其95%置信区间,并在存在显著异质性时使用随机效应模型。我们使用GRADE方法评估总体证据质量。
我们纳入了1996年至2000年发表的四项试验,这些试验将563名年龄在5个月至15岁之间的儿童(465名可评估)随机分为间歇性每周两次与每日抗结核治疗组。两项试验来自印度,一项来自南非,一项来自土耳其。所有试验都使用了利福平和异烟肼,三项试验使用了吡嗪酰胺,一项试验使用了链霉素。试验之间的药物组合以及间歇性和每日治疗的持续时间各不相同,且没有试验使用目前推荐用于儿童结核病的药物组合和用药方案。没有试验报告是否有儿童为HIV阳性。在每周两次与每日抗结核治疗方案的比较中,试验未发现治愈患者数量存在差异,但试验规模较小,且对照方案不标准(四项试验,465名儿童;证据质量极低)。试验没有足够的效力来提供关于死亡(两项试验,213名参与者,证据质量极低)复发(一项试验,214名参与者,证据质量极低)和导致治疗受限的不良事件(四项试验,441名参与者,证据质量极低)的估计。报告的治疗依从性相似(87%对84%;四项试验,458名儿童,证据质量极低)。我们未找到将常用的每周三次抗结核短程治疗方案与每日治疗方案进行比较的试验。
迄今为止进行的试验不足以支持或反驳在儿童结核病中使用间歇性每周两次或三次的短程治疗方案优于每日短程治疗方案。在结核病高传播地区进行进一步的随机试验将有助于为政策和实践提供信息。