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儿童肠道土源性蠕虫驱虫药物:对营养指标、血红蛋白及学业表现的影响

Deworming drugs for soil-transmitted intestinal worms in children: effects on nutritional indicators, haemoglobin, and school performance.

作者信息

Taylor-Robinson David C, Maayan Nicola, Soares-Weiser Karla, Donegan Sarah, Garner Paul

机构信息

Department of Public Health and Policy, University of Liverpool, Liverpool, Merseyside, UK.

出版信息

Cochrane Database Syst Rev. 2015 Jul 23;2015(7):CD000371. doi: 10.1002/14651858.CD000371.pub6.

Abstract

BACKGROUND

The World Health Organization (WHO) recommends treating all school children at regular intervals with deworming drugs in areas where helminth infection is common. As the intervention is often claimed to have important health, nutrition, and societal effects beyond the removal of worms, we critically evaluated the evidence on benefits.

OBJECTIVES

To summarize the effects of giving deworming drugs to children to treat soil-transmitted helminths on weight, haemoglobin, and cognition; and the evidence of impact on physical well-being, school attendance, school performance, and mortality.

SEARCH METHODS

We searched the Cochrane Infectious Diseases Group Specialized Register (14 April 2015); Cochrane Central Register of Controlled Trials (CENTRAL), published in the Cochrane Library (2015, Issue 4); MEDLINE (2000 to 14 April 2015); EMBASE (2000 to 14 April 2015); LILACS (2000 to 14 April 2015); the metaRegister of Controlled Trials (mRCT); and reference lists, and registers of ongoing and completed trials up to 14 April 2015.

SELECTION CRITERIA

We included randomized controlled trials (RCTs) and quasi-RCTs comparing deworming drugs for soil-transmitted helminths with placebo or no treatment in children aged 16 years or less, reporting on weight, haemoglobin, and formal tests of intellectual development. We also sought data on school attendance, school performance, and mortality. We included trials that combined health education with deworming programmes.

DATA COLLECTION AND ANALYSIS

At least two review authors independently assessed the trials, evaluated risk of bias, and extracted data. We analysed continuous data using the mean difference (MD) with 95% confidence intervals (CIs). Where data were missing, we contacted trial authors. We used outcomes at time of longest follow-up. The evidence quality was assessed using GRADE. This edition of the Cochrane Review adds the DEVTA trial from India, and draws on an independent analytical replication of a trial from Kenya.

MAIN RESULTS

We identified 45 trials, including nine cluster-RCTs, that met the inclusion criteria. One trial evaluating mortality included over one million children, and the remaining 44 trials included a total of 67,672 participants. Eight trials were in children known to be infected, and 37 trials were carried out in endemic areas, including areas of high (15 trials), moderate (12 trials), and low prevalence (10 trials). Treating children known to be infectedTreating children known to be infected with a single dose of deworming drugs (selected by screening, or living in areas where all children are infected) may increase weight gain over the next one to six months (627 participants, five trials, low quality evidence). The effect size varied across trials from an additional 0.2 kg gain to 1.3 kg. There is currently insufficient evidence to know whether treatment has additional effects on haemoglobin (247 participants, two trials, very low quality evidence); school attendance (0 trials); cognitive functioning (103 participants, two trials, very low quality evidence), or physical well-being (280 participants, three trials, very low quality evidence). Community deworming programmesTreating all children living in endemic areas with a dose of deworming drugs probably has little or no effect on average weight gain (MD 0.04 kg less, 95% CI 0.11 kg less to 0.04 kg more; trials 2719 participants, seven trials, moderate quality evidence), even in settings with high prevalence of infection (290 participants, two trials). A single dose also probably has no effect on average haemoglobin (MD 0.06 g/dL, 95% CI -0.05 lower to 0.17 higher; 1005 participants, three trials, moderate quality evidence), or average cognition (1361 participants, two trials, low quality evidence).Similiarly, regularly treating all children in endemic areas with deworming drugs, given every three to six months, may have little or no effect on average weight gain (MD 0.08 kg, 95% CI 0.11 kg less to 0.27 kg more; 38,392 participants, 10 trials, low quality evidence). The effects were variable across trials; one trial from a low prevalence setting carried out in 1995 found an increase in weight, but nine trials carried out since then found no effect, including five from moderate and high prevalence areas.There is also reasonable evidence that regular treatment probably has no effect on average height (MD 0.02 cm higher, 95% CI 0.14 lower to 0.17 cm higher; 7057 participants, seven trials, moderate quality evidence); average haemoglobin (MD 0.02 g/dL lower; 95% CI 0.08 g/dL lower to 0.04 g/dL higher; 3595 participants, seven trials, low quality evidence); formal tests of cognition (32,486 participants, five trials, moderate quality evidence); exam performance (32,659 participants, two trials, moderate quality evidence); or mortality (1,005,135 participants, three trials, low quality evidence). There is very limited evidence assessing an effect on school attendance and the findings are inconsistent, and at risk of bias (mean attendance 2% higher, 95% CI 4% lower to 8% higher; 20,243 participants, two trials, very low quality evidence).In a sensitivity analysis that only included trials with adequate allocation concealment, there was no evidence of any effect for the main outcomes.

AUTHORS' CONCLUSIONS: Treating children known to have worm infection may have some nutritional benefits for the individual. However, in mass treatment of all children in endemic areas, there is now substantial evidence that this does not improve average nutritional status, haemoglobin, cognition, school performance, or survival.

摘要

背景

世界卫生组织(WHO)建议,在蠕虫感染常见的地区,定期对所有学童使用驱虫药物进行治疗。由于人们常称这种干预措施除了能清除蠕虫外,还会对健康、营养和社会产生重要影响,因此我们对相关益处的证据进行了严格评估。

目的

总结给儿童使用驱虫药物治疗土源性蠕虫感染对体重、血红蛋白和认知的影响;以及对身体健康、上学出勤率、学业成绩和死亡率影响的证据。

检索方法

我们检索了Cochrane传染病组专业注册库(2015年4月14日);Cochrane系统评价数据库(CENTRAL),发表于Cochrane图书馆(2015年第4期);MEDLINE(2000年至2015年4月14日);EMBASE(2000年至2015年4月14日);拉丁美洲和加勒比卫生科学数据库(LILACS,2000年至2015年4月14日);对照试验元注册库(mRCT);以及参考文献列表,并检索了截至2015年4月14日的正在进行和已完成试验的注册库。

选择标准

我们纳入了随机对照试验(RCT)和半随机对照试验,这些试验比较了16岁及以下儿童使用土源性蠕虫驱虫药物与安慰剂或不治疗的效果,并报告了体重、血红蛋白和智力发育的正式测试结果。我们还收集了关于上学出勤率、学业成绩和死亡率的数据。我们纳入了将健康教育与驱虫计划相结合的试验。

数据收集与分析

至少两名综述作者独立评估试验、评估偏倚风险并提取数据。我们使用平均差(MD)及95%置信区间(CI)分析连续数据。数据缺失时,我们与试验作者联系。我们采用最长随访期的结果。使用GRADE评估证据质量。本版Cochrane系统评价纳入了来自印度的DEVTA试验,并借鉴了对肯尼亚一项试验的独立分析复现。

主要结果

我们确定了45项符合纳入标准的试验,其中包括9项整群随机对照试验。一项评估死亡率的试验纳入了超过100万名儿童,其余44项试验共纳入了67,672名参与者。8项试验针对已知感染的儿童,37项试验在流行地区开展,包括高流行区(15项试验)、中度流行区(12项试验)和低流行区(10项试验)。治疗已知感染的儿童给已知感染的儿童单次使用驱虫药物(通过筛查选择,或生活在所有儿童均感染的地区),可能会在接下来的1至6个月内增加体重(627名参与者,5项试验,低质量证据)。各试验的效应量有所不同,额外增加的体重从0.2千克到1.3千克不等。目前尚无足够证据表明治疗对血红蛋白(247名参与者,2项试验,极低质量证据)、上学出勤率(0项试验)、认知功能(103名参与者,2项试验,极低质量证据)或身体健康(280名参与者,3项试验,极低质量证据)有额外影响。社区驱虫计划给流行地区的所有儿童服用一剂驱虫药物,可能对平均体重增加几乎没有影响或没有影响(平均差为少0.04千克,95%置信区间为少0.11千克至多0.04千克;7项试验,2719名参与者,中等质量证据),即使在感染率高的地区也是如此(2项试验,290名参与者)。单次用药可能对平均血红蛋白(平均差为0.06克/分升,95%置信区间为低0.05克/分升至高0.17克/分升;3项试验,1005名参与者,中等质量证据)或平均认知也没有影响(2项试验,1361名参与者,低质量证据)。同样,每三至六个月定期给流行地区的所有儿童使用驱虫药物,可能对平均体重增加几乎没有影响或没有影响(平均差为0.08千克,95%置信区间为少0.11千克至多0.27千克;10项试验,38,392名参与者,低质量证据)。各试验的效应存在差异;1995年在低流行地区开展的一项试验发现体重增加,但此后开展的9项试验均未发现有影响,其中包括5项来自中度和高度流行地区的试验。也有合理证据表明,定期治疗可能对平均身高没有影响(平均差为高0.02厘米,95%置信区间为低0.14厘米至高0.17厘米;7项试验,7057名参与者,中等质量证据);对平均血红蛋白没有影响(平均差为低0.02克/分升;95%置信区间为低0.08克/分升至高0.04克/分升;7项试验,3595名参与者,低质量证据);对认知的正式测试没有影响(5项试验,32,486名参与者,中等质量证据);对考试成绩没有影响(2项试验,32,659名参与者;中等质量证据);或对死亡率没有影响(3项试验,1,005,135名参与者,低质量证据)。评估对上学出勤率影响的证据非常有限,且结果不一致,存在偏倚风险(平均出勤率高2%,95%置信区间为低4%至高8%;2项试验,20,243名参与者,极低质量证据)。在一项仅纳入分配隐藏充分的试验的敏感性分析中,没有证据表明主要结局有任何影响。

作者结论

治疗已知有蠕虫感染的儿童可能对个体有一些营养益处。然而,在对流行地区所有儿童进行大规模治疗时,现在有大量证据表明这并不能改善平均营养状况、血红蛋白、认知、学业成绩或生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/6464696/aab23f823542/nCD000371-AFig-FIG01.jpg

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