Huertas-Ceballos A, Logan S, Bennett C, Macarthur C
EGA Hospital, Neonatal Unit, UCLH, Huntley Street, London, UK WC1E 6DH.
Cochrane Database Syst Rev. 2008 Jan 23(1):CD003017. doi: 10.1002/14651858.CD003017.pub2.
BACKGROUND: Between 4% and 25% of school-age children complain of recurrent abdominal pain (RAP) of sufficient severity to interfere with daily activities. For the majority no organic cause for their pain can be found on physical examination or investigation and although most children are likely managed by reassurance and simple measures, a large range of interventions have been recommended. OBJECTIVES: To determine the effectiveness of medication for recurrent abdominal pain in school-age children. SEARCH STRATEGY: The Cochrane Library (CENTRAL) 2006 (Issue 4), MEDLINE (1966 to Dec 2006), EMBASE (1980 to Dec 2006), CINAHL (1982 to Dec 2007), ERIC (1966 to Dec 2006), PsycINFO (1872 to Dec 2006), LILACS (1982 to Dec 2006), SIGLE (1980 to March 2005), and JICST (1985 to 06/2000) were searched with appropriate filters SELECTION CRITERIA: Studies on school age children with RAP (Apley or the Rome II criteria for gastrointestinal diseases) allocated by random or quasi-random methods to a drug treatment vs. placebo/ no treatment were included. DATA COLLECTION AND ANALYSIS: References identified by the searches were screened against the inclusion criteria by two independent reviewers. Data was extracted and analysed using RevMan 4.2.10. MAIN RESULTS: Three trials met the inclusion criteria. Symon et al report a cross-over trial comparing pizotifen and placebo in 16 children with "abdominal migraine". Data before cross-over was not available. Results for 14 children showed Mean fewer days in pain of 8.21 (95% CI 2.93, 13.48) while taking the active drug. Kline et al compared peppermint oil capsules with placebo in a randomised trial in 50 children with RAP and IBS. 42 children completed the study. OR for improvement was 3.33 (95% CI 0.93-12.1)See et al compared famotidine with placebo in a randomised cross-over trial in 25 children with RAP and dyspepsia. OR for improvement before cross-over was 11 (95%CI 1.6, 75.5). AUTHORS' CONCLUSIONS: This review provides weak evidence of benefit on medication in children with RAP. The lack of clear evidence of effectiveness for any of the recommended drugs suggests that there is little reason for their use outside of clinical trials. Clinicians may choose to prescribe drugs in children with severe symptoms that have not responded to simple management. However, if using drugs as a "therapeutic trial", clinicians should be aware that, RAP is a fluctuating condition and any "response" may reflect the natural history of the condition or a placebo effect rather than drug efficacy.
背景:4%至25%的学龄儿童主诉反复出现腹痛(RAP),严重程度足以干扰日常活动。对于大多数儿童,体格检查或检查未发现疼痛的器质性原因,尽管大多数儿童可能通过安慰和简单措施进行处理,但仍推荐了大量干预措施。 目的:确定药物治疗学龄儿童反复腹痛的有效性。 检索策略:检索了Cochrane图书馆(CENTRAL)2006年第4期、MEDLINE(1966年至2006年12月)、EMBASE(1980年至2006年12月)、CINAHL(1982年至2007年12月)、ERIC(1966年至2006年12月)、PsycINFO(1872年至2006年12月)、LILACS(1982年至2006年12月)、SIGLE(1980年至2005年3月)和JICST(1985年至2000年6月),并使用了适当的筛选条件。 选择标准:纳入采用随机或半随机方法将患有RAP(阿普利或罗马II胃肠疾病标准)的学龄儿童分配至药物治疗组与安慰剂/未治疗组的研究。 数据收集与分析:两名独立评审员根据纳入标准对检索到的参考文献进行筛选。使用RevMan 4.2.10提取和分析数据。 主要结果:三项试验符合纳入标准。西蒙等人报告了一项交叉试验,比较了匹莫齐特与安慰剂在16名“腹部偏头痛”儿童中的疗效。交叉前的数据不可用。14名儿童的结果显示,服用活性药物时平均疼痛天数减少8.21天(95%可信区间2.93,I3.48)。克莱因等人在一项针对50名患有RAP和IBS的儿童的随机试验中,将薄荷油胶囊与安慰剂进行了比较。42名儿童完成了研究。改善的比值比为3.33(95%可信区间0.93-12.1)。西等人在一项针对25名患有RAP和消化不良的儿童的随机交叉试验中,将法莫替丁与安慰剂进行了比较。交叉前改善的比值比为11(95%可信区间1.6,75.5)。 作者结论:本综述提供了药物治疗RAP儿童有益的微弱证据。缺乏任何推荐药物有效性的确切证据表明,在临床试验之外几乎没有理由使用这些药物。临床医生可能会选择为症状严重且对简单处理无反应的儿童开药。然而,如果将药物用作“治疗试验”,临床医生应意识到,RAP是一种波动的病症,任何“反应”可能反映的是病情的自然发展或安慰剂效应,而非药物疗效。
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