Gluckman Steven, Karpelowsky Jonathan, Webster Angela C, McGee Richard G
University of Sydney, Sydney Adventist Hospital, Wahroonga NSW 2076, Sydney, Australia.
Cochrane Database Syst Rev. 2017 Jun 1;6(6):CD006476. doi: 10.1002/14651858.CD006476.pub3.
Intussusception is a common abdominal emergency in children with significant morbidity. Prompt diagnosis and management reduces associated risks and the need for surgical intervention. Despite widespread agreement on the use of contrast enema as opposed to surgery for initial management in most cases, debate persists on the appropriate contrast medium, imaging modality, pharmacological adjuvant, and protocol for delayed repeat enema, and on the best approach for surgical management for intussusception in children.
To assess the safety and effectiveness of non-surgical and surgical approaches in the management of intussusception in children.
We searched the following electronic databases: Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 8) in the Cochrane Library; Ovid MEDLINE (1950 to September 2016); Ovid Embase (1974 to September 2016); Science Citation Index Expanded (via Web of Science) (1900 to September 2016); and BIOSIS Previews (1969 to September 2016).We examined the reference lists of all eligible trials to identify additional studies. To locate unpublished studies, we contacted content experts, searched the World Health Organization International Clinical Trials Registry Platform (ICTRP) and ClinicalTrials.gov (September 2016), and explored proceedings from meetings of the British Association of Paedatric Surgeons (BAPS), the American Soceity of Pediatric Surgery, and the World Congress of Pediatric Surgery.
We included all randomised controlled trials comparing contrast media, imaging modalities, pharmacological adjuvants, protocols for delayed repeat enema, and/or surgical approaches for the management of intussusception in children. We applied no language, publication date, or publication status restrictions.
Two review authors independently conducted study selection and data extraction and assessed risk of bias using a standardised form. We resolved disagreements by consensus with a third review author when necessary. We reported dichotomous outcomes as risk ratios (RRs) with 95% confidence intervals (CIs). We analysed data on an intention-to-treat basis and evaluated the overall quality of evidence supporting the outcomes by using GRADE criteria.
We included six randomised controlled trials (RCTs) with a total of 822 participants. Two trials compared liquid enema reduction plus glucagon versus liquid enema alone. One trial compared liquid enema plus dexamethasone versus liquid enema alone. Another trial compared air enema plus dexamethasone versus air enema alone, and two trials compared use of liquid enema versus air enema. We identified three ongoing trials.We judged all included trials to be at risk of bias owing to omissions in reported methods. We judged five of six trials as having high risk of bias in at least one domain. Therefore, the quality of the evidence (GRADE) for outcomes was low. Interventions and data presentation varied greatly across trials; therefore meta-analysis was not possible for most review outcomes. Enema plus glucagon versus enema alone It is uncertain whether use of glucagon improves the rate of successful reduction of intussusception when compared with enema alone (reported in two trials, 218 participants; RR 1.09, 95% CI 0.94 to 1.26;low quality of evidence). No trials in this comparison reported on the number of children with bowel perforation(s) nor on the number of children with recurrent intussusception. Enema plus dexamethasone versus enema alone Use of the adjunct, dexamethasone, may be beneficial in reducing intussusception recurrence with liquid or air enema (two trials, 299 participants; RR 0.14, 95% CI 0.03 to 0.60; low quality of evidence). This equates to a number needed to treat for an additional beneficial outcome of 13 (95% CI 8 to 37). It is uncertain whether use of the adjunct, dexamethasone, improves the rate of successful reduction of intussusception when compared with enema alone (reported in two trials, 356 participants; RR 1.01, 95% CI 0.92 to 1.10;low quality of evidence). Air enema versus liquid enema Air enema may be more successful than liquid enema for reducing intussusception (two trials, 199 participants; RR 1.28, 95% CI 1.10 to 1.49; low quality of evidence). This equates to a number needed to treat for an additional beneficial outcome of 6 (95% CI 4 to 19). No trials in this comparison reported on the number of children with bowel perforation(s) or on the number of children with recurrent intussusception nor any intraoperative complications, such as bowel perforation, or other adverse effects. Only one trial reported postoperative complications, but owing to the method of reporting used, a quantitative analysis was not possible. We identified no studies that exclusively evaluated surgical interventions for management of intussusception.
AUTHORS' CONCLUSIONS: This review identified a small number of trials that assessed a variety of interventions. All included trials provided evidence of low quality and were subject to serious concerns about imprecision, high risk of bias, or both. Air enema may be superior to liquid enema for successfully reducing intussusception in children; however, this finding is based on a few studies including small numbers of participants. Dexamethasone as an adjuvant may be more effective in reducing intussusception recurrence rates following air enema or liquid enema, but these results are also based on a few studies of small numbers of participants. This review highlights several points that need to be addressed in future studies, including reducing the risk of bias and including relevant outcomes. Specifically, surgical trials are lacking, and future research is needed to address this evidence gap.
肠套叠是儿童常见的腹部急症,发病率较高。及时诊断和治疗可降低相关风险及手术干预的必要性。尽管在大多数情况下,对于采用造影灌肠而非手术进行初始治疗已达成广泛共识,但对于合适的造影剂、成像方式、药物辅助剂、延迟重复灌肠方案以及儿童肠套叠手术治疗的最佳方法仍存在争议。
评估非手术和手术方法治疗儿童肠套叠的安全性和有效性。
我们检索了以下电子数据库:Cochrane图书馆中的Cochrane对照试验中心注册库(CENTRAL;2016年第8期);Ovid MEDLINE(1950年至2016年9月);Ovid Embase(1974年至2016年9月);科学引文索引扩展版(通过Web of Science)(1900年至2016年9月);以及BIOSIS Previews(1969年至2016年9月)。我们查阅了所有符合条件试验的参考文献列表以识别其他研究。为查找未发表的研究,我们联系了相关领域专家,检索了世界卫生组织国际临床试验注册平台(ICTRP)和ClinicalTrials.gov(2016年9月),并查阅了英国小儿外科医师协会(BAPS)、美国小儿外科学会和世界小儿外科学大会会议记录。
我们纳入了所有比较造影剂、成像方式、药物辅助剂、延迟重复灌肠方案和/或儿童肠套叠治疗手术方法的随机对照试验。我们未设置语言、发表日期或发表状态限制。
两位综述作者独立进行研究选择和数据提取,并使用标准化表格评估偏倚风险。必要时,我们与第三位综述作者通过协商解决分歧。我们将二分法结局报告为风险比(RRs)及95%置信区间(CIs)。我们基于意向性分析数据,并使用GRADE标准评估支持结局的证据的总体质量。
我们纳入了6项随机对照试验(RCTs),共822名参与者。两项试验比较了液体灌肠复位加胰高血糖素与单纯液体灌肠。一项试验比较了液体灌肠加地塞米松与单纯液体灌肠。另一项试验比较了空气灌肠加地塞米松与单纯空气灌肠,两项试验比较了液体灌肠与空气灌肠的使用。我们确定了3项正在进行的试验。由于报告方法存在遗漏,我们判定所有纳入试验均存在偏倚风险。我们判定6项试验中的5项在至少一个领域存在高偏倚风险因此,结局证据的质量(GRADE)较低干预措施和数据呈现方式在各试验中差异很大;因此,对于大多数综述结局无法进行荟萃分析。灌肠加胰高血糖素与单纯灌肠相比与单纯灌肠相比,使用胰高血糖素是否能提高肠套叠成功复位率尚不确定(两项试验报告,218名参与者;RR 1.09,95% CI 0.94至1.26;证据质量低)。该比较中没有试验报告肠穿孔儿童数量或复发性肠套叠儿童数量。灌肠加地塞米松与单纯灌肠相比使用辅助药物地塞米松可能有助于减少液体或空气灌肠后肠套叠的复发(两项试验,299名参与者;RR 0.14,95% CI 0.03至0.60;证据质量低)。这相当于为获得额外有益结局所需治疗的人数为13(95% CI 8至37)。与单纯灌肠相比,使用辅助药物地塞米松是否能提高肠套叠成功复位率尚不确定(两项试验报告,356名参与者;RR 1.01,95% CI 0.92至1.10;证据质量低)。空气灌肠与液体灌肠相比空气灌肠在减少肠套叠方面可能比液体灌肠更成功(两项试验,199名参与者;RR 1.28,95% CI 1.10至1.49;证据质量低)。这相当于为获得额外有益结局所需治疗的人数为6(95% CI 4至19)。该比较中没有试验报告肠穿孔儿童数量、复发性肠套叠儿童数量或任何术中并发症,如肠穿孔或其他不良反应。只有一项试验报告了术后并发症,但由于所使用的报告方法,无法进行定量分析。我们未发现专门评估肠套叠手术干预的研究。
本综述识别出少数评估多种干预措施的试验。所有纳入试验提供的证据质量较低,且存在对不精确性、高偏倚风险或两者的严重担忧。空气灌肠在成功减少儿童肠套叠方面可能优于液体灌肠;然而,这一发现基于少数研究,参与者数量较少。地塞米松作为辅助药物在减少空气灌肠或液体灌肠后肠套叠复发率方面可能更有效,但这些结果同样基于少数参与者数量较少的研究。本综述突出了未来研究需要解决的几个要点包括降低偏倚风险和纳入相关结局。具体而言,缺乏手术试验,未来需要开展研究以填补这一证据空白。