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Recommendations and evidence for reporting items in pediatric clinical trial protocols and reports: two systematic reviews

机译:儿科临床试验方案和报告中报告项目的建议和证据:两项系统评价

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Background Complete and transparent reporting of clinical trial protocols and reports ensures that these documents are useful to all stakeholders, that bias is minimized, and that the research is not wasted. However, current studies repeatedly conclude that pediatric trial protocols and reports are not appropriately reported. Guidelines like SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) and CONSORT (Consolidated Standards of Reporting Trials) may improve reporting, but do not offer guidance on issues unique to pediatric trials. This paper reports two systematic reviews conducted to build the evidence base for the development of pediatric reporting guideline extensions: 1) SPIRIT-Children (SPIRIT-C) for pediatric trial protocols, and 2) CONSORT-Children (CONSORT-C) for pediatric trial reports. Method MEDLINE, the Cochrane Methodology Register, and reference lists of included studies were searched. Publications of any type were eligible if they included explicit recommendations or empirical evidence for the reporting of potential items in a pediatric protocol (SPIRIT-C systematic review) or trial report (CONSORT-C systematic review). Study characteristics, recommendations and evidence for pediatric extension items were extracted. Recurrent themes in the recommendations and evidence were identified and synthesized. All steps were conducted by two reviewers. Results For the SPIRIT-C and CONSORT-C systematic reviews 366 and 429 publications were included, respectively. Recommendations were identified for 48 of 50 original reporting items and sub-items from SPIRIT, 15 of 20 potential SPIRIT-C reporting items, all 37 original CONSORT items and sub-items, and 16 of 22 potential CONSORT-C reporting items. The following overarching themes of evidence to support or refute the utility of reporting items were identified: transparency; reproducibility; interpretability; usefulness; internal validity; external validity; reporting bias; publication bias; accountability; scientific soundness; and research ethics. Conclusion These systematic reviews are the first to systematically gather evidence and recommendations for the reporting of specific items in pediatric protocols and trials. They provide useful and translatable evidence on which to build pediatric extensions to the SPIRIT and CONSORT reporting guidelines. The resulting SPIRIT-C and CONSORT-C will provide guidance to the authors of pediatric protocols and reports, respectively, helping to alleviate concerns of inappropriate and inconsistent reporting, and reduce research waste.
机译:背景技术完整,透明的临床试验方案和报告报告可确保这些文件对所有利益相关者都有用,可以将偏见降到最低,并且不会浪费研究资源。但是,当前的研究反复得出结论,没有适当地报告儿科试验方案和报告。诸如SPIRIT(标准方案项目:介入试验的建议)和CONSORT(报告试验的合并标准)之类的指南可能会改善报告质量,但不会提供有关儿科试验独有问题的指导。本文报告了两项系统的审查,以建立扩展儿科报告指南扩展的证据基础:1)SPIRIT-Children(SPIRIT-C)用于儿科试验方案,以及2)CONSORT-Children(CONSORT-C)用于儿科试验报告。搜索方法MEDLINE,Cochrane方法学注册簿和纳入研究的参考文献清单。如果任何类型的出版物均包含明确的建议或经验证据,以用于儿科规程(SPIRIT-C系统评价)或试验报告(CONSORT-C系统评价)中潜在项目的报告,则它们是合格的。提取了儿童扩展项目的研究特征,建议和证据。在建议和证据中反复出现的主题已得到识别和综合。所有步骤均由两名审核员进行。结果对于SPIRIT-C和CONSORT-C,系统评价分别包括366和429种出版物。确定了SPIRIT的50个原始报告项目和子项目中的48个建议,20个SPIRIT-C潜在报告项目中的15个,CONSORT原始项目和子项目中的所有37个,以及CONSORT-C 22个潜在报告项目中的16个。确定了以下支持或反驳报告项目效用的总体证据主题:透明度;再现性可解释性;用处;内部有效性外部有效性;报告偏见;出版偏见问责制;科学的健全性;和研究伦理。结论这些系统评价是第一个系统地收集证据和建议的儿童和儿童试验方案和试验中的特定项目的报告。它们为在SPIRIT和CONSORT报告指南中建立儿科扩展提供了有用且可翻译的证据。由此产生的SPIRIT-C和CONSORT-C将分别为儿科方案和报告的作者提供指导,帮助减轻对报告不适当和不一致的担忧,并减少研究浪费。

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