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Comparative effectiveness of inhaled corticosteroids for paediatric asthma: protocol for a systematic review and Bayesian network meta-analysis

机译:吸入性糖皮质激素治疗小儿哮喘的比较有效性:系统评价方案和贝叶斯网络荟萃分析

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Introduction Use of inhaled corticosteroid (ICS) is the mainstream maintenance therapy for paediatric asthma. Several forms of ICS are available, but the relative effectiveness among ICS has not been well investigated in published, randomised, controlled trials. The paucity of direct comparisons between ICS may have resulted in insufficient estimation in former systematic reviews/meta-analyses. To supplement the information on the comparative effectiveness of ICS for paediatric asthma, we plan to conduct a network meta-analysis that will enable summary of direct and indirect evidence. Methods and analysis We will retrieve randomised, controlled trials that examined the effectiveness of ICS for paediatric asthma from the PubMed and Cochrane Central Register of Controlled Trials. After one author scans the title and abstract for eligible studies, two authors will independently review study data and assess the quality of the study. Studies of children (≤18?years old) with chronic asthma or recurrent wheezing episodes will be included if they used ICS for ≥4?weeks. We will define a priori core outcomes and supplemental outcomes of paediatric asthma, including exacerbation, healthcare use and pulmonary function. Studies reporting a minimum of one core outcome will be entered into the systematic review. After the systematic review is performed, extracted data of relevant studies will be synthesised in the Bayesian framework using a random-effects model. Ethics and dissemination The results will be disseminated through peer-reviewed publications and conference presentations. Protocol registration number UMIN (000016724) and PROSPERO (CRD42015025889).
机译:简介吸入糖皮质激素(ICS)的使用是小儿哮喘的主流维持疗法。可以使用几种形式的ICS,但是尚未在已发表的随机对照试验中很好地研究ICS之间的相对有效性。 ICS之间直接比较的匮乏可能导致以前的系统评价/元分析的估计不足。为了补充有关ICS对小儿哮喘的相对有效性的信息,我们计划进行网络荟萃分析,以汇总直接和间接证据。方法和分析我们将从PubMed和Cochrane中央对照试验登记册中检索检查ICS对小儿哮喘的有效性的随机对照试验。一位作者扫描了符合条件的研究的标题和摘要后,两位作者将独立查看研究数据并评估研究质量。如果他们使用ICS≥4周,则对儿童(≤18岁)患有慢性哮喘或反复发作​​的哮喘进行研究。我们将定义小儿哮喘的先验核心结局和补充结局,包括病情加重,医疗保健使用和肺功能。报告至少一项核心结果的研究将进入系统评价。完成系统评价后,将使用随机效应模型在贝叶斯框架中综合提取相关研究的数据。道德与传播结果将通过同行评审的出版物和会议演讲进行传播。协议注册号UMIN(000016724)和PROSPERO(CRD42015025889)。

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