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Reporting and interpreting missing health-related quality of life data in intensive care trials: Protocol for a systematic review

机译:报告和解释缺失的健康相关的生命数据质量,在重症监护审判中:系统审查的议定书

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Background Health-related quality of life is often used as a patient-important outcome in randomized clinical trials in the intensive care unit setting. Missing data are a challenge in randomized clinical trials as they hamper the interpretation of the results, but the extent and handling of missing health-related quality of life data are unknown. Therefore, we aim to describe and evaluate the extent, pattern, and handling of missing health-related quality of life data in randomized clinical trials conducted in the intensive care unit setting. Methods We will conduct a systematic review of randomized clinical trials in intensive care patients that report health-related quality of life. We will systematically search the Cochrane Library, PubMed, excerpta medica database ovid, and cumulative index to nursing and allied health literature for relevant literature. We will follow the recommendations by the Cochrane Collaboration and the preferred reporting items for systematic review and meta-analysis statement. We will extract information about missing data, including how the analyses and reporting of missing data were performed. We will assess the risk of systematic errors (bias) and compare the number of nonresponders vs responders in (a) low vs high risk of bias trials and in (b) small (n 100). Discussion With this outlined systematic review, we will describe the handling of missing health-related quality of life data in randomized clinical trials in the intensive care unit setting and the impact on the interpretation of results. Systematic review registration International Prospective Register of Systematic Reviews (PROSPERO): reg. no.: CRD42019118932.
机译:背景技术相关的健康生活质量通常被用作重症监护单元环境中随机临床试验中的患者重要的结果。缺少数据在随机临床试验中是一个挑战,因为它们妨碍了对结果的解释,但缺少健康相关生活质量数据的程度和处理是未知的。因此,我们的目标是描述和评估在重症监护单元环境中进行的随机临床试验中缺失健康相关质量数据的程度,模式和处理。方法,我们将对报告与健康有关的生活质量的密集护理患者进行随机临床试验进行系统评价。我们将系统地搜索Cochrane图书馆,PubMed,Excerpta Medica Database Ovid和累积指数,以获得相关文献的护理和盟军健康文学。我们将遵循Cochrane合作的建议以及系统审查和Meta-Analysis陈述的首选报告项目。我们将提取有关缺失数据的信息,包括如何执行缺失数据的分析和报告。我们将评估系统错误(偏见)的风险,并比较(a)低与偏差试验的高风险和(b)小(n 100)中的非反应者对响应者的数量。讨论了这一概述的系统审查,我们将描述在重症监护单元环境中随机临床试验中缺失的健康相关质量数据的处理,以及对结果解释的影响。系统审查注册国际潜在课程评价(Prospero):reg。不。:CRD42019118932。

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