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A cross-sectional study of the reporting quality of pilot or feasibility trials in high-impact anesthesia journals

机译:高影响麻醉期刊中试点或可行性试验报告质量的横截面研究

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Purpose Pilot trials inform the design and conduct of larger scale trials. Using the Consolidated Standards of Reporting Trials (CONSORT) pilot extension guidelines, we assessed reporting quality in five high-impact anesthesia journals and explored factors associated with reporting quality. Methods The five highest-impact anesthesia journals were screened for randomized-controlled trials published as pilot or feasibility trials between 2006 and 2016. A pair of reviewers independently screened citations, extracted data, and assessed reporting quality using the CONSORT pilot trial extension checklists for abstracts and full texts. We reported the percentage adherence for each item, along with the median [interquartile range (IQR)] or mean (standard deviation [SD]) for all items. The factors considered to influence reporting were: 1) trial registration, 2) industry funding, 3) trial identification as a pilot or feasibility in the title or abstract, 4) primary objective as “feasibility”, and 5) the specific journal. The association was estimated using generalized estimating equations and reported as incidence rate ratios with 99% confidence intervals. Results Of 364 citations, 58 articles were eligible. The median [IQR] number of CONSORT abstract items reported was 5 [4-7], and the mean (SD) number of full text items reported was 13 (5). Significantly poor reporting was associated with “not registering the trial” (both abstracts and full texts), “trial not identified as a pilot” (abstracts), and “using clinical hypothesis as the primary objective” (full texts). Conclusion The reporting quality of pilot trials published in leading anesthesia journals is poor. Journal editorial boards can encourage improved reporting by supporting adherence to the CONSORT extension for pilot trials.
机译:目的试验试验可通知设计和进行更大的规模试验。利用综合报告试验标准(共配)试验延期准则,我们评估了五个高冲击麻醉期刊和与报告质量相关的因素的报告质量。方法对2006年至2016年之间的试验或可行性试验发布的随机对照试验的五种最高影响麻醉期刊。一对审阅人员独立筛选引文,提取数据,并使用加盟试验试验摘要清单进行摘要,评估报告质量和全文。我们报告了每个项目的依从性,以及所有物品的中位数[四分位数范围(IQR)]或平均值(标准偏差[SD])。被认为会报告的因素是:1)审判登记,2)行业资金,3)试验识别作为标题或抽象的试点或可行性,4)主要目标是“可行性”,以及5)具体日记。使用广义估计方程估计该关联,并报告为99%置信区间的发病率比。结果364引文,58条有资格。报告的中位数[IQR]报告的分配项目数为5 [4-7],平均(SD)报告的全文项目数为13(5)。显着差的报告与“未注册审判”(摘要和全文)有关,“未定名未被确定为试验”(摘要),以及“使用临床假设作为主要目标”(全文)。结论领先麻醉期刊出版的试验试验报告质量差。编辑委员会可以通过支持遵守飞行员试验的联席会延期来鼓励改进的报告。

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