Trauma, Emergency and Critical Care Research Program, Evaluative Clinical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
Department of Surgery, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
BMJ Open. 2018 May 9;8(5):e021750. doi: 10.1136/bmjopen-2018-021750.
Quality improvement (QI) is mandatory in trauma centres but there is no prescription for doing successful QI. Considerable variation in implementation strategies and inconsistent use of evidence-based protocols therefore exist across centres. The quality of reporting on these strategies may limit the transferability of successful initiatives across centres. This systematic review will assess the quality of reporting on guideline, protocol or algorithm implementation within a trauma centre in terms of the Revised Standards for Quality Improvement Reporting Excellence (SQUIRE 2.0).
We will search for English language articles published after 2010 in EMBASE, MEDLINE, CINAHL electronic databases and the Cochrane Central Register of Controlled Trials. The database search will be supplemented by searching trial registries and grey literature online. Included studies will evaluate the effectiveness of guideline implementation in terms of change in clinical practice or improvement in patient outcomes. The primary outcome will be a global score reporting the proportion of studies respecting at least 80% of the SQUIRE 2.0 criteria and will be obtained based on the 18-items identified in the SQUIRE 2.0 guidelines. Secondary outcome will be the risk of bias assessed with the Risk Of Bias In Non-randomised Studies- of Interventions tool for observational cohort studies and with the Cochrane Collaboration tool for randomised controlled trials. Meta-analyses will be conducted in randomised controlled trials to estimate the effectiveness of guideline implementation if studies are not heterogeneous. If meta-analyses are conducted, we will combine studies according to the risk of bias (low, moderate or high/unclear) in subgroup analyses. All study titles, abstracts and full-text screening will be completed independently and in duplicate by the review team members. Data extraction and risk of bias assessment will also be done independently and in duplicate.
Results will be disseminated through scientific publication and conferences.
CRD42018084273.
质量改进(QI)在创伤中心是强制性的,但成功进行 QI 没有规定的方法。因此,各个中心之间在实施策略方面存在相当大的差异,并且对基于证据的协议的使用也不一致。这些策略报告的质量可能限制了成功举措在中心之间的可转移性。本系统评价将根据修订后的质量改进报告卓越标准(SQUIRE 2.0)评估创伤中心内指南、协议或算法实施的报告质量。
我们将搜索 2010 年后发表的英文文章,检索范围包括 EMBASE、MEDLINE、CINAHL 电子数据库和 Cochrane 对照试验中心注册库。数据库搜索将辅以试验登记处和在线灰色文献搜索。纳入的研究将根据临床实践的变化或患者结局的改善来评估指南实施的有效性。主要结局将是一个全球评分,报告至少有 80%的 SQUIRE 2.0 标准的研究比例,并根据 SQUIRE 2.0 指南中确定的 18 个项目获得。次要结局将是使用非随机干预观察队列研究的风险偏倚评估工具(RoBINS-I)和随机对照试验的 Cochrane 协作工具评估风险偏倚。如果研究没有异质性,将进行随机对照试验的荟萃分析以估计指南实施的有效性。如果进行荟萃分析,我们将根据偏倚风险(低、中或高/不明确)在亚组分析中合并研究。所有研究标题、摘要和全文筛选都将由审查团队成员独立重复完成。数据提取和风险偏倚评估也将独立重复进行。
结果将通过科学出版物和会议进行传播。
PROSPERO 注册号:CRD42018084273。