School of Medical Sciences, Bangor University, Bangor, UK
Medicine, Ysbyty Gwynedd, Bangor, UK.
BMJ Open. 2021 Jan 13;11(1):e047446. doi: 10.1136/bmjopen-2020-047446.
Review available evidence for impact of electronic health records (EHRs) on predefined patient safety outcomes in interventional studies to identify gaps in current knowledge and design interventions for future research.
Scoping review to map existing evidence and identify gaps for future research.
PubMed, the Cochrane Library, EMBASE, Trial registers.
Eligibility criteria: We conducted a scoping review of bibliographic databases and the grey literature of randomised and non-randomised trials describing interventions targeting a list of fourteen predefined areas of safety. The search was limited to manuscripts published between January 2008 and December 2018 of studies in adult inpatient settings and complemented by a targeted search for studies using a sample of EHR vendors. Studies were categorised according to methodology, intervention characteristics and safety outcome.Results from identified studies were grouped around common themes of safety measures.
The search yielded 583 articles of which 24 articles were included. The identified studies were largely from US academic medical centres, heterogeneous in study conduct, definitions, treatment protocols and study outcome reporting. Of the 24 included studies effective safety themes included medication reconciliation, decision support for prescribing medications, communication between teams, infection prevention and measures of EHR-specific harm. Heterogeneity of the interventions and study characteristics precluded a systematic meta-analysis. Most studies reported process measures and not patient-level safety outcomes: We found no or limited evidence in 13 of 14 predefined safety areas, with good evidence limited to medication safety.
Published evidence for EHR impact on safety outcomes from interventional studies is limited and does not permit firm conclusions regarding the full safety impact of EHRs or support recommendations about ideal design features. The review highlights the need for greater transparency in quality assurance of existing EHRs and further research into suitable metrics and study designs.
综述干预性研究中电子健康记录(EHR)对预先设定的患者安全结果的影响的现有证据,以确定当前知识的差距,并为未来的研究设计干预措施。
范围综述以绘制现有证据并确定未来研究的差距。
PubMed、Cochrane 图书馆、EMBASE、试验登记处。
纳入标准:我们对文献数据库和灰色文献进行了范围综述,纳入了描述针对安全性的 14 个预先设定领域的干预措施的随机和非随机试验。搜索仅限于 2008 年 1 月至 2018 年 12 月期间发表的、成人住院患者环境中进行的研究的手稿,并辅以针对使用电子病历供应商样本的研究的有针对性搜索。研究根据方法学、干预措施特征和安全结果进行分类。从确定的研究中获得的结果围绕安全措施的共同主题进行了分组。
搜索产生了 583 篇文章,其中 24 篇文章被纳入。确定的研究主要来自美国学术医疗中心,在研究实施、定义、治疗方案和研究结果报告方面存在差异。在纳入的 24 项研究中,有效的安全主题包括药物重整、药物处方决策支持、团队之间的沟通、感染预防和电子病历特定伤害的措施。干预措施和研究特征的异质性排除了系统的荟萃分析。大多数研究报告的是过程措施,而不是患者层面的安全结果:我们在 14 个预先设定的安全领域中的 13 个领域中没有或仅有有限的证据,药物安全性方面的证据较好。
干预性研究中关于电子病历对安全结果影响的发表证据有限,不能就电子病历的全部安全影响得出确定的结论,也不能支持关于理想设计特征的建议。该综述强调了提高现有电子病历质量保证透明度以及进一步研究合适的指标和研究设计的必要性。