Suppr超能文献

一项旨在提高急诊科对循证肺栓塞诊断依从性的质量改进项目的可行性。

Feasibility of a quality improvement project to increase adherence to evidence-based pulmonary embolism diagnosis in the emergency department.

作者信息

Germini Federico, Hu Yang, Afzal Sarah, Al-Haimus Fayad, Puttagunta Srikanth A, Niaz Saghar, Chan Teresa, Clayton Natasha, Mondoux Shawn, Thabane Lehana, de Wit Kerstin

机构信息

Department of Health Research Methods, Evidence, and Impact, Health Information Research Unit (HIRU), Communication Research Laboratory (CRL), McMaster University, 1280 Main Street West, Hamilton, ON, L8S 4K1, Canada.

Department of Medicine, McMaster University, Hamilton, ON, Canada.

出版信息

Pilot Feasibility Stud. 2021 Jan 4;7(1):4. doi: 10.1186/s40814-020-00741-8.

Abstract

BACKGROUND

Many evidence-based clinical decision tools are available for the diagnosis of pulmonary embolism (PE). However, these clinical decision tools have had suboptimal uptake in the everyday clinical practice in emergency departments (EDs), despite numerous implementation efforts. We aimed to test the feasibility of a multi-faceted intervention to implement an evidence-based PE diagnosis protocol.

METHODS

We conducted an interrupted time series study in three EDs in Ontario, Canada. We enrolled consecutive adult patients accessing the ED with suspected PE from January 1, 2018, to February 28, 2020. Components of the intervention were as follows: clinical leadership endorsement, a new pathway for PE testing, physician education, personalized confidential physician feedback, and collection of patient outcome information. The intervention was implemented in November 2019. We identified six criteria for defining the feasibility outcome: successful implementation of the intervention in at least two of the three sites, capturing data on ≥ 80% of all CTPAs ordered in the EDs, timely access to electronic data, rapid manual data extraction with feedback preparation before the end of the month ≥ 80% of the time, and time required for manual data extraction and feedback preparation ≤ 2 days per week in total.

RESULTS

The intervention was successfully implemented in two out of three sites. A total of 5094 and 899 patients were tested for PE in the period before and after the intervention, respectively. We captured data from 90% of CTPAs ordered in the EDs, and we accessed the required electronic data. The manual data extraction and individual emergency physician audit and feedback were consistently finalized before the end of each month. The time required for manual data extraction and feedback preparation was ≤ 2 days per week (14 h).

CONCLUSIONS

We proved the feasibility of implementing an evidence-based PE diagnosis protocol in two EDs. We were not successful implementing the protocol in the third ED.

REGISTRATION

The study was not registered.

摘要

背景

有许多基于证据的临床决策工具可用于诊断肺栓塞(PE)。然而,尽管进行了大量实施工作,但这些临床决策工具在急诊科(ED)的日常临床实践中的采用情况并不理想。我们旨在测试实施基于证据的PE诊断方案的多方面干预措施的可行性。

方法

我们在加拿大安大略省的三个急诊科进行了一项中断时间序列研究。我们纳入了2018年1月1日至2020年2月28日期间因疑似PE而进入急诊科的连续成年患者。干预措施的组成部分如下:临床领导认可、PE检测的新途径、医生教育、个性化的保密医生反馈以及患者结局信息的收集。干预措施于2019年11月实施。我们确定了六个定义可行性结果的标准:在三个地点中的至少两个成功实施干预措施、获取急诊科所有CTPA检查中≥80%的数据、及时获取电子数据、在月底前≥80%的时间内快速进行人工数据提取并准备反馈、人工数据提取和反馈准备所需的时间每周总计≤2天。

结果

干预措施在三个地点中的两个成功实施。在干预前和干预后期间,分别有5094例和899例患者接受了PE检测。我们获取了急诊科90%的CTPA检查数据,并获取了所需的电子数据。人工数据提取以及对每位急诊医生的审核和反馈在每个月底前均能完成。人工数据提取和反馈准备所需的时间为每周≤2天(14小时)。

结论

我们证明了在两个急诊科实施基于证据的PE诊断方案的可行性。我们未能在第三个急诊科成功实施该方案。

注册情况

该研究未注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef8d/7780666/9e7fe904188e/40814_2020_741_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验