Implementation of delirium management during the pandemic: lessons learned

Peter Nydahl, Friederike Baumgarte, Daniela Berg, Christoph Borzikowsky, Diana Green, Anisa Hannig, Hans-Christian Hansen, Uta Hansen, Rahel Istel, Norma Krämer, Karita Krause, Mohammad Mohammadzadeh-Vazifeh, Jürgen Osterbrink, Frederick Palm, Telse Petersen, Fidan Rasmussen, Bernd Schöller, Henning Stolze, J. Meyne, Nils G Margraf
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Abstract

During the covid-19 pandemic, a non-funded, nurse-led quality improvement project on delirium management was in progress on four Stroke Units (SU). Two sites experienced pandemic-related delays; we set out to learn lessons based on the impact for delivering multicentre trials. Secondary analysis of a prospective quality improvement project. We compared data quality from centres with vs. without delay. Unplanned modifications in study management were classified as a) fatal modifications (ending the study), b) serious modifications (requiring a revision of the registration and/or ethic approval, c) moderate modifications (revising study management), d) minor modifications (improving study performance). Local study coordinators summarised lessons learned. The study had an overall delay of 14 months. Centres without delay delivered better data quality and had less loss of patients due to missing primary outcome data in 0.3% vs 28.8% in centres with delay (p<0.001). There were no fatal modifications, two serious (exchange of study centre, adding new outcome parameters), six moderate (e.g. delayed start in two centres, change from in-person to virtual meetings), and one minor modification (four local study coordinators taking parental leave). Lessons learned were frequent communication with study coordinators, attention to data quality, protocolisation of recruitment rates, and adapted education in quality improvement projects. Pandemic-related disruption can be substantial, with poorer data quality, but only in a few cases were registration and/or ethic approval modifications required. Facilitators are flexible, including changed time frames, frequent virtual communication, and critical reflection.
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在大流行病期间实施谵妄管理:经验教训
在科维德-19 大流行期间,由护士领导的谵妄管理质量改进项目在四个卒中单元(SU)进行,该项目没有资金支持。其中有两家医院出现了与大流行相关的延误;我们试图从这对开展多中心试验的影响中吸取经验教训。对前瞻性质量改进项目进行二次分析。我们比较了有延误和无延误中心的数据质量。研究管理中的计划外修改分为:a) 致命修改(终止研究);b) 严重修改(需要修改注册和/或伦理批准;c) 中等修改(修改研究管理);d) 小修改(提高研究绩效)。当地研究协调员总结了经验教训。研究总体延迟了 14 个月。未延期的中心提供的数据质量更高,因主要结果数据缺失而造成的患者损失更少,缺失率为 0.3%,而延期中心的缺失率为 28.8%(P<0.001)。没有致命的修改,有两项严重修改(交换研究中心、增加新的结果参数),六项中度修改(如两个中心推迟启动、从面对面会议改为虚拟会议),一项小修改(四名当地研究协调员休育儿假)。从中吸取的经验教训包括与研究协调员的频繁沟通、对数据质量的关注、招募率的协议化以及质量改进项目中的适应性教育。与大流行病相关的干扰可能很大,数据质量也较差,但只有少数情况下需要修改注册和/或伦理审批。促进者具有灵活性,包括改变时间框架、频繁的虚拟交流和批判性反思。
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