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Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework

机译:减轻健康风险在Covid-19大流行期间重新打开临床研究实验室:框架

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Background The COVID-19 pandemic has led to many countries implementing lockdown procedures, resulting in the suspension of laboratory research. With lockdown measures now easing in some areas, many laboratories are preparing to reopen. This is particularly challenging for clinical research laboratories due to the dual risk of patient samples carrying the virus that causes COVID-19, SARS-CoV-2, and the risk to patients being exposed to research staff during clinical sampling. To date, no confirmed transmission of the virus has been confirmed within a laboratory setting; however, operating processes and procedures should be adapted to ensure safe working of samples of positive, negative, or unknown COVID-19 status. Objective In this paper, we propose a framework for reopening a clinical research laboratory and resuming operations with the aim to maximize research capacity while minimizing the risk to research participants and staff. Methods This framework was developed by consensus among experienced laboratory staff who have prepared to reopen a clinical research laboratory. Results Multiple aspects need to be considered to reopen a clinical laboratory. We describe our process to stratify projects by risk, including assessment of donor risk and COVID-19 clinical status, the COVID-19 status of the specific sample type, and how to safely process each sample type. We describe methods to prepare the laboratory for safe working including maintaining social distancing through signage, one-way systems and access arrangements for staff and patients, limiting staff numbers on site and encouraging home working for all nonlaboratory tasks including data analysis and writing. Shared equipment usage was made safe by adapting booking systems to allow for the deployment of cleaning protocols. All risk assessments and standard operating procedures were rewritten and approved by local committees, and staff training was initiated to ensure compliance. Conclusions Laboratories can adopt and adapt this framework to expedite reopening a clinical laboratory during the current COVID-19 pandemic while mitigating the risk to research participants and staff.
机译:背景COVID-19的盛行已导致许多国家实行锁定程序,导致在悬挂实验室研究。随着锁定措施,如今在部分地区缓解,许多实验室正在准备重新开放。这对于临床研究实验室尤其具有挑战性,由于携带导致COVID-19,SARS-COV-2病毒的患者样本的双重风险,并且给患者的风险临床采样期间暴露于研究人员。迄今为止,该病毒没有确认的传播已经确认实验室环境内;然而,操作流程和程序应适应,以确保正,负或未知COVID-19状态的样品的安全工作。目的在本文中,我们提出了重开临床研究实验室和恢复操作,目的是最大限度地提高研究能力,同时尽量减少风险,研究参与者和工作人员提供一个框架。方法这个框架是由已经准备重开临床研究实验室谁之间有经验的实验室工作人员的共识发展。结果多个方面需要考虑重新临床实验室。我们描述我们的工艺,以分层项目的风险,包括捐助者的风险和COVID-19的临床状况,具体的样品类型的COVID-19的地位,以及如何安全地处理每个样品类型的评估。我们描述的是制备实验室的安全工作,包括保持通过标牌社会距离,单程系统和工作人员和病人的访问安排,在现场限制员工人数,并鼓励家庭所有非实验室任务,包括数据分析和撰写工作。共用设备的使用提出了通过调整订票系统,以允许清洗协议的部署安全。所有的风险评估和标准作业程序被改写,并通过当地的委员会的批准后,开始工作人员的培训,以确保遵守。结论实验室可以采用和适应这个框架,以加快当前COVID-19大流行期间重开临床实验室同时减轻风险研究参与者和工作人员。

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