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重症监护病房的多研究操作:一种基于疫情信息的跨专业方法。

Multistudy Research Operations in the ICU: An Interprofessional Pandemic-Informed Approach.

作者信息

Cook Deborah J, Duan Erick H, Clarke France J, Matic Karlo, Culgin Sarah, Kelly Laurel, Nelson Katlynne S, Wallace Christine V, Soth Mark D, Lewis Kimberley A, Rudkowski Jill C, Perri Dan, Ligori Tania L, Jaeschke Roman Z, Chagla Zain, Chaudhuri Dipayan, Wright Angela E, Fu Zoe Y, Reeve Brenda K, Lee Hilary M, Overington Jeffrey D, Rozenberg Anna, Bloomfield Kimberly A, Love Katryn, Gain Jennifer L, Zytaruk Nicole L, Cheung Jason H, Thabane Lehana, Kho Michelle E

机构信息

Department of Critical Care, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, ON, Canada.

出版信息

Crit Care Explor. 2022 Dec 1;4(12):e0808. doi: 10.1097/CCE.0000000000000808. eCollection 2022 Dec.

Abstract

UNLABELLED

Proliferation of COVID-19 research underscored the need for improved awareness among investigators, research staff and bedside clinicians of the operational details of clinical studies. The objective was to describe the genesis, goals, participation, procedures, and outcomes of two research operations committees in an academic ICU during the COVID-19 pandemic.

DESIGN

Two-phase, single-center multistudy cohort.

SETTING

University-affiliated ICU in Hamilton, ON, Canada.

PATIENTS

Adult patients in the ICU, medical stepdown unit, or COVID-19 ward.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

An interprofessional COVID Collaborative was convened at the pandemic onset within our department, to proactively coordinate studies, help navigate multiple authentic consent encounters by different research staff, and determine which studies would be suitable for coenrollment. From March 2020 to May 2021, five non-COVID trials continued, two were paused then restarted, and five were launched. Over 15 months, 161 patients were involved in 215 trial enrollments, 110 (51.1%) of which were into a COVID treatment trial. The overall informed consent rate (proportion agreed of those eligible and approached including a priori and deferred consent models) was 83% (215/259). The informed consent rate was lower for COVID-19 trials (110/142, 77.5%) than other trials (105/117, 89.7%; = 0.01). Patients with COVID-19 were significantly more likely to be coenrolled in two or more studies (29/77, 37.7%) compared with other patients (13/84, 15.5%; = 0.002). Review items for each new study were collated, refined, and evolved into a modifiable checklist template to set up each study for success. The COVID Collaborative expanded to a more formal Department of Critical Care Research Operations Committee in June 2021, supporting sustainable research operations during and beyond the pandemic.

CONCLUSIONS

Structured coordination and increased communication about research operations among diverse research stakeholders cultivated a sense of shared purpose and enhanced the integrity of clinical research operations.

摘要

未标注

新冠疫情研究的激增凸显了提高研究人员、研究人员和床边临床医生对临床研究操作细节认识的必要性。目的是描述新冠疫情期间一所学术重症监护病房(ICU)中两个研究操作委员会的起源、目标、参与情况、程序和结果。

设计

两阶段、单中心多研究队列。

地点

加拿大安大略省汉密尔顿市一所大学附属ICU。

患者

ICU、医疗降级病房或新冠病房的成年患者。

干预措施

无。

测量指标和主要结果

疫情爆发时,我们部门召集了一个跨专业的新冠协作组,以积极协调研究,帮助应对不同研究人员进行的多次真实同意过程,并确定哪些研究适合联合入组。2020年3月至2021年5月,5项非新冠试验继续进行,2项暂停后重启,5项启动。在15个月内,161名患者参与了215次试验入组,其中110例(51.1%)进入新冠治疗试验。总体知情同意率(包括先验同意和延期同意模式下符合条件并被邀请者中同意的比例)为83%(215/259)。新冠试验的知情同意率(110/142,77.5%)低于其他试验(105/117,89.7%;P = 0.01)。与其他患者相比,新冠患者更有可能同时参与两项或更多项研究(29/77,37.7%对比13/84,15.5%;P = 0.002)。对每项新研究的审查项目进行整理、完善,并演变成一个可修改的清单模板,为每项研究的成功开展做好准备。2021年6月,新冠协作组扩展为一个更正式的重症监护研究操作委员会,在疫情期间及之后支持可持续的研究操作。

结论

不同研究利益相关者之间就研究操作进行结构化协调和加强沟通,培养了共同目标意识,提高了临床研究操作的完整性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc0/9722625/d897fceb70aa/cc9-4-e0808-g001.jpg

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