Building capacity in critical care research coordination in Saudi Arabia: The role of the Saudi critical care trials group

A. Deeb, E. Al Qasim, Lara Y. Afesh, S. Abdukahil, M. Sadat, Y. Arabi
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引用次数: 2

Abstract

Critical care research is growing around the world including Saudi Arabia. The objective of this review is to discuss the building capacity in critical care research coordination in Saudi Arabia as a part of the research strategy of the Saudi Critical Care Trials Group (SCCTG). The SCCTG was developed to promote high impact critical care research in Saudi Arabia and to facilitate collaboration in national and international clinical research. Well-organized coordination between all parties is necessary by the presence of qualified clinical research coordinator (CRC). Critical care has unique features that make clinical research conduct more complex and demanding. It is a high-risk area with increased potentiality of error or adverse events occurrence. Critical care providers such as critical care nurses, critical care pharmacists, respiratory therapists, critical care physiotherapists, or intensive care unit physicians with added skills may be appropriate candidates to handle CRC roles in critical care setting. These skills include but not limited to data collection, obtaining consent, patient assessment, patient screening for the study eligibility, data entry, ethics submissions, providing teaching regarding the study protocol and research topics to clinical staff, attending to regulatory requirements, and designing data collection tools. The SCCTG shall focus on training the clinical research coordination skills through providing specialized courses and workshops that enable different hospitals to conduct and participate in clinical research. It will also help developing network group to connect critical care CRCs in Saudi Arabia and worldwide.
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沙特阿拉伯重症监护研究协调能力建设:沙特重症监护试验组的作用
包括沙特阿拉伯在内的世界各地都在进行重症监护研究。本综述的目的是讨论沙特阿拉伯重症监护研究协调能力建设,作为沙特重症监护试验组(SCCTG)研究战略的一部分。制定SCCTG是为了促进沙特阿拉伯的高影响力重症监护研究,并促进国家和国际临床研究方面的合作。通过合格的临床研究协调员(CRC)的存在,各方之间组织良好的协调是必要的。重症监护具有独特的特点,使临床研究更加复杂和苛刻。这是一个高风险区域,发生错误或不良事件的可能性增加。重症监护提供者,如重症监护护士、重症监护药剂师、呼吸治疗师、重症监护物理治疗师或重症监护病房医生,具有额外技能,可能是在重症监护环境中处理结直肠癌角色的合适人选。这些技能包括但不限于数据收集、获得同意、患者评估、患者筛选研究资格、数据录入、伦理提交、向临床工作人员提供有关研究方案和研究主题的教学、遵守监管要求以及设计数据收集工具。SCCTG应重点培训临床研究协调技能,通过开设专业课程和讲习班,使不同医院能够开展和参与临床研究。它还将帮助建立网络小组,以连接沙特阿拉伯和世界各地的重症监护中心。
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