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临床试验中的疼痛评估:一项叙述性综述。

Pain assessment in clinical trials: a narrative review.

作者信息

Puljak Livia, Boric Krste, Dosenovic Svjetlana

机构信息

Center for Evidence-Based Medicine and Health Care, Catholic University of Croatia, Zagreb, Croatia.

Department of Surgery, University Hospital Center Split, Split, Croatia.

出版信息

Ann Transl Med. 2021 Jan;9(2):188. doi: 10.21037/atm-20-3451.

Abstract

Pain is a symptom measured in many clinical trials. For pain as an outcome domain, trialists need to choose adequate outcome measure(s), as there are myriad outcome measures for pain to choose from. To ensure consistency and uniformity in clinical trials and systematic reviews, core outcome sets (COS) have been defined; COS includes a predefined minimal list of core outcomes that should be measured within a trial, to ensure their consistency and comparability. COS is defined via consensus procedure, which includes relevant stakeholders such as experts from a specific field and patients. Along with outcomes, outcome measures for each outcome need to be defined to make sure that the outcomes will be measured consistently and uniformly. Hereby we reviewed studies that have examined use of recommended core outcome domains and outcome measures in clinical trials that would be expected to measure pain. Despite the existence of COS and defined core outcome measures (COMs), multiple studies have shown that these are not necessarily used in clinical trials, or in the relevant systematic reviews, which further increases heterogeneity of existing evidence, hinders evidence synthesis and trial comparability, and assessment of comparative effectiveness of interventions. Trialists are encouraged to use COS and COMs when designing clinical trials. Research community is encouraged to design interventions that will help with identifying barriers for using COS and COMs and interventions to foster their uptake. Use of consistent pain outcomes and pain outcome measures is in the interest of patients, research community, healthcare workers and decision-makers. For clinical conditions for which there are no COS and COMs, efforts to design them would be beneficial.

摘要

疼痛是许多临床试验中测量的一种症状。对于疼痛作为一个结局领域,试验者需要选择适当的结局指标,因为有无数种疼痛结局指标可供选择。为确保临床试验和系统评价的一致性和统一性,已定义了核心结局集(COS);COS包括一份预先确定的核心结局最小清单,应在试验中进行测量,以确保其一致性和可比性。COS通过共识程序定义,该程序包括相关利益相关者,如特定领域的专家和患者。除了结局,还需要为每个结局定义结局指标,以确保结局能够得到一致和统一的测量。在此,我们回顾了一些研究,这些研究考察了在预期测量疼痛的临床试验中推荐的核心结局领域和结局指标的使用情况。尽管存在COS和已定义的核心结局指标(COM),但多项研究表明,这些指标在临床试验或相关系统评价中不一定会被使用,这进一步增加了现有证据的异质性,阻碍了证据综合和试验可比性,以及对干预措施比较效果的评估。鼓励试验者在设计临床试验时使用COS和COM。鼓励研究界设计有助于识别使用COS和COM的障碍的干预措施,以及促进其采用的干预措施。使用一致的疼痛结局和疼痛结局指标符合患者、研究界、医护人员和决策者的利益。对于没有COS和COM的临床情况,努力设计它们将是有益的。

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