Institute of Translational Medicine, University of Liverpool, Liverpool, Merseyside, United Kingdom.
Department of Health Services Research, Institute of Population Health Sciences, University of Liverpool, Liverpool, Merseyside, United Kingdom.
PLoS One. 2020 Jan 10;15(1):e0225907. doi: 10.1371/journal.pone.0225907. eCollection 2020.
Cauda Equina Syndrome (CES) is an emergency condition that requires acute intervention and can lead to permanent neurological deficit in working age adults. A Core Outcome Set (COS) is the minimum set of outcomes that should be reported by a research study within a specific disease area. There is significant heterogeneity in outcome reporting for CES, which does not allow data synthesis between studies. The hypothesis is that a COS for CES can be developed for future research studies using patients and healthcare professionals (HCPs) as key stakeholders.
Qualitative semi-structured interviews with CES patients were audio-recorded, transcribed and analysed using NVivo to identify the outcomes of importance. These were combined with the outcomes obtained from a published systematic literature review of CES patients. The outcomes were grouped into a list of 37, for rating through two rounds of an international Delphi survey according to pre-set criteria. The Delphi survey had an overall response rate of 63% and included 172 participants (104 patients, 68 HCPs) from 14 countries who completed both rounds. Thirteen outcomes reached consensus at the end of the Delphi survey and there was no attrition bias detected. The results were discussed at an international consensus meeting attended by 34 key stakeholders (16 patients and 18 HCPs) from 8 countries. A further three outcomes were agreed to be included. There was no selection bias detected at the consensus meeting. There are 16 outcomes in total in the CESCOS.
This is the first study in the literature that has determined the core outcomes in CES using a transparent international consensus process involving healthcare professionals and CES patients as key stakeholders. This COS is recommended as the most important outcomes to be reported in any research study investigating CES outcomes and will allow evidence synthesis in CES.
马尾综合征(CES)是一种紧急情况,需要进行急性干预,如果发生在成年工作人群中,可能会导致永久性神经功能缺损。核心结局集(COS)是特定疾病领域的研究报告中应报告的最小结果集。CES 的结局报告存在显著异质性,无法在研究之间进行数据综合。该假设是,通过将患者和医疗保健专业人员(HCP)作为关键利益相关者,可针对 CES 开发一个 COS,用于未来的研究。
对 CES 患者进行定性半结构式访谈,使用 NVivo 对访谈录音进行转录和分析,以确定重要的结局。将这些与从 CES 患者的已发表系统文献综述中获得的结局相结合。根据预先设定的标准,将这些结局分为 37 个列表,用于两轮国际 Delphi 调查的评分。Delphi 调查的总体回复率为 63%,共有来自 14 个国家的 172 名参与者(104 名患者,68 名 HCP)完成了两轮调查。在 Delphi 调查结束时,有 13 个结局达成共识,且未发现衰减偏倚。结果在由来自 8 个国家的 34 名关键利益相关者(16 名患者和 18 名 HCP)参加的国际共识会议上进行了讨论。又有 3 个结局被同意纳入。在共识会议上未发现选择偏倚。CESCOS 共有 16 个结局。
这是文献中首次使用透明的国际共识过程,通过将医疗保健专业人员和 CES 患者作为关键利益相关者,确定 CES 中的核心结局。该 COS 被推荐为研究 CES 结局的任何研究报告中最重要的结局,这将允许在 CES 中进行证据综合。