Department of Obstetrics and Gynaecology, University of Melbourne, Melbourne, Australia.
Obstetrics and Gynaecology, Eastern Virginia Medical School, Norfolk, VA.
Menopause. 2021 Apr 26;28(8):852-858. doi: 10.1097/GME.0000000000001787.
Vasomotor symptoms (VMS) (hot flashes and night sweats) affect most women over the menopause transition. Comparing the safety and effectiveness of treatments for vasomotor symptoms is limited by the use of inconsistent outcome measures, and uncertainty as to which outcomes are most important to symptomatic women. To address this, we have developed a Core Outcome Set (COS) for use in clinical trials of treatments for VMS.
We systematically reviewed the primary outcomes measured in randomized controlled trials of treatments for VMS. These were refined and entered into a two-round modified Delphi survey completed by clinicians, researchers, and postmenopausal women between November 2019 and March 2020. Outcomes were scored on a nine-point scale from "not important" to "critically important." Two international consensus meetings were held to finalize the COS.
Based on the systematic review, 13 separate outcomes were included in the Delphi process. This was completed by 227 participants of whom 58% were postmenopausal women, 34% clinicians, and 8% researchers. Predefined thresholds were applied to categorize importance scores obtained during Round 2 of the Delphi survey. These informed discussions at the consensus meetings which were attended by 56 participants from 28 countries. The final COS includes six outcomes: 1) frequency of VMS, 2) severity of VMS, 3) distress, bother or interference caused by VMS, 4) impact on sleep, 5) satisfaction with treatment, and 6) side-effects of treatment.
Implementation of this COS will: better enable research studies to accurately reflect the joint priorities of postmenopausal women, clinicians and researchers, standardize outcome reporting, and facilitate combining and comparing results from different studies, and ultimately improve outcomes for women with bothersome VMS.
血管舒缩症状(VMS)(热潮和盗汗)影响大多数绝经过渡中的女性。比较 VMS 治疗的安全性和有效性受到使用不一致的结局测量方法的限制,并且不确定哪些结局对有症状的女性最重要。为了解决这个问题,我们为 VMS 治疗的临床试验制定了一个核心结局集(COS)。
我们系统地回顾了 VMS 治疗的随机对照试验中测量的主要结局。这些结局经过精炼并纳入了 2019 年 11 月至 2020 年 3 月期间由临床医生、研究人员和绝经后妇女完成的两轮修改后的 Delphi 调查。结局在从“不重要”到“至关重要”的九点量表上进行评分。召开了两次国际共识会议以敲定 COS。
基于系统评价,Delphi 过程中纳入了 13 项单独的结局。这项工作由 227 名参与者完成,其中 58%是绝经后妇女,34%是临床医生,8%是研究人员。应用预定的阈值对 Delphi 调查第二轮获得的重要性得分进行分类。这为在 28 个国家/地区的 56 名参与者参加的共识会议上的讨论提供了信息。最终的 COS 包括六个结局:1)VMS 的频率,2)VMS 的严重程度,3)VMS 引起的困扰、烦恼或干扰,4)对睡眠的影响,5)对治疗的满意度,以及 6)治疗的副作用。
实施这个 COS 将:更好地使研究准确反映绝经后妇女、临床医生和研究人员的共同重点,标准化结局报告,并促进从不同研究中组合和比较结果,最终改善有困扰的 VMS 女性的结局。