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dc.contributor.authorLensen S
dc.contributor.authorParamanandam V.S
dc.contributor.authorGabes M
dc.contributor.authorKann G
dc.contributor.authorDonhauser T
dc.contributor.authorWaters N.F
dc.contributor.authorLi A.D
dc.contributor.authorPeate M
dc.contributor.authorSusanto N.S
dc.contributor.authorCaughey L.E
dc.contributor.authorRangoonwal F
dc.contributor.authorLiu J
dc.contributor.authorCondron P
dc.contributor.authorAnagnostis P
dc.contributor.authorArcher D.F
dc.contributor.authorAvis N.E
dc.contributor.authorBell R.J
dc.contributor.authorCarpenter J.S
dc.contributor.authorChedraui P
dc.contributor.authorChristmas M
dc.contributor.authorDavies M
dc.contributor.authorHillard T
dc.contributor.authorHunter M.S
dc.contributor.authorIliodromiti S
dc.contributor.authorJaff N.G
dc.contributor.authorJaisamrarn U
dc.contributor.authorJoffe H.
dc.date.accessioned2024-10-09T14:28:24Z
dc.date.available2024-10-09T14:28:24Z
dc.date.issued2024
dc.identifier.issn10723714
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85197340097&doi=10.1097%2fGME.0000000000002370&partnerID=40&md5=24fe4377ecfbf7e3179b0582ebcd764d
dc.identifier.urihttp://hdl.handle.net/10818/61944
dc.description.abstractObjective The aim of the study is to identify suitable definitions and patient-reported outcome measures (PROMs) to assess each of the six core outcomes previously identified through the COMMA (Core Outcomes in Menopause) global consensus process relating to vasomotor symptoms: frequency, severity, distress/bother/interference, impact on sleep, satisfaction with treatment, and side effects. Methods A systematic review was conducted to identify relevant definitions for the outcome of side-effects and PROMs with acceptable measurement properties for the remaining five core outcomes. The consensus process, involving 36 participants from 16 countries, was conducted to review definitions and PROMs and make final recommendations for the measurement of each core outcome. Results A total of 21,207 publications were screened from which 119 reporting on 40 PROMs were identified. Of these 40 PROMs, 36 either did not adequately map onto the core outcomes or lacked sufficient measurement properties. Therefore, only four PROMs corresponding to two of the six core outcomes were considered for recommendation. We recommend the Hot Flash Related Daily Interference Scale to measure the domain of distress, bother, or interference of vasomotor symptoms and to capture impact on sleep (one item in the Hot Flash Related Daily Interference Scale captures interference with sleep). Six definitions of "side effects"were identified and considered. We recommend that all trials report adverse events, which is a requirement of Good Clinical Practice. Conclusions We identified suitable definitions and PROMs for only three of the six core outcomes. No suitable PROMs were found for the remaining three outcomes (frequency and severity of vasomotor symptoms and satisfaction with treatment). Future studies should develop and validate PROMs for these outcomes. © Wolters Kluwer Health, Inc. All rights reserved.en
dc.formatapplication/pdfes_CO
dc.language.isoenges_CO
dc.publisherMenopausees_CO
dc.relation.ispartofseriesMenopause Vol. 31 N° 7
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceUniversidad de La Sabanaes_CO
dc.sourceIntellectum Repositorio Universidad de La Sabanaes_CO
dc.subject.otherCore outcome seten
dc.subject.otherCOSMINen
dc.subject.otherMenopauseen
dc.subject.otherPatient-reported outcome measure (PROM)en
dc.subject.otherSystematic reviewen
dc.subject.otherVasomotoren
dc.titleRecommended measurement instruments for menopausal vasomotor symptoms: the COMMA (Core Outcomes in Menopause) consortiumen
dc.typejournal articlees_CO
dc.type.hasVersionpublishedVersiones_CO
dc.rights.accessRightsopenAccesses_CO
dc.identifier.doi10.1097/GME.0000000000002370


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