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dc.contributor.authorHo, Iris S S
dc.contributor.authorAzcoaga-Lorenzo, Amaya
dc.contributor.authorAkbari, Ashley
dc.contributor.authorDavies, Jim
dc.contributor.authorKhunti, Kamlesh
dc.contributor.authorKadam, Umesh T
dc.contributor.authorLyons, Ronan A
dc.contributor.authorMcCowan, Colin
dc.contributor.authorMercer, Stewart W
dc.contributor.authorNirantharakumar, Krishnarajah
dc.contributor.authorStaniszewska, Sophie
dc.contributor.authorGuthrie, Bruce
dc.date.accessioned2022-08-10T15:30:29Z
dc.date.available2022-08-10T15:30:29Z
dc.date.issued2022-07-27
dc.identifier279760116
dc.identifier1261ac95-b6c7-433c-b70d-2b53bc0e7e0d
dc.identifier.citationHo , I S S , Azcoaga-Lorenzo , A , Akbari , A , Davies , J , Khunti , K , Kadam , U T , Lyons , R A , McCowan , C , Mercer , S W , Nirantharakumar , K , Staniszewska , S & Guthrie , B 2022 , ' Measuring multimorbidity in research : Delphi consensus study ' , BMJ Medicine , vol. 1 , no. 1 , e000247 . https://doi.org/10.1136/bmjmed-2022-000247en
dc.identifier.issn2754-0413
dc.identifier.otherRIS: urn:84E8FCFF73B5F025234CB3E0AC0E43B2
dc.identifier.otherORCID: /0000-0002-9466-833X/work/116597532
dc.identifier.otherORCID: /0000-0003-3307-878X/work/116598377
dc.identifier.otherRIS: urn:84E8FCFF73B5F025234CB3E0AC0E43B2
dc.identifier.urihttps://hdl.handle.net/10023/25814
dc.description.abstractObjective To develop international consensus on the definition and measurement of multimorbidity in research. Design Delphi consensus study. Setting International consensus; data collected in three online rounds from participants between 30 November 2020 and 18 May 2021. Participants Professionals interested in multimorbidity and people with long term conditions were recruited to professional and public panels. Results 150 professional and 25 public participants completed the first survey round. Response rates for rounds 2/3 were 83%/92% for professionals and 88%/93% in the public panel, respectively. Across both panels, the consensus was that multimorbidity should be defined as two or more long term conditions. Complex multimorbidity was perceived to be a useful concept, but the panels were unable to agree on how to define it. Both panels agreed that conditions should be included in a multimorbidity measure if they were one or more of the following: currently active; permanent in their effects; requiring current treatment, care, or therapy; requiring surveillance; or relapsing-remitting conditions requiring ongoing care. Consensus was reached for 24 conditions to always include in multimorbidity measures, and 35 conditions to usually include unless a good reason not to existed. Simple counts were preferred for estimating prevalence and examining clustering or trajectories, and weighted measures were preferred for risk adjustment and outcome prediction. Conclusions Previous multimorbidity research is limited by inconsistent definitions and approaches to measuring multimorbidity. This Delphi study identifies professional and public panel consensus guidance to facilitate consistency of definition and measurement, and to improve study comparability and reproducibility.
dc.format.extent1745901
dc.language.isoeng
dc.relation.ispartofBMJ Medicineen
dc.subjectRA Public aspects of medicineen
dc.subjectNDASen
dc.subject.lccRAen
dc.titleMeasuring multimorbidity in research : Delphi consensus studyen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Sir James Mackenzie Institute for Early Diagnosisen
dc.contributor.institutionUniversity of St Andrews. Population and Behavioural Science Divisionen
dc.identifier.doihttps://doi.org/10.1136/bmjmed-2022-000247
dc.description.statusPeer revieweden


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