Protocol for the development of the Wales Multimorbidity e-Cohort (WMC): data sources and methods to construct a population-based research platform to investigate multimorbidity.
Protocol for the development of the Wales Multimorbidity e-Cohort (WMC): data sources and methods to construct a population-based research platform to investigate multimorbidity.
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DOI:
10.1136/bmjopen-2020-047101
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发表时间:
2021-01-19
期刊:
影响因子:
2.9
通讯作者:
Lyons RA
中科院分区:
文献类型:
--
作者:
Lyons J;Akbari A;Agrawal U;Harper G;Azcoaga-Lorenzo A;Bailey R;Rafferty J;Watkins A;Fry R;McCowan C;Dezateux C;Robson JP;Peek N;Holmes C;Denaxas S;Owen R;Abrams KR;John A;O'Reilly D;Richardson S;Hall M;Gale CP;Davies J;Davies C;Cross L;Gallacher J;Chess J;Brookes AJ;Lyons RA
Multimorbidity is widely recognised as the presence of two or more concurrent long-term conditions, yet remains a poorly understood global issue despite increasing in prevalence. We have created the Wales Multimorbidity e-Cohort (WMC) to provide an accessible research ready data asset to further the understanding of multimorbidity. Our objectives are to create a platform to support research which would help to understand prevalence, trajectories and determinants in multimorbidity, characterise clusters that lead to highest burden on individuals and healthcare services, and evaluate and provide new multimorbidity phenotypes and algorithms to the National Health Service and research communities to support prevention, healthcare planning and the management of individuals with multimorbidity. The WMC has been created and derived from multisourced demographic, administrative and electronic health record data relating to the Welsh population in the Secure Anonymised Information Linkage (SAIL) Databank. The WMC consists of 2.9 million people alive and living in Wales on the 1 January 2000 with follow-up until 31 December 2019, Welsh residency break or death. Published comorbidity indices and phenotype code lists will be used to measure and conceptualise multimorbidity. Study outcomes will include: (1) a description of multimorbidity using published data phenotype algorithms/ontologies, (2) investigation of the associations between baseline demographic factors and multimorbidity, (3) identification of temporal trajectories of clusters of conditions and multimorbidity and (4) investigation of multimorbidity clusters with poor outcomes such as mortality and high healthcare service utilisation. The SAIL Databank independent Information Governance Review Panel has approved this study (SAIL Project: 0911). Study findings will be presented to policy groups, public meetings, national and international conferences, and published in peer-reviewed journals.
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影响因子:
15.8
作者:
Hall M;Dondo TB;Yan AT;Mamas MA;Timmis AD;Deanfield JE;Jernberg T;Hemingway H;Fox KAA;Gale CP
通讯作者:
Gale CP
影响因子:
3.5
作者:
Lyons RA;Jones KH;John G;Brooks CJ;Verplancke JP;Ford DV;Brown G;Leake K
通讯作者:
Leake K
影响因子:
3
作者:
Elixhauser, A;Steiner, C;Coffey, RN
通讯作者:
Coffey, RN
影响因子:
4.5
作者:
Jones, Kerina H.;Ford, David V.;Jones, Chris;Dsilva, Rohan;Thompson, Simon;Brooks, Caroline J.;Heaven, Martin L.;Thayer, Daniel S.;McNerney, Cynthia L.;Lyons, Ronan A.
通讯作者:
Lyons, Ronan A.
影响因子:
3.7
作者:
Lyons, Ronan A.;Turner, Samantha;Jones, Sarah J.
通讯作者:
Jones, Sarah J.