Show simple item record

dc.contributor.authorValderas Martinez, JM
dc.contributor.authorViolan, C
dc.contributor.authorFoguet-Boreu, Q
dc.contributor.authorFernandez-Bertolin, S
dc.contributor.authorGuisado-Clavero, M
dc.contributor.authorCabrera-Bean, M
dc.contributor.authorFormiga, F
dc.contributor.authorValderas Martinez, JM
dc.contributor.authorRoso-Llorach, A
dc.date.accessioned2019-08-30T12:14:53Z
dc.date.issued2019-08-30
dc.description.abstractObjectives The aim of this study was to identify, with soft clustering methods, multimorbidity patterns in the electronic health records of a population ≥65 years, and to analyse such patterns in accordance with the different prevalence cut-off points applied. Fuzzy cluster analysis allows individuals to be linked simultaneously to multiple clusters and is more consistent with clinical experience than other approaches frequently found in the literature. Design A cross-sectional study was conducted based on data from electronic health records. Setting 284 primary healthcare centres in Catalonia, Spain (2012). Participants 916 619 eligible individuals were included (women: 57.7%). Primary and secondary outcome measures We extracted data on demographics, International Classification of Diseases version 10 chronic diagnoses, prescribed drugs and socioeconomic status for patients aged ≥65. Following principal component analysis of categorical and continuous variables for dimensionality reduction, machine learning techniques were applied for the identification of disease clusters in a fuzzy c-means analysis. Sensitivity analyses, with different prevalence cut-off points for chronic diseases, were also conducted. Solutions were evaluated from clinical consistency and significance criteria. Results Multimorbidity was present in 93.1%. Eight clusters were identified with a varying number of disease values: nervous and digestive; respiratory, circulatory and nervous; circulatory and digestive; mental, nervous and digestive, female dominant; mental, digestive and blood, female oldest-old dominant; nervous, musculoskeletal and circulatory, female dominant; genitourinary, mental and musculoskeletal, male dominant; and non-specified, youngest-old dominant. Nuclear diseases were identified for each cluster independently of the prevalence cut-off point considered. Conclusions Multimorbidity patterns were obtained using fuzzy c-means cluster analysis. They are clinically meaningful clusters which support the development of tailored approaches to multimorbidity management and further research.en_GB
dc.description.sponsorshipCarlos III Institute of Health, Ministry of Economy and Competitiveness (Spain)en_GB
dc.description.sponsorship(European Regional Development Funden_GB
dc.description.sponsorshipDepartment of Health of the Catalan Governmenten_GB
dc.description.sponsorshipCatalan Governmenten_GB
dc.identifier.citationVol. 9, article e029594en_GB
dc.identifier.doi10.1136/bmjopen-2019-029594
dc.identifier.grantnumberPI16/00639en_GB
dc.identifier.grantnumberSLT002/16/00058en_GB
dc.identifier.grantnumberAGAUR 2017 SGR 578en_GB
dc.identifier.urihttp://hdl.handle.net/10871/38493
dc.language.isoenen_GB
dc.publisherBMJ Publishing Groupen_GB
dc.rights© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.en_GB
dc.titleSoft clustering using real-world data for the identification of multimorbidity patterns in an elderly population: cross-sectional study in a Mediterranean populationen_GB
dc.typeArticleen_GB
dc.date.available2019-08-30T12:14:53Z
dc.descriptionThis is the final version. Available on open access from BMJ Publishing Group via the DOI in this recorden_GB
dc.identifier.eissn2044-6055
dc.identifier.journalBMJ Openen_GB
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/en_GB
dcterms.dateAccepted2019-07-29
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-08-30
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-08-30T12:08:39Z
refterms.versionFCDVoR
refterms.dateFOA2019-08-30T12:14:58Z
refterms.panelAen_GB


Files in this item

This item appears in the following Collection(s)

Show simple item record

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Except where otherwise noted, this item's licence is described as © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.