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dc.contributor.authorMULTIPAP group
dc.contributor.authorAragon MultiPAP Group
dc.contributor.authorMadrid MultiPAP Group: Marta Alcaraz-Borrajo
dc.contributor.authorLopez-Rodriguez, Juan A.
dc.contributor.authorSanz-Cuesta, Teresa
dc.contributor.authorAza-Pascual-Salcedo, Mercedes
dc.contributor.authorBujalance-Zafra, M. Jose
dc.contributor.authorCura-Gonzalez, Isabel
dc.contributor.authorHernández-Santiago, Virginia
dc.contributor.authorRico-Blázquez, Milagros
dc.contributor.authorTello-Bernabé, M. Eugenia
dc.contributor.authorRumayor-Zarzuelo, Mercedes
dc.date.accessioned2021-03-25T12:30:12Z
dc.date.available2021-03-25T12:30:12Z
dc.date.issued2020-03-03
dc.identifier.citationMULTIPAP group , Aragon MultiPAP Group , Madrid MultiPAP Group: Marta Alcaraz-Borrajo , Lopez-Rodriguez , J A , Sanz-Cuesta , T , Aza-Pascual-Salcedo , M , Bujalance-Zafra , M J , Cura-Gonzalez , I , Hernández-Santiago , V , Rico-Blázquez , M , Tello-Bernabé , M E & Rumayor-Zarzuelo , M 2020 , ' Use of an electronic clinical decision support system in primary care to assess inappropriate polypharmacy in young seniors with multimorbidity : Observational, descriptive, cross-sectional study ' , Journal of Medical Internet Research , vol. 8 , no. 3 , e14130 . https://doi.org/10.2196/14130en
dc.identifier.issn1439-4456
dc.identifier.otherPURE: 272337674
dc.identifier.otherPURE UUID: d6b0a7e3-9d1f-41ba-a5f9-c8fba96b3085
dc.identifier.otherScopus: 85097112301
dc.identifier.otherORCID: /0000-0002-8544-1483/work/86987228
dc.identifier.urihttps://hdl.handle.net/10023/21715
dc.descriptionThis study was funded by National Institute for Health Research ISCIII (Grant numbers PI15/00276 (APT), PI15/00572 (ICG), PI15/00996 (JDPT), RD16/0001/0004 (ICG), RD16/0001/0005 (APT), RD16/0001/0006 (JDPT)) Co-funded by European Regional Development Fund, (ERDF) “A way of shaping Europe”. National Plan I+D+I 2013-2016.en
dc.description.abstractBackground: Multimorbidity is a global health problem that is usually associated with polypharmacy, which increases the risk of potentially inappropriate prescribing (PIP). PIP entails higher hospitalization rates and mortality and increased usage of services provided by the health system. Tools exist to improve prescription practices and decrease PIP, including screening tools and explicit criteria that can be applied in an automated manner. Objective: This study aimed to describe the prevalence of PIP in primary care consultations among patients aged 65-75 years with multimorbidity and polypharmacy, detected by an electronic clinical decision support system (ECDSS) following the 2015 American Geriatrics Society Beers Criteria, the European Screening Tool of Older Person’s Prescription (STOPP), and the Screening Tool to Alert doctors to Right Treatment (START). Methods: This was an observational, descriptive, cross-sectional study. The sample included 593 community-dwelling adults aged 65-75 years (henceforth called young seniors), with multimorbidity (3 diseases) and polypharmacy (5 medications), who had visited their primary care doctor at least once over the last year at 1 of the 38 health care centers participating in the Multimorbidity and Polypharmacy in Primary Care (Multi-PAP) trial. Sociodemographic data, clinical and pharmacological treatment variables, and PIP, as detected by 1 ECDSS, were recorded. A multivariate logistic regression model with robust estimators was built to assess the factors affecting PIP according to the STOPP criteria.  Results: PIP was detected in 57.0% (338/593; 95% CI 53-61) and 72.8% (432/593; 95% CI 69.3-76.4) of the patients according to the STOPP criteria and the Beers Criteria, respectively, whereas 42.8% (254/593; 95% CI 38.9-46.8) of the patients partially met the START criteria. The most frequently detected PIPs were benzodiazepines (BZD) intake for more than 4 weeks (217/593, 36.6%) using the STOPP version 2 and the prolonged use of proton pump inhibitors (269/593, 45.4%) using the 2015 Beers Criteria. Being a woman (odds ratio [OR] 1.43, 95% CI 1.01-2.01; P.04), taking a greater number of medicines (OR 1.25, 95%CI 1.14-1.37; P.04), working in the primary sector (OR 1.91, 95% CI 1.25-2.93; P.003), and being prescribed drugs for the central nervous system (OR 3.75, 95% CI 2.45-5.76; P<.001) were related to a higher frequency of PIP. Conclusions: There is a high prevalence of PIP in primary care as detected by an ECDSS in community-dwelling young seniors with comorbidity and polypharmacy. The specific PIP criteria defined by this study are consistent with the current literature. This ECDSS can be useful for supervising prescriptions in primary health care consultations.
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofJournal of Medical Internet Researchen
dc.rightsCopyright © Eloisa A Rogero-Blanco, Juan A Lopez-Rodriguez, Teresa Sanz-Cuesta, Mercedes Aza-Pascual-Salcedo, M Jose Bujalance-Zafra, Isabel Cura-Gonzalez, MultiPAP Group. Originally published in JMIR Medical Informatics (http://medinform.jmir.org), 03.03.2020. This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Medical Informatics, is properly cited. The complete bibliographic information, a link to the original publication on http://medinform.jmir.org/, as well as this copyright and license information must be included.en
dc.subjectClinical decision support systemsen
dc.subjectMultimorbidityen
dc.subjectPolypharmacyen
dc.subjectPotentially inappropriate medication listen
dc.subjectPrimary careen
dc.subjectRM Therapeutics. Pharmacologyen
dc.subjectHealth Informaticsen
dc.subjectDASen
dc.subject.lccRMen
dc.titleUse of an electronic clinical decision support system in primary care to assess inappropriate polypharmacy in young seniors with multimorbidity : Observational, descriptive, cross-sectional studyen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.2196/14130
dc.description.statusPeer revieweden


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