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Clinical complexity and impact of the ABC (Atrial fibrillation Better Care) pathway in patients with atrial fibrillation: a report from the ESC-EHRA EURObservational Research Programme in AF General Long-Term Registry

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dc.contributor.author Romiti, Giulio-Francesco
dc.contributor.author Proietti, Marco
dc.contributor.author Vitolo, Marco
dc.contributor.author Bonini, Niccolo
dc.contributor.author Fawzy, Ameenathul-Mazaya
dc.contributor.author Ding, Wern-Yew
dc.contributor.author Fauchier, Laurent
dc.contributor.author Marín, Francisco
dc.contributor.author Nabauer, Michael
dc.contributor.author Dan, Gheorghe-Andrei
dc.contributor.author Potpara, Tatjana-S
dc.contributor.author Boriani, Giuseppe
dc.contributor.author Lip, Gregory-YH
dc.date.accessioned 2025-11-20T07:15:49Z
dc.date.available 2025-11-20T07:15:49Z
dc.date.issued 2022-09
dc.identifier.citation Romiti GF, Proietti M, Vitolo M, Bonini N, Fawzy AM, Ding WY, et al. Clinical complexity and impact of the ABC (Atrial fibrillation Better Care) pathway in patients with atrial fibrillation: a report from the ESC-EHRA EURObservational Research Programme in AF General Long-Term Registry. BMC Med. 2 de septiembre de 2022;20(1):326.
dc.identifier.issn 1741-7015
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21494
dc.description.abstract BACKGROUND: Clinical complexity is increasingly prevalent among patients with atrial fibrillation (AF). The 'Atrial fibrillation Better Care' (ABC) pathway approach has been proposed to streamline a more holistic and integrated approach to AF care; however, there are limited data on its usefulness among clinically complex patients. We aim to determine the impact of ABC pathway in a contemporary cohort of clinically complex AF patients. METHODS: From the ESC-EHRA EORP-AF General Long-Term Registry, we analysed clinically complex AF patients, defined as the presence of frailty, multimorbidity and/or polypharmacy. A K-medoids cluster analysis was performed to identify different groups of clinical complexity. The impact of an ABC-adherent approach on major outcomes was analysed through Cox-regression analyses and delay of event (DoE) analyses. RESULTS: Among 9966 AF patients included, 8289 (83.1%) were clinically complex. Adherence to the ABC pathway in the clinically complex group reduced the risk of all-cause death (adjusted HR [aHR]: 0.72, 95%CI 0.58-0.91), major adverse cardiovascular events (MACEs; aHR: 0.68, 95%CI 0.52-0.87) and composite outcome (aHR: 0.70, 95%CI: 0.58-0.85). Adherence to the ABC pathway was associated with a significant reduction in the risk of death (aHR: 0.74, 95%CI 0.56-0.98) and composite outcome (aHR: 0.76, 95%CI 0.60-0.96) also in the high-complexity cluster; similar trends were observed for MACEs. In DoE analyses, an ABC-adherent approach resulted in significant gains in event-free survival for all the outcomes investigated in clinically complex patients. Based on absolute risk reduction at 1 year of follow-up, the number needed to treat for ABC pathway adherence was 24 for all-cause death, 31 for MACEs and 20 for the composite outcome. CONCLUSIONS: An ABC-adherent approach reduces the risk of major outcomes in clinically complex AF patients. Ensuring adherence to the ABC pathway is essential to improve clinical outcomes among clinically complex AF patients.
dc.language.iso eng
dc.publisher BMC
dc.rights http://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.rights.uri Atribución-NoComercial-SinDerivadas 3.0 España *
dc.subject.mesh Anticoagulants/therapeutic use
dc.subject.mesh Atrial Fibrillation/drug therapy/epidemiology
dc.subject.mesh Humans
dc.subject.mesh Registries
dc.subject.mesh Risk Factors
dc.subject.mesh Stroke/complications
dc.title Clinical complexity and impact of the ABC (Atrial fibrillation Better Care) pathway in patients with atrial fibrillation: a report from the ESC-EHRA EURObservational Research Programme in AF General Long-Term Registry
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 36056426
dc.relation.publisherversion https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-022-02526-7
dc.identifier.doi 10.1186/s12916-022-02526-7
dc.journal.title Bmc Medicine


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