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Article: Adverse Events and Clinical Correlates in Asian Patients with Atrial Fibrillation and Diabetes Mellitus: A Report from Asia Pacific Heart Rhythm Society Atrial Fibrillation Registry

TitleAdverse Events and Clinical Correlates in Asian Patients with Atrial Fibrillation and Diabetes Mellitus: A Report from Asia Pacific Heart Rhythm Society Atrial Fibrillation Registry
Authors
KeywordsAsians
atrial fibrillation
cardiovascular events
diabetes
major bleedings
Issue Date1-Mar-2024
PublisherMDPI
Citation
Journal of Clinical Medicine, 2024, v. 13, n. 5 How to Cite?
Abstract

Aims. To evaluate the adverse events (and its clinical correlates) in a large prospective cohort of Asian patients with atrial fibrillation (AF) and diabetes mellitus (DM). Material and Methods. We recruited patients with atrial fibrillation (AF) from the Asia-Pacific Heart Rhythm Society (APHRS) AF Registry and included those for whom the diabetic mellitus (DM) status was known. We used Cox-regression analysis to assess the 1-year risk of all-cause death, thromboembolic events, acute coronary syndrome, heart failure and major bleeding. Results. Of 4058 patients (mean age 68.5 ± 11.8 years; 34.4% females) considered for this analysis, 999 (24.6%) had DM (age 71 ± 11 years, 36.4% females). Patients with DM had higher mean CHA2DS2-VASc (2.3 ± 1.6 vs. 4.0 ± 1.5, p < 0.001) and HAS-BLED (1.3 ± 1.0 vs. 1.7 ± 1.1, p < 0.001) risk scores and were less treated with rhythm control strategies compared to patients without DM (18.7% vs. 22.0%). After 1-year of follow-up, patients with DM had higher incidence of all-cause death (4.9% vs. 2.3%, p < 0.001), cardiovascular death (1.3% vs. 0.4%, p = 0.003), and major bleeding (1.8% vs. 0.9%, p = 0.002) compared to those without DM. On Cox regression analysis, adjusted for age, sex, heart failure, coronary and peripheral artery diseases and previous thromboembolic event, DM was independently associated with a higher risk of all-cause death (HR 1.48, 95% CI 1.00–2.19), cardiovascular death (HR 2.33, 95% CI 1.01–5.40), and major bleeding (HR 1.91, 95% 1.01–3.60). On interaction analysis, the impact of DM in determining the risk of all-cause death was greater in young than in older patients (p int = 0.010). Conclusions. Given the high rates of adverse outcomes in these Asian AF patients with DM, efforts to optimize the management approach of these high-risk patients in a holistic or integrated care approach are needed.


Persistent Identifierhttp://hdl.handle.net/10722/348447
ISSN
2023 Impact Factor: 3.0
2023 SCImago Journal Rankings: 0.882
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorBucci, Tommaso-
dc.contributor.authorNabrdalik, Katarzyna-
dc.contributor.authorShantsila, Alena-
dc.contributor.authorRomiti, Giulio Francesco-
dc.contributor.authorTeo, Wee-Siong-
dc.contributor.authorPark, Hyung-Wook-
dc.contributor.authorShimizu, Wataru-
dc.contributor.authorTse, Hung-Fat-
dc.contributor.authorProietti, Marco-
dc.contributor.authorChao, Tze-Fan-
dc.contributor.authorLip, Gregory Y H-
dc.contributor.authorAsia-Pacific Heart Rhythm Society Atrial Fibrillation Registry Investigators-
dc.date.accessioned2024-10-09T00:31:33Z-
dc.date.available2024-10-09T00:31:33Z-
dc.date.issued2024-03-01-
dc.identifier.citationJournal of Clinical Medicine, 2024, v. 13, n. 5-
dc.identifier.issn2077-0383-
dc.identifier.urihttp://hdl.handle.net/10722/348447-
dc.description.abstract<p><strong>Aims.</strong> To evaluate the adverse events (and its clinical correlates) in a large prospective cohort of Asian patients with atrial fibrillation (AF) and diabetes mellitus (DM). <strong>Material and Methods.</strong> We recruited patients with atrial fibrillation (AF) from the Asia-Pacific Heart Rhythm Society (APHRS) AF Registry and included those for whom the diabetic mellitus (DM) status was known. We used Cox-regression analysis to assess the 1-year risk of all-cause death, thromboembolic events, acute coronary syndrome, heart failure and major bleeding. <strong>Results.</strong> Of 4058 patients (mean age 68.5 ± 11.8 years; 34.4% females) considered for this analysis, 999 (24.6%) had DM (age 71 ± 11 years, 36.4% females). Patients with DM had higher mean CHA<sub>2</sub>DS<sub>2</sub>-VASc (2.3 ± 1.6 vs. 4.0 ± 1.5, p < 0.001) and HAS-BLED (1.3 ± 1.0 vs. 1.7 ± 1.1, p < 0.001) risk scores and were less treated with rhythm control strategies compared to patients without DM (18.7% vs. 22.0%). After 1-year of follow-up, patients with DM had higher incidence of all-cause death (4.9% vs. 2.3%, p < 0.001), cardiovascular death (1.3% vs. 0.4%, p = 0.003), and major bleeding (1.8% vs. 0.9%, p = 0.002) compared to those without DM. On Cox regression analysis, adjusted for age, sex, heart failure, coronary and peripheral artery diseases and previous thromboembolic event, DM was independently associated with a higher risk of all-cause death (HR 1.48, 95% CI 1.00–2.19), cardiovascular death (HR 2.33, 95% CI 1.01–5.40), and major bleeding (HR 1.91, 95% 1.01–3.60). On interaction analysis, the impact of DM in determining the risk of all-cause death was greater in young than in older patients (p int = 0.010). <strong>Conclusions.</strong> Given the high rates of adverse outcomes in these Asian AF patients with DM, efforts to optimize the management approach of these high-risk patients in a holistic or integrated care approach are needed.<br></p>-
dc.languageeng-
dc.publisherMDPI-
dc.relation.ispartofJournal of Clinical Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAsians-
dc.subjectatrial fibrillation-
dc.subjectcardiovascular events-
dc.subjectdiabetes-
dc.subjectmajor bleedings-
dc.titleAdverse Events and Clinical Correlates in Asian Patients with Atrial Fibrillation and Diabetes Mellitus: A Report from Asia Pacific Heart Rhythm Society Atrial Fibrillation Registry-
dc.typeArticle-
dc.identifier.doi10.3390/jcm13051274-
dc.identifier.scopuseid_2-s2.0-85187444521-
dc.identifier.volume13-
dc.identifier.issue5-
dc.identifier.eissn2077-0383-
dc.identifier.isiWOS:001183361700001-
dc.identifier.issnl2077-0383-

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