Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис: http://hdl.handle.net/20.500.12188/27251
DC FieldValueLanguage
dc.contributor.authorSimovic, Sen_US
dc.contributor.authorTaleski Jen_US
dc.contributor.authorTodorovic, Zen_US
dc.contributor.authorKircanski, Ben_US
dc.date.accessioned2023-07-31T07:05:57Z-
dc.date.available2023-07-31T07:05:57Z-
dc.date.issued2023-05-24-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/27251-
dc.description.abstract<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Funding Acknowledgements</jats:title> <jats:p>Type of funding sources: None.</jats:p> </jats:sec> <jats:sec> <jats:title>Background</jats:title> <jats:p>Atrial High Rates Episodes (AHRE) are associated with progression to clinical atrial fibrillation (AF), stroke, increased risk of MACE and increased mortality (1-4). Although oral anticoagulation should be initiated in patients with CHADs-VASc score ≥ 2 and episode duration ≥ 24h, treatment of AHRE with antiarrhythmics was not investigated so far.</jats:p> </jats:sec> <jats:sec> <jats:title>Purpose</jats:title> <jats:p>This study aimed to assess the effects of antiarrhythmic treatment on AHRE and its impact on the progression to clinical AF and AHRE burden.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>This study included patients with AHRE duration ≥ 24h detected by dual-chamber pacemakers, without a previous diagnosis of AF and treatment with antiarrhythmics. Nominal settings with high atrial rate criterion programmed to 200 beats/min were used for AHRE detection. Patients were randomized to the Intervention (n=169) and Control Group (n=138). Patients in the Intervention Group received antiarrhythmic treatment (Ic antiarrhythmics (n=54), beta-blockers (n=58) and amiodarone (n=57)). The primary endpoint was progression to clinical AF and the secondary endpoint was AHRE burden.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>A total of 307 were included in the study, with a mean age of 71.4±8.15, 166 (54.07%) females and a mean follow-up 20.84±5.04 months. The baseline characteristics did not differ significantly between groups. During the follow-up, 50 patients (36.23%) from the Control group developed clinical AF. In groups of patients treated with Ic antiarrhythmics, beta-blockers and amiodarone, clinical AF developed in 11 (20.37%), 25 (25.86%) and 5 (8.77%) patients, respectively (p&lt;0.001). Average time to clinical AF progression was significantly longer in groups of patients treated with antiarrhythmics (Ic antiarrhythmics, beta-blockers and amiodarone) compared to the Control group (17.7, 17.2, 19.0 vs 15.9 months, respectively, p&lt;0.001). The Kaplan-Meier plot of freedom from clinical AF is given in Figure 1. Amiodarone prolonged the time to clinical AF progression significantly compared to beta-blockers (p=0.017), while a trend was observed compared to Ic antiarrhythmics (p=0.057). No significant differences between Ic antiarrhythmics and beta-blockers were observed in time to clinical AF progression (p=0.567). The AHRE burden was significantly lower in the Intervention group compared to the Control group (6.9% vs 15.4%, p&lt;0.001). Amiodarone was superior in lowering the AHRE burden when compared to Ic antiarrhythmics and beta-blockers (2.1% vs 5.6% and 7.8%, respectively, p&lt;0.001), while no significant differences were observed between Ic antiarrhythmics and beta-blockers (p=0.18)</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Initiating antiarrhythmics for AHRE episodes leads to a lower AHRE burden and progression to clinical AF. Randomized clinical trials are needed to investigate further the early antiarrhythmic treatment of AHRE without clinical AF.</jats:p> </jats:sec>en_US
dc.language.isoenen_US
dc.publisherOxford University Press (OUP)en_US
dc.relation.ispartofEuropaceen_US
dc.titleEffects of antiarrhythmics on atrial high rate episodes and progression to clinical atrial fibrillation (ANTI-AHRE)en_US
dc.typeArticleen_US
dc.identifier.doi10.1093/europace/euad122.066-
dc.identifier.urlhttps://academic.oup.com/europace/article-pdf/25/Supplement_1/euad122.066/50427957/euad122.066.pdf-
dc.identifier.urlhttps://academic.oup.com/europace/article-pdf/25/Supplement_1/euad122.066/50427957/euad122.066.pdf-
dc.identifier.volume25-
dc.identifier.issueSupplement_1-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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