학술논문

Patterns of anticoagulation and clinical outcomes in atrial fibrillation: insights from a single institution registry.
Document Type
Article
Source
Cardiologia Croatica. Oct2019, Vol. 14 Issue 9/10, p239-239. 1p.
Subject
*ATRIAL fibrillation
*CORONARY disease
*CEREBRAL embolism & thrombosis
Language
ISSN
1848-543X
Abstract
Aim: To investigate clinical outcomes in patients with atrial fibrillation exposed to different types of anticoagulant drugs within a single institution retrospective registry. Patients and Methods: A cohort of 758 consecutive patients with non- valvular atrial fibrillation receiving anticoagulation therapy after first referral to our institution in a period from 2012 to 2018. We analyzed demographic and clinical data, first choice anticoagulation therapy and time of any of the following clinical outcomes: death, thromboembolic event, and major bleeding and performed univariate and multivariate analyses. Results: There were 434 (57%) patients receiving warfarin, and 178 (23%) and 146 (20%) patients receiving dabigatran and AntiXa, respectively. There was a statistically significant trend of increase in frequency of DOAC use over time (P=0.002). Patients anticoagulated with warfarin were significantly older, had lower eGFR and LVEF, had more frequent chronic heart failure, coronary artery disease, permanent atrial fibrillation, higher CHA2DS2VASC and higher HAS-BLED scores than DOAC receiving patients (P<0.05 for all comparisons). Only 11% of patients on warfarin had acceptable recorded time in therapeutic range values. Univariately, there were significantly more events in patients treated with warfarin than with DOACs (p<0,001 for all events). After adjusting for age, eGFR, and EFLV time to death (HR=5.08, 95% CI (2.23-11.61), P<0.001) and time to thromboembolic event (HR=3.38, 95% CI (1.30-11.12), P=0.045) were significantly shorter in warfarin then in DOAC treated patients, whereas time to major bleeding (HR=1.01, 95% CI (0.84-2.55), P=0.110) did not differ significantly. Conclusion: Patients with higher risk received warfarin more frequently, possibly due to reimbursement issues. Patients receiving warfarin experience significantly higher adjusted risks of thrombosis and death, probably reflecting differences in patients' characteristics and predetermined risks for stroke or other cardiovascular events at baseline. Although the use of DOACS increased over time, changes in DOAC availability for all patients should be made to optimize patterns of anticoagulation in atrial fibrillation. [ABSTRACT FROM AUTHOR]