The impact of atrial fibrillation and long-term oral anticoagulant use on all-cause and cardiovascular mortality: A 12-year evaluation of the prospective Brazilian Study of Stroke Mortality and Morbidity

被引:16
|
作者
Goulart, Alessandra C. [1 ,3 ]
Olmos, Rodrigo Diaz [1 ,3 ]
Santos, Itamar S. [1 ,3 ]
Tunes, Gisela [2 ]
Alencar, Airlane P. [2 ]
Thomas, Neil [4 ]
Lip, Gregory Y. H. [5 ,6 ,7 ]
Lotufo, Paulo A. [1 ,3 ]
Bensenor, Isabela M. [1 ,3 ]
机构
[1] Univ Sao Paulo, Hosp Univ, Ctr Clin & Epidemiol Res, Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Math & Stat, Sao Paulo, Brazil
[3] Univ Sao Paulo, Sch Med, Sao Paulo, Brazil
[4] Univ Birmingham, Inst Appl Hlth Res, Birmingham, W Midlands, England
[5] Univ Liverpool, Liverpool Ctr Cardiovasc Sci, Liverpool, Merseyside, England
[6] Liverpool Heart & Chest Hosp, Liverpool, Merseyside, England
[7] Aalborg Univ, Dept Clin Med, Aalborg Thrombosis Res Unit, Aalborg, Denmark
基金
巴西圣保罗研究基金会; 瑞典研究理事会;
关键词
Stroke epidemiology; stroke in developing countries; stroke prevention; IMMORTAL TIME BIAS; ISCHEMIC-STROKE; CUMULATIVE INCIDENCE; RISK; SURVIVAL; THERAPY; COHORT;
D O I
10.1177/1747493021995592
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Atrial fibrillation is a predictor of poor prognosis after stroke. Aims To evaluate atrial fibrillation and all-cause and cardiovascular mortality in a stroke cohort with low socioeconomic status, taking into consideration oral anticoagulant use during 12-year follow-up. Methods All-cause mortality was analyzed by Kaplan-Meier survival curve and Cox regression models to estimate hazard ratios and 95% confidence intervals (95% CI). For specific mortality causes, cumulative incidence functions were computed. A logit link function was used to calculate odds ratios (OR) with 95% CIs. Full models were adjusted by age, sex, oral anticoagulant use (as a time-dependent variable) and cardiovascular risk factors. Results Of 1121 ischemic stroke participants, 17.8% had atrial fibrillation. Overall, 654 deaths (58.3%) were observed. Survival rate was lower (median days, interquartile range-IQR) among those with atrial fibrillation (531, IQR: 46-2039) vs. non-atrial fibrillation (1808, IQR: 334-3301), p-log rank < 0.0001). Over 12-year follow-up, previous atrial fibrillation was associated with increased mortality: all-cause (multivariable hazard ratios, 1.82; 95% CI: 1.43-2.31) and cardiovascular mortality (multivariable OR, 2.07; 95% CI: 1.36-3.14), but not stroke mortality. In the same multivariable models, oral anticoagulant use was inversely associated with all-cause mortality (oral anticoagulant time-dependent effect: multivariable hazard ratios, 0.47; 95% CI: 0.30-0.50, p = 0.002) and stroke mortality (oral anticoagulant time-dependent effect >= 6 months: multivariable OR, 0.09; 95% CI: 0.01-0.65, p-value = 0.02), but not cardiovascular mortality. Conclusions Among individuals with low socioeconomic status, atrial fibrillation was an independent predictor of poor survival, increasing all-cause and cardiovascular mortality risk. Long-term oral anticoagulant use was associated with a markedly reduced risk of all-cause and stroke mortality.
引用
收藏
页码:48 / 58
页数:11
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