Perera Kanjana S, Pearce Lesly A, Sharma Mukul, Benavente Oscar, Connolly Stuart J, Hart Robert G
Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
Minot, North Dakota.
Am J Cardiol. 2018 Mar 1;121(5):584-589. doi: 10.1016/j.amjcard.2017.11.028. Epub 2017 Dec 11.
The mortality rate of most patients with atrial fibrillation (AF) exceeds the stroke rate, but predictors of mortality have not been well defined. The Atrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events (ACTIVE A) recruited patients with AF who were unsuitable to receive vitamin K-antagonists and were randomized to aspirin alone versus aspirin plus clopidogrel. We investigated independent predictors of all-cause mortality by multivariable Cox regression analysis and explored interactions with assigned antiplatelet therapy. Of the 7,554 patients enrolled with a mean age of 71 years, 1,687 (22%) patients died during the median follow-up of 3.7 years (annualized mortality rate 6.4%/year). Assignment to dual antiplatelet therapy had no effect on mortality (hazard ratio [HR] 0.99, 95% confidence interval [CI] 0.90 to 1.1) or on vascular and nonvascular death. Independent predictors of all-cause mortality were advancing age, lower body mass index (HR 1.4 < 25 kg/m, 95% CI 1.3 to 1.6), diabetes mellitus, Latin American ethnicity (HR 1.4, 95% CI 1.1 to 1.6), previous stroke or transient ischemic attack, peripheral artery disease, increased resting heart rate (HR 1.3, 95% CI 1.1 to 1.4 per 30 bpm), lower diastolic blood pressure, coronary artery disease, heart failure, left ventricular systolic dysfunction, hemoglobin level of <13 mg/dl, and reduced estimated glomerular filtration rate. In conclusion, in this large clinical trial cohort of patients with AF, treatment with clopidogrel plus aspirin versus aspirin monotherapy did not affect all-cause mortality, vascular death, or nonvascular death. Novel independent predictors of increased mortality included lower diastolic blood pressure and Latin American ethnicity.
大多数心房颤动(AF)患者的死亡率超过了卒中发生率,但死亡率的预测因素尚未明确界定。心房颤动氯吡格雷与厄贝沙坦预防血管事件试验(ACTIVE A)招募了不适于接受维生素K拮抗剂治疗的AF患者,并将其随机分为单独使用阿司匹林组与阿司匹林加氯吡格雷组。我们通过多变量Cox回归分析研究了全因死亡率的独立预测因素,并探讨了与指定抗血小板治疗的相互作用。在平均年龄为71岁的7554例入组患者中,1,687例(22%)患者在3.7年的中位随访期内死亡(年化死亡率6.4%/年)。接受双联抗血小板治疗对死亡率(风险比[HR]0.99,95%置信区间[CI]0.90至1.1)或血管性和非血管性死亡均无影响。全因死亡率的独立预测因素包括年龄增长、较低的体重指数(HR 1.4,<25 kg/m²,95% CI 1.3至1.6)、糖尿病、拉丁裔种族(HR 1.4,95% CI 1.1至1.6)、既往卒中或短暂性脑缺血发作、外周动脉疾病、静息心率增加(每30次心跳HR 1.3,95% CI 1.1至1.4)、较低的舒张压、冠状动脉疾病、心力衰竭、左心室收缩功能障碍、血红蛋白水平<13 mg/dl以及估算肾小球滤过率降低。总之,在这个大型AF患者临床试验队列中,氯吡格雷加阿司匹林治疗与单药阿司匹林治疗相比,对全因死亡率、血管性死亡或非血管性死亡均无影响。死亡率增加的新的独立预测因素包括较低的舒张压和拉丁裔种族。