Pokorney Sean D, Piccini Jonathan P, Stevens Susanna R, Patel Manesh R, Pieper Karen S, Halperin Jonathan L, Breithardt Günter, Singer Daniel E, Hankey Graeme J, Hacke Werner, Becker Richard C, Berkowitz Scott D, Nessel Christopher C, Mahaffey Kenneth W, Fox Keith A A, Califf Robert M
Duke Clinical Research Institute, Duke University Medical Center, Durham, NC
Duke Clinical Research Institute, Duke University Medical Center, Durham, NC.
J Am Heart Assoc. 2016 Mar 8;5(3):e002197. doi: 10.1161/JAHA.115.002197.
Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions.
In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intention-to-treat population. The median age was 73 years, and the mean CHADS2 score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P<0.0001) and age ≥75 years (hazard ratio 1.69, 95% CI 1.51-1.90, P<0.0001) were associated with higher all-cause mortality. Multiple additional characteristics were independently associated with higher mortality, with decreasing creatinine clearance, chronic obstructive pulmonary disease, male sex, peripheral vascular disease, and diabetes being among the most strongly associated (model C-index 0.677).
In a large population of patients anticoagulated for nonvalvular atrial fibrillation, ≈7 in 10 deaths were cardiovascular, whereas <1 in 10 deaths were caused by nonhemorrhagic stroke or systemic embolism. Optimal prevention and treatment of heart failure, renal impairment, chronic obstructive pulmonary disease, and diabetes may improve survival.
URL: https://www.clinicaltrials.gov/. Unique identifier: NCT00403767.
心房颤动与较高的死亡率相关。确定死亡原因及全因死亡率的当代危险因素可能有助于指导干预措施。
在利伐沙班每日一次口服直接抑制Xa因子与维生素K拮抗剂预防心房颤动患者中风和栓塞的试验(ROCKET AF)中,非瓣膜性心房颤动患者被随机分为利伐沙班组或剂量调整的华法林组。采用逐步回归的Cox比例风险回归分析确定了意向性治疗人群中14171名参与者在随机分组时与全因死亡率独立相关的因素。中位年龄为73岁,平均CHADS2评分为3.5。在中位随访1.9年期间,1214名(8.6%)患者死亡。Kaplan-Meier法计算的1年死亡率为4.2%,2年死亡率为8.9%。大多数分类死亡(1081例)为心血管原因(72%),而非出血性中风或全身性栓塞仅占6%。利伐沙班组和华法林组之间未观察到全因死亡率的显著差异(P = 0.15)。心力衰竭(风险比1.51,95%置信区间1.33 - 1.70,P < 0.0001)和年龄≥75岁(风险比1.69,95%置信区间1.51 - 1.90,P < 0.0001)与较高的全因死亡率相关。多个其他特征也与较高死亡率独立相关,肌酐清除率降低、慢性阻塞性肺疾病、男性、外周血管疾病和糖尿病是相关性最强的因素(模型C指数为0.677)。
在大量接受抗凝治疗的非瓣膜性心房颤动患者中,约十分之七的死亡为心血管原因,而十分之一以下的死亡由非出血性中风或全身性栓塞引起。对心力衰竭、肾功能损害、慢性阻塞性肺疾病和糖尿病进行最佳预防和治疗可能会提高生存率。