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首页> 外文期刊>BMC Cardiovascular Disorders >Incidence of Atrial Fibrillation in Patients with either Heart Failure or Acute Myocardial Infarction and Left Ventricular Dysfunction: A Cohort Study
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Incidence of Atrial Fibrillation in Patients with either Heart Failure or Acute Myocardial Infarction and Left Ventricular Dysfunction: A Cohort Study

机译:心力衰竭或急性心肌梗死合并左心室功能不全患者房颤发生率的一项队列研究

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Background We examined the incidence of new-onset atrial fibrillation in patients with left ventricular dysfunction. Patients either had a recent myocardial infarction (with or without clinical heart failure) or symptomatic heart failure (without a recent MI). Patients were with and without treatment with the class III antiarrhythmic drug dofetilide over 36 months. Methods The Danish Investigations of Arrhythmia and Mortality ON Dofetilide (DIAMOND) studies included 2627 patients without atrial fibrillation at baseline, who were randomised to treatment with either dofetilide or placebo. Results The competing risk analyses estimated the cumulative incidences of atrial fibrillation during the 42 months of follow-up to be 9.6% in the placebo-treated heart failure-group, and 2.9% in the placebo-treated myocardial infarction-group. Cox proportional hazard regression found a 42% significant reduction in the incidence of new-onset AF when assigned to dofetilide compared to placebo (hazard ratio 0.58, 95% confidence interval 0.40-0.82) and there was no interaction with study (p = 0.89). In the heart failure-group, the incidence of atrial fibrillation was significantly reduced to 5.6% in the dofetilide-treated patients (hazard ratio 0.57, 95% confidence interval 0.38-0.86). In the myocardial infarction-group the incidence of atrial fibrillation was reduced to 1.7% with the administration of dofetilide. This reduction was however not significant (hazard ratio 0.61, 95% confidence interval 0.30-1.24). Conclusion In patients with left ventricular dysfunction the incidence of AF in 42 months was 9.6% in patients with heart failure and 2.9% in patients with a recent MI. Dofetilide significantly reduced the risk of developing atrial fibrillation compared to placebo in the entire study group and in the subgroup of patients with heart failure. The reduction in the subgroup with recent MI was not statistically significant, but the hazard ratio was similar to the hazard ratio for the heart failure patients, and there was no difference between the effect in the two studies (p = 0.89 for interaction).
机译:背景我们检查了左心功能不全患者新发房颤的发生率。患者或者有最近的心肌梗塞(有或没有临床心力衰竭)或有症状的心力衰竭(无近期心梗)。在36个月内,患者接受或不接受III类抗心律不齐药物多非利特的治疗。方法丹麦关于多非利特的心律失常和死亡率调查(DIAMOND)包括2627例基线时无房颤的患者,随机分为多非利特或安慰剂治疗。结果竞争风险分析估计,在42个月的随访中,以安慰剂治疗的心力衰竭组的心房纤颤累积发生率为9.6%,在以安慰剂治疗的心肌梗塞组的发生率为2.9%。 Cox比例风险回归发现,与安慰剂相比,分配给多非利特的新发房颤发生率显着降低42%(风险比0.58,95%置信区间0.40-0.82),且与研究无交互作用(p = 0.89) 。在心力衰竭组中,多芬利肽治疗的患者的房颤发生率显着降低至5.6%(危险比0.57,95%置信区间0.38-0.86)。在心肌梗死组中,多芬利特的使用使心房颤动的发生率降低至1.7%。但是,这种降低并不明显(危险比0.61,95%置信区间0.30-1.24)。结论在左心功能不全的患者中,心力衰竭患者在42个月内发生AF的发生率为9.6%,而最近发生心梗的患者则为2.9%。与安慰剂相比,在整个研究组和心力衰竭患者亚组中,多非利特显着降低了发生房颤的风险。最近发生心肌梗死的亚组减少量无统计学意义,但危险比与心力衰竭患者的危险比相似,两项研究之间的影响无差异(相互作用p = 0.89)。

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