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首页> 外文期刊>The American heart journal >Atorvastatin prevents atrial fibrillation in patients with bradyarrhythmias and implantation of an atrial-based or dual-chamber pacemaker: a prospective randomized trial.
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Atorvastatin prevents atrial fibrillation in patients with bradyarrhythmias and implantation of an atrial-based or dual-chamber pacemaker: a prospective randomized trial.

机译:阿托伐他汀预防患有心律失常的患者发生房颤,并植入基于心房或双室起搏器的前瞻性随机试验。

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摘要

BACKGROUND: Increasing evidence suggests that atrial fibrillation (AF) is an inflammatory disease. Statins is an anti-inflammatory agent. The present study was conducted to test the efficacy of atorvastatin in preventing paroxysmal AF or atrial high rate episodes (AHEs) in patients with bradyarrhythmias and implantation of an atrial-based or dual-chamber pacemaker. METHODS: The effect of atorvastatin on time to the first attack of AF or AHE (> or =180 per minute and > or =1 or 10 minutes), which was accurately detected by pacemaker interrogation, was evaluated in an open-label prospective randomized design for 1 year of follow-up. RESULTS: Fifty-two patients (23 males, 70 +/- 13 years old) were randomized to the statin group (atorvastatin 20 mg/d) and 54 (25 males, 72 +/- 13 years old) to the nonstatin group. Event-free survivals from AHE > or =1 minute were not significantly different between the 2 groups (log-rank P = .410). However, patients in the nonstatin group were more likely to develop AHE > or =10 minutes than those in the statin group (log-rank P = .028). Atrial high rate episode > or =10 minutes occurred in 3 (5.8%) of 51 patients in the statin group after 1 year of follow-up, and 10 (19.2%) of 52 patients (odds ratio 0.26, P = .041) in the nonstatin group. The mean left atrial volume of the statin group was significantly lower than that of the nonstatin group at the end of follow-up (39.7 +/- 1.7 vs 43.7 +/- 1.9 mL, P < .0001). CONCLUSIONS: The present study demonstrated the efficacy of atorvastatin in preventing significant AF (> or =10 minutes) and left atrial enlargement in patients with bradyarrhythmias and implantation of a pacemaker.
机译:背景:越来越多的证据表明,房颤(AF)是一种炎症性疾病。他汀类药物是一种抗炎药。进行本研究以测试阿托伐他汀在预防心律失常患者阵发性房颤或房颤高发生率(AHE)以及植入基于心房或双腔起搏器的功效。方法:在开放标签的前瞻性随机研究中评估了阿托伐他汀对AF或AHE首次发作的时间(>或= 180每分钟和>或= 1或10分钟)的影响,通过起搏器询问可以准确地检测出这种影响。设计为期一年的随访。结果:52例患者(23名男性,70 +/- 13岁)被随机分配到他汀类药物组(阿托伐他汀20 mg / d),54例患者(25名男性,72 +/- 13岁)进入非他汀类药物组。两组之间AHE>或= 1分钟的无事件生存率无显着差异(log-rank P = .410)。但是,非他汀类药物组的患者发生AHE≥10分钟的可能性大于他汀类药物组(对数秩P = .028)。随访一年后,他汀类组51例患者中有3例(5.8%)发生了≥10分钟的心房高发生率,52例患者中有10例(19.2%)发生了房颤(赔率0.26,P = .041)在非他汀类药物组中。在随访结束时,他汀类药物组的平均左心房容积显着低于非他汀类药物组(39.7 +/- 1.7 vs 43.7 +/- 1.9 mL,P <.0001)。结论:本研究证明了阿托伐他汀在预防缓慢性心律失常和植入起搏器患者中显着预防房颤(≥10分钟)和左房扩大的功效。

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