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通过Ⅲ类药物预处理增强电复律并预防血流动力学有害的心房颤动立即复发。

Enhancing electrical cardioversion and preventing immediate reinitiation of hemodynamically deleterious atrial fibrillation with class III drug pretreatment.

作者信息

Hayashi Meiso, Tanaka Keiji, Kato Takao, Morita Norishige, Sato Naoki, Yasutake Masahiro, Kobayashi Yoshinori, Takano Teruo

机构信息

Intensive Care Unit, Nippon Medical School, Tokyo, Japan.

出版信息

J Cardiovasc Electrophysiol. 2005 Jul;16(7):740-7. doi: 10.1046/j.1540-8167.2005.40748.x.

Abstract

UNLABELLED

Nifekalant for shock-resistant atrial fibrillation.

INTRODUCTION

In severely ill patients, the development of atrial fibrillation (AF) may provoke lethal hemodynamic instability requiring immediate electrical defibrillation, which often is unsuccessful. Using the novel potassium channel blocking agent nifekalant, we prospectively assessed the hypothesis that class III antiarrhythmic drugs facilitate electrical cardioversion and suppress the immediate recurrence of hemodynamically deleterious AF.

METHODS AND RESULTS

Among 1896 adults admitted to the intensive care unit for cardiovascular diseases, hemodynamically destabilizing new-onset AF (systolic blood pressure<90 mm Hg) resistant to conventional electrical cardioversion occurred in 27 patients, and of these, 24 patients (70+/-12 years) were enrolled. Twenty-one patients had congestive heart failure and 11 patients had been mechanically ventilated. After three failed transthoracic cardioversions due to failure of conversion to SR (11 patients) or immediate reinitiation (13 patients), nifekalant (0.25+/-0.04 mg/kg) was administered intravenously, and electrical defibrillation was reattempted. In 18 patients (75%), sinus rhythm was restored and maintained after nifekalant infusion (6 patients) or subsequent transthoracic cardioversion (12 patients). Nifekalant administration significantly decreased the heart rate and increased systolic blood pressure during AF (P<0.001), and successful cardioversion rapidly further ameliorated these parameters (P<0.001). Logistic regression analysis showed that atrial defibrillation failure (relative risk [RR] 19.34, P=0.05) and age of >75 years (RR 15.25, P=0.03) were independent predictors of in-hospital death.

CONCLUSION

Nifekalant renders electrical defibrillation and the prevention of the early recurrence of hemodynamically unstable AF more successful without deteriorating hemodynamics, and successful defibrillation is associated with a more favorable patient outcome. Pretreatment with other class III drugs, e.g., ibutilide or dofetilide, would also be efficacious in patients with failed urgent electrical cardioversion.

摘要

未标记

尼非卡兰用于抗休克性心房颤动。

引言

在重症患者中,心房颤动(AF)的发生可能会引发致命的血流动力学不稳定,需要立即进行电除颤,但往往不成功。我们使用新型钾通道阻滞剂尼非卡兰,前瞻性地评估了Ⅲ类抗心律失常药物有助于电复律并抑制血流动力学有害的AF即刻复发这一假设。

方法与结果

在1896名因心血管疾病入住重症监护病房的成年人中,27例患者出现了对传统电复律有抵抗的血流动力学不稳定的新发AF(收缩压<90mmHg),其中24例患者(70±12岁)被纳入研究。21例患者患有充血性心力衰竭,11例患者接受了机械通气。在因未能转复为窦性心律(11例患者)或即刻复发(13例患者)导致三次经胸电复律失败后,静脉注射尼非卡兰(0.25±0.04mg/kg),并再次尝试电除颤。在18例患者(75%)中,输注尼非卡兰后(6例患者)或随后的经胸电复律后(12例患者)恢复并维持了窦性心律。尼非卡兰给药显著降低了AF期间的心率并升高了收缩压(P<0.001),成功复律迅速进一步改善了这些参数(P<0.001)。逻辑回归分析表明,心房除颤失败(相对风险[RR]19.34,P=0.05)和年龄>75岁(RR 15.25,P=0.03)是院内死亡的独立预测因素。

结论

尼非卡兰使电除颤以及预防血流动力学不稳定的AF早期复发更成功,且不会使血流动力学恶化,成功除颤与更有利的患者预后相关。用其他Ⅲ类药物,如伊布利特或多非利特进行预处理,对紧急电复律失败的患者也有效。

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