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口服和注射氟卡尼对房室旁道患者的影响

[Effects of oral and injectable flecainide in patients with an accessory atrioventricular pathway].

作者信息

Fauchier J P, Cosnay P, Rouesnel P, Moquet B, Bonnet P, Scala P J, Demeyer J F

出版信息

Arch Mal Coeur Vaiss. 1985 Oct;78 Spec No:81-90.

PMID:3938264
Abstract

Flecainide, a new Vaughan-Williams Class Ic anti-arrhythmic agent, was used in 21 patients with an accessory AV conduction pathway which was apparent in 16 cases (WPW syndrome), latent in 1 case and concealed in 4 cases (block in the anterograde direction). Seventeen patients had spontaneous and inducible arrhythmias; 13 supraventricular tachycardias (SVT) due to orthodromic reentry including the accessory AV pathway and 4 atrial arrhythmias. Intravenous flecainide (2 mg/kg over 5 minute period) terminated the 13 cases of SVT in an average of 3 minutes by depressing then blocking retrograde conduction in the accessory pathway and 3 out of 4 cases of atrial arrhythmias. Conduction in the accessory pathway was blocked in the anterograde direction in 75% of cases and depressed in the rest; it was blocked in the retrograde direction in about half the cases and depressed in the rest. Intravenous flecainide completely prevented the induction or arrhythmias in 13 out of 17 patients (76%). Oral flecainide blocked the accessory pathway in the anterograde direction in 68.7%, and in the retrograde direction in 62% of patients, and prevented arrhythmias during provocative testing in 82% of patients (14 out of 17). With an average follow-up of 20.7 +/- 2.6 months with oral doses adapted to body weight and to the response to IV flecainide only one recurrence of atrial fibrillation was observed, a 100% prevention of spontaneous SVT and 94% prevention of all arrhythmias (16 out of 17 cases). The predictive value for the response to oral therapy of the tests of regularisation of SVT by IV flecainide and of the tests of non-provocation of SVT with oral or IV flecainide was excellent (100%). The cardiac tolerance was very good in these 21 patients (17 of whom had no valvular or myocardial lesion). There were 6 minor cases of general intolerance to oral therapy which were not dose related, only 1 of which required interruption of therapy. Flecainide appears one of the best choices for the treatment of preexcitation syndromes and their related arrhythmias at the present time.

摘要

氟卡尼是一种新型的 Vaughan-Williams Ic 类抗心律失常药物,应用于 21 例伴有房室旁道的患者,其中 16 例旁道明显(预激综合征),1 例旁道隐匿,4 例旁道隐匿(前传阻滞)。17 例患者有自发和可诱发的心律失常;13 例室上性心动过速(SVT)由包括房室旁道的顺向折返引起,4 例房性心律失常。静脉注射氟卡尼(5 分钟内 2mg/kg),通过抑制然后阻断旁道的逆向传导,平均 3 分钟内终止了 13 例 SVT,4 例房性心律失常中的 3 例也被终止。75%的病例旁道前传被阻断,其余病例旁道前传受到抑制;约一半病例旁道逆向传导被阻断,其余病例旁道逆向传导受到抑制。静脉注射氟卡尼使 17 例患者中的 13 例(76%)完全预防了心律失常的诱发。口服氟卡尼使 68.7%的患者旁道前传被阻断,62%的患者旁道逆向传导被阻断,82%的患者(17 例中的 14 例)在激发试验期间预防了心律失常。口服剂量根据体重和静脉注射氟卡尼的反应进行调整,平均随访 20.7±2.6 个月,仅观察到 1 例房颤复发,100%预防了自发 SVT,94%预防了所有心律失常(17 例中的 16 例)。静脉注射氟卡尼使 SVT 规律化试验以及口服或静脉注射氟卡尼不诱发 SVT 试验对口服治疗反应的预测价值极佳(100%)。这 21 例患者(其中 17 例无瓣膜或心肌病变)的心脏耐受性非常好。有 6 例口服治疗的轻度全身不耐受情况,与剂量无关,其中仅 1 例需要中断治疗。目前,氟卡尼似乎是治疗预激综合征及其相关心律失常的最佳选择之一。

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