Fauchier J P, Rouesnel P, Breuillac J C, Cosnay P, Scheck F, Garnier L F
Service de Cardiologie B, CHU Trousseau, Tours.
Ann Cardiol Angeiol (Paris). 1994 Apr;43(4):194-203.
Cibenzoline, a Vaughan-Williams Class I antiarrhythmic agent, was studied in 26 patients with orthodromic supraventricular tachycardia (SVT) by nodal reentry (n = 10) or an accessory pathway (AP) (n = 16). IV cibenzoline accelerated sinus rhythm, prolonged PR, AH, HV and QT, widened QRS and depressed or blocked anterograde and retrograde conduction in the accessory pathway, significantly, without significantly modifying conduction capacity in the AV node, nor atrial, nodal or ventricular refractory periods. It converted 6/10 of nodal reentries and 9/16 of reentries due to an AP, by a mean dose of 1 mg/kg, in 2 to 3 minutes, in 12 cases out of 16 by blocking retrograde conduction in the reentry circuit. It prevented reinduction of 12 of the 26 cases of SVT, significantly slowing the cycle of induced SVT in other patients. Oral cibenzoline (260 to 390 mg/day) prevented induced SVT in 11 cases out of 25 and spontaneous SVT in 14 cases out of 26, with a follow-up of 11 +/- 4 months (6 to 16), and this regardless of the reentry mechanisms. Intravenous cibenzoline was not associated with any clinical or hemodynamic intolerance but there was facilitation of episodes of SVT in one patient. Oral administration caused only one case of digestive intolerance, leading to lowering of the dose. Plasma levels showed no significant differences between successes and failures, for both the injection and oral formulations of cibenzoline, whether in terms of the conversion or prevention of episodes. Electrophysiological investigations had a 60% positive and 50% negative predictive value, a sensitivity of 64% and a specificity of 50%. Cibenzoline thus appears to be useful for the conversion and prevention of episodes, SVT, regardless of the reentry circuit, and seems justified, in view of its good safety/acceptability, as first line treatment in this diagnostic indication, measurement of plasma levels and electrophysiological investigations being of little apparent value in terms of guiding treatment and predicting its results.
昔苯唑啉是一种Ⅰ类抗心律失常药( Vaughan-Williams分类法),我们对26例通过房室结折返(n = 10)或旁路(AP)(n = 16)引起的顺向型室上性心动过速(SVT)患者进行了研究。静脉注射昔苯唑啉可使窦性心律加速,PR、AH、HV和QT间期延长,QRS波增宽,旁路的前向和逆向传导明显受抑制或阻滞,而对房室结的传导能力以及心房、房室结或心室的不应期无明显影响。平均剂量1mg/kg的昔苯唑啉可在2至3分钟内转复10例房室结折返性心动过速中的6例以及16例旁路介导的折返性心动过速中的9例,16例中有12例是通过阻断折返环路中的逆向传导实现转复的。它预防了26例SVT患者中12例的再次诱发,使其他患者诱发的SVT周期显著延长。口服昔苯唑啉(260至390mg/天)预防了25例患者中11例的诱发SVT以及26例患者中14例的自发性SVT,随访时间为11±4个月(6至16个月),且与折返机制无关。静脉注射昔苯唑啉未出现任何临床或血流动力学不耐受情况,但有1例患者的SVT发作增多。口服给药仅导致1例消化不耐受,需减少剂量。无论是注射剂型还是口服剂型的昔苯唑啉,在转复或预防发作方面,成功组和失败组的血浆水平均无显著差异。电生理检查的阳性预测值为60%,阴性预测值为50%,敏感性为64%,特异性为50%。因此,昔苯唑啉似乎对转复和预防SVT发作有效,无论折返环路如何,鉴于其良好的安全性/可接受性,作为该诊断指征的一线治疗似乎是合理的,血浆水平测定和电生理检查在指导治疗和预测结果方面似乎价值不大。