Wyndham C R, Pratt C M, Mann D E, Winkle R A, Somberg J, de Maria A N, Josephson M E
Department of Medicine, Baylor College of Medicine, Houston, Texas.
Am J Cardiol. 1987 Oct 16;60(11):67F-72F. doi: 10.1016/0002-9149(87)90724-7.
Moricizine HCl, an antiarrhythmic phenothiazine drug, was investigated for its efficacy against ventricular tachycardia (VT) in a group of 60 patients from 8 institutions using electrophysiologic testing before and after oral administration. Moricizine HCl significantly prolonged PR, QRS, AH and HV intervals and cycle length for atrioventricular nodal block, but had minimal or no effect on repolarization or cardiac refractory periods. Induction of sustained VT (in 33 patients) and nonsustained VT (in 14 patients) occurred at baseline. During moricizine HCl therapy, sustained VT was induced in 31 patients and nonsustained VT in 7 patients. In individual patients, suppression of VT induction was obtained in 18% of patients with sustained VT and in 27% of patients with nonsustained VT. Cycle length of induced VT was significantly prolonged by moricizine HCl therapy. During prospective follow-up of 37 patients, electrophysiologic study predicted recurrence of nonrecurrence of VT with a sensitivity value of 82% and specificity of 65%.
盐酸莫雷西嗪是一种抗心律失常的吩噻嗪类药物,在来自8个机构的60例患者中,通过口服给药前后的电生理测试研究了其对室性心动过速(VT)的疗效。盐酸莫雷西嗪显著延长了PR、QRS、AH和HV间期以及房室结阻滞的周期长度,但对复极化或心脏不应期影响极小或无影响。在基线时,33例患者发生持续性VT,14例患者发生非持续性VT。在盐酸莫雷西嗪治疗期间,31例患者诱发了持续性VT,7例患者诱发了非持续性VT。在个体患者中,18%的持续性VT患者和27%的非持续性VT患者的VT诱发得到抑制。盐酸莫雷西嗪治疗显著延长了诱发VT的周期长度。在对37例患者的前瞻性随访中,电生理研究预测VT复发或不复发的敏感性值为82%,特异性为65%。