Alpert J S, Benotti J R, Brady P M, McCue J E, Weiner B H, Ockene I S
Am J Cardiol. 1985 Mar 15;55(7):20C-24C. doi: 10.1016/0002-9149(85)90801-x.
Calcium-channel blockers are known to have depressant effects on atrioventricular (AV) nodal conduction and myocardial contractility. Because of these known depressant effects, bepridil hydrochloride, a new, long-acting, antianginal and antiarrhythmic calcium-channel blocker, was administered intravenously to patients without heart failure to determine acute hemodynamic effects. The patients studied had normal ventricular function, were without electrocardiographic conduction disturbances and were taking no drug except sublingual nitroglycerin for at least 24 hours before bepridil infusion. The study protocol included right- and left-sided cardiac catheterization with infusion of bepridil at 2 mg/kg for 15 minutes followed by 1 mg/kg for 15 minutes in 10 patients, and infusion of bepridil at 3 mg/kg for 15 minutes followed by 1 mg/kg for 15 minutes in 8 patients. Pressures, Fick cardiac output, resistances, left ventricular (LV) dP/dt, LV stroke work index and rate-pressure product of the left ventricle were monitored. There were no significant changes during bepridil infusion at either dose for cardiac output, systemic vascular and pulmonary vascular resistances, LV stroke work index, heart rate, arterial blood pressure and rate-pressure product. There was mild depression of LV dP/dt during bepridil infusion. Further, LV end-diastolic pressure, pulmonary capillary wedge pressure and pulmonary arterial pressures were significantly increased during bepridil infusion. There were no apparent changes in AV nodal or intraventricular conduction during bepridil infusion. We conclude that bepridil appears to be a safe drug for intravenous administration despite mild depression of myocardial function in patients with normal baseline hemodynamic function who are not receiving concomitant beta-blocker therapy.
已知钙通道阻滞剂对房室(AV)结传导和心肌收缩力有抑制作用。由于这些已知的抑制作用,将一种新型长效抗心绞痛和抗心律失常钙通道阻滞剂盐酸苄普地尔静脉注射给无心力衰竭的患者,以确定其急性血流动力学效应。所研究的患者心室功能正常,无心电图传导障碍,且在输注苄普地尔前至少24小时除舌下含服硝酸甘油外未服用其他药物。研究方案包括对10例患者进行左右心导管检查,先以2mg/kg的剂量输注苄普地尔15分钟,然后以1mg/kg的剂量输注15分钟;对8例患者先以3mg/kg的剂量输注苄普地尔15分钟,然后以1mg/kg的剂量输注15分钟。监测压力、Fick心输出量、阻力、左心室(LV)dP/dt、左心室每搏功指数和左心室率压乘积。在输注苄普地尔期间,两种剂量下的心输出量、体循环血管和肺循环血管阻力、左心室每搏功指数、心率、动脉血压和率压乘积均无显著变化。在输注苄普地尔期间左心室dP/dt有轻度降低。此外,在输注苄普地尔期间左心室舒张末期压力、肺毛细血管楔压和肺动脉压力显著升高。在输注苄普地尔期间房室结或心室内传导无明显变化。我们得出结论,对于基线血流动力学功能正常且未接受β受体阻滞剂治疗的患者,尽管苄普地尔会轻度抑制心肌功能,但它似乎是一种安全的静脉给药药物。