Serruys P W, Vanhaleweyk G, Van Den Brand M, Verdouw P, Lubsen J, Hugenholtz P G
Br J Clin Pharmacol. 1983 Jul;16(1):51-9. doi: 10.1111/j.1365-2125.1983.tb02143.x.
Flecainide acetate has been shown to be a potent antiarrhythmic agent which is active for more than 8 h, whether given intravenously or orally. However, the negative inotropic effect demonstrated in animal studies could hamper the potential clinical utility of the drug. Ten patients with coronary artery disease but without cardiac failure were given intravenous flecainide (2 mg/kg). Stroke index (SI), left ventricular systolic pressure (LVP), end diastolic pressure (EDP) and LV contractility indices (max dP/dt, VCE 40 mm Hg, peak VCE, Vmax from total pressure (TP] were measured immediately before and 10 min after flecainide, under resting conditions and during atrial pacing with heart rates up to 133 +/- 4.2 beats/min (mean +/- s.e. mean). It is demonstrated that flecainide has a negative inotropic effect, not only under resting conditions, but also less apparently during pacing-induced tachycardia. The effect appears to be dose-related and may result in a reduction of cardiac performance.
已证明醋酸氟卡尼是一种强效抗心律失常药物,无论静脉给药还是口服给药,其作用时间都超过8小时。然而,动物研究中显示的负性肌力作用可能会妨碍该药物的潜在临床应用。对10例冠心病但无心力衰竭的患者静脉注射氟卡尼(2mg/kg)。在静息状态下以及心房起搏心率高达133±4.2次/分钟(平均值±标准误)时,于注射氟卡尼前及注射后10分钟测量每搏输出量指数(SI)、左心室收缩压(LVP)、舒张末期压力(EDP)和左心室收缩性指数(最大dP/dt、VCE 40mmHg、VCE峰值、总压力(TP)下的Vmax)。结果表明,氟卡尼不仅在静息状态下有负性肌力作用,而且在起搏诱发的心动过速期间作用不太明显。这种作用似乎与剂量相关,可能导致心脏功能降低。