Tisdale J E, Gheorghiade M
College of Pharmacy and Allied Health Professions, Wayne State University, Detroit, Michigan.
Am J Cardiol. 1992 Jun 4;69(18):34G-47G. doi: 10.1016/0002-9149(92)91253-z.
Although digitalis preparations have been in use for greater than 200 years, it is only within the last 2 decades that the central hemodynamic and neurohumoral effects occurring over several hours following intravenous administration of digoxin have been investigated in patients with congestive heart failure (CHF). Although digoxin has been shown to stimulate myocardial contractility in tissue preparations, its positive inotropic activity does not consistently translate into improvements in hemodynamic measurements in humans. Digoxin given intravenously results in increased cardiac index and decreased heart rate, left ventricular filling pressure, and right atrial pressure, as well as in acute attenuation of neurohumoral abnormalities, in patients with chronic CHF who have abnormal baseline hemodynamic measurements. Unlike other drugs with positive inotropic activity, however, digoxin does not influence hemodynamics in normal volunteers or in CHF patients in whom hemodynamics have been normalized with other therapies. These differing effects may be related to the drug's diverse peripheral vascular effects in CHF patients in whom vasodilation may occur in comparison with those that occur in normal subjects in whom the peripheral vasoconstrictor effects may prevent the inotropic effects of the drug from being translated into an increase in cardiac output. The hemodynamic effects of digoxin in patients with chronic CHF due primarily to diastolic dysfunction have not been fully investigated. Intravenous digoxin produces hemodynamic effects in patients with CHF associated with acute myocardial infarction, but these changes are small compared with those resulting from the administration of dobutamine. Digoxin does not appear to influence hemodynamic measurements in patients with right ventricular dysfunction unless concomitant left ventricular failure is present. In patients with chronic left ventricular dysfunction, the hemodynamic effects of intravenous digoxin and vasodilators are enhanced when these agents are given in combination.
尽管洋地黄制剂已使用了200多年,但直到最近20年,才开始对充血性心力衰竭(CHF)患者静脉注射地高辛后数小时内发生的中心血流动力学和神经体液效应进行研究。尽管地高辛在组织制剂中已显示出能刺激心肌收缩力,但其正性肌力活性在人体血流动力学测量中并不总能转化为改善。对于基线血流动力学测量异常的慢性CHF患者,静脉注射地高辛可导致心脏指数增加,心率、左心室充盈压和右心房压力降低,以及神经体液异常的急性减轻。然而,与其他具有正性肌力活性的药物不同,地高辛对正常志愿者或已通过其他疗法使血流动力学正常化的CHF患者的血流动力学没有影响。这些不同的效应可能与该药物在CHF患者中的多种外周血管效应有关,与正常受试者相比,CHF患者可能会发生血管舒张,而正常受试者的外周血管收缩效应可能会阻止该药物的正性肌力效应转化为心输出量的增加。地高辛对主要由舒张功能障碍引起的慢性CHF患者的血流动力学效应尚未得到充分研究。静脉注射地高辛对与急性心肌梗死相关的CHF患者产生血流动力学效应,但与给予多巴酚丁胺所产生的变化相比,这些变化较小。除非伴有左心室衰竭,地高辛似乎对右心室功能障碍患者的血流动力学测量没有影响。在慢性左心室功能障碍患者中,静脉注射地高辛和血管扩张剂联合使用时,其血流动力学效应会增强。