Holubarsch C, Pieske B, Hasenfuss G, Just H
Medizinische Universitätsklinik, Abt. Kardiologie und Angiologie, Freiburg.
Z Kardiol. 1994;83 Suppl 2:21-5.
The phosphodiesterase inhibitor enoximone has both vasodilating and positive inotropic pharmacological properties. The balance between vasodilation and positive inotropism may be different between the various types of heart failure as well as the various stages of heart failure. Therefore, we investigated the effect of intravenous application of enoximone (1 mg/kg body weight) in a cohort of patients (n = 10) suffering from acute or subacute heart failure mainly due to ischemia or hypoxia. All patients had high left ventricular filling pressure, low cardiac output and were pretreated with intravenous dobutamine. Enoximone increased cardiac output from 3.2 +/- 1.2 to 5.5 +/- 2.2 l/min, increased heart rate from 94 +/- 20 to 100 +/- 18 beats/min, decreased systemic peripheral resistance from 1770 +/- 861 to 931 +/- 340 dyn.sec.cm-5 and decreased pulmonary wedge pressure from 24 +/- 5 to 20 +/- 6 mmHg, significantly. However, systolic aortic pressure, systolic pulmonary pressure and right atrial pressure were not significantly altered. We conclude that in a selected group of patients enoximone-given intravenously and acutely in the intensive care unity-can induce beneficial effects on central hemodynamics without critical falls in perfusion pressure.
磷酸二酯酶抑制剂依诺昔酮具有血管舒张和正性肌力的药理特性。血管舒张和正性肌力之间的平衡在不同类型的心力衰竭以及心力衰竭的不同阶段可能有所不同。因此,我们研究了静脉注射依诺昔酮(1mg/kg体重)对一组主要因缺血或缺氧导致急性或亚急性心力衰竭患者(n = 10)的影响。所有患者左心室充盈压高、心输出量低,并预先接受了静脉注射多巴酚丁胺治疗。依诺昔酮使心输出量从3.2±1.2升/分钟增加到5.5±2.2升/分钟,心率从94±20次/分钟增加到100±18次/分钟,全身外周阻力从1770±861降至931±340达因·秒·厘米⁻⁵,肺楔压从24±5降至20±6毫米汞柱,差异均有统计学意义。然而,收缩期主动脉压、收缩期肺动脉压和右心房压无明显改变。我们得出结论,在特定的一组患者中,在重症监护病房静脉内急性给予依诺昔酮可对中心血流动力学产生有益影响,而不会导致灌注压严重下降。