Kaukinen S, Ylitalo P, Pessi T, Vapaatalo H
Clin Pharmacol Ther. 1984 Oct;36(4):464-9. doi: 10.1038/clpt.1984.205.
Iloprost is a chemically stable derivative of carbaprostacyclin. We studied its hemodynamic effects in 10 patients in an intensive care unit. Iloprost was infused intravenously for 3 days for the treatment of advanced obliterative arterial disease of the lower extremities. Clinically significant hemodynamic responses were obtained with an infusion rate of 0.5 ng/kg/min. All subjects tolerated the dose of 4 ng/kg/min, which increased heart rate an average of 11% and cardiac index an average of 26%. This infusion rate decreased mean arterial pressure by 15%, total peripheral resistance by 31%, and pulmonary vascular resistance by 34%. Mean pulmonary arterial pressure, pulmonary capillary wedge pressure, left and right ventricular stroke work indices, and rate pressure product did not change. At higher doses of up to 8 ng/kg/min, responses were augmented only slightly, but side effects such as headache, nausea, and abdominal colics became more prominent. The data show iloprost to be a potent vasodilator that reduces both pre- and afterload and presumably induces a compensatory increase in cardiac output and heart rate, but does not increase the work load or oxygen demand of the heart.
依洛前列素是卡前列环素的化学稳定衍生物。我们在重症监护病房对10例患者研究了其血流动力学效应。依洛前列素静脉输注3天用于治疗晚期下肢闭塞性动脉疾病。输注速率为0.5纳克/千克/分钟时可获得具有临床意义的血流动力学反应。所有受试者均耐受4纳克/千克/分钟的剂量,该剂量使心率平均增加11%,心脏指数平均增加26%。该输注速率使平均动脉压降低15%,总外周阻力降低31%,肺血管阻力降低34%。平均肺动脉压、肺毛细血管楔压、左右心室每搏功指数及心率血压乘积未发生变化。在高达8纳克/千克/分钟的更高剂量下,反应仅略有增强,但头痛、恶心和腹部绞痛等副作用变得更加突出。数据表明依洛前列素是一种强效血管扩张剂,可降低前负荷和后负荷,并可能诱导心输出量和心率的代偿性增加,但不会增加心脏的工作负荷或需氧量。