Hülsmann M, Stanek B, Frey B, Berger R, Rödler S, Siegel A, Hartter E, Schuller M, Ogris E, Pacher R
Department of Cardiology, University of Vienna, Austria.
J Heart Lung Transplant. 1997 May;16(5):556-62.
Prostaglandins of the E type are potent endogenous vasodilators that also interfere with the activity of the sympathetic nervous system. Thus treating patients with end-stage heart failure with prostaglandin E1 (PGE1) infusions seems to accord well with the hypothesis that neurohumoral imbalance rather than hemodynamic derangements should be the priority in the treatment of heart failure.
We sought to investigate neurohumoral in addition to hemodynamic changes during long-term PGE1 infusion and determined plasma renin activity, atrial natriuretic peptide, norepinephrine, and big endothelin plasma levels in 13 male patients with heart failure whose symptoms remained severe in spite of optimized oral therapy with digitalis, nitrates, furosemide (185 +/- 72 mg/d) and enalapril (33 +/- 3 mg/d). PGE1 infusion rate was started with 2.5 ng/kg/min and stepwise increased to the maximum tolerated dose (26 +/- 4 ng/kg/min), which was halved for continuous infusion through the following 12 hours and further stepwise reduced to an average dose of 8 +/- 1 ng/kg/min. Right heart catheterization was performed for acute hemodynamic studies and after 4 weeks. All patients were discharged with a catheter that was connected to a portable pump for home therapy.
Acute effects of PGE1 were reductions in systemic blood pressure, (p < 0.05), right atrial pressure (p < 0.001), pulmonary artery pressure (p < 0.05), pulmonary capillary wedge pressure (p < 0.01), systemic and pulmonary vascular resistance index (both p < 0.01) and an increase in cardiac and stroke volume index (both p < 0.001) without a change in heart rate. After 4 weeks a persistent increase from baseline in cardiac index (from 1.9 +/- 0.1 to 2.5 +/- 0.2 L/min/m2; p < 0.01) and in pulmonary vascular resistance index (from 479 +/- 50 to 331 +/- 29 dynes x sec/cm5 x m2; p < 0.05) was observed. Atrial natriuretic peptide (p < 0.05) decreased, and norepinephrine and big endothelin showed a tendency to a lower level. Concomitantly, New York Heart Association functional class changed (p = 0.0001), with one patient's condition remaining class IV, the conditions of seven patients decreasing to class II, and the conditions of five patients decreasing to class III.
Thus long-term parenteral home therapy with PGE1 infusions in patients with severe end-stage heart failure elicited beneficial clinical and hemodynamic effects without activating neurohumoral counterregulatory systems.
E型前列腺素是强效的内源性血管舒张剂,也会干扰交感神经系统的活性。因此,对终末期心力衰竭患者输注前列腺素E1(PGE1)似乎与以下假设高度契合,即神经体液失衡而非血流动力学紊乱应成为心力衰竭治疗的首要关注点。
我们试图研究长期输注PGE1期间除血流动力学变化外的神经体液变化,并测定了13例男性心力衰竭患者的血浆肾素活性、心房利钠肽、去甲肾上腺素和大内皮素血浆水平。这些患者尽管接受了洋地黄、硝酸盐、呋塞米(185±72mg/d)和依那普利(33±3mg/d)的优化口服治疗,但症状仍很严重。PGE1输注速率从2.5ng/kg/min开始,逐步增加至最大耐受剂量(26±4ng/kg/min),在接下来的12小时内将其减半用于持续输注,并进一步逐步降至平均剂量8±1ng/kg/min。进行右心导管插入术以进行急性血流动力学研究,并在4周后再次进行。所有患者出院时均携带一根连接到便携式泵的导管,用于家庭治疗。
PGE1的急性作用包括全身血压降低(p<0.05)、右心房压力降低(p<0.001)、肺动脉压力降低(p<0.05)、肺毛细血管楔压降低(p<0.01)、全身和肺血管阻力指数降低(均p<0.01)以及心输出量和每搏输出量指数增加(均p<0.001),心率无变化。4周后,观察到心脏指数从基线持续增加(从1.9±0.1升至2.5±0.2L/min/m²;p<0.01),肺血管阻力指数从479±50降至331±29达因·秒/厘米⁵·米²(p<0.05)。心房利钠肽降低(p<0.05),去甲肾上腺素和大内皮素呈降低趋势。同时,纽约心脏协会功能分级发生变化(p = 0.0001),1例患者仍为IV级,7例患者的病情降至II级,5例患者的病情降至III级。
因此,对重度终末期心力衰竭患者进行长期家庭胃肠外PGE1输注治疗可产生有益的临床和血流动力学效果,且不会激活神经体液反调节系统。