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左西孟旦对急性肺栓塞所致右心室衰竭的影响。

Effects of levosimendan on acute pulmonary embolism-induced right ventricular failure.

作者信息

Kerbaul François, Gariboldi Vlad, Giorgi Roch, Mekkaoui Choukri, Guieu Régis, Fesler Pierre, Gouin François, Brimioulle Serge, Collart Frédéric

机构信息

Laboratory of Hemodynamics and Cardiovascular Mechanisms and the LERTIM, Faculty of Medicine, Marseille, France.

出版信息

Crit Care Med. 2007 Aug;35(8):1948-54. doi: 10.1097/01.CCM.0000275266.33910.8D.

Abstract

OBJECTIVE

Repeated episodes of pulmonary embolism can persistently increase pulmonary arterial pressure and depress right ventricular contractility. We investigated the effects of levosimendan on right ventricular-pulmonary arterial coupling in this model of right ventricular failure.

DESIGN

Prospective, controlled, randomized animal study.

SETTING

University research laboratory.

SUBJECTS

Fourteen anesthetized piglets.

INTERVENTIONS

Repeated acute pulmonary embolisms were induced with autologous blood clots to induce persistent right ventricular failure. Animals were randomly assigned to a control or levosimendan group. Levosimendan 20 microg/kg was administered in 10 mins followed by 0.2 microg/kg/min or same volumes of isotonic saline.

MEASUREMENTS AND MAIN RESULTS

Pulmonary artery distal resistance and proximal elastance by pressure-flow relationships and vascular impedance were measured. We noted right ventricle contractility by the end-systolic pressure-volume relationship (Ees), pulmonary artery effective elastance by the end-diastolic to end-systolic relationship (Ea), and right ventricular-pulmonary arterial coupling efficiency by the Ees/Ea ratio. The gradual pulmonary artery embolism increased pulmonary artery resistance and elastance, increased Ea from 1.01 +/- 0.17 to 5.58 +/- 0.37 mm Hg/mL, decreased Ees from 1.75 +/- 0.12 to 1.29 +/- 0.20 mm Hg/mL, and decreased Ees/Ea from 1.74 +/- 0.20 to 0.24 +/- 0.09. Compared with placebo, levosimendan decreased pulmonary arterial elastance and characteristic impedance. Right ventricular-pulmonary arterial coupling was restored by both an increase in right ventricular contractility and a decrease in right ventricular afterload.

CONCLUSIONS

A gradual increase in pulmonary artery pressure induced by pulmonary embolism persistently worsens pulmonary artery hemodynamics, right ventricular contractility, right ventricular-pulmonary arterial coupling, and cardiac output. Levosimendan restores right ventricular-pulmonary arterial coupling better than placebo, because of combined pulmonary vasodilation and increased right ventricular contractility.

摘要

目的

反复发生的肺栓塞可持续升高肺动脉压并降低右心室收缩力。我们在这种右心室衰竭模型中研究了左西孟旦对右心室 - 肺动脉耦合的影响。

设计

前瞻性、对照、随机动物研究。

地点

大学研究实验室。

对象

14只麻醉仔猪。

干预措施

用自体血凝块诱导反复急性肺栓塞以诱发持续性右心室衰竭。动物被随机分为对照组或左西孟旦组。在10分钟内给予左西孟旦20微克/千克,随后以0.2微克/千克/分钟的速度给药,或给予相同体积的等渗盐水。

测量指标及主要结果

通过压力 - 流量关系和血管阻抗测量肺动脉远端阻力和近端弹性。我们通过收缩末期压力 - 容积关系(Ees)记录右心室收缩力,通过舒张末期到收缩末期关系(Ea)记录肺动脉有效弹性,并通过Ees/Ea比值记录右心室 - 肺动脉耦合效率。逐渐发生的肺动脉栓塞增加了肺动脉阻力和弹性,使Ea从1.01±0.17毫米汞柱/毫升增加到5.58±0.37毫米汞柱/毫升,使Ees从1.75±0.12毫米汞柱/毫升降低到1.29±0.20毫米汞柱/毫升,并使Ees/Ea从1.74±0.20降低到0.24±0.09。与安慰剂相比,左西孟旦降低了肺动脉弹性和特性阻抗。右心室 - 肺动脉耦合通过右心室收缩力增加和右心室后负荷降低得以恢复。

结论

肺栓塞引起的肺动脉压力逐渐升高会持续恶化肺动脉血流动力学、右心室收缩力、右心室 - 肺动脉耦合和心输出量。由于联合了肺血管舒张和右心室收缩力增加,左西孟旦比安慰剂能更好地恢复右心室 - 肺动脉耦合。

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