Alghanem Fares, Bryner Benjamin S, Jahangir Emilia M, Fernando Uditha P, Trahanas John M, Hoffman Hayley R, Bartlett Robert H, Rojas-Peña Alvaro, Hirschl Ronald B
From the *Extracorporeal Life Support Laboratory, University of Michigan, Ann Arbor, Michigan; †Section of Transplant Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, and ‡Section of Pediatric Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan.
ASAIO J. 2017 Mar/Apr;63(2):223-228. doi: 10.1097/MAT.0000000000000481.
Lung disease in children often results in pulmonary hypertension and right heart failure. The availability of a pediatric artificial lung (PAL) would open new approaches to the management of these conditions by bridging to recovery in acute disease or transplantation in chronic disease. This study investigates the efficacy of a novel PAL in alleviating an animal model of pulmonary hypertension and increased right ventricle afterload. Five juvenile lambs (20-30 kg) underwent PAL implantation in a pulmonary artery to left atrium configuration. Induction of disease involved temporary, reversible occlusion of the right main pulmonary artery. Hemodynamics, pulmonary vascular input impedance, and right ventricle efficiency were measured under 1) baseline, 2) disease, and 3) disease + PAL conditions. The disease model altered hemodynamics variables in a manner consistent with pulmonary hypertension. Subsequent PAL attachment improved pulmonary artery pressure (p = 0.018), cardiac output (p = 0.050), pulmonary vascular input impedance (Z.0 p = 0.028; Z.1 p = 0.058), and right ventricle efficiency (p = 0.001). The PAL averaged resistance of 2.3 ± 0.8 mm Hg/L/min and blood flow of 1.3 ± 0.6 L/min. This novel low-resistance PAL can alleviate pulmonary hypertension in an acute animal model and demonstrates potential for use as a bridge to lung recovery or transplantation in pediatric patients with significant pulmonary hypertension refractory to medical therapies.
儿童肺部疾病常导致肺动脉高压和右心衰竭。小儿人工肺(PAL)的出现将为这些病症的治疗开辟新途径,可用于急性疾病的恢复过渡或慢性疾病的移植治疗。本研究调查了一种新型PAL在缓解肺动脉高压动物模型及增加右心室后负荷方面的疗效。五只幼年羔羊(20 - 30千克)接受了肺动脉至左心房构型的PAL植入。疾病诱导包括暂时、可逆地阻断右主肺动脉。在1)基线、2)疾病和3)疾病 + PAL条件下测量血流动力学、肺血管输入阻抗和右心室效率。疾病模型以与肺动脉高压一致的方式改变了血流动力学变量。随后连接PAL改善了肺动脉压(p = 0.018)、心输出量(p = 0.050)、肺血管输入阻抗(Z.0 p = 0.028;Z.1 p = 0.058)和右心室效率(p = 0.001)。PAL的平均阻力为2.3±0.8毫米汞柱/升/分钟,血流量为1.3±0.6升/分钟。这种新型低阻力PAL可缓解急性动物模型中的肺动脉高压,并显示出在对药物治疗难治的严重肺动脉高压小儿患者中用作肺恢复或移植桥梁的潜力。