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Pediatric Artificial Lung: A Low-Resistance Pumpless Artificial Lung Alleviates an Acute Lamb Model of Increased Right Ventricle Afterload

机译:儿科人工肺:低电阻无泵人工肺缓解了右室后负荷增加的急性羔羊模型

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摘要

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 (A) baseline, (B) disease, and (C) 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 mmHg/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.
机译:儿童肺部疾病通常会导致肺动脉高压和右心衰竭。儿科人工肺(PAL)的可用性将为桥接这些疾病开辟新的途径,方法是过渡到急性疾病的恢复或慢性疾病的移植。这项研究调查了新型PAL在减轻肺动脉高压和右心室后负荷增加的动物模型中的功效。五只幼小羔羊(20-30 Kg)在肺动脉中植入了PAL至左心房构型。疾病的诱导涉及右主肺动脉的暂时性,可逆性阻塞。在(A)基线,(B)疾病和(C)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。随后的PAL附着改善了肺动脉压力(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 mmHg / L / min,血流量为1.3±0.6 L / min。这种新型的低阻力PAL可以减轻急性动物模型中的肺动脉高压,并证明有可能用作肺部恢复的桥梁患有严重肺动脉高压的小儿患者接受药物治疗或移植,但对药物治疗无效。

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