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A Model of Pediatric End-Stage Lung Failure in Small Lambs <20 kg

BD. Carr, CJ. Poling, P. Hala, M. Caceres Quinones, AR. Prater, JS. McLeod, RH. Bartlett, A. Rojas-Pena, RB. Hirschl,

. 2020 ; 66 (5) : 572-579. [pub] -

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc20028189

Grantová podpora
R01 HD015434 NICHD NIH HHS - United States

One in five children with end-stage lung failure (ESLF) die while awaiting lung transplant. No suitable animal model of ESLF exists for the development of artificial lung devices for bridging to transplant. Small lambs weighing 15.7 ± 3.1 kg (n = 5) underwent ligation of the left anterior pulmonary artery (PA) branch, and gradual occlusion of the right main PA over 48 hours. All animals remained hemodynamically stable. Over seven days of disease model conditions, they developed pulmonary hypertension (mean PA pressure 20 ± 5 vs. 33 ± 4 mm Hg), decreased perfusion (SvO2 66 ± 3 vs. 55 ± 8%) with supplemental oxygen requirement, and severe tachypneic response (45 ± 9 vs. 82 ± 23 breaths/min) (all p < 0.05). Severe right heart dysfunction developed (tricuspid annular plane systolic excursion 13 ± 3 vs. 7 ± 2 mm, fractional area change 36 ± 6 vs. 22 ± 10 mm, ejection fraction 51 ± 9 vs. 27 ± 17%, all p < 0.05) with severe tricuspid regurgitation and balloon-shaped dilation of the right ventricle. This model of pediatric ESLF reliably produces pulmonary hypertension, right heart strain, and impaired gas exchange, and will be used to develop a pediatric artificial lung.

Citace poskytuje Crossref.org

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$a One in five children with end-stage lung failure (ESLF) die while awaiting lung transplant. No suitable animal model of ESLF exists for the development of artificial lung devices for bridging to transplant. Small lambs weighing 15.7 ± 3.1 kg (n = 5) underwent ligation of the left anterior pulmonary artery (PA) branch, and gradual occlusion of the right main PA over 48 hours. All animals remained hemodynamically stable. Over seven days of disease model conditions, they developed pulmonary hypertension (mean PA pressure 20 ± 5 vs. 33 ± 4 mm Hg), decreased perfusion (SvO2 66 ± 3 vs. 55 ± 8%) with supplemental oxygen requirement, and severe tachypneic response (45 ± 9 vs. 82 ± 23 breaths/min) (all p < 0.05). Severe right heart dysfunction developed (tricuspid annular plane systolic excursion 13 ± 3 vs. 7 ± 2 mm, fractional area change 36 ± 6 vs. 22 ± 10 mm, ejection fraction 51 ± 9 vs. 27 ± 17%, all p < 0.05) with severe tricuspid regurgitation and balloon-shaped dilation of the right ventricle. This model of pediatric ESLF reliably produces pulmonary hypertension, right heart strain, and impaired gas exchange, and will be used to develop a pediatric artificial lung.
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$a Hala, Pavel $u From the Extracorporeal Life Support Laboratory, Department of Surgery. Department of Cardiology, Homolka Hospital. Department of Physiology, Charles University, Prague, Czech Republic. Department of Pediatric Anesthesia, Hospital Luis Calvo Mackenna, University of Chile.
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$a Caceres Quinones, Matias $u From the Extracorporeal Life Support Laboratory, Department of Surgery. Department of Anesthesia, Clínica Las Condes, Santiago, Chile. Department of Surgery, Section of Transplantation, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
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$a Rojas-Pena, Alvaro $u From the Extracorporeal Life Support Laboratory, Department of Surgery. Department of Surgery, Section of Transplantation, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
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