• Am J Transl Res · Jan 2016

    Extracorporeal membrane oxygenation improves survival in a novel 24-hour pig model of severe acute respiratory distress syndrome.

    • Joaquín Araos, Leyla Alegría, Patricio García, Felipe Damiani, Pablo Tapia, Dagoberto Soto, Tatiana Salomon, Felipe Rodriguez, Macarena Amthauer, Benjamín Erranz, Gabriel Castro, Pamela Carreño, Tania Medina, Jaime Retamal, Pablo Cruces, Guillermo Bugedo, and Alejandro Bruhn.
    • Departamento de Medicina Intensiva, Facultad de Medicina, Pontificia Universidad Católica de Chile Santiago, Chile.
    • Am J Transl Res. 2016 Jan 1; 8 (6): 2826-37.

    AbstractExtracorporeal membrane oxygenation (ECMO) is increasingly being used to treat severe acute respiratory distress syndrome (ARDS). However, there is limited clinical evidence about how to optimize the technique. Experimental research can provide an alternative to fill the actual knowledge gap. The purpose of the present study was to develop and validate an animal model of acute lung injury (ALI) which resembled severe ARDS, and which could be successfully supported with ECMO. Eighteen pigs were randomly allocated into three groups: sham, ALI, and ALI + ECMO. ALI was induced by a double-hit consisting in repeated saline lavage followed by a 2-hour period of injurious ventilation. All animals were followed up to 24 hours while being ventilated with conventional ventilation (tidal volume 10 ml/kg). The lung injury model resulted in severe hypoxemia, increased airway pressures, pulmonary hypertension, and altered alveolar membrane barrier function, as indicated by an increased protein concentration in bronchoalveolar fluid, and increased wet/dry lung weight ratio. Histologic examination revealed severe diffuse alveolar damage, characteristic of ARDS. Veno-venous ECMO was started at the end of lung injury induction with a flow > 60 ml/kg/min resulting in rapid reversal of hypoxemia and pulmonary hypertension. Mortality was 0, 66.6 and 16.6% in the SHAM, ALI and ALI + ECMO groups, respectively (p < 0.05). This is a novel clinically relevant animal model that can be used to optimize the approach to ECMO and foster translational research in extracorporeal lung support.

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