Scientific Reports (Oct 2021)

An innovative ovine model of severe cardiopulmonary failure supported by veno-arterial extracorporeal membrane oxygenation

  • Silver Heinsar,
  • Jae-Seung Jung,
  • Sebastiano Maria Colombo,
  • Sacha Rozencwajg,
  • Karin Wildi,
  • Kei Sato,
  • Carmen Ainola,
  • Xiaomeng Wang,
  • Gabriella Abbate,
  • Noriko Sato,
  • Wayne Bruce Dyer,
  • Samantha Annie Livingstone,
  • Leticia Pretti Pimenta,
  • Nicole Bartnikowski,
  • Mahe Jeannine Patricia Bouquet,
  • Margaret Passmore,
  • Bruno Vidal,
  • Chiara Palmieri,
  • Janice D. Reid,
  • Haris M. Haqqani,
  • Daniel McGuire,
  • Emily Susan Wilson,
  • Indrek Rätsep,
  • Roberto Lorusso,
  • Jacky Y. Suen,
  • Gianluigi Li Bassi,
  • John F. Fraser

DOI
https://doi.org/10.1038/s41598-021-00087-y
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 11

Abstract

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Abstract Refractory cardiogenic shock (CS) often requires veno-arterial extracorporeal membrane oxygenation (VA-ECMO) to sustain end-organ perfusion. Current animal models result in heterogenous cardiac injury and frequent episodes of refractory ventricular fibrillation. Thus, we aimed to develop an innovative, clinically relevant, and titratable model of severe cardiopulmonary failure. Six sheep (60 ± 6 kg) were anaesthetized and mechanically ventilated. VA-ECMO was commenced and CS was induced through intramyocardial injections of ethanol. Then, hypoxemic/hypercapnic pulmonary failure was achieved, through substantial decrease in ventilatory support. Echocardiography was used to compute left ventricular fractional area change (LVFAC) and cardiac Troponin I (cTnI) was quantified. After 5 h, the animals were euthanised and the heart was retrieved for histological evaluations. Ethanol (58 ± 23 mL) successfully induced CS in all animals. cTnI levels increased near 5000-fold. CS was confirmed by a drop in systolic blood pressure to 67 ± 14 mmHg, while lactate increased to 4.7 ± 0.9 mmol/L and LVFAC decreased to 16 ± 7%. Myocardial samples corroborated extensive cellular necrosis and inflammatory infiltrates. In conclusion, we present an innovative ovine model of severe cardiopulmonary failure in animals on VA-ECMO. This model could be essential to further characterize CS and develop future treatments.