Comparison of propofol and isoflurane anesthesia in orthotopic pig-to-baboon cardiac xenotransplantation

• Published in: Xenotransplantation (Københaven) 2007-05, Vol.14 (3), p.249-254
• Main Authors: Bauer, Andreas, Baschnegger, Heiko, Renz, Vivian, Brandl, Ulrike, Brenner, Paolo, Thein, Eckart, Reichart, Bruno, Schmoeckel, Michael, Christ, Frank
• Format: Article
• Language: English
• Subjects: anesthesia; Anesthesia, General - methods; Anesthesia, General - veterinary; Anesthetics, Inhalation - pharmacology; Anesthetics, Intravenous - pharmacology; Animals; baboon; Blood Pressure - drug effects; Central Venous Pressure - drug effects; Disease Models, Animal; Heart Rate - drug effects; Heart Transplantation - methods; isoflurane; Isoflurane - pharmacology; Male; Papio; Papio anubis; Papio hamadryas; pig; Primates; propofol; Propofol - pharmacology; Sus scrofa; Transplantation, Heterologous - methods; xenotransplantation
• ISSN: 0908-665X; 1399-3089
• DOI: 10.1111/j.1399-3089.2007.00383.x

: Background:  Orthotopic pig‐to‐baboon xenogeneic heart transplantation (oXHTx) is the only accepted preclinical animal model for cardiac xenotransplantation. We compared the hemodynamic stability of a propofol‐ and isoflurane‐based anesthetic regimen during oXHTx. Methods:  Hearts from 12 hDAF or hCD46 transgenic pigs (Sus scrofa; body weight 7 to 32 kg) were transplanted into baboons (Papio anubis and Papio hamadryas; body weight 9 to 26 kg) in the orthotopic life‐supporting position. Animals received a propofol‐based intravenous regimen or inhalation anesthesia with isoflurane. Analgesia was achieved with fentanyl in both groups. Systemic hemodynamic variables were measured before, during and after cardiopulmonary bypass (CPB) and the need for inotropic or vasoactive pharmacological support was compared before and after CPB. Results:  Global hemodynamic variables [i.e. heart rate, mean arterial pressure (MAP) and cardiac output] were not significantly different in propofol‐anesthetized baboons compared to baboons anesthetized with isoflurane. Baboons anesthetized with isoflurane showed a trend towards less pharmacological support required to achieve an adequate MAP of >60 mmHg after CPB (propofol: epinephrine 0.13 [0.05; 0.16] and norepinephrine 0.15 [0.02; 0.16] μg/kg/min vs. isoflurane: epinephrine 0.05 [0.02; 0.08] and norepinephrine 0.06 [0.02; 0.19] μg/kg/min; no significant difference). Conclusions:  Propofol and isoflurane appear to provide equal hemodynamic stability in orthotopic cardiac pig‐to‐baboon xenotransplantation prior to the start of CPB. The trend of a reduced catecholamine support needed after CPB, however, suggests that isoflurane may be the preferred drug for maintenance of anesthesia in this primate model.