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Effect of Subnormothermic Machine Perfusion on the Preservation of Vascularized Composite Allografts After Prolonged Warm Ischemia.
Charlès, Laura; Filz von Reiterdank, Irina; Lancia, Hyshem H; Shamlou, Austin Alana; Berkane, Yanis; Rosales, Ivy; Mink van der Molen, Aebele B; Coert, J H; Cetrulo, Curtis L; Lellouch, Alexandre G; Uygun, Korkut.
Affiliation
  • Charlès L; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation Laboratory, Massachusetts General Hospital, Boston, MA.
  • Filz von Reiterdank I; Department of Surgery, Harvard Medical School, Boston, MA.
  • Lancia HH; Department of Research, Shriners Children's Boston, Boston, MA.
  • Shamlou AA; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation Laboratory, Massachusetts General Hospital, Boston, MA.
  • Berkane Y; Department of Surgery, Harvard Medical School, Boston, MA.
  • Rosales I; Department of Research, Shriners Children's Boston, Boston, MA.
  • Mink van der Molen AB; Department of General Surgery, Center for Engineering in Medicine and Surgery, Massachusetts General Hospital, Boston, MA.
  • Coert JH; Department of Plastic, Reconstructive and Hand Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Cetrulo CL; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation Laboratory, Massachusetts General Hospital, Boston, MA.
  • Lellouch AG; Department of Surgery, Harvard Medical School, Boston, MA.
  • Uygun K; Department of Research, Shriners Children's Boston, Boston, MA.
Transplantation ; 2024 May 09.
Article in En | MEDLINE | ID: mdl-38722685
ABSTRACT

BACKGROUND:

Warm ischemia time (WIT) and ischemia-reperfusion injury are limiting factors for vascularized composite allograft (VCA) transplantation. Subnormothermic machine perfusion (SNMP) has demonstrated the potential to extend WIT in organ transplantation. This study evaluates the effect of SNMP on VCA viability after prolonged WIT.

METHODS:

Rat hindlimbs underwent WIT for 30, 45, 60, 120, 150, or 210 min, followed by 3-h SNMP. Monitoring of perfusion parameters and outflow determined the maximum WIT compatible with limb viability after SNMP. Thereafter, 2 groups were assessed a control group with inbred transplantation (Txp) after 120 min of WIT and an experimental group that underwent WIT + SNMP + Txp. Graft appearance, blood gas, cytokine levels, and histology were assessed for 21 d.

RESULTS:

Based on potassium levels, the limit of WIT compatible with limb viability after SNMP is 120 min. Before this limit, SNMP reduces potassium and lactate levels of WIT grafts to the same level as fresh grafts. In vivo, the control group presented 80% graft necrosis, whereas the experimental group showed no necrosis, had better healing (P = 0.0004), and reduced histological muscle injury (P = 0.012). Results of blood analysis revealed lower lactate, potassium levels, and calcium levels (P = 0.048) in the experimental group. Both groups presented an increase in interleukin (IL)-10 and IL-1b/IL-1F2 with a return to baseline after 7 to 14 d.

CONCLUSIONS:

Our study establishes the limit of WIT compatible with VCA viability and demonstrates the effectiveness of SNMP in restoring a graft after WIT ex vivo and in vivo, locally and systemically.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Transplantation Year: 2024 Document type: Article Affiliation country: Marruecos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Transplantation Year: 2024 Document type: Article Affiliation country: Marruecos Country of publication: Estados Unidos