Your browser doesn't support javascript.
loading
Machine perfusion and the prevention of ischemic type biliary lesions following liver transplant: What is the evidence?
Durán, Manuel; Calleja, Rafael; Hann, Angus; Clarke, George; Ciria, Ruben; Nutu, Anisa; Sanabria-Mateos, Rebeca; Ayllón, María Dolores; López-Cillero, Pedro; Mergental, Hynek; Briceño, Javier; Perera, M Thamara P R.
Afiliação
  • Durán M; Department of Liver Transplantation, Reina Sofía University Hospital, Córdoba 14004, Spain.
  • Calleja R; Department of Liver Transplantation, Reina Sofía University Hospital, Córdoba 14004, Spain.
  • Hann A; The Liver Unit, Queen Elizabeth Hospital Birmingham, Birmingham B15 2TH, United Kingdom.
  • Clarke G; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham B15 2TH, United Kingdom.
  • Ciria R; The Liver Unit, Queen Elizabeth Hospital Birmingham, Birmingham B15 2TH, United Kingdom.
  • Nutu A; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham B15 2TH, United Kingdom.
  • Sanabria-Mateos R; Department of Liver Transplantation, Reina Sofía University Hospital, Córdoba 14004, Spain.
  • Ayllón MD; The Liver Unit, Queen Elizabeth Hospital Birmingham, Birmingham B15 2TH, United Kingdom.
  • López-Cillero P; The Liver Unit, Queen Elizabeth Hospital Birmingham, Birmingham B15 2TH, United Kingdom.
  • Mergental H; Department of Liver Transplantation, Reina Sofía University Hospital, Córdoba 14004, Spain.
  • Briceño J; Department of Liver Transplantation, Reina Sofía University Hospital, Córdoba 14004, Spain.
  • Perera MTPR; The Liver Unit, Queen Elizabeth Hospital Birmingham, Birmingham B15 2TH, United Kingdom.
World J Gastroenterol ; 29(20): 3066-3083, 2023 May 28.
Article em En | MEDLINE | ID: mdl-37346149
The widespread uptake of different machine perfusion (MP) strategies for liver transplant has been driven by an effort to minimize graft injury. Damage to the cholangiocytes during the liver donation, preservation, or early posttransplant period may result in stricturing of the biliary tree and inadequate biliary drainage. This problem continues to trouble clinicians, and may have catastrophic consequences for the graft and patient. Ischemic injury, as a result of compromised hepatic artery flow, is a well-known cause of biliary strictures, sepsis, and graft failure. However, very similar lesions can appear with a patent hepatic artery and these are known as ischemic type biliary lesions (ITBL) that are attributed to microcirculatory dysfunction rather than main hepatic arterial compromise. Both the warm and cold ischemic period duration appear to influence the onset of ITBL. All of the commonly used MP techniques deliver oxygen to the graft cells, and therefore may minimize the cholangiocyte injury and subsequently reduce the incidence of ITBL. As clinical experience and published evidence grows for these modalities, the impact they have on ITBL rates is important to consider. In this review, the evidence for the three commonly used MP strategies (abdominal normothermic regional perfusion [A-NRP], hypothermic oxygenated perfusion [HOPE], and normothermic machine perfusion [NMP] for ITBL prevention has been critically reviewed. Inconsistencies with ITBL definitions used in trials, coupled with variations in techniques of MP, make interpretation challenging. Overall, the evidence suggests that both HOPE and A-NRP prevent ITBL in donated after circulatory death grafts compared to cold storage. The evidence for ITBL prevention in donor after brain death grafts with any MP technique is weak.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Biliar / Transplante de Fígado Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Biliar / Transplante de Fígado Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article