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N-acetylcysteine: a novel approach to methaemoglobinaemia in normothermic liver machine perfusion.
Clarke, George; Mao, Jingwen; Fan, Yiyu; Hann, Angus; Gupta, Amita; Nutu, Anisa; Buckel, Erwin; Kayani, Kayani; Murphy, Nicholas; Bangash, Mansoor N; Casey, Anna L; Wootton, Isla; Lawson, Alexander J; Dasari, Bobby V M; Perera, M Thamara P R; Mergental, Hynek; Afford, Simon C.
Affiliation
  • Clarke G; Liver Unit, Queen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, B15 2TH, UK. George.Clarke@uhb.nhs.uk.
  • Mao J; Birmingham Biomedical Research Centre, National Institute for Health Research (NIHR), University of Birmingham and University Hospitals Birmingham NHS Foundation Trust, Birmingham, B15 2TH, UK. George.Clarke@uhb.nhs.uk.
  • Fan Y; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, B15 2TH, UK. George.Clarke@uhb.nhs.uk.
  • Hann A; Birmingham Biomedical Research Centre, National Institute for Health Research (NIHR), University of Birmingham and University Hospitals Birmingham NHS Foundation Trust, Birmingham, B15 2TH, UK.
  • Gupta A; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, B15 2TH, UK.
  • Nutu A; Birmingham Biomedical Research Centre, National Institute for Health Research (NIHR), University of Birmingham and University Hospitals Birmingham NHS Foundation Trust, Birmingham, B15 2TH, UK.
  • Buckel E; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, B15 2TH, UK.
  • Kayani K; Liver Unit, Queen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, B15 2TH, UK.
  • Murphy N; Birmingham Biomedical Research Centre, National Institute for Health Research (NIHR), University of Birmingham and University Hospitals Birmingham NHS Foundation Trust, Birmingham, B15 2TH, UK.
  • Bangash MN; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, B15 2TH, UK.
  • Casey AL; Ochre-Bio Ltd, Oxford, UK.
  • Wootton I; Liver Unit, Queen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, B15 2TH, UK.
  • Lawson AJ; Liver Unit, Queen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, B15 2TH, UK.
  • Dasari BVM; Birmingham Biomedical Research Centre, National Institute for Health Research (NIHR), University of Birmingham and University Hospitals Birmingham NHS Foundation Trust, Birmingham, B15 2TH, UK.
  • Perera MTPR; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, B15 2TH, UK.
  • Mergental H; Queen Elizabeth Hospital Birmingham, Birmingham, B15 2TH, UK.
  • Afford SC; Intensive Care Unit, Queen Elizabeth Hospital Birmingham, Birmingham, B15 2TH, UK.
Sci Rep ; 13(1): 19022, 2023 11 03.
Article in En | MEDLINE | ID: mdl-37923778
Extended duration of normothermic machine perfusion (NMP) provides opportunities to resuscitate suboptimal donor livers. This intervention requires adequate oxygen delivery typically provided by a blood-based perfusion solution. Methaemoglobin (MetHb) results from the oxidation of iron within haemoglobin and represents a serious problem in perfusions lasting > 24 h. We explored the effects of anti-oxidant, N-acetylcysteine (NAC) on the accumulation of methaemoglobin. NMP was performed on nine human donor livers declined for transplantation: three were perfused without NAC (no-NAC group), and six organs perfused with an initial NAC bolus, followed by continuous infusion (NAC group), with hourly methaemoglobin perfusate measurements. In-vitro experiments examined the impact of NAC (3 mg) on red cells (30 ml) in the absence of liver tissue. The no-NAC group sustained perfusions for an average of 96 (range 87-102) h, universally developing methaemoglobinaemia (≥ 2%) observed after an average of 45 h, with subsequent steep rise. The NAC group was perfused for an average of 148 (range 90-184) h. Only 2 livers developed methaemoglobinaemia (peak MetHb of 6%), with an average onset of 116.5 h. Addition of NAC efficiently limits formation and accumulation of methaemoglobin during NMP, and allows the significant extension of perfusion duration.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liver Transplantation / Methemoglobinemia Limits: Humans Language: En Journal: Sci Rep Year: 2023 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liver Transplantation / Methemoglobinemia Limits: Humans Language: En Journal: Sci Rep Year: 2023 Type: Article