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Thomas Vogel

Researcher at University of Oxford

Publications -  27
Citations -  820

Thomas Vogel is an academic researcher from University of Oxford. The author has contributed to research in topics: Transplantation & Liver transplantation. The author has an hindex of 10, co-authored 20 publications receiving 666 citations.

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Journal ArticleDOI

Liver Transplantation After Ex Vivo Normothermic Machine Preservation: A Phase 1 (First-in-Man) Clinical Trial

TL;DR: This first report of liver transplantation using NMP‐preserved livers demonstrates the safety and feasibility of using this technology from retrieval to transplantation, including transportation, and may be valuable in increasing the number of donor livers and improving the function of transplantable organs.
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The role of normothermic extracorporeal perfusion in minimizing ischemia reperfusion injury

TL;DR: Normothermic machine perfusion might transpire to be the ideal vehicle to deliver other therapeutic interventions during preservation to modulate and optimize the graft before transplantation by restoring function in marginal donor organs and enabling the clinician to appraise its viability, the donor pool might be greatly expanded.
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The 24-hour normothermic machine perfusion of discarded human liver grafts.

TL;DR: Normothermic perfusion preservation of human livers for 24 hours was shown to be technically feasible and positive correlation between instantly available perfusion parameters and generally accepted predictors of posttransplant graft survival was found.
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Ex-vivo normothermic liver perfusion: an update.

TL;DR: Avoidance of cold ischaemic preservation damage and repair of injury sustained during warm ischaemia and organ procurement would potentially allow many livers from extended criteria donors to be transplanted reliably.
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Novel approaches to preventing ischemia-reperfusion injury during liver transplantation.

TL;DR: A balanced overview on how machine preservation technologies, the coagulation system, antioxidants, cytoprotective agents, cytokines, preservation solutions, and the innate and adaptive immune system can be targeted to prevent IRI in liver transplantation is presented.