Continuous Resuscitation for Porcine Liver Transplantation From Donor After Cardiac Death
To solve the serious donor shortage, the demand is increasing for developing a new method to use the marginal donors, including donors after cardiac death (DCD). Continuous machine perfusion from ex vivo to in situ is a novel technique to overcome warm ischemia during organ grafting as an ischemia-f...
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Veröffentlicht in: | Transplantation proceedings 2019-06, Vol.51 (5), p.1463-1467 |
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creator | Yoshimoto, Syuhei Torai, Shinji Yoshioka, Masaki Nadahara, Soichi Kobayashi, Eiji |
description | To solve the serious donor shortage, the demand is increasing for developing a new method to use the marginal donors, including donors after cardiac death (DCD). Continuous machine perfusion from ex vivo to in situ is a novel technique to overcome warm ischemia during organ grafting as an ischemia-free transplantation. Herein, we tested orthotopic and heterotopic ischemia-free liver transplantation in pigs and evaluated the perfusion characteristics of DCD grafts from ex vivo preservation to implantation.
The demonstration of ischemia-free transplantation was conducted using both orthotopic and heterotopic transplantation models. Warm ischemia time (WIT) was set at 60 minutes or 120 minutes in the DCD models. Recipients were humanely killed 3 days after transplant. Flow rates of portal vein and hepatic artery were set to 0.06 to 0.15 mL/min/g and 0.04 to 0.06 mL/min/g for the liver weight ratio, respectively.
Under the stable perfusion rate by machine perfusion, the average hepatic artery pressure of the liver graft after a WIT of 120 minutes was approximately 80 mm Hg higher than after WIT of 60 minutes. The recipient with liver graft of WIT of 60 minutes could not survive overnight. In heterotopic model, the recipient with 1 hour DCD liver survived until humanely killed.
The results of pressure monitoring in our DCD liver graft model indicate that pressures are influenced not only by thrombus formation but also by postmortem rigidity at 2 hours after cardiac death.
•We studied the use of continuous perfusion of DCD liver grafts in a porcine model.•Machine perfusion of DCD liver grafts was successfully continued from ex vivo state.•Mean hepatic artery perfusion pressure was increased after 2 h of warm ischemia.•Mean hepatic artery perfusion pressure was not increased after 1 h of warm ischemia.•Thrombus formation and postmortem rigidity 2 h after cardiac death affect pressures. |
doi_str_mv | 10.1016/j.transproceed.2019.03.016 |
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The demonstration of ischemia-free transplantation was conducted using both orthotopic and heterotopic transplantation models. Warm ischemia time (WIT) was set at 60 minutes or 120 minutes in the DCD models. Recipients were humanely killed 3 days after transplant. Flow rates of portal vein and hepatic artery were set to 0.06 to 0.15 mL/min/g and 0.04 to 0.06 mL/min/g for the liver weight ratio, respectively.
Under the stable perfusion rate by machine perfusion, the average hepatic artery pressure of the liver graft after a WIT of 120 minutes was approximately 80 mm Hg higher than after WIT of 60 minutes. The recipient with liver graft of WIT of 60 minutes could not survive overnight. In heterotopic model, the recipient with 1 hour DCD liver survived until humanely killed.
The results of pressure monitoring in our DCD liver graft model indicate that pressures are influenced not only by thrombus formation but also by postmortem rigidity at 2 hours after cardiac death.
•We studied the use of continuous perfusion of DCD liver grafts in a porcine model.•Machine perfusion of DCD liver grafts was successfully continued from ex vivo state.•Mean hepatic artery perfusion pressure was increased after 2 h of warm ischemia.•Mean hepatic artery perfusion pressure was not increased after 1 h of warm ischemia.•Thrombus formation and postmortem rigidity 2 h after cardiac death affect pressures.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2019.03.016</identifier><identifier>PMID: 31155180</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Blood Pressure - physiology ; Death ; Hepatic Artery - physiology ; Liver - blood supply ; Liver Transplantation - methods ; Organ Preservation - methods ; Perfusion - methods ; Swine ; Tissue Donors ; Warm Ischemia</subject><ispartof>Transplantation proceedings, 2019-06, Vol.51 (5), p.1463-1467</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-85812b4693907a04165116b75d7dca77da5b2c1713c6487afff42d696f3ee3be3</citedby><cites>FETCH-LOGICAL-c380t-85812b4693907a04165116b75d7dca77da5b2c1713c6487afff42d696f3ee3be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041134518318244$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31155180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoshimoto, Syuhei</creatorcontrib><creatorcontrib>Torai, Shinji</creatorcontrib><creatorcontrib>Yoshioka, Masaki</creatorcontrib><creatorcontrib>Nadahara, Soichi</creatorcontrib><creatorcontrib>Kobayashi, Eiji</creatorcontrib><title>Continuous Resuscitation for Porcine Liver Transplantation From Donor After Cardiac Death</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>To solve the serious donor shortage, the demand is increasing for developing a new method to use the marginal donors, including donors after cardiac death (DCD). Continuous machine perfusion from ex vivo to in situ is a novel technique to overcome warm ischemia during organ grafting as an ischemia-free transplantation. Herein, we tested orthotopic and heterotopic ischemia-free liver transplantation in pigs and evaluated the perfusion characteristics of DCD grafts from ex vivo preservation to implantation.
The demonstration of ischemia-free transplantation was conducted using both orthotopic and heterotopic transplantation models. Warm ischemia time (WIT) was set at 60 minutes or 120 minutes in the DCD models. Recipients were humanely killed 3 days after transplant. Flow rates of portal vein and hepatic artery were set to 0.06 to 0.15 mL/min/g and 0.04 to 0.06 mL/min/g for the liver weight ratio, respectively.
Under the stable perfusion rate by machine perfusion, the average hepatic artery pressure of the liver graft after a WIT of 120 minutes was approximately 80 mm Hg higher than after WIT of 60 minutes. The recipient with liver graft of WIT of 60 minutes could not survive overnight. In heterotopic model, the recipient with 1 hour DCD liver survived until humanely killed.
The results of pressure monitoring in our DCD liver graft model indicate that pressures are influenced not only by thrombus formation but also by postmortem rigidity at 2 hours after cardiac death.
•We studied the use of continuous perfusion of DCD liver grafts in a porcine model.•Machine perfusion of DCD liver grafts was successfully continued from ex vivo state.•Mean hepatic artery perfusion pressure was increased after 2 h of warm ischemia.•Mean hepatic artery perfusion pressure was not increased after 1 h of warm ischemia.•Thrombus formation and postmortem rigidity 2 h after cardiac death affect pressures.</description><subject>Animals</subject><subject>Blood Pressure - physiology</subject><subject>Death</subject><subject>Hepatic Artery - physiology</subject><subject>Liver - blood supply</subject><subject>Liver Transplantation - methods</subject><subject>Organ Preservation - methods</subject><subject>Perfusion - methods</subject><subject>Swine</subject><subject>Tissue Donors</subject><subject>Warm Ischemia</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1LAzEQhoMotlb_giyevOyaSfar3kprVSgoUg-eQjY7iyndTU2yBf-9qW3Bo6cwvM9kZh5CboAmQCG_WyXeys5trFGIdcIojBPKkxCdkCGUBY9ZzvgpGVKaQgw8zQbkwrkVDTVL-TkZcIAsg5IOycfUdF53veld9Iaud0p76bXposbY6NVYpTuMFnqLNlr-Tl3L7kDMrWmjmekCOGl8AKbS1lqqaIbSf16Ss0auHV4d3hF5nz8sp0_x4uXxeTpZxIqX1MdlVgKr0nzMx7SQYeE8A8irIquLWsmiqGVWMQUFcJWnZSGbpklZnY_zhiPyCvmI3O7_DT6-enRetNopXIc9MVwlGONpWjKAMqD3e1RZ45zFRmysbqX9FkDFTq1Yib9qxU6toFyEKDRfH-b0VRuyY-vRZQBmewDDtVuNVgSZ2CmstUXlRW30f-b8AC5Bkcw</recordid><startdate>201906</startdate><enddate>201906</enddate><creator>Yoshimoto, Syuhei</creator><creator>Torai, Shinji</creator><creator>Yoshioka, Masaki</creator><creator>Nadahara, Soichi</creator><creator>Kobayashi, Eiji</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201906</creationdate><title>Continuous Resuscitation for Porcine Liver Transplantation From Donor After Cardiac Death</title><author>Yoshimoto, Syuhei ; Torai, Shinji ; Yoshioka, Masaki ; Nadahara, Soichi ; Kobayashi, Eiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-85812b4693907a04165116b75d7dca77da5b2c1713c6487afff42d696f3ee3be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Blood Pressure - physiology</topic><topic>Death</topic><topic>Hepatic Artery - physiology</topic><topic>Liver - blood supply</topic><topic>Liver Transplantation - methods</topic><topic>Organ Preservation - methods</topic><topic>Perfusion - methods</topic><topic>Swine</topic><topic>Tissue Donors</topic><topic>Warm Ischemia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshimoto, Syuhei</creatorcontrib><creatorcontrib>Torai, Shinji</creatorcontrib><creatorcontrib>Yoshioka, Masaki</creatorcontrib><creatorcontrib>Nadahara, Soichi</creatorcontrib><creatorcontrib>Kobayashi, Eiji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshimoto, Syuhei</au><au>Torai, Shinji</au><au>Yoshioka, Masaki</au><au>Nadahara, Soichi</au><au>Kobayashi, Eiji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Continuous Resuscitation for Porcine Liver Transplantation From Donor After Cardiac Death</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2019-06</date><risdate>2019</risdate><volume>51</volume><issue>5</issue><spage>1463</spage><epage>1467</epage><pages>1463-1467</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>To solve the serious donor shortage, the demand is increasing for developing a new method to use the marginal donors, including donors after cardiac death (DCD). Continuous machine perfusion from ex vivo to in situ is a novel technique to overcome warm ischemia during organ grafting as an ischemia-free transplantation. Herein, we tested orthotopic and heterotopic ischemia-free liver transplantation in pigs and evaluated the perfusion characteristics of DCD grafts from ex vivo preservation to implantation.
The demonstration of ischemia-free transplantation was conducted using both orthotopic and heterotopic transplantation models. Warm ischemia time (WIT) was set at 60 minutes or 120 minutes in the DCD models. Recipients were humanely killed 3 days after transplant. Flow rates of portal vein and hepatic artery were set to 0.06 to 0.15 mL/min/g and 0.04 to 0.06 mL/min/g for the liver weight ratio, respectively.
Under the stable perfusion rate by machine perfusion, the average hepatic artery pressure of the liver graft after a WIT of 120 minutes was approximately 80 mm Hg higher than after WIT of 60 minutes. The recipient with liver graft of WIT of 60 minutes could not survive overnight. In heterotopic model, the recipient with 1 hour DCD liver survived until humanely killed.
The results of pressure monitoring in our DCD liver graft model indicate that pressures are influenced not only by thrombus formation but also by postmortem rigidity at 2 hours after cardiac death.
•We studied the use of continuous perfusion of DCD liver grafts in a porcine model.•Machine perfusion of DCD liver grafts was successfully continued from ex vivo state.•Mean hepatic artery perfusion pressure was increased after 2 h of warm ischemia.•Mean hepatic artery perfusion pressure was not increased after 1 h of warm ischemia.•Thrombus formation and postmortem rigidity 2 h after cardiac death affect pressures.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31155180</pmid><doi>10.1016/j.transproceed.2019.03.016</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Blood Pressure - physiology Death Hepatic Artery - physiology Liver - blood supply Liver Transplantation - methods Organ Preservation - methods Perfusion - methods Swine Tissue Donors Warm Ischemia |
title | Continuous Resuscitation for Porcine Liver Transplantation From Donor After Cardiac Death |
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