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Comparison of HTK and Hypertonic Citrate to Intraarterial Cooling in Human Non–Heart-Beating Kidney Donors
Abstract Intraarterial cooling (IAC) of non–heart-beating donors (NHBD) for renal donation requires a cheap, low-viscosity solution. HTK contains a high hydrogen ion buffer level that theoretically should reduce the observable acidosis associated with ongoing anaerobic metabolism. A retrospective co...
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Published in: | Transplantation proceedings 2007-03, Vol.39 (2), p.351-352 |
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creator | Wilson, C.H Asher, J.F Gupta, A Vijayanand, D Wyrley-Birch, H Stamp, S Rix, D.A Soomro, N Manas, D.M Jaques, B.C Peaston, R Talbot, D |
description | Abstract Intraarterial cooling (IAC) of non–heart-beating donors (NHBD) for renal donation requires a cheap, low-viscosity solution. HTK contains a high hydrogen ion buffer level that theoretically should reduce the observable acidosis associated with ongoing anaerobic metabolism. A retrospective comparison of all retrieved NHBD kidneys as well as of viability on the Organ Recovery Systems Lifeporter machine perfusion circuit was performed with respect to the preservation solution HTK or Marshall’s HOC. Forty-two NHBD kidneys (19 HTK and 23 HOC) were machine perfused between February 2004 and May 2005. Most of the HTK kidneys were obtained from uncontrolled donors (12 vs 5; Fisher exact test, P = .01). As a consequence, the glutathione- s -transferase viability assay (411 vs 292 IU/L, P = .12) and the lactate concentrations (2.33 vs 1.94 mmol/L, P = .13) were higher among the HTK cohort. There was evidence of greater buffering capacity in HTK, since the lactate:hydrogen ion ratios were consistently lower during the first 2 perfusion hours (1 hour P = .03, 2 hour P = .02). A linear regression analysis confirmed that this was related to the IAC solution (ANCOVA, P < .001). All controlled donor kidneys passed viability testing and were transplanted. In contrast, 83% (10/12) of the uncontrolled donor kidneys preserved with HTK passed the viability test and were transplanted, compared with only 20% (1/5) of the HOC-treated comparators (Fisher exact test, P = .03). It may be concluded that the postulated advantages of improved pH buffering with HTK appear to have clinical relevance. |
doi_str_mv | 10.1016/j.transproceed.2007.01.012 |
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HTK contains a high hydrogen ion buffer level that theoretically should reduce the observable acidosis associated with ongoing anaerobic metabolism. A retrospective comparison of all retrieved NHBD kidneys as well as of viability on the Organ Recovery Systems Lifeporter machine perfusion circuit was performed with respect to the preservation solution HTK or Marshall’s HOC. Forty-two NHBD kidneys (19 HTK and 23 HOC) were machine perfused between February 2004 and May 2005. Most of the HTK kidneys were obtained from uncontrolled donors (12 vs 5; Fisher exact test, P = .01). As a consequence, the glutathione- s -transferase viability assay (411 vs 292 IU/L, P = .12) and the lactate concentrations (2.33 vs 1.94 mmol/L, P = .13) were higher among the HTK cohort. There was evidence of greater buffering capacity in HTK, since the lactate:hydrogen ion ratios were consistently lower during the first 2 perfusion hours (1 hour P = .03, 2 hour P = .02). A linear regression analysis confirmed that this was related to the IAC solution (ANCOVA, P < .001). All controlled donor kidneys passed viability testing and were transplanted. In contrast, 83% (10/12) of the uncontrolled donor kidneys preserved with HTK passed the viability test and were transplanted, compared with only 20% (1/5) of the HOC-treated comparators (Fisher exact test, P = .03). It may be concluded that the postulated advantages of improved pH buffering with HTK appear to have clinical relevance.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2007.01.012</identifier><identifier>PMID: 17362727</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Cohort Studies ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Glucose ; Heart Arrest ; Humans ; Hypertonic Solutions ; Kidney ; Male ; Mannitol ; Medical sciences ; Middle Aged ; Organ Preservation Solutions ; Patient Selection ; Perfusion ; Potassium Chloride ; Procaine ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. 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HTK contains a high hydrogen ion buffer level that theoretically should reduce the observable acidosis associated with ongoing anaerobic metabolism. A retrospective comparison of all retrieved NHBD kidneys as well as of viability on the Organ Recovery Systems Lifeporter machine perfusion circuit was performed with respect to the preservation solution HTK or Marshall’s HOC. Forty-two NHBD kidneys (19 HTK and 23 HOC) were machine perfused between February 2004 and May 2005. Most of the HTK kidneys were obtained from uncontrolled donors (12 vs 5; Fisher exact test, P = .01). As a consequence, the glutathione- s -transferase viability assay (411 vs 292 IU/L, P = .12) and the lactate concentrations (2.33 vs 1.94 mmol/L, P = .13) were higher among the HTK cohort. There was evidence of greater buffering capacity in HTK, since the lactate:hydrogen ion ratios were consistently lower during the first 2 perfusion hours (1 hour P = .03, 2 hour P = .02). A linear regression analysis confirmed that this was related to the IAC solution (ANCOVA, P < .001). All controlled donor kidneys passed viability testing and were transplanted. In contrast, 83% (10/12) of the uncontrolled donor kidneys preserved with HTK passed the viability test and were transplanted, compared with only 20% (1/5) of the HOC-treated comparators (Fisher exact test, P = .03). It may be concluded that the postulated advantages of improved pH buffering with HTK appear to have clinical relevance.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Glucose</subject><subject>Heart Arrest</subject><subject>Humans</subject><subject>Hypertonic Solutions</subject><subject>Kidney</subject><subject>Male</subject><subject>Mannitol</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Organ Preservation Solutions</subject><subject>Patient Selection</subject><subject>Perfusion</subject><subject>Potassium Chloride</subject><subject>Procaine</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. 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Psychology</topic><topic>Fundamental immunology</topic><topic>Glucose</topic><topic>Heart Arrest</topic><topic>Humans</topic><topic>Hypertonic Solutions</topic><topic>Kidney</topic><topic>Male</topic><topic>Mannitol</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Organ Preservation Solutions</topic><topic>Patient Selection</topic><topic>Perfusion</topic><topic>Potassium Chloride</topic><topic>Procaine</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Tissue and Organ Harvesting - methods</topic><topic>Tissue Donors</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilson, C.H</creatorcontrib><creatorcontrib>Asher, J.F</creatorcontrib><creatorcontrib>Gupta, A</creatorcontrib><creatorcontrib>Vijayanand, D</creatorcontrib><creatorcontrib>Wyrley-Birch, H</creatorcontrib><creatorcontrib>Stamp, S</creatorcontrib><creatorcontrib>Rix, D.A</creatorcontrib><creatorcontrib>Soomro, N</creatorcontrib><creatorcontrib>Manas, D.M</creatorcontrib><creatorcontrib>Jaques, B.C</creatorcontrib><creatorcontrib>Peaston, R</creatorcontrib><creatorcontrib>Talbot, D</creatorcontrib><collection>Pascal-Francis</collection><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>Wilson, C.H</au><au>Asher, J.F</au><au>Gupta, A</au><au>Vijayanand, D</au><au>Wyrley-Birch, H</au><au>Stamp, S</au><au>Rix, D.A</au><au>Soomro, N</au><au>Manas, D.M</au><au>Jaques, B.C</au><au>Peaston, R</au><au>Talbot, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of HTK and Hypertonic Citrate to Intraarterial Cooling in Human Non–Heart-Beating Kidney Donors</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2007-03-01</date><risdate>2007</risdate><volume>39</volume><issue>2</issue><spage>351</spage><epage>352</epage><pages>351-352</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>Abstract Intraarterial cooling (IAC) of non–heart-beating donors (NHBD) for renal donation requires a cheap, low-viscosity solution. HTK contains a high hydrogen ion buffer level that theoretically should reduce the observable acidosis associated with ongoing anaerobic metabolism. A retrospective comparison of all retrieved NHBD kidneys as well as of viability on the Organ Recovery Systems Lifeporter machine perfusion circuit was performed with respect to the preservation solution HTK or Marshall’s HOC. Forty-two NHBD kidneys (19 HTK and 23 HOC) were machine perfused between February 2004 and May 2005. Most of the HTK kidneys were obtained from uncontrolled donors (12 vs 5; Fisher exact test, P = .01). As a consequence, the glutathione- s -transferase viability assay (411 vs 292 IU/L, P = .12) and the lactate concentrations (2.33 vs 1.94 mmol/L, P = .13) were higher among the HTK cohort. There was evidence of greater buffering capacity in HTK, since the lactate:hydrogen ion ratios were consistently lower during the first 2 perfusion hours (1 hour P = .03, 2 hour P = .02). A linear regression analysis confirmed that this was related to the IAC solution (ANCOVA, P < .001). All controlled donor kidneys passed viability testing and were transplanted. In contrast, 83% (10/12) of the uncontrolled donor kidneys preserved with HTK passed the viability test and were transplanted, compared with only 20% (1/5) of the HOC-treated comparators (Fisher exact test, P = .03). It may be concluded that the postulated advantages of improved pH buffering with HTK appear to have clinical relevance.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17362727</pmid><doi>10.1016/j.transproceed.2007.01.012</doi><tpages>2</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Child Cohort Studies Female Fundamental and applied biological sciences. Psychology Fundamental immunology Glucose Heart Arrest Humans Hypertonic Solutions Kidney Male Mannitol Medical sciences Middle Aged Organ Preservation Solutions Patient Selection Perfusion Potassium Chloride Procaine Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Tissue and Organ Harvesting - methods Tissue Donors Tissue, organ and graft immunology |
title | Comparison of HTK and Hypertonic Citrate to Intraarterial Cooling in Human Non–Heart-Beating Kidney Donors |
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