A novel dextran 40‐based preservation solution
Although the University of Wisconsin (UW) solution has become the standard solution for the preservation of kidneys for transplantation, the importance of the colloid hydroxyethylstarch (HES), one of the key compounds of the UW solution, has been questioned repeatedly. It is now established that HES...
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Veröffentlicht in: | Transplant international 1996-01, Vol.9 (1), p.32-37 |
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description | Although the University of Wisconsin (UW) solution has become the standard solution for the preservation of kidneys for transplantation, the importance of the colloid hydroxyethylstarch (HES), one of the key compounds of the UW solution, has been questioned repeatedly. It is now established that HES is not necessary for routine kidney preservation. However, colloids may still be advantageous in UW like solutions for the purpose of multiorgan procurements and the preservation of organs from marginal donors. It has been shown in various experimental models that dextran 40 may successfully substitute for HES. Dextran 40 is not only cheaper but also has a variety of biological effects that may be beneficial during the graft reperfusion phase. The aim of this clinical study was to examine the efficacy of a dextran 40‐based preservation solution (Dex‐PS) for its use in human kidney graft preservation and to compare the transplantation results with kidneys preserved with UW solution. A total of 87 kidneys were preserved with Dex‐PS and matched with 87 kidneys preserved with UW solution. Both groups were comparable in terms of donor and recipient characteristics and both had a high proportion of kidneys from non‐heart‐beating donors. Patient survival and graft survival after 1 year were 95 % and 86 % for the Dex‐PS group and 94 % and 90 % for the UW group, respectively (P= NS). Primary nonfunction, delayed graft function, postoperative need for dialysis, and follow‐up of serum creat‐inine were statistically comparable between these two groups. We conclude that dextran 40 can safely replace HES in UW solution for the purpose of clinical kidney preservation. There were no statistically detectable differences in graft performance between the kidneys preserved with UW and those preserved with Dex‐PS. |
doi_str_mv | 10.1111/j.1432-2277.1996.tb00849.x |
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R. ; Schlumpf, Rolf</creator><creatorcontrib>Candinas, Daniel ; Largiadèr, Felix ; Binswanger, Ulrich ; Sutherland, David E. R. ; Schlumpf, Rolf</creatorcontrib><description>Although the University of Wisconsin (UW) solution has become the standard solution for the preservation of kidneys for transplantation, the importance of the colloid hydroxyethylstarch (HES), one of the key compounds of the UW solution, has been questioned repeatedly. It is now established that HES is not necessary for routine kidney preservation. However, colloids may still be advantageous in UW like solutions for the purpose of multiorgan procurements and the preservation of organs from marginal donors. It has been shown in various experimental models that dextran 40 may successfully substitute for HES. Dextran 40 is not only cheaper but also has a variety of biological effects that may be beneficial during the graft reperfusion phase. The aim of this clinical study was to examine the efficacy of a dextran 40‐based preservation solution (Dex‐PS) for its use in human kidney graft preservation and to compare the transplantation results with kidneys preserved with UW solution. A total of 87 kidneys were preserved with Dex‐PS and matched with 87 kidneys preserved with UW solution. Both groups were comparable in terms of donor and recipient characteristics and both had a high proportion of kidneys from non‐heart‐beating donors. Patient survival and graft survival after 1 year were 95 % and 86 % for the Dex‐PS group and 94 % and 90 % for the UW group, respectively (P= NS). Primary nonfunction, delayed graft function, postoperative need for dialysis, and follow‐up of serum creat‐inine were statistically comparable between these two groups. We conclude that dextran 40 can safely replace HES in UW solution for the purpose of clinical kidney preservation. There were no statistically detectable differences in graft performance between the kidneys preserved with UW and those preserved with Dex‐PS.</description><identifier>ISSN: 0934-0874</identifier><identifier>EISSN: 1432-2277</identifier><identifier>DOI: 10.1111/j.1432-2277.1996.tb00849.x</identifier><identifier>PMID: 8748408</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine - chemistry ; Adult ; Allopurinol - chemistry ; Biological and medical sciences ; Colloids ; Creatinine - blood ; dextran 40 ; dextran 40. Dextran 40 ; Dextrans ; Female ; Glutathione - chemistry ; Graft Survival ; Humans ; Hydroxyethyl Starch Derivatives ; Insulin - chemistry ; Kidney preservation ; kidney preservation. UW solution ; Kidney Transplantation - methods ; Kidney Transplantation - physiology ; Male ; Medical sciences ; Middle Aged ; Organ Preservation - methods ; Organ Preservation Solutions ; Raffinose - chemistry ; Solutions ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system</subject><ispartof>Transplant international, 1996-01, Vol.9 (1), p.32-37</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3122-ca1deed5c29eef0790a3d46b7a5bd16c83b630a40beacd7b62e7ee5002366bb3</citedby><cites>FETCH-LOGICAL-c3122-ca1deed5c29eef0790a3d46b7a5bd16c83b630a40beacd7b62e7ee5002366bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2955800$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8748408$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Candinas, Daniel</creatorcontrib><creatorcontrib>Largiadèr, Felix</creatorcontrib><creatorcontrib>Binswanger, Ulrich</creatorcontrib><creatorcontrib>Sutherland, David E. R.</creatorcontrib><creatorcontrib>Schlumpf, Rolf</creatorcontrib><title>A novel dextran 40‐based preservation solution</title><title>Transplant international</title><addtitle>Transpl Int</addtitle><description>Although the University of Wisconsin (UW) solution has become the standard solution for the preservation of kidneys for transplantation, the importance of the colloid hydroxyethylstarch (HES), one of the key compounds of the UW solution, has been questioned repeatedly. It is now established that HES is not necessary for routine kidney preservation. However, colloids may still be advantageous in UW like solutions for the purpose of multiorgan procurements and the preservation of organs from marginal donors. It has been shown in various experimental models that dextran 40 may successfully substitute for HES. Dextran 40 is not only cheaper but also has a variety of biological effects that may be beneficial during the graft reperfusion phase. The aim of this clinical study was to examine the efficacy of a dextran 40‐based preservation solution (Dex‐PS) for its use in human kidney graft preservation and to compare the transplantation results with kidneys preserved with UW solution. A total of 87 kidneys were preserved with Dex‐PS and matched with 87 kidneys preserved with UW solution. Both groups were comparable in terms of donor and recipient characteristics and both had a high proportion of kidneys from non‐heart‐beating donors. Patient survival and graft survival after 1 year were 95 % and 86 % for the Dex‐PS group and 94 % and 90 % for the UW group, respectively (P= NS). Primary nonfunction, delayed graft function, postoperative need for dialysis, and follow‐up of serum creat‐inine were statistically comparable between these two groups. We conclude that dextran 40 can safely replace HES in UW solution for the purpose of clinical kidney preservation. There were no statistically detectable differences in graft performance between the kidneys preserved with UW and those preserved with Dex‐PS.</description><subject>Adenosine - chemistry</subject><subject>Adult</subject><subject>Allopurinol - chemistry</subject><subject>Biological and medical sciences</subject><subject>Colloids</subject><subject>Creatinine - blood</subject><subject>dextran 40</subject><subject>dextran 40. Dextran 40</subject><subject>Dextrans</subject><subject>Female</subject><subject>Glutathione - chemistry</subject><subject>Graft Survival</subject><subject>Humans</subject><subject>Hydroxyethyl Starch Derivatives</subject><subject>Insulin - chemistry</subject><subject>Kidney preservation</subject><subject>kidney preservation. UW solution</subject><subject>Kidney Transplantation - methods</subject><subject>Kidney Transplantation - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Organ Preservation - methods</subject><subject>Organ Preservation Solutions</subject><subject>Raffinose - chemistry</subject><subject>Solutions</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><issn>0934-0874</issn><issn>1432-2277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkN1KwzAUx4Moc04fQSgi3rWefLRpBS_G8GMwEGT3IUlPoaNrZ9Ppducj-Iw-iSkruzc3J5z_7ySHHyE3FCLqz_0qooKzkDEpI5plSdQZgFRk0e6EjI_RKRlDxkUIqRTn5MK5FQCwNIYRGflWKiAdE5gGdfOJVZDjrmt1HQj4_f4x2mEebFp02H7qrmzqwDXVtr9ckrNCVw6vhjohy-en5ew1XLy9zGfTRWg5ZSy0muaIeWxZhliAzEDzXCRG6tjkNLEpNwkHLcCgtrk0CUOJGPsFeZIYwyfk7vDspm0-tug6tS6dxarSNTZbp2TKEiEF9-DDAbRt41yLhdq05Vq3e0VB9bbUSvVKVK9E9bbUYEvt_PD18MvWrDE_jg56fH475NpZXRVekC3dEWNZHKcAHns8YF9lhft_LKCW73PO-B-484df</recordid><startdate>199601</startdate><enddate>199601</enddate><creator>Candinas, Daniel</creator><creator>Largiadèr, Felix</creator><creator>Binswanger, Ulrich</creator><creator>Sutherland, David E. R.</creator><creator>Schlumpf, Rolf</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Publishing</general><scope>IQODW</scope><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>199601</creationdate><title>A novel dextran 40‐based preservation solution</title><author>Candinas, Daniel ; Largiadèr, Felix ; Binswanger, Ulrich ; Sutherland, David E. R. ; Schlumpf, Rolf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3122-ca1deed5c29eef0790a3d46b7a5bd16c83b630a40beacd7b62e7ee5002366bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adenosine - chemistry</topic><topic>Adult</topic><topic>Allopurinol - chemistry</topic><topic>Biological and medical sciences</topic><topic>Colloids</topic><topic>Creatinine - blood</topic><topic>dextran 40</topic><topic>dextran 40. Dextran 40</topic><topic>Dextrans</topic><topic>Female</topic><topic>Glutathione - chemistry</topic><topic>Graft Survival</topic><topic>Humans</topic><topic>Hydroxyethyl Starch Derivatives</topic><topic>Insulin - chemistry</topic><topic>Kidney preservation</topic><topic>kidney preservation. UW solution</topic><topic>Kidney Transplantation - methods</topic><topic>Kidney Transplantation - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Organ Preservation - methods</topic><topic>Organ Preservation Solutions</topic><topic>Raffinose - chemistry</topic><topic>Solutions</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Candinas, Daniel</creatorcontrib><creatorcontrib>Largiadèr, Felix</creatorcontrib><creatorcontrib>Binswanger, Ulrich</creatorcontrib><creatorcontrib>Sutherland, David E. R.</creatorcontrib><creatorcontrib>Schlumpf, Rolf</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>Transplant international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Candinas, Daniel</au><au>Largiadèr, Felix</au><au>Binswanger, Ulrich</au><au>Sutherland, David E. R.</au><au>Schlumpf, Rolf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel dextran 40‐based preservation solution</atitle><jtitle>Transplant international</jtitle><addtitle>Transpl Int</addtitle><date>1996-01</date><risdate>1996</risdate><volume>9</volume><issue>1</issue><spage>32</spage><epage>37</epage><pages>32-37</pages><issn>0934-0874</issn><eissn>1432-2277</eissn><abstract>Although the University of Wisconsin (UW) solution has become the standard solution for the preservation of kidneys for transplantation, the importance of the colloid hydroxyethylstarch (HES), one of the key compounds of the UW solution, has been questioned repeatedly. It is now established that HES is not necessary for routine kidney preservation. However, colloids may still be advantageous in UW like solutions for the purpose of multiorgan procurements and the preservation of organs from marginal donors. It has been shown in various experimental models that dextran 40 may successfully substitute for HES. Dextran 40 is not only cheaper but also has a variety of biological effects that may be beneficial during the graft reperfusion phase. The aim of this clinical study was to examine the efficacy of a dextran 40‐based preservation solution (Dex‐PS) for its use in human kidney graft preservation and to compare the transplantation results with kidneys preserved with UW solution. A total of 87 kidneys were preserved with Dex‐PS and matched with 87 kidneys preserved with UW solution. Both groups were comparable in terms of donor and recipient characteristics and both had a high proportion of kidneys from non‐heart‐beating donors. Patient survival and graft survival after 1 year were 95 % and 86 % for the Dex‐PS group and 94 % and 90 % for the UW group, respectively (P= NS). Primary nonfunction, delayed graft function, postoperative need for dialysis, and follow‐up of serum creat‐inine were statistically comparable between these two groups. We conclude that dextran 40 can safely replace HES in UW solution for the purpose of clinical kidney preservation. There were no statistically detectable differences in graft performance between the kidneys preserved with UW and those preserved with Dex‐PS.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8748408</pmid><doi>10.1111/j.1432-2277.1996.tb00849.x</doi><tpages>6</tpages></addata></record> |
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subjects | Adenosine - chemistry Adult Allopurinol - chemistry Biological and medical sciences Colloids Creatinine - blood dextran 40 dextran 40. Dextran 40 Dextrans Female Glutathione - chemistry Graft Survival Humans Hydroxyethyl Starch Derivatives Insulin - chemistry Kidney preservation kidney preservation. UW solution Kidney Transplantation - methods Kidney Transplantation - physiology Male Medical sciences Middle Aged Organ Preservation - methods Organ Preservation Solutions Raffinose - chemistry Solutions Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system |
title | A novel dextran 40‐based preservation solution |
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