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How Long Should Initiation of Calcineurin Inhibitors Be Delayed to Protect Renal Function in Liver Transplantation?
Abstract Background and aim Delayed introduction of calcineurin inhibitors (CNI) in liver transplantation (OLT) seeks to protect renal function, although the optimal length of the delay is not well established. The aim of this study was to analyze the effects on renal function of CNI initiation on d...
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Published in: | Transplantation proceedings 2011-04, Vol.43 (3), p.697-698 |
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description | Abstract Background and aim Delayed introduction of calcineurin inhibitors (CNI) in liver transplantation (OLT) seeks to protect renal function, although the optimal length of the delay is not well established. The aim of this study was to analyze the effects on renal function of CNI initiation on different days after OLT. Methods We reviewed the charts of 260 OLT recipients. Group D1-a ( n = 36) underwent the standard initial immunosuppression at our center: namely, CNI introduction on day 1 with further daily administration to achieve target levels of 8 to 15 ng/mL for tacrolimus or 150 to 300 ng/mL for cyclosporine. Due to renal concerns, 126 patients (group D1-b) had CNI introduced on day 1 either not daily or at doses to achieve less than the target on at least two occasions. In 43 patients (group D2), CNI were introduced on day 2 in 23 on day 3 (group D3), in 12 on day 4 (group D4), and at least at day 5 in 20 others (group D5). In periods without CNI treatment, patients received mycophenolate mofetil. Steroids were administered to all patients. The study period included the first 3 months post-OLT. Renal function was estimated as creatinine clearance (CrCl) using the Cockcroft-Gault equation. Results Changes in CrCl from pre-OLT to month 3 were −19% ± 28% in group D1-a; −27% ± 19% in group D1-b; −29% ± 19% in group D2; −23% ± 26% in group D3; −4% ± 38% in group D4, and +4% ± 33% in group D5 ( P < .05 vs groups D1-a, D1-b, D2, and D3). On multivariate analysis, CNI introduction at day ≥5 was protective for kidneys when adjusted for other variables that potentially influence renal function. Conclusion CNI should be introduced at day 5 after OLT to protect renal function. |
doi_str_mv | 10.1016/j.transproceed.2011.01.091 |
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The aim of this study was to analyze the effects on renal function of CNI initiation on different days after OLT. Methods We reviewed the charts of 260 OLT recipients. Group D1-a ( n = 36) underwent the standard initial immunosuppression at our center: namely, CNI introduction on day 1 with further daily administration to achieve target levels of 8 to 15 ng/mL for tacrolimus or 150 to 300 ng/mL for cyclosporine. Due to renal concerns, 126 patients (group D1-b) had CNI introduced on day 1 either not daily or at doses to achieve less than the target on at least two occasions. In 43 patients (group D2), CNI were introduced on day 2 in 23 on day 3 (group D3), in 12 on day 4 (group D4), and at least at day 5 in 20 others (group D5). In periods without CNI treatment, patients received mycophenolate mofetil. Steroids were administered to all patients. The study period included the first 3 months post-OLT. Renal function was estimated as creatinine clearance (CrCl) using the Cockcroft-Gault equation. Results Changes in CrCl from pre-OLT to month 3 were −19% ± 28% in group D1-a; −27% ± 19% in group D1-b; −29% ± 19% in group D2; −23% ± 26% in group D3; −4% ± 38% in group D4, and +4% ± 33% in group D5 ( P < .05 vs groups D1-a, D1-b, D2, and D3). On multivariate analysis, CNI introduction at day ≥5 was protective for kidneys when adjusted for other variables that potentially influence renal function. Conclusion CNI should be introduced at day 5 after OLT to protect renal function.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2011.01.091</identifier><identifier>PMID: 21486577</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adult ; Biological and medical sciences ; Calcineurin Inhibitors ; Drug Administration Schedule ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Immunosuppressive Agents - administration & dosage ; Kidney - physiopathology ; Kidney Function Tests ; Liver Transplantation ; Liver, biliary tract, pancreas, portal circulation, spleen ; Male ; Medical Audit ; Medical sciences ; Middle Aged ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the digestive system ; Tacrolimus - administration & dosage ; Tissue, organ and graft immunology</subject><ispartof>Transplantation proceedings, 2011-04, Vol.43 (3), p.697-698</ispartof><rights>Elsevier Inc.</rights><rights>2011 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-50451e80f35577e228a7b65aa3a4a67e6f0facc4d5cf79ef99d6f8c43145e8cc3</citedby><cites>FETCH-LOGICAL-c464t-50451e80f35577e228a7b65aa3a4a67e6f0facc4d5cf79ef99d6f8c43145e8cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24108674$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21486577$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rafael-Valdivia, L</creatorcontrib><creatorcontrib>Mendoza, M.A</creatorcontrib><creatorcontrib>Martinez-Saldivar, B</creatorcontrib><creatorcontrib>Sanchez-Fueyo, A</creatorcontrib><creatorcontrib>Brunet, M</creatorcontrib><creatorcontrib>Garcia-Valdecasas, J.C</creatorcontrib><creatorcontrib>Rimola, A</creatorcontrib><title>How Long Should Initiation of Calcineurin Inhibitors Be Delayed to Protect Renal Function in Liver Transplantation?</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract Background and aim Delayed introduction of calcineurin inhibitors (CNI) in liver transplantation (OLT) seeks to protect renal function, although the optimal length of the delay is not well established. The aim of this study was to analyze the effects on renal function of CNI initiation on different days after OLT. Methods We reviewed the charts of 260 OLT recipients. Group D1-a ( n = 36) underwent the standard initial immunosuppression at our center: namely, CNI introduction on day 1 with further daily administration to achieve target levels of 8 to 15 ng/mL for tacrolimus or 150 to 300 ng/mL for cyclosporine. Due to renal concerns, 126 patients (group D1-b) had CNI introduced on day 1 either not daily or at doses to achieve less than the target on at least two occasions. In 43 patients (group D2), CNI were introduced on day 2 in 23 on day 3 (group D3), in 12 on day 4 (group D4), and at least at day 5 in 20 others (group D5). In periods without CNI treatment, patients received mycophenolate mofetil. Steroids were administered to all patients. The study period included the first 3 months post-OLT. Renal function was estimated as creatinine clearance (CrCl) using the Cockcroft-Gault equation. Results Changes in CrCl from pre-OLT to month 3 were −19% ± 28% in group D1-a; −27% ± 19% in group D1-b; −29% ± 19% in group D2; −23% ± 26% in group D3; −4% ± 38% in group D4, and +4% ± 33% in group D5 ( P < .05 vs groups D1-a, D1-b, D2, and D3). On multivariate analysis, CNI introduction at day ≥5 was protective for kidneys when adjusted for other variables that potentially influence renal function. Conclusion CNI should be introduced at day 5 after OLT to protect renal function.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Calcineurin Inhibitors</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Kidney - physiopathology</subject><subject>Kidney Function Tests</subject><subject>Liver Transplantation</subject><subject>Liver, biliary tract, pancreas, portal circulation, spleen</subject><subject>Male</subject><subject>Medical Audit</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the digestive system</subject><subject>Tacrolimus - administration & dosage</subject><subject>Tissue, organ and graft immunology</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqNUmFrFDEQDaLYs_oXJAjST3tOdrPZXT8o9Wpt4UCx9XPIZSc2515Sk2zl_r3ZuystfhIGQpj33jzeDCFvGMwZMPFuPU9BuXgbvEbs5yUwNodcHXtCZqxtqqIUZfWUzAA4K1jF6yPyIsY15H_Jq-fkqGS8FXXTzEi88H_o0ruf9OrGj0NPL51NViXrHfWGLtSgrcMxWJc7N3Zlkw-RfkJ6hoPaYk-Tp9-CT6gT_Y5ODfR8dHpHz5SlvcNAr3duB-XSTvfjS_LMqCHiq8N7TH6cf75eXBTLr18uF6fLQnPBU1EDrxm2YKo6W8WybFWzErVSleJKNCgMGKU172ttmg5N1_XCtJpXjNfYal0dk5O9bk7q94gxyY2NGofsBP0YZStKgAY4z8j3e6QOPsaARt4Gu1FhKxnIKXO5lo8zl1PmEnJ1LJNfH8aMq03u3VPvQ86AtweAiloNJgtpGx9wnEErmsnF2R6HOZQ7i0FGbdFp7G3I-cre2__z8-EfGT1YZ_PkX7jFuPZjyHuKkslYSpBX05VMR8IYAGvqtvoLdNG8wA</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>Rafael-Valdivia, L</creator><creator>Mendoza, M.A</creator><creator>Martinez-Saldivar, B</creator><creator>Sanchez-Fueyo, A</creator><creator>Brunet, M</creator><creator>Garcia-Valdecasas, J.C</creator><creator>Rimola, A</creator><general>Elsevier Inc</general><general>Elsevier</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>20110401</creationdate><title>How Long Should Initiation of Calcineurin Inhibitors Be Delayed to Protect Renal Function in Liver Transplantation?</title><author>Rafael-Valdivia, L ; Mendoza, M.A ; Martinez-Saldivar, B ; Sanchez-Fueyo, A ; Brunet, M ; Garcia-Valdecasas, J.C ; Rimola, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-50451e80f35577e228a7b65aa3a4a67e6f0facc4d5cf79ef99d6f8c43145e8cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Calcineurin Inhibitors</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Kidney - physiopathology</topic><topic>Kidney Function Tests</topic><topic>Liver Transplantation</topic><topic>Liver, biliary tract, pancreas, portal circulation, spleen</topic><topic>Male</topic><topic>Medical Audit</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the digestive system</topic><topic>Tacrolimus - administration & dosage</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rafael-Valdivia, L</creatorcontrib><creatorcontrib>Mendoza, M.A</creatorcontrib><creatorcontrib>Martinez-Saldivar, B</creatorcontrib><creatorcontrib>Sanchez-Fueyo, A</creatorcontrib><creatorcontrib>Brunet, M</creatorcontrib><creatorcontrib>Garcia-Valdecasas, J.C</creatorcontrib><creatorcontrib>Rimola, A</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>Rafael-Valdivia, L</au><au>Mendoza, M.A</au><au>Martinez-Saldivar, B</au><au>Sanchez-Fueyo, A</au><au>Brunet, M</au><au>Garcia-Valdecasas, J.C</au><au>Rimola, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>How Long Should Initiation of Calcineurin Inhibitors Be Delayed to Protect Renal Function in Liver Transplantation?</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>43</volume><issue>3</issue><spage>697</spage><epage>698</epage><pages>697-698</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>Abstract Background and aim Delayed introduction of calcineurin inhibitors (CNI) in liver transplantation (OLT) seeks to protect renal function, although the optimal length of the delay is not well established. The aim of this study was to analyze the effects on renal function of CNI initiation on different days after OLT. Methods We reviewed the charts of 260 OLT recipients. Group D1-a ( n = 36) underwent the standard initial immunosuppression at our center: namely, CNI introduction on day 1 with further daily administration to achieve target levels of 8 to 15 ng/mL for tacrolimus or 150 to 300 ng/mL for cyclosporine. Due to renal concerns, 126 patients (group D1-b) had CNI introduced on day 1 either not daily or at doses to achieve less than the target on at least two occasions. In 43 patients (group D2), CNI were introduced on day 2 in 23 on day 3 (group D3), in 12 on day 4 (group D4), and at least at day 5 in 20 others (group D5). In periods without CNI treatment, patients received mycophenolate mofetil. Steroids were administered to all patients. The study period included the first 3 months post-OLT. Renal function was estimated as creatinine clearance (CrCl) using the Cockcroft-Gault equation. Results Changes in CrCl from pre-OLT to month 3 were −19% ± 28% in group D1-a; −27% ± 19% in group D1-b; −29% ± 19% in group D2; −23% ± 26% in group D3; −4% ± 38% in group D4, and +4% ± 33% in group D5 ( P < .05 vs groups D1-a, D1-b, D2, and D3). On multivariate analysis, CNI introduction at day ≥5 was protective for kidneys when adjusted for other variables that potentially influence renal function. Conclusion CNI should be introduced at day 5 after OLT to protect renal function.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>21486577</pmid><doi>10.1016/j.transproceed.2011.01.091</doi><tpages>2</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Calcineurin Inhibitors Drug Administration Schedule Female Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Immunosuppressive Agents - administration & dosage Kidney - physiopathology Kidney Function Tests Liver Transplantation Liver, biliary tract, pancreas, portal circulation, spleen Male Medical Audit Medical sciences Middle Aged Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system Tacrolimus - administration & dosage Tissue, organ and graft immunology |
title | How Long Should Initiation of Calcineurin Inhibitors Be Delayed to Protect Renal Function in Liver Transplantation? |
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