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A comparison between cyclosporine and tacrolimus-based immunosuppression for renal allografts: renal function and blood pressure after 5 years
The choice of initial immunosuppressive therapy (IST) following solid organ transplant remains a source of some controversy. Cyclosporine A (CsA) has been the basis of most IST protocols over the past two decades but has recently been supplanted in many centers by the use of tacrolimus (TAC)-based p...
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Published in: | Transplantation proceedings 2003-11, Vol.35 (7), p.2391-2394 |
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description | The choice of initial immunosuppressive therapy (IST) following solid organ transplant remains a source of some controversy. Cyclosporine A (CsA) has been the basis of most IST protocols over the past two decades but has recently been supplanted in many centers by the use of tacrolimus (TAC)-based protocols. Renal allograft recipients in London may receive either CsA or TAC based IST, along with prednisone and azathioprine or (since 1999) mycophenolate mofetil (MMF). The decision is based on criteria such as age, gender, diabetic status, and lipid levels, which are felt to be impacted by the delivery of CsA or TAC based IST. The present analysis focuses on the results of BP and renal function in renal transplant patients receiving CsA or TAC based initial therapy during the period January 1, 1996 to June 30, 2002. Patients receiving TAC based IST were significantly younger than those receiving CsA (44 ± 13.9 vs 50.5 ± 12.3 years;
P < .004). Mean arterial pressure (MAP) was lower in the TAC patients at 1 month (97.8 ± 13.1 vs 103.2 ± 11.8 mm Hg;
P = .035), but became equivalent to CsA-treated patients for the balance of the follow-up period of up to 60 m. Serum creatinine was not significantly different between groups at any time during up to 60 months of follow-up. Based on these results, it seems apparent that the choice of calcineurin inhibitor may not influence renal function or blood pressure in long-term renal allograft survivors. |
doi_str_mv | 10.1016/j.transproceed.2003.09.094 |
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P < .004). Mean arterial pressure (MAP) was lower in the TAC patients at 1 month (97.8 ± 13.1 vs 103.2 ± 11.8 mm Hg;
P = .035), but became equivalent to CsA-treated patients for the balance of the follow-up period of up to 60 m. Serum creatinine was not significantly different between groups at any time during up to 60 months of follow-up. Based on these results, it seems apparent that the choice of calcineurin inhibitor may not influence renal function or blood pressure in long-term renal allograft survivors.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2003.09.094</identifier><identifier>PMID: 14611965</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Biological and medical sciences ; Blood Pressure - drug effects ; Creatinine - blood ; Cyclosporine - therapeutic use ; Diabetes Mellitus - epidemiology ; Drug toxicity and drugs side effects treatment ; Female ; Follow-Up Studies ; Humans ; Immunosuppressive Agents - therapeutic use ; Isoantibodies - blood ; Kidney Function Tests ; Kidney Transplantation - immunology ; Kidney Transplantation - physiology ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Postoperative Complications - epidemiology ; Retrospective Studies ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Tacrolimus - therapeutic use ; Time Factors ; Toxicity: urogenital system</subject><ispartof>Transplantation proceedings, 2003-11, Vol.35 (7), p.2391-2394</ispartof><rights>2003 Elsevier Science Inc.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-ffd3896ff18976ed8fca2de504f9c355e49387336a950be849706d50fe3690ef3</citedby><cites>FETCH-LOGICAL-c406t-ffd3896ff18976ed8fca2de504f9c355e49387336a950be849706d50fe3690ef3</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=15285890$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14611965$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muirhead, N</creatorcontrib><creatorcontrib>House, A</creatorcontrib><creatorcontrib>Hollomby, D.J</creatorcontrib><creatorcontrib>Jevnikar, A.M</creatorcontrib><title>A comparison between cyclosporine and tacrolimus-based immunosuppression for renal allografts: renal function and blood pressure after 5 years</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>The choice of initial immunosuppressive therapy (IST) following solid organ transplant remains a source of some controversy. Cyclosporine A (CsA) has been the basis of most IST protocols over the past two decades but has recently been supplanted in many centers by the use of tacrolimus (TAC)-based protocols. Renal allograft recipients in London may receive either CsA or TAC based IST, along with prednisone and azathioprine or (since 1999) mycophenolate mofetil (MMF). The decision is based on criteria such as age, gender, diabetic status, and lipid levels, which are felt to be impacted by the delivery of CsA or TAC based IST. The present analysis focuses on the results of BP and renal function in renal transplant patients receiving CsA or TAC based initial therapy during the period January 1, 1996 to June 30, 2002. Patients receiving TAC based IST were significantly younger than those receiving CsA (44 ± 13.9 vs 50.5 ± 12.3 years;
P < .004). Mean arterial pressure (MAP) was lower in the TAC patients at 1 month (97.8 ± 13.1 vs 103.2 ± 11.8 mm Hg;
P = .035), but became equivalent to CsA-treated patients for the balance of the follow-up period of up to 60 m. Serum creatinine was not significantly different between groups at any time during up to 60 months of follow-up. Based on these results, it seems apparent that the choice of calcineurin inhibitor may not influence renal function or blood pressure in long-term renal allograft survivors.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Creatinine - blood</subject><subject>Cyclosporine - therapeutic use</subject><subject>Diabetes Mellitus - epidemiology</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Isoantibodies - blood</subject><subject>Kidney Function Tests</subject><subject>Kidney Transplantation - immunology</subject><subject>Kidney Transplantation - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Postoperative Complications - epidemiology</subject><subject>Retrospective Studies</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Tacrolimus - therapeutic use</subject><subject>Time Factors</subject><subject>Toxicity: urogenital system</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkcGOFCEQhonRuLOjr2CIid56hKZhmr1tVl1NNvGiZ0JDYZh0Q0t1a-YlfGYZZ6IeTSohwPf_BX8R8pKzHWdcvTnslmITziU7AL9rGRM7pmt1j8iG93vRtKoVj8mGsY43XHTyilwjHljdt514Sq54pzjXSm7Iz1vq8jTbEjEnOsDyAyBRd3RjxjmXmIDa5OliXcljnFZsBovgaZymNWVc57kAYqzakAstkOxI7Tjmr8WGBW8uJ2FNbjlBJ69hzNnT37q1VPuwQKGSHsEWfEaeBDsiPL-sW_Ll_bvPdx-ah0_3H-9uHxrXMbU0IXjRaxUC7_Vege-Ds60HybqgnZASOi1qDkJZLdkAfaf3THnJAgilGQSxJa_PvjXEbyvgYqaIDsbRJsgrmj0XkonqsCU3Z7D-H7FAMHOJky1Hw5k5TcMczL_TMKdpGKZrdVX84tJlHaZ690d6ib8Cry6ARWfHUI1cxL-cbHvZa1a5t2cOaibfIxSDLkJy4GMBtxif4_-85xcc4rOA</recordid><startdate>20031101</startdate><enddate>20031101</enddate><creator>Muirhead, N</creator><creator>House, A</creator><creator>Hollomby, D.J</creator><creator>Jevnikar, A.M</creator><general>Elsevier Inc</general><general>Elsevier Science</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>20031101</creationdate><title>A comparison between cyclosporine and tacrolimus-based immunosuppression for renal allografts: renal function and blood pressure after 5 years</title><author>Muirhead, N ; House, A ; Hollomby, D.J ; Jevnikar, A.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-ffd3896ff18976ed8fca2de504f9c355e49387336a950be849706d50fe3690ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Creatinine - blood</topic><topic>Cyclosporine - therapeutic use</topic><topic>Diabetes Mellitus - epidemiology</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Isoantibodies - blood</topic><topic>Kidney Function Tests</topic><topic>Kidney Transplantation - immunology</topic><topic>Kidney Transplantation - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Postoperative Complications - epidemiology</topic><topic>Retrospective Studies</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Tacrolimus - therapeutic use</topic><topic>Time Factors</topic><topic>Toxicity: urogenital system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muirhead, N</creatorcontrib><creatorcontrib>House, A</creatorcontrib><creatorcontrib>Hollomby, D.J</creatorcontrib><creatorcontrib>Jevnikar, A.M</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>Muirhead, N</au><au>House, A</au><au>Hollomby, D.J</au><au>Jevnikar, A.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A comparison between cyclosporine and tacrolimus-based immunosuppression for renal allografts: renal function and blood pressure after 5 years</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2003-11-01</date><risdate>2003</risdate><volume>35</volume><issue>7</issue><spage>2391</spage><epage>2394</epage><pages>2391-2394</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>The choice of initial immunosuppressive therapy (IST) following solid organ transplant remains a source of some controversy. Cyclosporine A (CsA) has been the basis of most IST protocols over the past two decades but has recently been supplanted in many centers by the use of tacrolimus (TAC)-based protocols. Renal allograft recipients in London may receive either CsA or TAC based IST, along with prednisone and azathioprine or (since 1999) mycophenolate mofetil (MMF). The decision is based on criteria such as age, gender, diabetic status, and lipid levels, which are felt to be impacted by the delivery of CsA or TAC based IST. The present analysis focuses on the results of BP and renal function in renal transplant patients receiving CsA or TAC based initial therapy during the period January 1, 1996 to June 30, 2002. Patients receiving TAC based IST were significantly younger than those receiving CsA (44 ± 13.9 vs 50.5 ± 12.3 years;
P < .004). Mean arterial pressure (MAP) was lower in the TAC patients at 1 month (97.8 ± 13.1 vs 103.2 ± 11.8 mm Hg;
P = .035), but became equivalent to CsA-treated patients for the balance of the follow-up period of up to 60 m. Serum creatinine was not significantly different between groups at any time during up to 60 months of follow-up. Based on these results, it seems apparent that the choice of calcineurin inhibitor may not influence renal function or blood pressure in long-term renal allograft survivors.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>14611965</pmid><doi>10.1016/j.transproceed.2003.09.094</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Blood Pressure - drug effects Creatinine - blood Cyclosporine - therapeutic use Diabetes Mellitus - epidemiology Drug toxicity and drugs side effects treatment Female Follow-Up Studies Humans Immunosuppressive Agents - therapeutic use Isoantibodies - blood Kidney Function Tests Kidney Transplantation - immunology Kidney Transplantation - physiology Male Medical sciences Middle Aged Pharmacology. Drug treatments Postoperative Complications - epidemiology Retrospective Studies Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Tacrolimus - therapeutic use Time Factors Toxicity: urogenital system |
title | A comparison between cyclosporine and tacrolimus-based immunosuppression for renal allografts: renal function and blood pressure after 5 years |
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