Prevalence and risk factors of recurrent cytomegalovirus infection in kidney transplant recipients
Recurrence of cytomegalovirus (CMV) infection following solid organ transplantation causes mortality and morbidity in allograft recipients. The aim of this study was to evaluate prevalence and risk factors of recurrent CMV infection in kidney transplant patients. Four hundred and twenty-seven consec...
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Veröffentlicht in: | Iranian journal of kidney diseases 2014-05, Vol.8 (3), p.231 |
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creator | Nafar, Mohsen Roshan, Azamosadat Pour-Reza-Gholi, Fatemeh Samadian, Fariba Ahmadpoor, Pedram Samavat, Shiva Abbasi, Mohammad Amin |
description | Recurrence of cytomegalovirus (CMV) infection following solid organ transplantation causes mortality and morbidity in allograft recipients. The aim of this study was to evaluate prevalence and risk factors of recurrent CMV infection in kidney transplant patients.
Four hundred and twenty-seven consecutive kidney transplant recipients were included in this retrospective cohort study. Both donors and recipients were CMV seropositive. Recurrent CMV infection (symptomatic or asymptomatic) was defined as detection of CMV infection in a patient who has had previously documented infection and who had not have virus detected for an interval of at least 4 weeks during active surveillance.
Of 427 recipients, 71 (16.6%) had CMV infection, of which 19 (4.4%) were recurrent infection. Donor source, dialysis duration before transplantation, recipient and donor age and sex, and administration of antithymocyte globulin and prophylactic treatment ganciclovir were not associated with CMV infection or recurrence. The use of tacrolimus in the immunosuppressive regimen as compared to cyclosporine was an independent risk factor for CMV infection but not recurrent infection.
Intensive immunosuppressive regimen, such as using tacrolimus, might be associated with a higher risk for CMV infection, but this study was not able to document the same association for recurrent CMV disease. In patients receiving immunosuppressive regimens that include tacrolimus and antithymocyte globulin, prophylactic treatment for CMV disease with ganciclovir is recommended. |
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Four hundred and twenty-seven consecutive kidney transplant recipients were included in this retrospective cohort study. Both donors and recipients were CMV seropositive. Recurrent CMV infection (symptomatic or asymptomatic) was defined as detection of CMV infection in a patient who has had previously documented infection and who had not have virus detected for an interval of at least 4 weeks during active surveillance.
Of 427 recipients, 71 (16.6%) had CMV infection, of which 19 (4.4%) were recurrent infection. Donor source, dialysis duration before transplantation, recipient and donor age and sex, and administration of antithymocyte globulin and prophylactic treatment ganciclovir were not associated with CMV infection or recurrence. The use of tacrolimus in the immunosuppressive regimen as compared to cyclosporine was an independent risk factor for CMV infection but not recurrent infection.
Intensive immunosuppressive regimen, such as using tacrolimus, might be associated with a higher risk for CMV infection, but this study was not able to document the same association for recurrent CMV disease. In patients receiving immunosuppressive regimens that include tacrolimus and antithymocyte globulin, prophylactic treatment for CMV disease with ganciclovir is recommended.</description><identifier>ISSN: 1735-8582</identifier><identifier>EISSN: 1735-8604</identifier><identifier>PMID: 24878947</identifier><language>eng</language><publisher>Iran: Iranian Society of Nephrology</publisher><subject>Adolescent ; Adult ; Aged ; Antilymphocyte Serum - adverse effects ; Antiviral Agents - therapeutic use ; Cytomegalovirus Infections - etiology ; Cytomegalovirus Infections - prevention & control ; Female ; Ganciclovir - therapeutic use ; Humans ; Immunosuppressive Agents - adverse effects ; Kidney Transplantation - adverse effects ; Male ; Middle Aged ; Postoperative Complications - etiology ; Postoperative Complications - prevention & control ; Recurrence ; Retrospective Studies ; Risk Factors ; Secondary Prevention - methods ; Tacrolimus - adverse effects ; Young Adult</subject><ispartof>Iranian journal of kidney diseases, 2014-05, Vol.8 (3), p.231</ispartof><rights>Copyright Iranian Society of Nephrology May 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24878947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nafar, Mohsen</creatorcontrib><creatorcontrib>Roshan, Azamosadat</creatorcontrib><creatorcontrib>Pour-Reza-Gholi, Fatemeh</creatorcontrib><creatorcontrib>Samadian, Fariba</creatorcontrib><creatorcontrib>Ahmadpoor, Pedram</creatorcontrib><creatorcontrib>Samavat, Shiva</creatorcontrib><creatorcontrib>Abbasi, Mohammad Amin</creatorcontrib><title>Prevalence and risk factors of recurrent cytomegalovirus infection in kidney transplant recipients</title><title>Iranian journal of kidney diseases</title><addtitle>Iran J Kidney Dis</addtitle><description>Recurrence of cytomegalovirus (CMV) infection following solid organ transplantation causes mortality and morbidity in allograft recipients. The aim of this study was to evaluate prevalence and risk factors of recurrent CMV infection in kidney transplant patients.
Four hundred and twenty-seven consecutive kidney transplant recipients were included in this retrospective cohort study. Both donors and recipients were CMV seropositive. Recurrent CMV infection (symptomatic or asymptomatic) was defined as detection of CMV infection in a patient who has had previously documented infection and who had not have virus detected for an interval of at least 4 weeks during active surveillance.
Of 427 recipients, 71 (16.6%) had CMV infection, of which 19 (4.4%) were recurrent infection. Donor source, dialysis duration before transplantation, recipient and donor age and sex, and administration of antithymocyte globulin and prophylactic treatment ganciclovir were not associated with CMV infection or recurrence. The use of tacrolimus in the immunosuppressive regimen as compared to cyclosporine was an independent risk factor for CMV infection but not recurrent infection.
Intensive immunosuppressive regimen, such as using tacrolimus, might be associated with a higher risk for CMV infection, but this study was not able to document the same association for recurrent CMV disease. In patients receiving immunosuppressive regimens that include tacrolimus and antithymocyte globulin, prophylactic treatment for CMV disease with ganciclovir is recommended.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antilymphocyte Serum - adverse effects</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Cytomegalovirus Infections - etiology</subject><subject>Cytomegalovirus Infections - prevention & control</subject><subject>Female</subject><subject>Ganciclovir - therapeutic use</subject><subject>Humans</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Postoperative Complications - etiology</subject><subject>Postoperative Complications - prevention & control</subject><subject>Recurrence</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Secondary Prevention - methods</subject><subject>Tacrolimus - adverse effects</subject><subject>Young Adult</subject><issn>1735-8582</issn><issn>1735-8604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNo1UFtLwzAYDaK4Wf0LEvC5kFuT9FGGl8FAH_S5JE0q2dqkJulg_96A29N3PjgXzrkCayxoU0uO2PUFN5KswF1Ke4Q4bRm6BSvCpJAtE2ugP6M9qtH63kLlDYwuHeCg-hxigmGA0fZLjNZn2J9ymOyPGsPRxSVB5wfbZxd8QfDgjLcnmKPyaR5VoRehm10RpntwM6gx2YfzrcD368vX5r3efbxtN8-7eiaI57rFmjFEiehbzY2VlAksGiy1ZkYrRZFBWBFuBMZNi1pJSCmAePmkwZwrWoGnf985ht_FptztwxJ9iexwQwWSkhT_CjyeWYuerOnm6CYVT91lEvoHCLReXg</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>Nafar, Mohsen</creator><creator>Roshan, Azamosadat</creator><creator>Pour-Reza-Gholi, Fatemeh</creator><creator>Samadian, Fariba</creator><creator>Ahmadpoor, Pedram</creator><creator>Samavat, Shiva</creator><creator>Abbasi, Mohammad Amin</creator><general>Iranian Society of Nephrology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20140501</creationdate><title>Prevalence and risk factors of recurrent cytomegalovirus infection in kidney transplant recipients</title><author>Nafar, Mohsen ; Roshan, Azamosadat ; Pour-Reza-Gholi, Fatemeh ; Samadian, Fariba ; Ahmadpoor, Pedram ; Samavat, Shiva ; Abbasi, Mohammad Amin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p206t-91b440327c9b6de834717518bb4dbaa30d01a26d7115909822947061158d166a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antilymphocyte Serum - adverse effects</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Cytomegalovirus Infections - etiology</topic><topic>Cytomegalovirus Infections - prevention & control</topic><topic>Female</topic><topic>Ganciclovir - therapeutic use</topic><topic>Humans</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Postoperative Complications - etiology</topic><topic>Postoperative Complications - prevention & control</topic><topic>Recurrence</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Secondary Prevention - methods</topic><topic>Tacrolimus - adverse effects</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nafar, Mohsen</creatorcontrib><creatorcontrib>Roshan, Azamosadat</creatorcontrib><creatorcontrib>Pour-Reza-Gholi, Fatemeh</creatorcontrib><creatorcontrib>Samadian, Fariba</creatorcontrib><creatorcontrib>Ahmadpoor, Pedram</creatorcontrib><creatorcontrib>Samavat, Shiva</creatorcontrib><creatorcontrib>Abbasi, Mohammad Amin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Iranian journal of kidney diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nafar, Mohsen</au><au>Roshan, Azamosadat</au><au>Pour-Reza-Gholi, Fatemeh</au><au>Samadian, Fariba</au><au>Ahmadpoor, Pedram</au><au>Samavat, Shiva</au><au>Abbasi, Mohammad Amin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence and risk factors of recurrent cytomegalovirus infection in kidney transplant recipients</atitle><jtitle>Iranian journal of kidney diseases</jtitle><addtitle>Iran J Kidney Dis</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>8</volume><issue>3</issue><spage>231</spage><pages>231-</pages><issn>1735-8582</issn><eissn>1735-8604</eissn><abstract>Recurrence of cytomegalovirus (CMV) infection following solid organ transplantation causes mortality and morbidity in allograft recipients. The aim of this study was to evaluate prevalence and risk factors of recurrent CMV infection in kidney transplant patients.
Four hundred and twenty-seven consecutive kidney transplant recipients were included in this retrospective cohort study. Both donors and recipients were CMV seropositive. Recurrent CMV infection (symptomatic or asymptomatic) was defined as detection of CMV infection in a patient who has had previously documented infection and who had not have virus detected for an interval of at least 4 weeks during active surveillance.
Of 427 recipients, 71 (16.6%) had CMV infection, of which 19 (4.4%) were recurrent infection. Donor source, dialysis duration before transplantation, recipient and donor age and sex, and administration of antithymocyte globulin and prophylactic treatment ganciclovir were not associated with CMV infection or recurrence. The use of tacrolimus in the immunosuppressive regimen as compared to cyclosporine was an independent risk factor for CMV infection but not recurrent infection.
Intensive immunosuppressive regimen, such as using tacrolimus, might be associated with a higher risk for CMV infection, but this study was not able to document the same association for recurrent CMV disease. In patients receiving immunosuppressive regimens that include tacrolimus and antithymocyte globulin, prophylactic treatment for CMV disease with ganciclovir is recommended.</abstract><cop>Iran</cop><pub>Iranian Society of Nephrology</pub><pmid>24878947</pmid></addata></record> |
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subjects | Adolescent Adult Aged Antilymphocyte Serum - adverse effects Antiviral Agents - therapeutic use Cytomegalovirus Infections - etiology Cytomegalovirus Infections - prevention & control Female Ganciclovir - therapeutic use Humans Immunosuppressive Agents - adverse effects Kidney Transplantation - adverse effects Male Middle Aged Postoperative Complications - etiology Postoperative Complications - prevention & control Recurrence Retrospective Studies Risk Factors Secondary Prevention - methods Tacrolimus - adverse effects Young Adult |
title | Prevalence and risk factors of recurrent cytomegalovirus infection in kidney transplant recipients |
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