A Hybrid Strategy for the Prevention of Cytomegalovirus-Related Complications in Pediatric Liver Transplantation Recipients
This single center, retrospective study describes experience with a hybrid prevention strategy combining short-course antiviral prophylaxis and preemptive cytomegalovirus (CMV) polymerase chain reaction (PCR) monitoring. One hundred twenty-two pediatric liver transplantation recipients were followed...
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Veröffentlicht in: | Transplantation 2009-05, Vol.87 (9), p.1318-1324 |
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creator | MADAN, Rebecca P CAMPBELL, Andrew L SHUST, Gail F KAHN, Alissa R WISTINGHAUSEN, Birte POSADA, Roberto KERKAR, Nanda SHNEIDER, Benjamin L EMRE, Sukru HEROLD, Betsy C |
description | This single center, retrospective study describes experience with a hybrid prevention strategy combining short-course antiviral prophylaxis and preemptive cytomegalovirus (CMV) polymerase chain reaction (PCR) monitoring.
One hundred twenty-two pediatric liver transplantation recipients were followed up for a median of 2.3 years posttransplantation. Subjects received a minimum of 14 days of postoperative ganciclovir, followed by monthly CMV PCR monitoring.
Forty-three CMV seronegative recipients received seropositive grafts and were considered high risk for CMV; 79 subjects were routine risk. CMV was detected by PCR in the absence of symptoms in 34.4% of subjects and was more likely in high risk than in routine risk recipients (58.1% vs. 21.8%, P=0.0001). Twelve subjects (9.8%) developed CMV disease (8 high risk vs. 4 routine risk, P=0.03). Three subjects developed acute rejection in the 6 months after detection of CMV, but CMV was preceded by rejection in 13 subjects. There were no mortalities secondary to CMV. A total of 38.5% of subjects were spared antiviral medications beyond their initial postoperative prophylaxis.
These results suggest that a hybrid preventative approach for CMV is a reasonable alternative to prolonged antiviral prophylaxis and may reduce unnecessary exposure to antiviral therapy. However, patients who receive intensified immunosuppression after acute rejection are at increased risk for CMV and may require extended prophylaxis and closer monitoring. |
doi_str_mv | 10.1097/TP.0b013e3181a19cda |
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One hundred twenty-two pediatric liver transplantation recipients were followed up for a median of 2.3 years posttransplantation. Subjects received a minimum of 14 days of postoperative ganciclovir, followed by monthly CMV PCR monitoring.
Forty-three CMV seronegative recipients received seropositive grafts and were considered high risk for CMV; 79 subjects were routine risk. CMV was detected by PCR in the absence of symptoms in 34.4% of subjects and was more likely in high risk than in routine risk recipients (58.1% vs. 21.8%, P=0.0001). Twelve subjects (9.8%) developed CMV disease (8 high risk vs. 4 routine risk, P=0.03). Three subjects developed acute rejection in the 6 months after detection of CMV, but CMV was preceded by rejection in 13 subjects. There were no mortalities secondary to CMV. A total of 38.5% of subjects were spared antiviral medications beyond their initial postoperative prophylaxis.
These results suggest that a hybrid preventative approach for CMV is a reasonable alternative to prolonged antiviral prophylaxis and may reduce unnecessary exposure to antiviral therapy. However, patients who receive intensified immunosuppression after acute rejection are at increased risk for CMV and may require extended prophylaxis and closer monitoring.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/TP.0b013e3181a19cda</identifier><identifier>PMID: 19424031</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adolescent ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Child ; Child, Preschool ; Cytomegalovirus ; Cytomegalovirus - genetics ; Cytomegalovirus Infections - epidemiology ; Cytomegalovirus Infections - prevention & control ; DNA, Viral - analysis ; Follow-Up Studies ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Ganciclovir - therapeutic use ; Humans ; Infant ; Liver Transplantation - adverse effects ; Liver, biliary tract, pancreas, portal circulation, spleen ; Medical sciences ; Polymerase Chain Reaction - methods ; Postoperative Complications - prevention & control ; Postoperative Complications - virology ; Prevention and actions ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Retrospective Studies ; Risk Assessment ; Risk Reduction Behavior ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the digestive system ; Time Factors ; Tissue, organ and graft immunology ; Viremia - epidemiology</subject><ispartof>Transplantation, 2009-05, Vol.87 (9), p.1318-1324</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-38e776c8873b1a3d977d12f849de73675f48dbda9c4fce7e0e8c03ea3349ebfb3</citedby><cites>FETCH-LOGICAL-c441t-38e776c8873b1a3d977d12f849de73675f48dbda9c4fce7e0e8c03ea3349ebfb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21526722$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19424031$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MADAN, Rebecca P</creatorcontrib><creatorcontrib>CAMPBELL, Andrew L</creatorcontrib><creatorcontrib>SHUST, Gail F</creatorcontrib><creatorcontrib>KAHN, Alissa R</creatorcontrib><creatorcontrib>WISTINGHAUSEN, Birte</creatorcontrib><creatorcontrib>POSADA, Roberto</creatorcontrib><creatorcontrib>KERKAR, Nanda</creatorcontrib><creatorcontrib>SHNEIDER, Benjamin L</creatorcontrib><creatorcontrib>EMRE, Sukru</creatorcontrib><creatorcontrib>HEROLD, Betsy C</creatorcontrib><title>A Hybrid Strategy for the Prevention of Cytomegalovirus-Related Complications in Pediatric Liver Transplantation Recipients</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>This single center, retrospective study describes experience with a hybrid prevention strategy combining short-course antiviral prophylaxis and preemptive cytomegalovirus (CMV) polymerase chain reaction (PCR) monitoring.
One hundred twenty-two pediatric liver transplantation recipients were followed up for a median of 2.3 years posttransplantation. Subjects received a minimum of 14 days of postoperative ganciclovir, followed by monthly CMV PCR monitoring.
Forty-three CMV seronegative recipients received seropositive grafts and were considered high risk for CMV; 79 subjects were routine risk. CMV was detected by PCR in the absence of symptoms in 34.4% of subjects and was more likely in high risk than in routine risk recipients (58.1% vs. 21.8%, P=0.0001). Twelve subjects (9.8%) developed CMV disease (8 high risk vs. 4 routine risk, P=0.03). Three subjects developed acute rejection in the 6 months after detection of CMV, but CMV was preceded by rejection in 13 subjects. There were no mortalities secondary to CMV. A total of 38.5% of subjects were spared antiviral medications beyond their initial postoperative prophylaxis.
These results suggest that a hybrid preventative approach for CMV is a reasonable alternative to prolonged antiviral prophylaxis and may reduce unnecessary exposure to antiviral therapy. However, patients who receive intensified immunosuppression after acute rejection are at increased risk for CMV and may require extended prophylaxis and closer monitoring.</description><subject>Adolescent</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus - genetics</subject><subject>Cytomegalovirus Infections - epidemiology</subject><subject>Cytomegalovirus Infections - prevention & control</subject><subject>DNA, Viral - analysis</subject><subject>Follow-Up Studies</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Ganciclovir - therapeutic use</subject><subject>Humans</subject><subject>Infant</subject><subject>Liver Transplantation - adverse effects</subject><subject>Liver, biliary tract, pancreas, portal circulation, spleen</subject><subject>Medical sciences</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Postoperative Complications - prevention & control</subject><subject>Postoperative Complications - virology</subject><subject>Prevention and actions</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Reduction Behavior</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the digestive system</subject><subject>Time Factors</subject><subject>Tissue, organ and graft immunology</subject><subject>Viremia - epidemiology</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0cFu1DAQBmALgei28ARIyBfglOLJOHF8rFaFIq3EqiznyLEnxSiJg51dacXL47YrkDjAyZdv_hn5Z-wViEsQWr3fbS9FJwAJoQED2jrzhK2gQlnUohFP2UoICQUgqjN2ntJ3IUSFSj1nZ6BlKQXCiv284jfHLnrHvyzRLHR35H2IfPlGfBvpQNPiw8RDz9fHJYx0Z4Zw8HGfilsaMnd8HcZ58Nbcu8T9xLfkvFmit3zjDxT5LpopzYOZlgfDb8n62efg9II9682Q6OXpvWBfP1zv1jfF5vPHT-urTWGlhKXAhpSqbdMo7MCg00o5KPtGakcKa1X1snGdM9rK3pIiQY0VSAZRaur6Di_Yu8fcOYYfe0pLO_pkacg3UdinVslKo6wQs3z7T1mrUoCu9X9hCVBCVUOG-AhtDClF6ts5-tHEYwuiva-x3W3bv2vMU69P8ftuJPdn5tRbBm9OwCRrhj7_sfXpt8u7y3xrib8Ad42pQw</recordid><startdate>20090515</startdate><enddate>20090515</enddate><creator>MADAN, Rebecca P</creator><creator>CAMPBELL, Andrew L</creator><creator>SHUST, Gail F</creator><creator>KAHN, Alissa R</creator><creator>WISTINGHAUSEN, Birte</creator><creator>POSADA, Roberto</creator><creator>KERKAR, Nanda</creator><creator>SHNEIDER, Benjamin L</creator><creator>EMRE, Sukru</creator><creator>HEROLD, Betsy C</creator><general>Lippincott Williams & Wilkins</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>7T5</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090515</creationdate><title>A Hybrid Strategy for the Prevention of Cytomegalovirus-Related Complications in Pediatric Liver Transplantation Recipients</title><author>MADAN, Rebecca P ; CAMPBELL, Andrew L ; SHUST, Gail F ; KAHN, Alissa R ; WISTINGHAUSEN, Birte ; POSADA, Roberto ; KERKAR, Nanda ; SHNEIDER, Benjamin L ; EMRE, Sukru ; HEROLD, Betsy C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-38e776c8873b1a3d977d12f849de73675f48dbda9c4fce7e0e8c03ea3349ebfb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus - genetics</topic><topic>Cytomegalovirus Infections - epidemiology</topic><topic>Cytomegalovirus Infections - prevention & control</topic><topic>DNA, Viral - analysis</topic><topic>Follow-Up Studies</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Ganciclovir - therapeutic use</topic><topic>Humans</topic><topic>Infant</topic><topic>Liver Transplantation - adverse effects</topic><topic>Liver, biliary tract, pancreas, portal circulation, spleen</topic><topic>Medical sciences</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Postoperative Complications - prevention & control</topic><topic>Postoperative Complications - virology</topic><topic>Prevention and actions</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Reduction Behavior</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the digestive system</topic><topic>Time Factors</topic><topic>Tissue, organ and graft immunology</topic><topic>Viremia - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MADAN, Rebecca P</creatorcontrib><creatorcontrib>CAMPBELL, Andrew L</creatorcontrib><creatorcontrib>SHUST, Gail F</creatorcontrib><creatorcontrib>KAHN, Alissa R</creatorcontrib><creatorcontrib>WISTINGHAUSEN, Birte</creatorcontrib><creatorcontrib>POSADA, Roberto</creatorcontrib><creatorcontrib>KERKAR, Nanda</creatorcontrib><creatorcontrib>SHNEIDER, Benjamin L</creatorcontrib><creatorcontrib>EMRE, Sukru</creatorcontrib><creatorcontrib>HEROLD, Betsy C</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>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MADAN, Rebecca P</au><au>CAMPBELL, Andrew L</au><au>SHUST, Gail F</au><au>KAHN, Alissa R</au><au>WISTINGHAUSEN, Birte</au><au>POSADA, Roberto</au><au>KERKAR, Nanda</au><au>SHNEIDER, Benjamin L</au><au>EMRE, Sukru</au><au>HEROLD, Betsy C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Hybrid Strategy for the Prevention of Cytomegalovirus-Related Complications in Pediatric Liver Transplantation Recipients</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2009-05-15</date><risdate>2009</risdate><volume>87</volume><issue>9</issue><spage>1318</spage><epage>1324</epage><pages>1318-1324</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><coden>TRPLAU</coden><abstract>This single center, retrospective study describes experience with a hybrid prevention strategy combining short-course antiviral prophylaxis and preemptive cytomegalovirus (CMV) polymerase chain reaction (PCR) monitoring.
One hundred twenty-two pediatric liver transplantation recipients were followed up for a median of 2.3 years posttransplantation. Subjects received a minimum of 14 days of postoperative ganciclovir, followed by monthly CMV PCR monitoring.
Forty-three CMV seronegative recipients received seropositive grafts and were considered high risk for CMV; 79 subjects were routine risk. CMV was detected by PCR in the absence of symptoms in 34.4% of subjects and was more likely in high risk than in routine risk recipients (58.1% vs. 21.8%, P=0.0001). Twelve subjects (9.8%) developed CMV disease (8 high risk vs. 4 routine risk, P=0.03). Three subjects developed acute rejection in the 6 months after detection of CMV, but CMV was preceded by rejection in 13 subjects. There were no mortalities secondary to CMV. A total of 38.5% of subjects were spared antiviral medications beyond their initial postoperative prophylaxis.
These results suggest that a hybrid preventative approach for CMV is a reasonable alternative to prolonged antiviral prophylaxis and may reduce unnecessary exposure to antiviral therapy. However, patients who receive intensified immunosuppression after acute rejection are at increased risk for CMV and may require extended prophylaxis and closer monitoring.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>19424031</pmid><doi>10.1097/TP.0b013e3181a19cda</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Antiviral Agents - therapeutic use Biological and medical sciences Child Child, Preschool Cytomegalovirus Cytomegalovirus - genetics Cytomegalovirus Infections - epidemiology Cytomegalovirus Infections - prevention & control DNA, Viral - analysis Follow-Up Studies Fundamental and applied biological sciences. Psychology Fundamental immunology Ganciclovir - therapeutic use Humans Infant Liver Transplantation - adverse effects Liver, biliary tract, pancreas, portal circulation, spleen Medical sciences Polymerase Chain Reaction - methods Postoperative Complications - prevention & control Postoperative Complications - virology Prevention and actions Public health. Hygiene Public health. Hygiene-occupational medicine Retrospective Studies Risk Assessment Risk Reduction Behavior Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system Time Factors Tissue, organ and graft immunology Viremia - epidemiology |
title | A Hybrid Strategy for the Prevention of Cytomegalovirus-Related Complications in Pediatric Liver Transplantation Recipients |
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