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
Hauptverfasser: 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
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container_end_page 1324
container_issue 9
container_start_page 1318
container_title Transplantation
container_volume 87
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. 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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 &amp; 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. 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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. 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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 &amp; 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. 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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. 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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 &amp; 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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