Ganciclovir for Cytomegalovirus: a Call for Indefinite Prophylaxis in Lung Transplantation

Background Universal ganciclovir (GCV) prophylaxis is a strategy aimed at reducing cytomegalovirus (CMV) infection and delaying the development of bronchiolitis obliterans syndrome (BOS). However, the optimal duration of GCV prophylaxis remains unclear. We report our experience with GCV prophylaxis...

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Veröffentlicht in:The Journal of heart and lung transplantation 2008-08, Vol.27 (8), p.875-881
Hauptverfasser: Valentine, Vincent G., MD, FACP, Weill, David, MD, Gupta, Meera R., MD, Raper, Brad, MD, LaPlace, Stephanie G., RNC, BSN, Lombard, Gisele A., RNC, BSN, Bonvillain, Ryan W., BS, Taylor, David E., MD, Dhillon, Gundeep S., MD
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container_end_page 881
container_issue 8
container_start_page 875
container_title The Journal of heart and lung transplantation
container_volume 27
creator Valentine, Vincent G., MD, FACP
Weill, David, MD
Gupta, Meera R., MD
Raper, Brad, MD
LaPlace, Stephanie G., RNC, BSN
Lombard, Gisele A., RNC, BSN
Bonvillain, Ryan W., BS
Taylor, David E., MD
Dhillon, Gundeep S., MD
description Background Universal ganciclovir (GCV) prophylaxis is a strategy aimed at reducing cytomegalovirus (CMV) infection and delaying the development of bronchiolitis obliterans syndrome (BOS). However, the optimal duration of GCV prophylaxis remains unclear. We report our experience with GCV prophylaxis administered indefinitely and its effect on CMV pneumonitis, BOS and survival after lung transplantation (LT). Methods One hundred fifty-one patients surviving >100 days after LT were analyzed. GCV was given to 130 CMV donor- or recipient-seropositive patients. Data from 90 patients who received indefinite GCV prophylaxis (IND) and 40 patients who discontinued their GCV prophylaxis (STOP) were compared. Results CMV pneumonitis occurred in 16%, 8%, 17% and 19% of patients in the D+ R+ , D− R+ , D+ R− and D− R− groups, respectively. In the STOP cohort, 15 of 40 patients developed CMV pneumonitis (median time 79 days) after GCV was stopped. Ten of these 15 patients developed BOS (median time 116 days) after discontinuing GCV. The risk of CMV pneumonitis in the STOP cohort was significantly higher when GCV prophylaxis was discontinued within the first year. Cumulative incidence of CMV pneumonitis in the IND and STOP groups at 5 years was 2% and 57%, respectively ( p < 0.001). BOS-free survival and survival were similar across both groups. Conclusions Indefinite GCV prophylaxis prevents CMV pneumonitis in 98% of LT recipients. Thirty-eight percent of patients discontinuing prophylaxis developed CMV pneumonitis, 50% of whom progressed to BOS within 1 year. Continuing ganciclovir prophylaxis indefinitely after lung transplantation should be considered.
doi_str_mv 10.1016/j.healun.2008.05.009
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However, the optimal duration of GCV prophylaxis remains unclear. We report our experience with GCV prophylaxis administered indefinitely and its effect on CMV pneumonitis, BOS and survival after lung transplantation (LT). Methods One hundred fifty-one patients surviving &gt;100 days after LT were analyzed. GCV was given to 130 CMV donor- or recipient-seropositive patients. Data from 90 patients who received indefinite GCV prophylaxis (IND) and 40 patients who discontinued their GCV prophylaxis (STOP) were compared. Results CMV pneumonitis occurred in 16%, 8%, 17% and 19% of patients in the D+ R+ , D− R+ , D+ R− and D− R− groups, respectively. In the STOP cohort, 15 of 40 patients developed CMV pneumonitis (median time 79 days) after GCV was stopped. Ten of these 15 patients developed BOS (median time 116 days) after discontinuing GCV. The risk of CMV pneumonitis in the STOP cohort was significantly higher when GCV prophylaxis was discontinued within the first year. Cumulative incidence of CMV pneumonitis in the IND and STOP groups at 5 years was 2% and 57%, respectively ( p &lt; 0.001). BOS-free survival and survival were similar across both groups. Conclusions Indefinite GCV prophylaxis prevents CMV pneumonitis in 98% of LT recipients. Thirty-eight percent of patients discontinuing prophylaxis developed CMV pneumonitis, 50% of whom progressed to BOS within 1 year. Continuing ganciclovir prophylaxis indefinitely after lung transplantation should be considered.</description><identifier>ISSN: 1053-2498</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2008.05.009</identifier><identifier>PMID: 18656801</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Bronchiolitis Obliterans - prevention &amp; control ; Cardiology. Vascular system ; Cohort Studies ; Cytomegalovirus Infections - prevention &amp; control ; Dose-Response Relationship, Drug ; Female ; Ganciclovir - therapeutic use ; Humans ; Immunosuppression - methods ; Infectious diseases ; Lung Transplantation ; Male ; Medical sciences ; Middle Aged ; Opportunistic Infections - prevention &amp; control ; Pneumonia - prevention &amp; control ; Retrospective Studies ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. 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However, the optimal duration of GCV prophylaxis remains unclear. We report our experience with GCV prophylaxis administered indefinitely and its effect on CMV pneumonitis, BOS and survival after lung transplantation (LT). Methods One hundred fifty-one patients surviving &gt;100 days after LT were analyzed. GCV was given to 130 CMV donor- or recipient-seropositive patients. Data from 90 patients who received indefinite GCV prophylaxis (IND) and 40 patients who discontinued their GCV prophylaxis (STOP) were compared. Results CMV pneumonitis occurred in 16%, 8%, 17% and 19% of patients in the D+ R+ , D− R+ , D+ R− and D− R− groups, respectively. In the STOP cohort, 15 of 40 patients developed CMV pneumonitis (median time 79 days) after GCV was stopped. Ten of these 15 patients developed BOS (median time 116 days) after discontinuing GCV. The risk of CMV pneumonitis in the STOP cohort was significantly higher when GCV prophylaxis was discontinued within the first year. Cumulative incidence of CMV pneumonitis in the IND and STOP groups at 5 years was 2% and 57%, respectively ( p &lt; 0.001). BOS-free survival and survival were similar across both groups. Conclusions Indefinite GCV prophylaxis prevents CMV pneumonitis in 98% of LT recipients. Thirty-eight percent of patients discontinuing prophylaxis developed CMV pneumonitis, 50% of whom progressed to BOS within 1 year. Continuing ganciclovir prophylaxis indefinitely after lung transplantation should be considered.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bronchiolitis Obliterans - prevention &amp; control</subject><subject>Cardiology. Vascular system</subject><subject>Cohort Studies</subject><subject>Cytomegalovirus Infections - prevention &amp; control</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Ganciclovir - therapeutic use</subject><subject>Humans</subject><subject>Immunosuppression - methods</subject><subject>Infectious diseases</subject><subject>Lung Transplantation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Opportunistic Infections - prevention &amp; control</subject><subject>Pneumonia - prevention &amp; control</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. 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Vascular system</topic><topic>Cohort Studies</topic><topic>Cytomegalovirus Infections - prevention &amp; control</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Ganciclovir - therapeutic use</topic><topic>Humans</topic><topic>Immunosuppression - methods</topic><topic>Infectious diseases</topic><topic>Lung Transplantation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Opportunistic Infections - prevention &amp; control</topic><topic>Pneumonia - prevention &amp; control</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the heart</topic><topic>Treatment Outcome</topic><topic>Viral diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valentine, Vincent G., MD, FACP</creatorcontrib><creatorcontrib>Weill, David, MD</creatorcontrib><creatorcontrib>Gupta, Meera R., MD</creatorcontrib><creatorcontrib>Raper, Brad, MD</creatorcontrib><creatorcontrib>LaPlace, Stephanie G., RNC, BSN</creatorcontrib><creatorcontrib>Lombard, Gisele A., RNC, BSN</creatorcontrib><creatorcontrib>Bonvillain, Ryan W., BS</creatorcontrib><creatorcontrib>Taylor, David E., MD</creatorcontrib><creatorcontrib>Dhillon, Gundeep S., MD</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>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valentine, Vincent G., MD, FACP</au><au>Weill, David, MD</au><au>Gupta, Meera R., MD</au><au>Raper, Brad, MD</au><au>LaPlace, Stephanie G., RNC, BSN</au><au>Lombard, Gisele A., RNC, BSN</au><au>Bonvillain, Ryan W., BS</au><au>Taylor, David E., MD</au><au>Dhillon, Gundeep S., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ganciclovir for Cytomegalovirus: a Call for Indefinite Prophylaxis in Lung Transplantation</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>27</volume><issue>8</issue><spage>875</spage><epage>881</epage><pages>875-881</pages><issn>1053-2498</issn><eissn>1557-3117</eissn><abstract>Background Universal ganciclovir (GCV) prophylaxis is a strategy aimed at reducing cytomegalovirus (CMV) infection and delaying the development of bronchiolitis obliterans syndrome (BOS). However, the optimal duration of GCV prophylaxis remains unclear. We report our experience with GCV prophylaxis administered indefinitely and its effect on CMV pneumonitis, BOS and survival after lung transplantation (LT). Methods One hundred fifty-one patients surviving &gt;100 days after LT were analyzed. GCV was given to 130 CMV donor- or recipient-seropositive patients. Data from 90 patients who received indefinite GCV prophylaxis (IND) and 40 patients who discontinued their GCV prophylaxis (STOP) were compared. Results CMV pneumonitis occurred in 16%, 8%, 17% and 19% of patients in the D+ R+ , D− R+ , D+ R− and D− R− groups, respectively. In the STOP cohort, 15 of 40 patients developed CMV pneumonitis (median time 79 days) after GCV was stopped. Ten of these 15 patients developed BOS (median time 116 days) after discontinuing GCV. The risk of CMV pneumonitis in the STOP cohort was significantly higher when GCV prophylaxis was discontinued within the first year. Cumulative incidence of CMV pneumonitis in the IND and STOP groups at 5 years was 2% and 57%, respectively ( p &lt; 0.001). BOS-free survival and survival were similar across both groups. Conclusions Indefinite GCV prophylaxis prevents CMV pneumonitis in 98% of LT recipients. Thirty-eight percent of patients discontinuing prophylaxis developed CMV pneumonitis, 50% of whom progressed to BOS within 1 year. Continuing ganciclovir prophylaxis indefinitely after lung transplantation should be considered.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18656801</pmid><doi>10.1016/j.healun.2008.05.009</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Antiviral Agents - therapeutic use
Biological and medical sciences
Bronchiolitis Obliterans - prevention & control
Cardiology. Vascular system
Cohort Studies
Cytomegalovirus Infections - prevention & control
Dose-Response Relationship, Drug
Female
Ganciclovir - therapeutic use
Humans
Immunosuppression - methods
Infectious diseases
Lung Transplantation
Male
Medical sciences
Middle Aged
Opportunistic Infections - prevention & control
Pneumonia - prevention & control
Retrospective Studies
Surgery
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the heart
Treatment Outcome
Viral diseases
title Ganciclovir for Cytomegalovirus: a Call for Indefinite Prophylaxis in Lung Transplantation
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