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Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation
BACKGROUND: The incidence of cytomegalovirus (CMV) syndrome/disease after adult solid organ transplantation in the era effective antiviral therapy has not been fully assessed. OBJECTIVE: To determines the incidence of CMV syndrome/disease after solid organ transplantation in the UK. STUDY DESIGN: A...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355300/ https://www.ncbi.nlm.nih.gov/pubmed/22445261 http://dx.doi.org/10.1016/j.jcv.2012.02.020 |
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author | Emery, Vincent C. Asher, Kevin Sanjuan, Cristina de Juan |
author_facet | Emery, Vincent C. Asher, Kevin Sanjuan, Cristina de Juan |
author_sort | Emery, Vincent C. |
collection | PubMed |
description | BACKGROUND: The incidence of cytomegalovirus (CMV) syndrome/disease after adult solid organ transplantation in the era effective antiviral therapy has not been fully assessed. OBJECTIVE: To determines the incidence of CMV syndrome/disease after solid organ transplantation in the UK. STUDY DESIGN: A retrospective analysis of 1807 solid organ transplants from 12 UK solid organ transplant centres representing 32.7% of all transplant activity occurring in the UK between 1/04/2004 and 31/03/2006. Patients were categorised into those experiencing an episode of symptomatic CMV infection after transplant or those who remained free of symptoms. All patients were followed up for 2 years for the occurrence of CMV syndrome/disease. RESULTS: The majority of the transplant centres used valganciclovir prophylaxis in the high risk D+R− patients (91.6%) whereas management of the lower risk D+R+ and D−R+ patients was more variable with deployment of both prophylactic and pre-emptive strategies in ∼50% of centres. CMV syndrome/disease occurred in 20.5% of the D+R− patients representing 55 cases whereas the incidence was only 8.1% and 9% in the D+R+ and D−R+ group, respectively (p < 0.001 compared to the D+R− group), but representing a further 58 cases of CMV syndrome/disease. CMV viraemia in the D+R− group was associated with a high probability (65%) of CMV syndrome/disease in renal transplant recipients whereas this was less apparent in the intermediate risk groups. CONCLUSIONS: CMV syndrome/disease remains an important healthcare burden after solid organ transplantation with the intermediate risk groups contributing similar numbers of cases as the high risk group. |
format | Online Article Text |
id | pubmed-3355300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33553002012-06-01 Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation Emery, Vincent C. Asher, Kevin Sanjuan, Cristina de Juan J Clin Virol Article BACKGROUND: The incidence of cytomegalovirus (CMV) syndrome/disease after adult solid organ transplantation in the era effective antiviral therapy has not been fully assessed. OBJECTIVE: To determines the incidence of CMV syndrome/disease after solid organ transplantation in the UK. STUDY DESIGN: A retrospective analysis of 1807 solid organ transplants from 12 UK solid organ transplant centres representing 32.7% of all transplant activity occurring in the UK between 1/04/2004 and 31/03/2006. Patients were categorised into those experiencing an episode of symptomatic CMV infection after transplant or those who remained free of symptoms. All patients were followed up for 2 years for the occurrence of CMV syndrome/disease. RESULTS: The majority of the transplant centres used valganciclovir prophylaxis in the high risk D+R− patients (91.6%) whereas management of the lower risk D+R+ and D−R+ patients was more variable with deployment of both prophylactic and pre-emptive strategies in ∼50% of centres. CMV syndrome/disease occurred in 20.5% of the D+R− patients representing 55 cases whereas the incidence was only 8.1% and 9% in the D+R+ and D−R+ group, respectively (p < 0.001 compared to the D+R− group), but representing a further 58 cases of CMV syndrome/disease. CMV viraemia in the D+R− group was associated with a high probability (65%) of CMV syndrome/disease in renal transplant recipients whereas this was less apparent in the intermediate risk groups. CONCLUSIONS: CMV syndrome/disease remains an important healthcare burden after solid organ transplantation with the intermediate risk groups contributing similar numbers of cases as the high risk group. Elsevier Science 2012-06 /pmc/articles/PMC3355300/ /pubmed/22445261 http://dx.doi.org/10.1016/j.jcv.2012.02.020 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Emery, Vincent C. Asher, Kevin Sanjuan, Cristina de Juan Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
title | Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
title_full | Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
title_fullStr | Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
title_full_unstemmed | Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
title_short | Importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
title_sort | importance of the cytomegalovirus seropositive recipient as a contributor to disease burden after solid organ transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355300/ https://www.ncbi.nlm.nih.gov/pubmed/22445261 http://dx.doi.org/10.1016/j.jcv.2012.02.020 |
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