Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation

Background: Late-onset cytomegalovirus (CMV) infection (LCI) has been emerging mong solid-organ transplant recipients. We explored clinical characteristics, risk factors, and outcomes of LCI in kidney transplantation (KT) recipients. Methods: A retrospective study of all adult KT recipients with LCI...

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Main Authors: Sirapob Nuansri, Surasak Kantachuvesiri, Siriorn P. Watcharananan, Charat Thongprayoon, Wisit Cheungpasitporn, Jackrapong Bruminhent
其他作者: Faculty of Medicine Ramathibodi Hospital, Mahidol University
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出版: 2022
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spelling th-mahidol.779062022-08-04T16:14:08Z Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation Sirapob Nuansri Surasak Kantachuvesiri Siriorn P. Watcharananan Charat Thongprayoon Wisit Cheungpasitporn Jackrapong Bruminhent Faculty of Medicine Ramathibodi Hospital, Mahidol University Mayo Clinic Medicine Background: Late-onset cytomegalovirus (CMV) infection (LCI) has been emerging mong solid-organ transplant recipients. We explored clinical characteristics, risk factors, and outcomes of LCI in kidney transplantation (KT) recipients. Methods: A retrospective study of all adult KT recipients with LCIs (that occurred >6 months after transplant) from 2016 to 2018 was conducted. Clinical characteristics and outcomes were extracted. Risk factors of LCI were analyzed using Cox proportional hazards models. Results: A total of 518 KT recipients were included. Ninety-eight percent had donor CMV-seropositive and recipient CMV-seropositive status (D+/R+). Ten (2%) KT recipients developed LCI with a median onset of 14 (interquartile range, 8-15) months. Those included asymptomatic CMV infection (40%) and tissue-invasive disease (60%). CMV D+/R– serostatus and a prior episode of rejection within 6 months were associated with LCI (hazard ratio, 17.35; 95% confidence interval, 3.60-83.63; P < .001) and (hazard ratio, 38.15; 95% confidence interval, 6.15-236.72; P < .001), respectively. There was no difference in the rate of allograft failure and mortality in those with LCI compared with those with early-onset CMV infection. Conclusion: LCI is uncommon after KT. Those with CMV seromismatch and a prior episode of rejection were more likely to develop LCI. Clinical and allograft outcomes were not different among each group. 2022-08-04T09:14:08Z 2022-08-04T09:14:08Z 2021-09-01 Article Transplantation Proceedings. Vol.53, No.7 (2021), 2267-2271 10.1016/j.transproceed.2021.07.033 18732623 00411345 2-s2.0-85112574852 https://repository.li.mahidol.ac.th/handle/123456789/77906 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112574852&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Sirapob Nuansri
Surasak Kantachuvesiri
Siriorn P. Watcharananan
Charat Thongprayoon
Wisit Cheungpasitporn
Jackrapong Bruminhent
Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
description Background: Late-onset cytomegalovirus (CMV) infection (LCI) has been emerging mong solid-organ transplant recipients. We explored clinical characteristics, risk factors, and outcomes of LCI in kidney transplantation (KT) recipients. Methods: A retrospective study of all adult KT recipients with LCIs (that occurred >6 months after transplant) from 2016 to 2018 was conducted. Clinical characteristics and outcomes were extracted. Risk factors of LCI were analyzed using Cox proportional hazards models. Results: A total of 518 KT recipients were included. Ninety-eight percent had donor CMV-seropositive and recipient CMV-seropositive status (D+/R+). Ten (2%) KT recipients developed LCI with a median onset of 14 (interquartile range, 8-15) months. Those included asymptomatic CMV infection (40%) and tissue-invasive disease (60%). CMV D+/R– serostatus and a prior episode of rejection within 6 months were associated with LCI (hazard ratio, 17.35; 95% confidence interval, 3.60-83.63; P < .001) and (hazard ratio, 38.15; 95% confidence interval, 6.15-236.72; P < .001), respectively. There was no difference in the rate of allograft failure and mortality in those with LCI compared with those with early-onset CMV infection. Conclusion: LCI is uncommon after KT. Those with CMV seromismatch and a prior episode of rejection were more likely to develop LCI. Clinical and allograft outcomes were not different among each group.
author2 Faculty of Medicine Ramathibodi Hospital, Mahidol University
author_facet Faculty of Medicine Ramathibodi Hospital, Mahidol University
Sirapob Nuansri
Surasak Kantachuvesiri
Siriorn P. Watcharananan
Charat Thongprayoon
Wisit Cheungpasitporn
Jackrapong Bruminhent
format Article
author Sirapob Nuansri
Surasak Kantachuvesiri
Siriorn P. Watcharananan
Charat Thongprayoon
Wisit Cheungpasitporn
Jackrapong Bruminhent
author_sort Sirapob Nuansri
title Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
title_short Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
title_full Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
title_fullStr Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
title_full_unstemmed Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
title_sort clinical characteristics of late-onset cytomegalovirus infection after kidney transplantation
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/77906
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