Publication: Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation
dc.contributor.author | Sirapob Nuansri | en_US |
dc.contributor.author | Surasak Kantachuvesiri | en_US |
dc.contributor.author | Siriorn P. Watcharananan | en_US |
dc.contributor.author | Charat Thongprayoon | en_US |
dc.contributor.author | Wisit Cheungpasitporn | en_US |
dc.contributor.author | Jackrapong Bruminhent | en_US |
dc.contributor.other | Faculty of Medicine Ramathibodi Hospital, Mahidol University | en_US |
dc.contributor.other | Mayo Clinic | en_US |
dc.date.accessioned | 2022-08-04T09:14:08Z | |
dc.date.available | 2022-08-04T09:14:08Z | |
dc.date.issued | 2021-09-01 | en_US |
dc.description.abstract | 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. | en_US |
dc.identifier.citation | Transplantation Proceedings. Vol.53, No.7 (2021), 2267-2271 | en_US |
dc.identifier.doi | 10.1016/j.transproceed.2021.07.033 | en_US |
dc.identifier.issn | 18732623 | en_US |
dc.identifier.issn | 00411345 | en_US |
dc.identifier.other | 2-s2.0-85112574852 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/77906 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112574852&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Clinical Characteristics of Late-Onset Cytomegalovirus Infection After Kidney Transplantation | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112574852&origin=inward | en_US |