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Prevention of Cytomegalovirus Infection in Solid Organ Transplant Recipients: Guidelines by the Korean Society of Infectious Diseases and the Korean Society for Transplantationopen access

Authors
Huh, K.Lee, S.-O.Kim, J.Lee, S.J.Choe, P.G.Kang, J.-M.Yang, J.Sung, H.Kim, S.-H.Moon, C.Seok, H.Shi, H.J.Wi, Y.M.Jeong, S.J.Park, W.B.Kim, Y.J.Kim, J.Ahn, H.J.Kim, N.J.Peck, K.R.Kim, M.S.Kim, S.I.
Issue Date
Mar-2024
Publisher
Korean Society of Infectious Diseases, Korean Society for Antimicrobial Therapy, Korean Society for AIDS
Keywords
Cytomegalovirus; Organ transplantation; Prevention
Citation
Infection and Chemotherapy, v.56, no.1, pp 101 - 121
Pages
21
Journal Title
Infection and Chemotherapy
Volume
56
Number
1
Start Page
101
End Page
121
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/91101
DOI
10.3947/ic.2024.0016
ISSN
2093-2340
2092-6448
Abstract
Cytomegalovirus (CMV) is the most important opportunistic viral pathogen in solid organ transplant (SOT) recipients. The Korean guideline for the prevention of CMV infection in SOT recipients was developed jointly by the Korean Society for Infectious Diseases and the Korean Society of Transplantation. CMV serostatus of both donors and recipients should be screened before transplantation to best assess the risk of CMV infection after SOT. Seronegative recipients receiving organs from seropositive donors face the highest risk, followed by seropositive recipients. Either antiviral prophylaxis or preemptive therapy can be used to prevent CMV infection. While both strategies have been demonstrated to prevent CMV infection post-transplant, each has its own advantages and disadvantages. CMV serostatus, transplant organ, other risk factors, and practical issues should be considered for the selection of preventive measures. There is no universal viral load threshold to guide treatment in preemptive therapy. Each institution should define and validate its own threshold. Valganciclovir is the favored agent for both prophylaxis and preemptive therapy. The evaluation of CMV-specific cell-mediated immunity and the monitoring of viral load kinetics are gaining interest, but there was insufficient evidence to issue recommendations. Specific considerations on pediatric transplant recipients are included. Copyright © 2024 by The Korean Society of Infectious Diseases, Korean Society for Antimicrobial Therapy, and The Korean Society for AIDS.
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