Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/9498
Title: Ten-year epidemiology and risk factors of cytomegalovirus infection in hematopoietic stem cell transplantation patients in Taiwan
Authors: Huang, Yi-Che
Hsiao, Fei-Yuan
Guan, Shang-Ting
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Keywords: CMV disease
CMV infection
HSCT
Issue Date: Jun-2024
Publisher: Journal of Microbiology, Immunology and Infection
Series/Report no.: Original Article;365-374
Abstract: Background: Cytomegalovirus (CMV) can cause infection and critical diseases in hematopoietic stem cell transplantation (HSCT) recipients. This study aimed to explore the cumulative incidence and risk factors for CMV infection and disease among HSCT recipients in Taiwan. Methods: This retrospective cohort study using the Taiwan Blood and Marrow Transplantation Registry (TBMTR) included HSCT recipients between 2009 and 2018 in Taiwan. The primary outcome was cumulative incidence of CMV infection or disease at day 100 after HSCT. Secondary outcomes included day 180 cumulative incidence of CMV infection or disease, infection sites, risk factors for CMV infection or disease, survival analysis, and overall survival after CMV infection and disease. Results: There were 4394 HSCT recipients included in the study (2044 auto-HSCT and 2350 allo- HSCT). The cumulative incidence of CMV infection and disease was significantly higher in allo- HSCT than in auto-HSCT patients at day 100 (53.7% vs. 6.0%, P < 0.0001 and 6.1% vs. 0.9%, P < 0.0001). Use of ATG (HR 1.819, p < 0.0001), recipient CMV serostatus positive (HR 2.631, p < 0.0001) and acute GVHD grades II (HR 1.563, p < 0.0001) were risk factors for CMV infection, while matched donor (HR 0.856, p Z 0.0180) and myeloablative conditioning (MAC) (HR 0.674, p < 0.0001) were protective factors. Conclusion: The study revealed a significant disparity in terms of the incidence, risk factors, and clinical outcomes of CMV infection and disease between auto and allo-HSCT patients. These findings underscore the importance of considering these factors in the management of HSCT recipients to improve outcomes related to CMV infections.
URI: http://localhost:8080/xmlui/handle/123456789/9498
ISSN: 1684-1182
Appears in Collections:Vol. 57 No. 3 (2024)

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