4.1 Article

Efficacy and Safety According to the Dose of Valganciclovir for Cytomegalovirus Prophylaxis in Transplantation: Network Meta-analysis Using Recent Data

Journal

TRANSPLANTATION PROCEEDINGS
Volume 53, Issue 6, Pages 1945-1950

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.transproceed.2021.05.006

Keywords

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Funding

  1. Basic Science Research Program through the Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Korean government (MSIT) [SDH: NRF-2019M3E5D1A02069619]

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This study used network meta-analysis to identify the appropriate dose of valganciclovir for preventing CMV infection in kidney transplant patients. The results showed that 450 mg of valganciclovir had the highest probability of decreasing CMV infection, while the incidence of CMV infection did not differ significantly based on the dose. Additionally, the low dose of valganciclovir significantly reduced the incidence of leukopenia.
Background. Valganciclovir is used to prevent posttransplant cytomegalovirus (CMV) infection among patients undergoing kidney transplant. However, the optimal dose remains controversial because continuous use decreases kidney function and can induce leukopenia. The purpose of this study was to identify the appropriate dose of valganciclovir for preventing CMV using network meta-analysis. Methods. We searched the Cochrane Central Register, Ovid MEDLINE, EMBASE, Cumulative Index to Nursing and Allied Health, and Web of Science databases for studies published through April 15, 2017, evaluating 900-mg and 450-mg valganciclovir. We performed direct and indirect network meta-analysis using Bayesian models and generated rankings of different doses of valganciclovir by generating a mixed-treatment comparison. Results. Twenty-three studies involving 3478 participants were included. Compared with the control group, there was no difference in the incidence of CMV infection between the low-dose (450 mg) (odds ratio [OR], 0.79; 95% confidence interval [CI], 0.50-1.40) and high-dose (900 mg) (OR, 1.0; 95% CI, 0.61-1.60) groups. Low-dose valganciclovir had the best probability (71.1%) for decreasing CMV infection. Leukopenia was significantly more common in the highdose group than in the control group (OR, 4.3; 95% CI, 2.69-7.10) and in the low-dose group (OR, 2.9; 95% CI, 1.88-4.67), but there was no significant difference in the incidence of leukopenia between the low-dose and control groups (OR, 1.5; 95% CI, 0.99-2.20). Conclusions. The incidence of CMV was not different based on the dose of valganciclovir, although the tendency for CMV infection was decreased at 450 mg. However, the low dose of valganciclovir significantly reduced the incidence of leukopenia

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