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The efficacy and safety of valganciclovir vs. oral ganciclovir in the prevention of symptomatic CMV infection in children after solid organ transplantation
Author(s) -
LapidusKrol E.,
Shapiro R.,
Amir J.,
Davidovits M.,
Steinberg R.,
Mor E.,
Avitzur Y.
Publication year - 2010
Publication title -
pediatric transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 69
eISSN - 1399-3046
pISSN - 1397-3142
DOI - 10.1111/j.1399-3046.2010.01330.x
Subject(s) - valganciclovir , medicine , ganciclovir , transplantation , organ transplantation , intensive care medicine , cytomegalovirus , virology , human cytomegalovirus , herpesviridae , viral disease , human immunodeficiency virus (hiv) , virus
Lapidus‐Krol E, Shapiro R, Amir J, Davidovits M, Steinberg R, Mor E, Avitzur Y. The efficacy and safety of valganciclovir vs. oral ganciclovir in the prevention of symptomatic CMV infection in children after solid organ transplantation.
Pediatr Transplantation 2010: 14:753–760. © 2010 John Wiley & Sons A/S. Abstract:  Routine prophylaxis for CMV with valganciclovir is common in adult recipients but data to support its use in children are scarce. The aim of this study was to compare the efficacy and safety of valganciclovir vs. ganciclovir in a pediatric cohort. We performed a retrospective analysis of 92 children after KTx and/or LTx. All children have received IV ganciclovir for two wk, and then oral ganciclovir (TID; n = 41) before 2004, or valganciclovir (OD; n = 51) thereafter. Treatment was given for three months in R+/D+ or R+/D− recipients and for six months in R−/D+. Patients were followed for one yr post transplant. Both groups were comparable in their demographic and transplant‐related history. Symptomatic CMV infection/disease developed in 13.7% vs. 19.5% of valganciclovir and ganciclovir groups, respectively (P‐NS). Time‐to‐onset of CMV infection was comparable in both groups (P‐NS); rates of acute allograft rejection were similar in both groups (3.9% vs. 9.8%). Risk factors for CMV infection included young age, serostatus of R−/D+, and allograft from cadaver donor. No significant side effects were noted in both groups. As in adults, valganciclovir appears to be as efficacious and safe as oral ganciclovir. Valganciclovir should be considered as a possible prophylactic treatment for CMV in pediatric recipients of KTx or LTx.

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