(Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation.

Standard

(Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation. / Höcker, Britta; Böhm, Stephan; Fickenscher, Helmut; Küsters, Uta; Schnitzler, Paul; Pohl, Martin; John, Ulrike; Kemper, Markus J.; Fehrenbach, Henry; Wigger, Marianne; Holder, Martin; Schröder, Monika; Feneberg, Reinhard; Köpf-Shakib, Sabine; Tönshoff, Burkhard.

in: TRANSPL INT, Jahrgang 25, Nr. 7, 7, 2012, S. 723-731.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Höcker, B, Böhm, S, Fickenscher, H, Küsters, U, Schnitzler, P, Pohl, M, John, U, Kemper, MJ, Fehrenbach, H, Wigger, M, Holder, M, Schröder, M, Feneberg, R, Köpf-Shakib, S & Tönshoff, B 2012, '(Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation.', TRANSPL INT, Jg. 25, Nr. 7, 7, S. 723-731. <http://www.ncbi.nlm.nih.gov/pubmed/22533698?dopt=Citation>

APA

Höcker, B., Böhm, S., Fickenscher, H., Küsters, U., Schnitzler, P., Pohl, M., John, U., Kemper, M. J., Fehrenbach, H., Wigger, M., Holder, M., Schröder, M., Feneberg, R., Köpf-Shakib, S., & Tönshoff, B. (2012). (Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation. TRANSPL INT, 25(7), 723-731. [7]. http://www.ncbi.nlm.nih.gov/pubmed/22533698?dopt=Citation

Vancouver

Höcker B, Böhm S, Fickenscher H, Küsters U, Schnitzler P, Pohl M et al. (Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation. TRANSPL INT. 2012;25(7):723-731. 7.

Bibtex

@article{6a6e636900234f719b9065ce61b1a40d,
title = "(Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation.",
abstract = "Epstein-Barr virus (EBV) primary infection constitutes a serious risk for pediatric transplant recipients, particularly as regards the development of EBV-related post-transplant lymphoproliferative disease (PTLD). Currently, there is no established prophylactic regimen. We investigated the association between chemoprophylaxis with valganciclovir (VGCV) or ganciclovir (GCV) and the incidence of EBV viremia in EBV-na{\"i}ve pediatric renal transplant recipients (R-) who had received a graft from an EBV-positive donor (D+) and are therefore at high risk of EBV primary infection. In a prospective, multicenter trial (n = 114), we compared a cohort on chemoprophylaxis (n = 20) with a similar control cohort without chemoprophylaxis (n = 8). Over the 1-year study period, antiviral prophylaxis with VGCV/GCV was associated with a significantly decreased incidence of EBV primary infection: 9/20 patients (45%) in the prophylaxis group experienced an EBV primary infection compared to 8/8 controls (100%) (P < 0.0001). Chemoprophylaxis was associated with a significantly lower EBV viral load (P < 0.001). Type or intensity of immunosuppressive therapy did not influence the occurrence of EBV primary infection or the level/persistence of EBV viral load. Chemoprophylaxis with VGCV/GCV is associated with a reduced incidence of EBV viremia in high-risk pediatric kidney allograft recipients in the first year post-transplant. (ClinicalTrials.gov number: NCT00963248).",
keywords = "Adult, Humans, Male, Female, Prospective Studies, Cohort Studies, Child, Kidney Transplantation/*methods, Immunosuppressive Agents/therapeutic use, Antiviral Agents/therapeutic use, Chemoprevention/methods, Epstein-Barr Virus Infections/*prevention & control, Ganciclovir/*analogs & derivatives/*therapeutic use, Herpesvirus 4, Human/*metabolism, Lymphoproliferative Disorders/etiology, Pediatrics/methods, Adult, Humans, Male, Female, Prospective Studies, Cohort Studies, Child, Kidney Transplantation/*methods, Immunosuppressive Agents/therapeutic use, Antiviral Agents/therapeutic use, Chemoprevention/methods, Epstein-Barr Virus Infections/*prevention & control, Ganciclovir/*analogs & derivatives/*therapeutic use, Herpesvirus 4, Human/*metabolism, Lymphoproliferative Disorders/etiology, Pediatrics/methods",
author = "Britta H{\"o}cker and Stephan B{\"o}hm and Helmut Fickenscher and Uta K{\"u}sters and Paul Schnitzler and Martin Pohl and Ulrike John and Kemper, {Markus J.} and Henry Fehrenbach and Marianne Wigger and Martin Holder and Monika Schr{\"o}der and Reinhard Feneberg and Sabine K{\"o}pf-Shakib and Burkhard T{\"o}nshoff",
year = "2012",
language = "English",
volume = "25",
pages = "723--731",
journal = "TRANSPL INT",
issn = "0934-0874",
publisher = "Wiley-Blackwell",
number = "7",

}

RIS

TY - JOUR

T1 - (Val-)Ganciclovir prophylaxis reduces Epstein-Barr virus primary infection in pediatric renal transplantation.

AU - Höcker, Britta

AU - Böhm, Stephan

AU - Fickenscher, Helmut

AU - Küsters, Uta

AU - Schnitzler, Paul

AU - Pohl, Martin

AU - John, Ulrike

AU - Kemper, Markus J.

AU - Fehrenbach, Henry

AU - Wigger, Marianne

AU - Holder, Martin

AU - Schröder, Monika

AU - Feneberg, Reinhard

AU - Köpf-Shakib, Sabine

AU - Tönshoff, Burkhard

PY - 2012

Y1 - 2012

N2 - Epstein-Barr virus (EBV) primary infection constitutes a serious risk for pediatric transplant recipients, particularly as regards the development of EBV-related post-transplant lymphoproliferative disease (PTLD). Currently, there is no established prophylactic regimen. We investigated the association between chemoprophylaxis with valganciclovir (VGCV) or ganciclovir (GCV) and the incidence of EBV viremia in EBV-naïve pediatric renal transplant recipients (R-) who had received a graft from an EBV-positive donor (D+) and are therefore at high risk of EBV primary infection. In a prospective, multicenter trial (n = 114), we compared a cohort on chemoprophylaxis (n = 20) with a similar control cohort without chemoprophylaxis (n = 8). Over the 1-year study period, antiviral prophylaxis with VGCV/GCV was associated with a significantly decreased incidence of EBV primary infection: 9/20 patients (45%) in the prophylaxis group experienced an EBV primary infection compared to 8/8 controls (100%) (P < 0.0001). Chemoprophylaxis was associated with a significantly lower EBV viral load (P < 0.001). Type or intensity of immunosuppressive therapy did not influence the occurrence of EBV primary infection or the level/persistence of EBV viral load. Chemoprophylaxis with VGCV/GCV is associated with a reduced incidence of EBV viremia in high-risk pediatric kidney allograft recipients in the first year post-transplant. (ClinicalTrials.gov number: NCT00963248).

AB - Epstein-Barr virus (EBV) primary infection constitutes a serious risk for pediatric transplant recipients, particularly as regards the development of EBV-related post-transplant lymphoproliferative disease (PTLD). Currently, there is no established prophylactic regimen. We investigated the association between chemoprophylaxis with valganciclovir (VGCV) or ganciclovir (GCV) and the incidence of EBV viremia in EBV-naïve pediatric renal transplant recipients (R-) who had received a graft from an EBV-positive donor (D+) and are therefore at high risk of EBV primary infection. In a prospective, multicenter trial (n = 114), we compared a cohort on chemoprophylaxis (n = 20) with a similar control cohort without chemoprophylaxis (n = 8). Over the 1-year study period, antiviral prophylaxis with VGCV/GCV was associated with a significantly decreased incidence of EBV primary infection: 9/20 patients (45%) in the prophylaxis group experienced an EBV primary infection compared to 8/8 controls (100%) (P < 0.0001). Chemoprophylaxis was associated with a significantly lower EBV viral load (P < 0.001). Type or intensity of immunosuppressive therapy did not influence the occurrence of EBV primary infection or the level/persistence of EBV viral load. Chemoprophylaxis with VGCV/GCV is associated with a reduced incidence of EBV viremia in high-risk pediatric kidney allograft recipients in the first year post-transplant. (ClinicalTrials.gov number: NCT00963248).

KW - Adult

KW - Humans

KW - Male

KW - Female

KW - Prospective Studies

KW - Cohort Studies

KW - Child

KW - Kidney Transplantation/methods

KW - Immunosuppressive Agents/therapeutic use

KW - Antiviral Agents/therapeutic use

KW - Chemoprevention/methods

KW - Epstein-Barr Virus Infections/prevention & control

KW - Ganciclovir/analogs & derivatives/therapeutic use

KW - Herpesvirus 4, Human/metabolism

KW - Lymphoproliferative Disorders/etiology

KW - Pediatrics/methods

KW - Adult

KW - Humans

KW - Male

KW - Female

KW - Prospective Studies

KW - Cohort Studies

KW - Child

KW - Kidney Transplantation/methods

KW - Immunosuppressive Agents/therapeutic use

KW - Antiviral Agents/therapeutic use

KW - Chemoprevention/methods

KW - Epstein-Barr Virus Infections/prevention & control

KW - Ganciclovir/analogs & derivatives/therapeutic use

KW - Herpesvirus 4, Human/metabolism

KW - Lymphoproliferative Disorders/etiology

KW - Pediatrics/methods

M3 - SCORING: Journal article

VL - 25

SP - 723

EP - 731

JO - TRANSPL INT

JF - TRANSPL INT

SN - 0934-0874

IS - 7

M1 - 7

ER -