Single centre experience with basiliximab in paediatric renal transplantation.

Standard

Single centre experience with basiliximab in paediatric renal transplantation. / Pape, Lars; Strehlau, Juergen; Henne, Thomas; Latta, Kay; Nashan, Björn; Ehrich, Jochen H H; Klempnauer, Juergen; Offner, Gisela.

in: NEPHROL DIAL TRANSPL, Jahrgang 17, Nr. 2, 2, 2002, S. 276-280.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Pape, L, Strehlau, J, Henne, T, Latta, K, Nashan, B, Ehrich, JHH, Klempnauer, J & Offner, G 2002, 'Single centre experience with basiliximab in paediatric renal transplantation.', NEPHROL DIAL TRANSPL, Jg. 17, Nr. 2, 2, S. 276-280. <http://www.ncbi.nlm.nih.gov/pubmed/11812879?dopt=Citation>

APA

Pape, L., Strehlau, J., Henne, T., Latta, K., Nashan, B., Ehrich, J. H. H., Klempnauer, J., & Offner, G. (2002). Single centre experience with basiliximab in paediatric renal transplantation. NEPHROL DIAL TRANSPL, 17(2), 276-280. [2]. http://www.ncbi.nlm.nih.gov/pubmed/11812879?dopt=Citation

Vancouver

Pape L, Strehlau J, Henne T, Latta K, Nashan B, Ehrich JHH et al. Single centre experience with basiliximab in paediatric renal transplantation. NEPHROL DIAL TRANSPL. 2002;17(2):276-280. 2.

Bibtex

@article{1cf594d4606d47a99cab0641dd8a2ab8,
title = "Single centre experience with basiliximab in paediatric renal transplantation.",
abstract = "BACKGROUND: Introduction of IL-2-receptor antagonists has led to significantly decreasing numbers of acute rejection episodes in renal transplantation in adults. No data are available in paediatric recipients. METHODS: Between 1997 and 2000, 78 renal transplantations were performed in 77 children aged 0.5-16 years. Basiliximab, cyclosporin A (CsA) and prednisolone were administered in 48 children (age 7.8 +/- 5.3 years) and compared with 29 children (age 7.3 +/- 5.2 years) receiving CsA and prednisolone only. The number of acute rejections, survival, glomerular filtration rate (GFR) and side effects were determined for 3 years after transplantation. RESULTS: All 77 patients survived the observation period. One year graft survival in the basiliximab group was 95%, which is similar to the comparison group (93%). Children receiving basiliximab showed a lower incidence of acute rejection than the comparison group (14% vs 34%). The calculated GFR was lower in the basiliximab group when discharging from hospital, with 51 compared with 66 ml/min/1.73 m(2) in the non-basiliximab group. This was associated with higher CsA trough levels (214 vs 174 ng/ml) in the basiliximab patients. After 1 year the GFR was comparable in both groups (58 vs 52 ml/min/1.73 m(2)). CONCLUSIONS: Basiliximab offers excellent allograft survival, a lower incidence of acute rejections and almost no side effects. Therefore it can be recommended for routine immunosuppressive therapy in paediatric renal transplantation.",
author = "Lars Pape and Juergen Strehlau and Thomas Henne and Kay Latta and Bj{\"o}rn Nashan and Ehrich, {Jochen H H} and Juergen Klempnauer and Gisela Offner",
year = "2002",
language = "Deutsch",
volume = "17",
pages = "276--280",
journal = "NEPHROL DIAL TRANSPL",
issn = "0931-0509",
publisher = "Oxford University Press",
number = "2",

}

RIS

TY - JOUR

T1 - Single centre experience with basiliximab in paediatric renal transplantation.

AU - Pape, Lars

AU - Strehlau, Juergen

AU - Henne, Thomas

AU - Latta, Kay

AU - Nashan, Björn

AU - Ehrich, Jochen H H

AU - Klempnauer, Juergen

AU - Offner, Gisela

PY - 2002

Y1 - 2002

N2 - BACKGROUND: Introduction of IL-2-receptor antagonists has led to significantly decreasing numbers of acute rejection episodes in renal transplantation in adults. No data are available in paediatric recipients. METHODS: Between 1997 and 2000, 78 renal transplantations were performed in 77 children aged 0.5-16 years. Basiliximab, cyclosporin A (CsA) and prednisolone were administered in 48 children (age 7.8 +/- 5.3 years) and compared with 29 children (age 7.3 +/- 5.2 years) receiving CsA and prednisolone only. The number of acute rejections, survival, glomerular filtration rate (GFR) and side effects were determined for 3 years after transplantation. RESULTS: All 77 patients survived the observation period. One year graft survival in the basiliximab group was 95%, which is similar to the comparison group (93%). Children receiving basiliximab showed a lower incidence of acute rejection than the comparison group (14% vs 34%). The calculated GFR was lower in the basiliximab group when discharging from hospital, with 51 compared with 66 ml/min/1.73 m(2) in the non-basiliximab group. This was associated with higher CsA trough levels (214 vs 174 ng/ml) in the basiliximab patients. After 1 year the GFR was comparable in both groups (58 vs 52 ml/min/1.73 m(2)). CONCLUSIONS: Basiliximab offers excellent allograft survival, a lower incidence of acute rejections and almost no side effects. Therefore it can be recommended for routine immunosuppressive therapy in paediatric renal transplantation.

AB - BACKGROUND: Introduction of IL-2-receptor antagonists has led to significantly decreasing numbers of acute rejection episodes in renal transplantation in adults. No data are available in paediatric recipients. METHODS: Between 1997 and 2000, 78 renal transplantations were performed in 77 children aged 0.5-16 years. Basiliximab, cyclosporin A (CsA) and prednisolone were administered in 48 children (age 7.8 +/- 5.3 years) and compared with 29 children (age 7.3 +/- 5.2 years) receiving CsA and prednisolone only. The number of acute rejections, survival, glomerular filtration rate (GFR) and side effects were determined for 3 years after transplantation. RESULTS: All 77 patients survived the observation period. One year graft survival in the basiliximab group was 95%, which is similar to the comparison group (93%). Children receiving basiliximab showed a lower incidence of acute rejection than the comparison group (14% vs 34%). The calculated GFR was lower in the basiliximab group when discharging from hospital, with 51 compared with 66 ml/min/1.73 m(2) in the non-basiliximab group. This was associated with higher CsA trough levels (214 vs 174 ng/ml) in the basiliximab patients. After 1 year the GFR was comparable in both groups (58 vs 52 ml/min/1.73 m(2)). CONCLUSIONS: Basiliximab offers excellent allograft survival, a lower incidence of acute rejections and almost no side effects. Therefore it can be recommended for routine immunosuppressive therapy in paediatric renal transplantation.

M3 - SCORING: Zeitschriftenaufsatz

VL - 17

SP - 276

EP - 280

JO - NEPHROL DIAL TRANSPL

JF - NEPHROL DIAL TRANSPL

SN - 0931-0509

IS - 2

M1 - 2

ER -