Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation.

Standard

Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation. / Kemper, Markus J.; Spartà, Giuseppina; Laube, Guido F; Miozzari, Marco; Neuhaus, Thomas J.

in: CLIN TRANSPLANT, Jahrgang 17, Nr. 2, 2, 2003, S. 130-134.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Kemper, MJ, Spartà, G, Laube, GF, Miozzari, M & Neuhaus, TJ 2003, 'Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation.', CLIN TRANSPLANT, Jg. 17, Nr. 2, 2, S. 130-134. <http://www.ncbi.nlm.nih.gov/pubmed/12709079?dopt=Citation>

APA

Kemper, M. J., Spartà, G., Laube, G. F., Miozzari, M., & Neuhaus, T. J. (2003). Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation. CLIN TRANSPLANT, 17(2), 130-134. [2]. http://www.ncbi.nlm.nih.gov/pubmed/12709079?dopt=Citation

Vancouver

Kemper MJ, Spartà G, Laube GF, Miozzari M, Neuhaus TJ. Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation. CLIN TRANSPLANT. 2003;17(2):130-134. 2.

Bibtex

@article{fe11138f5c2942c281adb28b1263e079,
title = "Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation.",
abstract = "Calcineurin inhibition with tacrolimus has been used after renal transplantation (RTPL) as rescue therapy for insufficient immunological control or if cyclosporin A (CSA) toxicity occurred. Neurologic side-effects occur but are rare in children, usually presenting as tremor; however, serious complications, e.g. the posterior leukoencephalopathy syndrome are also documented. Twenty children (10 girls) were switched to tacrolimus: 11 (55%) for immunological reasons (n = 9: steroid-resistant rejection; n = 2: recurrent rejections) and nine for CSA side-effects. Tacrolimus was started at a median of 8 wk (range 10 d to 8.7 yr) after RTPL and was continued for a median of 2.5 yr (range 5 wk to 4.6 yr). Renal function significantly improved over a period of 12 months following conversion to tacrolimus (glomerular filtration rate 56 +/- 19 vs. 66 +/- 16 mL/min/1.73 m2; p < 0.03; n = 13). Fifteen of 20 (75%) patients tolerated tacrolimus well. The most frequent side-effects were neuropsychological and behavioral symptoms in three children, ranging from anorexia nervosa-like symptoms with weight loss, amenorrhea, depression and school problems to severe insomnia and to aggressive and anxious behavior in one child. Only the latter child was exposed to toxic tacrolimus blood levels. All side-effects were fully reversible after discontinuation of tacrolimus. In conclusion, tacrolimus had a beneficial effect on renal function and was well tolerated in the majority of pediatric patients. However, neuropsychologic and behavioral side-effects are important and maybe underrecognized in children.",
keywords = "Humans, Male, Female, Adolescent, Child, Drug Resistance, *Kidney Transplantation, Immunosuppressive Agents/*adverse effects, Weight Loss, Abdominal Pain/chemically induced, Aggression, Amenorrhea/chemically induced, Child Behavior Disorders/chemically induced, Cyclosporine/adverse effects, Depression/chemically induced, Diabetes Mellitus/chemically induced, Gingival Hyperplasia/chemically induced, Graft Rejection/prevention & control, Hypertrichosis/chemically induced, Kidney Diseases/chemically induced, Sleep Initiation and Maintenance Disorders/chemically induced, Tacrolimus/*adverse effects, Humans, Male, Female, Adolescent, Child, Drug Resistance, *Kidney Transplantation, Immunosuppressive Agents/*adverse effects, Weight Loss, Abdominal Pain/chemically induced, Aggression, Amenorrhea/chemically induced, Child Behavior Disorders/chemically induced, Cyclosporine/adverse effects, Depression/chemically induced, Diabetes Mellitus/chemically induced, Gingival Hyperplasia/chemically induced, Graft Rejection/prevention & control, Hypertrichosis/chemically induced, Kidney Diseases/chemically induced, Sleep Initiation and Maintenance Disorders/chemically induced, Tacrolimus/*adverse effects",
author = "Kemper, {Markus J.} and Giuseppina Spart{\`a} and Laube, {Guido F} and Marco Miozzari and Neuhaus, {Thomas J}",
year = "2003",
language = "English",
volume = "17",
pages = "130--134",
journal = "CLIN TRANSPLANT",
issn = "0902-0063",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Neuropsychologic side-effects of tacrolimus in pediatric renal transplantation.

AU - Kemper, Markus J.

AU - Spartà, Giuseppina

AU - Laube, Guido F

AU - Miozzari, Marco

AU - Neuhaus, Thomas J

PY - 2003

Y1 - 2003

N2 - Calcineurin inhibition with tacrolimus has been used after renal transplantation (RTPL) as rescue therapy for insufficient immunological control or if cyclosporin A (CSA) toxicity occurred. Neurologic side-effects occur but are rare in children, usually presenting as tremor; however, serious complications, e.g. the posterior leukoencephalopathy syndrome are also documented. Twenty children (10 girls) were switched to tacrolimus: 11 (55%) for immunological reasons (n = 9: steroid-resistant rejection; n = 2: recurrent rejections) and nine for CSA side-effects. Tacrolimus was started at a median of 8 wk (range 10 d to 8.7 yr) after RTPL and was continued for a median of 2.5 yr (range 5 wk to 4.6 yr). Renal function significantly improved over a period of 12 months following conversion to tacrolimus (glomerular filtration rate 56 +/- 19 vs. 66 +/- 16 mL/min/1.73 m2; p < 0.03; n = 13). Fifteen of 20 (75%) patients tolerated tacrolimus well. The most frequent side-effects were neuropsychological and behavioral symptoms in three children, ranging from anorexia nervosa-like symptoms with weight loss, amenorrhea, depression and school problems to severe insomnia and to aggressive and anxious behavior in one child. Only the latter child was exposed to toxic tacrolimus blood levels. All side-effects were fully reversible after discontinuation of tacrolimus. In conclusion, tacrolimus had a beneficial effect on renal function and was well tolerated in the majority of pediatric patients. However, neuropsychologic and behavioral side-effects are important and maybe underrecognized in children.

AB - Calcineurin inhibition with tacrolimus has been used after renal transplantation (RTPL) as rescue therapy for insufficient immunological control or if cyclosporin A (CSA) toxicity occurred. Neurologic side-effects occur but are rare in children, usually presenting as tremor; however, serious complications, e.g. the posterior leukoencephalopathy syndrome are also documented. Twenty children (10 girls) were switched to tacrolimus: 11 (55%) for immunological reasons (n = 9: steroid-resistant rejection; n = 2: recurrent rejections) and nine for CSA side-effects. Tacrolimus was started at a median of 8 wk (range 10 d to 8.7 yr) after RTPL and was continued for a median of 2.5 yr (range 5 wk to 4.6 yr). Renal function significantly improved over a period of 12 months following conversion to tacrolimus (glomerular filtration rate 56 +/- 19 vs. 66 +/- 16 mL/min/1.73 m2; p < 0.03; n = 13). Fifteen of 20 (75%) patients tolerated tacrolimus well. The most frequent side-effects were neuropsychological and behavioral symptoms in three children, ranging from anorexia nervosa-like symptoms with weight loss, amenorrhea, depression and school problems to severe insomnia and to aggressive and anxious behavior in one child. Only the latter child was exposed to toxic tacrolimus blood levels. All side-effects were fully reversible after discontinuation of tacrolimus. In conclusion, tacrolimus had a beneficial effect on renal function and was well tolerated in the majority of pediatric patients. However, neuropsychologic and behavioral side-effects are important and maybe underrecognized in children.

KW - Humans

KW - Male

KW - Female

KW - Adolescent

KW - Child

KW - Drug Resistance

KW - Kidney Transplantation

KW - Immunosuppressive Agents/adverse effects

KW - Weight Loss

KW - Abdominal Pain/chemically induced

KW - Aggression

KW - Amenorrhea/chemically induced

KW - Child Behavior Disorders/chemically induced

KW - Cyclosporine/adverse effects

KW - Depression/chemically induced

KW - Diabetes Mellitus/chemically induced

KW - Gingival Hyperplasia/chemically induced

KW - Graft Rejection/prevention & control

KW - Hypertrichosis/chemically induced

KW - Kidney Diseases/chemically induced

KW - Sleep Initiation and Maintenance Disorders/chemically induced

KW - Tacrolimus/adverse effects

KW - Humans

KW - Male

KW - Female

KW - Adolescent

KW - Child

KW - Drug Resistance

KW - Kidney Transplantation

KW - Immunosuppressive Agents/adverse effects

KW - Weight Loss

KW - Abdominal Pain/chemically induced

KW - Aggression

KW - Amenorrhea/chemically induced

KW - Child Behavior Disorders/chemically induced

KW - Cyclosporine/adverse effects

KW - Depression/chemically induced

KW - Diabetes Mellitus/chemically induced

KW - Gingival Hyperplasia/chemically induced

KW - Graft Rejection/prevention & control

KW - Hypertrichosis/chemically induced

KW - Kidney Diseases/chemically induced

KW - Sleep Initiation and Maintenance Disorders/chemically induced

KW - Tacrolimus/adverse effects

M3 - SCORING: Journal article

VL - 17

SP - 130

EP - 134

JO - CLIN TRANSPLANT

JF - CLIN TRANSPLANT

SN - 0902-0063

IS - 2

M1 - 2

ER -