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P0299 - Atypical antipsychotics and their metabolic impact on psychiatrically hospitalized children and adolescents

Published online by Cambridge University Press:  16 April 2020

R.R. Silva
Affiliation:
Department of Child and Adolescent Psychiatry, New York University School of Medicine, New York, NY, USA
M. Ghaffari
Affiliation:
Department of Child and Adolescent Psychiatry, New York University School of Medicine, New York, NY, USA
N. Martinez
Affiliation:
Department of Child and Adolescent Psychiatry, New York University School of Medicine, New York, NY, USA
E. Teitel
Affiliation:
Department of Child and Adolescent Psychiatry, New York University School of Medicine, New York, NY, USA
M. Pappagallo
Affiliation:
Department of Child and Adolescent Psychiatry, New York University School of Medicine, New York, NY, USA
G. Gosselin
Affiliation:
Department of Psychiatry, Harvard Medical School, Children's Hospital, Boston, MA, USA

Abstract

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Objective:

Atypical antipsychotic use in youth has increased. Adverse metabolic effects on weight, lipids, and glucose are evident in adults, but inadequately studied in youth. This report focuses on the metabolic effects of these agents in psychiatrically hospitalized youth.

Methods:

Inpatient subjects were assessed at admission, 3 weeks, and discharge. Weight, body mass index, blood pressure, fasting glucose levels, high and low density lipoproteins (HDL and LDL, respectively), and triglycerides were measured.

Results:

N=112 subjects, diagnosed as: Affective Disorders (26.4%), Disruptive Behavior Disorders (32.6%), Pervasive Development Disorders (9.3%), Psychotic Disorders (5.4%), and Others (26.3%). Ages ranged from 4-17 years. Patients received: risperidone (N=41), olanzapine (N=13), quetiapine (N= 15), aripiprazole (N=22), while 34 patients received no medication. Average length of hospital stay (LOS) was 55.9 days (1-289). For the sample as a whole, trends of statistical differences were noted in weight at the time of discharge (+3.79 lbs). Weight gain at discharge was significantly correlated with only olanzapine (r=.553, p<0.0001), multiple regression analysis controlling for LOS is also significant (Beta .558, p < 0.0001) for olanzapine. For the medication treated group, statistically significant increases in HDL are noted at three weeks (+ 5 mgs/dl, p = 0.023); at discharge the difference was not significant. A similar trend was observed for glucose. There was a statistical trend for decrease in triglycerides at 3 weeks (15 mg/dl, p = 0.054), discharge difference was non-significant (-9 mg/dl).

Conclusion:

Certain agents may carry greater propensity for inducing certain metabolic changes, but further study is required.

Type
Poster Session I: Neuroleptics and Antipsychotics
Copyright
Copyright © European Psychiatric Association 2008
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