TY - JOUR
T1 - Incidence of adverse events in antipsychotic-naïve children and adolescents treated with antipsychotic drugs
T2 - Results of a multicenter naturalistic study (ETAPE)
AU - Menard, Marie Line
AU - Thümmler, Susanne
AU - Giannitelli, Marianna
AU - Cruzel, Coralie
AU - Bonnot, Olivier
AU - Cohen, David
AU - Askenazy, Florence
AU - Boublil, Michel
AU - Chambry, Jean
AU - Charvet, Dorothée
AU - Cseterky, Mona
AU - Fontas, Eric
AU - Fourneret, Pierre
AU - Gicquel, Ludovic
AU - Kabuth, Bernard
AU - Leroy, Bernard
AU - Maria, Fanny
AU - Moceri, Pamela
AU - Parassol-Girard, Nadege
AU - Ravis, Brigitte
AU - Raynaud, Jean Philippe
AU - Roche, Jean Francois
AU - Rochet, Thierry
N1 - Publisher Copyright:
© 2019 Elsevier B.V. and ECNP
PY - 2019/12
Y1 - 2019/12
N2 - The main objective of ETAPE study was to determine the incidence of adverse events (AEs) potentially related to antipsychotic (AP) during a 12-months observational study of naturalistic treatment. ETAPE is a naturalistic prospective multicenter study conducted between April 2013 and May 2016. 200 patients were included. The mean age was 12 ± 3 years, with 73.6% being males. Patients presented a significant clinical improvement over time. At baseline, 92% of patients received a second generation AP, 74% AP monotherapy and 79.5% off-label AP prescriptions. Clinical diagnoses were heterogeneous including psychosis, anxiety, mood and neurodevelopmental disorders. The overall AE incidence rate was 11.52 AEs per person-years. Among AEs potentially attributable to AP, 15.4% were neuromotor, 14.8% gastroenterological, 12.2% metabolic and 11.8% general symptoms. Weight and body mass index increased significantly. More than half of AE appeared during the first 3 months, but onset of AE was noted all over follow-up. The presence of AEs was stable over time. ETAPE study highlights a high incidence rate of AE in children treated with AP. A careful and continuous clinical and biological monitoring is required to adapt treatment decisions based on benefice-risk-analysis. Moreover, additional research is warranted, also in regard of high proportion of off-label prescriptions.
AB - The main objective of ETAPE study was to determine the incidence of adverse events (AEs) potentially related to antipsychotic (AP) during a 12-months observational study of naturalistic treatment. ETAPE is a naturalistic prospective multicenter study conducted between April 2013 and May 2016. 200 patients were included. The mean age was 12 ± 3 years, with 73.6% being males. Patients presented a significant clinical improvement over time. At baseline, 92% of patients received a second generation AP, 74% AP monotherapy and 79.5% off-label AP prescriptions. Clinical diagnoses were heterogeneous including psychosis, anxiety, mood and neurodevelopmental disorders. The overall AE incidence rate was 11.52 AEs per person-years. Among AEs potentially attributable to AP, 15.4% were neuromotor, 14.8% gastroenterological, 12.2% metabolic and 11.8% general symptoms. Weight and body mass index increased significantly. More than half of AE appeared during the first 3 months, but onset of AE was noted all over follow-up. The presence of AEs was stable over time. ETAPE study highlights a high incidence rate of AE in children treated with AP. A careful and continuous clinical and biological monitoring is required to adapt treatment decisions based on benefice-risk-analysis. Moreover, additional research is warranted, also in regard of high proportion of off-label prescriptions.
KW - Adverse events
KW - Antipsychotics
KW - Child and adolescent psychiatry
KW - Pediatric population
KW - Psychotropics
UR - http://www.scopus.com/inward/record.url?scp=85074844302&partnerID=8YFLogxK
U2 - 10.1016/j.euroneuro.2019.10.006
DO - 10.1016/j.euroneuro.2019.10.006
M3 - Article
C2 - 31699516
AN - SCOPUS:85074844302
SN - 0924-977X
VL - 29
SP - 1397
EP - 1407
JO - European Neuropsychopharmacology
JF - European Neuropsychopharmacology
IS - 12
ER -