Tolerability, Safety, and Benefits of Risperidone in Children and Adolescents with Autism: 21-Month Follow-up After 8-Week Placebo-Controlled Trial

dc.contributor.authorAman, Michael
dc.contributor.authorRettiganti, Mallikarjuna
dc.contributor.authorNagaraja, Haikady N.
dc.contributor.authorHollway, Jill A.
dc.contributor.authorMcCracken, James
dc.contributor.authorMcDougle, Christopher J.
dc.contributor.authorTierney, Elaine
dc.contributor.authorScahill, Lawrence
dc.contributor.authorArnold, L. Eugene
dc.contributor.authorHellings, Jessica
dc.contributor.authorPosey, David J.
dc.contributor.authorSwiezy, Naomi B.
dc.contributor.authorGuhman, Jaswinder
dc.contributor.authorGrados, Marco
dc.contributor.authorShah, Bhavik
dc.contributor.authorVitiello, Benedetto
dc.contributor.departmentDepartment of Psychiatry, IU School of Medicineen_US
dc.date.accessioned2017-05-30T14:36:43Z
dc.date.available2017-05-30T14:36:43Z
dc.date.issued2015-08-01
dc.description.abstractOBJECTIVE: Risperidone has demonstrated efficacy for acute (8 week) and intermediate length (6 month) management of severe irritability and aggression in children and adolescents with autism. Less is known about the long-term effects of risperidone exposure in this population. We examined the tolerability, safety, and therapeutic benefit of risperidone exposure over a 1-2 year follow-up period. METHODS: In a naturalistic study, 84 children and adolescents 5-17 years of age (from an original sample of 101) were assessed an average of 21.4 months after initial entry into a placebo-controlled 8 week trial of risperidone for children and adolescents with autism and severe irritability. They were assessed at baseline and at follow-up on safety and tolerability measures (blood, urinalysis, electrocardiogram [ECG], medical history, vital signs, neurological symptoms, other adverse events), developmental measures (adaptive behavior, intelligence quotient [IQ]), and standardized rating instruments. Treatment over the follow-up period, after completion of protocol participation, was uncontrolled. Statistical analyses assessed outcome over time with or without prolonged risperidone therapy. RESULTS: Two-thirds of the 84 subjects continued to receive risperidone (mean 2.47 mg/day, S.D. 1.29 mg). At follow-up, risperidone was associated with more enuresis, more excessive appetite, and more weight gain, but not more adverse neurological effects. No clinically significant events were noted on blood counts, chemistries, urinalysis, ECG, or interim medical history. Regardless of drug condition at follow-up, there was considerable improvement in maladaptive behavior compared with baseline, including core symptoms associated with autism. Height and weight gains were elevated with risperidone. Social skills on Vineland Adaptive Behavior Scale (VABS) improved with risperidone. Parent-rated Aberrant Behavior Checklist (ABC) Irritability subscale scores were reduced in those taking risperidone at follow-up. Several other measures of maladaptive behavior (some related to socialization) also showed improved functioning in association with risperidone on the ABC or on the Modified Real Life Rating Scale. CONCLUSIONS: Increased appetite, weight gain, and enuresis are risks associated with long-term risperidone. Our data suggest that these risks were balanced by longer-term behavioral and social benefits for many children over 1.8 years of ongoing treatment.en_US
dc.identifier.citationAman, M., Rettiganti, M., Nagaraja, H. N., Hollway, J. A., McCracken, J., McDougle, C. J., … Vitiello, B. (2015). Tolerability, Safety, and Benefits of Risperidone in Children and Adolescents with Autism: 21-Month Follow-up After 8-Week Placebo-Controlled Trial. Journal of Child and Adolescent Psychopharmacology, 25(6), 482–493. http://doi.org/10.1089/cap.2015.0005en_US
dc.identifier.urihttps://hdl.handle.net/1805/12773
dc.language.isoen_USen_US
dc.publisherMary Ann Liebert, Inc.en_US
dc.relation.isversionof10.1089/cap.2015.0005en_US
dc.relation.journalJournal of Child and Adolescent Psychopharmacologyen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectAggressionen_US
dc.subjectAntipsychotic Agentsen_US
dc.subjectAutistic Disorderen_US
dc.subjectIrritable Mooden_US
dc.subjectRisperidoneen_US
dc.subjectWeight Gainen_US
dc.titleTolerability, Safety, and Benefits of Risperidone in Children and Adolescents with Autism: 21-Month Follow-up After 8-Week Placebo-Controlled Trialen_US
dc.typeArticleen_US
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545698/en_US
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