Risperidone versus aripiprazole fracture risk in children and adolescents with autism spectrum disorders

Autor: Joop P. W. van den Bergh, Frank de Vries, Richard Houghton, Kiely Law, Yutong Liu
Přispěvatelé: Clinical Pharmacy, RS: Carim - V01 Vascular complications of diabetes and metabolic syndrome, Interne Geneeskunde, RS: NUTRIM - R3 - Respiratory & Age-related Health, MUMC+: DA KFT Medische Staf (9)
Rok vydání: 2021
Předmět:
Male
Pediatrics
SEROTONIN REUPTAKE INHIBITORS
medicine.medical_treatment
ANTIPSYCHOTIC MEDICATION
Cohort Studies
Fractures
Bone

DOUBLE-BLIND
0302 clinical medicine
Child
Genetics (clinical)
General Neuroscience
05 social sciences
Hazard ratio
fractures
OPEN-LABEL
PSYCHOTROPIC MEDICATIONS
Cohort
Female
Aripiprazole
IRRITABILITY
BONE-MINERAL DENSITY
Antipsychotic Agents
050104 developmental & child psychology
medicine.drug
medicine.medical_specialty
Adolescent
autism spectrum disorder
Lower risk
03 medical and health sciences
aripiprazole
medicine
Humans
0501 psychology and cognitive sciences
Antipsychotic
SERUM PROLACTIN
Retrospective Studies
risperidone
Risperidone
PEDIATRIC-PATIENTS
business.industry
medicine.disease
United States
Confidence interval
antipsychotics
ADHD SYMPTOMS
Autism
Neurology (clinical)
business
030217 neurology & neurosurgery
Zdroj: Autism Research, 14(8), 1800-1814. Wiley
ISSN: 1939-3806
1939-3792
DOI: 10.1002/aur.2541
Popis: Risperidone and aripiprazole, commonly used antipsychotics in children with autism spectrum disorder (ASD), have previously been associated with elevated fracture risk in other populations. The aim of this study was to evaluate and compare the risk of fracture among children with ASD using risperidone or aripiprazole. This was a retrospective, propensity-score matched cohort study, set between January 2013 and December 2018. We used the MarketScan Medicaid insurance data, which covers multiple states of the United States. We included ASD children aged 2-18 years, who were new users of aripiprazole or risperidone and with no prior history of antipsychotic use or fractures. The main exposure was the continued use of aripiprazole or risperidone. The incidence rates of any fracture during follow-up were evaluated, and the risk between aripiprazole and risperidone was compared via Cox-proportional hazard models. Results were stratified by age, sex, duration of exposure and fracture site. In total, 3312 patients (78% male; mean [SD] age 11.0 [3.7] years) were identified for each cohort. Over the full duration of follow-up, fracture incidence rates per 1000 patient-years were 23.2 for risperidone and 38.4 for aripiprazole (hazard ratio and 95% confidence interval: 0.60 [0.44-0.83]). Risks were similar between cohorts throughout the first 180 days on treatment, but significantly higher in the aripiprazole group thereafter. Extremity fractures drove most of the increased risk, with the biggest differences in lower leg and ankle fractures. Differences widened for children aged 10 years or younger (HR [95% CI]: 0.47 [0.30-0.74]). In conclusion, compared to aripiprazole, risperidone was associated with 40% lower risk of fracture. Further analysis on the mechanism and long-term bone health of antipsychotic-treated children with ASD is warranted.Lay summary We compared the risk of bone fractures among 6624 children with autism spectrum disorder (ASD), half of whom used risperidone and half of whom used aripiprazole. Taking other factors into account, risks were similar between the two groups throughout the first 180 days on treatment, but significantly higher in the aripiprazole group thereafter. The biggest differences were in lower leg and ankle fractures. Overall, compared with aripiprazole, risperidone was associated with 40% lower risk of fracture.
Databáze: OpenAIRE