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Table 1 Characteristics of included studies

From: Pharmacological interventions for challenging behaviour in children with intellectual disabilities: a systematic review and meta-analysis

Study

Diagnosis

Targeted CBa(measure)

Intervention (dose mg/day)

Comparison (dose mg/day)

Treatment duration

Akhondzadeh 2008

ASD

Severely disruptive symptoms (ABC total)

Piracetam (800) + risperidone (3)

Placebo + risperidone (3)

10 weeks

Aman 2002

Mild to moderate ID

Conduct problems (NCBRF conduct)

Risperidone (1.2)

Placebo

6 weeks

Ghanizadeh 2013

ASD

Irritability (ABC-I)

Aripiprazole (5.5)

Risperidone (1.1)

8 weeks

Hardan 2012

ASD

Irritability (ABC-I)

N-acetylcysteine (2700)

Placebo

12 weeks

Hellings 2005

ASD + IDb

Irritability (ABC-I)

Valproate (20)c

Placebo

8 weeks

Hollander 2010

ASDd

Irritability (ABC-I)

Valproate (375)

Placebo

8 weeks

Kent 2013e

ASD

Irritability (ABC-I)

Risperidone (1.8)f

Placebo

6 weeks

Malone 2001

ASD + mild to severe IDg

Hyperactivity (CPRS-H)

Olanzapine (10)f

Haloperidol (2.5)

6 weeks

Marcus 2009

ASD

Irritability (ABC-I)

Aripiprazole (10)h

Placebo

8 weeks

Owen 2009

ASD

Irritability (ABC-I)

Aripiprazole (8.9)

Placebo

8 weeks

Rezaei 2010

ASD

Irritability (ABC-I)

Topiramate (200) + risperidone (2)f

Placebo + risperidone (2)f

8 weeks

RUPP 2002i

ASD + mild to severe ID

Irritability (ABC-I)

Risperidone (1.8)

Placebo

8 weeks

Shea 2004

ASD + mild to moderate ID

Conduct problems (NCBRF conduct)

Risperidone (1.5)

Placebo

8 weeks

Snyder 2002

Mild to moderate IDj

Conduct problems (NCBRF conduct)

Risperidone (1)

Placebo

6 weeks

  1. Notes: ASD = autism spectrum disorder; CB = challenging behaviour; ID = intellectual disability; N = number randomised; ABC total = Aberrant Behaviour Checklist total score; ABC-I = Aberrant Behaviour Checklist: Irritability; CGI-I = Clinical Global Impressions: Improvement; CPRS-H Children’s Psychiatric Rating Scale: Hyperactivity; NCBRF = Nisonger Child Behaviour Rating Form: Conduct problems. a Primary outcome measure for meta-analysis; b 13 % of sample had borderline to average intelligence; 87 % were diagnosed with ID; c 20 mg/kg/day; d15% of sample had Asperger’s syndrome; e Three armed trial: high dose risperidone and placebo arms used in meta-analysis; f Maximum dose; g 8 % of participants had normal cognitive functioning, all others had mild to severe ID; h Data from high, moderate and low dose conditions combined in meta-analyses; i Research Units on Pediatric psychopharmacology (RUPP) Autism Spectrum Disorder Network; j 2 % of participants had borderline intellectual functioning; all others had mild to moderate ID.