Author, year | Long-acting MPH formulation and dosinga | Sample size Age range | Diagnosis | Comorbid conditions | Outcome measures |
---|---|---|---|---|---|
Pharmacokinetic studies | |||||
Gonzalez et al., 2002 [20] | Concerta® (18, 36, 54 mg) | n = 36 | Not applicable | Not stated | PK parameters for 24 hours post-dose, including bioequivalence |
Equasym XL® (20, 40, 60 mg) | 21–40 years | ||||
Haessler et al., 2008 [26] | Ritalin LA® (40 mg) | n = 28 | Not applicable | Not stated | PK parameters for 24 hours post-dose, including bioequivalence |
Medikinet® retard (40 mg) | 18–30 years | ||||
Markowitz et al., 2003 [22] | Concerta® (18 mg) | n = 20 | Not applicable | Not stated | PK parameters for 24 hours post-dose, including bioequivalence |
Ritalin LA® (20 mg) | 21–34 years | ||||
Modi et al., 2000 [23] | Concerta® (18 mg) | n = 36 | Not applicable | Not stated | PK parameters for 30 hours post-dose |
Ritalin SR® (20 mg) | 18–41 years | ||||
Pierce et al., 2010 [24] | Concerta® (18, 27, 36, 54 mg) | n = 71 | ADHD according to DSM-IV-TR criteria | Possibly ODD | PK properties of d,l-MPH after single, multiple, fixed and escalating doses of Concerta® and Daytrana® |
Daytrana® (10, 15, 20, 30 mg/9 hours) | 6–17 years | ||||
Reiz et al., 2008 [25] | Concerta® (18 mg) | n = 24 | Not applicable | Not stated | PK parameters for 24 hours post-dose, including bioequivalence |
Biphentin® (20 mg) | 19–25 years | ||||
Schutz et al., 2009 [28] | Equasym XL® (20 mg) | n = 14 | Not applicable | Not stated | PK parameters for 24 hours post-dose, including bioequivalence |
Medikinet® retard (20 mg) | 22–43 years | ||||
Spencer et al., 2010 [21] | Concerta® (36 mg) | n = 21 | Not applicable | Not stated | PET imaging |
Equasym XL® (40 mg) | 18–55 years | ||||
Tuerck et al., 2007 [27] | Focalin XR® (20 mg) | n = 25 | Not applicable | Not stated | PK parameters for 24 hours post-dose, including bioequivalence |
Ritalin LA® (40 mg) | 19–45 years | ||||
Laboratory school studies | |||||
Lopez et al., 2003 [31] | Concerta® (18, 36 mg) | n = 36 | ADHD according to C-DISC criteria | Not stated | SKAMP-Attention; SKAMP-Deportment; SKAMP-Combined; Math-Attempted; Math-Correct |
Ritalin LA® (20 mg) | 6–12 years | ||||
Muniz et al., 2008 [33] | Concerta® (36, 54 mg) | n = 84 | Combined-type ADHD (89%); Inattentive-type ADHD (11%) according to DSM-IV criteria, established by C-DISC | Not stated | SKAMP-Combined; SKAMP-Attention; SKAMP-Deportment; Math-Attempted; Math-Correct; CPRS |
Focalin XR® (20, 30 mg) | 6–12 years | ||||
Schulz et al., 2010 [38] | Ritalin LA® (20 mg) | n = 147 | Combined-type ADHD (55%); Inattentive-type ADHD (37%); Hyperactive/impulsive-type ADHD according to DSM-IV criteria, confirmed by K-SADS | Disturbance in social behaviour (n = 4), initial insomnia (n = 2), ODD (n = 2), dysphemia (n = 1), encopresis (n = 1) | SKAMP-Combined; Math-Attempted; Math-Correct; NCBRF-TIQ |
Medikinet® retard (20 mg) | 6–14 years | ||||
Silva et al., 2005 [32] | Concerta® (18 mg) | n = 54 | Combined inattentive/hyperactive-type ADHD (70%); Inattentive-type ADHD (28%); Hyperactive/impulsive-type ADHD (2%) according to DSM-IV criteria | Not stated | SKAMP-Attempted; SKAMP-Deportment; SKAMP-Combined; Math-Attempted; Math-Correct |
Ritalin LA® (20 mg) | 6–12 years | ||||
Silva et al., 2008 [18] | Concerta® (36, 54 mg) Focalin XR® (20, 30 mg) | n = 82 6–12 years | Combined-type ADHD (94%); Inattentive-type (6%) according to DSM-IV criteria | Not stated | SKAMP-Attention; SKAMP-Deportment; SKAMP-Combined; Math-Attempted; Math-Correct; CPRS |
Sonuga-Barke et al., 2004 [34] | Concerta® (18, 36, 54 mg) Equasym XL® (20, 40, 60 mg) | n = 184 6–12 years | Combined-type (82%); Inattentive-type (13%); Hyperactive/impulsive-type (5%) according to DSM-IV criteria and confirmed by DISC | Comorbid condition (25%), including anxiety and ODD | Placebo-adjusted SKAMP-Combined |
Post-hoc study of COMACS [37] | Â | ||||
Sonuga-Barke et al., 2007 [35] | Concerta® (18, 36, 54 mg) Equasym XL® (20, 40, 60 mg) | n = 184 6–12 years | Females: Combined-type (77%); Inattentive-type (15%); Hyperactive/impulsive-type (8%). Males: Combined-type (84%); Inattentive-type (12.4%); Hyperactive/impulsive-type (4%) | Comorbid condition (25%), including anxiety and ODD | SKAMP-Combined; PERMP |
Post-hoc study of COMACS [37] | Â | ||||
Sonuga-Barke et al., 2008 [36] | Concerta® (18, 36, 54 mg) | n = 184 | Combined-type (82%); Inattentive-type (13%); Hyperactive/impulsive-type (5%) according to DSM-IV criteria, confirmed by DISC | Comorbid condition (25%), including anxiety and ODD | GMM analysis |
Equasym XL® (20, 40, 60 mg) | 6–12 years | ||||
Post-hoc study of COMACS [37] | |||||
Swanson et al., 2004 [37] | Concerta® (18, 36, 54 mg) | n = 184 | Combined-type (82%); Inattentive-type (13%); Hyperactive/impulsive-type (5%) according to DSM-IV criteria, confirmed by DISC | Comorbid condition (25%), including anxiety and ODD | SKAMP-Attention; SKAMP-Deportment; PERMP |
Equasym XL® (20, 40, 60 mg) | 6–12 years | ||||
COMACS study | |||||
Randomized controlled trials | |||||
Doepfner et al., 2011 [42] | Concerta® (18, 36 mg) | n = 113 | Combined-type ADHD according to DSM-IV, confirmed by interview (DCL-ADHD) | ODD or conduct disorder (36%) | SKAMP-D; DAYAS; FBB-ADHD |
Medikinet® retard (10, 20, 30 mg) | 6–16 years | ||||
Findling et al., 2008 [43] | Concerta® (18, 27, 36, 54 mg) | n = 282 | Combined-type ADHD (71–86%); Inattentive-type ADHD (11–26%); Hyperactive/impulsive-type ADHD (1–2%) according to DSM-IV-TR criteria | Possibly ODD | ADHD-RS-IV mean total score; CTRS-R; CPRS-R; CGI–S; CGI–I; PGA; MPH plasma concentrations at 7.5, 9 and 10 hours post-dose |
Daytrana® (10, 15, 20, 30 mg) | 6–12 years | ||||
Switching studies | |||||
Arnold et al., 2010 [46] | Concerta® (18, 27, 36, 45, 54 mg) | n = 171 | Combined-type ADHD (77%); Inattentive-type ADHD (21%); Hyperactive/impulsive -type ADHD (2%) according to DSM-IV-TR criteria | Possibly ODD | ADHD-RS-IV mean total scores; CGI–I; PGA, CPRS-R; CGI–S |
Ritalin LA® (10, 20, 30, 40, 50 mg) | 6–12 years | ||||
Equasym XL® (10, 15, 20, 30, 40, 50 mg) | |||||
Daytrana® (10, 15, 20, 30 mg) | |||||
Bukstein et al., 2009 [47] | Concerta® (18, 27, 36, 45, 54 mg) | n = 171 | See Arnold et al., 2010 [46] | Possibly ODD | AIM-C; MSS |
Ritalin LA® (10, 20, 30, 40, 50 mg) | 6–12 years | ||||
Equasym XL® (10, 15, 20, 30, 40, 50 mg) | |||||
Daytrana® (10, 15, 20, 30 mg) | |||||
Dirksen et al., 2002 [48] | Equasym XL® (20, 40, 60 mg) | n = 308 | ADHD according to DSM-IV criteria (diagnostic code 314.01) | Not stated | CGI–I; CGI–S; CGI-Efficacy Index |
Concerta® (18, 36, 54, 72 mg) | 6–17 years | ||||
Other long-acting MPH (excluding Concerta®; dose not stated) | |||||
Observational studies | |||||
Doepfner et al., 2011 [49] | Equasym XL® (10–120 mg) | n = 822 | Disturbance of activity/attention (F90.0; 55%); hyperkinetic conduct disorder (F90.1; 36%); other hyperkinetic disorders (F90.8; 8%) according to ICD-10 criteria | Not stated | CGI–S; CGI–I; FBB-ADHD; DAYAS; SDQ-P |
Other long-acting MPH (most commonly Medikinet® retard; approximately 0.85 mg/kg/day) | 6–17 years | ||||
OBSEER study | |||||
Doepfner et al., 2011 [50] | Equasym XL® (10–120 mg) | n = 782 | For total study sample (n = 822) see Doepfner et al., 2011 [49] | Not stated | FBB-ADHD; CGI–S; DAYAS; KINDL |
Other long-acting MPH (mean [SD] 29.2 [11.28] mg) | 6–17 years | ||||
Post-hoc study of OBSEER [49] | |||||
Rothenberger et al., 2011 [51] | See Doepfner et al., 2011 [49] | n = 822 6–17 years | See Doepfner et al., 2011 [49] | Not stated | KINDL; SAMS |
Post-hoc study of OBSEER [49] | |||||
Meta-analyses | |||||
Faraone et al., 2006 [55] | Equasym XL®; Ritalin LA®; | n = 29 articles |  |  | Effect size expressed as SMD |
Concerta®; Daytrana® | Children and adolescents | ||||
Faraone and Buitelaar, 2010 [56] | Equasym XL®; Ritalin LA®; | n = 23 articles |  |  | Effect size expressed as SMD |
Concerta®; Daytrana® | Children and adolescents | ||||
Faraone and Glatt, 2010 [57] | Concerta®; | n = 18 articles |  |  | Effect size expressed as SMD |
Focalin XR® | Adults | ||||
Peterson et al., 2008 [58] | Concerta®; | n = 22 articles |  |  | Ratio of relative risks |
Focalin XR® | Adults | ||||
Systematic reviews | |||||
Banaschewski et al., 2006 [52] | Concerta®; Ritalin LA®; Equasym XL®; Medikinet® retard | Not stated |  |  | Effect size expressed as SMD |
Brams et al., 2008 [53] | Concerta®; Daytrana®; Focalin XR®; Equasym XL®; Ritalin LA® | n = 18 articles |  |  | SKAMP, CADS-T, IOWA Conners’ Rating Scale, ADHD-RS-IV, PERMP, CGIS-T |
Children and adolescents | |||||
Brams et al., 2010 [19] | Concerta®; Focalin XR®; Equasym XL®; Ritalin LA® | n = 15 articles |  |  | PERMP |
Children, adolescents and adults | |||||
Swanson et al., 2002 [54] | Concerta®; Equasym XL®; Ritalin LA® | Not stated |  |  | SKAMP, 10-Minute Math Test, PK measures, effect size |