PMID- 38280948 OWN - NLM STAT- Publisher LR - 20240127 IS - 1433-8491 (Electronic) IS - 0940-1334 (Linking) DP - 2024 Jan 27 TI - Long-term medication for ADHD (LMA) trial: 2-year prospective observational study in children and adolescents. Core symptoms, daily functioning, and comorbidity outcomes. LID - 10.1007/s00406-023-01744-1 [doi] AB - More knowledge is needed about long-term ADHD medication and symptom, daily functioning, comorbidity, and tolerability outcomes. This "Long-term Medication for ADHD (LMA) trial" was a prospective observational 2-year trial in children and adolescents aged 6-18 years (extension of 1-year trial). Participants met criteria for DSM-5 ADHD (inattentive or combined), with complex comorbidities; autism spectrum disorder (31%), autistic traits (24%), oppositional symptoms (59%), anxiety (32%), dyslexia/language disorder (16%), borderline intellectual functioning (17%). Medication was individually tailored and followed-up at clinical visits (1, 2, 3, 6, 12, 18, 24 months). Primary outcome: Clinical Global Impression-Severity and Improvement scales (CGI-S, CGI-I). Secondary outcomes: Investigator-rated ADHD-Rating Scale, Weiss Functional Impairment Rating Scale-Parent report (WFIRS-P; Family, School Learning and Behavior, Life Skills, Self-Concept, Social Activities, and Risky Activities domains), comorbidity symptoms and adverse events (AEs). One hundred twenty-eight participants were enrolled (1-year trial only n = 27, LMA trial n = 101). Of these 29 (23%) discontinued, mainly due to AEs (n = 7), moving (n = 7), or no longer needing medication (n = 6). Main AEs were poor appetite, low mood, anxiety, irritability, fatigue. Improvements from baseline to 2 years were large in CGI-S (effect size (ES) 2.28), ADHD-RS (ES 2.06), and moderate to large in WFIRS-P (ES total 0.73, learning 0.4, family 0.67). Overall, the trial showed robust and sustained improvements in ADHD symptom severity and daily functioning over a period of 2 years of ADHD medication in children and adolescents with ADHD and complex comorbidities. Most AEs were mild. Comorbidity symptoms were improved after 1 year, particularly oppositional symptoms, depression, and anxiety. CI - (c) 2024. The Author(s). FAU - Johnson, M AU - Johnson M AUID- ORCID: 0000-0001-5195-3379 AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. mats.johnson@gnc.gu.se. FAU - Johnels, J Asberg AU - Johnels JA AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. FAU - Ostlund, S AU - Ostlund S AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. FAU - Jakobsson, K AU - Jakobsson K AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. FAU - Hogstedt, J AU - Hogstedt J AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. FAU - Larsson, P Javid AU - Larsson PJ AD - Habilitation and Health, Region Vastra Gotaland, Gothenburg, Sweden. FAU - Gillberg, C AU - Gillberg C AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. FAU - Billstedt, E AU - Billstedt E AD - Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. LA - eng PT - Journal Article DEP - 20240127 PL - Germany TA - Eur Arch Psychiatry Clin Neurosci JT - European archives of psychiatry and clinical neuroscience JID - 9103030 SB - IM OTO - NOTNLM OT - ADHD OT - Autism OT - Comorbidities OT - Daily functioning OT - Long-term medication EDAT- 2024/01/28 07:44 MHDA- 2024/01/28 07:44 CRDT- 2024/01/27 23:19 PHST- 2023/04/12 00:00 [received] PHST- 2023/12/11 00:00 [accepted] PHST- 2024/01/28 07:44 [medline] PHST- 2024/01/28 07:44 [pubmed] PHST- 2024/01/27 23:19 [entrez] AID - 10.1007/s00406-023-01744-1 [pii] AID - 10.1007/s00406-023-01744-1 [doi] PST - aheadofprint SO - Eur Arch Psychiatry Clin Neurosci. 2024 Jan 27. doi: 10.1007/s00406-023-01744-1.