Attention Deficit Hyperactivity Disorder (ADHD)
Summary
Attention Deficit Hyperactivity Disorder (ADHD) is a neurodevelopmental condition characterised by persistent patterns of inattention, hyperactivity, and impulsivity that interfere with functioning and development. Symptoms must be present before age 12 and occur in multiple settings (home, school, work). ADHD affects 5-7% of children and persists into adulthood in 50-65% of cases. Early diagnosis and multimodal treatment (behavioural interventions plus medication) significantly improve long-term outcomes including academic achievement, employment, and mental health.
Key Facts
- Prevalence: 5-7% of children; 2.5-4% of adults
- Male:Female ratio: 3:1 in childhood; 1.5:1 in adulthood (females underdiagnosed)
- Persistence: 50-65% continue to have symptoms into adulthood
- Heritability: 70-80% (highly genetic)
- Key management: Behavioural interventions first; medication (stimulants) for moderate-severe
- Comorbidities: Anxiety (25%), depression (20%), conduct disorder (40%), learning difficulties (30%)
Clinical Pearls
The Triad Varies by Age: Hyperactivity often decreases by adolescence, but inattention and impulsivity persist. Adult ADHD manifests as disorganisation, poor time management, and emotional dysregulation.
The Female Presentation: Girls often present with inattentive subtype — "dreamy" rather than disruptive. They are frequently diagnosed later and have higher rates of comorbid anxiety and depression.
The 6-Month Rule: Symptoms must be present for at least 6 months, start before age 12, and cause impairment in at least 2 settings to meet diagnostic criteria.
Why This Matters Clinically
Untreated ADHD significantly impacts academic achievement, employment, relationships, and mental health. Children with ADHD are at higher risk of academic failure, substance misuse, accidents, and criminal behaviour. Early identification and treatment markedly improve outcomes and reduce these risks.
Incidence & Prevalence
- Childhood prevalence: 5-7% globally
- Adult prevalence: 2.5-4%
- UK prevalence: 3-5% of children (likely underdiagnosed)
- Trend: Increasing diagnosis rates (improved recognition)
Demographics
| Factor | Details |
|---|---|
| Age | Onset before 12 years; often recognised age 6-9 |
| Sex | Male:Female 3:1 (children); 1.5:1 (adults) |
| Ethnicity | Similar across ethnic groups when assessed consistently |
| Geography | Higher reported rates in developed countries |
Risk Factors
Non-Modifiable:
- Family history (first-degree relative: 5-10x risk)
- Preterm birth (particularly less than 32 weeks)
- Low birth weight
- Male sex
Modifiable:
| Risk Factor | Relative Risk |
|---|---|
| Maternal smoking in pregnancy | 2-3x |
| Maternal alcohol in pregnancy | 2x |
| Lead exposure | 2x |
| Early childhood adversity | 1.5-2x |
Mechanism
Step 1: Genetic Predisposition
- Highly heritable (70-80%)
- Polygenic: Multiple genes of small effect (dopamine transporter DAT1, dopamine receptors DRD4/DRD5)
- Gene-environment interactions important
Step 2: Dopaminergic Dysfunction
- Reduced dopamine signalling in prefrontal cortex and striatum
- Impaired executive functions (attention, planning, impulse control)
- Reward pathway alterations (delay aversion)
Step 3: Neurodevelopmental Changes
- Delayed cortical maturation (particularly prefrontal cortex)
- Reduced grey matter volume in key regions
- Altered connectivity in attention networks
Step 4: Behavioural Expression
- Inattention: Difficulty sustaining focus, easily distracted
- Hyperactivity: Excessive motor activity, restlessness
- Impulsivity: Difficulty waiting, interrupting, risk-taking
Classification
| Presentation | Definition | Clinical Features |
|---|---|---|
| Predominantly Inattentive | 6+ inattention symptoms; fewer than 6 hyperactive-impulsive | "Dreamy", forgetful, loses things, poor concentration |
| Predominantly Hyperactive-Impulsive | 6+ hyperactive-impulsive symptoms; fewer than 6 inattention | Fidgety, talks excessively, interrupts, cannot wait |
| Combined | 6+ symptoms in both domains | Most common; mixed picture |
| Adult ADHD | Symptoms persist from childhood | Disorganisation, procrastination, emotional dysregulation |
Anatomical Considerations
- Prefrontal cortex: Executive function, attention control
- Striatum (caudate, putamen): Motor control, reward processing
- Cerebellum: Timing, coordination
- Default Mode Network: Alterations contribute to mind-wandering
Symptoms
Inattention (6+ required for diagnosis):
Hyperactivity-Impulsivity (6+ required for diagnosis):
Atypical Presentations:
Signs
Red Flags
[!CAUTION] Red Flags — Urgent assessment required if:
- Suicidal ideation or self-harm (particularly in adolescents on medication)
- Severe aggression or conduct disorder
- Psychotic symptoms
- Substance misuse
- Cardiovascular symptoms on stimulant medication (chest pain, palpitations)
Structured Approach
General:
- Observe behaviour during consultation (restlessness, distractibility)
- Note interaction style (interrupting, impulsivity)
- Assess emotional state (anxiety, low mood common)
Developmental Assessment:
- Gross and fine motor skills
- Language development
- Academic achievement relative to IQ
- Social skills and peer relationships
Physical Examination:
- Growth (height, weight) — baseline before stimulants
- Cardiovascular: HR, BP — baseline and monitoring on treatment
- Neurological: Exclude alternative diagnoses
Special Tests
| Test | Technique | Positive Finding | Sensitivity/Specificity |
|---|---|---|---|
| Conners Rating Scales | Parent/teacher questionnaire | T-score greater than 65 | 80-90% / 70-80% |
| SNAP-IV | 18-item DSM-based rating | Elevated symptom counts | Good for screening |
| QB Test | Computer-based attention/activity | Abnormal attention, increased movement | Adjunct to clinical assessment |
| DIVA 2.0 | Structured diagnostic interview | Meets DSM-5 criteria | Clinical interview gold standard |
First-Line (Bedside)
- Structured interview — Parent, child, teacher input
- Rating scales — Conners, SNAP-IV, Vanderbilt
- School reports — Academic performance, behaviour reports
- Observations — Structured observation (school/clinic)
Laboratory Tests
| Test | Expected Finding | Purpose |
|---|---|---|
| Height/Weight | Baseline centile | Monitor growth on stimulants |
| BP and HR | Normal baseline | Cardiovascular monitoring |
| TFTs | Normal (rule out thyroid disease) | If suspected alternative diagnosis |
| Lead level | If exposure history | Rule out lead toxicity |
Imaging
| Modality | Findings | Indication |
|---|---|---|
| MRI Brain | Not routinely indicated | If neurological abnormality suspected |
| EEG | Not routinely indicated | If seizure disorder suspected |
Diagnostic Criteria
DSM-5 Criteria:
- A: 6+ symptoms of inattention and/or hyperactivity-impulsivity for 6+ months
- B: Symptoms present before age 12
- C: Symptoms present in 2+ settings (home, school, work)
- D: Clear evidence of functional impairment
- E: Not better explained by another mental disorder
NICE NG87 Pathway:
- Primary care: Screen using validated rating scales
- Refer to specialist ADHD team (paediatrics, CAMHS, adult psychiatry)
- Full assessment including multiple informants
- Physical health assessment
- Diagnosis made by specialist
Management Algorithm
SUSPECTED ADHD
↓
┌─────────────────────────────────────────┐
│ INITIAL ASSESSMENT │
│ Rating scales, history, school input │
└─────────────────────────────────────────┘
↓
┌─────────────────────────────────────────┐
│ SPECIALIST REFERRAL │
│ CAMHS / Paediatrics / Adult ADHD │
└─────────────────────────────────────────┘
↓
┌─────────────────────────────────────────┐
│ DIAGNOSIS CONFIRMED │
├─────────────────────────────────────────┤
│ MILD → Non-pharmacological only │
│ MODERATE/SEVERE → Add medication │
└─────────────────────────────────────────┘
↓
┌─────────────────────────────────────────┐
│ MEDICATION SELECTION │
├─────────────────────────────────────────┤
│ FIRST LINE: Methylphenidate (child) │
│ Lisdexamfetamine (adult) │
│ SECOND LINE: Lisdexamfetamine (child) │
│ Atomoxetine (non-stim) │
└─────────────────────────────────────────┘
↓
┌─────────────────────────────────────────┐
│ ONGOING MONITORING │
│ Growth, HR, BP, side effects, efficacy │
└─────────────────────────────────────────┘
Acute/Emergency Management
- Not applicable (chronic condition)
- Acute presentations may relate to comorbid mental health crisis — manage accordingly
Conservative Management
- Environmental modifications: Reduce distractions, structured routines, visual schedules
- Parent training programmes: Triple P, Incredible Years (first-line for preschoolers)
- Educational support: Individual Education Plan (IEP), classroom accommodations
- CBT: For emotional dysregulation and comorbid anxiety/depression
- Exercise: Regular physical activity improves symptoms
Medical Management
| Drug Class | Drug | Dose | Duration |
|---|---|---|---|
| Stimulant (1st line child) | Methylphenidate (Concerta, Equasym) | Start 5mg BD, titrate to effect | Long-term |
| Stimulant (1st line adult) | Lisdexamfetamine (Elvanse) | Start 30mg OD, titrate | Long-term |
| Stimulant (alternative) | Dexamfetamine | Start 2.5mg BD, titrate | Long-term |
| Non-stimulant | Atomoxetine | 0.5mg/kg OD, increase to 1.2mg/kg | Long-term |
| Non-stimulant (2nd) | Guanfacine (Intuniv) | Start 1mg OD | Long-term |
Medication Monitoring:
- Height and weight every 6 months (children)
- HR and BP before each dose increase and every 6 months
- Monitor for tics, mood changes, appetite suppression, sleep disturbance
Disposition
- Admit if: Severe comorbid mental health crisis, suicidal ideation
- Discharge if: Routine — managed in outpatient specialist services
- Follow-up: Monthly during titration; 3-6 monthly when stable; annual comprehensive review
Immediate (Treatment-Related)
| Complication | Incidence | Presentation | Management |
|---|---|---|---|
| Appetite suppression | 30-50% | Weight loss, reduced eating | Take medication with meals; drug holiday if needed |
| Sleep disturbance | 20-40% | Insomnia, delayed sleep onset | Give medication earlier; melatonin if needed |
| Tics | 5-10% | New or worsening tics | Consider non-stimulant alternative |
Early (Weeks-Months)
- Growth suppression: 1-2cm height deficit over 3 years — monitor; usually catch-up growth
- Mood changes: Irritability, emotional lability — dose adjustment or drug switch
- Cardiovascular: Mild HR/BP increases — monitor; rare serious events
Late (Years)
- Academic underachievement: If untreated
- Substance misuse: Higher risk if untreated; treatment is protective
- Mental health comorbidity: Anxiety, depression, personality disorder
- Relationship and employment difficulties: If unmanaged
Natural History
- Untreated ADHD associated with significant functional impairment
- Hyperactivity tends to decrease with age; inattention persists
- 50-65% continue to meet criteria in adulthood
- High rates of comorbid mental health conditions
Outcomes with Treatment
| Variable | Outcome |
|---|---|
| Symptom improvement on medication | 70-80% respond to stimulants |
| Academic improvement | Significant improvement in treated children |
| Substance misuse risk | Reduced by 50% with treatment |
| Employment outcomes | Improved with treatment |
Prognostic Factors
Good Prognosis:
- Early diagnosis and treatment
- Higher IQ
- Supportive family environment
- Fewer comorbidities
- Good response to medication
Poor Prognosis:
- Late diagnosis
- Comorbid conduct disorder
- Family dysfunction
- Substance misuse
- Poor treatment adherence
Key Guidelines
- NICE NG87 (2018) — Attention deficit hyperactivity disorder: diagnosis and management. NICE NG87
- SIGN 112 — Management of attention deficit and hyperkinetic disorders in children and young people.
- CADDRA Guidelines (2020) — Canadian ADHD Resource Alliance clinical practice guidelines.
Landmark Trials
MTA Study (1999) — Multimodal Treatment Study of Children with ADHD
- 579 children randomised to 4 treatment arms
- Key finding: Medication alone or with behavioural therapy superior to behavioural alone or community care
- Clinical Impact: Established medication as effective treatment for moderate-severe ADHD
PATS Study (2006) — Preschool ADHD Treatment Study
- 303 preschoolers with ADHD
- Key finding: Methylphenidate effective in preschoolers but with more side effects
- Clinical Impact: Behavioural interventions first-line in preschoolers
OROS-MPH Studies — Long-acting methylphenidate formulations
- Multiple RCTs
- Key finding: Once-daily formulations effective and improve adherence
- Clinical Impact: Long-acting stimulants now standard of care
Evidence Strength
| Intervention | Level | Key Evidence |
|---|---|---|
| Methylphenidate for children | 1a | Cochrane review, MTA Study |
| Lisdexamfetamine | 1b | Multiple RCTs |
| Parent training (preschool) | 1b | PATS Study, NICE recommendation |
| Atomoxetine | 1b | Multiple RCTs |
What is ADHD?
ADHD stands for Attention Deficit Hyperactivity Disorder. It is a condition where the brain works differently in ways that make it harder to concentrate, sit still, and control impulses. Think of it like a car with a very sensitive accelerator and weaker brakes — the brain has lots of energy but finds it harder to slow down and focus.
Why does it matter?
Without support, ADHD can make school, work, and relationships much harder. Children may struggle at school, get into trouble, and feel frustrated. Adults may have difficulty keeping jobs, managing time, or maintaining relationships. The good news is that with the right support and sometimes medication, people with ADHD can thrive.
How is it treated?
- Understanding and support: Learning about ADHD helps you and your family understand what is happening and reduces frustration.
- Changes at home and school: Structured routines, fewer distractions, and breaking tasks into smaller steps help enormously.
- Parent training: Programmes teach strategies to manage behaviour positively.
- Medication: If symptoms are moderate to severe, medication (usually methylphenidate or lisdexamfetamine) can significantly improve concentration and reduce hyperactivity.
What to expect
- Getting a diagnosis takes time — involving assessments with you, your child, and teachers
- Medication, if used, is usually taken long-term and monitored carefully
- Many children continue to do well into adulthood, especially with ongoing support
- Height, weight, and heart rate are checked regularly if on medication
When to seek help
Contact your doctor or specialist if:
- Symptoms are affecting school, friendships, or family life
- Your child seems very unhappy, anxious, or talking about harming themselves
- Medication side effects are causing problems (not eating, not sleeping, mood changes)
- New symptoms develop (tics, chest pain, palpitations)
Primary Guidelines
- National Institute for Health and Care Excellence. Attention deficit hyperactivity disorder: diagnosis and management (NG87). 2018. NICE NG87
Key Trials
- MTA Cooperative Group. A 14-month randomized clinical trial of treatment strategies for attention-deficit/hyperactivity disorder. Arch Gen Psychiatry. 1999;56(12):1073-86. PMID: 10591283
- Greenhill L, et al. Efficacy and safety of immediate-release methylphenidate treatment for preschoolers with ADHD. J Am Acad Child Adolesc Psychiatry. 2006;45(11):1284-93. PMID: 17023867
- Cortese S, et al. Comparative efficacy and tolerability of medications for attention-deficit hyperactivity disorder in children, adolescents, and adults: a systematic review and network meta-analysis. Lancet Psychiatry. 2018;5(9):727-738. PMID: 30097390
Further Resources
- ADDISS (National ADHD Support): addiss.co.uk
- Young Minds: youngminds.org.uk
- NHS ADHD Information: nhs.uk/conditions/attention-deficit-hyperactivity-disorder-adhd
Last Reviewed: 2025-12-24 | MedVellum Editorial Team
Medical Disclaimer: MedVellum content is for educational purposes and clinical reference. Clinical decisions should account for individual patient circumstances. Always consult appropriate specialists.