The Australian Clinical Practice Guideline for ADHD: A Summary for Clinicians
The Australian Clinical Practice Guideline for ADHD is a comprehensive guide to diagnosing, treating and managing ADHD.
This guideline provides evidence-based best practice recommendations for the assessment, diagnosis, and management of ADHD in children and adolescents. It also provides guidance for health professionals on managing the long-term effects of ADHD and offering support for those affected.
The Psych Scene Hub has summarised the main points of the Australian Clinical Practice Guideline for ADHD, so that readers can quickly and easily understand the key points of the guideline.
This summary will provide an overview of the most important aspects of the guideline and will be useful for those looking for more information on the diagnosis and treatment of ADHD.
The prevalence of adult ADHD in Australia is between 2% and 6% (similar to international prevalence)
The social and economic costs of ADHD are estimated at $20.42 billion per year or $25,071 per individual with ADHD per annum. [Deloitte Access Economics. (2019). The social and economic costs of ADHD in Australia. Retrieved from Canberra]
This article summarises the key recommendations from the Australian Evidence-Based Clinical Practice Guidelines for Attention Deficit Hyperactivity Disorder (ADHD). [AADPA]
This summary is best read in combination with other articles we have previously covered for a comprehensive overview of ADHD.
Neurobiology of Attention Deficit Hyperactivity Disorder (ADHD) – A Primer
Diagnosis and Management of Attention Deficit Hyperactivity Disorder (ADHD) – Focus on Adult ADHD
Evidence-Based Summary of the ADHD International Consensus Statement
ADHD and Comorbidities – Management Principles
OUTCOMES OF ADHD IN AUSTRALIA
Outcomes of ADHD in Australia are similar to outcomes shown internationally from systematic reviews and meta-analyses.
A community-based cohort study tracking children with ADHD from age 7 to age 10 found that ADHD was associated with poorer academic functioning, poorer emotional and behavioural functioning, poorer social functioning, and higher rates of co-occurring internalising and externalising mental health disorders compared to children without ADHD. [Efron et al., 2020]; [Zendarski et al., 2022]
This study found that the best predictors of outcomes at age 10 were the following at age 7: [Efron et al., 2020], [Zendarski et al., 2017], [Zendarski et al., 2017]
- Measures of working memory (academic functioning)
- The severity of ADHD symptoms (parent and teacher-reported emotional and behavioural functioning)
- Autism symptom severity (parent-reported emotional functioning and parent-reported social functioning)
A cohort study from Victoria, which examined outcomes for adolescents with ADHD in the early years of high school, found: [Zendarski et al., 2017]
- Poorer academic performance across multiple domains
- Poorer school engagement
- Increased school suspensions compared with state averages.
A Western Australian study identified a similar impact on academic performance in both genders. [Silva et al., 2020]
Risk of school suspension in ADHD:
Low risk of suspension:
- Higher cognitive ability
- Higher neighbourhood socio-economic status
- Attending an independent school
Increased risk of Suspension:
- Higher levels of conduct and ADHD symptoms
Children with ADHD also had an increased risk of early hospitalisations before the age of 4. [Silva et al., 2014]
There were also increased odds of having a community correction or an incarceration record [Silva et al., 2014]
The odds of having a community correction or incarceration record were higher for girls with ADHD compared to girls without ADHD. The most common reason for the first justice record was for the offences of burglary and breaking and entering.
DIAGNOSTIC INDICATORS - WHEN SHOULD ONE SUSPECT ADHD?
Clinicians should be aware of the following indicators in children, adolescents, and adults that may indicate the presence of ADHD.
Diagnostic indicators in High-Risk groups:
Children:
- In and out of home care
- Diagnosed with oppositional defiant disorder or conduct disorder
Children and adolescents:
- Diagnosed with anxiety disorders
- Diagnosed with epilepsy
- History of substance abuse
Adults:
- Any mental health disorder (including substance use disorders, borderline personality disorder, intermittent explosive disorder, internet addiction, psychotic disorders, binge eating disorder, gambling disorder)
- Presence of suicidal behaviour or ideation
All ages:
- Individuals with neurodevelopmental disorders, including autism spectrum disorder, intellectual disability, tic disorders, language disorders and specific learning disorders
- Preterm birth
- A close family member diagnosed with ADHD
- Prenatal exposure to substances, including alcohol and other drugs
- Acquired brain injury
- Imprisonment
- Low birth weight
- Presence of anxiety, depressive or bipolar and related disorders
- Sleep disorders
- Females may be less likely to be diagnosed or misdiagnosed [Gender differences in ADHD]
DIAGNOSIS OF ADHD - KEY POINTS FROM THE AUSTRALIAN GUIDELINES FOR ADHD
- A diagnosis of ADHD should not be made solely based on rating scales or observational data.
- Observations from more than one setting and reporter (e.g. a teacher, in the case of children) should be used to confirm if symptoms, function and participation difficulties occur in more than one setting.
- ADHD should be considered a possible diagnosis in all age groups, including adults over 65 years.
- Consider the varied presentations of ADHD. [See red flags in adults]
- Children and adults may not present with the most visible symptoms of hyperactivity/impulsivity. [See gender differences]
- Inattentive symptoms may not be identified until secondary school (or later), following increased demands for organisation and independent study or work.
- Individuals may have developed compensation strategies that may mask symptoms.
- Neuropsychological testing is not required to diagnose ADHD. A review by The Canadian ADHD Resource Alliance Advisory Council (CADDRA) found no other strategies achieved additional benefit beyond that of clinician interview in combination with rating scales.
- Direct observations such as observing children in their educational setting, neuropsychological and psychoeducational assessments, computerised cognitive assessments, neuroimaging and electroencephalography (EEG) did not increase the accuracy of diagnosis.
Indications for Psychometric/neuropsychological evaluation:
- Identifying differential and co-occurring conditions when there is diagnostic uncertainty.
- Identifying specific language and learning disorders.
- Assistance with treatment planning and identifying and targeting intervention strategies to specific domains based on the cognitive strengths and challenges of the person.
Recommended Screening Scales:
Young children:
- Achenbach System of Empirically Based Assessment – Attention Problems scale
- Child Behaviour Checklist DSM Oriented ADHD subscale
Children and adolescents
- Achenbach System of Empirically Based Assessment – Attention Problems scale
- Child Behaviour Checklist – DSM Oriented ADHD subscale
- Strengths and Difficulties Questionnaires (Hyperactivity subscale)
- Conners’ 3 short form
- Swanson, Nolan and Pelham (SNAP) scale
- ADHD Rating Scale 5
- Vanderbilt ADHD Diagnostic Rating Scale
Adults
- WHO Adult ADHD Self Report Scale (ASRS) (Part A)
- Conners’ Adult ADHD Rating Scale – Short
- Wender Utah Rating Scale (WURS) – Short
Recommended Diagnostic scales
Young children
- Achenbach System of Empirically Based Assessment – Attention Problems scale
- Child Behaviour Checklist – DSM Oriented ADHD subscale
- Brown Attention Deficit Disorder Symptom Assessment Scale (BADDS)
Children and adolescents
- Vanderbilt ADHD Diagnostic Rating Scale
- Conners’ 3
- Swanson, Nolan and Pelham (SNAP) scale
- ADHD Rating Scale 5
- Brown Attention Deficit Disorder Symptom Assessment Scale (BADDS)
Adults
- WHO Adult ADHD Self Report Scale (ASRS) (Part A + B)
- Conners Adult ADHD Rating Scale
- Wender Utah Rating Scale (WURS)
- Brown Attention Deficit Disorder Symptom Assessment Scale
- Barkley Adult ADHD Rating Scale-IV
Rule out medical conditions:
- Sleep disorders
- Hearing or vision impairment
- Thyroid disease
- Anaemia
- Epilepsy
- Acquired brain injury
- Foetal alcohol spectrum disorder
- Medications: Cognitive dulling (e.g., SSRIs, anticholinergic medications, mood stabilisers), psychomotor activation (e.g. decongestants, asthma medication, non-prescribed stimulants like caffeine).
Psychiatric Comorbidities:
Read in detail: ADHD and Comorbidities – Management Principles
Children and Adolescents with ADHD:
The most common co-occurring disorders are:
- Oppositional defiant disorder
- Language disorders
- Autism spectrum disorders
- Anxiety disorders
- Depressive disorders
- Substance use disorders emerging in adolescence.
- Specific learning disorders ( involving reading, written expression or mathematics difficulties).
For adults with ADHD, the most common co-occurring mental health disorders are:
- Depressive disorders
- Bipolar disorders
- Anxiety disorders
- Personality disorders
- Substance use disorders
- Medical conditions (see above)
TREATMENT PRINCIPLES IN ADHD
General principles of management
Read more on non-pharmacological strategies in ADHD.
Lifestyle measures:
- Diet
- Exercise or activity levels.
- Sleep patterns
Clinicians should offer guidance on lifestyle factors to help people with ADHD, including:
- Asking about sleep, offering strategies, and/or a referral to assist with sleep if indicated. [Diagnosis and Management of Insomnia]
- Individuals with ADHD have high rates of comorbid sleep disorders. Primer on Neurobiology and Neuropsychiatry of Sleep – Application to Clinical Practice
- Asking about diet and physical activity levels and offering strategies and/or referrals to assist with any challenges if needed.
Cognitive Behavioural Interventions:
The term refers to a broad range of approaches that use cognitive and/or behavioural interventions to minimise the day-to-day impact on functioning from ADHD symptoms.
- Can reduce ADHD symptom severity indirectly
- Can impact broader functioning and wellbeing
- Cognitive-behavioural interventions can be offered to children with ADHD.
- Cognitive-behavioural interventions should be offered to adolescents and adults with ADHD.
- Younger children may benefit from a foundational focus on emotional literacy, proactive help-seeking, problem-solving and self-esteem growth.
- Children approaching adolescence may benefit from simple behavioural techniques. Through adolescence, increasingly sophisticated behavioural and cognitive restructuring techniques may be of benefit.
Adults :
- Interventional strategies include adjusting the environment (home, school and/ or work, social settings) to maximise the chances of success for the person with ADHD.
- Preventing or removing challenges likely to result from ADHD symptoms or enabling increased use of personal strengths and interests.
- Assisting the person to understand and recognise the impact of ADHD symptoms on their day-to-day lives:
- Cognitive processes involved in symptom experiences.
- Symptom fluctuation and difficulties due to external and environmental factors, e.g. stressors, sleep, exercise and hormones (for women), and relationships.
- Positive and negative impacts of compensatory measures and coping strategies the person has developed over time.
Parent and Family Training for Parents/families of young children with ADHD:
Under 5 and 5-17:
- More intensive parent/family training programs should be offered to parents/families of children with ADHD who have a co-occurring oppositional defiant disorder or conduct disorder.
- Modifications can be designed and/or implemented by the person with ADHD or others in a supportive role. They can involve modifying: expected tasks and routines and the surrounding physical space, including its sensory elements.
- Communication and engagement strategies for others living with the person with ADHD.
- Neurofeedback (NF), also known as EEG (electroencephalography) biofeedback, applies principles of operant conditioning to teach self-modification of cortical electrical activity.
- Neurofeedback requires EEG electrodes on the scalp to detect neural activity, which is transferred to a computer.
- The software converts the EEG patterns into visual and auditory rewards, which are ‘feedback to the participant to learn to inhibit or increase specific EEG frequencies of neural firing.
- There are several different types of neurofeedback and various treatment regimes.
- Based on the evidence review, the evidence of benefits of neurofeedback over waitlist/usual care for parent- or teacher-reported ADHD was inconsistent in children and adolescents.
- There were benefits for ADHD inattention symptoms based on parent reports but not a teacher or clinician report, and no benefits for parents or teacher-reported ADHD hyperactivity/impulsivity symptoms. In adults, the evidence was inconclusive.
- ADHD Treatment via QEEG-Informed Neurofeedback Treatment Stratification and Predictors of Response: Awaiting Multi-Centre Replication
ADHD Coaching:
ADHD coaching combines three key coaching skill sets [Wright, 2014]:
- Collaborative, client-centred, client-driven process to support the person’s empowerment
- Education about ADHD and related topics, as well as tools and resources
- Skills coaching to build on the person’s strengths and resources and develop conscious competence in new systems and strategies.
PRINCIPLES OF MEDICATION MANAGEMENT IN ADHD
Read medication management in detail.
Prescribing for children and adolescents:
- Paediatricians and child psychiatrists may prescribe for persons under 18 years of age.
Prescribing for adults:
- Psychiatrists are primarily authorised to prescribe psychostimulants.
- In some circumstances, such as in regional/rural settings with no access to specialists, a general practitioner with appropriate training and authorisation may be authorised to initiate psychostimulant medication.
Medication management:
Individuals with ADHD should be referred for a cardiology opinion before commencing stimulant medication if any of the following is present:
- History of congenital heart disease or previous cardiac surgery
- History of sudden death in a first-degree relative under 40 years suggesting a cardiac disease
- Shortness of breath on exertion
- Fainting on exertion
- Palpitations that are rapid, regular and start and stop suddenly
- Chest pain suggesting a cardiac origin
- Heart murmur (not including innocent heart murmurs in children)
- Hypertension.
Principles of medication management in children:
- If ADHD symptoms cause significant impairment in more than one setting, a specialist with expertise in child development and treatment of ADHD in young children (either a paediatrician or a child psychiatrist) should assess the child to identify suitable treatment options.
- Medication should be used cautiously and monitored closely in children under 5 years.
- First-line medication for children aged 6 years and over should be stimulants.
Principles of medication management in adolescents and adults:
Methylphenidate, dexamphetamine, or lisdexamfetamine should be offered as the first-line pharmacological treatment for people with ADHD, where ADHD symptoms are causing significant impairment.
The decision to start with a short or long-acting stimulant formulation should be based on a clinical decision, together with the wishes of the person with ADHD or their parent/carer/family, by considering the advantages and disadvantages of each. For example:
- Short-acting formulation may be preferred when close monitoring is required
- Long-acting formulation may be preferred for convenience or when there is a medical contraindication
- Consideration of any potential cost implications
Modified-release once-daily preparations could be offered for any of the following reasons:
- Convenience
- Improving adherence
- Reducing stigma by removing the need to take medication at school or in the workplace
- Reducing problems of storing and administering controlled drugs at school or work
- Risk of stimulant misuse and diversion with immediate-release preparations
- Pharmacokinetic profile offers an advantage for symptom improvement.
- To extend the duration of effect: Short-acting and long-acting stimulants could be offered together to optimise the effect (e.g. a modified-release preparation of methylphenidate in the morning and an immediate-release preparation of methylphenidate at another time of the day to extend the duration of the effect). Consider risks if medications are used in combination.
- Some short-acting stimulants contain gluten and/or lactose; a long-acting preparation free of these should be used in someone with gluten or lactose intolerance.
Evidence-based stimulants available in Australia:
- Short-acting: Immediate-release Methylphenidate (Ritalin) or Dexamfetamine (dexamphetamine).
- Long-acting: Modified-release Methylphenidate (Ritalin LA, Concerta XR) or lisdexamfetamine (Vyvanse).
Indications for atomoxetine or guanfacine in adults with ADHD:
- Stimulants are contraindicated
- Cannot tolerate methylphenidate, lisdexamfetamine or dexamfetamine
- Symptoms have not responded to separate trials of dexamfetamine or lisdexamfetamine and methylphenidate at adequate doses.
- The clinician considers that the medications may be beneficial as an adjunct to the current regimen.
Clinicians should apply the same recommendations and principles of prescribing for adults over 65 years as for adults below 65, with careful monitoring of side effects.
Other recommended options for adults with ADHD (in no particular order):
• Bupropion
• Clonidine
• Modafinil
• Reboxetine
• Venlafaxine
Other recommendations based on expert consensus for adults with ADHD (in no particular order):
Pharmaceutical Benefits Scheme (PBS) restrictions:
- Subsidy for ADHD treatments differs according to the age at which the person received the diagnosis.
- Guanfacine and atomoxetine are subsidised only for those diagnosed between the ages of 6 and 17 years.
- Subsidy for long-acting methylphenidate, lisdexamfetamine and atomoxetine is restricted to those diagnosed between the ages of 6 and 18 years.
- A retrospective diagnosis to fulfil the PBS criteria for a diagnosis between the ages of 6 and 18 is permitted for lisdexamfetamine.
- Age restrictions do not apply to PBS listings for dexamfetamine and methylphenidate short-acting formulations.
- These restrictions may result in increased costs to people for whom ADHD was not diagnosed before 18 years.
Initiating medication:
- Before starting, record baseline ADHD symptoms and level of functioning.
- Monitor and record adverse effects during titration at each dose change.
- Review progress regularly during the dose-titration period.
- Titrate dose taking into account symptoms, level of functioning and adverse effects until the optimal dose has been identified (i.e. the dose at which symptoms are reduced and functional outcomes are improved, with minimal adverse effects).
Indications for slower dose titration and/or more frequent monitoring:
- Neurodevelopmental disorders (e.g. autism spectrum disorder, tic disorders, intellectual disability)
- Comorbid mental health conditions include anxiety disorders, schizophrenia or bipolar disorder, depression, personality disorders, eating disorders, post-traumatic stress disorder and substance misuse.
- Medical conditions (e.g. cardiac disease, epilepsy or acquired brain injury).
Titration of medication:
Different schedules have been used to optimise the dose in titrating initial medication. [Huss et l, 2017]
Children:
Methylphenidate:
Titration to a maximum dose (flexible) and a fixed dose regimen considering body weight has been used. [Simonoff et al., 2013]
The Australian Therapeutic Guidelines includes age- and weight-based maximum doses, recommending up to 1 mg/kg/d or 60 mg/d in children aged 4 years or older and a dose titration of extended-release or OROS methylphenidate of 0.5 to 2.0 mg/kg/d in children older than 6 years. [Therapeutic Guidelines Limited].
The Australian Medicines Handbook states that in children aged 2 to 12 years, doses of immediate-release methylphenidate may be titrated up to 1 mg/kg/day to a maximum of 40 mg/day or 60 mg/day in children older than 12 years. Modified-release methylphenidate may be increased to 72 mg/day (for OROS) or 80 mg/day (for extended release). [ Australian Medicines Handbook].
A meta-analysis concluded: [Ching, 2019]
If the individual’s optimal dose can be established by finding the best balance of therapeutic advantages and tolerability, having a maximum dose may be unnecessary.
Fixed dose trials: [Farhat et al., 2022]
- Meta-analyses of fixed-dose trials in children and adolescents with ADHD for methylphenidate and amphetamine demonstrated increased efficacy. They raised the likelihood of discontinuation due to adverse effects (AEs) with increasing doses of stimulants.
- The incremental benefits of stimulants in terms of efficacy decreased beyond 30 mg of methylphenidate or 20 mg of amphetamine in fixed-dosed trials.
Flexible dose trials:[Farhat et al, 2022]
- Meta-analyses of flexible-dose trials for both methylphenidate and amphetamine demonstrated increased efficacy and reduced likelihood of discontinuations for any reason with increasing stimulant doses.
- The incremental benefits of stimulants in terms of efficacy remained constant across the FDA-licensed dose range for methylphenidate and amphetamine in flexible-dose trials.
Thus, recommendations are to consider flexible titration as it is associated with improved efficacy and acceptability because practitioners can increase/reduce doses based on control of ADHD symptoms/dose-limiting adverse effects.
From a practical perspective, there is significant variability in doses of methylphenidate for optimal efficacy. The rule of thumb is that patients should not be prescribed methylphenidate at doses exceeding 150 mg/day. [Jaeschke, 2021]
In the position paper by members of the International Multicentre Persistent ADHD Collaboration, it was implied that ‘doses around 1 mg/kg [per body mass] of methylphenidate are correlated with better efficacy, yet are rarely achieved in studies of adult patients. [Franke et al., 2018]
Monitoring :
- Once the medication is titrated and stabilised, clinicians should proactively arrange individualised monitoring based on a chronic disease management model.
- People receiving treatment for ADHD should have regular reviews and follow-ups according to the severity of their condition, regardless of whether or not they are taking medication.
Monitor the following:
- Height and weight
- Cardiovascular function
- Tics
- Sexual function
- Seizures
- Sleep Quality
- Worsening symptoms
- Worsening of mood
- Increased anxiety
- Risk of stimulant diversion
- Other side-effects.
For children and adolescents, monitor:
- Plot height and weight on a growth chart
- Measure height every 6 months
- For children of any age, measure weight 3 and 6 months after starting treatment and 6 months after that, or more often if concerns arise.
Management of specific situations:
Addressing reduced growth rate in children or adolescents:
- Consider a planned break in treatment over school holidays to allow ‘catch-up’ growth
- Switch to alternate medication
- Consider non-medication causes.
Managing acute psychotic or manic episodes during treatment with stimulant medication:
- Stop stimulants and review other medications for ADHD
- Treat the psychotic or manic episode
- Consider the introduction of a mood stabiliser
- Consider alternate treatment for ADHD after the episode has resolved
- Consider the risks and benefits of reintroducing stimulant medication. If stimulant medication is to be reintroduced, take extra precautions in monitoring, such as admitting the person to a hospital/clinic for observation.
If weight loss/insufficient weight gain in children is a clinical concern, consider the following strategies:
- Taking medication either with or after food rather than before meals.
- Taking additional meals or snacks early in the morning or late in the evening when stimulant effects have worn off.
- Obtaining dietician advice
- Consuming high-calorie foods of good nutritional value
- Taking a planned break from treatment
- Changing or stopping the medication.
- Consider the impact of appetite suppression due to stimulant treatment when people have a co-occurring eating disorder or other medical conditions contributing to weight loss.
Risk of diversion or misuse:
- Exercise caution when prescribing stimulants if there is a risk of diversion for cognitive enhancement.
- Clinicians should not offer immediate or modified-release stimulants that can be easily injected or inhaled if there is a risk of misuse or diversion.
Comorbidities:
- Treatment approaches for co-occurring conditions should follow best-practice guidelines for each co-occurring condition but with treatment delivery methods adjusted to account for ADHD symptoms.
- ADHD and Comorbidities – Management Principles
ADHD AND SUBSTANCE USE
- Stimulant treatment in people with ADHD can result in positive outcomes for those with co-occurring substance use disorders, including reduced substance use.
- Read more on SUD and ADHD.
- Stimulant treatment for ADHD does not increase the risk of substance use disorders compared with people with ADHD who do not access stimulant medication. [Fluyau et al.,2021].
- Clinicians should be aware of and monitor the risk of misuse and diversion of psychostimulant medication. To minimise the risk of diversion and misuse, the use of long-acting, rather than short-acting, psychostimulants should be considered.
- Before starting stimulant pharmacotherapy in people with concurrent ADHD and substance use disorders, it is essential that the person is abstinent or has reduced/stabilised their substance use.
- If this is not the case, the clinician should consider non-stimulant pharmacotherapy (e.g. atomoxetine, guanfacine, or bupropion)
- Pharmacological treatment of ADHD requires careful titration and monitoring of its effect and possible adverse effects.
- Higher doses of stimulants may be required in people with ADHD and concurrent substance use disorders than those without substance use disorders to achieve a favourable effect on ADHD symptoms and reduce substance use.
ADHD AND THE CRIMINAL JUSTICE SYSTEM
ADHD in the correctional system:
- Screening and assessment processes should be established to identify the presence of ADHD and co-occurring conditions
- Custodial staff and those within the criminal justice system (e.g. police, magistrates) should receive ADHD awareness training.
- Treatment in custodial settings should include pharmacological and non-pharmacological approaches equivalent to the treatment available in the community.
- Prisons should establish safe processes for administering long-acting stimulant medications to those with ADHD (similar to administering other controlled drugs and ensuring the safety of the person in prison receiving stimulant medication).
- Before administering stimulant medication, specific screening for comorbid substance use disorders should be undertaken.
CONCLUSION
There is now greater recognition of the importance of a timely diagnosis and management of ADHD across the lifespan.
There continue to be barriers and challenges in accessing treatment in the Australian setting.
The guidelines recommend the following changes at a systemic level:
- Funding should be made available to expand services for people with ADHD to deliver timely and accessible assessment, support and intervention, and an ADHD helpline accessible to all Australians.
- Laws and regulations for prescribing ADHD stimulant medications and shared care should be uniform between the states and territories in Australia.
- Training should be available for all clinicians working with people with ADHD.
- Further ADHD research is needed to understand many aspects of ADHD better and to improve the quality of life for people living with ADHD.