
Diagnose ADHD from DSM-5 criteria with rating scales from at least two settings, plus a screen for coexisting conditions, in any patient aged 4 to 18 with academic or behavioral problems (AAP 2019) and in adults with a lifelong pattern. Treatment depends on age: parent training in behavior management first for preschoolers, FDA-approved medication plus behavioral and school supports for ages 6 to 18, and stimulants as usual first-line drugs in adults without contraindications. Stimulants are Schedule II, so no refills, up to a 90-day supply through sequential prescriptions, a PDMP check and state rules apply.
ADHD is a primary care diagnosis made from DSM-5 criteria, information from more than one setting and a screen for conditions that mimic or coexist with it. The AAP 2019 guideline tells the provider to evaluate any child or adolescent aged 4 to 18 with academic or behavioral problems and symptoms of inattention, hyperactivity or impulsivity, then to treat by age: parent training in behavior management first for preschoolers, and FDA-approved medication with behavioral and school supports from age 6. In adults, stimulants are the usual first-line drugs, and because they are Schedule II, prescribing follows DEA rules that the exam tests directly.
The AAP guideline asks the provider to gather reports from parents or guardians, teachers and other school personnel, and mental health clinicians involved in the child's care, usually through validated rating scales such as the Vanderbilt scales. For adolescents, collect information from at least two teachers and from the adolescent, because symptoms are often less visible and substance use and other conditions become more likely.
The evaluation must also screen for coexisting conditions: emotional and behavioral (anxiety, depression, oppositional defiant disorder, conduct disorder, substance use), developmental (learning and language disorders, autism spectrum disorder) and physical (tics, sleep apnea). A hearing and vision check and a sleep history belong in every evaluation.
Adult ADHD requires the same DSM-5 criteria, including evidence that symptoms began before 12, which usually means collateral history from a parent or partner and old school records. The 6-item WHO Adult ADHD Self-Report Scale (ASRS v1.1) screener is the common primary care entry tool; four or more responses in the shaded boxes is a positive screen that leads to a full diagnostic interview, not a diagnosis.
Adult differentials to rule out before prescribing a stimulant:
Before a stimulant, ask about fainting or chest pain with exercise, palpitations, known heart disease, and family history of sudden or unexplained death at a young age, cardiomyopathy or inherited arrhythmia. Measure blood pressure and heart rate and examine the heart. A routine ECG is not required for every patient; a positive history or abnormal examination calls for an ECG or cardiology evaluation first.
| Age group | AAP 2019 first-line | Medication role | Other required supports |
|---|---|---|---|
| 4 years to 6th birthday | Evidence-based parent training in behavior management (PTBM) and/or behavioral classroom interventions | Methylphenidate if behavioral treatment does not give significant improvement and moderate to severe disturbance continues | Preschool or Head Start programs, early childhood special education |
| 6 to 11 years | FDA-approved medication plus PTBM and/or behavioral classroom intervention, preferably both | Stimulants have the strongest evidence; then atomoxetine, extended-release guanfacine, extended-release clonidine | Educational interventions and an IEP or 504 plan |
| 12 to 18 years | FDA-approved medication with the adolescent's assent, plus training interventions and/or behavioral therapy | Same drug order; plan for driving safety and diversion risk | School supports, transition planning |
| Adults | Medication is the core of treatment; stimulants first-line absent contraindications | Nonstimulant (atomoxetine, viloxazine) if stimulants are unsuitable | Psychoeducation, CBT for ADHD, workplace accommodations |
The AAP also directs the provider to titrate medication to the dose that gives maximum benefit with tolerable adverse effects, and to treat ADHD as a chronic condition using the chronic care model and medical home.
| Feature | Stimulants (methylphenidate, amphetamine) | Atomoxetine, viloxazine | Alpha-2 agonists (extended-release guanfacine, clonidine) |
|---|---|---|---|
| Effect size | Highest | Moderate | Moderate |
| Onset | Same day | Several weeks | 1 to 2 weeks or more |
| Controlled substance | Schedule II | No | No |
| Key adverse effects | Appetite loss, weight and growth effects, insomnia, raised blood pressure and heart rate, irritability, tics may worsen | Boxed warnings for suicidal thoughts (check each label for the age groups covered), GI upset; atomoxetine liver injury (rare) | Sedation, hypotension, bradycardia, rebound hypertension if stopped suddenly |
| Good choice when | Most patients | Substance use history, diversion risk, coexisting anxiety or tics, stimulant intolerance | Tics, sleep problems, oppositional symptoms, adjunct to a stimulant |
| What | When | Why |
|---|---|---|
| Symptom and function ratings from home and school (or work) | During titration, then at each follow-up | Confirms response and guides dose |
| Blood pressure and heart rate | Baseline, with dose changes, then periodically | Sympathomimetic effects |
| Height, weight, growth curve (children) | Baseline and each visit | Appetite suppression and growth slowing |
| Sleep, mood, tics, psychosis | Each visit | Adverse effects and coexisting conditions |
| Suicidal thoughts | Each visit on atomoxetine or viloxazine | Boxed warning |
| Prescription drug monitoring program (PDMP) | Before starting and per state rules | Duplicate prescriptions, diversion |
| Misuse and diversion | Each visit; pill counts or urine testing when concern exists | Boxed warning, Schedule II status |
During titration, contact is usually every 1 to 2 weeks, then at least every few months once stable; state rules for controlled substances may require more frequent visits. Drug holidays on weekends or summers can be discussed when growth is a concern.
Some states limit NP Schedule II prescribing (for example by supply length, a collaborative agreement or a physician co-signature), require PDMP checks at set intervals or require controlled-substance agreements. The exam expects awareness that state law can be stricter than federal law, and that the stricter rule applies.
The Ryan Haight Act generally requires an in-person medical evaluation before a controlled substance is prescribed through telemedicine. DEA and HHS have repeatedly extended a temporary waiver of that requirement; the fourth extension runs through December 31, 2026. A permanent special registration rule was under federal review in late 2026. Confirm the current rule before prescribing a stimulant to a patient never seen in person.
A 7-year-old boy is evaluated for ADHD. Vanderbilt rating scales from his mother and his teacher both show seven inattentive and six hyperactive-impulsive symptoms for more than a year, with failing grades and frequent classroom removals. Hearing and vision are normal. He has no history of syncope or chest pain, and there is no family history of sudden cardiac death. Blood pressure and cardiac examination are normal. Which of the following is the most appropriate management?
Answer: B. For a child aged 6 to 11 with ADHD confirmed from two settings, the AAP 2019 guideline recommends FDA-approved medication together with parent training and/or behavioral classroom interventions, preferably both, plus school supports. Option A is the first-line approach for preschoolers aged 4 to 5, not for a 7-year-old. Option C orders cardiac testing that is not indicated when the personal and family cardiac history and the examination are negative. Option D uses a drug with weaker evidence than stimulants as the first choice without a reason such as tics, substance misuse risk or stimulant intolerance.
Common follow-up questions on Mental Health in Primary Care.
Not routinely. Take a personal cardiac history (syncope, chest pain with exertion, palpitations) and a family history of sudden death or inherited arrhythmia, and examine the heart; obtain an ECG or cardiology input when that screen is positive.
No. Schedule II prescriptions cannot be refilled. Federal rules allow multiple prescriptions written on the same day with earliest fill dates, totaling up to a 90-day supply, if state law permits.
Under the fourth DEA and HHS extension, the in-person evaluation requirement remains waived through December 31, 2026, while a permanent special registration rule is pending. Confirm the current rule and your state's requirements before prescribing.
APSARD has developed US adult ADHD guidelines, but as of late 2026 they were described as about to launch. Until they are final, adult care draws on DSM-5, NICE NG87 and drug labeling.
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