📋 Key Information Summary
- Headache affects approximately 15% of Australians at any given time and is the most common neurological reason for GP consultation.
- Use the SNOOP mnemonic (Systemic symptoms, Neurological signs, Onset sudden, Older age, Pattern change) to screen for secondary (dangerous) headaches.
- Primary headaches — migraine, tension-type headache (TTH), and cluster headache — account for >90% of presentations; a structured history is the single most important diagnostic tool.
- Migraine: unilateral, pulsating, 4–72 h, with nausea/vomiting or photo-/phonophobia; ± aura (visual, sensory, or speech disturbance lasting 5–60 min).
- Tension-type headache: bilateral, pressing/tightening (non-pulsating), mild–moderate, no nausea; most common primary headache worldwide.
- Cluster headache: strictly unilateral orbital/superotemporal pain with autonomic features (lacrimation, rhinorrhoea, ptosis, miosis), 15–180 min per attack, occurring in bouts.
- Thunderclap headache (peak intensity within 1 minute) is subarachnoid haemorrhage until proven otherwise — urgent CT brain ± LP required.
- Acute migraine: first-line is oral NSAID or paracetamol; triptans (sumatriptan, eletriptan) are first-line for moderate–severe attacks or when simple analgesia fails.
- Preventive migraine therapy should be considered when attacks occur ≥4 days/month or cause significant disability; options include propranolol, amitriptyline, topiramate, and CGRP monoclonal antibodies (PBS authority-required).
- Headache in pregnancy requires a low threshold for neuroimaging — paracetamol is first-line; aspirin and triptans require specialist guidance; avoid ergots entirely.
- New-onset headache in patients aged ≥50 years must prompt evaluation for giant cell arteritis (temporal artery biopsy + ESR/CRP) and space-occupying lesions.
- Aboriginal and Torres Strait Islander peoples experience headache at higher rates but face barriers to specialist access; culturally safe care and remote telehealth pathways are essential.
Introduction & Australian Epidemiology
Headache is one of the most prevalent human conditions and the most frequent neurological symptom presenting to Australian general practice. The International Classification of Headache Disorders, 3rd edition (ICHD-3) divides headaches into primary (the headache itself is the disorder) and secondary (the headache is a symptom of an underlying condition). Accurate classification depends on a meticulous history, targeted examination, and judicious investigation.
In Australia, headache accounts for an estimated 4–5% of all GP encounters annually, and migraine alone affects approximately 4.9 million Australians (AIHW, 2023). The economic burden exceeds billion per year when direct healthcare costs, lost productivity, and carer burden are included. Tension-type headache is the most common primary headache globally, while migraine ranks as the second most disabling neurological condition measured by years lived with disability (GBD 2019 Neurology Collaborators).
Cluster headache, though less prevalent (0.1–0.4% lifetime prevalence), causes some of the most severe pain known in medicine. Secondary headaches — including subarachnoid haemorrhage, meningitis, space-occupying lesions, giant cell arteritis, and idiopathic intracranial hypertension — must be identified promptly, as delayed diagnosis carries significant morbidity and mortality.
Headache Diagnostic Model
The diagnostic approach to headache proceeds in three steps: (1) identify red flags for secondary headache; (2) apply ICHD-3 criteria to classify the primary headache phenotype; and (3) recognise comorbidities and medication-overuse headache (MOH).
Step 1 — Red-Flag Screening (SNOOP Mnemonic)
Step 2 — Detailed History for Primary Headache Classification
A structured headache history should cover:
- Location: unilateral vs bilateral; orbital/periorbital vs diffuse
- Quality: pulsating, pressing/tightening, stabbing, burning
- Intensity: mild / moderate / severe (numeric rating scale 0–10)
- Duration: minutes, hours, or days per attack
- Frequency: attacks per month; episodic vs chronic
- Associated features: nausea, vomiting, photo-/phonophobia, aura, autonomic features, restlessness
- Triggers: stress, sleep disturbance, alcohol, menstrual cycle, weather
- Medication use: analgesic frequency (≥15 days/month = possible MOH)
- Family history: migraine has strong genetic component (60–80% heritability)
Step 3 — Physical Examination
A focused neurological examination should be performed in all new-onset headaches. Assess:
- Vital signs (hypertension, fever, tachycardia)
- Fundoscopy — papilloedema (IIH, mass lesion), subhyaloid haemorrhage (SAH)
- Pupillary reflexes — relative afferent pupillary defect (optic neuritis)
- Cranial nerve examination — CN III, IV, VI palsy (pituitary apoplexy, aneurysm)
- Motor, sensory, coordination, and gait assessment
- Temporal artery palpation — tenderness, thickening, reduced pulse (GCA)
- Neck range of motion and meningeal signs if indicated
Medication-Overuse Headache (MOH)
MOH is diagnosed when headache occurs on ≥15 days/month in a patient with a pre-existing headache disorder and regular overuse of acute medications for >3 months. Overuse thresholds: simple analgesics ≥15 days/month; triptans, opioids, or combination analgesics ≥10 days/month. Management involves withdrawal of the overused agent, bridge therapy (e.g., naproxen, prednisolone), and initiation of preventive treatment.
Migraine vs Tension vs Cluster Headache Comparison
| Feature | Migraine | Tension-Type Headache | Cluster Headache |
|---|---|---|---|
| Prevalence (Australia) | ~12–15% (♀ 3:1) | ~38–46% | 0.1–0.4% |
| Location | Unilateral (60%); can be bilateral | Bilateral, band-like | Strictly unilateral, orbital/superotemporal |
| Quality | Pulsating / throbbing | Pressing / tightening (non-pulsating) | Stabbing / boring / excruciating |
| Severity | Moderate to severe | Mild to moderate | Very severe (10/10); "suicide headache" |
| Duration | 4–72 h | 30 min – 7 days | 15–180 min |
| Frequency | 1–4/month (episodic); ≥15 d/month (chronic) | <1 d/month to daily (chronic) | Every other day – 8/day during bouts |
| Autonomic features | None (± lacrimation in severe attacks) | None | Ipsilateral lacrimation, conjunctival injection, rhinorrhoea, ptosis, miosis, eyelid oedema |
| Nausea / vomiting | Yes (80%) | No | Rare |
| Photo-/phonophobia | Yes (both) | One or neither | Rare |
| Restlessness | Prefers to lie still | No restlessness | Pacing, rocking, agitation |
| Aura | 25–30% (visual most common) | None | None |
| Circadian pattern | Morning predominance | Afternoon / evening | Nocturnal (1–2 AM); clock-like regularity |
| Alcohol trigger | Occasional | Not typical | During bouts (always) |
| Sex predilection | Female (3:1) | Slight female predominance | Male (3:1) |
Acute Treatment Comparison
Preventive Treatment Overview
Thunderclap Headache & Red Flags
Causes of Thunderclap Headache
| Aetiology | Key Features | Initial Investigation |
|---|---|---|
| Subarachnoid haemorrhage | Worst headache ever, meningism, ± LOC, vomiting | Non-contrast CT → LP (xanthochromia) → CT angiography |
| Cerebral venous sinus thrombosis | Progressive or thunderclap; may be subacute; risk in pregnancy, COCP, prothrombotic states | CT venography or MR venography |
| Reversible cerebral vasoconstriction syndrome | Recurrent thunderclap headaches over days; often triggered by exertion, vasoactive drugs, postpartum | CT angiography (segmental vasoconstriction) |
| Arterial dissection (carotid/vertebral) | Unilateral headache/neck pain, Horner syndrome, focal ischaemic signs | CT angiography or MRA neck |
| Meningitis / encephalitis | Fever, meningism, altered consciousness, rash (meningococcal) | Blood cultures → LP → CT head if focal signs |
| Pituitary apoplexy | Sudden headache, visual field defects, ophthalmoplegia, endocrine collapse | Urgent MRI pituitary, cortisol, TFTs, FBC |
| Spontaneous intracranial hypotension | Orthostatic headache (worse upright, better supine); history of LP or spinal procedure | MRI brain with gadolinium (pachymeningeal enhancement) |
| Acute hypertensive crisis | Severe headache with systolic BP > 180 mmHg; target organ damage | BP measurement, fundoscopy, CT head, troponin, UEC |
Other Red-Flag Features Requiring Urgent Investigation
Giant Cell Arteritis (GCA) — Specific Red Flag in the Elderly
Headache in Pregnancy & the Elderly
Headache in Pregnancy
Headache during pregnancy requires careful evaluation because the differential diagnosis broadens significantly. Pre-existing migraine often improves (especially in the 2nd and 3rd trimesters) due to stable oestrogen levels, but new-onset or worsening headache demands a low threshold for investigation.
| Treatment | Safety in Pregnancy | Notes |
|---|---|---|
| Paracetamol | Safe in all trimesters | First-line acute treatment; max 4 g/day |
| Ibuprofen / Naproxen | Avoid after 30 weeks (ductus arteriosus closure) | May be used in 2nd trimester with caution |
| Aspirin (low-dose) | Safe at 75–150 mg/day for pre-eclampsia prophylaxis | Not for acute headache treatment |
| Sumatriptan | Not teratogenic in registry data but not formally PBS-approved in pregnancy | May be considered under specialist advice for severe, refractory migraine |
| Ergotamine / dihydroergotamine | Contraindicated — uterotonic | Absolutely contraindicated in pregnancy and breastfeeding |
| Propranolol | Generally safe; monitor neonate for bradycardia | Preferred migraine preventive in pregnancy |
| Amitriptyline | Use if benefits outweigh risks | Monitor neonate for withdrawal effects |
| Topiramate | Avoid — teratogenic (cleft palate) | Contraindicated; switch to propranolol or amitriptyline |
| Sodium valproate | Contraindicated — neural tube defects | Absolutely contraindicated in pregnancy of childbearing potential |
Headache in the Elderly (≥65 Years)
New-onset headache in older adults is more likely to be secondary compared to younger patients. The most important causes to exclude are:
- Giant cell arteritis: temporal headache, jaw claudication, visual loss, ESR >50 mm/h — treat empirically with prednisolone and refer for temporal artery biopsy
- Space-occupying lesion: progressive headache worse in morning, worse with Valsalva, with focal neurology or cognitive change — CT/MRI with contrast
- Idiopathic intracranial hypertension: rare in elderly but possible with obesity and tetracycline use
- Medication-related: nitrates, PDE5 inhibitors, calcium-channel blockers, NSAIDs
- Occipital neuralgia and cervicogenic headache: increasingly common with cervical spondylosis
Acute and preventive treatment in the elderly requires dose adjustment for renal and hepatic function, increased sensitivity to CNS side effects, and awareness of polypharmacy. Start low, go slow. NSAIDs should be used with caution due to GI bleeding risk. Propranolol is relatively contraindicated in severe COPD and heart failure; candesartan or amitriptyline may be preferred alternatives.
Investigations
Primary headaches are diagnosed clinically and do not require neuroimaging. Investigations are indicated when red flags are present or a secondary cause is suspected.
Acute Management of Primary Headache
Migraine — Acute Treatment Ladder
Tension-Type Headache — Acute Treatment
- First-line: Paracetamol 1 g PO stat or aspirin 600–900 mg PO stat or ibuprofen 400 mg PO stat
- Combination analgesics (e.g., paracetamol/codeine) should be limited to ≤2 days/week due to MOH risk
- Triptans are not indicated for TTH
- Non-pharmacological strategies: stress management, physiotherapy, regular sleep, exercise, cognitive behavioural therapy
Cluster Headache — Acute Treatment
Cluster Headache — Transitional and Preventive Therapy
- Transitional (bridge): Prednisolone 1 mg/kg/day (max 60 mg) for 5 days then taper over 2–3 weeks; or greater occipital nerve block (bupivacaine + corticosteroid)
- Episodic cluster prophylaxis: Verapamil 80 mg TDS, titrate to 240–480 mg/day with ECG monitoring (risk of QT prolongation/heart block at higher doses)
- Refractory cluster: Lithium 300 mg BD–TDS (monitor levels), galcanezumab 300 mg SC monthly (PBS authority-required for specialist-initiated chronic cluster)
- TACs (SUNCT/SUNA): Lamotrigine 25–200 mg/day is first-line
Migraine Preventive Therapy
Preventive therapy should be considered when migraine occurs on ≥4 days/month, causes significant disability despite acute treatment, or when acute medications are contraindicated or overused. A minimum 2–3 month trial at adequate dose is required before judging efficacy.
| Drug | Starting Dose | Target Dose | Key Side Effects | PBS Status |
|---|---|---|---|---|
| Propranolol | 20 mg BD | 40–80 mg BD | Fatigue, bradycardia, bronchospasm | General Benefit |
| Candesartan | 4 mg daily | 16–32 mg daily | Hyperkalaemia, hypotension, cough | General Benefit |
| Amitriptyline | 10 mg nocte | 25–75 mg nocte | Sedation, dry mouth, weight gain, cardiac conduction | General Benefit |
| Topiramate | 25 mg nocte | 50–100 mg BD | Cognitive slowing, paraesthesia, renal stones, weight loss | Authority Required |
| Erenumab | 70 mg SC monthly | 70–140 mg SC monthly | Injection-site reactions, constipation | Authority Required (Specialist) |
| Fremanezumab | 225 mg SC monthly or 675 mg quarterly | Same as starting | Injection-site reactions | Authority Required (Specialist) |
| Galcanezumab | 120 mg SC monthly (after 240 mg loading) | Same as starting | Injection-site reactions | Authority Required (Specialist) |
Special Populations
Pregnancy & Breastfeeding
Paediatrics
Elderly (≥65 years)
Renal Impairment
Hepatic Impairment
Immunocompromised
Aboriginal and Torres Strait Islander Health Considerations
📚 References
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- 2. Australian Institute of Health and Welfare (AIHW). Headache in Australia. Cat. no. PHE 323. Canberra: AIHW; 2023.
- 3. Steiner TJ, Stovner LJ, Jensen R, et al. Migraine remains second among the world's causes of disability, and first among young women: findings from GBD2019. J Headache Pain. 2020;21(1):137.
- 4. Royal Australian College of General Practitioners (RACGP). Diagnostic approach to headache in primary care. RACGP Clinical Guide. Melbourne: RACGP; 2023.
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- 9. National Health and Medical Research Council (NHMRC). Evidence review: headache management in primary care. Canberra: NHMRC; 2022.
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- 13. Royal Australian and New Zealand College of Obstetricians and Gynaecologists (RANZCOG). Guideline: Hypertensive disorders of pregnancy. Melbourne: RANZCOG; 2023.
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