What is the best course of action for a patient with a 2-month history of headaches?

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Evaluation and Management of 2-Month Headache

A patient with 2 months of continuous or near-daily headache requires urgent evaluation to exclude secondary causes—particularly giant cell arteritis if age ≥50 years, intracranial pathology, or spontaneous intracranial hypotension—before diagnosing and treating a primary headache disorder such as chronic migraine, new daily persistent headache, or chronic tension-type headache. 1, 2, 3

Initial Red Flag Assessment

First, determine if urgent neuroimaging or specialist evaluation is needed by screening for these red flags 2, 4, 5:

  • Age ≥50 years with new-onset headache: Giant cell arteritis must be excluded, as headache is the most frequent presenting symptom and prompt corticosteroid treatment prevents permanent vision loss 6, 7, 3
  • Thunderclap or sudden-onset headache: Suggests subarachnoid hemorrhage or other vascular catastrophe 2, 4
  • Orthostatic features (worse when upright, better lying down): Evaluate for spontaneous intracranial hypotension with brain and spine MRI with contrast 4
  • Progressive worsening pattern or headache awakening patient from sleep: Raises concern for mass lesion or increased intracranial pressure 2, 3
  • Focal neurological deficits: Requires immediate neuroimaging 2, 5
  • Worsening with Valsalva or lying down: Suggests increased intracranial pressure 2
  • History of cancer or immunosuppression: Higher risk of metastatic disease or opportunistic infection 5, 3

Diagnostic Classification After Excluding Secondary Causes

If no red flags are present, classify the primary headache disorder based on frequency and phenotype 1, 4:

Chronic Migraine (Most Common)

  • ≥15 headache days per month for >3 months, with migraine features on ≥8 days/month 1, 8
  • Migraine features include: moderate-to-severe unilateral throbbing pain, nausea/vomiting, photophobia, phonophobia, worsening with physical activity 1, 5
  • Critical pitfall: Only 20% of patients meeting chronic migraine criteria are correctly diagnosed because patients often underreport milder headache days 1
  • Ask directly: "Do you feel like you have a headache of some type on 15 or more days per month?" 1

New Daily Persistent Headache

  • Patient can pinpoint the exact day the daily headache began 4
  • Headache becomes continuous and unremitting from onset 4
  • Must exclude spontaneous intracranial hypotension with brain and spine MRI with contrast if any orthostatic features present 4

Chronic Tension-Type Headache

  • Bilateral, pressing/tightening (non-pulsating) quality 2
  • Mild-to-moderate intensity 2
  • Not aggravated by routine physical activity 2
  • No nausea/vomiting (though photophobia or phonophobia may occur) 2

Medication Overuse Headache Assessment

Before initiating preventive treatment, evaluate for medication overuse headache, which perpetuates chronic daily headache 8:

  • Triptans, ergots, or combination analgesics: ≥10 days/month for ≥3 months 8
  • Simple analgesics (acetaminophen, NSAIDs): ≥15 days/month for ≥3 months 8
  • If medication overuse is present, withdrawal is necessary for preventive therapy to be effective 1

Preventive Treatment Strategy

For Chronic Migraine (First-Line)

CGRP monoclonal antibodies (erenumab, fremanezumab, or galcanezumab) are first-line preventive treatment for chronic migraine, with strong evidence demonstrating 2-4.8 fewer migraine days per month and favorable tolerability 8:

  • Administered as monthly subcutaneous injections 8
  • Minimal systemic side effects compared to traditional preventives 8
  • Monitor blood pressure with erenumab due to postmarketing reports of hypertension development or worsening 8
  • Fremanezumab should be avoided in patients with history of stroke, subarachnoid hemorrhage, coronary heart disease, inflammatory bowel disease, COPD, or impaired wound healing 1

Alternative first-line option: Topiramate 50-100 mg daily 1, 8:

  • The only traditional preventive with randomized controlled trial evidence specifically in chronic migraine 8
  • Start at 25 mg daily, titrate slowly to minimize side effects 8
  • Common adverse effects: cognitive slowing, paresthesias, weight loss, nephrolithiasis 1, 8
  • Absolutely contraindicated in pregnancy and women of childbearing potential without reliable contraception 1

Third-line option: OnabotulinumtoxinA 1, 8:

  • FDA-approved specifically for chronic migraine (≥15 headache days/month) 8
  • 155-195 units injected into 31-39 sites every 12 weeks 1
  • Consider if CGRP antibodies and topiramate fail or are contraindicated 1

For New Daily Persistent Headache

Treat based on predominant phenotype since no controlled trials exist specifically for NDPH 4:

  • Migraine-like phenotype: Use CGRP monoclonal antibodies or topiramate as above 4
  • Tension-type phenotype: Use amitriptyline as below 4

For Chronic Tension-Type Headache

Amitriptyline is the drug of first choice for chronic tension-type headache prophylaxis 2, 4:

  • Start 10 mg at night, titrate to 10-100 mg based on response and tolerability 1
  • Particularly beneficial if comorbid depression or sleep disturbances present 4
  • Contraindicated in age <6 years, heart failure, concurrent monoamine oxidase inhibitors or SSRIs, glaucoma 1

Alternative: Beta-blockers (propranolol, metoprolol) if comorbid hypertension 2

Non-Pharmacologic Interventions

Recommend for all patients regardless of headache type 2, 4:

  • Regular aerobic exercise or progressive strength training 2, 4
  • Cognitive-behavioral therapy and biofeedback 4
  • Physical therapy for tension-type headache 2

Monitoring and Follow-Up

Implement headache diary immediately to track frequency, severity, triggers, and acute medication use 1, 2, 4:

  • Headache calendars require minimal time if completed only on symptomatic days 1
  • Essential for monitoring medication overuse and treatment response 1

Evaluate treatment response at 2-3 months after initiating or changing preventive therapy 1, 8, 2:

  • Full benefit may take 2-3 months to manifest; do not abandon therapy prematurely 8
  • Key outcome measures: attack frequency, severity, and migraine-related disability 1
  • Use validated tools: Migraine Treatment Optimization Questionnaire (mTOQ-4) for acute medication effectiveness, HURT questionnaire for preventive effectiveness 1

Continue appropriate acute therapy alongside preventive treatment 8:

  • Acute migraine treatment: NSAIDs, triptans, gepants (rimegepant, ubrogepant), or lasmiditan 5
  • Monitor for medication overuse headache development 2

Refer to headache specialist if 1, 2, 4:

  • No improvement after 2-3 months of optimized preventive therapy 1
  • Diagnostic uncertainty persists 2, 4
  • Complex medication management needed 1

Special Population Considerations

Age ≥50 years 2, 3:

  • Lower threshold for neuroimaging, as migraine typically remits with age while secondary headaches increase substantially 2
  • Greater caution with medication side effects and drug interactions 2
  • Higher suspicion for giant cell arteritis or intracranial mass lesion 3

Women of childbearing potential 1, 2:

  • Absolutely avoid topiramate and valproate due to teratogenic effects 1, 2
  • Consider pregnancy plans when selecting prophylactic medication 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Treatment of Chronic Tension-Type Headache

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

New Daily Persistent Headache Diagnosis and Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Giant cell (temporal) arteritis.

Neurologic clinics, 1997

Research

[Headache due to temporal arteritis].

Pathologie-biologie, 2000

Guideline

Medications for Chronic Migraine Prevention

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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