Scope of this summary
Adolescents and adults with a clinically established episodic or chronic migraine phenotype. This page does not cover status migrainosus infusion protocols, hemiplegic or retinal migraine, pregnancy-specific prescribing, pediatric dosing or cluster headache. Product choice requires current FDA labeling, contraindications and insurance criteria in addition to the 2023 VA/DoD evidence review.
sources for this section:VA/DoD headache 2023
The Bottom Line
- Treat attacks early with an individualized plan that considers severity, nausea, route, previous response, cardiovascular disease, pregnancy and interactions rather than cycling randomly through rescue products.
- VA/DoD supports selected triptans and nonopioid analgesics for acute migraine and suggests oral gepants for appropriate patients; choose within current FDA labeling and patient-specific safety constraints.
- Offer prevention when attack frequency, disability, prolonged attacks, medication overuse or patient preference justifies it, and select among source-supported oral, injectable and behavioral options through shared decision-making.
- Set a measurable target using monthly migraine days, acute-medication days and function, allow an adequate trial at a tolerated dose and reassess benefit before continuing indefinitely.
sources for this section:VA/DoD headache 2023
Practical clinical workflow
1
Confirm migraine features and aura, record baseline frequency and disability, identify nausea or allodynia, review cardiovascular and pregnancy risk, and reconcile every acute medicine including caffeine combinations.
2
Build a stepped home rescue plan with a primary agent, route, timing, repeat or backup instructions and a limit on medication days; address hydration, sleep and predictable triggers pragmatically.
3
Discuss prevention options by evidence, comorbidity, weight, blood pressure, mood, reproductive plans, adherence, cost and route; titrate one change at a time when feasible.
4
Review diary outcomes and adverse effects after an appropriate interval, taper ineffective preventive therapy safely and escalate refractory chronic migraine or diagnostic uncertainty to headache expertise.
sources for this section:VA/DoD headache 2023
Safety boundaries and escalation
- A first aura with motor weakness, persistent deficit, abrupt maximal-onset pain or a materially different attack requires evaluation for stroke, hemorrhage or another secondary cause.
- Check vasoconstrictor contraindications and interactions before triptans or ergot derivatives; do not infer that a newer drug is safe in pregnancy or vascular disease without current labeling.
- Frequent use of triptans, combination analgesics, opioids or simple analgesics can sustain medication-overuse headache; prevention and a structured withdrawal plan may be necessary.
- Suicidal thinking, severe depression, uncontrolled hypertension, pregnancy planning or serious treatment adverse effects should change the preventive choice and follow-up intensity.
sources for this section:VA/DoD headache 2023
Localization
US preventive access is strongly shaped by FDA indications and payer step requirements, which are not clinical evidence thresholds. The 2023 VA/DoD guideline predates some subsequent label expansions, so every prescribed product needs a live label check.
sources for this section:VA/DoD headache 2023
Source documents
Use the linked source documents for complete recommendations, evidence grading, exclusions and implementation detail.
- U.S. Department of Veterans Affairs and U.S. Department of Defense Evidence-Based Practice Work GroupVA/DoD Clinical Practice Guideline for Management of Headache2023 guideline; official page updated 2025-07-11 路 published 2023-09-01 路 updated 2025-07-11 路 accessed 2026-08-20view source
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