45-Year-old male patient, a known case of migraine without... Aura. Presented with severe, initially global headache. Followed by right-sided headache since evening, and global headache was since morning. It was associated with vomiting and nausea in the office afternoon. He was non-compliant with medication and had skipped his medications since the past one day. He has come to my emergency. His initial vitals, BP was high, but after 15 minutes when we checked it again, the BP was normal, pulse is normal, SpO2 was normal. Please tell me what treatment to give. I am a general medicine, medicine resident. Also, tell me what not to miss and what should I check.

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"Migraine Disorders"[MeSH Terms] AND emergency treatment

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acute migraine emergency department treatment guideline red flags ACEP headache

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PMID: 41321235

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"Migraine Disorders"[MeSH Terms] AND prochlorperazine

Do not label this as uncomplicated migraine until you establish that today’s headache is typical for him and the neurologic examination is normal. A history of migraine does not exclude SAH, dissection, infection, hemorrhage, or another secondary headache.

Immediate ED approach

  1. ABC, monitoring, IV access
    • Recheck BP manually after analgesia/antiemetic and document both readings.
    • Check temperature, GCS/mental status, pain score, glucose.
    • Keep NPO initially if vomiting or possible need for imaging/LP.
    • Dark, quiet room and IV fluids if clinically dehydrated from emesis. Routine large-volume fluids alone are not migraine treatment.
  2. Focused history, before treating if possible
    • Exact time and speed of onset: Did it peak within seconds to 1 minute? Was it “first/worst” or maximal at onset?
    • Is this the same as prior migraine: location, severity, evolution, associated symptoms, duration, and response to prior rescue therapy?
    • Precipitant: exertion, sex, Valsalva, trauma, neck manipulation, cocaine/amphetamines/cannabis, anticoagulants/antiplatelets, infection, immunosuppression.
    • Medication details: what preventive medication was missed, usual acute drugs, number of analgesic/triptan days per month, and any recent medication changes.
    • Ask specifically about neck pain, fever, rash, visual loss/red painful eye, diplopia, weakness/numbness, dysarthria, seizure, syncope, confusion, positional component, and severe hypertension history.
  3. Examination
    • Full neurological examination, including gait if safe.
    • Funduscopy for papilledema, pupils/EOMs, visual fields.
    • Neck stiffness and neck tenderness/Horner syndrome.
    • Eye examination including visual acuity, red eye/corneal haze, and IOP if acute angle closure is plausible.
    • Skin/rash and sinus/ear/dental exam only if suggested clinically.
    • Repeat neurologic exam after initial treatment.

When to image or investigate now

For this patient, a new severe global headache with later unilateral predominance and vomiting may still be migraine, but I would have a low threshold for imaging if the pattern is not convincingly identical to his established attacks.
Obtain urgent non-contrast CT head if any of the following:
  • Thunderclap or abrupt maximal-at-onset headache
  • First or worst headache, important change in established migraine pattern, or progressive severity
  • Focal deficit, seizure, confusion, reduced consciousness, papilledema
  • Fever/meningism
  • Persistent or unexplained vomiting
  • Anticoagulant use, trauma, immunosuppression, malignancy
  • Exertional/sexual/Valsalva onset, neck pain, Horner syndrome
  • Persistent severe BP elevation with neurologic symptoms or end-organ injury
If true thunderclap/SAH remains a concern:
  • A good-quality non-contrast CT performed within 6 hours of onset in a neurologically intact patient can be sufficient to exclude SAH in the appropriate setting.
  • If presentation is beyond 6 hours, CT is nondiagnostic, or clinical suspicion remains significant, proceed with LP or CTA using your local pathway and shared decision-making. ACEP recommends LP or CTA for patients still at risk after a negative CT. The ACEP headache policy summary supports this approach.
  • Consider CTA head/neck for dissection/RCVS, and CTV/MRV if CVT is plausible. MRI is preferable for many nonhemorrhagic structural, inflammatory, or posterior-fossa processes. Bradley and Daroff's Neurology in Clinical Practice, CT/MRI discussion, pp. 2673-77 in the library extract.

If examination is normal and this is a typical migraine attack

For a severe migraine with nausea/vomiting, use a non-opioid parenteral regimen.

A practical first-line regimen

  • Prochlorperazine 10 mg IV, slow administration
    Consider diphenhydramine 25 mg IV if your departmental protocol uses it or if akathisia/EPS risk occurs.
  • Ketorolac 15 mg IV or 30 mg IV/IM, if no renal impairment, active GI bleeding/ulcer, NSAID allergy, significant dehydration, or high bleeding risk.
  • IV crystalloid only as needed for volume depletion from vomiting.
An alternative if prochlorperazine is unavailable/contraindicated:
  • Metoclopramide 10 mg IV over 10-15 minutes, with treatment/observation for akathisia or dystonia.
The 2025 AHS evidence assessment found IV prochlorperazine to be a Level A treatment to offer for eligible adults. IV metoclopramide and IV ketorolac were Level B treatments to offer when appropriate. It specifically states that IV hydromorphone must not be offered for ED migraine. See Robblee et al., AHS ED migraine guideline, PMID: 41321235. Rosen also lists dopamine antagonists, triptans/DHE, and parenteral NSAIDs as initial options for moderate-severe attacks, and notes akathisia as a key adverse effect. ROSEN's Emergency Medicine: Concepts and Clinical Practice, “Management,” pp. 4652-54 in the library extract.

If incomplete response

  • Reassess at 30-60 minutes and repeat neurologic examination.
  • Consider dexamethasone 10 mg IV once, particularly if recurrence risk is high. It is primarily for reducing relapse after discharge, not rapid analgesia.
  • SC sumatriptan 6 mg can be useful if this is clearly migraine and there is no vascular contraindication. Avoid it if BP remains uncontrolled, or if you have concern for stroke/TIA, CAD/vasospasm, dissection, or an unexcluded secondary vascular headache.
  • DHE is another specialist/protocol-dependent option, but do not combine with a triptan within 24 hours and avoid in vascular disease/uncontrolled hypertension.

What not to do

  • Do not give opioids, especially hydromorphone, for presumed migraine. They have poorer migraine outcomes, contribute to medication-overuse headache, and can increase return visits. The updated AHS recommendation is Level A “must not offer” for IV hydromorphone.
  • Do not acutely lower BP solely because it was initially high during severe pain/vomiting if it normalizes and there is no end-organ injury. Pain and nausea commonly elevate BP. Treat a hypertensive emergency only if BP remains markedly elevated with objective acute target-organ injury.
  • Do not use a normal neurologic examination alone to rule out SAH if onset was thunderclap or history is concerning.
  • Do not use an oral drug as the main initial therapy while he is actively vomiting.
  • Do not simply restart or alter his preventive regimen in the ED without confirming the actual drug, dose, adherence issue, contraindications, and outpatient plan.

Suggested ED documentation/disposition

If symptoms resolve substantially, repeat BP and neuro exam are normal, there are no red flags, and he can tolerate oral intake:
  • Document why this attack is consistent with his established migraine phenotype.
  • Discharge with a clear rescue plan, antiemetic if needed, and prompt follow-up for preventive-medication adherence.
  • Give return precautions for thunderclap recurrence, new focal symptoms, fever/neck stiffness, persistent vomiting, altered consciousness, visual loss, or a new atypical headache.
Bottom line: If he is neurologically intact and this is truly his usual migraine, prochlorperazine 10 mg IV plus ketorolac, with fluids if depleted, is a reasonable ED regimen. But if “severe global headache since morning” represents a new phenotype, abrupt peak, or unexplained persistent vomiting, investigate for secondary headache before concluding it is migraine.

Find the latest guidelines on acute migraine treatment

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"Migraine Disorders"[MeSH Terms] AND emergency treatment

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2025 2026 acute migraine treatment guideline emergency department American Headache Society guideline parenteral pharmacotherapies

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site:americanheadachesociety.org guideline acute treatment migraine triptans gepants ditans 2025 2026

Latest acute migraine guideline for adults in the ED

The most current high-quality guideline is the American Headache Society 2025 update, published in Headache in 2026:
Robblee et al., AHS ED acute migraine guideline, Headache 2026;66:53-76. PMID: 41321235. It updates the 2016 AHS parenteral-therapy guideline and was affirmed as valuable by the AAN.
This applies to adults with an established migraine attack requiring parenteral treatment in the ED, after appropriate evaluation for secondary headache.
AHS recommendation levelTreatment
Level A: must offerProchlorperazine IV; greater occipital nerve block
Level A: must not offerHydromorphone IV
Level B: should offer when appropriateKetorolac IV, dexketoprofen IV, metoclopramide IV, sumatriptan SC, supraorbital nerve block
Level C: may offerChlorpromazine IV, dexamethasone IV, valproate IV
Level C: should not offerParacetamol/acetaminophen IV
Insufficient evidence for an ED recommendationNormal saline alone, ketamine, lidocaine, propofol, caffeine, granisetron, ibuprofen IV, sphenopalatine ganglion block
The AHS summary of the guideline is available here.

Practical ED implication

For a typical severe migraine with vomiting and a normal neurological examination after exclusion of red flags, a reasonable evidence-aligned approach is:
  • Prochlorperazine 10 mg IV, usually with monitoring for sedation, dystonia, or akathisia
  • Consider diphenhydramine 25 mg IV according to local protocol or to treat EPS/akathisia
  • Add ketorolac IV/IM if no renal dysfunction, significant dehydration, GI bleed/ulcer risk, anticoagulation-related bleeding concern, or NSAID allergy
  • Alternatively, metoclopramide 10 mg IV if prochlorperazine is unavailable or unsuitable
  • Consider dexamethasone IV mainly to reduce post-discharge recurrence, not as the main immediate analgesic
  • Use SC sumatriptan only if diagnosis is secure and there is no uncontrolled hypertension, coronary/cerebrovascular disease, vasospastic disease, or concern for dissection/RCVS/secondary vascular headache.
Avoid opioids, especially hydromorphone. The guideline now uses the strongest wording, “must not offer,” due to inferior migraine outcomes and risks of ongoing opioid use and medication-overuse headache.

For outpatient acute therapy

There has not been a newer, equally definitive US guideline that supersedes the general AHS outpatient acute-treatment framework. The contemporary approach remains stratified:
  1. Mild to moderate attacks: NSAID or acetaminophen early in the attack, with an antiemetic when nausea is prominent.
  2. Moderate to severe attacks or NSAID failure: a triptan is generally the main migraine-specific option if no vascular contraindication.
  3. If triptan is contraindicated, ineffective, or poorly tolerated: consider a nonvasoconstrictive agent:
    • Gepants: ubrogepant, rimegepant, zavegepant nasal spray
    • Ditan: lasmiditan, noting major driving/impairment restrictions
  4. Use a non-oral route when vomiting or marked gastric stasis makes oral absorption unreliable.
  5. Avoid frequent acute-medication use. A practical threshold for reassessment is use on more than 2 to 3 days per week or escalating monthly acute-medication days, because of medication-overuse headache risk.
For an ED resident, the key update is that IV prochlorperazine is now the clearest first-line pharmacologic choice, with metoclopramide and ketorolac as strong alternatives or adjuncts, and hydromorphone specifically discouraged. The 2025 network meta-analysis also supports the general direction but notes low-to-very-low certainty for many comparative rankings: deSouza et al. 2025, systematic review, PMID: 39674934.
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