Drug Guide
Dihydroergotamine Mesylate
Classification
Therapeutic: Migraine abortive agent
Pharmacological: Vasoconstrictor, serotonin receptor agonist
FDA Approved Indications
- Acute treatment of migraine headaches with or without aura
Mechanism of Action
Dihydroergotamine acts as an agonist at serotonin 5-HT1B and 5-HT1D receptors on cranial blood vessels and sensory nerves, leading to vasoconstriction and inhibition of pro-inflammatory neuropeptide release, thus relieving migraine symptoms.
Dosage and Administration
Adult: 4 mg inhaled starting dose, repeat every 15 minutes as needed, up to 2 administrations within 24 hours; for nasal spray, typically 1 spray per nostril, may repeat after at least 15 minutes and up to 2 sprays per nostril in 24 hours.
Pediatric: Not approved for pediatric use.
Geriatric: Use with caution; start at lower end of dosage range due to increased sensitivity.
Renal Impairment: Adjust dosage; use with caution as clearance might be reduced.
Hepatic Impairment: Use with caution; hepatic impairment may increase systemic exposure.
Pharmacokinetics
Absorption: Bioavailability varies; oral bioavailability is low (~2%), nasal and injectable forms provide higher bioavailability.
Distribution: Widely dispersed, crosses the blood-brain barrier.
Metabolism: Hepatic via oxidative dealkylation.
Excretion: Primarily in feces, some in urine.
Half Life: Approximately 2 hours.
Contraindications
- Coronary artery disease or history of myocardial infarction
- Uncontrolled hypertension
- Vomiting or nausea with potential aspiration risk
- Use within 24 hours of another ergot or triptan
- Known hypersensitivity to ergot alkaloids
Precautions
- Use cautiously in elderly, hepatic or renal impairment, or ischemic heart disease; monitor blood pressure; avoid in pregnancy unless benefits outweigh risks.
Adverse Reactions - Common
- Nausea (Common)
- Vasoconstriction effects such as cold extremities, numbness (Common)
- Dizziness, vertigo (Common)
Adverse Reactions - Serious
- Ischemic stroke (Rare)
- Severe hypertension (Rare)
- Ergotism (prolonged vasoconstriction) (Rare)
Drug-Drug Interactions
- Other vasoconstrictors, including triptans and other ergot alkaloids; CYP3A4 inhibitors such as macrolides, azole antifungals, and protease inhibitors may increase levels.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood pressure before and after administration; assess for history of cardiovascular disease; check blood flow to extremities.
Diagnoses:
- Risk for ischemic events
- Impaired tissue perfusion
Implementation: Administer as prescribed; instruct patient to report chest pain, cold extremities, tingling, or numbness.
Evaluation: Evaluate relief of migraine symptoms and monitor for adverse effects.
Patient/Family Teaching
- Instruct patient to report chest pain, cold extremities, or unusual numbness or tingling.
- Use at the first signs of migraine for best efficacy.
- Do not use more frequently than prescribed.
- Inform about possible side effects and when to seek medical help.
Special Considerations
Black Box Warnings:
- Vasospasm leading to ischemic events; avoid in patients with coronary artery disease.
- Use with caution in pregnancy unless clearly indicated.
Genetic Factors: No specific genetic testing recommended.
Lab Test Interference: May slightly elevate serum enzyme levels or affect vascular assessments.
Overdose Management
Signs/Symptoms: Prolonged vasospasm, ischemia, cool extremities, numbness, tingling, chest pain.
Treatment: Discontinue drug; provide supportive care; administer vasodilators like nitroglycerin if indicated and under medical supervision.
Storage and Handling
Storage: Store at room temperature, away from direct light and moisture.
Stability: Stable up to the expiration date on the package.