Drugs for Headache Disorders



Drugs for Headache Disorders

I. Classification of Headache

A. Primary headache disorders

a. Cluster- No aura, are recurring (can use tryptans)

b. Migraine- associated with nausea, vomiting, diarrhea, and vertigo

c. Tension- episodic; may be stress related, can be exacerbated by fatigue, noise, or glare

i. Most common type of recurring headache

B. Secondary headache disorders- management focuses on underlying disorder

a. Arise from other disorders

i. Hemorrhage

ii. Infection

iii. Neuropathy

iv. Stroke

v. Tumor

II. Pathogenesis of Migraine Headaches

A. Neurovascular dysfunction

a. Imbalance of excitatory and inhibitory neurotransmitter activity in CNS

i. Serotonin is the primary neurotransmitter for migraine

ii. Norepinephrine and dopamine can also be considered

iii. Trigeminal nerve is anatomical epicenter

b. The imbalance may be triggered by

i. Hormones- estrogen, hormone replacement therapy, menstruation, ovulation, and oral contraceptives

ii. Stress

iii. Lack of sleep

iv. Food

1. Alcohol(red wine)

2. Aspartame

3. Coffee

4. Nuts

5. Chocolate

6. MSG

7. Nitrites/nitrates

8. Pickled meats

v. Drugs

1. Danazol (Danocrine)

a. Anti-gonadotropic drug- used form endometriosis, fibrolytic breast disease, angioedema

2. Oral contraceptives

3. H2 blockers

vi. Sensorial

1. Bright or flickering lights

2. Odors

B. Phases of migraine attack

a. First phase

i. Characterized by cerebral vasoconstriction and ischemia

ii. Release of 5-HT from CNS neurons and circulating platelets contribute to this phase

1. Use anti-platelet drugs and serotonin antagonists

b. Second phase (longer than first phase)

i. Cerebral vasodilation and pain

1. Trigeminal neurovascular system has central role

2. Neurons in trigeminal complex release peptides, including substance P and Calcitonin gene-related peptide (CGRP)

3. Peptides trigger vasodilation and inflammation of dural vessels- stimulates nociceptive fibers of trigeminal nerve- pain

c. AURA of migraine headaches- result of vasoconstriction and ischemia

i. Occur in 15% of patients- lasts 15-20 minutes

ii. May be visual or sensory

iii. Migraine without aura- aka common headache- may be accompanied by photophobia, nausea and vomiting

III. General approach to treatment of migraines

A. Goals of long term migraine treatment (prophylaxis)

a. Reduce frequency, severity, and disability of migraine

b. Reduce reliance on poorly tolerated medications

c. Improve quality of life (QOL)

d. Avoid increased headache medication use

e. Educate patients to manage their disease

f. Select medication based on side-effect profile and patient’s underlying disease states Medication should be used for at least 2-3 months to assess efficacy

B. Goals of acute/abortive migraine treatment

a. Treat migraine attacks rapidly and consistently without recurrence

b. Restore the patients ability to function

c. Minimize the use of backup and rescue medications

d. Optimize self-care for overall management

e. Be cost effective in overall management

f. Cause minimal or no adverse effects

IV. Drugs for Migraine Headaches

A. Prophylactic drugs

a. Anticonvulsants

b. Antidepressants

c. NSAIDS

d. Beta blockers and calcium channel blockers

e. 5-HT2 receptor blockers

i. Serotonin receptors are widely distributed in CNS, smooth muscles, and platelets to mediate platelet aggregation

ii. 5-HT2 blockers prevent vasoconstriction

B. Abortive (symptomatic drugs)- reverse vasodilative phase and pain/inflammation

a. Dihydroergotamine and ergotamine

b. 5-HT 1d/1b receptor agonist (triptans)

i. Predominant 5-HT receptor in CNS, presynaptic autoreceptor to prevent release of 5-HT

ii. Mediates cerebral vasoconstriction

c. Miscellaneous- NSAIDS, corticosteroids, narcotic analgesics

V. Prophylactic drugs to prevent migraine

A. Anticonvulsants

a. Onset 2-3 weeks

b. ADRs- weight gain, sedation, and tremor

c. Examples

i. Divalproex Na (Depakote, Depakote ER) - most common epileptic drug used for migraine

ii. Topiramate (Topamax) - just FDA approved

C. Antidepressants

a. Onset of efficacy is 3-4 weeks

b. MOA for prevention of migraine no fully understood- may stabilize seroternergic neurotransmission by anatagonizing down regulation of 5-HT2 receptors

c. Examples

i. Selective serotonin reuptake inhibitors (SSRI) (Prozac and others)

1. More efficacious with migraines associated with depression- increases serotonin levels

2. May increase phase 1 effects

3. ADR- anxiety, GI effects, Sexual dysfunction

ii. Tricyclic antidepressants (TCA)

1. ADRs- drowsiness, tremor and anticholinergic side effects

2. Amitriptyline (Elavil)- most common drug in this class

iii. Monoamine oxidase inhibitors (MAO inhibitors)

1. ADRs- hypertensive crisis with tyramine containing foods, sympathomimetic amine drugs

D. NSAIDS

a. MOA- inhibit thromboxane synthesis and platelet aggregation- reduce release of serotonin

b. Can also be used for the treatment of migraines

c. Examples

i. Aspirin, naproxen, ibuprofen, diclofenac

ii. ADRs- GI effects, bleeding, Na and H2O retention, antagonize antihypertensive effects

E. Beta Blockers

a. Must be without ISA (intrinsic sympathomimetic activity) activity (timolol, Propanolol)

b. MOA- may block beta 2 mediated vasodilation and reduce platelet aggregation (uncertain)

F. Calcium channel blockers

a. Less effective than other prophylactic migraine drugs

b. Verapimil primarily used

G. 5-HT2 receptor antagonists

a. Methysergide (Sansert) (X)- ergot alkaloid

i. MOA- blocks 5-HT2 receptor- prevents vasoconstrictive phase of migraine

ii. Associated with several potentially life threatening ADRs- retroperitoneal, pleural and cardiac valve fibrosis

iii. Rarely used, limit to 6 months of use, monitor serum creatinine and chest x-ray

H. Miscellaneous agents

a. Feverfew- herbal preparation. Contraindicated in pregnancy

i. Inhibit prostaglandin and leukotriene migration

b. Magnesium

c. Riboflavin

VI. Abortive drugs to treat migraines

A. Dihydroergotamine (DHE) and ergotamine- both pregnancy category X

a. Used for migraine and cluster headaches

b. Ergot alkaloids- derived from fungus that grows on rye

c. MOA- activate serotonin 5-HT1d/1b receptors in trigeminal neurovascular system- produces vasoconstriction- reverses vasodilation and reduces throbbing. Also inhibits release of peptides that cause vasodilation, inflammation, and pain. Also prevents activation of trigeminal nerves involved in migraine

d. Contraindicated in CAD, PVD, uncontrolled HTN, and in patients using MAO inhibitors

e. Must follow strict dosing guidelines and maximum dosing recommendations

f. ADRs- N,V,D muscle cramps,. More serious- severe cerebral vasoconstriction, ischemia, rebound vasodilation and headache

g. Ergotamine

i. PO, SC, PR

ii. Combined with caffeine (Cafergot)

1. Increases absorption

h. DHE

i. Intranasal, INJ

ii. INJ often combined with Metoclopramide to prevent N/V

B. 5-HT 1d/1b receptor agonists (triptans) (C)

a. Structural analogs of 5-HT

b. MOA- similar to ergotamine and DHE

c. Sumatriptan (Imitrex) (SC, PO, nasal_

i. Newer version has rapid release and is used to compete with newer triptans

d. Newer triptans- Zolmitriptan (Zomig), Rizatriptan (Maxalt)

i. More lipophilic with increased bioavailability

ii. May be more effective than Imitrex with less recurrence of headaches

iii. Examples

1. Almotriptan (Axert)

2. Eletriptan (Replax)

3. Frovatriptan (Frova)

4. Naratriptan (Amerge)

5. Rizatriptan (Maxalt)

6. Zolmitriptan (Zomig)

e. Contraindicated in CAD, PVD, uncontrolled HTN, and in patients using MAO inhibitors

f. All have specific dosing recommendations with maximum doses

g. ADRs- chest tightness, weakness, dizziness, paresthesias, nausea

i. More serious- coronary vasospasm

h. Use injections during morning migraines, vomiting, or unable to take PO

C. Miscellaneous agents

a. Non-narcotic analgesics: First line for abortive treatment

i. Acetaminophen and aspirin; also combine with caffeine in OTC products like Excedrin

ii. NSAIDS

1. Ketorlac IM (Toradol)

a. Very effective

b. Limit use < 5 days due to ADRs (GI bleeding, renal effects)

iii. Narcotic analgesics

1. Opiods effective to relieve pain. Less commonly used.

2. Pregnancy C/D

3. Good for acute migraine when sedation will not put patient at risk

4. Examples

a. Butorphanol nasal spray (Stadol NS)

b. Hydrocodone/ APAP (Vicodin)

5. Barbituate hypnotics

a. Pregnancy Category D

b. Avoid due to overuse and misuse. Max daily dose = 6 doses per day

c. Examples

i. Butalbital/APAP/Caffeine (Fioricet)

ii. Butalbital/ASA/Caffeine (Fiorinal) C2

6. Steroids

a. Good for status migrainosus

b. Most common is dexamethasone IM

7. Isometheptene

a. Works like sympathomimetic to treat migraine

b. Available as combo product with APAP and mild sedative dichlorphenazone (Midrin)

c. Good for mild-moderate headaches

VII. Treatment of tension and cluster headaches

A. Tension headaches

a. Prophylaxis: TCA antidepressants

b. Abortive: NSAIDS

B. Cluster headaches- similar to migraine treatment

a. Prophylaxis: CCBs, ergots, steroids

b. Abortive: triptans, ergots, oxygen

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