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Some Drugs for Prevention of Migraine Page 110 Treatment Guidelines Published by The Medical Letter, Inc.. Sumatriptan nasal spray has produced relief in about 60% of patients after 2 ho

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Treatment Guidelines

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IN THIS ISSUE (starts on next page)

Drugs for Migraine p 107

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Drugs for Migraine

Tables

1 Triptans: Onset of Action Page 108

2 Some Drugs for Treatment of Migraine Page 109

3 Some Drugs for Prevention of Migraine Page 110

Treatment Guidelines

Published by The Medical Letter, Inc • 145 Huguenot Street, New Rochelle, NY 10801 • A Nonprofit Publication

Volume 11 (Issue 136) December 2013

www.medicalletter.org

TREATMENT OF MIGRAINE

Treatment of migraine in the emergency department,

which may involve use of intravenous drugs, is not

discussed here.

ANALGESICS — Treatment with a nonopioid

anal-gesic may be sufficient for mild-to-moderate episodes

of migraine without nausea, disability, or need for bed

rest Aspirin and acetaminophen1alone have been

shown to be effective Both are also available by

pre-scription in widely used combinations with

butal-bital and caffeine (Fiorinal, Fioricet, and others).

Butalbital has not been shown to be effective for

treatment of migraine in controlled trials and has been

associated with tolerance and dependence.

Oral combinations of aspirin or acetaminophen with

an opioid are effective for relief of migraine pain, but

they can cause the usual opioid adverse effects (such

as nausea, drowsiness, and constipation), and their use

can lead to tolerance, dependence, and addiction.

Nonsteroidal anti-inflammatory drugs (NSAIDs) such

as naproxen sodium (Aleve, and others) and ibuprofen (Advil, Motrin, and generics) have been effective in

relieving migraine pain.2,3Naproxen has a longer half-life and may have a longer duration of action than ibuprofen Diclofenac is available as a powder for oral

solution (Cambia) for treatment of migraine; it has a

rapid onset of action, but is much more expensive than generic NSAIDs.

SEROTONIN (5-HT1B/1D) RECEPTOR AGO-NISTS (“TRIPTANS”) — A triptan is the drug of

choice for treatment of moderate-to-severe migraine.4

Use of a triptan early in an attack when pain is still mild to moderate in intensity can improve outcomes.

Sumatriptan is available for subcutaneous (SC)

self-injection (with or without a needle),5as a nasal spray, and for oral administration, and has been approved by the FDA as a transdermal patch formulation The injectable and possibly the nasal-spray formulations may be useful for patients with nausea and/or vomit-ing, and they have a more rapid onset of action than the oral tablets SC sumatriptan produces relief within 2 hours in about 80% of patients with moderate-to-severe migraine Sumatriptan nasal spray has produced relief in about 60% of patients after 2 hours, about the same as oral sumatriptan, which has been effective in about 50% to 60% of patients with acute migraine after

2 hours and in about 70% after 4 hours.6 The transder-mal patch has not been compared to other formulations

of sumatriptan, but it will likely have a slower onset of action than the nasal spray or injectable formulations.

It frequently causes application-site reactions.7

A fixed-dose combination tablet containing

sumatrip-tan 85 mg and naproxen 500 mg (Treximet) provided

better pain relief than either agent taken alone in patients with moderate or severe migraine.8

A nonopioid analgesic may be effective for treatment

of mild-to-moderate migraine A triptan is the drug of

choice for treatment of moderate-to-severe migraine.

The short-acting oral triptans sumatriptan,

almotrip-tan, eletripalmotrip-tan, rizatripalmotrip-tan, and zolmitriptan are

simi-lar in their efficacy and speed of onset; naratriptan

and frovatriptan have a slower onset and longer

dura-tion of acdura-tion The nasal spray formuladura-tions of

suma-triptan and zolmisuma-triptan have a faster onset of action

than oral triptans Subcutaneous sumatriptan is the

fastest-acting and most effective triptan formulation.

Patients who do not respond to one triptan may

respond to another For prevention of migraine,

topi-ramate, valproate, propranolol, timolol, or

metopro-lol is recommended.

Related article(s) since publication

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Drugs for Migraine

Treatment Guidelines from The Medical Letter • Vol 11 ( Issue 136) • December 2013

The oral short-acting triptans almotriptan, eletriptan,

rizatriptan and zolmitriptan are similar in efficacy to

sumatriptan.9 Zolmitriptan, like sumatriptan, is also

available as a nasal spray; compared to sumatriptan,

fewer patients complain about its taste.10Naratriptan

and frovatriptan have longer half-lives and have a

slower onset of action and lower initial response rate

than other triptans.11

Recurrence – In patients with moderate-to-severe

migraine, the rate of recurrence within 24 hours after

treatment with a triptan is generally 20% to 40%; it

may be slightly lower with naratriptan and

frovatrip-tan Recurrences usually respond to a second dose of

the triptan.

Adverse Effects – Tingling, flushing, dizziness,

drowsi-ness, fatigue, and a feeling of heavidrowsi-ness, tightdrowsi-ness, or

pressure in the chest may occur with all triptans, but

most commonly with injectable sumatriptan A burning

sensation at the injection site is common with SC

suma-triptan CNS symptoms such as somnolence and

asthe-nia following triptan therapy may be part of the migraine

attack, unmasked by the successful treatment of pain,

rather than adverse effects of the drugs Angina,

myocar-dial infarction, cardiac arrhythmia, stroke, and death

have occurred rarely with triptans,12 which are

con-traindicated in patients with coronary, cerebrovascular or

other arterial disease, or uncontrolled hypertension.

They should be used with caution in patients with other

risk factors for vascular disease, particularly diabetes.

Drug Interactions – A triptan should generally not be

used within 24 hours after another triptan or an

ergot-containing drug because vasoconstriction could be

additive MAO inhibitors increase serum

concentra-tions of rizatriptan, sumatriptan, and zolmitriptan; they

should not be used within 2 weeks of each other.

Propranolol increases serum concentrations of

eletrip-tan, rizatripeletrip-tan, and zolmitriptan Inhibitors of

CYP3A4, including verapamil, can increase eletriptan

108

serum concentrations.13Triptans are frequently taken together with selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs); serotonin syndrome has been reported with concurrent use.14

ERGOTS — Ergotamine, a non-specific serotonin

agonist and vasoconstrictor, has been used for many years for treatment of moderate-to-severe migraine headache It is available alone in sublingual tablets and

in combination with caffeine in oral tablets and sup-positories Comparative studies have shown that oral ergotamine plus caffeine is less effective than a triptan for acute treatment of migraine.15

Dihydroergotamine, which can be injected

subcuta-neously, intramuscularly, or intravenously, or sprayed intranasally, is also effective in acute migraine treatment.

It can be effective in some patients who do not respond

to triptans Dihydroergotamine nasal spray relieves migraine after 2 hours in about 50% of patients with a 15% incidence of headache recurrence within 24 hours

Adverse Effects – Dihydroergotamine is a weaker

vasoconstrictor than ergotamine and causes fewer adverse effects Nausea and vomiting are fairly com-mon with ergotamine, but can be prevented by pre-treatment with or concurrent use of an antiemetic such

as metoclopramide (Reglan, and generics) Serious

adverse effects, such as vascular (including coronary) occlusion and gangrene, are rare and are usually asso-ciated with overdosage (>6 mg in 24 hours or 10 mg per week) Liver disease or fever can accelerate devel-opment of severe vasoconstriction Ergots are con-traindicated in patients with arterial disease or uncon-trolled hypertension.

Drug Interactions – The effects of ergots may be

potentiated by triptans, beta blockers, dopamine, nico-tine, or CYP3A4 inhibitors Ergots and triptans should not be taken within 24 hours of each other Use of ergots is contraindicated with strong CYP3A4

inhibitors such as clarithromycin (Biaxin, and gener-ics) or itraconazole (Sporanox, and genergener-ics).13

MEDICATION OVERUSE HEADACHE

Overuse of drugs for migraine, such as analgesics and triptans, but especially butalbital and opioids, can lead

to chronic headache with structural and functional changes in the brain Treatment of medication overuse headache involves withdrawing the overused drug(s) Abrupt withdrawal may require hospitalization and bridge therapy with other drugs Preventive medica-tions for migraine should be considered Future use of acute migraine treatments should be limited to <2 days

Onset Elimination

of action half-life

Almotriptan (Axert) 30-60 min 3-4 hrs

Eletriptan (Relpax) 30-60 min ~4 hrs

Frovatriptan (Frova) ~2 hrs ~25 hrs

Naratriptan (Amerge) 1-3 hrs ~6 hrs

Rizatriptan (Maxalt) 30-60 min 2-3 hrs

nasal spray 10-15 min

SC injection ~10 min

nasal spray 10-15 min

Table 1 Triptans: Onset of Action

Trang 4

per week.16,17 NSAIDs are less likely than other

anal-gesics to cause medication overuse headache.

PREVENTION

Patients with frequent or severe disabling migraine

headaches and those who cannot take vasoconstrictors

or are refractory to acute treatment should receive

pro-phylactic treatment.18,19Menstrual or other predictable

migraine attacks may sometimes be prevented by a

brief course of an NSAID or triptan, particularly nara-triptan or frovanara-triptan, taken, for example, for several days before and after the onset of menstruation.20,21

BETA BLOCKERS — For continuous prophylaxis,

beta blockers are commonly used Propranolol and timolol are the only beta blockers approved by the FDA for this indication, but metoprolol, nadolol

(Corgard, and generics) and atenolol (Tenormin, and

generics) have also been effective in preventing

Table 2 Some Drugs for Treatment of Migraine

Serotonin (5-HT 1B/1D ) Receptor Agonists ("Triptans")

Almotriptan – Axert (Janssen) 6.25, 12.5 mg tabs 6.25 or 12.5 mg PO; can be repeated $30.70

once after 2 hrs (max 25 mg/d) Eletriptan – Relpax (Pfizer) 20, 40 mg tabs 20 or 40 mg PO; can be repeated 30.90

after 2 hrs (max 80 mg/d) Frovatriptan – Frova (Endo) 2.5 mg tabs 2.5 mg PO; can be repeated after 34.10

2 hrs (max 7.5 mg/d) Naratriptan – generic 1, 2.5 mg tabs 2.5 mg PO; can be repeated once 14.50

Rizatriptan – generic 5, 10 mg tabs 5 or 10 mg PO; can be repeated 8.80

5, 10 mg orally disintegrating tabs after 2 hrs (max 30 mg/d)2 20.30

Sumatriptan – generic 25, 50, 100 mg tabs 50 or 100 mg PO; can be repeated 3.00

after 2 hrs (max 200 mg/d)

4, 6 mg/0.5 mL injectable kit, vials 6 mg SC; can be repeated once after 51.80

1 hr (max 12 mg/d) Alsuma (Pfizer) 6 mg/0.5 mL auto-injector 6 mg SC; can be repeated once after 91.60

1 hr (max 12 mg/d) Imitrex (GSK) 25, 50, 100 mg tabs 50 or 100 mg PO; can be repeated 33.60

after 2 hrs (max 200 mg/d)

5, 20 mg/0.1 mL nasal spray 5, 10 or 20 mg intranasally; can be 41.90

repeated once after 2 hrs (max 40 mg/d)

4, 6 mg/0.5 mL cartridges; 6 mg SC; can be repeated once after 97.90

6 mg/0.5 mL vials 1 hr (max 12 mg/d) Sumavel DosePro (Zogenix) 6 mg/0.5 mL SC (needle-free) 6 mg SC; can be repeated once after 1 hr 98.90

(max 12 mg/d) Zecuity (NuPathe) 6.5 mg transdermal patch 6.5 mg transdermally; a second patch can N.A

be applied after 2 hrs (max 2 patches/d) Zolmitriptan – generic 2.5, 5 mg tabs 2.5 or 5 mg PO; can be repeated 32.00

2.5, 5 mg orally disintegrating tabs after 2 hrs (max 10 mg/d) 32.00

Zomig nasal spray 2.5, 5 mg/0.1 mL nasal spray 2.5 or 5 mg intranasally; can be repeated 42.80

once after 2 hrs (max 10 mg/d)

Triptan Combination Product

Sumatriptan/naproxen – Treximet 85 mg/500 mg tabs 85 mg/500 mg PO; can be repeated 25.50

Ergots

Dihydroergotamine mesylate – 1 mg/mL ampules 1 mg IM or SC; can be repeated at

Migranal nasal spray (Valeant) 4 mg/mL nasal spray 1 spray (0.5 mg) into each nostril, 195.80

repeated 15 min later (2 mg/dose;

max 3 mg/d) Ergotamine tartrate – Ergomar 2 mg sublingual tabs 2 mg sublingually; can be repeated 15.00

Ergotamine/caffeine – generic 1 mg/100 mg tabs 2 tabs PO; can be repeated q 30 min x 4 1.80

N.A = Price not available

1 Approximate wholesale acquisition cost (WAC) of one dose at the lowest usual dosage Source: Analy$ource® Monthly (Selected from FDB MedKnowledge™) November 5, 2013 Reprinted with permission by FDB, Inc All rights reserved ©2013 www.fdbhealth.com/policies/drug-pricing-policy Actual retail prices may be higher.

2 Patients also taking propranolol should only use a 5-mg dose (max 15 mg/d).

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Drugs for Migraine

Treatment Guidelines from The Medical Letter • Vol 11 ( Issue 136) • December 2013

migraine.22All beta blockers can cause fatigue,

exer-cise intolerance, and orthostatic hypotension, and

should not be used in patients with decompensated

heart failure All are relatively contraindicated in

patients with asthma Patients with migraine often

have comorbid depression, which may be aggravated

by beta blockers.

ANTIEPILEPTIC DRUGS — Valproate and

topi-ramate have been effective in decreasing migraine

frequency and are approved by the FDA for migraine

prophylaxis About 50% of patients achieve a >50%

reduction in headache frequency with these drugs.23

In randomized double-blind studies, topiramate was

at least as effective as propranolol for migraine

pre-vention.24,25Topiramate has also reduced the number

of migraine headache days per month and improved

associated symptoms in patients with chronic

migraine (>15 headache days/month for >3 months)

results of clinical trials suggest that gabapentin

(Neurontin, and others) may not be effective for

migraine prophylaxis.28

110

Adverse effects of valproate include nausea, fatigue,

tremor, weight gain, and hair loss Acute hepatic failure, pancreatitis, and hyperammonemia (in patients with urea cycle disorders) occur rarely Other effects include polycystic ovary syndrome, hyperinsulinemia, lipid abnormalities, hirsutism, and menstrual

distur-bances Topiramate commonly causes paresthesias;

fatigue, language and cognitive impairment, taste perversion, and weight loss can also occur Topiramate can rarely cause secondary narrow-angle glaucoma, oligohydrosis, nephrolithiasis, and symptomatic meta-bolic acidosis.

ANTIDEPRESSANTS — Tricyclic antidepressants

can prevent migraine in some patients and may be given concurrently with other prophylactic agents, but they often cause sedation, dry mouth, and weight gain Amitriptyline is the only tricyclic shown to be effective

in clinical trials.29 Nortriptyline and imipramine

(Tofranil, and generics), which may have fewer adverse

effects than amitriptyline, are also frequently used.

Newer antidepressants such as the SNRI venlafaxine

may also be effective in preventing migraine.30

Table 3 Some Drugs for Prevention of Migraine

Beta Blockers

extended-release – generic 25, 50, 100, 200 mg tabs 100-200 mg once/d 32.90

Propranolol – generic 10, 20, 40, 60, 80 mg tabs 160-240 mg/d divided bid, 3.60

tid or qid extended-release – generic 60, 80, 120, 160 mg caps 160-240 mg once/d 51.90

Timolol – generic 5, 10, 20 mg tabs 10-15 mg bid or 20 mg once/d 39.60

Antiepileptic Drugs

Tricyclic Antidepressants 2

Amitriptyline – generic 10, 25, 50, 75, 100, 150 mg tabs 30-150 mg once/d 3.60

SNRI 2

Venlafaxine – generic 25, 37.5, 50, 75, 100 mg tabs 25-50 mg tid 69.30 extended-relese – generic 37.5, 75, 150 mg caps; 37.5, 75, 75-150 mg once/d 16.90

150, 225 mg tabs

Botulinum Toxin Type A 4

Onabotulinumtoxin A – Botox (Allergan) 50, 100, 200 unit vial 155 units IM every 12 weeks5 1050.006

1 Approximate wholesale acquisition cost (WAC) of 30 days’ treatment at the lowest usual dosage Source: Analy$ource® Monthly (Selected from FDB

MedKnowledge™) September 5, 2013 Reprinted with permission by FDB, Inc All rights reserved ©2013 www.fdbhealth.com/policies/drug-pricing-policy Actual retail prices may be higher.

2 Not FDA-approved for this indication.

3 Marketed as divalproex sodium (Depakote) and valproic acid (Depakene, and others) Only divalproex sodium is FDA-approved for prevention of migraine.

4 FDA-approved for prophylaxis of headaches in adult patients with chronic migraine.

5 Total dosage of 155 units is divided over 7 specific head/neck muscle areas (detailed information provided in package insert).

6 Cost of one 200-unit vial.

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OTHERS — Pericranial injections of

onabotuli-numtoxinA (Botox) may be marginally effective for

prophylaxis of headaches in adult patients with

chron-ic migraine.31Botulinum toxin is not recommended for

prevention of episodic migraine.

Calcium channel blockers are used for prevention of

migraine, but evidence for their effectiveness is weak.

Verapamil (Calan, and generics) was somewhat more

effective than placebo in some small studies.22

In small double-blind trials, the

angiotensin-convert-ing enzyme (ACE) inhibitor lisinopril (Prinivil, and

others) and the angiotensin receptor blocker (ARB)

candesartan (Atacand, and generics) have reduced

migraine frequency by about 30-35%; they have not

been compared to other, better-established

prophylac-tic agents.32

Nonsteroidal anti-inflammatory drugs (NSAIDs),

such as naproxen and ibuprofen, have been used for

short-term prevention of migraine, including

menstru-al migraine, and for aborting acute attacks.33

The dietary supplement petasites (butterbur; Petadolex)

100-150 mg per day reduced migraine attack frequency

by 36-60% in 2 randomized, placebo-controlled trials in

about 300 patients.33,34 Riboflavin, magnesium citrate,

coenzyme Q10, and feverfew have also been reported to

be effective in preventing migraine in small, randomized,

placebo-controlled trials.33,35-38

PREGNANCY

Acetaminophen and/or opioids are commonly used for

treatment of acute migraine attacks during pregnancy.

NSAIDs should not be used in the third trimester

because they can cause premature closure of the ductus

arteriosus Opioids should also be avoided late in the

third trimester because of the risk of neonatal

with-drawal The triptans are classified as category C

(embryo/fetal toxicity in animals; no adequate studies

in humans) for use during pregnancy, but sumatriptan,

which has been used the longest, and possibly

rizatrip-tan, eletriprizatrip-tan, and zolmitriprizatrip-tan, do not appear to be

associated with an increased risk of birth defects.39,40

All ergots are contraindicated (category X) during

pregnancy.

Preventive therapy is generally not recommended

during pregnancy Valproate sodium, valproic acid,

and divalproex sodium are contraindicated (category

X) for prevention of migraine in pregnant women; IQ

scores were lower in the children of mothers who took

these drugs during pregnancy.41 Topiramate has been

reported to increase the risk of cleft lip and cleft palate

in children whose mothers took the drug during preg-nancy Women should avoid ACE inhibitors and ARBs

if they become or are planning to become pregnant; drugs that act on the renin-angiotensin system can cause fetal and neonatal morbidity and death.

1 MJ Prior et al A randomized, placebo-controlled trial of acetamino-phen for treatment of migraine headache Headache 2010; 50:819

2 CC Suthisisang et al Meta-analysis of the efficacy and safety of naproxen sodium in the acute treatment of migraine Headache 2010; 50:808

3 C Suthisisang et al Efficacy of low-dose ibuprofen in acute migraine treatment: systematic review and meta-analysis Ann Pharmacother 2007; 41:1782

4 EA MacGregor In the clinic Migraine Ann Intern Med 2013; 159:ITC5-1

5 A sumatriptan needle-free injector for migraine Med Lett Drugs Ther 2010; 52:50

6 SD Silberstein Migraine Lancet 2004; 363:381

7 A sumatriptan patch (Zecuity) for migraine Med Lett Drugs Ther 2013; in press

8 RB Lipton et al Consistency of response to sumatriptan/naproxen sodium in a placebo-controlled crossover study Cephalalgia 2009; 29:826

9 MM Johnston and AM Rapoport Triptans for the management of migraine Drugs 2010; 70:1505

10 Zolmitriptan (Zomig) nasal spray for migraine Med Lett Drugs Ther 2004; 46:7

11 V Tullo et al Frovatriptan versus zolmitriptan for the acute treatment

of migraine: a double-blind, randomized, multicenter, Italian study Neurol Sci 2010; 31:S51

12 G Roberto et al Triptans and serious adverse vascular events: data mining of the FDA Adverse Event Reporting System database Cephalalgia 2013; Aug 6 (epub)

13 Inhibitors and inducers of CYP enzymes and P-glycoprotein Med Lett Drugs Ther 2013; 55:e44

14 FDA Public Health Advisory Combined use of 5-hydroxytryptamine receptor agonists (triptans), selective serotonin reuptake inhibitors (SSRIs) or selective serotonin/norepinephrine reuptake inhibitors (SNRIs) may result in life-threatening serotonin syndrome 7/19/2006 Last updated August 16, 2013 Available at www.fda.gov/Drugs/ DrugSafety/PostmarketDrugSafetyInformationforPatientsandProvider s/DrugSafetyInformationforHeathcareProfessionals/PublicHealthAdv isories/ucm124349.htm Accessed November 12, 2013

15 MJ Láinez et al Crossover, double-blind clinical trial comparing almotriptan and ergotamine plus caffeine for acute migraine therapy Eur J Neurol 2007; 14:269

16 JR Saper and AN DaSilva Medication overuse headache: history, fea-tures, prevention and management strategies CNS Drugs 2013; 27:867

17 SJ Tepper Medication-overuse headache Continuum (Minneap Minn) 2012; 18:807

18 SD Silberstein et al Evidence-based guideline update: pharmacologic treatment for episodic migraine prevention in adults: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society Neurology 2012; 78:1337

19 E Loder et al The 2012 AHS/AAN guidelines for prevention of episodic migraine: a summary and comparison with other recent clin-ical practice guidelines Headache 2012; 52:930

20 T Pringsheim et al Acute treatment and prevention of menstrually related migraine headache: evidence-based review Neurology 2008; 70:1555

21 EA MacGregor et al Safety and tolerability of frovatriptan in the acute treatment of migraine and prevention of menstrual migraine: results of

a new analysis of data from five previously published studies Gend Med 2010; 7:88

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Treatment Guidelines from The Medical Letter • Vol 11 ( Issue 136) • December 2013

112

Drugs for Migraine

22 V Limmroth and MC Michel The prevention of migraine: a critical

review with special emphasis on beta-adrenoceptor blockers Br J

Clin Pharmacol 2001; 52:237

23 V Shaygannejad et al Comparison of the effect of topiramate and

sodium valporate in migraine prevention: a randomized blinded

crossover study Headache 2006; 46:642

24 HC Diener et al Topiramate in migraine prophylaxis–results from a

placebo-controlled trial with propranolol as an active control J

Neurol 2004; 251:943

25 F Ashtari et al A double-blind, randomized trial of low-dose topiramate

vs propranolol in migraine prophylaxis Acta Neurol Scand 2008;

118:301

26 S Silberstein et al Topiramate treatment of chronic migraine: a

ran-domized, placebo-controlled trial of quality of life and other efficacy

measures Headache 2009; 49:1153

27 HC Diener et al Topiramate reduces headache days in chronic

migraine: a randomized, double-blind, placebo-controlled study

Cephalalgia 2007; 27:814

28 M Linde et al Gabapentin or pregabalin for the prophylaxis of

episod-ic migraine in adults Cochrane Database Syst Rev 2013;

6:CD010609

29 DW Dodick et al Topiramate versus amitriptyline in migraine

pre-vention: a 26-week, multicenter, randomized, blind,

double-dummy, parallel-group noninferiority trial in adult migraineurs Clin

Ther 2009; 31:542

30 S Tarlaci Escitalopram and venlafaxine for the prophylaxis of

migraine headache without mood disorders Clin Neuropharmacol

2009; 32:254

31 Botulinum toxin for chronic migraine Med Lett Drugs Ther 2011;

53:7

32 BJ Gales et al Angiotensin-converting enzyme inhibitors and

angiotensin receptor blockers for the prevention of migraines Ann

Pharmacother 2010; 44:360

33 S Holland et al Evidence-based guideline update: NSAIDs and other

complementary treatments for episodic migraine prevention in adults:

report of the Quality Standards Subcommittee of the American

Academy of Neurology and the American Headache Society

Neurology 2012; 78:1346

34 RB Lipton et al Petasites hybridus root (butterbur) is an effective

pre-ventive treatment for migraine Neurology 2004; 63:2240

35 J Schoenen et al Effectiveness of high-dose riboflavin in migraine

prophylaxis A randomized controlled trial Neurology 1998; 50:466

36 A Peikert et al Prophylaxis of migraine with oral magnesium: results

from a prospective, multi-center, placebo-controlled and double-blind

randomized study Cephalalgia 1996; 16:257

37 PS Sándor et al Efficacy of coenzyme Q10 in migraine prophylaxis:

a randomized controlled trial Neurology 2005; 64:713

38 HC Diener et al Efficacy and safety of 6.25 mg t.i.d feverfew

CO2-extract (MIG-99) in migraine prevention–a randomized,

double-blind, multicentre, placebo-controlled study Cephalalgia 2005;

25:1031

39 ML Hilaire et al Treatment of migraine headaches with sumatriptan

in pregnancy Ann Pharmacother 2004; 38:1726

40 K Nezvalová-Henriksen et al Triptan safety during pregnancy: a

Norwegian population registry study Eur J Epidemiol 2013; 28:759

41 In brief: warning against use of valproate for migraine prevention

dur-ing pregnancy Med Lett Drugs Ther 2013; 55:45

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Copyright 2013 ISSN 1541-2792

Treatment Guidelines

from The Medical Letter®

EDITOR IN CHIEF: Mark Abramowicz, M.D.

EXECUTIVE EDITOR: Gianna Zuccotti, M.D., M.P.H., F.A.C.P., Harvard Medical

School

EDITOR: Jean-Marie Pflomm, Pharm.D.

ASSISTANT EDITORS, DRUG INFORMATION: Susan M Daron, Pharm.D., Corinne Z Morrison, Pharm.D., Michael P Viscusi, Pharm.D.

CONSULTING EDITORS: Brinda M Shah, Pharm.D., F Peter Swanson, M.D CONTRIBUTING EDITORS:

Carl W Bazil, M.D., Ph.D., Columbia University College of Physicians and Surgeons Vanessa K Dalton, M.D., M.P.H., University of Michigan Medical School Eric J Epstein, M.D., Albert Einstein College of Medicine

Jane P Gagliardi, M.D., M.H.S., F.A.C.P., Duke University School of Medicine Jules Hirsch, M.D., Rockefeller University

David N Juurlink, BPhm, M.D., PhD, Sunnybrook Health Sciences Centre Richard B Kim, M.D., University of Western Ontario

Hans Meinertz, M.D., University Hospital, Copenhagen Sandip K Mukherjee, M.D., F.A.C.C., Yale School of Medicine Dan M Roden, M.D., Vanderbilt University School of Medicine Esperance A K Schaefer, M.D., M.P.H., Harvard Medical School

F Estelle R Simons, M.D., University of Manitoba Neal H Steigbigel, M.D., New York University School of Medicine Arthur M.F Yee, M.D., Ph.D., F.A.C.R, Weill Medical College of Cornell University SENIOR ASSOCIATE EDITOR: Amy Faucard

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Founded in 1959 by Arthur Kallet and Harold Aaron, M.D.

Correction: Drugs for Epilepsy (Treat Guidel Med

Lett 2013; 11:9)

The dosage of topiramate in Table 2 on page 11 has been

changed from 200-400 mg/day in 2 doses to 100-400 mg/day

in 2 doses The dosage recommendation in the labeling for

monotherapy is 400 mg per day, but Medical Letter consultants

have pointed out that in clinical practice, the usual dose of

top-iramate for monotherapy is 100-200 mg per day Higher doses

may be needed for adjunctive use

Coming Soon in Treatment Guidelines:

Drugs for Lipids – January 2014 Drugs for HIV Infection – February 2014

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1 Explain the current approach to the management of migraine.

2 Discuss the pharmacologic options available for treatment and prevention of migraine and compare them based on their efficacy, dosage and administration, potential adverse effects and drug interactions.

3 Determine the most appropriate therapy given the clinical presentation of an individual patient.

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Treatment Guidelines from The Medical Letter • Vol 11 ( Issue 136) • December 2013

1 Which of the following is least likely to cause medication overuse

headache in patients with migraine?

a a triptan

b acetaminophen

c an opioid

d an NSAID

2 The drug of choice for treatment of moderate-to-severe migraine

is:

a butalbital

b an NSAID

c a triptan

d an ergot

3 Subcutaneous injection of sumatriptan produces relief within 2

hours in about what percentage of patients with

moderate-to-severe migraine?

a 40%

b 60%

c 80%

d 100%

4 A 42-year old woman with episodic migraine has been taking oral

sumatriptan to treat her attacks, but often vomits after taking it

You could tell her that:

a sumatriptan nasal spray is about equally effective

b vomiting does not reduce the effectiveness of the oral drug

c oral sumatriptan has a faster onset of action than the nasal

spray

d all of the above

5 The sumatriptan formulation with the fastest onset of action is the:

a oral tablet

b transdermal patch

c nasal spray

d SC injection

6 The rate of recurrence of migraine within 24 hours after treatment

with a triptan is about:

a <10%

b 20-40%

c 50%

d 60-80%

7 The most worrisome adverse effects of triptans are:

a dermatologic

b renal

c cardiovascular

d gastrointestinal

8 Dihydroergotamine:

a is a weaker vasoconstrictor than ergotamine

b may be effective in patients who do not respond to triptans

c causes fewer adverse effects than ergotamine

d all of the above

9 A 26-year-old woman with mild-to-moderate migraine, which she usually treats with Fiorinal, has recently experienced a sharp increase in headache frequency, which has not responded to an increase in her intake of Fiorinal The most likely diagnosis is:

a glioblastoma

b medication overuse headache

c a hypertensive crisis

d fungal meningitis

10 The only beta-blockers approved by the FDA for prevention of migraine are:

a propranolol and timolol

b timolol and metoprolol

c metoprolol and nadolol

d nadolol and atenolol

11 Topiramate:

a has been effective in reducing migraine frequency

b has improved symptoms in patients with chronic migraine

c can cause cognitive impairment

d all of the above

12 Pericranial injections of onabotulinumtoxinA:

a can be used to treat migraine attacks

b are recommended for prevention of episodic migraine

c may be marginally effective for prevention of headaches in chronic migraine

d all of the above

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Issue 136 Questions

ACPE UPN: 0379-0000-13-136-H01-P; Release: November 2013, Expire: November 2014

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