Headache School provides education to help patients better manage migraine. Migraine is a very common neurological disorder that affects over 30 million Americans. Formal educational programs have been shown to produce better outcomes for patients with headache. The classes cover topics like different medication options, how diet can impact headaches, and headaches in women. Understanding the science behind migraine can help patients identify triggers to prevent attacks and choose effective treatment options.

1. Headache School
2013
Norton Headache and Concussion Center

2. Why Headache School?
• Headache is one of the most common reasons
for patients to seek medical attention
• Of patients seeking medical attention for
headache, the majority will be diagnosed with
migraine
• Migraine affects approximately 12% of the
population

3. Why Headache School?
• Formal educational programs have been
shown to produce better outcomes for
patients with headache
• Opportunity for patients to interact with
physicians and other patients in an informal
setting

4. What Can You Do?
• Come to classes
• Bring a friend, spouse, etc.
• Come with questions
• Share your story
– Interact with those around you
– Migraine is a lot more common than you think
– You are NOT the only one

5. Upcoming Classes
• Medication Maze
– April 11
• How Diet Affects Headaches
– May 16
• Women and Headaches
– June 13

6. What Is Migraine?

7. A Common Problem
• 45 million Americans with headache disorders
• 30 million Americans with migraine, the most
common disabling form of headache
• 12% of the US population has migraine
• 18% of women, 6% of men are affected by
migraine

8. One Year Prevalence of Migraine
Lipton R B et al. Neurology 2007;68:343-349

9. Migraine is more common than
diabetes and asthma combined!
Migraine 13%
Osteoarthritis 7%
Diabetes 6%
Asthma 7%
Rheumatoid
1%
Arthritis
0% 5% 10% 15% 20%

10. Commonly Mis- / Un-Diagnosed
Diagnosed Migraine 48%
39%
Undiagnosed
61% Migraine
52%
1999
1989 Lipton et al., 2001
American Migraine Study II

11. A Costly Problem
• Chronic headache disorders are among the
top 20 causes of disability in the US according
to the World Health Organization (WHO)
• 4% of Americans experience 4 hours of
headaches per day, at least 15 days per month
• Headache disorders are responsible for more
than $31B in economic costs in the US
annually

12. Diagnosis of Migraine Without Aura
• No single feature required or sufficient for diagnosis
• Characteristics (2/4)
– Unilateral (40% bilateral or generalized)
– Throbbing (50% non-pulsating)
– Moderate-severe intensity (~20% mild)
– Pain worsened by exertion (>95%)
• Associated symptoms (1/2)
– Nausea (86% – 95%) or vomiting (47% – 62%)
– Photophobia (82% – 95%), phonophobia (61% – 98%)
Russell MB et al. Cephalalgia. 1996.
Pryse-Phillips WEM et al. Can Med Assoc J. 1997.

13. Additional Features of Migraine
• Predictable timing around menstruation and
ovulation
• Stereotyped prodromal symptoms
• Characteristic triggers
• Improves with sleep (more effective in young pts)
• Positive family history
• Childhood precursors (cyclic vomiting, abdominal
“migraine”, episodic vertigo, probably motion
sickness)
• Osmophobia (smell sensitivity)

14. “I have sinus headaches”
Patients self diagnosing “sinus headaches”
86% Migraine
3% Sinus related headache
Eross E, Dodick D, Eross M. The sinus, allergy and migraine study (SAMS)

15. What Causes Migraine?
• The Vascular Theory
• Blood vessels constricting (aura)
Followed by
• Blood vessels dilating

16. The Vascular Theory
• Does not explain prodrome
• Not supported by blood flow studies
• There are effective nonvascular drugs, such as
NSAIDs
• Most patients do not have aura
• THIS IS NOT CORRECT

17. The Neurovascular Theory
• Referred pain from dura mater and blood
vessels
• Peripheral Neural Processing
• Central Neural Processing

18. Pain Perceiving Structures Inside the Skull
The most important structures that register pain in the head are the large cranial vessels,
proximal cerebral vessels and dural arteries and the large veins and venous sinuses

19. A More Sensitive Brain
Pain control mechanisms are partially defective in migraine patients

20. People with migraine process visual and auditory stimulation differently that people
without migraine. In this example with repeated stimulation non-migraine patients
have decreased response with repeated stimulation whereas migraine patients have
an increased response.
Wang, Schoenen. Cephalalgia. 1998.

21. Migraine Triggers
• Most frequently reported triggers
– Stress
– Menstruation
– Changes in sleep
– Skipping meals
– Changes in weather
– Diet (alcohol most frequent)
• Time from trigger to onset of headache can be up to
72 hours - hard to track

22. Migraine Triggers
If summation of triggers are greater than threshold – a headache happens

23. Migraine Aura

25. Migraine Aura
• A reversible focal neurological deficit
– Most commonly visual
• Cortical spreading depression
– Think a wave of activity moving across the brain
followed by decreased activity
– The part of the brain inactivated causes the
neurological deficit
• Occipital lobes = vision

26. Spreading Depression of Leão
EEG activity is suppressed and moves in a wave, correlates with symptoms

27. Aura is from brain cells (neurons)

28. The Pain

30. Neuropeptides
• Cranial levels of both substance P and
calcitonin gene-related peptide (CGRP) are
increased by stimulation of the trigeminal
ganglion in humans
• In migraine CGRP is elevated in external
jugular vein blood, whereas substance P is not
• CGRP infusions can trigger headache and
migraine

31. A Growing Snowball
• Trigeminal nerve and its blood supply
(neurovascular)
– Release of neuropeptides
• CGRP
• Substance P
• 5-HT (serotonin) --> “triptans”
• Nitric oxide
– Vasodilatation (CGRP) leads to further activation, and the
process spreads
– Brainstem, thalamus, cortex become activated leading to
“central sensitization”
• Amplified pain signaling in the central nervous system
– Allodynia: pain due to a non-noxious stimulant

32. Cutaneous Allodynia
Migraineurs develop increased
sensitivity to stimuli as a result of
increased nerve excitability
80% of migraine patients had
cutaneous allodynia during attacks
Non painful stimuli perceived as
painful
After allodynia occurs, triptans lose
effectiveness

33. 1-Peripheral
Trigeminal Sensitization 3-Forehead Allodynia
2-Central Trigeminal
Sensitization 4-Extracephalic
Allodynia
Burstein R, et al. Brain. 2000.

34. Importance of treating early
No Allodynia Allodynia
Pain free @2hrs 28 (93%) 5 (15%)
Not pain free @2hrs 2 (7%) 29 (85%)
30 34
R Burstein, 2003

35. Allodynia is a risk factor for
developing chronic migraine

36. Earliest Possible Treatment to Stop
Migraine Progression and Chronification
Inherited Medication
threshold for overuse
trigeminal
activation
Chronic
Ineffective migraine
pain
control
Triggers or
stressors
Increased
headache
Episodic frequency
migraine
Graphic adapted from: Calhoun AH. In: Headache Newsletter: American Headache Society
Committee for Headache Education; Veteran’s Day, 2010.

37. Medication Overuse Headache
• Headache present on ≥15 days/month
• Regular overuse for ≥3 months of one or more drugs
that can be taken for acute and/or symptomatic
treatment of headache
• Headache has developed or markedly worsened
during medication overuse
• Headache resolves or reverts to its previous pattern
within 2 months after discontinuation of overused
medication

38. Chronification of Migraine
Medication Overuse Headache
The Cleveland Clinic Manual of Headache Therapy p. 156
Bigal ME, et al. Headache. 2008;48:1157-1168.
Bigal ME, et al. Pain. 2009;142:179-182.

39. Medication Overuse Headache
• Simple analgesics: • Opiates:
• Acetaminophen (Tylenol) – Lortab (hydrocodone)
• Ibuprofen (Advil, Motrin)
– Percocet (oxycodone)
• Aspirin (Bayer)
• Naproxen (Aleve)
– Many others
• Combination products: • Triptans:
• Fioricet – Imitrex, Maxalt, Relpax,
• Excedrin Zomig, Frova, Amerge,
Axert, Treximet
• DHE

40. Why opiates are bad

41. Other Associated Symptoms

42. Nausea
• Gastroparesis occurs frequently,
both during and outside of acute
migraine attacks1-3
– May correlate with intensity of
headache, nausea, and photophobia4
• Absorption of orally administered
drugs used to treat migraine may be
delayed by gastroparesis,
postponing the drug’s onset of action1,5-7
1. Krymchantowski AV, et al. Cephalalgia. 2006;26(7):871-874; 2. Aurora SK, et al. Headache. 2006;46(1):57-63; 3.
Aurora S, et al. Headache. 2007;47(10):1443-1446; 4. Boyle R, et al. Br J Clin Pharmacol. 1990;30(3):405-409; 5.
Thomsen LL, et al. Cephalalgia. 1996;16(4):270-275; 6. Volans GN. Br J Clin Pharmacol. 1975;2(1):57-63; 7. Tokola
RA and Neuvonen PJ. Br J Clin Pharmacol. 1984;18(6):867-871; 8. Tfelt-Hansen P. Headache. 2007;47(6):929-930; 9.
Dahlöf C. Curr Opin Neurol. 2002;15:317-322; 10. Lychkova AE. Bull Exp Biol Med. 2004;138(2):127-130.

43. Other Associated Symptoms
• Blurry vision (29%)
• Neck pain (31%)
• Nasal congestion (28%)
• Sweating (30%)
• Dizziness (16%)

44. Why is it important to understand
the science of migraine?
• Treatment
– Prevention of triggers
– Preventative medications
– Rescue medications

45. Triggers
• We now understand that patients with
migraine have an “excitable” brain
– Need to be careful with:
• Sleep
• Diet
• Medication overuse
• Stress management

46. Preventative Medications
• Antiseizure drugs
– Topamax
– Depakote
• Antidepressants
– Amitriptyline (Elavil)
– Effexor
• Blood pressure medications
– Propranolol (Inderal)
– Verapamil

47. Rescue Medications
• Triptans
• NSAIDs
• DHE

48. Triptans
Selective agonists (activators) of serotonin
blocking the release of other inflammatory
chemicals during a migraine attack
Triptans work here

49. Triptans
• Prevent release of neuropeptides
• Once enough activation has occurred the
process of central sensitization begins
– Manifested by allodynia
– Remember 15% vs. 93% chance of success

50. NSAIDs
• Ketorolac infusion has been shown to reverse
central sensitization
• IV ketorolac is not practical in the outpatient
setting
• Further discussed next month

51. DHE
• Can also reverse central sensitization
• More side effects
• A little less convenient to give in the home
setting
• Will be discussed further next month

52. Summary
• Hyperexcitable brain: more susceptible to
triggers
• Aura: spreading excitation and depression
• Throbbing head pain: trigeminal inflammation
• Allodynia: common, important and due to
central sensitization

53. Future Classes
• Medication Maze
– April 11
• How Diet Affects Headaches
– May 16
• Women and Headaches
– June 13

54. Questions?
Thanks
NortonHealthcare.com/HeadacheandConcussion