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MANAGEMENT OF FIBROMYALGIC SYNDROME

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Title: MANAGEMENT OF FIBROMYALGIC SYNDROME


1
MANAGEMENT OF FIBROMYALGIC SYNDROME
Prof. A.V. SRINIVASAN Emeritus Professor The
Tamil Nadu Dr. MGR Medical University RAILWAY
HOSPITAL
30th July 2010
2
Prevalence
  • Familial
  • Young, healthy women FgtM 31
  • 17 18.2 of adult females
  • 6 6.5 adult males
  • 2-3rd decade onset can occur sooner
  • Peaks ages 22-55.
  • ½ migraine sufferers not diagnosed.
  • 94 pts seen in primary care settings for HA
    have migraines

3
  • Common misdiagnoses for migraine
  • Sinus HA
  • Stress HA
  • Referral to ENT for sinus disease and facial pain.

4
  • Migraineurs more likely to have motion sickness.
  • Half of Menieres patients claim to have
    migrainous symptoms.
  • BPPV

5
  • 13 billion/year in lost productivity
  • 1/3 participants in American Migraine Study II
    missed work in prior 3 months

6
Migraine Definition
  • IHS Diagnostic criteria migraine w/o aura
  • HA lasting for 4-72 hrs
  • HA w/2 of following
  • Unilateral
  • Pulsating
  • Mod/severe intensity.
  • Aggravated by routine physical activity.
  • During HA at least 1 of following
  • N/V
  • Photophobia
  • Phonophobia
  • IHS criteria Migraine/aura (3 out of 4)
  • One or more fully reversible aura symptoms
    indicates focal cerebral cortical or brainstem
    dysfunction.
  • At least one aura symptom develops gradually over
    more than 4 minutes.
  • No aura symptom lasts more than one hour.
  • HA follows aura w/free interval of less than one
    hour and may begin before or w/aura.
  • History, PE, Neuro exam show no other organic
    disease.
  • At least five attacks occur

7
Migraine Subtypes
  • Basilar type migraine
  • Dysarthria, vertigo, diplopia, tinnitus,
    decreased hearing, ataxia, bilateral
    paresthesias, altered consciousness.
  • Simultaneous bilateral visual symptoms.
  • No muscular weakness.
  • Retinal or ocular migraine
  • Repeated monocular scotomata or blindness lt 1 hr
  • Associated with or followed by a HA

8
Migraine Subtypes
  • Menstrual migraine
  • Hemiplegic migraine
  • Unilateral motor and sensory symptoms that may
    persist after the headache.
  • Complete recover
  • Familial hemiplegic migraine

9
Migrainous vertigo
  • Vertigo sole or prevailing symptom.
  • Benign paroxysmal vertigo of childhood.
  • Prevalence 7-9 of pts in referral dizzy and
    migraine clinics.
  • Not recognized by the IHS
  • Diagnosis (proposed criteria)
  • Recurrent episodic vestibular symptoms of at
    least moderate severity.
  • One of the following
  • Current of previous history of IHS migraine.
  • Migrainous symptoms during two or more attacks of
    vertigo.
  • Migraine-precipitants before vertigo in more than
    50 of attacks.
  • Response to migraine medications in more than 50
    of attacks

10
Migraine mechanism
  • Neurovascular theory.
  • Abnormal brainstem responses.
  • Trigemino-vascular system.
  • Calcitonin gene related peptide
  • Neurokinin A
  • Substance P
  • Extracranial arterial vasodilation.
  • Temporal
  • Pulsing pain.
  • Extracranial neurogenic inflammation.
  • Decreased inhibition of central pain
    transmission.
  • Endogenous opioids.

11
  • Important role in migraine pathogenesis.
  • Mechanism of action in migraines not well
    established.
  • Main target of pharmacotherapy.

12
Aura Mechanism
  • Cortical spreading depression
  • Self propagating wave of neuronal and glial
    depolarization across the cortex
  • Activates trigeminal afferents
  • Causes inflammation of pain sensitive meninges
    that generates HA through central/peripheral
    reflexes.
  • Alters blood-brain barrier.
  • Associated with a low flow state in the dural
    sinuses.

13
  • Auras
  • Vision most common neurologic symptom
  • Paresthesia of lips, lower face and fingers 2nd
    most common
  • Typical aura
  • Flickering uncolored zigzag line in center and
    then periphery
  • Motor hand and arm on one side
  • Auras (visual, sensory, aphasia) 1 hr
  • Prodrome
  • Lasts hours to days

14
Clinical manifestations
  • Clinical manifestations
  • Lateralized in severe attacks 60-70
  • Bifrontal/global HA 30
  • Gradual onset with crescendo pattern.
  • Limits activity due to its intensity.
  • Worsened by rapid head motion, sneezing,
    straining, constant motion or exertion.
  • Focal facial pain, cutaneous allodynia, GI
    dysfunction, facial flushing, lacrimation,
    rhinorrhea, nasal congestion and vertigo

15
Precipitating factors
  • stress
  • head and neck infection
  • head trauma/surgery
  • aged cheese
  • dairy
  • red wine
  • nuts
  • shellfish
  • caffeine withdrawal
  • vasodilators
  • perfumes/strong odors
  • irregular diet/sleep
  • light

16
Treatment
  • Abortive
  • Stepped
  • Stratified
  • Staged
  • Preventive

17
Abortive Therapy
  • Reduces headache recurrence.
  • Alleviation of symptoms.
  • Analgesics
  • Tylenol, opioids
  • Antiphlogistics
  • NSAIDs
  • Vasoconstrictors
  • Caffeine
  • Sympathomimetics
  • Serotoninergics
  • Selective - triptans
  • Nonselective ergots
  • Metoclopramide

18
Abortive care strategies
  • Stepped
  • Start with lower level drugs, then switch to more
    specific drugs if symptoms persist or worsen.
  • Analgesics Tylenol, NSAIDs
  • Vasoconstrictors sympathomimetics
  • Opioids (try to avoid) - Butorphanol
  • Triptans sumatriptan (oral, SQ, nasal),
    naratriptan, rizatripatan, zomatriptan.
  • Limited by patient compliance.
  • Stratified
  • Adjusts treatment according to symptom intensity.
  • Mild analgesics, NSAIDs
  • Moderate analgesic plus caffeine/sympathomimetic
  • Severe opioids, triptans, ergots
  • Severe sx treatment limited due to concomitant GI
    sxs.
  • Staged
  • Bases treatment on intensity and time of attacks.
  • HA diary reviewed with patient.
  • Medication plan and backup plans.

19
Preventive therapy
  • Consider if pt has more than 3-4 episodes/month.
  • Reduces frequency by 40 60.
  • Breakthrough headaches easier to abort.
  • Beta blockers
  • Amitriptyline
  • Calcium channel blockers
  • Lifestyle modification.
  • Biofeedback.

20
Botox
  • 51 migraineurs treated had complete prophylaxis
    for 4.1 months.
  • 38 had prophylaxis for 2.7 months.
  • Randomized trial showed significant improvement
    in headache frequency with multiple treatments.

21
Conclusions
  • Migraine is common but unrecognized.
  • Keep migraine and its variants in the
    differential diagnosis.

22
Dedicated to my family for making everything
worthwhile
23
(No Transcript)
24
READ not to contradict or confute Nor to Believe
and Take for Granted but TO WEIGH AND CONSIDER
THANK YOU

25
References
  1. Landy, S. Migraine throughout the Life Cycle
    Treatment through the Ages. Neurology. 2004 62
    (5) Supplement 2 S2-S8.
  2. Bailey, BJ. Head and Neck Surgery
    Otolaryngology 3rd Edition. 2001. Pgs. 221-235.
  3. Bajwa, ZH, Sabahat, A. Pathophysiology, Clinical
    Manifestations, and Diagnosis of Migraine in
    Adults. Up To Date online. 2005.
  4. Lipton, RB, Stewart, WF, Liberman, JN.
    Self-awareness of migraine Interpreting the
    labels that headache sufferers apply to their
    headaches. Neurology. 2002 58(9) Supplement 6
    S21-S26.
  5. Cady, RK, Schreiber, CP. Sinus headache or
    migraine? Considerations in making a
    differential diagnosis. Neurology. 2002 58 (9)
    Supplement 6 S10-S14.
  6. Perry, BF, Login, IS, Kountakis, SE.
    Nonrhinologic headache in a tertiary rhinology
    practice. Otolaryngology Head and Neck Surg
    2004 130 449-452.
  7. Daudia, AT, Jones, NS. Facial migraine in a
    rhinological setting. Clinical Otolaryngology
    and Allied Sciences. 2002 27(6) 521-525.
  8. Spierings, EL. Migraine mechanism and
    management. Otolarynogol Clin N Am 36 (2003)
    1063 1078.
  9. Avnon, y, Nitzan, M, Sprecher, E, Rogowski, Z,
    and Yarnitsky, D. Different patterns of
    parasympathetic activation in uni- and bilateral
    migraineurs. Brain. 2003 126 1660-1670.
  10. Stroud, RH, Bailey, BJ, Quinn, FB. Headache and
    Facial Pain. Dr. Quinns Online Textbook of
    Otolaryngology Grand Rounds Archive. 2001.
    http//www.utmb.edu/otoref/Grnds/HA-facial-pain-20
    01-0131/HA-facial-pain-2001.doc
  11. Ondo, WG, Vuong KD, Derman, HS. Botulinum toxin
    A for chronic daily headache a randomized,
    placebo-controlled, parallel design study.
    Cephalalgia 2004 (24) 60-65.
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