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Headache
Dr. Avatar Verma
KISTMCTH
076/03/06
• Headache is among the most common reasons to seek medical attention, and
responsible for more disability than any other neurologic problem
• Common and causes considerable worry, but rarely represents sinister disease
• Causes may be Primary (benign) or Secondary, and most have primary
syndromes
• Tempo of evolution is critical; Sudden-onset headache, maximal immediately,
is always a ‘red flag’ and prompt rapid assessment for possible subarachnoid
hemorrhage or other sinister causes, even only 10–25% serious pathology
• Evolves over hours to days is much less likely to be sinister
• The tempo of evolution of headache is critical; sudden-onset headache,
maximal immediately, is always a ‘red flag’ (Box 26.11) and should
prompt rapid assessment in hospital for possible subarachnoid
hemorrhage or other sinister causes, even though only 10–25% of
patients harbor serious pathology
• Clues to other possible causes (e.g. rash in meningitis) should be sought
(p. 1201)
• Headache that evolves over hours to days is much less likely to be
sinister
• Establish whether the headache comes and goes, with periods of no
headache in between (usually migraine), or present almost all the time
• Associated symptoms, such as preceding visual symptoms,
nausea/vomiting or photophobia/ phonophobia, support a diagnosis of
migraine, but progressive focal symptoms or constitutional upset like
weight loss or fever, may suggest a more sinister cause (e.g. cancer or
meningitis)
• Migraine patients typically retire to bed to sleep in a dark room, whereas
cluster headache often agitated and restless
• Headaches present for months or years are almost never sinister (although
paradoxically worry patients), whereas new-onset especially in elderly, more of
concern
• Over 60 years pain localised to one or both temples, temporal arteritis should be
considered, especially if temporal pulses are absent and/or arteries are enlarged and
tender
• Most outpatients will have migraine (intermittent, lasting a few hours, associated with
migrainous symptoms) or chronic daily headache syndrome (often present for months
to years, without associated symptoms and refractory to analgesia)
• Easy to recognise but patients are often worried, so elicit such concerns and explain
why sinister disease is unlikely and investigation is rarely required
• Sinusitis, ‘eye strain’, food allergies and uncomplicated hypertension are never the
explanation for persistent headache
CLINICAL EVALUATION OF ACUTE, NEW-
ONSET HEADACHE
• New, severe headache has a differential diagnosis that is quite different from
recurrent headaches over many years
• Have probability of finding a potentially serious cause is considerably greater
• Require prompt evaluation and appropriate treatment
• Serious causes include meningitis, subarachnoid hemorrhage, epidural or
subdural hematoma, glaucoma, tumor, and purulent sinusitis
• Careful neurologic examination is an essential first step
• Patients with an abnormal examination or a history of recent-onset headache
should be evaluated by a computed tomography (CT) or magnetic resonance
imaging (MRI) study of the brain
• As an initial screening procedure CT and MRI methods appear to be equally
sensitive
• In some LP is also required, unless a benign etiology can be otherwise
established.
• Evaluation include cranial arteries by palpation; cervical spine by the
effect of passive movement of the head and by imaging;
• Investigation of cardiovascular and renal status by blood pressure
monitoring and urine examination;
• Eyes by funduscopy, intraocular pressure measurement, and refraction
• Psychological state should also be evaluated because a relationship exists between head
pain, depression, and anxiety
• To identify comorbidity rather than explanation for the headache, because troublesome
headache is seldom simply caused by mood change
• Medicines with antidepressant actions are also effective in the preventive treatment of
both tension-type headache and migraine, each symptom must be treated optimally
• Recurrent headache disorders may be activated by pain that follows otologic or
endodontic surgical procedures
• Treatment of the headache is largely ineffective until the cause of the primary problem
is addressed
• Brain tumor is a rare cause of headache and even less commonly a cause of severe pain
Tension-type headache
• Most common type and is experienced to some degree by the majority
of the population
• Pathophysiology
• Incompletely understood
• Emotions and anxiety are common precipitants and sometimes
associated depressive illness
• Anxiety about the headache itself may lead to continuation
• Patients often become convinced of a serious underlying condition
• Muscular spasms may worsen this in some patients
Clinical features
• Characterized as ‘dull’, ‘tight’ or like a ‘pressure’, and there may be
sensation of a band round the head or pressure at the vertex
• Constant and generalised, but often radiates forwards from the
occipital region
• Pain can remain unabated for weeks or months without interruption,
although the severity may vary, and there is no associated vomiting or
photophobia
• Activities are usually continued and pain may be less noticeable when the
patient is occupied
• Less severe in the early part of the day, becoming more troublesome as the
day goes on
• Tenderness may be present over skull vault or in occiput but easily
distinguished from the triggered pains of trigeminal neuralgia and the
exquisite tenderness of temporal arteritis
• Analgesics may be taken with chronic regularity despite little effect, and may
serve to perpetuate the symptoms
Management
• Provide careful assessment, followed by discussion of likely precipitants
and reassurance that the prognosis is good
• Excessive use of analgesia, particularly containing codeine, may maintain
and exacerbate the headache
• Physiotherapy (with muscle relaxation and stress management) may help and
low-dose amitriptyline can provide benefit
• Evidence that patients benefit from a perception that their problem has been
taken seriously and rigorously assessed
• Investigation contribute to such reassurance, especially if concerns about
underlying lesion are strong, but should understand the purpose and likely
outcome of such imaging
Migraine
• Usually appears before middle age; affects about 20% of females and
6% of males at some point in life
• Some assume that migraine is a term encompassing any severe
headache but has a characteristic presentation
Pathophysiology
• Cause is unknown but increasing evidence that aura is due to dysfunction of
ion channels causing a spreading front of cortical depolarisation (excitation)
followed by hyperpolarization (depression of activity)
• Spreads over the cortex at a rate of about 3 mm/minute, corresponding to the
aura’s symptomatic spread
• The headache phase is associated with vasodilatation of extracranial vessels
and may be relayed by hypothalamic activity
• Activation of the trigemino vascular system is probably important
• Genetic contribution is implied by frequently positive family history, and
similar phenomena occurring in disorders such as CADASIL
• Female preponderance and the frequency of attacks at certain points in
menstrual cycle also suggest hormonal influences
• Oestrogen-containing oral contraception sometimes exacerbates migraine, and
increases the small risk of stroke in patients who suffer from migraine with
aura
• When psychological factors contribute, attack often occurs after a period of
stress, being more likely on Friday evening at the end of the working week or
at the beginning of a holiday
Clinical features
• Some report a prodrome of malaise, irritability or behavioural change for some hours or days
• Around 20% experience an aura, and are said to have migraine with aura (previously known
as classical migraine)
• Aura is most often visual, consisting of fortification spectra, which are shimmering, silvery
zigzag lines that march across the visual fields for up to 40 minutes, sometimes leaving a trail
of temporary visual field loss (scotoma)
• In some sensory aura of tingling followed by numbness, spreading over 20–30 minutes, from
one part of the body to another
• Dominant hemisphere involvement may cause transient speech disturbance
• 80% with characteristic headache but no ‘aura’ are said to have migraine without aura
• Usually severe and throbbing, with photophobia, phonophobia and vomiting
lasting from 4 to 72 hours
• Movement makes the pain worse, and patients prefer to lie in a quiet, dark room
• Caution should be taken when limb weakness or isolated aura without headache
to migraine
• In such cases, structural disorders of the brain, or even focal epilepsy, considered
• In some aura do not resolve, leaving more permanent neurological disturbance
• This persistent migrainous aura may occur with or without evidence of brain
infarction
Management
• Avoidance of identified triggers or exacerbating factors (chocolate, cheese,
redwine, combined contraceptive pill) may prevent attacks
• Treatment of acute attack consists of simple analgesia with aspirin, paracetamol or
non-steroidal anti-inflammatory agents
• Nausea may require an antiemetic such as metoclopramide or domperidone
• Severe attacks can be aborted by one of the increasing number of ‘triptans’ (e.g.
sumatriptan), which are potent 5-hydroxytryptamine (5-HT) agonists
• These can be administered orally, by subcutaneous injection or by nasal spray
• Avoid accelerating use
• Overuse of analgesia, including triptans, contribute to medication
overuse headache
• If frequent (more than 3–4 per month), prophylaxis considered
• Vasoactive drugs (calcium channel blockers and β-adrenoceptor
antagonists (β-blockers)), antidepressants (amitriptyline, dosulepin) and
anti-epileptic drugs (valproate, topiramate)
• Women with aura should avoid oestrogen treatment for either oral
contraception or hormone replacement, although the increased risk of
ischaemic stroke is minimal
Medication overuse headache
• With increasing availability of over-the-counter medication, headache
syndromes perpetuated by analgesia intake are becoming common
• Can complicate any other headache syndrome, especially associated
with migraine and tension headache
• Most common culprits are compound analgesia (particularly codeine
and other opiate-containing preparations) and triptans, and MOH is
usually associated with use on more than 10–15 days per month
Management
• Withdrawal of responsible analgesics
• Migraine prophylactics may be helpful in reducing the rebound
headaches
• In severe cases, hospital admission with or without a course of
corticosteroids may be helpful
Cluster headache
• Cluster headaches (also known as migrainous neuralgia) are much less
common than migraine
• 5 : 1 male predominance and onset is usually in the third decade
Pathophysiology
• Cause unknown, but differs from migraine in its character, lack of
genetic predisposition, lack of provoking dietary factors, opposing
gender imbalance and different drug effect
• Functional imaging studies have suggested abnormal hypothalamic
activity
• Patients are more often smokers with a higher than average alcohol
consumption
Clinical features
• Cluster headache is strikingly periodic, featuring runs of identical
headaches beginning at the same hour for weeks at a time (the
eponymous ‘cluster’)
• Patients may experience either one or several attacks within a 24-hour
period
• Severe, unilateral periorbital pain with autonomic features, such as
unilateral lacrimation, nasal congestion and conjunctival injection
(occasionally with the other features of Horner’s syndrome)
• Severe, is characteristically brief (30–90 minutes)
• Patients are often highly agitated during the headache phase
• Cluster period is typically a few weeks, followed by remission for
months to years, but a small proportion do not experience remission
Management
• Acute attacks: Subcutaneous injections of sumatriptan or inhalation of
100% oxygen
• Brevity of the attack probably prevents other migraine therapies from being
effective
• Migraine prophylaxis is often ineffective too but can be prevented in some
by sodium valproate, verapamil, methysergide or short courses of oral
corticosteroids
• Severe debilitating clusters can be helped with lithium therapy, although
this requires monitoring
Headaches associated with
specific activities
• These usually affect men in their thirties and forties
• Patients develop a sudden, severe headache with exertion, including sexual
activity
• Usually no vomiting and no neck stiffness, and the headache lasts less than
10–15 minutes, though a less severe dullness may persist for some hours
• Subarachnoid haemorrhage needs to be excluded by CT and/or CSF
examination after a first event
• The pathogenesis of these headaches is unknown
• Although frightening, attacks are usually brief and patients may only
need reassurance and simple analgesia for the residual headache
• The syndrome may recur, and prevention may be necessary with
propranolol or indomethacin
Other headache syndromes
• A number of rare headache syndromes produce pains about the eye
similar to cluster headaches
• These include chronic paroxysmal hemicrania and SUNCT (short-
lasting unilateral neuralgiform headaches with conjunctival injection
and tearing)
• The recognition of these syndromes is useful since they often respond
to specific treatments such as indomethacin.
Headache
Headache

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Headache

  • 2. • Headache is among the most common reasons to seek medical attention, and responsible for more disability than any other neurologic problem • Common and causes considerable worry, but rarely represents sinister disease • Causes may be Primary (benign) or Secondary, and most have primary syndromes • Tempo of evolution is critical; Sudden-onset headache, maximal immediately, is always a ‘red flag’ and prompt rapid assessment for possible subarachnoid hemorrhage or other sinister causes, even only 10–25% serious pathology • Evolves over hours to days is much less likely to be sinister
  • 3. • The tempo of evolution of headache is critical; sudden-onset headache, maximal immediately, is always a ‘red flag’ (Box 26.11) and should prompt rapid assessment in hospital for possible subarachnoid hemorrhage or other sinister causes, even though only 10–25% of patients harbor serious pathology • Clues to other possible causes (e.g. rash in meningitis) should be sought (p. 1201) • Headache that evolves over hours to days is much less likely to be sinister
  • 4.
  • 5.
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  • 7.
  • 8. • Establish whether the headache comes and goes, with periods of no headache in between (usually migraine), or present almost all the time • Associated symptoms, such as preceding visual symptoms, nausea/vomiting or photophobia/ phonophobia, support a diagnosis of migraine, but progressive focal symptoms or constitutional upset like weight loss or fever, may suggest a more sinister cause (e.g. cancer or meningitis) • Migraine patients typically retire to bed to sleep in a dark room, whereas cluster headache often agitated and restless
  • 9. • Headaches present for months or years are almost never sinister (although paradoxically worry patients), whereas new-onset especially in elderly, more of concern • Over 60 years pain localised to one or both temples, temporal arteritis should be considered, especially if temporal pulses are absent and/or arteries are enlarged and tender • Most outpatients will have migraine (intermittent, lasting a few hours, associated with migrainous symptoms) or chronic daily headache syndrome (often present for months to years, without associated symptoms and refractory to analgesia) • Easy to recognise but patients are often worried, so elicit such concerns and explain why sinister disease is unlikely and investigation is rarely required • Sinusitis, ‘eye strain’, food allergies and uncomplicated hypertension are never the explanation for persistent headache
  • 10. CLINICAL EVALUATION OF ACUTE, NEW- ONSET HEADACHE • New, severe headache has a differential diagnosis that is quite different from recurrent headaches over many years • Have probability of finding a potentially serious cause is considerably greater • Require prompt evaluation and appropriate treatment • Serious causes include meningitis, subarachnoid hemorrhage, epidural or subdural hematoma, glaucoma, tumor, and purulent sinusitis
  • 11. • Careful neurologic examination is an essential first step • Patients with an abnormal examination or a history of recent-onset headache should be evaluated by a computed tomography (CT) or magnetic resonance imaging (MRI) study of the brain • As an initial screening procedure CT and MRI methods appear to be equally sensitive • In some LP is also required, unless a benign etiology can be otherwise established.
  • 12. • Evaluation include cranial arteries by palpation; cervical spine by the effect of passive movement of the head and by imaging; • Investigation of cardiovascular and renal status by blood pressure monitoring and urine examination; • Eyes by funduscopy, intraocular pressure measurement, and refraction
  • 13. • Psychological state should also be evaluated because a relationship exists between head pain, depression, and anxiety • To identify comorbidity rather than explanation for the headache, because troublesome headache is seldom simply caused by mood change • Medicines with antidepressant actions are also effective in the preventive treatment of both tension-type headache and migraine, each symptom must be treated optimally • Recurrent headache disorders may be activated by pain that follows otologic or endodontic surgical procedures • Treatment of the headache is largely ineffective until the cause of the primary problem is addressed • Brain tumor is a rare cause of headache and even less commonly a cause of severe pain
  • 14. Tension-type headache • Most common type and is experienced to some degree by the majority of the population • Pathophysiology • Incompletely understood • Emotions and anxiety are common precipitants and sometimes associated depressive illness • Anxiety about the headache itself may lead to continuation
  • 15. • Patients often become convinced of a serious underlying condition • Muscular spasms may worsen this in some patients
  • 16. Clinical features • Characterized as ‘dull’, ‘tight’ or like a ‘pressure’, and there may be sensation of a band round the head or pressure at the vertex • Constant and generalised, but often radiates forwards from the occipital region • Pain can remain unabated for weeks or months without interruption, although the severity may vary, and there is no associated vomiting or photophobia
  • 17. • Activities are usually continued and pain may be less noticeable when the patient is occupied • Less severe in the early part of the day, becoming more troublesome as the day goes on • Tenderness may be present over skull vault or in occiput but easily distinguished from the triggered pains of trigeminal neuralgia and the exquisite tenderness of temporal arteritis • Analgesics may be taken with chronic regularity despite little effect, and may serve to perpetuate the symptoms
  • 18. Management • Provide careful assessment, followed by discussion of likely precipitants and reassurance that the prognosis is good • Excessive use of analgesia, particularly containing codeine, may maintain and exacerbate the headache
  • 19. • Physiotherapy (with muscle relaxation and stress management) may help and low-dose amitriptyline can provide benefit • Evidence that patients benefit from a perception that their problem has been taken seriously and rigorously assessed • Investigation contribute to such reassurance, especially if concerns about underlying lesion are strong, but should understand the purpose and likely outcome of such imaging
  • 20. Migraine • Usually appears before middle age; affects about 20% of females and 6% of males at some point in life • Some assume that migraine is a term encompassing any severe headache but has a characteristic presentation
  • 21. Pathophysiology • Cause is unknown but increasing evidence that aura is due to dysfunction of ion channels causing a spreading front of cortical depolarisation (excitation) followed by hyperpolarization (depression of activity) • Spreads over the cortex at a rate of about 3 mm/minute, corresponding to the aura’s symptomatic spread • The headache phase is associated with vasodilatation of extracranial vessels and may be relayed by hypothalamic activity
  • 22. • Activation of the trigemino vascular system is probably important • Genetic contribution is implied by frequently positive family history, and similar phenomena occurring in disorders such as CADASIL • Female preponderance and the frequency of attacks at certain points in menstrual cycle also suggest hormonal influences • Oestrogen-containing oral contraception sometimes exacerbates migraine, and increases the small risk of stroke in patients who suffer from migraine with aura • When psychological factors contribute, attack often occurs after a period of stress, being more likely on Friday evening at the end of the working week or at the beginning of a holiday
  • 23. Clinical features • Some report a prodrome of malaise, irritability or behavioural change for some hours or days • Around 20% experience an aura, and are said to have migraine with aura (previously known as classical migraine) • Aura is most often visual, consisting of fortification spectra, which are shimmering, silvery zigzag lines that march across the visual fields for up to 40 minutes, sometimes leaving a trail of temporary visual field loss (scotoma) • In some sensory aura of tingling followed by numbness, spreading over 20–30 minutes, from one part of the body to another • Dominant hemisphere involvement may cause transient speech disturbance • 80% with characteristic headache but no ‘aura’ are said to have migraine without aura
  • 24. • Usually severe and throbbing, with photophobia, phonophobia and vomiting lasting from 4 to 72 hours • Movement makes the pain worse, and patients prefer to lie in a quiet, dark room • Caution should be taken when limb weakness or isolated aura without headache to migraine • In such cases, structural disorders of the brain, or even focal epilepsy, considered • In some aura do not resolve, leaving more permanent neurological disturbance • This persistent migrainous aura may occur with or without evidence of brain infarction
  • 25.
  • 26. Management • Avoidance of identified triggers or exacerbating factors (chocolate, cheese, redwine, combined contraceptive pill) may prevent attacks • Treatment of acute attack consists of simple analgesia with aspirin, paracetamol or non-steroidal anti-inflammatory agents • Nausea may require an antiemetic such as metoclopramide or domperidone • Severe attacks can be aborted by one of the increasing number of ‘triptans’ (e.g. sumatriptan), which are potent 5-hydroxytryptamine (5-HT) agonists • These can be administered orally, by subcutaneous injection or by nasal spray
  • 27. • Avoid accelerating use • Overuse of analgesia, including triptans, contribute to medication overuse headache • If frequent (more than 3–4 per month), prophylaxis considered • Vasoactive drugs (calcium channel blockers and β-adrenoceptor antagonists (β-blockers)), antidepressants (amitriptyline, dosulepin) and anti-epileptic drugs (valproate, topiramate) • Women with aura should avoid oestrogen treatment for either oral contraception or hormone replacement, although the increased risk of ischaemic stroke is minimal
  • 28. Medication overuse headache • With increasing availability of over-the-counter medication, headache syndromes perpetuated by analgesia intake are becoming common • Can complicate any other headache syndrome, especially associated with migraine and tension headache • Most common culprits are compound analgesia (particularly codeine and other opiate-containing preparations) and triptans, and MOH is usually associated with use on more than 10–15 days per month
  • 29. Management • Withdrawal of responsible analgesics • Migraine prophylactics may be helpful in reducing the rebound headaches • In severe cases, hospital admission with or without a course of corticosteroids may be helpful
  • 30. Cluster headache • Cluster headaches (also known as migrainous neuralgia) are much less common than migraine • 5 : 1 male predominance and onset is usually in the third decade
  • 31. Pathophysiology • Cause unknown, but differs from migraine in its character, lack of genetic predisposition, lack of provoking dietary factors, opposing gender imbalance and different drug effect • Functional imaging studies have suggested abnormal hypothalamic activity • Patients are more often smokers with a higher than average alcohol consumption
  • 32. Clinical features • Cluster headache is strikingly periodic, featuring runs of identical headaches beginning at the same hour for weeks at a time (the eponymous ‘cluster’) • Patients may experience either one or several attacks within a 24-hour period • Severe, unilateral periorbital pain with autonomic features, such as unilateral lacrimation, nasal congestion and conjunctival injection (occasionally with the other features of Horner’s syndrome)
  • 33. • Severe, is characteristically brief (30–90 minutes) • Patients are often highly agitated during the headache phase • Cluster period is typically a few weeks, followed by remission for months to years, but a small proportion do not experience remission
  • 34. Management • Acute attacks: Subcutaneous injections of sumatriptan or inhalation of 100% oxygen • Brevity of the attack probably prevents other migraine therapies from being effective • Migraine prophylaxis is often ineffective too but can be prevented in some by sodium valproate, verapamil, methysergide or short courses of oral corticosteroids • Severe debilitating clusters can be helped with lithium therapy, although this requires monitoring
  • 35. Headaches associated with specific activities • These usually affect men in their thirties and forties • Patients develop a sudden, severe headache with exertion, including sexual activity • Usually no vomiting and no neck stiffness, and the headache lasts less than 10–15 minutes, though a less severe dullness may persist for some hours • Subarachnoid haemorrhage needs to be excluded by CT and/or CSF examination after a first event
  • 36. • The pathogenesis of these headaches is unknown • Although frightening, attacks are usually brief and patients may only need reassurance and simple analgesia for the residual headache • The syndrome may recur, and prevention may be necessary with propranolol or indomethacin
  • 37. Other headache syndromes • A number of rare headache syndromes produce pains about the eye similar to cluster headaches • These include chronic paroxysmal hemicrania and SUNCT (short- lasting unilateral neuralgiform headaches with conjunctival injection and tearing) • The recognition of these syndromes is useful since they often respond to specific treatments such as indomethacin.