Headaches Flashcards

1
Q

features of SAH

A
S:diffuse
O: reaches maximal intensity within a minute or two 
C: constant and throbbing
R: usually to the neck
A: photophobia, nausea, neck stiffness
T: lasts at least an hour, usually for many, many hours
E: non-specific
S: 10/10!!
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2
Q

order of layers of the brain

A

brain–>pia mater–>arachnoid–>dura mater (2 layers)

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3
Q

SAH

A
85% caused by ruptured aneurysm
1/3 die immediately
1/3 present with coma, seizures or focal deficit
1/3 present with isolated headache
20-30% re-bleed within first month

only 25% of those with thunderclap headache have SAH

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4
Q

SAH investigation

A

CT head - only 95% sensitive in the first 48h

if CT negative, all require a LP (if no contraindications)

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5
Q

CSF findings in SAH

A

uniformly bloody early on
becomes xanthochromic (yellow) after several hours due to breakdown products of Hb (bilirubin)
xanthochromia confirms that the bleed was due to a SAH rather than a continuous bleed from a ‘bloody tap’

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6
Q

SAH management

A

secure aneurysm
evacuate haematoma
relieve hydrocephalus

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7
Q

features of Temporal/Giant cell arteritis

A
S: temporal
O: gradual
C: constant
R: none
A: malaise, weight loss, visual loss, diplopia, jaw claudication, proximal limb pain, temporal artery thickening and pulselessness
T: subacute/chronic
E: none (hair brushing)
S: moderate
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8
Q

diagnosis can be difficult - requires urgent investigation

A

ESR traditionally used - normal in 5%, so also use CRP
temporal artery USS - only 40% sensitive, but very specific
temporal artery biopsy - gold standard, but still only 50-60% sensitive, especially if a small sample is taken
consider in anyone presenting with headache >50years old

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9
Q

GCA Tx

A

if suspicious, then treat! high risk of permanent visual loss
high dose oral steroids (prednisolone 60mg)
Sx should resolve within 2 days
after 1 month, slowly reduce dose
keep reducing until ESR starts to rise again, or Sx return

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10
Q

migraine diagnostic criteria

A

last between 3 and 72h
any 2 of - moderate or severe intensity; unilateral; aggravated with routine activity; throbbing in nature
either nausea/vomiting OR photophobia and phonophobia
these are often too strict however, for clinical practice

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11
Q

migraine aura

A
present in 25%
caused by spreading cortical depression
usually last 10-20mins
usually precede migraine headache
can occur without headache
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12
Q

location of aura and Sx

A

occipital lobe - visual distirbance
parietal lobe - marching sensory disturbance
frontal lobe - hemiparesis, dysphasia

these Sx come on gradually and spread over minutes, unlike stroke

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13
Q

migraine Tx

A
avoid dietary triggers (lacking in most)
regular meals
keep hydrated
regular sleep pattern
address anxiety and depression

avoid medication overuse!
regular analgesic use (10 time a month can be enough) leads to worsening of headaches. opiates and triptans are the worst, but paracetamol and NSAIDs also responsible

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14
Q

acute migraine Sx therapy

A

taken as soon as the headcahe starts
NSAIDs very effective in the majority
if not, triptans can be used
taken no more than twice weekly

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15
Q

triptans

A

e.g. sumatriptan

serotonin receptor agonist, leading to vasoconstriction in tyhe brain and reducing the subsequent neuropeptide release

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16
Q

migraine prophylaxis

A

1st line treatments include propranalol, topiramate (ant-epileptic) and amitriptyline (tri cyclic). need to persevere for 8 weeks with each to see an effect. aim for halving the freq if migraines and reduce the severity

17
Q

feature of raised ICP

A
S: diffuse
O: gradual
C: throbbing or constant
R: none
A: nausea, diplopia, other neuro deficits, seizures
T: subacute/chronic
E: mornings, straining
S: mild to moderate
18
Q

Raised ICP

A

brain tumours are rare and rarely present with headache, and almost never in the absemce of papilloedema or other focal signs
other causes include: cerebral venous sinus thrombosis and idiopathic intracranial HTN