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aMMS

  • 1+2: Age | DoB
  • 3+4: Year | Time
  • 5: Place
  • 6+7: Monarch | WWI
  • 8: 20->1 or WORLD<-
  • 9: Recogn 2
  • 10: 42 West St



Six Item Cognitive Impairment Test (6CIT)

Stroke Classification (OCSP)

  • {1|2|3}=unilat weakness and/or sensory deficit affecting {face | arm/hand | leg/foot}
  • 4=dysphasia
  • 5=visuospatial disorder (eg. sensory inattention)
  • 6=homonymous hemianopia
  • 7=brainstem/cerebellar signs
  • 8=other deficits
  • Total Anterior Circulation Stroke=TACS=1+2+3+{4|5}+6
  • LACunar Stroke=LacS=1+2+3 or 1+2 or 2+3
  • POsterior Cirulation Stroke=PoCS=6 or 7 or 6+7
  • Partial Anterior Circulation Stroke=PACS=other combinations exc. 7+8
    • TACS, LacS: 1:leg/foot--2:arm/hand--3:face
    • TACS             4:dysphasia--5:inattention
    • PoCS             6:hemianopia--7:brainstem/cerebell
    • PACS             8:other

Oculomotor nerve palsy = 3rd nerve palsy

  • eg Src: StudBMJ
  • Sy: horizontal and vertical binocular diplopia; ptosis
  • eye 'down-and-out', unable to move upwards/downwards/inwards
  • ptosis
  • large unreactive pupil='surgical palsy': possible post communic artery aneurysm
  • if pupillary sparing='medical palsy': usu microvascular ischaemia (eg DM, Htn)

Periodic Paralysis

  • periodic paralysis triggered by cold, heat, hi CHO meals, fasting, stress, etc
  • 'channelopathy'; AD with variable penetrance
  • eg {hypo-|hyper-}kalaemic periodic paralysis (=distribution problem, but overall K stores usu normal)
  • DD: hyperthyroidism

Guillian-Barre-syndrome=GBS

  • =acute inflammatory demyelinating neuropathy=AIDP: autoimmune disease affecting PNS, usu triggered by acute infectious process
  • ascending paralysis, areflexic, +/- dysaesthesias, loss of proprioception, pain
  • maybe lower CN involvment (weakness, oropharyngeal dysphagia)
  • sometimes respiratory weakness, 30% GBS require ventilation
  • Miller-Fisher variant: oculomotor weakness
  • Diagn: CSF: albumino-cytological dissociation; EMG/NCS
  • Diagnostic criteria
    • Required
      • Progressive, relatively symmetrical weakness of 2 or more limbs due to neuropathy
      • Areflexia
      • Disease course < 4 weeks [else: CIDP]
      • Exclusion of other causes (see below)
    • Supportive
      • relatively symmetric weakness accompanied by numbness and/or tingling
      • mild sensory involvement
      • facial nerve or other cranial nerve involvement
      • absence of fever
      • typical CSF findings obtained from lumbar puncture
      • electrophysiologic evidence of demyelination from electromyogram
    • Differential diagnosis
      • acute myelopathies with chronic back pain and sphincter dysfunction
      • botulism with early loss of pupillary reactivity
      • diphtheria with early oropharyngeal dysfunction
      • Lyme disease polyradiculitis and other tick-borne paralyses
      • porphyria with abdominal pain, seizures, psychosis
      • vasculitis neuropathy
      • poliomyelitis with fever and meningeal signs
      • CMV polyradiculitis in immunocompromised patients
      • critical illness neuropathy
      • myasthenia gravis
      • poisonings with organophosphate, poison hemlock, thallium, or arsenic
      • paresis caused by West Nile Virus
      • spinal astrocytoma
      • Motor Neurone Disease
  • Treatment
    • ventilation: early intubation if
      • VC<20mL/kg
      • Negative Inspiratory Force (NIF)< -25cmH20
      • 30% dcr in VC or NIF within 24h
      • rapid disease progression
      • autonomic instability
    • hi dose IV Ig or plasmapheresis ASAP (must be <2wk since onset of motor symptoms)
    • [Glucocorticoids: NOT effective]
 
Subpages (3): IIH PD Stroke
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Andreas Jostel,
3 Apr 2009, 08:40
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