Neurology Flashcards
Gullain Barre Syndrome:
What are some common causes of it?
How does it present?
What investigations should you do?
What is the treatment?
Causes:
Campylobacter Jejunum
Mycoplasma Pneumonia
EBV
Hep E - Genotype 3
**molecular mimicary
Presentation:
Symmetrical Weakness, proximal muslces affected.
- 20% devleop resipratory distress
Sensory changes
- Pain
- Distal Parasthesia
Weakness:
- Loss of reflexes
- Diploia
- Dysphasia
Autonomic dysfuncton
- postural hypotension
- Constipation
Investigations:
Nerve conduction studies
Peak Flow - to assess respiratory function - every 4 hrly.
Lumbar puncture:
- raised Protein
- Normal White cells
*if detioration admitt to ITU
Treatment:
IV immunoglobulins
Plasma Exchange
Respiratory Support
Pain management
Bell’s Palsy:
Lower Motor Neuron lesion of the fascial nerve.
Unkown eitology but thought to be associated with:
- latent HSV
*more common in pregnancy x3
*more common in DM x5
Clinical Features:
- abrupt onset - over night
- complete unilateral weakness
- ipsilateral pain around ear
- reduced taste (ageusia)
- hypersensitivity of sounds (stapedius palsy)
Differentials:
- Ramsay Hunt syndrome (VZV reactivation)
- Mengitits
- Braimstem lesions
- Cerebellopontine angle tumours - accoustic
- lymm disease (Borrelia)
Investigations:
To rule out other causes:
- VZV antibodies
- Borrelia antibodies
- ESR
- Glucose
*CT/MRI (tumours)
Mangagement:
within 72 hours - predisilone 60mg.
+72 hours - steroids but the evidence is not clear
**protection of th eye:
- dark glasses
- artificial tears
- use of tape on the eyes
- surgical eye closure if severe
Prognosis:
incomplete paralysis make full recover
- in a few weeks
complete paralysis - 80%
Myesthenia Crisis:
*Plasmaphresis
*Immunoglobulins
*ventilatory support
Myasthenia Gravis:
What can make this worse?
What is it associated with?
What investigations should be done?
How is it treated?
Autoimmune disease
-antibodies against nictonic receptor
Augmentors:
*climte change
* pregnancy
*hypokalamia
*gentamicin
*opiods
*Beta Blockers
Differentials:
Lambert- Eaton Syndrome
Polymyositis
Takayasu’s arteritis
botulism
Associations:
- SLE
- RA
Investigations:
- Anti- AChR antibodies
- Muscle Specific Tyrosine Kinase / MUSK antibodies
- Low density lipolipoprotein receptor related protein
- EMG studies
- CT for thyoma (as associated)
- Tensilon test (dangerous)
Treatment:
- Anti-cholinesterase (pyridostigamine)
- Immunosupression - steroids
- Thyectomy
Lambort Eaton Syndrome?
Compare and contrast with MG:
Neuromuscular disease that prevents the release of neurotransmitters on the pre-synptic membrane
- due to antibodies against the Ca2+ channel.
*associated with cancers
- small cell lung cancer
Clinical Features:
gait changes - this is well before changes to the muscles of the eye
Autonomic dysfunction
- dry eyes
- constipation
**weakness improves with exercise
this is contrasted with MG, which gets worse.
Treatment:
* cure underlying condition
* pyridostigamine
*Diaminopyridine
- this blocks K+ allowing Ca2+ to stay open for longer
*Immunoglobulins
Define Delierium:
A distrubanc of consciousness with reduced ability to focus, substain or shift attention.
It develops acutely (over hours to days) and tends to fluctate in its severity over that time
Evidence of a physiological cause induced by illness, trauma, medication or pyschological distress
Types:
* hypoactive
*hyperative
*mixed
What are some differentials to delierum?
And what are some common risk factors?
Dementia
Anxiety
Non- convulsive Status epilepticus
Primary mental illness - schizophrenia
Risk Factors:
>65 years old
Dementia
Hip fracture
Acute illness
Pyschological agitation (pain)
What is the management for Delerious patients?
Assessment:
*History
- any clues to underlying causes
*Examination
*Cognitive Assessment
- AMT
- MMSE
*Investigations
Investigations:
FBC
U&Es
Blood Glucose
ABG
Bone profile
- Ca2+
CRP
Spetic Screen
- urine dipstick
- CXR
- Blood cultures
- CT/ EEG
What is the management for delierum?
_**Resolve the causative factor_
_**Review medications_
_**Avoid constipation_
Reorientate the patient as best as possible
- clocks
- Calenders
Calm the patient with reassurance
Encourage physical movement
Maintain fluids
Sedation:
used only when patient is a risk to themselves and others:
1st line: Haloperidol
*avoid in parkinson’s
2nd line: Lorazepam
What is the Imaging investgiations can be done into Parkinson’s?
DAT SPECT scan
What is the treatment for cluster headaches?
100% oxgen. The to 80% as pain decreases
+
Triptans
Prophylaxis:
- verapmil
During a GCS assessment, the supraorbital is squeezed and the patient moves their arm to below their clavical, what does this count as?
M4 - normal flexition
it does not count as localisation as it is not above clavical
What are the treatment options for generalised seizures?
1st line:
- Sodium valporate
2nd line:
- Lamotrigrine
or - Carbamazepine
What are the treatment options for focal seizures?
1st line:
- Carbamezepine
- Lamotrigrine
- *2nd Line:**
- Sodium valporate
- Levetiracetum
What type of seizure is most associatted with Automatisms?
Complex focal seizure of temporal lobe
Automatisms include:
- lip smacking
- Dystonic limb movement
- undressing
- walking in circles
What are some typical features of a generalised seizure?
Photosensitivity - some people sensitivity to certain light frequency.
Usually with genetic in nature
Tend not to have the build up
Usually in early hours of the days
No Aura
If an EMG shows diminished respone to continual stimulation what is a likely diagnosis?
Mysthenia Gravis
How are migraines treated acutely?
1st line:
- Triptans
- NSAIDs - high dose aspirin
2nd line:
- Metaclopramide
- Non- oral NSAIDs
What is the propholyatic treatment for migraines?
Avoid triggers:
- caffiene
- Cholocate
- Hangovers
etc
1st:
- propranolol
or
- Topiramate
2nd:
- accupuncture - 10 courses
3rd:
- botulism injections
What is the diagnostic criteria for migraines?
Without aura:
>2 of the following:
- unilateral
- Pulsating
- Mod pain
- Aggrevated by activity
>5 attacks
Lasting 4-72 hours
N&V or Photophobia
With Aura:
>2 attacks
What are the antibodies investigated for in mysthenia gravis?
Acetlycholine Receptor
Muscle Specific Kinase - MuSK
Low Density Lipolipoproteins receptor related 4 - LRP4
How is Msythenia Gravis offocially diagnosed?
Autoantibodies
Edrophonium test
What type of ventilation is used in mysthenia gravis crisis?
BiPAP
or
Intubation
What are the most common causes of Guillian Barre syndrome?
Campylobacter
EBV
CMV
Hep E type 3
What is the criteria used for diagnosis of Guillian Barre syndrome?
and what additional tests can be done to support the diagnosis?
Brighton Criteria
- EMG studies - reduced signals
- LP rasied proteins