Guillain- Barre Syndrome Flashcards

(71 cards)

1
Q

what is gullian- barre syndrome?

A
  • acute symmetrical paralytic polyneuropathy
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2
Q

what does GBS affect?

A
  • affects the peripheral nervous system via ascending weakness
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3
Q

what are the possible triggers of GBS?

A
  • bacterial and viral infections
    e.g., camplobacter jejuni, cytomegalovirus, espstein- barr virus
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4
Q

what is the underlying mechanism of GBS?

A
  • molecular mimicry
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5
Q

what is molecular mimicry?

A
  • where the B cells of the immune system creates antibodies against the antigens on the pathogen that is causing the proceeding infection
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6
Q

what do the antibodies that the B cells produce also match? what does this target?

A
  • also matches the proteins on the nerve cells
  • targets myelin sheath or nerve axon causing damage to nerve cells and hence causing neuropathy and symptoms
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7
Q

what does GBS predominantly affect?

A
  • affects the schawnn cells
  • gradual destruction
    or the axons of peripheral nerves
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8
Q

is there a cure for the condition? what can it be described as?

A
  • no cure for the condition, only ways to manage the condition
  • described as auto- immune
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9
Q

what is the classic GBS onset?

A
  • ascending sensorimotor neuropathy
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10
Q

what are the symptoms like?

A
  • can range from mild to severe
  • very varied
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11
Q

what can severe cases of GBS result in?

A
  • respiratory paralysis
  • anatomic dysfunction
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12
Q

what does GBS start as?

A
  • starts as monopathy presentation
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13
Q

what are the 5 main symptoms of GBS?

A
  • symmetrical ascending weakness
  • lack of sensation
  • lack of reflexes
  • lack of function
  • neuropathic pain
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14
Q

what is the time period where symptoms normally start within?

A
  • normally start within 4 weeks of the infection
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14
Q

what can GBS progress to?

A
  • can progress to cranial nerves
  • causes facial nerve weakness
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15
Q

when do the symptoms peak?

A
  • symptoms peak at 2-4 weeks
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16
Q

how long does the recovery period last?

A
  • lasts months to years
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17
Q

what are the 3 phases of GBS?

A
  • acute
  • plateau
  • recovery
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18
Q

what does the acute phase involve? what is the time frame?

A
  • rapid onset of symptoms
  • escalating over a period of days to weeks
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19
Q

what does the plateau stage involve?

A
  • stabilisation of symptoms
  • no further deterioration
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20
Q

what does the recovery phase involve?

A
  • gradual improvement
  • full recovery may lead to residual deficits
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21
Q

how is GBS normally diagnosed?

A
  • diagnosed based on medical history, physical exam and tests like CSF examination and electrodiagnostic studies
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22
Q

what investigations support the diagnosis of GBS?

A
  • nerve conduction signals (reduced signal)
  • lumbar puncture (high CSF with normal cell count and glucose)
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23
Q

what two features are required for diagnosis?

A
  1. progressive bilateral weakness of arms and legs (initially, only legs may be involved) - ascending motor weakness
  2. absent or decreased tendon reflexes in affected limbs
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24
how long does the progressive phase last for?
- from days to 4 weeks - normally under 2 weeks
25
what can result from GBS? what does this mean?
- autonomic dysfunction - nerves of ANS are damaged
26
what can be a result of cranial nerve involvement? what is affected?
- bilateral facial palsy - usually affects vision
27
what are the five features that strongly support the diagnosis?
- relative symmetry of symptoms - relatively mild sensory symptoms and signs (absent in pure motor variant) - muscular or radicular back/ limb pain - increased CSF - electrodiagnostic features of motor or sensorimotor neuropathy
28
what are the two first line of treatment?
- intravenous immunoglobulin (IVIg) - plasma exchange
29
what does plasma exchange help with?
- helps to remove antibodies
30
why is IVIg and plasma exchange effective?
- because they are strong steroid based anti- inflammatory treatments
31
what are the steroids you could use in treatment?
- plasmapheresis - DVT prophylaxis
32
why would you use DVT prophylaxis?
- prevents blood clots as pulmonary embolism is the leading cause of death via GBS
33
what are the two pathways you can enter the hospital with GBS?
- come into hospital with understanding of neurological problem so neuro screening requested - other patients may have unclear signs
34
when would you admit a patient to ICU?
when one or more is present: - rapid progression of weakness - severe autonomic or swallowing dysfunction - evolving respiratory distress - EGRIS > 4
35
when would you start treatment of GBS?
when one or more present: - inability to walk >10m independently - rapid progression of weakness - severe autonomic or swallowing dysfunction - respiratory insufficiency
36
what are the four main factors to monitor for?
- muscle strength - respiratory function - swallowing function - autonomic function
37
what should you look for in respiratory function?
- weak cough - unable to clear secretions - tone
38
when is it especially important to monitor swallowing function?
- if bulbar symptoms present
39
what should you include when monitoring autonomic function?
- blood pressure - heart rate/ rhythm - bladder/ bowel control
40
what percentage of GBS patients fully recover?
- 80%
41
what percentage of GBS patients have some neurological disability?
- 15%
42
what percentage of GBS patients die?
- 5% die
43
what are the 15 early complications of GBS?
- chocking - cardiac arrhythmias - infections - deep vein thrombosis - pain - delirium - depression - urinary retention - constipation - corneal ulceration - dietary deficiency - hyponatraemia - pressure ulcers - compression neuropathy - limb contractures
44
what is cardiac arrhythmias?
- abnormal heart rhythm
45
what are the 8 key features of general intensive care?
- assisted cough - proper nutritional support - insulin infusion - adequate positioning - anticoagulants and compression stockings - maintenance of the functional position of limbs - early rehabilitation - psychological support
46
what could GBS patients suffer from?
- respiratory muscle weakness - reduced inspiration and expiration
47
what would respiratory muscle weakness lead to? (3)
- airway protection loss - ineffective cough - several pulmonary complications
48
what effects the ability to clear secretions in GBS patients? (2)
- bulbar palsy - dysautonomia
49
what does a reduced clearance of secretions cause?
- higher risk of respiratory failure and pulmonary infections
50
what should you monitor for bulbar palsy and dysautonomia?
- heart rate - blood pressure - respiratory rate
51
what is bulbar palsy?
- affects the brainstem's motor neurons especially those used for speech and swallowing
52
how often are patients monitored? what is monitored?
- monitored every 3-4 hours - monitored on forced vital capacity
53
what is forced vital capacity?
- maximum air volume exhaled after a deep breath
54
what are you monitoring in the FVC measurement? what do you compare it to?
- check for reduction in 20 to 25% of forced vital capacity - compare to guidelines
55
what percentage of GBS patients have affected respiratory muscles?
- 40% of patients
56
what do the affected respiratory muscles lead to?
- causes neuromuscular respiratory failure in 25%
57
when is it especially vital to evaluate respiratory muscle involvement?
- vital in those with rapid onset weakness in the bulbar/ shoulder girdle muscles
58
why would you evaluate respiratory muscle involvement?
- evaluate to see if there is a need for mechanical ventilation
59
what other tests should be completed to monitor respiratory muscle function?
- beside pulmonary function tests
60
what are other cardinal features of GBS?
- autonomic disturbances
61
what are the important symptoms to note of failing respiration? (5)
- rapid and significant muscle weakening - facial muscle weakness - bulbar palsy - shallow/ rapid breathing - reduced breath sounds
62
what are other signs of failing respiration? (3)
- staccato speech - inability to count above 10 - low FVC of 1 litre
63
what are some other symptoms of respiratory failure? (6)
- dysautonomia - tachycardia - brow sweating - paradoxical breathing - mental clouding - somnolence
64
what are some laboratory markers of failing respiration on ABG? (3)
- oxygen saturation less than 92% - p02 < 8kPa - C02 > 6kPa
65
what is the measurement of FVC indicative of failing respiration?
- FVC 30% of FVC from baseline within 24 hours - inconsistent/ failing values of FVC at a single test session
66
how does FVC indicate diaphragmatic weakness?
- decline in vital capacity by more than 15-20% in the supine position indicates diaphragmatic weakness
67
what monitoring should you do every 4 hours? (5)
- FVCs - pulse - blood pressure - respiratory rate - Sp02
68
when should you monitor FVC every 1-2 hours?
- when FVC is below 20mL/ Kg BW
69
what FVC will prompt urgent intensive care? what will this care involve?
- value of less than 15mL/kg should prompt urgent care referral - would include endotracheal intubation in anticipation of potential respiratory arrest
70
what should you check if clinical or laboratory signs of failing respiration are present? what does this give a sense of?
- check for ABGs - sense of acidity and homeostatic imbalance