Guillain- Barre Syndrome Flashcards

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
Q

how long does the progressive phase last for?

A
  • from days to 4 weeks
  • normally under 2 weeks
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25
Q

what can result from GBS? what does this mean?

A
  • autonomic dysfunction
  • nerves of ANS are damaged
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26
Q

what can be a result of cranial nerve involvement? what is affected?

A
  • bilateral facial palsy
  • usually affects vision
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27
Q

what are the five features that strongly support the diagnosis?

A
  • 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
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28
Q

what are the two first line of treatment?

A
  • intravenous immunoglobulin (IVIg)
  • plasma exchange
29
Q

what does plasma exchange help with?

A
  • helps to remove antibodies
30
Q

why is IVIg and plasma exchange effective?

A
  • because they are strong steroid based anti- inflammatory treatments
31
Q

what are the steroids you could use in treatment?

A
  • plasmapheresis
  • DVT prophylaxis
32
Q

why would you use DVT prophylaxis?

A
  • prevents blood clots as pulmonary embolism is the leading cause of death via GBS
33
Q

what are the two pathways you can enter the hospital with GBS?

A
  • come into hospital with understanding of neurological problem so neuro screening requested
  • other patients may have unclear signs
34
Q

when would you admit a patient to ICU?

A

when one or more is present:
- rapid progression of weakness
- severe autonomic or swallowing dysfunction
- evolving respiratory distress
- EGRIS > 4

35
Q

when would you start treatment of GBS?

A

when one or more present:
- inability to walk >10m independently
- rapid progression of weakness
- severe autonomic or swallowing dysfunction
- respiratory insufficiency

36
Q

what are the four main factors to monitor for?

A
  • muscle strength
  • respiratory function
  • swallowing function
  • autonomic function
37
Q

what should you look for in respiratory function?

A
  • weak cough
  • unable to clear secretions
  • tone
38
Q

when is it especially important to monitor swallowing function?

A
  • if bulbar symptoms present
39
Q

what should you include when monitoring autonomic function?

A
  • blood pressure
  • heart rate/ rhythm
  • bladder/ bowel control
40
Q

what percentage of GBS patients fully recover?

41
Q

what percentage of GBS patients have some neurological disability?

42
Q

what percentage of GBS patients die?

43
Q

what are the 15 early complications of GBS?

A
  • 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
Q

what is cardiac arrhythmias?

A
  • abnormal heart rhythm
45
Q

what are the 8 key features of general intensive care?

A
  • 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
Q

what could GBS patients suffer from?

A
  • respiratory muscle weakness
  • reduced inspiration and expiration
47
Q

what would respiratory muscle weakness lead to? (3)

A
  • airway protection loss
  • ineffective cough
  • several pulmonary complications
48
Q

what effects the ability to clear secretions in GBS patients? (2)

A
  • bulbar palsy
  • dysautonomia
49
Q

what does a reduced clearance of secretions cause?

A
  • higher risk of respiratory failure and pulmonary infections
50
Q

what should you monitor for bulbar palsy and dysautonomia?

A
  • heart rate
  • blood pressure
  • respiratory rate
51
Q

what is bulbar palsy?

A
  • affects the brainstem’s motor neurons especially those used for speech and swallowing
52
Q

how often are patients monitored? what is monitored?

A
  • monitored every 3-4 hours
  • monitored on forced vital capacity
53
Q

what is forced vital capacity?

A
  • maximum air volume exhaled after a deep breath
54
Q

what are you monitoring in the FVC measurement? what do you compare it to?

A
  • check for reduction in 20 to 25% of forced vital capacity
  • compare to guidelines
55
Q

what percentage of GBS patients have affected respiratory muscles?

A
  • 40% of patients
56
Q

what do the affected respiratory muscles lead to?

A
  • causes neuromuscular respiratory failure in 25%
57
Q

when is it especially vital to evaluate respiratory muscle involvement?

A
  • vital in those with rapid onset weakness in the bulbar/ shoulder girdle muscles
58
Q

why would you evaluate respiratory muscle involvement?

A
  • evaluate to see if there is a need for mechanical ventilation
59
Q

what other tests should be completed to monitor respiratory muscle function?

A
  • beside pulmonary function tests
60
Q

what are other cardinal features of GBS?

A
  • autonomic disturbances
61
Q

what are the important symptoms to note of failing respiration? (5)

A
  • rapid and significant muscle weakening
  • facial muscle weakness
  • bulbar palsy
  • shallow/ rapid breathing
  • reduced breath sounds
62
Q

what are other signs of failing respiration? (3)

A
  • staccato speech
  • inability to count above 10
  • low FVC of 1 litre
63
Q

what are some other symptoms of respiratory failure? (6)

A
  • dysautonomia
  • tachycardia
  • brow sweating
  • paradoxical breathing
  • mental clouding
  • somnolence
64
Q

what are some laboratory markers of failing respiration on ABG? (3)

A
  • oxygen saturation less than 92%
  • p02 < 8kPa
  • C02 > 6kPa
65
Q

what is the measurement of FVC indicative of failing respiration?

A
  • FVC 30% of FVC from baseline within 24 hours
  • inconsistent/ failing values of FVC at a single test session
66
Q

how does FVC indicate diaphragmatic weakness?

A
  • decline in vital capacity by more than 15-20% in the supine position indicates diaphragmatic weakness
67
Q

what monitoring should you do every 4 hours? (5)

A
  • FVCs
  • pulse
  • blood pressure
  • respiratory rate
  • Sp02
68
Q

when should you monitor FVC every 1-2 hours?

A
  • when FVC is below 20mL/ Kg BW
69
Q

what FVC will prompt urgent intensive care? what will this care involve?

A
  • value of less than 15mL/kg should prompt urgent care referral
  • would include endotracheal intubation in anticipation of potential respiratory arrest
70
Q

what should you check if clinical or laboratory signs of failing respiration are present? what does this give a sense of?

A
  • check for ABGs
  • sense of acidity and homeostatic imbalance