Guillain Bare Syndrome Flashcards

1
Q

what type of disease is GBS?

-2

A

autoimmune

polyneuropathy

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2
Q

what structure is damaged in GBS?

A

peripheral nerves

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3
Q

what happens to muscle?

A

flaccis paralysis

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4
Q

what happens to muscle tone?

A

↓tone

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5
Q

what happens to muscle strength?

A

weakness

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6
Q

patient’s antibodies attack what molecule in which system?

what are these antibodies caleld?

A

gangliosides
PNS

anti-ganglioside antibody

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7
Q

anti-GM1 antibody stands for what?

how many pt is it present in?
-% wise

A

anti-ganglioside antibody

25%

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8
Q

is inflammation acute or chronic?

A

acute

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9
Q

what are the 2 main subtypes of GBS?

A

Acute inflammatory demyelinating polyneuropathy

Acute motor axonal neuropathy

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10
Q

which subtype involved myelin destruction?

what cell destroys the myelin?

which cell activates the above cell?

A

Acute inflammatory demyelinating polyneuropathy

macrophages

T cell

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11
Q

which subtype involved a specific antibody attacking axons?

which immunoglobulin is it?

A

Acute motor axonal neuropathy

IgG

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12
Q

the pathophysiology of GBS has been given what term?

explain this pathophysiology?

A

molecular mimicry

infection –> some viruses have similar antigens to gangliosides –> antibodies confused and attack gangliosides

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13
Q

where on the neurones are gangliosides located?

A

axolemma

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14
Q

which bacteria has antigens similar to gangliosides?

A

campylobacter

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15
Q

which muscles groups become weak first?

A

legs

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16
Q

are the proximal or distal muscles affected first?

A

proximal first

17
Q

is the muscle weakness progressive or not?

A

progressive

18
Q

due to extraocular muscle weakness what symptoms can occur?

19
Q

due to oropharyngeal weakness what symptoms can occur?

A

speech problems

20
Q

what happens to reflexes?

A

Hyporeflexia

21
Q

what happens to muscle tone?

22
Q

where can paraesthesia occur?

is the paraesthesia mild or sever?

A

hands and feet

usually mild

23
Q

1st line Ix?
-2

result for each?

A

LP - ↑protein with normal WBC count

Nerve conduction study - slower

24
Q

what is the result on spirometry?

A

↓vital capacity

25
what is the result on LP? explain this result? how long would it take for these results to be seen on a CSF?
↑protein because of inflammation 3 days for protein to elevate in CSF
26
1st line Mx? -2 combining the above two Mx gives a synergistic effect. true or false?
Plasma exchange high dose IV immunoglobulin false (no synergistic effect)
27
what is prognosis? | good or bad
good recovery
28
2-5% of GBS patients die from what complication?
resp failure
29
Plasma exchange is oft abbreviated to what term? how does this procedure work?
PLEX remove their blood, centrifuge to separate, give back their rbc & wbc. give healthy donated FFP
30
which blood product contains the antibodies?
FFP
31
why do you not do IV immunoglobulin in IgA deficient patients ?
SE = anaphylaxis
32
list all symptoms of GBS? | -8
``` Progressive muscle weakness Leg/back pain 65% speech problems facial weakness diplopia hypotonia Hyporeflexia Paraesthesia hand & feet (80%) ```
33
complication of leg muscle weakness?
DVT
34
list complications?
Resp muscle weakness Cranial nerve involvement- diplopia Autonomic nerves effected DVT
35
if autonomic nerves are effected. what features will you see? -4
urinary retention, diarrhoea, BP or HR changes
36
how any GBS pts require ventilation at some point? %wise and why?
30% resp muscle weakness
37
what is typical history?
rapid acute onset of symptoms, lots of muscle weakness.
38
what does GBS stand for?
Guillain Barre Syndrome