Test 4 Ch. 29 - Gullain-Barre Syndrome Flashcards

1
Q

GBS is an _______ disease that causes acute peripheral nervous system disorder called polyneuropathy, that results in a flaccid paralysis of the skeletal muscles and loss of muscle reflexes.

A

Autoimmune

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the major pathological and structural changes of the lungs associated with poorly managed GBS?

A
  • Mucus accumulation
  • Airway obstruction
  • Alveolar consolidation
  • Atelectasis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

GBS occurs worldwide with an overall incidence of _______ per 100,000 people.

A

1 to 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Where is GBS slightly more frequent?

A

More frequent in males than females

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

The incidence of GBS is greater in what type of people?

A

Those over 50 years of age

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

GBS is ______% more common in whites than blacks.

A

50-60%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

In about ________ of the cases, the onset of GBS occurs 1-4 weeks after a febrile episode caused by a mild respiratory or GI viral or bacterial infection.

A

Two-thirds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the most common form of GBS in North America and Europe, representing about 75-80% of cases?

A

AIDP - Acute Inflammatory Demyelinating Polyradiculopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

_____________ is similar to AIDP, but without sensory symptoms, affects the motor axons of the nerves.

A

AMAN - Acute Motor Axonal Neuropathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

________________ is a severe variant of GBS that is more prevalent in Asia, Central America and South America. It causes severe, rapid destruction to nerves throughout the body.

A

AMSAN - Acute Motor and Sensory Axonal Neuropathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is Miller Fisher Syndrome (subtype of GBS) characterized by?

A
  • Double vision
  • Loss of appetite
  • Loss of deep tendon reflexes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

AIDP is caused by an immunologic attack that results in peripheral nerve demyelination and inflammation. ___________ and _____________ appear to attack an strip of the myelin sheath of the peripheral nerve and leave swelling and fragmentation of the neural axon.

A

Lymphocytes and macrophages

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

With AIDP, it is believed that the ________________ is the actual target of the immune attack.

A

Myelin sheath covering the peripheral nerves

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Although the precise infectious cause of GBS is not fully understood, it is known that many patients with GBS have had ____________ before developing GBS.

A

CMV infection and campylobacterjejuni

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Today, about ____% of patients with GBS will die.

A

2-3%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the general clinical history of patients with GBS?

A
  • Symmetric muscle weakness in the distal extremities accompanied by paresthesia (tingling, burning, shocklike sensations) or dysesthesias (unpleasant, abnormal sense of touch)
  • Pain (Throbbing, aching especially in lower back, buttocks and legs)
  • Numbness
17
Q

Muscle paralysis that spreads upward is called _____________.

A

Ascending paralysis

18
Q

With GBS, muscle paralysis generally peaks in about ______.

A

2 weeks

19
Q

With GBS, oculomotor weakness occurs in about ____% of cases.

A

15

20
Q

With GBS, more than ________ of patients experience severe pain.

A

HALF

21
Q

With GBS, about _________ of patients have autonomic symptoms.

A

two-thirds

22
Q

In ________% of GBS cases, respiratory muscle paralysis develops, followed by acute ventilatory failure (hypercapnic respiratory failure)

A

10-30%

23
Q

Although GB is typically an ascending paralysis — that is, moving from the lower portions of legs and body upward - in about ____% of cases, muscle paralysis affects the facial and arm muscles and then moves downward.

A

10

24
Q

Between _____% of GBS patients have permanent residual neurologic deficits.

A

10-20%

25
Q

About _____% of GBS patients make a full recovery, but recovery time may be as long as 3 years.

A

90

26
Q

The diagnosis of GBS is based on:

A
  1. Patient’s clinical history
  2. CSF findings (obtained through a lumbar puncture)
  3. Thorough neurophysiology studies by way of an EMG or nerve conduction studies
27
Q

In 80-90% of cases, the typical finding of CSF is an ______________.

A

Elevated protein level (100-1000 mg/dL) with a normal WBC.

28
Q

What is the physical examination of GBS look like?

A
  • RR varies with the degree of respiratory muscle paralysis
  • Apnea in severe cases
  • Anxiety
  • Cyanosis
  • Diminished breath sounds
  • Crackles
29
Q

What are the radiologic findings of GBS?

A
  • Normal or
  • Increased opacity (when atelectasis or consolidation are present)
30
Q

What are some autonomic nervous system dysfunctions associated with GBS?

A
  • Dysautonomia occurs in about 70% of cases. Symptoms include:
  • Cardiac arrythmias
  • Tachycardia - Most common
  • Bradycardia, ventricular tachycardia, atrial flutter, a-fib and asystole
  • Urinary retention
  • Hypertension alternating with hypotension
  • Orthostatic hypotension
  • Obstruction of the intestines (ileus)
  • Loss of sweating
31
Q

About _____% of GBS case develop acute ventilatory failure and require mechanical ventilation.

A

30

32
Q

The primary treatment of GBS should be directed at what?

A

Stabilization of vital signs and supportive care of the patient

33
Q

What should be closely monitored/frequently measured for patient with GBS?

A
  • FVC
  • MIP
  • MEP
  • Blood pressure
  • Oxygenation saturation
  • When indicated, ABGs
34
Q

What are good clinical indicators of impending acute ventilatory failure?

A
  • FVC <20mL/kg
  • MIP <-30 cmH2o
  • MEP <40
  • PaCO2 >45
  • pH <7.35
35
Q

What are primary treatment modalities for GBS?

A
  • Plasmapheresis (plasma exchange)
  • Intravenous immune globulin (IVIG)
36
Q

_____________ entails the removal of damaged antibodies from the patient’s blood plasma, followed by the transfusion of blood.

A

Plasmapheresis

37
Q

The effects of IVIG last between ____________.

A

2 weeks and 3 months

38
Q

With GBS, Nonsteroidal antiinflammatory agents are helpful for what?

A

Pain control

39
Q

What is commonly used to relieve pain and facilitate limb movement for GBS?

A

Hydrotherapy (Whirlpool therapy)

Full recovery make occur in as little as a few weeks or as long as 3 years.