Musculoskeletal quick hits Flashcards

1
Q

What disease should hyperthermia be avoided in? Why?

A

MS - Signs and symptoms can be exacerbated by heat

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2
Q

Which fluid should be avoided in patients with hypokalemic periodic paralysis?

A

D5W - dextrose can cause a shift of K into the cells and exacerbate skeletal muscle weakness

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3
Q

Which condition is similar to MH and is characterized by hyperkalemia and rhabdomyolysis?

A

Duchenne’s

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4
Q

Dosage for dantrolene?

A

2.5mg/kg IV every 5 minutes till hypermetabolism subsides

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5
Q

What is CREST syndrome?

A

Type of scleroderma

Calcinosis
Raynaud’s
Esophageal hypomotility
Sclerodactyly
Telangiectasia

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6
Q

How often must a charcoal filter be changed with a patient with MH

A

Every hour

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7
Q

What is Myasthenia Gravis? What disease is associated with it?

A

Autoimmune IgG

Nn receptor dysfunction on the post junctional receptor motor end plate

Thymoma

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8
Q

First line treatment for MG?

A

Oral pyridostigmine

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9
Q

What is the Tensilon test?

A

Edrophonium is given 1-2 mg IV

If muscle weakness is worse then in cholinergic crisis

If muscle weakness is better then the patient had an exacerbation of myasthenic symptoms

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10
Q

Treatment for cholinergic crisis?

A

Anticholinergic

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11
Q

How will paralytics affect MG?

A

Sensitive to non depolarizes

Resistant to Succ

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12
Q

What is Lambert Eaton syndrome? What disease is common with this?

A

Destruction of voltage gated calcium channels

Small cell lung carcinoma

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13
Q

How do paralytics affect Eaton Lambert ?

A

Increased sensitivity to Succ

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14
Q

Eaton Lambert or MG, AchE inhibitors have low efficacy?

A

Eaton Lambert

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15
Q

What is Guillain-Barre? (acute idiopathic polyneuritis)

A

Ascending paralysis that is preceded by flu like illness

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16
Q

What is Familial periodic paralysis?

A

Group of diseases that intermittently attacks skeletal muscle and causes weakness

Hypo and hyperkalemia

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17
Q

What is myotonic dystrophy?

A

Prolonged muscle contracture after a voluntary skeletal muscle movement

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18
Q

What is Charcot-Marie-Tooth?

A

Peripheral neuropathy that presents as weakness

Usually lower third of the legs

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19
Q

How is Guilian Barre treated?

A

IV IgG and Plasmapheresis

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20
Q

Do steroids or interferon improve outcomes on Guilian Barre?

21
Q

What anesthetic is preferred in GB? Should Succ be avoided?

A

General

Yes - avoid succ

22
Q

What is the treatment for both variants of periodic familial paralysis?

A

Acetazolamide

23
Q

Is glucose and beta 2 agonists safe in hypo or hyperkalemic periodic familial paralysis?

A

Safe in hyper because it shifts it lower. Don’t give in hypokalemia

24
Q

What must be avoided at all costs in periodic paralysis?

A

Hypothermia - MAINTAIN NORMOTHERMIA

25
MH affects which receptor ?
Ryanodine - RYR1
26
Is Duchenne's a risk factor for MH?
NO
27
What three diseases are risk factors for MH?
King Denborough Central core disease Multiminicore disease
28
What are three early signs of MH?
Masseter spasm Increased EtCO2 Tachycardia Tachypnea Warm soda lime
29
What is trismus?
A tight jaw that can be opened and responds to succ
30
What is masseter muscle rigidity?
Tight jaw that cannot be opened and does not respond to succ
31
Should dantrolene be D/C if venous irritation is observed?
NO
32
What drug class should be avoided with MH?
CCBs (verapamil)
33
What is Duchenne's? What lab value will be observed ? EKG findings?
Absence of dystrophin CK leaks through muscle cell and is elevated Deep Q waves in limb leads Increased R wave in lead I
34
What changes occur in the lung with Duchenne's? What doesn't happen?
Decreased pulmonary reserve from kyphoscoliosis Increased secretions and aspiration Respiratory muscle weakness NO PULMONARY FIBROSIS
35
Children with DMD are susceptible to what life threatening condition?
Hyperkalemia after Succ
36
What is Cobbs angle and go through each degree
Measurement of scoliosis 50- Need surgery 60-Pulmonary reserve decreases 70-Pulmonary symptoms appear 100- High risk of post op complications
37
*** What region of the spinal cord do somatosensory evoked potentials monitor?
Posterior or dorsal column
38
What is the most common RA airway complication?
Atlantoaxial subluxation and separation of the atlanto-odontoid articulation
39
What is the first line treatment of RA? What else is used?
NSAIDS Glucocorticoids
40
What three things will you see in patients with RA?
Anemia Pleural effusion Aortic regurgitation others: Bleeding (from aspirin) Hyperglycemia (from steroids) Restrictive lung disease
41
Treatment for lupus?
Hydrocortisone and cyclophosphamide NSAIDS Antimalarials
42
mnemonic for SLE?
Pissed Chimp
43
Which immunosuppressant increases the duration of succ?
Cyclophosphamide. inhibits plasma cholinesterase
44
What disease has spontaneous bleeding into the joints?
Ehlers - Danlos Procollagen and collagen disorder Careful with anything that punctures (regional, IM, line placement)
45
What disease has blue sclera and brittle bones?
Osteogenesis Imperfecta Connective tissue disorder BP cuff can cause a fracture Serum thyroxine is increased
46
Which disease has a high risk of spontaneous pneumothorax?
Marfan Also -Aortic regurgitation -Aortic dissection
47
Pagets disease has a risk of what?
Bone fracture Excess osteoblastic and clastic activity - causes thick and weak bones
48
Which disease has bulbar muscle dysfunction?
MS
49
How does scleroderma affect the airway?
Skin fibrosis - limits mouth mobility Telangiectasis - increased risk of mucosal bleeding