Skin & Musculoskeletal Dz Flashcards

1
Q

The main anesthetic concerns in pts with _________ center on the serious complications that can occur if proper precautions are not taken during any form of pt manipulation or instrumentation

A

Epidermolysis bullosa

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2
Q

Anesthetic concerns for epidermolysis bullosa:

A

Avoidance of trauma to the skin & mucous membrane is crucial;
Bulla formation can be caused by trauma from tape, BP cuff, tourniquets, adhesive electrodes, & rubbing of skin with alcohol wipes;
BP cuffs should be padded w/ a loose cotton dressing;
Electrodes should have the adhesive portion removed (petroleum jelly guaze to hold in place);
Anything that touches a pt should be well padded;
IV and art lines should be sutured in place or guaze wraps;
Nonadhesive pulse ox;
Place soft foam, sheepskin, or gel pad under pt

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3
Q

H1 & H2 receptor antagonist should be given preop to decrease clinical response to histamine relaese in ________?

A

Mastocytosis

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4
Q

What drugs should be avoided with mastocytosis? Why?

A

Morphine, benzylisoquiniloniums. B/c they stimulate histamine release

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5
Q

All pts with chronic urticaria should be advised to avoid which drugs?

A

ACE inhibitors, aspirin, & NSAIDs

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6
Q

Scleroderma is characterized by what 3 interrelated processes?

A

1) inflammation and autoimmunity;
2) vascular injury w/ eventual vascular obliteration;
3) fibrosis and accumulaiton of excess matrix in many organs & tissues

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7
Q

CREST syndrome a/w scleroderma

A

Calcinosis, Raynaud’s phenomenon, Esophageal hypo motility, Sclerodactyly, Telangiectasia

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8
Q

A connective tissue disorder d/t defects in large glycoprotein fibrillin-1 inherited as autosomal dominant . Pts have long tubular bones and an “Abe Lincoln” appearance

A

Marfan Syndrome

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9
Q

What is the main cause of all premature deaths in pts with Marfan syndrome?

A

Cardiovascular abnormalities

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10
Q

Management of anesthesia must consider the vulnerability of pts with polymyositis to _____

A

Pulmonary aspiration

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11
Q

Are NDNMBs and sux safe with polymyositis?

A

Responses are normal, however w/ skeletal muscle weakness there is concern. Give half dose and check tiwtches before giving more

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12
Q

A group of hereditary diseases characterized by PAINLESS degeneration of muslce fibers

A

Muscular dystrophy

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13
Q

What age does duchenne muscular dystrophy become apparent?

A

2-5 yr old boys

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14
Q

Children with duchenne muscular dystrophy are typically confined to a wheelchair by ______

A

8-10

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15
Q

Intellectual disability is often present with which muscular disorder?

A

Duchenne muscular dystrophy

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16
Q

_________, __________, & ________ are not able to prevent or relieve skeletal muscle contraction with myotonic dystrophy

A

General anesthesia, regional anesthesia, & nueromuscular blockade

17
Q

The inability of skeletal muscle to relax after voluntary contraction or stimulation results from _______? (Myotonic dystrophy)

A

Abnormal calcium metabolism

18
Q

Hereditary degenerativ diseases of skeletal muscle characterized by persistent contracture after voluntary contraction of a muscle or following electrical stimulation

A

Myotonic dystrophy

19
Q

A decrease in functional ACh receptors at the NMJ resulting from their destruciton or inactivation by circulating antibodies leading to marked sensitivity to non-depolarizing muscle relaxants

A

Myasthenia Gravis

20
Q

Who are most often affected by MG?

A

Women aged 20-30; men are often older than 60

21
Q

The clinical course of MG is marked by?

A

Periods of exacerbation & remission

22
Q

________, especially ________ can aggravate muscle weakness a/w MG

A

Antibiotics, aminoglycosides

23
Q

Anticholinesterase drugs effective in the treatment of MG do NOT produce improvement in which pts?

A

Eaton-Lambert Syndrome (myasthenic syndrome)

24
Q

Proximal limb weakness (legs > arms), exercise improves strength, muscle pain common, reflexes absent or decreased;
Affects males more than females;
Co-exists w/ small cell lung cancer;
Sensitive to Sux & NDNMB w/ poor response to anticholinesterase

A

Myasthenic Syndrome

25
Q

Extraocular, bulbar, & facial muscle weakness, exercise causes fatigue, muscle pain uncommon, reflexes normal;
Affects femals > males;
Co-exists w/ Thymoma;
Resistant to Sux but sensitive to NDNMB w/ good response to anticholinesterase

A

Myasthenia Gravis

26
Q

Pain usually present on motion and relieved by rest.
Stiffness tends to disappear rapidly with joint motion (physical therapy).
Pain can also be relieved w/ heat, acetaminophen, & anti-inflammatory drugs

A

Osteoarthritis

27
Q

What causes symptoms to worsen with Lumbar Spinal Stenosis? Improve?

A

Worsen with standing or walking; improve in flexed or supine position

28
Q

Hallmark of rheumatoid arthritis

A

Morning stiffness

29
Q

Management of aortic regurg in ankylosing spondylitis includes:

A

Keeping HR 90 or higher and SVR lower than normal

30
Q

Excessive osteoblastic & osteoclastic activity that results in abnormally thick but weak bones. Usually involves excess of ____ or deficiency of _____.

A

Paget’s Disease; PTH, calcitonin

31
Q

Most common symptom of Paget’s Disease

A

Bone pain

32
Q

Interscalene block may be problematic and is best avoided in which patients?

A

COPD or neuromsucular dz associated w/ weakness of the respiratory muscles

33
Q

How could succinylcholine result in fractures in pts with Osteogenesis Imperfecta?

A

The sux induced fasiculations

34
Q

Infrequent bu t potentially lethal postop complication most often a/w posterior fossa crainiotomy performed in the sitting position

A

Macroglossia