Musculoskeletal disorders Flashcards

1
Q

DMD is most common in what population?

A

male 2-5yo

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2
Q

How do you diagnose DMD?

A

you’ll see the patient falling, can not walk up stairs, waddling gait

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3
Q

pseudo-hypertrophy muscular dystrophy will have a ___ CK lab value

A

High
- leads to hyperkalemia and kidney failure

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4
Q

Muscular dystrophy EKG

A

prolongs PR interval
Tall R waves
Large Q waves in the limb leads

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5
Q

Muscular dystrophy pulmonary symptoms

A

weak cough, OSA, pulm HTN

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6
Q

How does having a weak cough alter anesthesia plan?

A
  • don’t over sedate
  • may was to avoid NMB (you want to use suggamedex)
  • Patient will usually need to stay on the ventilator for a prolonged time
  • will try and do a regional anesthetic
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7
Q

Muscular dystrophy patients are at increased risk of _____

A

aspiration due to delayed gastric emptying

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8
Q

avoid using _____ in Muscular dystrophy patients

A

Sux (no reversal)
- these patients have an increase risk of malignant hyperthermia (careful with volatiles)

this can also add to the hyperkalemia

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9
Q

What is a good medication for sedating a pediatric patient short term?

A

ketamine (disassociation) short term

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10
Q

Myasthenia Gravis is a _____

A

chronic autoimmune disorder developed in later adult hood

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11
Q

Getting up and walking around can cause exhaustion in a pt with _______

A

Myasthenia Gravis

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12
Q

Classifications of MG

A

type 1 involves the eyes and type 4 is a severe disbility

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13
Q

Symptoms of MG
Eyes
Secretions
Speaking
Movement
Cardiac

A

Ptosis, diplopia, and dysphagia​

Dysarthria and difficulty handling saliva​

Isolated respiratory failure ​

Arm, leg, or trunk muscle weakness​

Myocarditis​

Autoimmune diseases associated ​

RA, SLE, pernicious anemia, hyperthyroidism ​

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14
Q

MG crisis usually happens when a patient is ____

A

traveling

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15
Q

MG crisis presents with severe ___

A

muscle weakness
- looks like cholinergic crisis

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16
Q

What medications have cholinergic effects?

A

scopolamine
glycopyrolate
zofran
phenergen

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17
Q

Tensilon Test

A

Give 1-2 mg of edrophonium and if the muscle weakness gets better it is MG and not cholinergic crisis

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18
Q

What can you give to take out the muscle tone in a patient without using a NMB?

A

Robaxin, Spinal anesthesia

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19
Q

Treatment of MG

A

thymectomy
- this is a big surgery and can help with remission and wont need biologic agents. but this takes a while until you show improvement

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20
Q

What medications do MG patients usually take

A

corticosteroids (give the stress dose)
immunosuppressant
immunoglobuliln
plasmapheresis

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21
Q

_____ is a great alternative to sux in MG

A

Remifentanyl

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22
Q

Osteoarthritis is largely in what three joints?

A

knees, hips, shoulders

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23
Q

What causes Osteoarthritis ?

A

repetitive mechanical stress

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24
Q

Osteoarthritis vs rheumatoid arthritis symptoms

A

Osteoarthritis will have overuse of the joints while RA doesnt require that
- you will he heberden nodes

25
Q

Osteoarthritis treatment

A

exercise and PT
pain relief such as heat, NSAIDS, TENs unit, acupuncture, injection of stem cells, put dextrose in the joint, inject platelet rich plasma

26
Q

Osteoarthritis may cause ____ ____ ___ ____ during intubation

A

limited range of motion

27
Q

Rheumatoid arthritis tends to mainly affect what joints?

A

interphalangeal and metacarpophalangeal joints (hands and feet)

28
Q

What medications are RA usually on?

A

immunosuppressant’s
- viruses can be devastating to these patients

29
Q

RA is more common in ____ than _____

A

females than males

30
Q

is RA usually a single joint or multiple joints?

A

Could be both

31
Q

RA patients feel worse in the _____

32
Q

Osteoarthritis patients feel worse ____

A

in the evening

33
Q

_____ in RA can cause pain on opening their mouth

A

TMJ
- heat or PT can help with this

34
Q

RA is rarely seen in what place in the spine?

A

T and L
usually in the cervical spine

35
Q

Atlantoaxial subluxation is common in what patients?

A

Down syndrome or RA

36
Q

cricoarytenoid arthritis symptoms

A

Red arytenoid tissue, hoarseness, dyspena, stridor, anterior neck pain

37
Q

cricoarytenoid arthritis may cause what after intubation?

A

swelling and the patient may need to stay intubated

38
Q

RA symptoms
CV
Pulmonary
Hematology

A

CV: Pericarditis, accelerated coronary atherosclerosis​

Pulmonary: Restrictive lung changes, movement of the chest wall can cause pain​

Hematology: Anemia, neutropenia, elevated platelets​

Keratoconjunctivitis sicca and xerostomia​

39
Q

RA medications for treatment

A

DMARDS (methotrexate)
TNF inhibitors and IL-1 inhibitors work better than DMARDS but take a long time
TNF have severe side effects and will move to IL-1

40
Q

Anesthesia concerns with RA

A

Airway ​
- Atlantoaxial subluxation​
- TMJ limitation – video laryngescope​
- Cricoarytenoid joints​

Severe rheumatoid lung disease ​

Protect eyes ​

Stress dose​ steroids

41
Q

How would a lupus patient present with avascular necrosis?

A

pain in the hip, thigh, knee

42
Q

Lupus symptoms
CNS
CV
Pulmonary
Renal
Liver
NM
Hematology
Skin

A

Polyarthritis and dermatitis ​

Symmetrical arthritis ​

No spinal involvement​

Avascular necrosis of femoral head or condyle​

Hip pain, difficulty walking – need CT or MRI​

CNS: Cognitive dysfunction, psychological changes​

CV: Pericarditis, coronary atherosclerosis, Raynaud’s​

Pulmonary: Lupus pneumonia, restrictive lung disease, vanishing lung syndrome (diaphragm will move up into the chest) pleural effusions, hypoxic​

Renal: Glomerulonephritis, decreased GFR ​
GI/Liver: ABD pain, pancreatitis, elevated liver enzymes​

NM: Skeletal muscle weakness ​

Hematology: Thromboembolism, thrombocytopenia, hemolytic anemia ​

Skin: Butterfly-shaped malar rash, discoid lesions, alopecia​

43
Q

Vanishing lung syndrome in lupus

A

diaphragm is moved up into the chest

44
Q

Antimalarial drugs are used for what autoimmune disorder?

A

lupus
Hydroxychloroquine and quinacrine​

45
Q

Recurrent laryngeal nerve palsy presentation

A

hoarseness, unilateral
If bilateral the patient wont be able to breath

46
Q

What is the genetic mutations in malignant hyperthermia?

A

Ryanodine receptor - RYR1 gene​

Dihydropyridine receptor​

47
Q

What happens with calcium in MH?

A

uncontrolled elevation of calcium in the sarcoplasmic

48
Q

If the patient has a high RR and the CO2 is still rising worry about _____

49
Q

How to treat MH

A
  1. stop whatever caused is. If it is a volatile agent then take them off the vent entirely and hyperventilate the patient. Then get a new anesthesia machine
  2. Give Dantrolene (usually will have to give 10-20 vials)
  3. cool them off internally and externally
50
Q

what is the initial dose of dantrolene

A

2.5mg/kg to 10mg/kg

51
Q

Who can you call during an MH case?

A

Not ghost busters
1-800-MH-HYPER

52
Q

What is soda lime?

A

it absorbs the CO2

53
Q

Tensolin test improves what disease

54
Q

What is not a common manifestation of SLE?

A

asymmetric rash

55
Q

The mortality rate of MH is _____

56
Q

What agents are triggers for MH (2)

A

Anectine and isoflurane

57
Q

Horners syndrome occurs as a result of what blockade?

A

Stellate Ganglion is blocked with inter scalene block

58
Q

CREST syndrome stands for what?

A

Calcinosis, raynauds, esophageal dysfunction, sclerodactyl, telangiectasis