Neuromuscular Dz, TBI, Intracranial HTN, Brain death Flashcards

1
Q

Sx of ALS (Amyotrophic Lateral Sclerosis)?

A

Ascending paralysis with asymmetric limb involvement over months-years. Tongue fasiculations. Eye movement & sensation are normal.

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2
Q

Medical name of Lou Gehrig’s Dz?

A

ALS (Amyotrophic Lateral Sclerosis)

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3
Q

Muscle weakness w/ tongue fasiculations. Dz?

A

ALS (Amyotrophic Lateral Sclerosis)

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4
Q

Other name of Guillain-Barre Dz?

A

AIDP (Acute Inflammatory Demyelinating Polyneuropathy)

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5
Q

Sx of Guillaine-Barre?

A

Ascending, symmetrical weakness, sensory abnormalities, weeks after diarrhea. Autonomic abnormalities.

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6
Q

Muscle weakness w/ autonomic dysfunction. Dz?

A

Guiallain-Barre Dz

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7
Q

Pathophysiologiy of myasthenia gravis?

A

Post-synatpic AchR antibodies

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8
Q

weakness that gets worse with reptition. Dz?

A

Myasthenia gravis.

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9
Q

Thymoma associated with what weakness-causing disease?

A

myasthenia gravis

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10
Q

Muscle weakness w/ occulobulbar weakness. Dz?

A

Myasthenia gravis.

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11
Q

Mimic of myasthenia gravis? Differentiating feature?

A

Botulism. It has arelexia, dry mouth, ileus.

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12
Q

Sx of tick paralysis?

A

ascending paralysis, preserved sensation, areflexia, opthalmoplegia

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13
Q

Sx polio?

A

asymmetric weakness, legs > arms.

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14
Q

Sx Rabies?

A

Pharyngeal spasms, grimacing encephalitic agitation. Opisthontonos (paraspinal muscle spasms), then paralysis.

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15
Q

Paralysis with rash. Dz?

A

West Nile virus

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16
Q

Antibodies (+) in Guillain-Barre?

A

GM1, GD1a

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17
Q

Test of choice for Guillain Barre Dz?

A

-LP with increased protein & normal WBC. Nerve conduction studies or GM1, GD1a antibodies also plausible.

18
Q

Tx of Guillain-Barre Dz?

A

Anticholinesterase, IVIG, Plasma exchange. Corticosteroids. Thymectomy.

19
Q

Tests (2) for botulism?

A

Repetitive nerve stimulation shows presynaptic block. Toxin demonstration in blood, stool, wound.

20
Q

Test for rabies?

A

PCR from CSF shows viral RNA. Pleocytosis with increased protein.

21
Q

Test for polio?

A

PCR from CSF. Pleocytosis with increased protein.

22
Q

Mechanism of DAI?

A

axonal shear at grey/white interface is universal. Axon twisting.

23
Q

Test of choice for DAI?

A

MRI

24
Q

Indications for seizure ppx after TBI?

A

GCS<10, abnormal CT (defines moderate-severe)

25
Q

Duration of seizure ppx?

A

7 days

26
Q

CT definition of “mild” TBI?

A

Normal CT.

27
Q

CT definition of “moderate” / grade-IITBI?

A

cisterns open. <5mm shift. Small, high-density lesions.

28
Q

CT definition of “severe” / grade-III TBI?

A

Cisterns compressed

29
Q

CT definition of “severe” / grade-IV TBI?

A

Midline shift >5mm.

30
Q

Indications for surgery in SDH?

A

> 10mm or shift >5mm.

31
Q

Fluid choice in TBI?

A

isotonic, non-glucose containing fluids. Albumin caused harm. No evidence for/against prophylactic hypertonic saline or PRBCs.

32
Q

Normal intracranial pressure?

A

<15.

33
Q

Goal CPP (Cerebral perfusion pressure)?

A

50-70

34
Q

Indications for ICP monitoring in TBI?

A

Abnormal CT at admission. Normal CT, posturing, >40yo.

35
Q

Target Osm when using mannitol for TBI?

A

320

36
Q

Toxicity of mannitol?

A

renal failure

37
Q

Target Na when using hypertonic saline for TBI?

A

<155

38
Q

Elements of clinical braindeath exam? (6)

A
  1. Unresponsive to pain.
  2. No pupil response.
  3. Occulocephalic or occulovestibular reflex absent.
  4. No cornea reflex.
  5. No gag or cough reflex.
  6. Apena.
39
Q

Requirements of apnea testing for braindeath exam?

A

PaCo2 starts normal, then increases >60. No hypoxemia. 10 minute observation.

40
Q

Duration of flat EEG needed for braindeath exam?

A

30 minutes.