Neuromuscular Dz, TBI, Intracranial HTN, Brain death Flashcards

(40 cards)

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?

24
Q

Indications for seizure ppx after TBI?

A

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

25
Duration of seizure ppx?
7 days
26
CT definition of "mild" TBI?
Normal CT.
27
CT definition of "moderate" / grade-IITBI?
cisterns open. <5mm shift. Small, high-density lesions.
28
CT definition of "severe" / grade-III TBI?
Cisterns compressed
29
CT definition of "severe" / grade-IV TBI?
Midline shift >5mm.
30
Indications for surgery in SDH?
>10mm or shift >5mm.
31
Fluid choice in TBI?
isotonic, non-glucose containing fluids. Albumin caused harm. No evidence for/against prophylactic hypertonic saline or PRBCs.
32
Normal intracranial pressure?
<15.
33
Goal CPP (Cerebral perfusion pressure)?
50-70
34
Indications for ICP monitoring in TBI?
Abnormal CT at admission. Normal CT, posturing, >40yo.
35
Target Osm when using mannitol for TBI?
320
36
Toxicity of mannitol?
renal failure
37
Target Na when using hypertonic saline for TBI?
<155
38
Elements of clinical braindeath exam? (6)
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
Requirements of apnea testing for braindeath exam?
PaCo2 starts normal, then increases >60. No hypoxemia. 10 minute observation.
40
Duration of flat EEG needed for braindeath exam?
30 minutes.