Vertigo, Hearing Loss, N/V Flashcards

1
Q

What are otoxic and vestibulotoxic drugs

A

Amionglycosides - dose dependent, usually irreversible
Erythromycin
Minocycline
Fluoroquinolones
NSAIDs/salicylates - dose dependent
Loop Diuretics - dose dependent, can be irreversible
Cytostatic drugs - dose dependent, Irreversible
Antimalarials

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2
Q

What is the mechanism that aminoglycosides and cisplatin cause damage?

A
  • both end up inducing ROS to activate JNK to increase transcription of cell death proteins that act on the mitochondria to activate caspases – apoptosis
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3
Q

What is the mechanism that loop diuretics cause damage?

A
  • block the same channels in inner ear that disrupt fluid balance created by stria vascularis and cause edema of inner ear
  • dose dependent
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4
Q

What is short term treatment of Vertigo and their MOA

A
  1. meclizine hydrochloride - blocks H1 and M1
  2. Diphenhydramine - blocks H1 and M1
  3. Scopolamine transdermal patch - blocks M1
  4. Promethazine hydrochloride - blocks H1 and M1
  5. Diazepam - useful for psychosomatic vertigo
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5
Q

What are the CYP2D6 inhibitors

A

diphenhydramine and promethazine

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6
Q

Which should not be given to geriatric patients?

A

meclizine, diphenhydramine, scopolamine, promethazine b/c all have drowisness and dizziness as side effects

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7
Q

Promethazine ADE

A
  • BBW for injection use

- fatal respiratory depression in < 2 yo

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8
Q

ADE of scolopamine

A

xerostomia, ocular effects after touching patch and rubbing eyes

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9
Q

DDX for N/V

A
  • EtOH, NSAIDs, oral antibiotics, vestibular disorder, labyrinithitis, Meniere’s dz, motion sickness, migraine, anticipatory vomiting
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10
Q

vomiting process?

A
  1. pre-ejection
  2. Retching
  3. Ejection
    - accompanied by multiple autonomic phenomena including salivation, shivering, and vasomotor changes
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11
Q

Vomiting coordinated by what?

A
  • Central emesis center in lateral reticular formation of mid-brainstem next to both CTZ in area postrema and bottom of 4th ventricle and solitary tract nucleus
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12
Q

What works at solitary tract nucleus for emesis?

A

enkephalin, histamine, Ach, serotonin - vagal and sympathetic afferents as well as CN 5 and 9 afferents

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13
Q

What are the most potent antiemetics?

A

Serotonin Antagonists - setrons

  • works at CTZ and solitary tract nucleus
  • all undergo hepatic metabolism (only ondansetron needs adjustement)
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14
Q

What receptors are on CTZ

A

Serotonin, D2, M2

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15
Q

ADE of setrons

A

QT prolonation

- headache, constipation, diarrhea

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16
Q

What are the D2 receptor antagonists that work at CTZ?

A

Prochlorperazine, chlorpromazine - also possess antihistamine and anticholinergic activities

17
Q

ADE of prochlorperazine and chlorpromazine

A
  • chronic use –> bone marrow suppression
  • QT prolongation, and Torsades de pointes
  • Coadminstration w/ antipsyhcotics may increase CNS adverse effects
18
Q

What are the SubP/NK1 receptor antagonists that work at Solitary tract nucleus

A

Aprepitant and Fosaprepitant

- extensive hepaptic metabolism (CYp3A4 inhibitor)

19
Q

ADE of aprepitant and fosaprepitant

A
  • Headache, constipation, diarrhea

- numerous potential interactions w/ CYP

20
Q

What are the cannabinoid receptor agonist that work in medullary vomiting center and STN?

A

Dronabinol, THC –> also enhance appetite via effects in lateral hypothalamus

21
Q

Dronabinol details

A
  • Schedule III drug - slow and gradual onset

- produces high - elation and heightened awareness

22
Q

Which antineoplastics have high likelihood of emesis

A

Cisplatin, mechlorthamine, streptozotocin, cyclophsophamide

23
Q

What is the treatment of choice for prophylaxis against acute emesis

A

Serotonin receptor antagonists + corticosteroid + NK1 antagonist

24
Q

MOA of steroids for anti-emesis

A

act on steroid receptors in STN - might be due to decrease in 5HT