Aminoglycosides Flashcards

1
Q

Gentamicin/Tobramycin Peak dosing for uncomplicated lower UTIs

A

3-4 mcg/ml

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2
Q

Gentamicin/Tobramycin Peak dosing for gram-positive endocarditis (synergistic effects with PCN)

A

3-4 mcg/ml

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3
Q

Gentamicin/Tobramycin Peak dosing for gram-negative infxn (ex: sepsis)

A

6-8 mcg/ml

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4
Q

Gentamicin/Tobramycin Peak dosing for gram-negative pneumonia

A

8-10 mcg/ml

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5
Q

Gentamicin/Tobramycin Peak dosing for gram-negative pneumonia with CF

A

12-15 mcg/ml

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6
Q

Gentamicin/tobramycin trough

A

< 1-2 mcg/ml

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7
Q

Aminoglycosides time to sample for peak

A

Should be drawn 0.25 - 1 hour after a 1hr infusion

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8
Q

Aminoglycosides time to sample for trough

A

should be drawn 30 minutes or less before the next dose

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9
Q

Aminoglycosides time to sample for a random drawing after the first dose

A

The random should be drawn at least one half-life from the peak concentration

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10
Q

Aminoglycosides time to sample for a random drawing after dialysis

A

Wait at least 2 hours for redistribution to take place before drawing a concentration

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11
Q

AE and toxicity of Aminoglycosides

A

Nephrotoxicity, neurotoxicity, ototoxicity

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12
Q

Nephrotoxicity d/t aminoglycosides

A

May occur w/in 4-5 days
Non-oliguric
Reversible in most cases
Similar risk with gent, tobra, and amikacin
Risk factors: other disease states, age, other nephrotoxic drugs

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13
Q

Neurotoxicity d/t aminoglycosides

A

Muscle twitching, numbness, seizures, tingling

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14
Q

Ototoxicity d/t aminoglycosides

A

0.5-3% clinical incidence
Damage to 8th cranial nerve
Unilateral/bilateral
Variable onset

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15
Q

Cochlear ototoxicty

A

loss of hearing, tinnitus, feeling of ear fullness

Often irreversible

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16
Q

Vestibular ototoxicty

A

Vertigo, ataxia, nystagmus, dizziness, N/V, unsteadiness

Often irreversible

17
Q

Drug-drug interactions of aminoglycosides that can have a possible additive nephrotoxicity

A

Amphotericin B
Cisplatin
CsA
Lasix

18
Q

Drug-disease interactions with aminoglycosides: ascites

A

May increase Vd by greater than or equal to 25%

19
Q

Drug-drug interactions with aminoglycosides and skeletal muscle relaxants

A

Aminoglycosides are capable of producting neuromuscular blockade which can enhance the activity of the muscle relaxants

20
Q

Drug-disease interactions with aminoglycosides: Burns

A

Increase clearance and/or decrease t1/2

21
Q

Drug-disease interactions with aminoglycosides: cancer

A

Increased Vd

22
Q

Drug-disease interactions with aminoglycosides: Critically ill with sepsis

A

May increase or decrease Vd and clearance

23
Q

Drug-disease interactions with aminoglycosides: fever

A

Increased clearance

24
Q

Drug-disease interactions with aminoglycosides: hemodialysis/peritoneal dialysis

A

Increased clearance and decreased t1/2

25
Q

Drug-disease interactions with aminoglycosides: intensice care setting

A

may increase Vd up to 25-50%

26
Q

Drug-disease interactions with aminoglycosides: Post-op/mechanical ventilation

A

may increase Vd

27
Q

Drug-disease interactions with aminoglycosides: Postpartum

A

may increase Vd

28
Q

Drug-disease interactions with aminoglycosides: surgery

A

increases Vd

29
Q

Distribution of aminoglycosides

A
Rapid
Related to intracellular fluid
Low protein binding
Poor CSF penetration
High concentrations in kidney, liver and lung
Accumulation over time
Influenced by age, wt, dx/conditions
30
Q

Clearance of aminoglycosides

A

90-95% fraction excreted via kidney
Relationship b/n drug clearance and renal function (GFR, CrCl)
Dialyzable
Influenced by age, dx/conditions