Final Exam Flashcards

1
Q

Gent and tobra dose

A

7 mg/kg

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2
Q

Amikacin dose

A

15 mg/kg

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3
Q

When to draw AG peak

A

0.25 - 1 hour after 1 hour infusion

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4
Q

When to draw AG trough

A

30 minutes or less before the next dose

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5
Q

When to draw random AG

A

If drawn after 1st dose, should be at least one 1/2 life from the peak concentration
If drawing after dialysis, wait at least 2 hours for redistribution to take place before drawing a concentration

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6
Q

When to draw Vanc peak

A

At least 1-2 hours after the end of infusion

Avoids distributional phase which may result in erroneous calculations

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7
Q

When to draw Vanc trough

A

Less than 1 hour before next dose

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8
Q

When to draw Vanc random

A

At least one anticipated t1/2 from previous level obtained

To ensure accuracy in calculating elimination rate constant

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9
Q

What causes AG-induced nephrotoxicity

A

When the trough is too high

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10
Q

When does AG-induced nephrotoxicity occur

A

w/in 4-5 days

High risk associated w/long duration

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11
Q

Is AG-induced nephrotoxicity reversible?

A

Yes

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12
Q

AG-induced RF

A

other disease states, age, other nephrotoxic drugs

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13
Q

What happens to the urine production in AG-induced nephrotoxicity?

A

Non-oliguric

Will still be producing urine

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14
Q

What factors increase AG Vd

A
Ascites/pancreatitis
Cancer
CF
Intensive caare
Post-op/mechanical ventilation
Post partum
Surgery
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15
Q

What factors increase AG CL?

A

Burns
CF
Fever
HD/PD

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16
Q

What factors decrease AG half-life?

A

Burns
CF
HD/PD

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17
Q

What is oral vanc used for

A

Pseudomembraneous colitis

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18
Q

Are IM vanc injections considered?

A

No d/t severe pain

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19
Q

Vanc distribution

A

Widely into body tissues

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20
Q

What type of compartment model is used for Vanc?

A

1, 2 is most realistic

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21
Q

Vanc metabolism

A

Little to none

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22
Q

Vanc IV excretion

A

80-100% recovered in urine in first 24 hours in normal adults

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23
Q

Vanc in HD/PD

A

minimally removed

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24
Q

Vanc pts with increased clearance

A

Obese
Pediatrics
Burn pts

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25
Q

CAPD

A

Peritoneal dialysis
Moves along a fluid gradient
Less efficient than HD
Drugs can be added to PD

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26
Q

GFR in pts on CAPD

A

10-20

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27
Q

CAVH/CVVH

A

continuous renal replacement

Removes larger molecules than any other types of dialysis

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28
Q

GFR in pts on CAVH/CVVH

A

30

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29
Q

Concentration dependent abx

A

Amount of microbial killing depends on the max concentration of drug above the MIC

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30
Q

Concentration dependent abx PK/PD parameters

A

Peak MIC

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31
Q

Concentration dependent abx examples

A

AGs
FQs
Daptomycin
Metronidazole

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32
Q

Time dependent abx

A

Amount of microbial killing depends on the time the drug stays above the MIC

33
Q

Time dependent abx PK/PD parameters

A

T > MIC

34
Q

Time dependent abx examples

A
Beta-lactams
Macrolides
Clindamycin
Vanc
Linezolid
35
Q

Post-abx effect

A

Continued expression of bacterial growth after a short exposure to abx agents

36
Q

Drugs that increase risk of nephrotoxicity w/CSA/TAC

A

AGs
Amphotericin B
Vanc
NSAIDs

37
Q

Enzyme inducers and immunosuppressants

A

Prospectively increase CSA/TAC/EVR daily dose by 25%

Monitor CSA/TAC/EVR trough levels 4-7 days after initiation

38
Q

Conversion of PO TAC to IV TAC

A

IC TAC is 1/3 dose of PO dose

39
Q

Harvoni and Epclusa are not recommended with

A

Amiodarone
Rifampin, St. John’s wort
Carbamazepine, phenytoin, phenobarb, oxcarbazepine
Rosuvastatin (Harvoni only)

40
Q

Viekiera is C/I with

A

Carbamazepine, phenytoin, phenobarb
Rifampin, St John’s wort
Lovastatin, simvastatin
Sildenafil

41
Q

Zepatier is C/I with

A

Carbamazepine, Phenytoin
Rifampin
St. John’s wort
CsA

42
Q

Zepatier is not recommended with

A

3A4 inducers: nafcillin

3A4 inhibitors: ketoconazole, cobi

43
Q

EFV/NVP + rifampin PK result and recommendation

A

decreased EFV/NVP

Increase EFV dose

44
Q

EFV/NVP + statins PK result and recommendation

A

Decreased statins

Monitor cholesterol closely

45
Q

RPV + PPIs PK result and recommendation

A

Decreased RPV

Avoid PPIs

46
Q

ETV + unboosted PIs PK results

A

decreased PIs

47
Q

ETV + warfarin PK result and recommendation

A

Increased warfarin

Monitor INR carefully

48
Q

PI + rifampin PK result

A

Decreased PI, increased rifampin

49
Q

PI + St John’s Wort Pk result

A

Decreased PI

50
Q

PI + (midaz/triaz)/ergot/statin/pimozide

A

Increased second drug

51
Q

PI contraindicated with

A
Rifampin
Midaz/triaz
Lova/simva
ergot
St John Wort
Pimozide
52
Q

ATV + PPI PK result and recommendation

A

Decreased ATV
Max omep 20 mg/day
Always boost

53
Q

PI + amiodarone PK result and recommendation

A

Increase amiodarone
Avoid if possible
TDM

54
Q

PI + trazodone PK result and recommendation

A

Increased trazodone

Use lowest dose

55
Q

PI + immunosuppressants PK result and recommendation

A

Increased immunosuppressants

TDM

56
Q

PI + statins PK result and recommendation

A

Increased statins

Prava/atorv preferred

57
Q

PIs + fluticasone

A

Increased fluticasone

Use alternative inhaled/nasal glucocorticoid

58
Q

RAL + rifampin PK result and recommendation

A

Decreased RAL

Double RAL dose

59
Q

RAL + phenytoin/phenobarb PK result and recommendation

A

Potential decreased RAL

Use caution

60
Q

DTG + dofetilide PK result and recommendation

A

Increased dofetilide

C/I

61
Q

DTG + rifampin

A

decreased DTG

Increase DTG

62
Q

DTG + cations

A

Decreased DTG

Take DTG 2hrs before or 6 hours after cations

63
Q

Amiodarone level

A

0.5-2 mg/ml

Peak level at 3-7 hours

64
Q

Amiodarone MOA

A

Class III antiarrhythmic

Has properties of all classes

65
Q

Amiodarone absorption

A

Very slow

50-70%

66
Q

Amiodarone distribution

A

Mainly to lipophilic tissues

Tissue concentration 10-400x higher

67
Q

Amiodarone compartment model

A

2

68
Q

Amiodarone major metabolism site

A

Liver

3A4

69
Q

Amiodarone active metabolite

A

Desmthylamiodarone

70
Q

Amiodarone DDI by cyp enzymes

A
Warfarin - decrease dose by 25%
Digoxin - decrease dose by 50%
HMG-CoA reductase inhibitors
Phenytoin - increase phenytoin by 50%
Grapefruit juice may increase oral absorption - separate by 2 hours
71
Q

Amiodarone DDI by AV node conduction

A

NDH CCB
BB
Dig

72
Q

Amiodarone elimination

A

Biliary

73
Q

Adjustment of theophylline dosing based on ss concentration

A

For every 1 mg/kg of theophylline, blood concentrations will rise 2 mg/L

74
Q

Factors affecting drug absorption in the elderly

A
CV
CNS
Renal
GU
Endocrine
GI
Musculoskeletal
Immunology/hematology
75
Q

Absorption changes associated with aging

A

Intestinal permeability
Gastric acid secretion
GI motility
Transdermal/IM

76
Q

Distribution changes associated with aging

A

Protein binding

Body fat and body water

77
Q

Metabolism changes associated with aging

A

40% reduction of blood flow to the liver and reduction in liver mass
Phase 1 metabolism reduction

78
Q

Elimination changes associated with aging

A

Kidney mass decreases

Physiologic changes

79
Q

The aged kidney has…

A

Decreased ability to maximally concentrate or dilute urine
Decreased response to inadequate dietary daily
Impaired handling of potassium