THER.Intro to Abx I&II.9.1.15 Flashcards

1
Q

What is the “Time above MIC”?

A

The time at which the organism is being exposed to the antibiotics at a concentration that is greater than the minimum inhibitory concentration

Analogous to the AUC/MIC

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2
Q

Are the following drugs bactericidal or bacteriostatic?

Protein synthesis inhibitors (except aminoglycosides)

A

Bacteriostatic

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3
Q

Name the characteristics of the patient that will play a role in the effectiveness of the drug?

A

Allergy

Age: eldery have more fat may serve as a resevoir for drugs

Pregnancy: greater Clerance and Vd; will drug cross placenta?

Renal/hepatic fxn: decreased fxn leads to decreased clearance

Drug interactions: augment toxicity or effectiveness

Underlying disease: burn pts are predisposed to certain infections

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4
Q

Define Minimum inhibitory concentration (MIC)

A

The lowest concentration of antibiotic that inhibits the growth of an organism.

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5
Q

Define: AUC/MIC

A

Area over the MIC = Total amount exposure of an antibiotic at a concentration > MIC

This is more easily measured as the “time above MIC”

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6
Q

Define Time dependent killing

A
  • Killing depends on time of exposure above the MIC and NOT on higher serum concentrations
  • Usually associated with no PAE effects; give next dose immediately after concentration is below PAE
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7
Q

Describe the three traits of infection that will affect treatment with abx

A

Severity: may affect route of administration, dose, and choice of abx. Ex: for pts in shock, IV > oral becaue the person has diminished ciruclation and drug would never get to site of infection

Site: is the abx able to reach the brain (cross BBB) for treating meningitis?

Organism: sensitivity to drugs, combination therapy, etc.

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8
Q

Describe pharmacodynamics

A

“How drug effects the body”

Represented by the: Dose response curve

Concentration (x-axis) vs effect (y-axis)

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9
Q

Define Concentration dependent killing

A
  • Higher serum concentrations = More rapid and extensive killing
  • We often see abx with a long PAE here—- ex: aminoglycosides, we will see killing even after concentration is below MIC.
  • Prolonged PAE allows us to increase interval between doses
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10
Q

Define post-antibiotic effect

A

The amount of time it takes for bacterial growth to re-occur after the concentraion is below the MIC

gram neg: prolonged PAEs when treated with aminoglycosides and fluoroquinolones

gram positive: shorter PAE when treated with b-lactams

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11
Q

Bacteriostatic

A
  • Inhibits bacterial growth
  • Requires host immune defense to clear the pathogens
  • Inadequate host defense may lead to continued growth and resistance after abx are discontinued
  • ex: sulfonamide
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12
Q

Describe pharmacokinetics

A

What the body does to the drug: ADME

Represented by graph of: concentration of drug in body (y-axis) vs time (x-axis)

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13
Q

Describe the PK/PD combined curve

A

Tells us about the effect of the drug in the body over time

Effect: Y-axis

Time: X axis

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14
Q

Describe Bactericidal abx

A

Kills bacteria

Less dependent on host immune system (IS)

Ind for pts with inadequate or compromised IS

Required for treatment of:
»meningitis, endocarditis, osteomyelitis, febrile neutropenia

Ex: penicillin

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15
Q

Are the following drugs bactericidal or bacteriostatic?

Metabolic inhibitors

A

Bacteriostatic

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16
Q

Are the following drugs bactericidal or bacteriostatic?

Cell wall inhibitors (ex: penicilins)

A

Bactericidal

17
Q

Are the following drugs bactericidal or bacteriostatic?

Nucleic acid synthesis inhibitors

A

Bactericidal

18
Q

Factors to consider when choosing an appropriate abx

A
  • Predicted activity: consult measured susceptibility and clinical efficacy
  • “Drug of choice”: consult treatment guidelines and books
  • PK: is drug able to penetrate the infected tissues?
  • PD: do we need bactericidal or bacteriostatic drugs?
  • Side Effects: well tolerated?
  • Cost: IV drugs more effective and expensive