Antibiotic resistance Flashcards

1
Q

What are common causes of antibiotic therapy failure?

A

Unjustified therapy

Poor antibiotic selection.

Incorrect dose or regimen.

Suppressed host response.

Resistance.

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2
Q

What does C&AST stand for?

A

Culture and Antibiotic sensitivity testing

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3
Q

What are the methods for assessing resistance?

A

Liquid culture MIC determination

Disk diffusion (Kirby-Bauer) where diameter of zone inhibition for a genus is matched to a break point for MIC.

Detection of know resistance genes or mutations

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4
Q

What is the role of clinical breakpoints in determining antibiotic resistance?

A

Clinical breakpoints define whether bacteria are sensitive or resistant to antibiotics based on:

MIC (Minimum Inhibitory Concentration):
Sensitive: MIC < breakpoint.
Resistant: MIC > breakpoint.

Zone diameter in disc diffusion tests:
Sensitive: Diameter > breakpoint.
Resistant: Diameter < breakpoint.

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5
Q

Describe intrinsic resistance

A

An innate ability to resist activity of a particular antimicrobial agent through inherent structural or functional characteristics which allow tolerance of the drug

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6
Q

Describe acquired resistance

A

When a microorganism obtains the ability to resist the activity of a drug. Can be mutation or new gene acquisition.

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7
Q

Give examples of intrinsic bacteria

A

Poor permeability: Gram- -ve bacteria resist vancomycin

Lack of target: Mycoplasmas lack cell wall, making them resistant to beta-lactams

Different target: Enterococci resist cephalosporins due to low PBP affinity.

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8
Q

What are the mechanisms of acquired resistance?

A

Gene mutation: Alters antibiotic binding sites

Gene acquisition: Horizontal transfer via plasmids or other methods

Efflux pumps: Actively remove antibiotics from bacterial cells (e.g., tetracyclines)

Enzymatic degradation: Break down antibiotics (e.g., beta-lactamases)

Modification of targets: Changes to binding sites (e.g., methylation in ribosomal RNA).

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9
Q

What are common resistance mechanisms by antibiotic group?

A

Beta-lactams: Cleavage by beta-lactamases, altered PBPs.

Aminoglycosides: Enzymatic modification, efflux pumps.

Quinolones: Efflux, target mutations.

Tetracyclines: Efflux.

Rifamycins: Altered RNA polymerase.

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10
Q

What are factors that increase risk of selection?

A

Underdosing: Suboptimal concentrations fail to kill bacteria completely.

Length of selective exposure: Prolonged exposure increases resistance development.

Presence of resistant bacteria: Allows selection of resistant strains.

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11
Q

What is the difference between MDR, XDR, and PDR?

A

MDR (Multi-Drug Resistant): Resistant to ≥1 agent in ≥3 antimicrobial categories.

XDR (Extensively Drug Resistant): Resistant to ≥1 agent in all but ≥2 categories.

PDR (Pan-Drug Resistant): Resistant to all antimicrobial agents tested.

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12
Q

What are the key principles of good antibiotic stewardship?

A

Limit antibiotic use to necessary cases.

Use cytology and sensitivity testing where possible.

Prefer first-line agents over second-line or broad-spectrum antibiotics.

Administer concentration-dependent antibiotics at the highest effective dose.

Avoid underdosing or irregular administration.

Implement a practice-wide PROTECT plan.

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13
Q

What does the sensitivity grading “sssrR” indicate in an antimicrobial report?

A

It indicates very resistant sensitivity.

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14
Q

What is the significance of the disk content in antibiotic susceptibility testing?

A

It determines the breakpoints; changes in disk content can affect interpretive criteria.

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15
Q

What is the benefit of using Convenia (Cefovecin) in veterinary practice?

A

It is a long-acting injectable antibiotic, useful for hard-to-dose patients and treating skin and soft tissue infections.

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16
Q

What are the potential drawbacks of using systemic antibiotics for otitis externa?

A

Promotes antimicrobial resistance (AMR)

Exposes the whole animal unnecessarily

Low local concentration at the infection site