micro lecture 17 Flashcards

1
Q

what is the goal of antimicrobial therapy?

A

achieve maximum eradication of the causative organisms from the site of infection

to clinically reduce: deaths > complications > resistance > duration

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2
Q

what are the Principles of antibiotic prescribing

A
Know when to say ‘No’
Seek source control
Investigate judiciously
Cherish your normal flora
The need to be right
Right drug, right dose, right duration
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3
Q

concerning Catheter bacteruria how do you Treat the patient, not the result

A

50% urinary catheters colonised by day 10
Abx are unlikely to eradicate if catheter remains
Treatment will select out resistant organisms which will colonise the catheter
If the patient is not symptomatic, don’t send a urine and don’t treat (except pregnancy)

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4
Q

concerning chronic wounds how do you ​Treat the patient, not the result

A

Chronic wounds (e.g. leg ulcer)
Open wounds are like agar plates, bugs will grow!
Treat only if the patient is symptomatic

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5
Q

how do you find evidence of infection form clinical assessment clinically?

A

General signs/symptoms of infection

Peripheral / local

Systemic

Vital signs

Demographic considerations
Age, sex, occupation, pets

Pre-existing medical problems

Anatomical location – working diagnosis
Most likely pathogens will be known

Therefore can predict most suitable drug
from local pathogen knowledge
Route of administration to get it there
Topical, Oral, Injection, Inhalation

Previous results (grown something before ?)
Recent antibiotics (use something else)
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6
Q

how do you find evidence of infection from the laboratory?

A

tests

Haematology

Biochemistry

Microbiology

Confirmation of pathogen – identification
Microscopy, then indicative testing

Local epidemiological knowledge of
bug-drug susceptibility patterns
Selection of antimicrobial chemotherapy
Breakpoints: likely efficacy

MIC determination – more accurate but still “one colony”

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7
Q

what are the three ways to find evidence of infection?

A

clinical assessment: e.g. physical examination

from the laboratory

imaging: e.g. x-ray

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8
Q

what is the full meaning of MICs?

A

Minimum inhibitory concentrations

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9
Q

what are the three uses of MICs?

A

MICs have three uses

comparing likely effectiveness of antibiotics

observing trends of increasing MICs over time

predicting clinical efficacy in combination with pharmacodynamics

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10
Q

how is MIC determined?

A

Quantitative techniques

Chemically defined media

Governed by regularly updated guidelines

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11
Q

what are the quantitative techniques used to determine MIC?

A

Disk diffusion

Broth and agar dilution

E-tests

Other automated methods

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12
Q

what are the regularly updated guidelines
used to determine MIC?

what country for each one?

A

BSAC (UK),

EUCAST (EU),

CLSI (USA)

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13
Q

who makes the guidelines used to determine MIC for the UK?

A

British Society for Antimicrobial Chemotherapy. (BSAC)

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14
Q

MIC Interpretive Criteria = ____________________

A

BREAKPOINTS

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15
Q

what are are break points used to determine?

A

These are intended to predict CLINICAL efficacy

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16
Q

how are breakpoints determined?

A

MIC distribution

Animal models of efficacy

Pharmacokinetic/pharmacodynamic considerations

17
Q

what does S. pneumoniae baseline MICs show?

A

‘intrinsic’ penicillin G activity

Intrinsic activity of penicillin against ‘fully’ susceptible strains as found when penicillin was first introduced

18
Q

why is there S. pneumoniae resistance to penicillin g?

A

Resistance due to alterations in penicillin-binding proteins with decreased affinity for penicillin

19
Q

In Europe, S. pneumoniae typically shows high-level resistance to_____________

A

macrolides: eg erythromycin, roxithromycin, azithromycin and clarithromycin

20
Q

why does S. pneumoniae show resistance to macrolides in Europe?

A

Bimodal MIC distribution, with susceptible strains separated from resistant strains

21
Q

why does S. pneumoniae show resistance to macrolides in USA?

A

Tri-modal MIC distribution, with ‘fully’ susceptible strains separated from strains with ‘low’ and ‘high’ level resistance

22
Q

In the USA, S. pneumoniae typically shows both low-level and high-level resistance to___________

A

macrolides: eg erythromycin, roxithromycin, azithromycin and clarithromycin

23
Q

how can intrinsic MIC values be restored to amoxycillin when H. influenzae has developed resistance?

A

Intrinsic MIC values can be restored by the addition of clavulanate to amoxycilllin

24
Q

why is resistant to amoxycillin?

A

Intrinsic susceptibility (0.25–1 µg/ml). Resistant strains, due to β-lactamase production, have amoxycillin MICs of 8 µg/ml or higher, which are restored to ‘baseline’ values in the presence of a β-lactamase inhibitor