Antibiotics Flashcards

1
Q

What are some problems with antibiotic use?

A
  • Resistance

- C.dif

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2
Q

How does antibiotic resistance come about?

A

Antibiotics are mostly derived from micro-organisms. Therefore resistance mechanisms already exist in nature as bacteria and have been encountering antibiotics for billions of years.

Selection pressure from repeated exposure to antibiotics has greatly increased resistance.

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3
Q

What does emergence of resistance almost inevitably follow?

A

A novel agent

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4
Q

Why is C.dif a problem for antibiotic use?

A

When you kill lots of bacteria, you leave space for other bacteria, usually resistant and harder to kill.

C.dif is an eg of this, it lives harmlessly in the guts until we get rid of other bacteria, then it may cause bowel inflammation.

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5
Q

What does antibiotic stewardship aim to do?

A
  • Reduce antibiotic consumption
  • Restrict worst offender agents
  • Promotes logical antibiotic choices
  • Limits ‘co-lateral’ damage
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6
Q

In what ways can antibiotics be used?

A
  • Guided therapy
  • Empirical therapy
  • Prophylactic therapy
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7
Q

Describe guided therapy?

A

Depends on identifying cause of infection and selecting agent based on sensitivity testing.
Used for mild infection that can wait a few days to be treated.
Can also be used to rationalise therapy for patients previously on empirical therapy.

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8
Q

Describe empirical therapy?

A

Educated guess based on clinical/epidemiological acumen.
Used when patient has more serious infection and can’t wait for culture. As delay in therapy would result in worsening of condition, this therapy is used to cover all likely causes.

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9
Q

Describe prophylactic therapy?

A

Used for healthy people exposed to surgery, injury or infected material.
Also used for immunocompromised individuals eg HIV, transplantation or splenectomy patients
This is used to prevent infection before they start

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10
Q

Describe some more differences between empirical and guided therapy?

A

Guided:-Antibiotics have narrow spectrum

  • If possible they limit penetration to site of infection
  • Acheive clinical cure with as little impact on colonisation and resistance as possible.

Empirical:-Antibiotics have broad spectrum

  • Need to penetrate broadly throughout body
  • Impact on colonisation and resistance may be greater
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11
Q

What are the target effects of antibiotics?

A
  • Highly toxic to bacteria causing infection
  • Penetrate body area affected by infection
  • Limit release of toxins from bacteria
  • Convenient administration
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12
Q

What do we want to achieve with an antibiotic in terms of co-lateral damage?

A
  • Non-toxic to patient
  • Limited effect on colonising bacteria to reduce resistance and c.dif issues
  • Low potential for bacteria to escape treatment through developing resistance.
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13
Q

Can acheiving target effects and avoiding co-lateral damage be done together?

A

Yes, but they are often mutually exclusive so it becomes a balancing act.

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14
Q

In which ways can antibiotics act?

A
  • Bactericidal

- Bacteriostatic

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15
Q

Describe bactericidal action of antibiotics?

A

Achieve sterilisation of infected site by directly killing bacteria. Also prevents growth of bacteria.
Lysis of bacteria can lead to release of toxins and inflammatory material.

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16
Q

Describe bacteriostatic antibiotic action?

A

Supresses growth but does not directly sterilise infected site. Requires additional factors to clear bacteria - immune mediated killing.

17
Q

What structures can antibiotics target and give examples of each?

A
  • Cell wall peptidoglycan (penicillins, glycopeptides)
  • Ribosome (Macrolides, Aminoglycosides)
  • DNA (Quinolones)
  • Metabolism (trimethoprim)
18
Q

By which mechanisms can bacteria gain resistance to antibiotics?

A
  • Mutation/modification of target site
  • Inactivating enzymes
  • Limit access: -reduced permeability, -increased efflux
19
Q

Can genes mediating resistance be transferred?

A

Yes, often easily

20
Q

How do bacteria become resistant to beta-lactamases?

A

They cut hole in beta lactam ring of antibiotic, once this is gone, the antibiotic loses all activity.
Can be overcome by beta lactamase inhibitors or beta lactamase stable drugs.

21
Q

What is the action and downsides of penicillin?

A

Target penicillin binding proteins in and around cell wall. Insert into binding site and prevent peptidoglycan synthesis taking place.
Downside- allergy development (type 1 hypersensitivity)
They have rapid killing and low toxicity

22
Q

Describe role of vancomycin?

A

Cannot penetrate gram - cell wall.

Useful agains penicillin resistant bacteria eg.MRSA

23
Q

Describe role of ciprofloxaan?

A

Targets DNA replication

  • Broad spectrum
  • Resistance now widespread
24
Q

Describe role of trimethoprim?

A

Common resistance

  • target metabolism
  • Useful for non-severe UTI’s
25
Q

Describe role of clanthromycin and doxyclycine?

A

Target ribosome

Switch off protein production