Lecture 24 - Sterilsation And Infection Flashcards

0
Q

How can we break the chain of infection?

A
1\ aseptic technique
2\ antibiotics
3\ Immunisation
4\ Hand washing
5\ Isolate the patient
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1
Q

Where do microorganisms come from?

A

Hospital environment (instruments, fluid, air, medication)
Invasive devices (IVs, endoscopes, catheters)
Patient’s own flora
Other people

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2
Q

What can we do to the host to break the chain?

A

Immunisation

Antibiotics

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3
Q

How can we target entry to break the chain of infection?

A

Aseptic technique

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4
Q

How can we target transmission to break the chain of infection?

A

Handwashing

Aseptic technique

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5
Q

How can we target the source and pathogen to break the chain of infection?

A

Sterilising

Isolation of patient

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6
Q

What is aseptic technique?

A

Procedures that minimise transfer and contamination with potential pathogens

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7
Q

What are the standard (universal) precautions?

A

Don’t know what the patient has, but we use these precautions just incase

Protective equipment

  • masks
  • gloves
  • gowns
  • eyewear

When coming into direct contact with blood, mucous membranes, cuts, bodily fluids

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8
Q

What are the additional precautions?

A

Minimising risk of cross infection

  • single room accommodation (isolation)
  • special air filtration
  • special respiratory masks
  • restricted movement
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9
Q

Why do we encourage hand washing?

A

Very effective at stopping the spread of organisms

However, not everyone complies

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10
Q

When do we use standard precautions?

What about additional precautions?

A

Standard:
- all the time

Additional:

  • M. tuberculosis
  • influenza
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11
Q

When do we use positive and negative pressure rooms?

A

Positive pressure: highly immunocompromised patient

Negative pressure: TB patients

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12
Q

What are the improvents made in hand hygiene?

A

Washing: time consuming
Alcohol hand gels: better compliance
DeBug: Austin hospital, even better compliance

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13
Q

What has increased use of antibiotics in hospitals lead to?

A

Antibiotics resistance:

MRSA
VRE
Acinetobacter spp.
ESBL Klebsiella, E. coli

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14
Q

How can we stem emergence of resistance?

A

Prudent use of antimicrobials

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15
Q

What do plasmids often carry?

A

Genes for multiple resistance

Transfer

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16
Q

How does prudent use help?

A

Avoids selection of mutants

Avoid selection of certain bacteria in the gut

Minimise risk of antibiotic associated diarrhoea (C. difficile)

17
Q

How can we prevent the spread of infection?

A

Vaccination

18
Q

What does disinfection do?

A

Removes pathogens from an article

19
Q

What happens when we wash our hands?

A

Removal of pathogens that have been transiently picked up

We aren’t removing the normal flora that are always there

20
Q

What is sterilation?

How is this different from sterilisation?

A

Removal of all living micro-organisms, spores and infectious agents

Wipes out the normal flora as well

21
Q

What do we call the things that we use for disinfectants?

A

Disinfectants

22
Q

What is the difference between biocidal and biostatic?

A

Biostatic: prevents growth. When removed, they continue to grow

Biocidal: kills bacteria

23
Q

How do we go about disinfection?

A

Washing
Hot water, steam
Chemical disinfectants (bleach, alcohols, chlorhexidine, phenols)
- different efficacy against different pathogens

24
How do we kill spores?
Must use bleach and washing to physically remove the spores Alcohol is not sufficient
25
What so we need to think about when disinfecting?
- concentration - appropriate agent - appropriate conditions (pH and temperature) - adequate contact: physical and time
26
How do we perform sterilisation?
Heat: steam (autoclaves), hot air oven Filtration: if it is a liquid we are sterilising Chemical: H2O2, halogens, per acetic acid Ionizing radiation: for plastic etc.
27
What do we need to think about when sterilising?
- type of contamination - rate of biocidal action - level of assurance
28
How do we determine the level of contamination?
Viable count 1. Dilute out bacteria 2. Spread out bacteria on media 3. Incubation 4. Count the colonies 5. Determine initial microbial load
29
When do we want to mostly affect the bacteria?
In log growth phase
30
What is the D value?
Time taken to reduce the population tenfold (90%) at a particular temperature Decimal reduction time
31
What is sterility assurance?
Probability that a microorganism will survive the killing process
32
How do we decide on the sterility that is required?
Think about the function of the thing For example Bandaid: can accept a lower sterility assurance: 1/1000 Syringe: require higher sterility assurance: 1/1000000
33
Describe the sterilisation cycle
``` Preparation Penetration Holding Safety margin Cool down / drying / aeration ```
34
What is the sterilisation time?
Penetration + holding
35
How does heat kill microbes?
Physical and chemical change Dry: oxidation Moist: coagulation
36
Which type of heat is more effective?
Moist heat Because liberates intense latent heat Contract is volume --> draws in more heat
37
Is heat sterilisation good?
- Reliable and available - economical - the material must be stable
38
What can't we use moist heat for?
Things at risk of Corrosion Metals
39
What can we use dry heat for?
Oils, solids, metals