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
Q

How do we kill spores?

A

Must use bleach and washing to physically remove the spores

Alcohol is not sufficient

25
Q

What so we need to think about when disinfecting?

A
  • concentration
  • appropriate agent
  • appropriate conditions (pH and temperature)
  • adequate contact: physical and time
26
Q

How do we perform sterilisation?

A

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
Q

What do we need to think about when sterilising?

A
  • type of contamination
  • rate of biocidal action
  • level of assurance
28
Q

How do we determine the level of contamination?

A

Viable count

  1. Dilute out bacteria
  2. Spread out bacteria on media
  3. Incubation
  4. Count the colonies
  5. Determine initial microbial load
29
Q

When do we want to mostly affect the bacteria?

A

In log growth phase

30
Q

What is the D value?

A

Time taken to reduce the population tenfold (90%) at a particular temperature

Decimal reduction time

31
Q

What is sterility assurance?

A

Probability that a microorganism will survive the killing process

32
Q

How do we decide on the sterility that is required?

A

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
Q

Describe the sterilisation cycle

A
Preparation
Penetration
Holding
Safety margin
Cool down / drying / aeration
34
Q

What is the sterilisation time?

A

Penetration + holding

35
Q

How does heat kill microbes?

A

Physical and chemical change
Dry: oxidation
Moist: coagulation

36
Q

Which type of heat is more effective?

A

Moist heat

Because liberates intense latent heat
Contract is volume –> draws in more heat

37
Q

Is heat sterilisation good?

A
  • Reliable and available
  • economical
  • the material must be stable
38
Q

What can’t we use moist heat for?

A

Things at risk of Corrosion

Metals

39
Q

What can we use dry heat for?

A

Oils, solids, metals