Healthcare Acquired Infections, Diseases, Yr 3, Wk 1 Flashcards

1
Q

What does HAI mean?

A
  • Healthcare Associated Infection
  • they are infections that were not present or in the pre-symptomatic phase at the time of admission to hospital
  • which arise > or equal to 48 hrs after admission or within 48 hrs of discharge
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2
Q

List some possible outcomes of HAI:

A
  • Extended length of stay, pain, discomfort, permanent disability, death
  • Increased cost: 33% decrease in HAI in Scotland would lead to savings of £55 million
  • Litigation (taking legal action)
  • Loss of public confidence and decreased staff morale
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3
Q

Whats the a) most common cause of a HAI

b)What are the most common sites of HAI?

A

a) Proportion of HAIs are due to different infections
b) -UTI (22.6% of all HAI)- mainly related to catheterisation
- Surgical Site Infection (18.6%)
- Respiratory Tract Infection (17.5%)- intubation accounted for about 1/4 of these
- Bloodstream Infections (10.8%)- many central venous catheter (CVC) related
- Gastrointestinal infection (6.8% versus 15.4%)
- Skin and soft tissue infection (4.0%)

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4
Q

Give context to Bacteria versus Humans:

A
  • Approx 10 to the power of 14 bacteria in adult human
  • Approx 10 bacterial cells to every human cell
  • Human beings carry >1Kg of bacteria in their gut alone
  • 500 different species of bacteria have been isolated from human stool
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5
Q

List some of Nature’s defence mechanisms (1st line of defence):

A

1st line of defence:

  • Intact skin
  • ‘Normal’ bacteria flora e.g. skin, GIT
  • Body secretions e.g. tears containing antibodies/ enzymes, coughing
  • Gastric Acid
  • Flushing e.g. urination
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6
Q

List the body’s 2nd line of defence:

A

Immune system

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7
Q

Everyone and everything harbours microbes that may pose a risk…..Patients in hospital are……(finish this sentence)

A

…….Patients in hospital are more vulnerable to microbial colonisation AND infection

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8
Q

What is the fundamental question in clinical microbiology?

A

Colonisation versus Infection

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9
Q

Who discovered Staphylococcus aureus, (aka SA)?

A

Alexander Ogston

credited with introducing carbolic antiseptic spray to Aberdeen

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10
Q

What percentage of the population are colonised with SA in their nose (this includes patients, staff and relatives)?

A

30%

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11
Q

What type of SA are most people colonised with?

A

Most are colonised with the METICILLIN SENSITIVE Staphylococcus aureus (MSSA)

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12
Q

The same strain of Staphylococcus aureus can that is COLONISING can also cause INFECTION through:

A
  • Break in skin e.g. surgical site infection
  • Vascular device e.g. PVC, CVC
  • Catheter associated urinary tract infection (CAUTI)
  • Ventilator associated pneumonia (VAP)
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13
Q

Generally, what is the most common cause of a HAI?

A

Disturbance in bacterial-host equilibrium leads to most HAI

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14
Q

What are some factors related to MICROBIAL which tip the balance towards infection?

A

INCREASED:
-Resistance

  • Virulence
  • Transmissibility
  • Increased survival ability
  • Increased ability to evade host defences
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15
Q

What are some factors related to HOST which tip the balance towards infection?

A
  • Devices: PVC, CVC, Urinary catheter, Ventilation
  • Antibiotics
  • Break in the skin surface
  • Foreign body
  • Immunosuppression
  • Gastric Acid suppression
  • Age extremes
  • Overcrowding
  • Increased opportunity for transmission e.g. Interventions, Hands !!
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16
Q

Number of bacteria required to cause infection if
a) No SILK SUTURE?

b) SILK SUTURE present?

A

(Silk suture is a surgical suture used to hold skin together)

a) 6.5 million bacteria
b) 100 bacteria

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17
Q

List some means of transmission microbes:

A
  • Direct contact: e.g. SA, coliforms
  • Respiratory/Droplet: e.g. neisseria meningitidis, Mycobacteria tuberculosis
  • Faecal-Oral: e.g. Clostridium difficile, Salmonella sp.
  • Penetrating injury: e.g. Group A streptococcus, Bloodborne viruses
18
Q

List some ways of breaking the chain of infection:

A
  • Risk awareness
  • Standard Infection Prevention and Control Precautions (SICPs)
  • Hand hygiene
  • Appropriate PPE
  • Vaccination
  • Post exposure Prophylaxis
  • Environment
19
Q

Give the meaning of Cleaning:

A

Physical removal of organic material and decrease in microbial load

20
Q

Give the meaning of Disinfection:

A

Large reduction in microbe numbers- spore may remain

21
Q

Give the meaning of Sterilisation:

A

Removal/ Destruction of ALL microbes and spores

22
Q

Cleaning, Disinfection, Sterilisation:

List some;

a) Low risk categories and how they should be treated:
b) Medium risk categories and how they should be treated:
c) High risk categories and how they should be treated:

A

a) Low risk: Intact skin contact e.g. stethoscopes, cots, Mattresses: Cleaning compatible with manufacturer’s instructions
b) Medium risk: Mucous membrane contact e.g. bedpans, vaginal specula, Endoscopes: Disinfection or sterilisation as appropriate
c) High risk e.g. surgical instruments: Sterilisation

23
Q

Describe CLEANING and how it should be carried out:

A
  • Manufacturer’s instructions
  • Detergent and water
  • DRYING IS AN IMPORTANT PART OF THE PROCESS!
  • Cleaning essential PRIOR to disinfection and Sterilisation if these are required
24
Q

Give 2 methods of Disinfection and describe them:

A

Heat:

  • Pasteurisation (e.g. bedpans, linen, dishwashers)
  • Boiling (vaginal specula, ear syringes)

Chemical:

  • Chemicals vary in their organism activity range
  • Needs to be equipment compatible
  • Examples: Alcohol chlorhexidine, hypochlorites, hydrogen peroxide

(This is disinfection, NOT sterilisation)

25
List some Methods of Sterilisation:
- Steam under pressure (autoclave) - Hot Air Oven - Gas (ethylene dioxide) Ionising Radiation
26
List the 2 types of surveillance:
Local surveillance:- Laboratory Based -Ward/ Clinical Area Based National Surveillance
27
Give some advantages of Local surveillance (Lab based):
Laboratory detects an organism and notifies IPCT and clinicians: Advantages: -Know what organism is and specific recommendations can be made
28
Give some disadvantages of Local surveillance (Lab based):
Disadvantages: -Depends on samples being sent - Time taken to detect organism - Tests not 100% accurate
29
List some advantages of Local Surveillance (Clinical Area Based):
Clinical area staff notify Infection Prevention and Control Team (IPCT) Advantages: -Detect potential problem sooner -Can ensure correct samples sent
30
List some disadvantages of Local Surveillance (Clinical Area Based):
Disadvantages: -Causative microbe not known -IPC measures need to be more general
31
Describe OUTBREAKS- Definition and Identification:
-An outbreak of an infection is defined as 2 or more cases of infection linked in time and place N.B.: -1st purpose of IPCT is to PREVENT individual infections AND outbreaks!! -Purpose of surveillance is to DETECT and IDENTIFY a possible outbreak at the earliest opportunity
32
How do you act in an outbreak and describe 'typing' :
- Have to act in suspicion - Typing necessary to determine if the same strain present i.e. an outbreak Typing methods: - Antiobiogram (antibiotic sensitivity pattern) - Phase typing (e.g. SA) - Pyocin typing (Pseudomonas) - Serotyping (Salmonella, Pseudomonas) - Molecular typing (DNA typing) (Exam question: Give 2 typing methods)
33
In an OUTBREAK, list some Control Measures:
- Single room isolation - Cohorting of cases (group of people with shared characteristic) - Clinical Area/ Ward Closure - Re-inforcement of IPC measures - Staff exclusion (e.g. colonised staff in case of MRSA; non-immune staff in case of VZV, measles etc.) - Staff decolonisation or other measures
34
Give some Clinical Characteristics of C difficile infection:
- Diarrhoea - Faeces have a characteristic odour - May have abdominal pain, pyrexia, raised white cell count - Pseudomembranous colitis (PMC)
35
What is C difficile?
- Part of the normal gut flora in approx 2% of adults - Carriage rate increases with age - Approx 30% of the elderly are colonised - Can survive in environment- importance of cleaning - 2 toxins produced- Toxin negative strains DO NOT cause disease
36
Give more information about C. Difficile:
- IMBALANCE in gut flora - Endogenous or exogenous source - Variable in severity - Elderly most susceptible - N.B. UNDER DIAGNOSED IN THE COMMUNITY
37
List some laboratory tests that can be used in C. Difficile: N.B. Clinical Interpretation is required!
- Positive Toxin Test DOES NOT ALWAYS MEAN DISEASE! | - Diarrhoeal symptoms NEED TO BE PRESENT for diagnosis of CDI!
38
Why is CDI still occurring?
- Not possible to prevent all cases - All antibiotics can predispose to CDI although some are more predisposing than others - New strains? - Less handwashing because more handgelling? - Environmental contamination may still be an issue? - Increased no. of vulnerable patients close together? - Increased throughput of patients? - Other drugs having an effect e.g. PPIs?
39
Why have there been a reduction in incidence and explain this:
New Antibiotic Guidelines (ARI 2009) developed to: - Treat infection but also to - reduce incidence of C diff!!! -Available in ARI on INTRANET
40
What is the the treatment used in C. Difficile infection?
-STOP THE ANTIBIOTICS PREDISPOSING TO C difficile IF POSSIBLE! IF SYMPTOMATIC, treatment: -Oral metronidazole - Oral vancomycin if severe or failure to improve on metronidazole - Oral fidaxomicin if 2nd episode (Scottish Medicines Consortium (SMC) Guidance 2012) - N.B. DO NOT TREAT THE SYMPTOM FREE! - Any antibiotic can cause CDI including Metronidazole and Vancomyin