Week 5 - Medical device infections Flashcards

1
Q

What is a medical device?

A

Organic or inorganic medical object designed to be implanted into a normally sterile area

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2
Q

What are some types of medical devices?

A
  • Catheters/tubes, which introduce or drain fluid
  • Stents/grafts - restore a blocked tube
    Orthopaedic
    Cardiac
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3
Q

What are two types of orthopaedic devices?

A

Fracture fixation

Joitn replacementq

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4
Q

What are two types of cardiac medical devices?

A

Electrical - pacemakers etc

Mechanical - prosthetic/heart valves etc

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5
Q

What are cochlear implants for?

A

Deafness

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6
Q

When is the most common time for a device to become infected?

A

Time of insertion - skin flora/GIT/environment

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7
Q

How could a MD become infected after insertion?

A

From contamination at insertion, or from blood-bourne organisms in bacteraemia

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8
Q

Why do MDs become infected?

A
  1. Immune evasion - decreased vascularity from disruption of putting it in. Inhibition of complement, opsonization, phagocytosis by device components
  2. Biofilm formation
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9
Q

What are the two microorganism states? Describe them

A

Planktonic - float in liquid, actively replicate and actively motile
Sessile - attached to surface/another microbe. Less metabolically active, longer dividing time and preferred state for most microbes

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10
Q

What is a biofilm?

A

A community of sessile microbes attached to a surface, or each other

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11
Q

What do the bacteria produce for a biofilm?

A

Extracellular polymeric substance (EPS) –> slime, which the organisms embed themselves into

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12
Q

WHat % of bacteria are in a biofilm?

A

99.9%

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13
Q

What are sessile microbes?

A

Bacteria fungi and protozoa

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14
Q

What are the components of EPS?

A

polysaccharide & glycoproteins

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15
Q

On which surfaces do biofilms form?

A

Organic - blood vessels & bone

Inorganic - plastic, metal, rubber and silicone

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16
Q

What is the first step of biofilm formation?

A

‘Docking”

- Microbe/surface approximation and surface conditioning are required

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17
Q

What is microbe/surface conditioning composed of?

A

Organism needs to get to surface - needs fluid flow, chemotaxis, motility, hydrophobic/electrostatic interactions, temperature and pH

18
Q

What conditions a surface for docking?

A

It’s prepared by platelets and fibronectin

19
Q

What’s teh second step of biofilm formation?

A

‘Locking’

- Firms up teh connection

20
Q

What performs ‘locking’?

A

On the surface - toxin receptors and polysaccharides
The microbe - has pili, and fimbriae and produces things on it’s surface called microbial surface components recognising adhesion matrix molecules - MSCRAMMS

21
Q

What are MSCRAMMS and what do they do?

A

They mediate the initial attachment of bacteria to a surface
Critical step
usually bind to fibrinogen - also fibronectin and antibodies aka protein A, clumping factor A

22
Q

What is the third step of biofilm formation?

A

Maturation -
Planktonic microbes adhere to sessile ones. The organic/inorganic substances of the environment also adhere
Microbes then start secreting extracellular products to protect themselves

23
Q

Describe staphylococcus epidermis biofilm process

A

Staph sits to surface

  • Forms polysaccharide
  • Other bugs stick to it
  • Critical concentration of bugs allows them to secrete glycocalyx, which protects them
24
Q

Describe pseudomonas aeruginosa biofilm process

A
  1. Sticks to surface - uses flagella
  2. Migrates across surface and uses pili to aggregate community
  3. Produces exopolysaccharide
25
Describe biofilm structure
73-98% water content Has a coral reef like structure - water channels etc It's fraible at the edges
26
What can penetrate into the biofilm?
There's free diffusion of low molecular weight compounds - nutrients and toxins But Larger molecules like proteins can't get through
27
What limits size of biofilm?
Nutrient availability and efficiency of waste removal
28
Which of the first few biofilm stages are reversible?
Docking | Locking is irreversible
29
What's the function of a biofilm?
Physical barrier to things like antibiotics Allows attachment and division of labour - once in there they can stop producing their toxins/metabolic functions etc, but still doing ESP
30
What is advantageous about the biofilm for avoiding antibiotics?
It's hard to kill bugs that aren't metabolically active - and once they're in there, they switch off most metabolic functions
31
How does virulence of bugs increase once in a biofilm?
They can exchange genes/virulence factors
32
When does a biofilm cause systemic problems?
When it gets so big that it breaks apart and bacteria can spread to other areas of the body
33
What is Quorum?
The minimum number of members of a body necessary to conduct business of that group
34
What is Quorum sensing?
A population-dependent gene expression mechanism in some bugs
35
How does Quorum sensing occur?
Bacteria produce small signal molecules, different between Gram pos and neg. They can sense how many other organisms by concentration of the signal
36
What activities are regulated by quorum sensing?
- Extracellular products i.e. toxins - Replication - Bioluminescence
37
What activities are regulated by quorum sensing?
- Extracellular products i.e. toxins - Replication - Bioluminescence
38
In which step of biofilm formation is quorum important?
Step 2 - a quorum of bacteria is reached
39
In which step of biofilm formation is quorum important?
Step 2 - a quorum of bacteria is reached
40
Which step of biofilm formation is REGULATED by quorum sensing?
Step 3 - exopolysaccharide production