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DeBug Infection Prevention Program

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Hand Hygiene Learning Package


Surveillance

Regular and ongoing surveillance in sentinel wards provided feedback on the success of program interventions at Austin Health. The following outcomes were measured before and after the introduction of the DeBug Infection Prevention Program:

     Patients – Clinical MRSA infections, MRSA colonisation and acquisition

     Staff – MRSA colonisation

     Environment – MRSA contamination

     Hand Hygiene compliance

     Vancomycin usage

     Usage of DeBug and other Hand Hygiene products

 

Laboratory methods for culturing MRSA

Swabs taken from patients, staff and the environment are cultured on agar plates. They are incubated at 35° Celsius.
The bacterial colonies are visible within one to two days.

 

 

Identifying MRSA

As there are thousands of different organisms on the skin it is difficult to differentiate the S.aureus without using “selective” media to take advantage of the specific characteristics of the bacteria.

One such selective agar is mannitol salt agar (MSA) containing methicillin.

S.aureus, unlike many bacteria, is salt tolerant. Using media that contains a high salt concentration will therefore allow growth of S.aureus while inhibiting many of the other organisms.

Further selection can be achieved by adding methicillin or similar antibiotics to the agar.

Mannitol (a carbohydrate) is a useful agar additive because S.aureus utilises it to produce an acidic byproduct, which changes the colour of the agar around colonies from pink to yellow.

The scientist can then readily identify probable MRSA colonies by
their yellow colour. Further tests are performed to confirm the culture results.


  



Nose and groin swabs cultured on MSA
Nose and groin swabs cultured on MSA







Staphylococcus aureus on mannitol salt agar
Staphylococcus aureus on mannitol salt agar





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