Safety and specimen management Flashcards
What are methods of sterilisation?
Dry heat
Moist heat
Filtration
Ionising gamma radiation/ UV
What is difference between sterilisation and disinfection?
Sterilisation kills all microbes including spores
Disinfection kills most, but not all microbes
Hazard coding system is a square with 4 boxes.
What do they represent?
top - flammable temperature
left - health hazard e.g hazardous, extreme danger, deadly
right - instability e.g unstable if heated, may detonate
bottom - specific information e.g oxidiser, acidic, corrosive
T/F
- chlorhexidine gluconate can be used to cleanse skin before drawing blood
- fume hoods filter air, and remove pathogens before discharging it outside
- chlorhexidine gluconate can be used to cleanse skin before drawing blood T
- fume hoods filter air, and remove pathogens before discharging it outside F
Standard precautions include the following except…
A hand washing after removing gloves
B using PPE when handling specimens
C wearing lab coat to cafeteria
D using automatic pipettor
C wearing lab coat to cafeteria
Routine clinical specimens should be handled with precautions designated for…
- biosafety level 1
- biosafety level 2
- biosafety level 3
- biosafety level 4
- biosafety level 2
- biosafety 1 is suitable for undergraduate science
- 3/4 if for potentially infectious pathogens
Microbiologists must be careful not to generate infectious aerosols. Practice that generate aerosols include the following except….
A hot looping (trying to quickly cool an innouclating loop by inserting into agar)
B votexing
C streaking a plate
D grinding tissue
C streaking a plate
T/F
- bronchoscopy specimens should be centrifuged and sediment used to inoculate culture media
- urine culture represent semiquantitative technique
- bronchoscopy specimens should be centrifuged and sediment used to inoculate culture media T - this is to break down epithelial cells of lung
- urine culture represent semiquantitative technique F this is a quantitative technique, as know volume of liquid using specific inoculating loop
What are three sources of laboratory contamination, during molecular testing?
Carryover contamination - PCR products of previous samples, can be aerosolised during pipetting, and travel over benches/ equipment contaminating clean lab equipment
Sample-sample contamination - manipulating sample in MSC Class I cabinet can contaminate cabinets, consumables and gloves
Template DNA - contamination from environment from lab staff, or reagents used in PCR assay
How to reduce risk of lab contamination in molecular testing?
General -
- Unidirectional workflow - pre-amp to amp
- Use dedicated equipment e.g pipettes for each section
Specimens -
- Do not keep tubes/ reagents longer than necessary
- All reagents/ reaction tubes should be clearly labelled
- Centrifuge samples to remove droplets from lids
Cleaning -
- Clean regularly - e.g DNA away, UV-irradiation, sodium hypochlorite
- Environmental swabs for regular testing for contamination
Staff -
- Wash hands/ use gloves
- Lab coats
- training