manual and US cleaning Flashcards
before using US bath:
should be filled to required level
chemicals added FMIs for volume
before any cycles are ran a degass cycle must first be ran
same loading recommendations should be followed as per the WD
handpieces should not be processed within the US
always check MIs before processing instruments
what lid should be used for US bath and why?
need to use US bath with interlocking lid otherwise aerosol production
cleaning definition
physical removal of organic matter and infectious agents
why is cleaning essential to ensure effective disinfection and/or sterilisation?
organic matter on surgical instruments can inhibit disinfectant, sterilant or steam contacting microbial cells and therefore reduce its activity and effectiveness
Sinner circle
interactions of these elements - cleaning process 4 main elements chemicals temp time energy
chemicals
detergents (surfactants, enzymes etc)
lots of research to determine the optimum formulation to remove abnormal prion protein from surgical instruments
temp
optimise chemical reactions for the detergent agents
ensure that in the initial wash stages the temp does not exceed 40 degrees which will start to coagulate the proteins remaining on the instrument resulting in difficulties on their removal
time
how long does it take for the detergents/jet wash to take effect
length of time needed to clean an instrument should be confirmed during the validation process
energy
brushing as in manual cleaning
use of US energy
water jets in the WD
when should decon be started?
immediately after use or as soon as reasonably practicable
transporting instruments to decon room
regular collections
all items appropriately containerised to prevent damage during transit
ensure staff safety
what instruments should be decontaminated?
all reusable surgical instruments that are used in the clinical env should be decontaminated without exception
unacceptable to only process those instruments that come into direct pt contact
- all instruments and instrument trays opened in the clinical env should be decontaminated between uses
sorting of used instruments
sort reusable from non-reusable devices and dispose of consumable items such as napkins and cotton wool rolls, in the correct waste streams
manual cleaning processing env
area should be dedicated for the purpose and not shared with other activities
- dedicate sink to cleaning process
- where possible a 2nd sink for rinsing
- segregate dirty from clean by appropriate workflow patterns and practices
PPE for manual cleaning and safety
gloves, facemasks, waterproof apron, goggles/visor
first aid kit and eye wash bottle nearby
drying items
hand drying - clean, disposable, absorbent, non-shedding (low linting) cloths
mechanical drying facility
cleaning materials supply
routinely decontaminated/discarded at freq detailed in the documentation
env i.e. air and surfaces
requires an appropriate level of particulate and microbiological control
= purpose of env control is to minimise the possibility of re-contamination and as such, microbiological/infection control advice as to the appropriateness of the reprocessing env should be sought
non-immersion methods
for certain items which will become compromised by soaking in (aq)
e.g. handpieces, electrical and electronic equipment
clean in accordance with MIs
factors affecting manual cleaning
water temp - protein starts to coagulate at >40 degrees, so water above this must not be used for initial immersion of devices prior to cleaning
detergent conc
nature of soil and method of removal
accessibility of fluid to the item
what determines whether immersion/non-immersion?
construction of device
immersion method - how do you minimise risk to operator?
avoid splashing
avoid creation of aerosols - under water surface at all times