Question: I am an OR
nurse manager and have instituted procedures to curtail the routine
flashing of surgical sets. I have been working with our CPD manager to
implement a method to accelerate turn around times especially when OR
scheduling requires a fast turn around of certain sets for back-to-back
procedures. My preference is to have all instrument sets go to CPD for
reprocessing and terminal sterilization. I am not asking for any short
cuts or steps to be rushed or skipped in the cleaning, inspection,
assembly or sterilization process. I just would like CPD to prioritize
designated sets and when requested or needed to expedite their
processing. There are many times we have called for sets to be sent back
to us following a fast turn around request and the CPD manager has
stated the sets can not be released for use until they are totally
cooled down. If I insist upon the sets being returned he will open the
sterilized sets and tell us they will need to be flashed. The sets in
question are in sealed sterilization containers and I see no reason why
they cannot be released prior to "total" cooling for immediate use. He
maintains that the release of hot instrumentation would be a breach in
technique, as condensate would create excessive moisture inside the
container and cause contamination. We are at an impasse here and I would
appreciate your thoughts and any information you may be able to offer
that may help resolve this issue.
Answer: Certainly best
practice would be to allow all sterilized goods to be thoroughly cooled
prior to handling, or releasing for distribution or use. Goods wrapped
in woven textiles or non woven disposable packaging materials should
never be handled or released for use until they have thoroughly cooled
and must be considered contaminated if any moisture is present on the
inside or outside of the package. If your sealed sterilization container
has offset perforations between the filter retention plates in
containers lid and base which creates a torturous path, minimizing the
risk of microbial strike through, under the circumstances you described
the sets may possibly be released prior to complete cooling for your
immediate use. Since there are great variations in container design and
technology I would suggest that you consult with your specific container
manufacturer for advice and documentation. To ensure sterile integrity
and sterility maintenance protocols should be implemented which will
minimize the degree of handling and detail the care, movement and
logistics of sterile packages. There are rigid metallic sealed
sterilization containers now available which have FDA 510k clearance for
use in Flash Sterilization and Express abbreviated cycles which can be
processed in remote locations i.e. CPD and safely transported to the OR
prior to total cooling without the risk of contamination.
Question: We are doing
some major renovations in our OR and CPD areas and are considering a
case cart system. There are three issues we are debating and would
appreciate any assistance you might offer.
1. How many case carts
are required?
2. How much space is
required for a case cart system?
3. Are open or closed
case carts better?
Answer: 1.Number of carts
required
There is no one set
answer that will work for all institutions. The answer will vary among
organizations depending on procedures, processes, type of hospital,
procedure case load, physical design, logistics and the services and
specialties offered. The goal is to have enough carts to run at peak
capacity. Some sources recommend you have 3 carts per OR – 1 in use, a
2nd ready for the next case and a 3rd in processing. Some hospitals plan
for a case cart for each surgical procedure ( #cases per OR per day x #ORs
= # case carts required ) plus 2 C section carts and 1 case cart per
specialty e.g. emergency, cardiac, ortho, neuro, trauma etc…
2. Determining space
requirements –
Approximately 10 NSF is
commonly allocated for each cart in the assembly and holding areas i.e.
OR, Decontamination, staging etc. ( you will need to project the maximum
number of carts likely to be in these areas at one specific time period)
Here again there is no
fast formula – more or less space may be needed based on uniqueness of
each individual hospital and types of carts selected e.g. tall, short
,wide narrow and the like. Measurements of carts can be taken (include
all appenditures such as bumpers, handles, door swings etc.) project the
anticipated maximum number of carts to be in given area at one time
allow for a 10% variance and a clearance of at least 1 – 1.5’ around
cart and adjust specifications accordingly.
3. Open vs. Closed Case
Carts – From a practice perspective both designs are acceptable and both
have advantages and disadvantages. The decision basically gets down to
user and facility preference based on needs and uniqueness of their
facility’s design, policies and procedures. Some advantages and
disadvantages to consider in the selection process include the
following:
Open Case Cart
• Lighter in weight
• Lower in cost
• Provides visibility
•
Easier to clean; facilitates better drying
• Requires covering in
transit
• Increased potential for
compromising technique and sterile integrity
• More difficult to
contain contents
Closed Case Cart
• Maximum security and
protection of contents
• Minimizes the risk of
environmental contamination
• May need larger size as
there’s no give for expansion
• Heavier weight
• Higher cost
• More challenging to
clean and dry
• Doors require more
space for opening
• Working mechanisms and
doors prone to damage; greater maintenance may be required. HPN
Ray Taurasi is Director
of Professional Services for Case Medical Inc., Ridgefield, New Jersey.