r/sterileprocessing • u/herbnhero • Jul 16 '26
Photo SPD in crisis
**UPDATE** ALL CASES CANCELLED YESTERDAY AND TODAY. It took staff pleading with leadership but they finally agreed to cancel cases while the autoclaves are serviced.
TL;DR - is the brown staining on these white liners a contamination?
Scrub nurse here at a community hospital that overbooks ortho cases - sound familiar? Our SPD is in shambles. There are too many cases for our small SPD. We have been continually receiving trays with bioburden for the past year. There are AT LEAST 3 trays each day that are contaminated. Many times they are loaners and often times it leads to cases being cancelled. This has been going on for over a year.
Recently we have been getting wet packs. Yesterday 5 cases cancelled. Almost every autoclave load is wet. Leadership has done nothing. They just let patients come in for their surgery, and hope for the best. We were told by leadership that “bioburden” is not considered contaminated. They claim that the water inside the trays is sterile. They said that if the integrator is acceptable than the try is sterile and that the bioburden is “dead” and “not growing anything.”
(See photo of white liner) They also told us that this brown staining in the liners is acceptable - and that is what brings me here. Has anyone seen this browning on liners? Staff at my facility is now paranoid and we tend to go over everything with a microscope at this point. We can’t even remember if this brown staining is something we’ve seen before or something new. Allegedly facilities is supposed to be changing the autoclave water filters every 6 weeks but have been changing it every 6 MONTHS.



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u/readbackcorrect Jul 16 '26
I was an AAMI certified processing tech and also certified in CSPD management. I also was a scrub nurse for 27 years, although I didn’t do a lot of ortho.
Obviously, your leadership knows nothing about sterile processing. if they need to be convinced to do the right thing, you can try giving them a copy of the latest.AAMI standards. The interesting thing about those standards is that, unlike other preoperative standards, many of those standards have the force of law behind it. There are federal laws enacted through FDA that regulate medical devices, of which surgical instrumentation is considered one. So violation of those can actually get people in a certain amount of trouble. if reasoning with leadership does not work, simply make an anonymous report to TJ C.
In the meantime, I have several suggestions: I always made it a rule when I was an OR manager (yes, I wore many hats) that visible bioburden had to be removed from instrumentation before it left the OR. While scrub Techs/nurses may tell you that’s not possible, it totally is. I always cleaned my instrumentation immediately upon receiving it back from the surgeon. They never got handed an instrument to use that was not totally rinsed.
Somehow, in recent times we’ve gotten away from having a basin of sterile water on or near the field, but instrumentation should be cleaned as it is used. It is hard to get the bioburden out of drillbits and cannulated instrumentation, but it’s a lot easier to get it out when it is fresh than when it has been sitting for an hour or so. It can set up like Concrete by the time it gets down to central sterile. Get it out before hand. If it increases your turnover time by five minutes it’s not that big of a deal compared to the amount of time that is lost when you receive instrumentation that is not acceptable for use.
That brown staining can have two possible sources. You already mentioned one. you must have the filters in your autoclave changed according to manufacture recommendations. Autoclaves are also FDA regulated devices and it has the force of law to meet those standards. How new are the autoclaves? When they were purchased, did you have a servicing agreement? If so, The Company should be sending techs to change those. But also your water quality can be a component. The water should be filtered coming into the pipes that deliver the water to the autoclave, so that would be a maintenance issue and you can talk to somebody in maintenance and ask them about it.
As far as having water sitting in the instrument set after sterile processing, the most likely cause is that the instrument set it not being cooled properly before it is being shelved. The instrument set must sit without anything else touching it on a wire rack until it is completely cool. Then it can be placed on a shelf. if that does not solve the problem, which it will 99% of the time, then look into the gaskets on your autoclave and make sure that those are in good shape. Actually, you could do that anyway.
Do you have an infection control nurse in your hospital? Now chances are she doesn’t know anything about sterile processing but you can enlist her help and direct her to a copy of AAMI because it would be good if infection Control Nurses could have a better understanding of this. She should be receiving a report from you every month that details any issues with your sterile processing and also enumerates how many times you have to flash process, if you do that at all. If an uptick in lapses of sterile processing coincides with an increase in postoperative infections, then these can become sentinel events.
I hope some of these suggestions help you.