HMS Plus QC Management Plan
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Hello!
I am hoping to find another facility that has 5 or more HMS Plus instruments in their OR settings (Perfusion or Anesthesia) to get some QC management strategies.
We are a CAP accredited facility that has 6 HMS Plus devices that are run by our Anesthesia Techs. I am looking to gain some insight on better ways to manage the new lot CAP QC requirements due to the very short outdate of the HMS cartridges. We currently run the HR-ACT, HDR, Tan HPT, Blue HPT and Red HPT cartridges. Each device is in its own OR room and has a cart stocked with supplies. This leads to multiple different lots in use at one time because each room has different utilization amounts. The cartridges outdate is typically a month to 6 weeks so that is bringing in constant new lots. If you are a large site with multiple instruments, how are you managing to QC each device every 7 days, as well as each new lot/shipment of reagents and also staying in compliance with QCing each "in use" lot every 7 days?
Are your devices interfaced? if so, what middleware system do you use? Does the interface help in managing QC requirements?
We are not interfaced currently. The tech performing QC has a manual log that he records the lot information for cartridge and QC and the values. I have recently noticed that the information documented on the QC form does not match the lot information that is on the printout/entered into the device. Looking to build a better process to ensure accurate record keeping, all necessary QC runs are performed, and that we are ensuring excellent patient care!
Thank you in advance for your feedback!!
I am hoping to find another facility that has 5 or more HMS Plus instruments in their OR settings (Perfusion or Anesthesia) to get some QC management strategies.
We are a CAP accredited facility that has 6 HMS Plus devices that are run by our Anesthesia Techs. I am looking to gain some insight on better ways to manage the new lot CAP QC requirements due to the very short outdate of the HMS cartridges. We currently run the HR-ACT, HDR, Tan HPT, Blue HPT and Red HPT cartridges. Each device is in its own OR room and has a cart stocked with supplies. This leads to multiple different lots in use at one time because each room has different utilization amounts. The cartridges outdate is typically a month to 6 weeks so that is bringing in constant new lots. If you are a large site with multiple instruments, how are you managing to QC each device every 7 days, as well as each new lot/shipment of reagents and also staying in compliance with QCing each "in use" lot every 7 days?
Are your devices interfaced? if so, what middleware system do you use? Does the interface help in managing QC requirements?
We are not interfaced currently. The tech performing QC has a manual log that he records the lot information for cartridge and QC and the values. I have recently noticed that the information documented on the QC form does not match the lot information that is on the printout/entered into the device. Looking to build a better process to ensure accurate record keeping, all necessary QC runs are performed, and that we are ensuring excellent patient care!
Thank you in advance for your feedback!!
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What new CAP requirement are you referring to? As we have been getting pushback from the perfusionists to move Liquid QC to every 30 days with EQC every 8 hours.
We do not have a back up analyzer in the lab/POC office unfortunately, all devices are in use for cases. However, we just purchased 6 new devices to replace our old ones and are in the process of validating them. Thanks to your feedback, maybe we would be able to keep one of the old devices that would ultimately be sunset to have in our office for new lot performance. Our OR orders their own supplies and it gets delivered to them directly. We do have a fridge in the lab that they house supplies for the ABL90 and Hemochron that they can come grab so there may be potential to store their cartridges and QC down here. That would be taking on a whole new process for us and unfortunately the HMS is NOT a small analyzer to have in our small office but its an idea at least.
How do you manage having them enter the correct lot information into the device? Do you still see fallouts with this even though some of you are "checking out" the supplies?
I am also learning that most places this is run by Perfusion so I am not entirely sure why this is run by our Anesthesia Techs. I will have to dive into that as well.
Deborah, how are you able to have 30 Days for an IQCP plan? Ours is every 7 still even with an IQCP. I have personally never written an IQCP, just inherited all of the ones I have. I would love to hear more about/see your IQCP if you don't mind sharing. Even being able to drop the frequency down to every 30 days I think would drastically help!
Thank you all for your awesome feedback!