ACT result complaints - looking for advice!
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We currently run HR-ACT on the Medtronic ACT+ (will shortly be converting to iSTAT, we are in the middle of the validation). I hardly ever hear a peep from ECMO, perfusion, cath lab with complaints on results. In the last week, the Cath Lab medical director has decided that the Medtronic meter they are using, "doesn't work". He thinks for the dose of heparin he is giving, he's not getting the ACT he expects.
There is nothing functionally wrong with the instrument - no EQC or AQC issues, it recently passed a PT event right on this mean, no errors, no nothing.
I'm currently working through laying out patient results with cartridge lot numbers, etc. Any chance this could be from a change in heparin lot or manufacturer? Is that still an issue?
Someone from nursing is supposed to be checking with pharmacy.
There is nothing functionally wrong with the instrument - no EQC or AQC issues, it recently passed a PT event right on this mean, no errors, no nothing.
I'm currently working through laying out patient results with cartridge lot numbers, etc. Any chance this could be from a change in heparin lot or manufacturer? Is that still an issue?
Someone from nursing is supposed to be checking with pharmacy.
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As far as I know, the iSTAT ACTc/ACtk will work with all heparin doses. Good luck!
Myself and an iSTAT applications manager have walked through their process with them in depth and provided feedback for best practices. Oh the things you discover when you spend more time with them... The timing of their post-heparin dose ACT was all over the place. Anywhere from 25 minutes to almost an hour. So we're trying to get them to clean that up and test at specific times but that's easier said than done.
At this point, we're just trying to get switched over to iSTAT ASAP because the providers "like those results better".
Especially in house patients receiving heparin therapy; they can end up deficient in ATIII and then heparin can't do its job properly.