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pbaker

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Posts posted by pbaker

  1. We keep our transfusion orders in a binder and place a unit number sticker on the paper when we issue a unit.  When the patient is discharged or the specimen expires, the order is removed from the binder.

    When we went to electronic issue, we were able to decrease our routine inventory significantly because we no longer moved units back and forth from XM to available to XM to available.  We are still working to teach the physicians not to order products until they actually need to transfuse.  However, we did get the "keep ahead" order removed from the order set.  Baby steps ;)

  2. The "issued by" is captured at the time of issue by who is logged on and performing the task.  We scan employee badges to capture the "issued to" employee.  We do not assign/XM/dispense anything until the courier is at the window to pick it up. Cerner does that for you when you use computer issue.  (Unless it is a RBC for patient with an antibody, then full XM ahead of issue) 

  3. About half of our surgery patients are first timers to the blood bank.  Since we need two independent types, we use the pre admit type and screen as the first type and a heads up for any antibodies.  They always get redrawn the day of surgery for the type and screen we will crossmatch with.  That may be 28 days later or the next day.  We then have 2 independent types for our ABO/Rh confirmation.  We do not extend sample dates past 3 days without a really, really good reason and pathology approval.

  4. We use encounter (visit) for platelets and plasma.  If they go home in the morning and come back in the evening, that is a new encounter, so a new blood type.  We do not require a screen for plasma products.  We do have lots of oncology patients that get a recurring encounter that is good for 30 days.  After that 30 days we do another type.  Red cell products require every 3 days or new encounter, whichever comes first.

  5. We are adding weak D testing to our automation menu and are attempting our validations.  We have plenty of weak D negative specimens to run, but no weak D positive specimens.  I contacted our blood supplier, but they send their specimen processing out, so they no longer have samples to share with us.  Does anyone no of a way to manufacture a weak D positive cell?  Or any other suggestions where we might be able to obtain some for our validation.

  6. When ice builds up in our freezer, the defrost temp tends to peak much higher, sometimes out of range.  If we let that go on too long, the freezer dies completely.  After we do a manual defrost, the defrost temp stays much lower.  So I think your maintenance guys are right that it only needs a small defrost range.

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