Hi, everyone,
We have a hospital system with two campuses about five miles apart. Each
campus has its own blood bank under its lab's own CAP number, but there is
one manager and one director (me) over both blood banks. Patients are
frequently transferred from one campus to another. In some cases, blood
products have been crossmatched or otherwise assigned for transfusion, but
not yet transfused, at time of transfer. We have required that when a
patient is transferred from campus A to campus B, their assigned blood
products are sent with them only if they are "hanging" (being transfused) at
the time. Any other units being held for them are de-assigned, and the
patient is redrawn for compatibility testing at campus B.
I'm not sure what the regulatory requirements are. CAP staff was
characteristically
delphic when our manager called. We called other
hospitals nearby, and they do what we do. Our nursing staff is complaining
that the patient has to be redrawn and retested after transfer, and this is
redundant, since we have already prepared the units at campus A. I would
like to not repeat testing, and instead send the assigned products over with
the patient, but I know that blood bank rules are insane and defy logic. Any
suggestions?
Thanks!
Ed
Ed Uthman, MD
Pathologist, Houston/Richmond, Texas, USA
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Date: Fri, 17 Apr 2015
I'd transfer the blood products and, if you
do not share a computer system (which would make the issue moot, so I'm assuming
you do not), the compatibility testing records for those transferred units
(perhaps a screen dump or printout). If you use the same techniques and general
approach, I see no rational reason for repeating the work.
If you share a computer system (Wyndgate and Soft, as we do with a sister
hospital), the patients and compatibility records are identical and there is no
need for retesting. It's obviously suboptimal patient care to redraw patients
who do not need to be redrawn, and a waste of everyone's time, energy and
resources.
Blood Bank rules are made to protect patients, not for
mindless bureaucracy (one hopes),
so as long as you document that the i's have been dotted and the t's crossed
sufficiently to protect the patient, you're golden, in my view. Do the right
thing rather than what some possibly
arbitrary not very nuanced regulatory or accreditation inspector suggests.
You can quote me on that :).
Hope this helps,
Neil