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Medical Forum / General / Laboratory / February 2004

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High APTT levels

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Sargum - 09 Feb 2004 21:44 GMT
Hello,

We are conducting an animal study where we want to measure APTT and PT
levels in dogs every week.  We have been sending citrated plasma to
laboratories that deal with human specimens and have gotten clotting
times of >150 for APTT.  I have spoken with some vets and they say
that taking the sample to human lab should not really make a
difference except that the clot detection time needs to be adjusted to
an earlier reading (say 5 seconds instead of 10 seconds) since dogs
clot faster.  Other suggestions include:

(1)filling blue-top with blood all the way to the top
(2)invert tubes 5X immediately
(3)freeze plasma if >2 hours, else put on ice and run test w/i 2 hours

The dogs are given tranquilizer before a blood draw so they hold
still.  There are no anticoagulants given.  Can someone give us
insight as to why the APTT levels are off the charts?  Drugs?
Coagulation reagant differences? The dogs are not hemophiliacs; they
heal well after surgery.

Any help will be greatly appreciated.  

Sue
Manky Badger - 09 Feb 2004 22:37 GMT
> Hello,
>
[quoted text clipped - 16 lines]
> Coagulation reagant differences? The dogs are not hemophiliacs; they
> heal well after surgery.

If the APTTs are ALL high then there is a problem with the samples.
Either under or overfilling the sample bottles, or the samples are becoming
activated prior to analysis.

MB
al.green - 09 Feb 2004 23:03 GMT
We had similar problems because we were getting coag errors on samples.  It
appears to the machine it did not clot because it did not detect since it
clots prior to the analyzer reading the turbidity.  In actuality, the result
is probably a "Less Than" instead of a "Greater Than"

We use an ACL7000 coag analyzer.  If you check your rotors after it gives
you a no coag result, check the rotor manually to see if there was a clot
formed.  If there is, the clot probably formed prior to the analyzer being
able to detect the clot.

Al
> Hello,
>
[quoted text clipped - 20 lines]
>
> Sue
Robert - 10 Feb 2004 00:05 GMT
> We had similar problems because we were getting coag errors on samples.  It
> appears to the machine it did not clot because it did not detect since it
[quoted text clipped - 31 lines]
> >
> > Sue

I would agree with that.  Depending on the machine you use, it is always
wise to check the optical curve on where it starts and ends up at.
The alternative would be to use non optical machines and more mechanical
ones such as old fashion fibrometer.
al.green - 09 Feb 2004 23:06 GMT
I also forgot to mention, we see the same problem with PT's because the
times are less than human times.

al
> Hello,
>
[quoted text clipped - 20 lines]
>
> Sue
ES - 11 Feb 2004 02:19 GMT
>(1)filling blue-top with blood all the way to the top
>(2)invert tubes 5X immediately

Those two should not be just a suggestion but are absolutely
necessary.
Penn - 13 Feb 2004 01:39 GMT
I'm a little late getting this thread, but have all pre-analytical
variables been examined? I know it sounds stupid, but if the blood was
drawn via some sort of lock or catheter, there may be a tiny amount of
heparin in the reservior (i.e. standard practice when starting an I.V.
catheter without infusing anything is to inject a small amount of heparin
into the catheter to keep it from plugging up with a clots, then tubing
can be attached later for infusion of saline, etc.) I don't imagine
bleeding a dog is easy, nor would starting an I.V., so I was thinking this
might be the case in vetrinary medicine also. Perhaps someone else can
speak to that.  I do, however, remember several occassions where a bad
venipuncture caused erroneous results even in the absence of visible
hemolysis. Just some random thoughts.

> Hello,
>
[quoted text clipped - 20 lines]
>
> Sue
kuhnfucius - 23 Feb 2004 02:58 GMT
I know that the human setting on Ca analyzers reads the PTT at 50%
completion on the curve.  For animals it is usually set at 75%.  To make
this change for a human lab is not practical and you may not get the results
that are right for you.

Signature

Detective Tom Polhaus:  " Heavy.  What
is it?"
Sam Spade:  "The, uh, stuff that dreams
are made of."

> I'm a little late getting this thread, but have all pre-analytical
> variables been examined? I know it sounds stupid, but if the blood was
[quoted text clipped - 33 lines]
> >
> > Sue
Robert - 24 Feb 2004 04:57 GMT
> I know that the human setting on Ca analyzers reads the PTT at 50%
> completion on the curve.  For animals it is usually set at 75%.  To make
> this change for a human lab is not practical and you may not get the results
> that are right for you.

We are involved in the Polyheme study involving out in the field infusion of
a hemoglobin solution.  Samples collected from these patients will all show
moderate to severe hemolysis and as a result a limited menu of testing will
be done on these patients when they are brought in to the ER. We will be
dusting off our old Fibrometers and performing PT and PTT's. If the results
on this patients are promising then more labs will have to use old fashion
clot detectors instead of optical ones for these patients.
kuhnfucius - 25 Feb 2004 21:12 GMT
there is an instrument on the market that does both automated photo-optical
and electro-mechanical.

Signature

Detective Tom Polhaus:  " Heavy.  What
is it?"
Sam Spade:  "The, uh, stuff that dreams
are made of."

>
> > I know that the human setting on Ca analyzers reads the PTT at 50%
[quoted text clipped - 10 lines]
> on this patients are promising then more labs will have to use old fashion
> clot detectors instead of optical ones for these patients.
 
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