Print

Print


        Theory may not always match reality and I do not think you can
assume that whole blood levels will always equal plasma results when
using electrodes for measurements.

        We have several ABL 725 analyzers and perform monthly
comparisons on a few samples to confirm agreement. (whole blood versus
plasma from those whole blood samples).  The glucose results from the
ABL match the plasma glucose levels reliably, in our experience.  (I
don't have data handy, but can forward comparison data at a later date).
The close match of the results is likely a result of electrode design
and the calibrators.

        On the other hand, glucose meters are  (or  were) notorious for
generating different results on whole blood and plasma and only recent
changes to the design of the test strips reduced the impact of
hematocrit on some meter models.  There are a number of reports
published on the impact of hematocrit on electrolyte measurements by
ISE. It may be that glucose enzymatic-biosensors are less prone to
hematocrit effects that potentiometric electrodes, but I'm certain that
generalization can be made.  Those are my thoughts...... Regards, Andrew

Dr. Andrew W. Lyon
Univ. Calgary, Calgary, AB, Canada





-----Original Message-----
From: clinical biochemistry discussion list
[mailto:[log in to unmask]] On Behalf Of John Whitfield
Sent: May 7, 2002 7:05 PM
To: [log in to unmask]
Subject: Glucose measurements in blood gas analysers - whole blood or
plasma?


I have been asked whether glucose results from our blood gas analyser
are equivalent to plasma glucose or whole blood glucose. This arose from
a discussion of whether we should quote a different reference range
depending on the method of analysis.

My preliminary scientific answer is that the electrode is in contact
with the plasma phase of the whole blood and therefore the result given
is the plasma glucose (just as the potassium result is the plasma
potassium).

On the less scientific and more practical side, one could say that since
no-one is going to run their GTTs through this kind of system, and
anyone who gets a blood gas sample analysed is pretty sick, a few
percent difference doesn't really matter anyway.

The system in question is the Radiometer ABL 725, but the principle
should apply to any electrode-based system. Does anyone have a contrary
opinion, or data, so we don't have to do a comparison?

thanks

John Whitfield
Clinical Biochemistry
Royal Prince Alfred Hospital
Sydney, Australia


Phone (+61) 2 9515 5246
Fax (+61) 2 9515 7931

Disclaimer:
This message is intended for the named addressee and may contain
confidential information. If you are not the intended recipient, please
disregard it. Views are those of the sender and not necessarily those of
Royal Prince Alfred Hospital or Central Sydney Area Health Service.

------ACB discussion List Information--------
This is an open discussion list for the academic and clinical community
working in clinical biochemistry. Please note, archived messages are
public and can be viewed via the internet. Views expressed are those of
the individual and they are responsible for all message content.

ACB Web Site
http://www.acb.org.uk
List Archives http://www.jiscmail.ac.uk/lists/ACB-CLIN-CHEM-GEN.html
List Instructions (How to leave etc.) http://www.jiscmail.ac.uk/

------ACB discussion List Information--------
This is an open discussion list for the academic and clinical
community working in clinical biochemistry.
Please note, archived messages are public and can be viewed
via the internet. Views expressed are those of the individual and
they are responsible for all message content.

ACB Web Site
http://www.acb.org.uk
List Archives
http://www.jiscmail.ac.uk/lists/ACB-CLIN-CHEM-GEN.html
List Instructions (How to leave etc.)
http://www.jiscmail.ac.uk/