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/