Arterial blood gas accuracy in the pulmonary function lab.
There are steps we can take to make sure that the accuracy of the arterial blood gas sample is maintained. It is important that the sample be of purely arterial content. Even the smallest amount of venous blood can change the results radically. For example, a not uncommon error is to observe the flash of blood in the hub of the needle and seeing that the blood is a very dark and is probably venous, withdrawing the needle slightly and repositioning and then pushing the needle in again to find the artery. If the artery is then found successfully, although the vast bulk of the syringe volume will be arterial blood, the small amount of venous blood mixed in, will result in significant changes in most of the values, especially P[O.sub.2], even if the venous sample volume was very small compared to the arterial sample volume.
Arterial samples should be completely anaerobic. Whatever type of syringe is used, as soon as withdrawing the sample is complete, the syringe should be held upright and the room air bubble should be burped out of the syringe by flicking the syringe with a finger to get the bubble on top in the neck of the syringe and then pushing the barrel to extrude the bubble into the needle and out into the cap. New syringes have self sealing barrels which seal when contact with blood is made. During the actual blood gas draw, these self sealing barrels allow the sample to rise up into syringe and seal without a risk of aerobic contamination.
Calibration standard of the common brand of arterial blood gas analyzers are documented in the Clinical and Laboratory Standard Institute. For P[O.sub.2] and PC[O.sub.2] electrodes, gas calibrations should be performed often and quality assurance involves analyzing either manufactures or laboratory tonometered test samples. If calibration and quality assurance is not performed as indicated then blood gas results will be inaccurate and patient safety will be compromised.
It is true that air contamination of arterial blood specimens can alter blood gas values. Room air at sea level has a P[O.sub.2] of approximately 150 mmHg and a PC[O.sub.2] of near zero.
[P.sub.1][O.sub.2] = FI[O.sub.2] (PB-47)
= 0.21 (760-47
= 0.21 (713)
[P.sub.1][O.sub.2] = partial pressure of inspired [O.sub.2]
[F.sub.1][O.sub.2] = fractional % of inspired [O.sub.2]
[P.sub.B] = barometric pressure
47 = partial pressure of water vapor
If air bubbles are present in a blood gas sample, equilibrium of gases between the sample and air occurs, but no matter how large the bubble or no matter how much mixing is done, the combined P[O.sub.2] and PC02 can not exceed 150 mmHg at sea level and at normal barometric pressure. Reporting arterial blood gas results with combined P[O.sub.2] and PC[O.sub.2] of over 150 mmHg is the most common error in blood gas analysis. When the blood gas results are returned from the laboratory in which they were analyzed and if the sum of P[O.sub.2] and PC[O.sub.2] exceeds 150 mmHg, then we know that there must have been an error in the machine analysis, since with normal barometric pressures at sea level, the maximum sum can only be 150 mmHg. There just is not enough oxygen in the room air bubble to result in the sum of P[O.sub.2] and PC[O.sub.2] being higher.
A question was raised in our institution as to whether or not an arterial blood gas sample might see a change in partial pressure of either oxygen or carbon dioxide if the sample is placed into a pneumatic tube system with or without a bubble. The thought is that the sudden increase or decrease in barometric pressure might force oxygen from the air in the bubble present in the sample into solution and result in a change in partial pressure. We have done systematic trials with samples being sent through pneumatic tubes and found that no changes in partial pressure are evident. In any case the laws of physics described in the above paragraph dictate that any bubble, no matter what the barometric pressure change, will not cause any changes in partial pressure of oxygen or carbon dioxide.
We are often advised that arterial blood gas samples should be analyzed within 20 minutes of drawing and if the analysis is delayed, the metabolism of cellular components will draw down oxygen and add carbon dioxide. The fact is that despite the caveats about leukocyte and erythrocyte metabolism, even after one hour, there are no significant changes in either P[O.sub.2] or PC[O.sub.2].
Also, as discussed in my article published in the March/April 2007 issue of Focus, blood gas samples in plastic syringes should never be placed in ice or in ice slush. If an arterial blood sample in a plastic syringe is placed in ice slush for even fifteen minutes, the partial pressure can cause an increase in P[O.sub.2] of up to 20 mmHg or higher. Any false increase in P[O.sub.2] can be critical in pulmonary diagnostic tests involving respiratory care patients. An arterial sample kept in a glass syringe in ice slush will not result in an increase in P[O.sub.2] since glass is not permeable to oxygen. It is unfortunate that sixteen years after word went out that arterial blood gas samples in plastic syringes should not be stored in ice slush before analysis, many pulmonary function technologists and respiratory therapists are still icing arterial blood gas samples.
The drawing of arterial blood gas samples and their analysis, whether we perform the analysis or not, are very important for patient care and are a crucial component of pulmonary function testing.
Jim Harvey RRT, RPFT
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|Title Annotation:||PULMONARY FUNCTION|
|Publication:||FOCUS: Journal for Respiratory Care & Sleep Medicine|
|Date:||Jun 22, 2016|
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