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Arterial blood gas test

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Arterial-blood gas test
MeSHD001784
MedlinePlus003855
LOINC24336-0

An arterial blood gas (ABG) test, or arterial blood gas analysis (ABGA) measures the amounts of arterial gases, such as oxygen and carbon dioxide. An ABG test requires that a small volume of blood be drawn from the radial artery with a syringe and a thin needle,[1] but sometimes the femoral artery in the groin or another site is used. The blood can also be drawn from an arterial catheter.

An ABG test measures the blood gas tension values of the arterial partial pressure of oxygen (PaO2), and the arterial partial pressure of carbon dioxide (PaCO2), and the blood's pH. In addition, the arterial oxygen saturation (SaO2) can be determined. Such information is vital when caring for patients with critical illnesses or respiratory disease. Therefore, the ABG test is one of the most common tests performed on patients in intensive-care units. In other levels of care, pulse oximetry plus transcutaneous carbon-dioxide measurement is a less invasive, alternative method of obtaining similar information.[citation needed]

An ABG test can indirectly measure the level of bicarbonate in the blood. The bicarbonate level is calculated using the Henderson-Hasselbalch equation. Many blood-gas analyzers will also report concentrations of lactate, hemoglobin, several electrolytes, oxyhemoglobin, carboxyhemoglobin, and methemoglobin. ABG testing is mainly used in pulmonology and critical-care medicine to determine gas exchange across the alveolar-capillary membrane. ABG testing also has a variety of applications in other areas of medicine. Combinations of disorders can be complex and difficult to interpret, so calculators,[2] nomograms, and rules of thumb[3] are commonly used.

ABG samples originally were sent from the clinic to the medical laboratory for analysis. Newer equipment lets the analysis be done also as point-of-care testing, depending on the equipment available in each clinic.

Sampling and analysis

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Bench top analyzer ABL800 FLEX - Radiometer Medical
Modern, blood gas analyzer. This device is capable of reporting pH, pCO2, pO2, SatO2, Na+, K+, Cl, Ca2+, Hemoglobin (total and derivatives: O2Hb, MetHb, COHb, HHb, CNHb, SHb ), Hematocrit, Total bilirubin, Glucose, Lactate and Urea. (Cobas b 221 - Roche Diagnostics).

Arterial blood for blood-gas analysis is usually drawn by a respiratory therapist and sometimes a phlebotomist, a nurse, a paramedic or a doctor.[4] Blood is most commonly drawn from the radial artery because it is easily accessible, can be compressed to control bleeding, and has less risk for vascular occlusion. The selection of which radial artery to draw from is based on the outcome of an Allen's test. The brachial artery (or less often, the femoral artery) is also used, especially during emergency situations or with children. Blood can also be taken from an arterial catheter already placed in one of these arteries.[5]

There are plastic and glass syringes used for blood gas samples.[6] Most syringes come pre-packaged and contain a small amount of heparin, to prevent coagulation. Other syringes may need to be heparinised, by drawing up a small amount of liquid heparin and squirting it out again to remove air bubbles. Once the sample is obtained,[7] care is taken to eliminate visible gas bubbles, as these bubbles can dissolve into the sample and cause inaccurate results. The sealed syringe is taken to a blood gas analyzer.[8] If a plastic blood gas syringe is used, the sample should be transported and kept at room temperature and analyzed within 30 min. If prolonged time delays are expected (i.e., greater than 30 min) prior to analysis, the sample should be drawn in a glass syringe and immediately placed on ice.[9] Standard blood tests can also be performed on arterial blood, such as measuring glucose, lactate, hemoglobins, dyshemoglobins, bilirubin and electrolytes.[citation needed]

Derived parameters include bicarbonate concentration, SaO2, and base excess. Bicarbonate concentration is calculated from the measured pH and PCO2 using the Henderson-Hasselbalch equation. SaO2 is derived from the measured PO2 and calculated based on the assumption that all measured hemoglobin is normal (oxy- or deoxy-) hemoglobin.[10]

Calculations

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Detail of measurement chamber of a modern blood gas analyzer showing the measurement electrodes. (Cobas b 121 - Roche Diagnostics)

The machine used for analysis aspirates this blood from the syringe and measures the pH and the partial pressures of oxygen and carbon dioxide. The bicarbonate concentration is also calculated. These results are usually available for interpretation within five minutes.[citation needed]

Two methods have been used in medicine in the management of blood gases of patients in hypothermia: pH-stat method and alpha-stat method. Recent studies suggest that the α-stat method is superior.[citation needed]

  • pH-stat: The pH and other ABG results are measured at the patient's actual temperature. The goal is to maintain a pH of 7.40 and the arterial carbon dioxide tension (paCO2) at 5.3 kPa (40 mmHg) at the actual patient temperature. It is necessary to add CO2 to the oxygenator to accomplish this goal.
  • α-stat (alpha-stat): The pH and other ABG results are measured at 37 °C, despite the patient's actual temperature. The goal is to maintain the arterial carbon dioxide tension at 5.3 kPa (40mmHg) and the pH at 7.40 when measured at +37 °C.

Both the pH-stat and alpha-stat strategies have theoretical disadvantages. α-stat method is the method of choice for optimal myocardial function. The pH-stat method may result in loss of autoregulation in the brain (coupling of the cerebral blood flow with the metabolic rate in the brain). By increasing the cerebral blood flow beyond the metabolic requirements, the pH-stat method may lead to cerebral microembolisation and intracranial hypertension.[10]

Guidelines

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  1. A 1 mmHg change in PaCO2 above or below 40 mmHg results in 0.008 unit change in pH in the opposite direction.[11]
  2. The PaCO2 will decrease by about 1 mmHg for every 1 mEq/L reduction in [HCO
    3
    ] below 24 mEq/L
  3. A change in [HCO
    3
    ] of 10 mEq/L will result in a change in pH of approximately 0.15 pH units in the same direction.
  4. Assess relation of pCO2 with pH: If pCO2 & pH are moving in opposite directions i.e., pCO2 ↑ when pH is <7.4 or pCO2 ↓ when pH > 7.4, it is a primary respiratory disorder. If pCO2 & pH are moving in same direction i.e., pCO2 ↑when pH is >7.4 or pCO2 ↓ when pH < 7.4, it is a primary metabolic disorder.[12]

Parameters and reference ranges

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These are typical reference ranges, although various analysers and laboratories may employ different ranges.

Analyte Range Interpretation
pH 7.34–7.44[13] The pH or H+ indicates if a person is acidemic (pH < 7.35; H+ >45) or alkalemic (pH > 7.45; H+ < 35).
H+ 35–45 nmol/L (nM)
Arterial oxygen partial pressure (PaO2) 10–13 kPa
75–100 mmHg[13]
A low PaO2 indicates abnormal oxygenation of blood and a person is known as having hypoxemia. (Note that a low PaO2 is not required for the person to have hypoxia as in cases of Ischemia, a lack of oxygen in tissues or organs as opposed to arterial blood.) At a PaO2 of less than 60 mm Hg, supplemental oxygen should be administered.
Arterial carbon dioxide partial pressure (PaCO2) 4.7–6.0 kPa
35–45 mmHg[13]
The carbon dioxide partial pressure (PaCO2) is an indicator of CO2 production and elimination: for a constant metabolic rate, the PaCO2 is determined entirely by its elimination through ventilation.[14] A high PaCO2 (respiratory acidosis, alternatively hypercapnia) indicates underventilation (or, more rarely, a hypermetabolic disorder), a low PaCO2 (respiratory alkalosis, alternatively hypocapnia) hyper- or overventilation.
HCO3 22–26 mEq/L The HCO3 ion indicates whether a metabolic problem is present (such as ketoacidosis). A low HCO3 indicates metabolic acidosis, a high HCO3 indicates metabolic alkalosis. As this value when given with blood gas results is often calculated by the analyzer, correlation should be checked with total CO2 levels as directly measured (see below).
SBCe 21 to 27 mmol/L the bicarbonate concentration in the blood at a CO2 of 5.33 kPa, full oxygen saturation and 37 Celsius.[15]
Base excess −2 to +2 mmol/L The base excess is used for the assessment of the metabolic component of acid-base disorders, and indicates whether the person has metabolic acidosis or metabolic alkalosis. Contrasted with the bicarbonate levels, the base excess is a calculated value intended to completely isolate the non-respiratory portion of the pH change.[16]

There are two calculations for base excess (extra cellular fluid - BE(ecf); blood - BE(b)). The calculation used for the BE(ecf) = [HCO3]− 24.8 + 16.2 × (pH − 7.4). The calculation used for BE(b) = (1 − 0.014 × Hgb) × ([HCO3]− 24.8 + (1.43 × Hgb + 7.7) × (pH − 7.4).

total CO2 (tCO2 (P)c) 23–30 mmol/L[17]
100–132 mg/dL[18]
This is the total amount of CO2, and is the sum of HCO3 and PCO2 by the formula: tCO2 = [HCO3] + α×PCO2, where α=0.226 mM/kPa, HCO3 is expressed in millimolar concentration (mM) (mmol/L) and PCO2 is expressed in kPa
O2 Content (CaO2, CvO2, CcO2) 94-100%[19]
(mL O2/dL blood)
This is the sum of oxygen dissolved in plasma and chemically bound to hemoglobin as determined by the calculation: CaO2 = (PaO2 × 0.003) + (SaO2 × 1.34 × Hgb) where hemoglobin concentration is expressed in g/dL.[20]

Contamination of the sample with room air will result in abnormally low carbon dioxide and possibly elevated oxygen levels, and a concurrent elevation in pH. Delaying analysis (without chilling the sample) may result in inaccurately low oxygen and high carbon dioxide levels as a result of ongoing cellular respiration.

pH

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Pathophysiology sample values
BMP/ELECTROLYTES:
Na+ = 140 Cl = 100 BUN = 20 /
Glu = 150
\
K+ = 4 CO2 = 22 PCr = 1.0
ARTERIAL BLOOD GAS:
HCO3 = 24 paCO2 = 40 paO2 = 95 pH = 7.40
ALVEOLAR GAS:
pACO2 = 36 pAO2 = 105 A-a g = 10
OTHER:
Ca = 9.5 Mg2+ = 2.0 PO4 = 1
CK = 55 BE = −0.36 AG = 16
SERUM OSMOLARITY/RENAL:
PMO = 300 PCO = 295 POG = 5 BUN:Cr = 20
URINALYSIS:
UNa+ = 80 UCl = 100 UAG = 5 FENa = 0.95
UK+ = 25 USG = 1.01 UCr = 60 UO = 800
PROTEIN/GI/LIVER FUNCTION TESTS:
LDH = 100 TP = 7.6 AST = 25 TBIL = 0.7
ALP = 71 Alb = 4.0 ALT = 40 BC = 0.5
AST/ALT = 0.6 BU = 0.2
AF alb = 3.0 SAAG = 1.0 SOG = 60
CSF:
CSF alb = 30 CSF glu = 60 CSF/S alb = 7.5 CSF/S glu = 0.6

The normal range for pH is 7.35–7.45. As the pH decreases (< 7.35), it implies acidosis, while if the pH increases (> 7.45) it implies alkalosis. In the context of arterial blood gases, the most common occurrence will be that of respiratory acidosis. Carbon dioxide is dissolved in the blood as carbonic acid, a weak acid; however, in large concentrations, it can affect the pH drastically. Whenever there is poor pulmonary ventilation, the carbon dioxide levels in the blood are expected to rise. This leads to a rise of carbonic acid, leading to a decrease in pH. The first buffer of pH will be the plasma proteins, since these can accept some H+ ions to try to maintain acid-base homeostasis. As carbon dioxide concentrations continue to increase (PaCO2 > 45 mmHg), a condition known as respiratory acidosis occurs. The body tries to maintain homeostasis by increasing the respiratory rate, a condition known as tachypnea. This allows much more carbon dioxide to escape the body through the lungs, thus increasing the pH by having less carbonic acid. If a person is in a critical setting and intubated, one must increase the number of breaths mechanically.[citation needed]

Respiratory alkalosis (Pa CO2 < 35 mmHg) occurs when there is too little carbon dioxide in the blood. This may be due to hyperventilation or else excessive breaths given via a mechanical ventilator in a critical care setting. The action to be taken is to calm the person and try to reduce the number of breaths being taken to normalize the pH. The respiratory pathway tries to compensate for the change in pH in a matter of 2–4 hours. If this is not enough, the metabolic pathway takes place.[citation needed]

Under normal conditions, the Henderson–Hasselbalch equation will give the blood pH

where:

The kidney and the liver are two main organs responsible for the metabolic homeostasis of pH. Bicarbonate is a base that helps to accept excess hydrogen ions whenever there is acidaemia. However, this mechanism is slower than the respiratory pathway and may take from a few hours to 3 days to take effect. In acidaemia, the bicarbonate levels rise, so that they can neutralize the excess acid, while the contrary happens when there is alkalaemia. Thus when an arterial blood gas test reveals, for example, an elevated bicarbonate, the problem has been present for a couple of days, and metabolic compensation took place over a blood acidaemia problem.[citation needed]

In general, it is much easier to correct acute pH derangement by adjusting respiration. Metabolic compensations take place at a much later stage. However, in a critical setting, a person with a normal pH, a high CO2, and a high bicarbonate means that, although there is a high carbon dioxide level, there is metabolic compensation. As a result, one must be careful as to not artificially adjust breaths to lower the carbon dioxide. In such case, lowering the carbon dioxide abruptly means that the bicarbonate will be in excess and will cause a metabolic alkalosis. In such a case, carbon dioxide levels should be slowly diminished.[citation needed]

Arterial versus venous blood

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Since the advent of pulse oximetry which measures oxygen saturation transcutaneously and is non-invasive, arterial blood is seldom used for the determination of oxygenation outside the ICU. Acid base status can be determined with venous blood precluding the pain and inconvenience of arterial blood sampling in most cases. When an indwelling arterial line catheter is present, arterial blood is easy to obtain and still used. Venous blood is generally used otherwise, usually from a peripheral vein, such as a forearm vein. The values of pH and HCO3 of venous blood are close enough to arterial blood for direct comparison. The pCO2 of venous blood is less reliably compared to arterial blood but may be used in some cases. The PO2 level of venous blood is always significantly lower that arterial and should be reported, labeled and interpreted as venous PO2. [21]

See also

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References

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  1. ^ Dr Colin Tidy (26 Jan 2015). "Arterial Blood Gases - Indications and Interpretation". Patient. Reviewed by Dr Adrian Bonsall. Retrieved 2017-01-02.
  2. ^ Baillie K. "Arterial Blood Gas Interpreter". prognosis.org. Archived from the original on 2013-03-12. Retrieved 2007-07-05. - Online arterial blood gas analysis
  3. ^ Baillie, JK (2008). "Simple, easily memorised 'rules of thumb' for the rapid assessment of physiological compensation for acid-base disorders". Thorax. 63 (3): 289–90. doi:10.1136/thx.2007.091223. PMID 18308967.
  4. ^ Aaron SD, Vandemheen KL, Naftel SA, Lewis MJ, Rodger MA (2003). "Topical tetracaine prior to arterial puncture: a randomized, placebo-controlled, clinical trial". Respir. Med. 97 (11): 1195–1199. doi:10.1016/S0954-6111(03)00226-9. PMID 14635973.
  5. ^ Hager, Heather H.; Burns, Bracken (2024), "Artery Cannulation", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 29489243, retrieved 2024-06-28
  6. ^ Wiwanitkit, Viroj (January 2006). "Glass syringes are better than plastic for preserving arterial blood gas for oxygen partial pressure determination: an explanation based on nanomaterial composition". International Journal of Nanomedicine. 1 (2): 223–224. doi:10.2147/nano.2006.1.2.223. PMC 2426785. PMID 17722540.
  7. ^ Potter, Lewis (7 January 2014). "How to take an Arterial Blood Gas (ABG) - OSCE Guide". Geeky Medics. Retrieved 24 February 2023.
  8. ^ Horn, Klaus; Gruber, Rudolf; Ugele, Bernhard; Küster, Helmut; Rolinski, Boris (1 October 2001). "Total Bilirubin Measurement by Photometry on a Blood Gas Analyzer: Potential for Use in Neonatal Testing at the Point of Care". Clinical Chemistry. 47 (10): 1845–1847. doi:10.1093/clinchem/47.10.1845. PMID 11568098.
  9. ^ Procedures for the Collection of Arterial Blood Specimens; Approved Standard—Fourth Edition (Procedures for the Collection of Arterial Blood Specimens; Approved Standard—Fourth Edition ). Clinical and Laboratory Standards Institute. 2004. ISBN 978-1-56238-545-3. Archived from the original on 2015-05-11. Retrieved 2015-04-27.
  10. ^ a b Kofstad J (1996). "Blood Gases and Hypothermia: Some Theoretical and Practical Considerations". Scand J Clin Lab Invest Suppl. 224: 21–26. doi:10.3109/00365519609088622. PMID 8865418.
  11. ^ Stoelting: Basics of Anesthesia, 5th ed. p 321.
  12. ^ "Arterial Blood Gas (ABG) In 4 Steps". www.edulanche.com/. EduLanche. Retrieved 2016-05-13.
  13. ^ a b c Normal Reference Range Table from The University of Texas Southwestern Medical Center at Dallas. Used in Interactive Case Study Companion to Pathologic basis of disease.
  14. ^ Baillie K, Simpson A. "Altitude oxygen calculator". Apex (Altitude Physiology Expeditions). Archived from the original on 2017-06-11. Retrieved 2006-08-10. - Online interactive oxygen delivery calculator
  15. ^ "Acid Base Balance (page 3)". June 13, 2002. Archived from the original on 2002-06-13.
  16. ^ "RCPA Manual: Base Excess (arterial blood)".
  17. ^ "ABG (Arterial Blood Gas)". Brookside Associates. Retrieved 2017-01-02.
  18. ^ Derived from molar values using molar mass of 44.010 g/mol
  19. ^ "Blood Gases". Retrieved 2023-04-18.
  20. ^ "Hemoglobin and Oxygen Transport Charles L". www.meddean.luc.edu.
  21. ^ Byrne, Anthony L; Bennett, Michael; Chatterji, Robindro; Symons, Rebecca; Pace, Nathan L; Thomas, Paul S (January 2014). "Peripheral venous and arterial blood gas analysis in adults: are they comparable? A systematic review and meta‐analysis". Respirology. 19 (2): 168–175. doi:10.1111/resp.12225. ISSN 1323-7799.
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