Table of Contents
Alveolar Gas Equation
The partial pressure of oxygen in the alveoli can be calculated using the following alveolar gas equation:
PAO2 = PiO2 – (PaCO2/R)
PAO2 = Partial pressure of oxygen in alveoli
PiO2 = Partial pressure of oxygen in inspired air
PaCO2 = Partial pressure of CO2 in arterial blood
R = Respiratory quotient
where PAO2 is the partial pressure of oxygen in the alveoli, PiO2 is the partial pressure of oxygen in inspired air, PaCO2 denotes the partial pressure of CO2 in arterial blood, and R represents the respiratory quotient.
This is the simplest form of the alveolar gas equation provided by Rossier and Mean. Other versions of the alveolar gas equation are as follows:
- West: PAO2 = PiO2 – (PaCO2/R) + K
where K = FiO2 x PaCO2 x [(1–R)/R]
Under most clinical conditions, the value of K is not large enough to make a difference in the value of PAO2, and hence can be neglected.
- Riley: PAO2 = PiO2 – (PaCO2/R) x [1 – Fi2(1–R)]
The difference between the values of PAO2 calculated using the above 2 equations is only due to inert gas exchange; hence, they can be used to calculate the concentration effect.
- Selkurt: PAO2 = PiO2 – PaCO2 x [FiO2 + (1 – FiO2)/R]
- Filley, MacIntosh & Wright: PAO2 = PiO2 – PaCO2 x [(PiO2 – PĒO2)/PĒCO2]
This equation facilitates the disequilibria of inert gases. Therefore, it can be used during induction or recovery from anesthesia. Important assumptions for the above equation are:
- Metabolic minute production of carbon dioxide is constant.
- PACO2 = PaCO2, as the alveolar membrane is thin and carbon dioxide is highly diffusible.
- Alveolar and inspired gasses follow the ideal gas law (PV = nRT).
- Inspired gas contains no CO2 or water.
- All other gases except oxygen in the inspired gas are in equilibrium with their dissolved states in the blood.
- The alveolar gas is saturated with water.
- Note that PiO2 = (Patm – PH2O) x FiO2.
Patm = Atmospheric pressure (760 mm Hg at sea level)
PH2O = Water vapor pressure (47 mm Hg at body temperature)
FiO2 = Fraction of inspired oxygen (0.21 in room air)
Thus, at normal body temperature, while breathing room air at sea level,
PiO2 = (760 – 47) x 0.21 = 149.7 mm Hg
Respiratory quotient is the amount of CO2 produced divided by the amount of oxygen consumed by tissue metabolism.
- Normally, R is 0.8, when cells use both glucose and free fatty acids as fuel.
- R is 1.0 when the fuel is only glucose (for example, patient on intravenous glucose).
- R is 0.7 when the fuel includes only free fatty acids (for example, a hypoglycemic or a diabetic patient).
A-a gradient is the difference between alveolar oxygen pressure and arterial oxygen pressure. A-a gradient can be used to investigate the different causes of hypoxemia.
Hypoxemia is defined as a decrease in arterial PO2, while hypoxia indicates decreased oxygen delivery to the tissues. PO2 can be calculated using the alveolar gas equation (discussed above). The patient may develop hypoxia in the presence of normal PaO2, as in carbon monoxide poisoning or decreased hemoglobin (anemia).
A-a O2 gradient = PAO2 – PaO2
For a patient with PaCO2 = 40 mm Hg, PaO2 = 97 mm Hg, PAO2 can be derived from alveolar gas equation (Rossier and Mean) as follows:
PAO2 = PiO2 – (PaCO2/R) = 149.7 – (40/0.8) if PaCO2 is 40 mm Hg
= 99.7 mm Hg
Thus, A-a O2 gradient = PAO2 – PaO2
= 99.7 – 97 if PaO2 is 97 mm Hg
= 2.7 mm Hg
Assuming that the patient is breathing room air at sea level, with normal body temperature:
- Normal A-a O2 gradient suggests a normal gas exchange between the alveoli and blood. Values < 15 mm Hg are considered normal.
- Increased A-a O2 gradient (> 15 mm Hg) suggests an abnormal gas exchange between alveoli and blood, which may be due to V/Q mismatch, shunting, or thickened diffusion barrier.
Factors affecting A-a O2 Gradient
The A-a O2 gradient increases by 3 mm Hg for each decade over 30 years of age.
As the shape of the oxygen dissociation curve is non-linear, greater the PAO2, greater is the A-a O2 gradient, provided the rest of the factors remain the same.
Magnitude of venous admixture
Venous admixture reduces arterial O2 content and increases arterial CO2 content. As PaO2 is usually based on the hemoglobin dissociation curve, a small reduction in the O2 level induces a large reduction in PaO2, thereby increasing A-a O2 gradient.
The CO2 dissociation curve is steep and a further linear increase in arterial CO2 content does not significantly increase the PaCO2 level. Under clinical settings, compensatory hyperventilation is more than adequate to offset the small increase in PaCO2. Therefore, PaCO2 is often decreased, rather than increased.
The cardiac output is inversely proportional to A-a O2 gradient provided the venous admixture remains the same. However, reduced cardiac output is associated with a reduction in venous admixture and shunt fraction. Therefore, PaO2 and A-a O2 gradient remain almost unchanged.
Hemoglobin concentration does not affect the arterial oxygen content, but increased hemoglobin concentration slightly reduces the arterial oxygen tension.
Increased alveolar ventilation increases both PAO2 and A-a O2 gradient.
Etiology of Hypoxemia
There are 5 important pathophysiological causes of hypoxemia and respiratory failure.
The minute ventilation depends on the respiratory rate and tidal volume, which is the amount of inspired air during each normal breath at rest.
Minute ventilation = respiratory rate x tidal volume
The normal respiratory rate is about 12 breaths per minute and the normal tidal volume is about 500 mL. Therefore, the minute respiratory volume normally averages about 6 L/min.
Hypoventilation occurs when the respiratory rate and tidal volume are decreased so that the amount of air exchanged per minute is decreased. A decreased oxygen entry within the alveoli and the arteries leads to decreased PaO2. As already described, PaCO2 is inversely proportional to the ventilation; hence, hypoventilation increases PaCO2. The A-a gradient is normal and less than 10 mm Hg in the absence of abnormal diffusion of gas. In these cases, ventilation or the oxygen concentration can be increased to correct the abnormal behavior of blood gases.
Impaired diffusion is attributed to structural defects within the lung. A decreased surface area (as in emphysema), or increased thickness of alveolar membranes (as in fibrosis and restrictive lung diseases) that impairs the diffusion of gases across the alveoli increases the A-a gradient. Under increased A-a gradient, the alveolar PO2 is normal or increased, but the arterial PO2 is decreased. A greater structural defect leads to higher alveolar-arterial gradient.
Since the diffusion of gases is directly proportional to the gas concentrations, increasing the concentration of inhaled oxygen corrects PaO2. However, the increased A-a gradient persists as long as the structural problem remains.
In a pulmonary shunt, also known as a right-to-left shunt, the venous deoxygenated blood from the right side enters the left side of the heart and systemic circulation without getting oxygenated within the alveoli. Thus, a shunt refers to ‘normal perfusion, poor ventilation’.
The lungs carry a normal blood supply, but under decreased or zero ventilation no gas exchange occurs with the incoming deoxygenated blood. The ventilation-perfusion (V/Q) ratio is close to zero, especially in atelectasis and cyanotic heart diseases. In atelectasis, the collapsed lung is not ventilated and blood within that segment fails to oxygenate. In cyanotic heart diseases, the blood from the right side bypasses (shunts) the lungs and enters the left side, causing hypoxemia and cyanosis.
The A-a gradient is increased as deoxygenated blood enters the arterial (systemic) circulation, which decreases the PaO2.
Since venous blood does not oxygenate in the pulmonary shunt, increasing the oxygen concentration does not correct the hypoxemia. The blood will bypass the lungs regardless of the increased oxygen concentrations. This failure to increase PaO2 after oxygen administration is very important in distinguishing impaired diffusion from other causes of hypoxemia that are corrected with supplemental oxygen.
Ventilation-perfusion (V/Q) mismatch
V/Q is the ratio of alveolar ventilation (V) to pulmonary blood flow (Q). A V/Q match facilitates adequate exchange of oxygen and carbon dioxide within the alveoli. The V/Q ratio in normal individuals is around 0.8, but this ratio is altered in the presence of significant ventilation or perfusion defects.
Within the lungs, all the alveoli do not exhibit uniform ventilation and perfusion due to the effects of gravity.
At the apex of the lung, the alveoli are large and completely inflated, while they are small at the base. Similarly, the blood supply is higher at the base of the lung than at the apex, which creates physiological ventilation (V) – perfusion (Q) mismatch between different alveoli.
The decreased V/Q ratio (< 0.8) may occur either due to decreased ventilation (airway or interstitial lung disease) or as a result of over-perfusion. The blood is wasted in these cases and fails to oxygenate adequately. In extreme conditions, when ventilation is significantly decreased and the V/Q approaches zero, it behaves as a pulmonary shunt.
The increased V/Q ratio (> 0.8) occurs when perfusion is decreased, for e.g., in pulmonary embolism preventing blood flow distal to obstruction or under excessive ventilation. The air is wasted in these cases and fails to diffuse through the blood. In extreme conditions, when perfusion is significantly decreased and V/Q approaches 1, the alveoli act as dead space and no diffusion of gases occurs.
Therefore, the increased V/Q mismatch within the lung impairs the gas exchange mechanisms and ultimately leads to hypoxemia and respiratory failure.
High altitude effect
At high altitudes, the barometric pressure (PB) is decreased, which leads to decreased alveolar PO2 as in the following equation:
PAO2 = FIO2 × (PB – PH2O) – PACO2/R
The decreased alveolar PAO2 leads to decreased arterial PaO2 and hypoxemia but the A–a gradient remains normal as there is no defect within the gas exchange mechanism. Under these conditions, supplemental oxygen therapy (elevated FIO2) increases the PAO2 and corrects the hypoxemia.
When a person suddenly ascends to high altitude, the body responds to hypoxemia via hyperventilation causing respiratory alkalosis. The concentrations of 2, 3-diphosphoglycerate (DPG) are increased, shifting the oxygen-hemoglobin dissociation curve to the right.
Under chronic conditions, acclimatization occurs and the body responds by increasing the oxygen-carrying capacity of the blood (polycythemia). The kidneys excrete bicarbonates and maintain the pH level within normal limits.
|Causes of Hypoxemia|
|Cause||PaO2||A-a gradient||Response of PaO2 to supplemental oxygen|
|Shunt||Decreased||Increased||Does not increase|
|V/Q Mismatch||Decreased||Increased||Increases usually (depends on V/Q mismatch type)|
Factors Associated with Increased A-a O2 Gradient
- Pulmonary atelectasis
- Pulmonary consolidation/infection/neoplasm
- Alveolar destruction
- Extrapulmonary shunting
- Drugs such as vasodilators and volatile anesthetics
- Hepatic failure