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PaO2, SaO2 and Oxygen Content

The following section is adapted from Chapter 5 of Dr. Martin's book All You Really Need to Know to
Interpret Arterial Blood Gases, 2nd edition, published February 1999 by Lippincott Williams & Wilkins.
Click on the title to see the Preface and Table of Contents. The book is available for purchase from the
publisher at 1-800-638-0672 or 1-410-528-4223 and also at the following web sites:
Lippincott Williams & Wilkins and

How much oxygen is in the blood? The Differences Between

PaO2, SaO2 and Oxygen Content.
In the field of blood gas interpretation, confusion about PaO2, SaO2 and oxygen content is second only to
confusion about mixed acid-base disturbances.
Arterial PO2 (little 'a')gives us valuable information about adequacy of gas exchange within the lungs, when
(and only when) it is subtracted from the calculated alveolar PO2 (big A). We use the Alveolar Gas
Equation to calculate PAO2. The difference between measured PaO2 and calculated PAO2 is called the
Alveolar-arterial PO2 difference or 'A-a Gradient' for short. The A-a gradient answers the important
question: Are the lungs transferring oxygen properly from the atmosphere to the pulmonary circulation? If the
A-a gradient is elevated, the answer is NO. If the A-a gradient is normal is YES. (The A-a gradient is
discussed in detail in Chapter 4).
There is a second, equally important question concerning oxygen and gas exchange, which is the subject of
this section:

How much oxygen is in the blood, and is it adequate for the patient?
The answer here must obviously be based on some oxygen value, but which one? After all, blood gases give
us three different oxygen values:
Oxygen content (CaO 2)
Of these three values, PaO2, or oxygen pressure, is the least helpful to answer the question about oxygen
adequacy in the blood. The other two values --oxygen saturation and oxygen content -- are more useful
for this purpose. I will briefly define these three terms and then present a more detailed discussion of each,
with emphasis on their inter-relationships.
Oxygen molecules dissolved in plasma (i.e., not bound to hemoglobin) are free to impinge on the measuring
oxygen electrode. This "impingement" of free O2 molecules is reflected as the partial pressure of oxygen; if the
sample being tested is arterial blood, then it is the PaO2. Although the number of O2 molecules dissolved in
plasma determines, along with other factors, how many molecules will bind to hemoglobin, once bound the

oxygen molecules no longer exert any pressure (bound oxygen molecules are no longer free to impinge on
the measuring electrode). Since PaO2 reflects only free oxygen molecules dissolved in plasma and not those
bound to hemoglobin, PaO2 cannot tell us "how much" oxygen is in the blood; for that you need to know how
much oxygen is also bound to hemoglobin, information given by the SaO2 and hemoglobin content.
Binding sites for oxygen are the heme groups, the Fe++-porphyrin portions of the hemoglobin molecule. There
are four heme sites, and hence four oxygen binding sites, per hemoglobin molecule. Heme sites occupied by
oxygen molecules are said to be "saturated" with oxygen. The percentage of all the available heme binding
sites saturated with oxygen is the hemoglobin oxygen saturation (in arterial blood, the SaO2). Note that SaO 2
alone doesn't reveal how much oxygen is in the blood; for that we also need to know the hemoglobin content.
Tissues need a requisite amount of O 2 molecules for metabolism. Neither the PaO2 nor the SaO2 provide
information on the number of oxygen molecules, i.e., of how much oxygen is in the blood. (Note that neither
PaO2 nor SaO2 have units that denote any quantity.) Of the three values used for assessing blood oxygen
levels, how much is provided only by the oxygen content, CaO2 (units ml O 2/dl). This is because CaO2 is the
only value that incorporates the hemoglobin content. Oxygen content can be measured directly or calculated
by the oxygen content equation (introduced in Chapter 2):
CaO2 = Hb (gm/dl) x 1.34 ml O 2/gm Hb x SaO2 + PaO2 x (.003 ml O 2/mm Hg/dl).

More on the definitions and distinctions of PaO2, SaO2 and

You wish it was this simple, huh? I have shown the 3 short paragraphs above to dozens of students, interns,
residents; almost all will say they understand the differences, no problem. But, when given questions to test
their understanding, they flub. So more instruction is needed (and, yes, a few problems along the way).
Understanding the differences between PaO2, SaO2 and CaO2 is essential to proper blood gas interpretation.
By the end of this and the next chapter -- if you work on all the problems -- you should be able to teach the
PaO2 , the partial pressure of oxygen in the plasma phase of arterial blood, is registered by an electrode that
senses randomly-moving, dissolved oxygen molecules. The amount of dissolved oxygen in the plasma phase - and hence the PaO2 -- is determined by alveolar PO2 and lung architecture only, and is unrelated to
anything about hemoglobin. (With one exception: when there is both anemia and a sizable right to left shunt of
blood through the lungs. In this situation a sufficient amount of blood with low venous O 2 content can enter
the arterial circulation and lead to a reduced PaO2. However, with a normal amount of shunting, anemia and
hemoglobin variables do not affect PaO2.)
Oxygen molecules that pass through the thin alveolar-capillary membrane enter the plasma phase as dissolved
(free) molecules; most of these molecules quickly enter the red blood cell and bind with hemoglobin (Figure

5-1). There is a dynamic equilibrium between the freely dissolved and the hemoglobin-bound oxygen
molecules. However, the more dissolved molecules there are (i.e., the greater the PaO2) the more will bind to
available hemoglobin; thus SaO2 always depends, to a large degree, on the concentration of dissolved oxygen
molecules (i.e., on the PaO2).
Figure 5-1. Oxygen pressure, saturation and content. Schematic shows cross section of
lungs and pulmonary circulation. (CO2, nitrogen and other gas molecules are omitted for clarity.)
PaO2 is always slightly lower than PAO2 because of normal venous admixture, here represented
by a connection between the venous and pulmonary circulations. See text for discussion. Click on
figure to obtain larger image.

In this figure:
Hemoglobin content = 15 gm/dl
Alveolar partial pressure of oxygen (PAO2) = 102 mm Hg
Venous partial pressure of oxygen (PvO2) = 40 mm Hg
Venous hemoglobin oxygen saturation (SvO2) = 75%
Arterial partial pressure of oxygen (PaO2) = 95 mm Hg
Arterial hemoglobin oxygen saturation (SaO2) = 97%

Because there is a virtually unlimited supply of oxygen molecules in the atmosphere, the dissolved O 2
molecules that leave the plasma to bind with hemoglobin are quickly replaced by others; once bound, oxygen
no longer exerts a gas pressure. Thus hemoglobin is like an efficient sponge that soaks up oxygen so more
can enter the blood. Hemoglobin continues to soak up oxygen molecules until it becomes saturated with the
maximum amount it can hold - an amount that is largely determined by the PaO2. Of course this whole
process is near instantaneous and dynamic; at any given moment a given O 2 molecule could be bound or
dissolved. However, depending on the PaO2 and other factors, a certain percentage of all O 2 molecules will
be dissolved and a certain percentage will be bound (Figure 5-1). In Figure 5-1, the free or dissolved oxygen
molecules register a partial pressure of 95 mm Hg and the red blood cells contain a total hemoglobin content
of 15 gm/dl.
Each hemoglobin molecule has four Fe++heme sites for binding oxygen. If there is no interference (as from
carbon monoxide, for example), the free O2 molecules bind to these sites with great avidity. The total
percentage of sites actually bound with O 2 is constant for a given set of conditions, and is the 'saturation of
blood with oxygen'. This is called SvO2 and SaO2 in the venous and arterial circulations, respectively; in
Figure 5-1, the respective values are 75% and 97%. An SaO2 of 97% simply means that of every 100
hemoglobin binding sites, 97 are occupied with an oxygen molecule and the other three are either bound to
something else or are unbound.

In summary, PaO2 is determined by alveolar PO 2 and the state of the alveolar-capillary interface, not by the
amount of hemoglobin available to soak them up. PaO2, in turn, determines the oxygen saturation of
hemoglobin (along with other factors that affect the position of the O 2-dissociation curve, discussed below).
The SaO2, plus the concentration of hemoglobin (15 gm/dl in this example), determine the total amount of
oxygen in the blood or CaO2 (see equation for CaO2). For the variables shown in Figure 5-1, the CaO2 is
20 ml O 2/dl.
Clinical Problem 5-1. At 10 a.m. a patient has a PaO2 of 85 mm Hg, an SaO2 of 98%, and a
hemoglobin of 14 gm/dl. At 10:05 a.m. she suffers a severe hemolytic reaction that suddenly
leaves her with a hemoglobin of only 7 gm/dl. Assuming no lung disease occurs from the
hemolytic reaction, what will be her new PaO2, SaO2, and CaO2?
(NOTE: Answers to all Clinical Problems are provided at end of this section.)
a) PaO2 unchanged, SaO2 unchanged, CaO2 unchanged
b) PaO2 unchanged, SaO2 unchanged, CaO2 reduced
c) PaO2 reduced, SaO2 unchanged, CaO 2 reduced
d) PaO2 reduced, SaO2 reduced, CaO2 reduced
From the forgoing discussion the following observations should now be apparent.
the less hemoglobin available to bind the dissolved oxygen molecules, the fewer total number of oxygen
molecules will the blood contain; and
the more hemoglobin available to bind the dissolved oxygen molecules, the greater total number of
oxygen molecules will the blood contain.
Neither the amount of hemoglobin, nor the binding characteristics of hemoglobin, should affect the amount of
dissolved oxygen, and hence should not affect the PaO2). Stated another way, the number of dissolved
oxygen molecules is independent of the amount of hemoglobin or what is bound to it. To repeat one more
time (because it is so important), PaO2 is not a function of hemoglobin content or of its characteristics, but
only of the alveolar PO2 and the lung architecture (alveolar-capillary interface). This explains why, for
example, patients with severe anemia or carbon monoxide poisoning or methemoglobinemia can (and often
do) have a normal PaO2.
The most common physiologic disturbance of lung architecture, and hence of a reduced PaO 2, is ventilationperfusion (V-Q) imbalance. Less common causes are reduced alveolar ventilation, diffusion block, and
anatomic right to left shunting of blood.
Clinical Problem 5.2 State which of the following situations would be expected to lower PaO2.
a) anemia.
b) carbon monoxide toxicity.

c) an abnormal hemoglobin that holds oxygen with half the affinity of normal hemoglobin.
d) an abnormal hemoglobin that holds oxygen with twice the affinity of normal hemoglobin.
e) lung disease with intra-pulmonary shunting.
SaO2 is determined mainly by PaO2. The relationship between the two variables is the familiar oxygen
dissociation curve (Figure 5-2A). The dissociation curve is experimentally determined from in vitro titration
of blood with increasing partial pressures of oxygen. At low oxygen pressures there is relatively little increase
in SaO2 for a given change in PaO2. Above a PaO2 of 20 mm Hg, the rate of change of SaO2 increases
markedly, then slows again beyond a PaO2 of 60 mm Hg.
PaO2 is the most important (but not the only) determinant of SaO2. Other determinants of SaO2 for a given
PaO2 are conditions that shift the position of the oxygen dissociation curve left or right, such as temperature,
pH, PaCO2 and level of 2,3-DPG in the blood. Shifts of the O2-dissociation curve will be discussed further in
the next chapter.
For now, consolidate your understanding of the difference between PaO2 and SaO2. Think of PaO2 as the
driving pressure for oxygen molecules entering the red blood cell and chemically binding to hemoglobin; the
higher the PaO2, the higher the SaO2. Whatever the SaO2, its value is simply the percentage of total binding
sites on arterial hemoglobin that are bound with oxygen, and can never be more than 100%.
Figure 5-2.

The oxygen dissociation curve, showing PaO2 vs. SaO2 and PaO2 vs. oxygen content for two different
hemoglobin values. P50 is the PaO2 at which hemoglobin is 50% saturated with oxygen; normal value is 27
mm Hg. (X represents blood gas values of a case presented in Chapter 6).
The Arterial oxygen content is shown for two hemoglobin vaues, 15 gm/dl and 10 gm/dl. The relationship
between SaO2 and CaO2 for any given hemoglobin content is linear (excluding the minor influence of
dissolved oxygen with normal PO 2 values).
Clinical Problem 5-3. Using Figure 5-2 to determine SaO2, calculate O2 content of a patient
with hemoglobin 12 gms/dl, PaO2 50 mm Hg, pH 7.40.
The so-called "steep part" of the O2 dissociation curve is between 20 and 60 mm Hg PaO2. Compared with
the flatter portions, small increases in PaO2 in this region have a much greater effect on improving SaO2 and
therefore O2 content. Figure 5-2A shows the oxygen dissociation curve for PaO2 plotted against oxygen
content for two hemoglobin concentrations, 15 gm% and 10 gm%. Note that the shape and position of the

curve are the same irrespective of the hemoglobin content.

SaO2 is unaffected by the hemoglobin content, so anemia does not lower SaO 2. The more hemoglobin, the
more oxygen molecules will be bound in a given volume of blood, but the percentage of available hemoglobin
sites bound to oxygen (the SaO 2) depends only on the PaO2 and curve-shifting factors. Thus, a patient can
have a normal PaO2 and SaO2, but still have a low CaO2 (e.g., with anemia).
CaO2 , unlike either PaO 2 or SaO2, directly reflects the total number of oxygen molecules in arterial blood,
both bound and unbound to hemoglobin. In contrast to the other two variables, CaO2 depends on the
hemoglobin content and is directly related to it; other determinants of CaO2 are the SaO2 (in turn dependent
on PaO2 and position of the oxygen dissociation curve), and the amount of dissolved oxygen (the PaO2).
Since the dissolved oxygen contributes minimally to CaO2 under physiologic conditions, CaO2 is determined
almost entirely by hemoglobin content and SaO2, and is related linearly to either variable (Figure 5-2B).
Normal CaO2 ranges from 16 to 22 ml O 2/dl. Because PaO2 and/or SaO2 can be normal in certain
conditions associated with hypoxemia, one should always make sure CaO2 is adequate when assessing
oxygenation. About 98% of the normal O 2 content is carried bound to hemoglobin.
The CaO2 component bound to hemoglobin can be calculated by (Hb x 1.34 x SaO 2) and the dissolved
component by (.003 x PaO2). This equation can be used to calculate oxygen content of any blood or plasma
Figure 5-3 shows two beakers containing liquid open to the atmosphere. Beaker 1 contains blood with a Hb
content of 15 grams%. Beaker 2 contains only plasma (no hemoglobin). Assuming a barometric pressure of
760 mm Hg (and no water vapor pressure), calculate the oxygen content in each beaker.

Figure 5-3.
Beaker 1 contains blood with a hemoglobin content of 15 grams%; beaker 2 contains pure plasma, no
hemoglobin. Both beakers are open to the atmosphere (dry air; barometric pressure 760 mm Hg).

Beaker 1 contains hemoglobin that will combine chemically with oxygen; hence the oxygen content in beaker
1 consists of bound and unbound (dissolved) oxygen molecules. In beaker 2 there is no hemoglobin, just pure
plasma; all of its oxygen content must come from dissolved oxygen.
Dissolved oxygen in both beakers is determined by the PO2 to which the liquid is exposed and the solubility
of oxygen in plasma. The solubility is .003 ml O 2/dl plasma/mm Hg. But what is the PO2? Because there is no
CO2 exchange taking place in either beaker (as there is in our lungs) and the surface of the liquid is in free
contact with the atmosphere, the PO2 in solution is simply the PO2 above the solution. Given a barometric
pressure of 760 mm Hg (dry air), the PO2 in both beakers is
FIO2 x PB = .21 x 760 mm Hg = 160 mm Hg.
Since the PO2 is equal in both beakers, the O 2 content represented by dissolved oxygen is also the same in
both beakers; this content is

a) .48 ml O 2/dl
b) 2.0 ml O 2/dl
c) 4.8 ml O 2/dl
To calculate content from dissolved oxygen, substitute the values for oxygen solubility and PO2:
O 2 content of dissolved O 2 = .003 ml O 2/dl/mm Hg x 160 mm Hg
= .48 ml O 2/dl
There is no hemoglobin in beaker 2 so the entirety of its O 2 content comes from dissolved oxygen and = .48
ml O 2/dl. There is far more oxygen content in beaker 1 because oxygen molecules combine chemically with
hemoglobin. Once combined, O 2 molecules no longer exert any pressure. As O 2 molecules are taken up by
hemoglobin, additional molecules enter the plasma portion of the blood from the atmosphere. (Remember:
Hemoglobin is like a sponge that soaks up free oxygen molecules and allows many more to enter the
surrounding plasma.) Thus the difference in oxygen content between the two beakers is the amount of oxygen
bound to hemoglobin.
The oxygen content represented by hemoglobin-bound oxygen in beaker 1 is

a) .48 ml O 2/dl
b) 15 ml O 2/dl
c) 19.9 ml O 2/dl
O 2 content is calculated by the oxygen content equation, which in turn requires knowledge of SaO2, the
saturation of hemoglobin with oxygen. SaO2 is determined by the PO2 to which the blood is exposed in the

lungs (in this case 160 mm Hg) and the position of the oxygen dissociation curve. With a normally-positioned
curve, the SaO2 at this level of PO2 is approximately 99%. Thus,
Oxygen content (Hb-bound) = Hb x 1.34 x SaO2
= 15 x 1.34 x .99
= 19.9 ml O 2/dl

What is the total oxygen content of beaker 1? By what factor is this content greater than that in beaker 2?
The total oxygen content of beaker 1 is of course the sum of the dissolved and bound fractions, or .48 + 19.9
= 20.38 ml O2/dl. The total oxygen content of beaker 2 (.48 ml O 2/dl) is thus only about 2.4% of that
contained in beaker 1. Put another way, beaker 1 contains about 42 times more oxygen than beaker 2.
Clinical Problem 5-4. A healthy man is in the same room as the two beakers shown in Figure 5-3. If his
PaO2 = 100 mm Hg and Hb content = 15 gms%, what percent of his oxygen content is carried in dissolved
To summarize much of the forgoing discussion:
Although almost all of the oxygen content is chemically bound to hemoglobin, this quantity is
unrevealed by knowing only the PaO2.
Without knowledge of the hemoglobin content, the PaO2 does not even give a hint of the total oxygen
We need to calculate CaO2 to know the amount of oxygen in the blood.
Because the body needs a requisite oxygen content for survival, and PaO2 alone does not indicate
oxygen content, a patient can have normal PaO2 and be starved for oxygen.
Clinical Problem 5-5. For each of the four conditions below, give the expected changes (increased,
decreased, or normal) for PaO2, SaO2 and CaO2. Assume the subject is breathing ambient air, that each
situation occurred acutely (in less than 24 hours), and that there is no other abnormal condition.



Severe Anemia
CO Poisoning
Severe V-Q Imbalance
High Altitude

Clinical Problem 5-6. Which patient is more hypoxemic?

Patient A: PaO2 85 mm Hg, SaO2 95%, Hb 7 gm%


Patient B: PaO2 55 mm Hg, SaO2 85%, Hb 15 gm%

Clinical Problem 5-7. Test your understanding by answering the following statements a-h as either True or
a. If the lungs and heart are normal, then PaO2 is affected only by the alveolar PO2.
b. In a person with normal heart and lungs, anemia should not lower the PaO 2.
c. PaO2 will go up in a patient with hemolysis of red blood cells, as dissolved oxygen is given off when the
cells lyse.
d. As the oxygen dissociation curve shifts to the right, PaO2 rises since less oxygen is bound to hemoglobin.
e. An anemic patient who receives a blood transfusion should experience a rise in both SaO 2 and CaO2.
f. The PaO 2 in a cup of water is zero since there is no blood perfusing the water.
g. The SaO2 in a cup of water is zero since there is no hemoglobin present.
h. The CaO2 in a cup of water is zero since there is no hemoglobin present.
Lawrence Martin, M.D.
Answers to Problems
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