(Chest. 2001;120:625-633.)
© 2001
American College of Chest Physicians
Overnight Pulse Oximetry for Sleep-Disordered Breathing in Adults*
A Review
Nikolaus Netzer, MD;
Arn H. Eliasson, MD, FCCP;
Cordula Netzer, MD and
David A. Kristo, MD, FCCP
*
From the Pulmonary and Critical Care Medicine Service, Department of Medicine, Walter Reed Army Medical Center, Washington DC.
Correspondence to: Arn H. Eliasson, MD, FCCP, Pulmonary and Critical Care Medicine Service, Department of Medicine, Walter Reed Army Medical Center, Building 2, Ward 77, 6900 Georgia Ave, Washington, DC 20307; e-mail: aheliasson{at}aol.com
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Abstract
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Pulse oximetry is a well-established tool routinely used in many
settings of modern medicine to determine a patients arterial oxygen
saturation and heart rate. The decreasing size of pulse oximeters over
recent years has broadened their spectrum of use. For diagnosis and
treatment of sleep-disordered breathing, overnight pulse oximetry helps
determine the severity of disease and is used as an economical means to
detect sleep apnea. In this article, we outline the clinical utility
and economical benefit of overnight pulse oximetry in sleep and
breathing disorders in adults and highlight the controversies regarding
its limitations as presented in published studies.
Key Words: COPD desaturation pulse oximetry sleep sleep apnea syndromes upper airway resistance syndrome
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Introduction
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Pulse
oximetry is one of the most widely used tools to determine a patients
cardiorespiratory stability. Over the last 40 years, it has often
replaced arterial blood gas analysis because the arterial oxygen
saturation (SaO2) frequently gives a
sufficient amount of information about a persons respiratory
patterns.1
2
In the early years of pulmonary medicine,
pulse oximetry was the key means to identify patients with pickwickian
syndrome or severe sleep apnea syndrome by detecting the saw-tooth
pattern on oxygen desaturation waveforms (waveform derived as a plot of
SaO2 vs time).3
Very few
clinics had access to other devices such as pneumotachographs,
esophageal catheters, and respiratory effort belts. With the broader
use of nocturnal polysomnography (NPSG) in sleep medicine, pulse
oximetry has kept its key role in the interpretation of NPSG but has
lost its status as the sole objective diagnostic parameter for
respiratory disturbance events.4
5
In the past 5 years, debate has centered on the effectiveness of
overnight pulse oximetry as a screening tool to identify patients with
sleep-disordered breathing from the larger group of patients with
simple snoring and those with excessive daytime sleepiness from other
causes.6
7
8
This controversial discussion has arisen from
needs to reduce the cost for diagnostic procedures in sleep disorders
while technologic advances have made pulse oximeters handier, cheaper,
and more reliable.9
10
Using keywords, we found 1,558 articles listed in the PubMed database
over the last 5 years that are related to pulse oximetry. One
individual reviewed these publications by evaluating the abstracts.
Screening these publications for relevance revealed that 79 of these
articles contained useful information to outline the actual role of
overnight pulse oximetry in the diagnosis and treatment of
sleep-disordered breathing. We reviewed the full text of these 79
articles. Eleven key articles from previous years were also reviewed
for important background information. All articles were studied for
strategies to use in the interpretation of data gathered during
overnight pulse oximetry.
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Interpretation and Technical Aspects of Overnight Pulse Oximetry
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Common sense dictates that pulse oximetry can be a useful tool
only if the user knows how to interpret the oximetry data. In a survey
performed in 1997 with 203 respondents, only 36% of intensive care
nurses, 4% of medical technicians, and 50% of anesthesia technicians
believed that they had received adequate training in interpreting pulse
oximetry data. Only 68.5% correctly stated what pulse oximeters
actually measure.11
These survey results were found
despite the fact that practice guidelines for pulse oximetry were
published in 1991 by the American Association for Respiratory
Care.12
The interpretation skills of overnight pulse oximetry start with a
knowledge of normal oxygen saturation values during sleep. In a key
validation study published in 1996 in CHEST, the authors
noted a normal overnight mean (the so-called Sat 50)
SaO2 of 96.5% (± 1.5%)
in 350 healthy subjects.13
SaO2 decreased slightly
with increasing age, the values ranging from 96.8% in the age group of
1- to 10-year-old patients to 95.1% in the age group > 60 years
(Table 1
). Ethnicity, gender, and weight did not significantly influence normal
values. In a group of 21 asthmatic patients,
SaO2 did not decrease
significantly, but significantly lower values were found in a group of
25 patients with obstructive sleep apnea (OSA) where mean "lowest
SaO2" of 65.9%
(± 22.6%) was measured vs 90.4% (± 3.1%) in normal subjects and
89.0% (± 5.3%) in asthmatic subjects.
Normal SaO2 values at night differ
with altitude of course. In six healthy subjects, normal mean
SaO2 values of 97.3%, 83.0%, and
71.0% were measured respectively at 500 m, 4,200 m, and 6,400 m
(three subjects) of altitude during sleep.14
The high-quality, portable pulse oximeters of today deliver accurate
values of SaO2 that differ from
arterial blood gas probes by < 0.5% (± 1.8%); there are no
significant differences if probes measure at the fingertips or
ears.15
Due to the fact that measurements are taken by
performing a "running average" with a moving window that varies
from 1 to 15 s in length, the speed of response to onset of oxygen
breathing is on average 9 to 10 s with finger and ear
probes.15
16
However, the speed of response is markedly
slower with toe probes.15
The default settings for the
averaging time are different for various pulse oximeters, and must be
known by the user. For overnight pulse oximetry in sleep medicine, it
is important that the oximeter be set to the shortest time interval for
measurement.16
The typical cyclical drop in
SaO2 in patients with OSA lags 45 to
60 s behind a respiratory event and should be accurately detected
at this measurement speed.15
Due to movements during
sleep, the artifact rate is higher in overnight pulse oximetry,
compared to daytime SaO2
measurements. With measurement intervals set on high speed, artifacts
are recognized by most pulse oximeters due to a missing pulse signal,
although this is controversial. In a validation study of three
different oximeters, Barker and Shah17
revealed that one
oximeter displayed the SaO2 value
within 7% of control only 76% of the time after patient motion;
another oximeter did so 87% of the time; and only one of the three
oximeters did so 99% of the time. Another study18
also
showed that pulse oximeters detect only 18% (± 11%) of all
artifacts in infants.
There is no universally accepted definition of an oxygen desaturation
in sleep-disordered breathing. However, in most publications, an oxygen
desaturation is defined as a decrease of
4% from baseline
SaO2.6
19
20
21
22
Rauscher
et al19
tested the detection of apneas and hypopneas by
searching for rapid resaturations of
3%
SaO2 within 10 s at the end of a
respiratory event vs detecting a decrease
4%
SaO2 in a 40-s interval. They found
the resaturation to be a more accurate sign of respiratory events than
the actual desaturation.19
Taha et al23
defined an oxygen desaturation as a fall in oxyhemoglobin
saturation of
2% if the rate of descent was > 0.1%/s but
< 4%/s.
Whereas one definition of an oxygen desaturation is in common use, no
such uniform definition exists for a normal or abnormal oxygen
desaturation index (ODI; oxygen desaturations per hour of sleep). There
are generally three cutoff points for an abnormal ODI that appear to
mirror the definition of an abnormal apnea-hypopnea index (AHI; apneas
and hypopneas per hour of sleep) for that study. The threshold for an
abnormal ODI is either
5 desaturations per
hour,6
20
21
24
25
10 desaturations per
hour,7
8
22
or
15 desaturations per
hour.26
27
28
29
30
There is little evidence of one definition
having greater validity than the others.
To properly interpret overnight oximetry data, an understanding of the
SaO2 vs time waveform morphologies is
essential.31
32
The waveforms can help discriminate
between obstructive apneas and hypopneas, as well as between
obstructive and central apneas, and can give evidence of Cheyne-Stokes
respiration.33
While obstructive apneas show the typical
saw-tooth waveform with a rapid increase in
SaO2 during or after the arousal, the
"teeth" are not as sharp in hypopneas and are sometimes completely
missing in central apneas (Fig 1
, 2
). Central apneas can act as the great masquerader of oximetry
waveforms. Especially when part of Cheyne-Stokes respiration, they show
a more regular symmetrical wave due to the more regular breathing
pattern, compared to those of obstructive apneas. However, single
central apneas not in conjunction with Cheyne-Stokes respiration can
also have a saw-tooth configuration in the oximetry waveform.

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Figure 1. Respiratory patterns during a 3-min time period
for a patient with OSA syndrome showing obstructive apneas with typical
saw-tooth morphology of the pulse oximetry curve.
Flowna = nasal and oral airflow;
Respth = thoracic respiratory effort;
Respabd = abdominal respiratory effort;
Respsum = sum signal of thoracic and abdominal
respiratory effort; O = obstructive apnea.
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Figure 2. Respiratory patterns during a 3-min time period
for a patient with OSA syndrome showing obstructive hypopneas with a
more regular up-and-down waveform of the pulse oximetry curve.
H = hypopnea; see Figure 1
legend for definition of abbreviations.
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The length of the desaturation waveform can also help to distinguish
desaturations due to COPD from desaturations caused by obstructive
apneas or hypopneas. The desaturations secondary to COPD tend to last
much longer and have a much lesser degree of slope in the
waveform.34
35
This is also important for the diagnosis of
OSA in the presence of COPD, the so-called overlap syndrome.
The automatic interpretation of the
SaO2 waveform is often a part of
modern NPSG and portable oximetry software. However, the programs are
not yet able to replace interpretation by hand. The same may be true
for the interpretation of heart rate variability, but here the
experience with automatic analysis is much greater because of the long
experience with automatic analysis in ECG-Holter systems. The heart
rate slows during and at the end of an upper-airway obstruction (apnea
or hypopnea) due to a reflex bradycardia with high negative
intrathoracic pressure (involuntary Mueller maneuver). There is a rapid
increase in the pulse with rebreathing during the arousal. This
strategy does not apply to the interpretation of central apneas,
because there is no negative intrathoracic pressure during a central
apnea. Adult criteria for the interpretation of overnight pulse
oximetry may not be valid for the evaluation of sleep-disordered
breathing in children and adolescents due to different patterns of
normal respiration and gas exchange.36
37
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Sensitivity and Specificity of Overnight Pulse Oximetry in
Screening for Sleep-Disordered Breathing
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Over the last decade, a debate in the literature has questioned
whether or not pulse oximetry could effectively screen patients for
sleep-disordered breathing and possibly replace NPSG in many patients.
Deegan and McNicholas28
reported 250 consecutive Irish
patients who underwent NPSG. In one third of these patients, patient
history and pulse oximetry data would have been sufficient to make a
diagnosis. In the other two thirds, a final diagnosis could be
established only by NPSG.28
Other studies38
39
are more encouraging about the use of
overnight oximetry as a less expensive substitute for NPSG. In 1991,
Cooper et al25
studied a group of 41 patients with
suspected sleep apnea and found that the sensitivity and specificity of
pulse oximetry for identifying OSA was dependent on the AHI. For
patients with an AHI
25 events per hour, the sensitivity was 100%
and the specificity 95%. For patients with AHI
15 events per hour,
these values decreased to 75% and 86%; for patients with AHI
5
events per hour, to 60% and 80%, respectively. The authors concluded
that pulse oximetry is an effective tool for screening patients with
moderate-to-severe sleep apnea. In the same year, Williams et
al7
reported a sensitivity of 78% and specificity of
100% when screening patients with an AHI
10 events per hour. In a
study of 116 subjects, Rauscher et al8
reported a
sensitivity of 94% and a specificity of 45% for detecting OSA with an
AHI
10 events per hour and 95% and 45% with an AHI
20 events
per hour, respectively. Within the past 5 years, 11 articles on this
topic were published, revealing a broad range of sensitivity and
specificity values for pulse oximetry as a screening tool for
sleep-disordered breathing.26
27
29
30
40
41
42
43
44
45
46
The values
for sensitivity range from 31 to 98% and for specificity from 41 to
100% (Table 2
). These validation studies deserve critical comment. Some authors used
methods of pulse oximetry that are not yet available to the general
public. The utility of these new technologies may not be borne out with
further investigation.30
Other authors looked only at a
limited patient group in the spectrum of severity of OSA. Findings from
these studies may not be applicable to OSA patients with different
levels of severity from those studied.
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Table 2. Sensitivity and Specificity of Pulse Oximetry When
Used To Screen for OSA Compared to NPSG: Results From 11 Published
Studies *
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Overnight Pulse Oximetry in Combination With Other Parameters
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Pulse oximetry is the most important parameter for identifying
sleep-disordered breathing in many portable multichannel sleep apnea
screening devices. The next most commonly measured parameters are
snoring sound via microphone,47
48
oronasal airflow
measured via thermistor or nasal pressure cannula,49
50
51
and ECG recording.52
One author52
argues that
the full ECG provides information about the comorbidity of
cardiovascular disease in sleep apnea better than pulse oximetry alone.
In 1998, Lojander et al53
described pulse oximetry in
combination with a bed sensitive to static charge in order to measure
body movements. However, if compared to the sensitivity and specificity
values of pulse oximetry alone as a screening tool, the combination of
other parameters with pulse oximetry does not offer much
improvement.49
51
Another interesting strategy may be the combination of a validated
questionnaire with overnight pulse oximetry. Chervin and
Aldrich54
state that the addition of the Epworth
Sleepiness Scale alone does not appear to be helpful for the diagnosis
of sleep-disordered breathing compared to NPSG and oximetry. However,
there is a report42
that the combination of a
questionnaire and pulse oximetry doubles the specificity of oximetry as
a screening tool for sleep apnea. This approach invites further
validation.
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Other Applications
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Overnight pulse oximetry is frequently being used to assess the
response to the surgical interventions for OSA as well as the
effectiveness of therapy with continuous positive airway pressure.
However, this clinical practice is not established in the literature,
and validation of its use for this indication is lacking. Continuous
pulse oximetry is also in frequent use in a variety of other settings,
including preoperative evaluations, the operating room, postanesthesia
recovery suites, ICUs, and stroke units.55
56
57
58
59
60
61
This has
led to an increasing awareness of sleep-disordered breathing as a
comorbidity in patients being treated for other diagnoses or as a
symptom of other diseases, such as stroke,60
61
neuromuscular diseases,62
63
and cardiovascular
diseases.64
65
66
As continuous pulse oximetry has become
more accessible and more widely employed, physicians in specialties
other than sleep medicine have become accustomed to recognizing
oximetry waveforms suggestive of sleep apneas. These coincidental
observations are frequently leading to patient referrals for definitive
diagnosis and treatment of OSA.
Attempts have been made to capitalize on the continuous measurement of
heart rate provided by pulse oximetry. Computerized analysis of the
heart rate variability makes it possible to detect sleep apnea syndrome
via the pulse signal.67
68
Using this method, Keyl et
al68
report a sensitivity of 90% and a specificity of
77% for the detection of OSA in patients with daytime sleepiness. Some
authors69
70
believe that the interpretation of heart rate
changes delivers a better pulse oximetry indicator for OSA than
interpretation of the SaO2 signal,
especially if it is done using automation. Another aspect used by some
investigators is the waveform generated by the displacement of
capillary walls by the intermittent pulse signal or so-called
"plethysmographic" pulse. Shamir et al71
and Schnall
et al72
describe that apneas lead to transient peripheral
vasoconstriction. Schnall et al72
conclude in their
publication that pulsatile finger blood flow patterns can be clearly
diagnostic of OSA and other conditions of sleep-disordered breathing.
Future developments with pulse oximetry will undoubtedly show marked
improvements in artifact detection. Signal delivery will become more
reliable and less vulnerable to interruptions by movement using the
same technique employed in portable compact disk players to memorize
signals (using new paradigms for oximeter signal
processing).17
73
The spectral analysis of oximetry data
facilitates precise analysis with a reported sensitivity of 94% and
specificity of 65% for OSA.74
Photon density wave
differentials and noninvasive optical oximetry with a living tissue
oximeter may allow monitoring of regional tissue oxygenation in the
heart or brain in conjunction with sleep apnea.75
76
Another promising innovation is the improvement of adhesive probes that
would allow for pulse oximetry in sites other than digits and
ears.77
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Limitations
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While pulse oximetry is a useful clinical tool in sleep medicine,
it suffers from major limitations due to the nature of the parameters
that are monitored.78
79
80
Limitations result from problems
with blood flow, hemoglobin, or a lack of change in oxygen saturation.
Pulse oximetry relies on pulsatile blood flow for its measurements and
is vulnerable to the effects of poor peripheral arterial blood flow.
Therefore, body movements, vasoconstriction, and hypotension can cause
artifacts through an interruption of the pulse signal. In sleep
medicine, movement artifacts are common since patients often have
fragmented sleep with a lot of body movements. Oximeters do not always
detect movement artifacts, and this would tend to overestimate
desaturations.17
Changes in the hemoglobin structure and quantity will also cause
artificially high (in cases of methemoglobinemia and
carboxyhemoglobinemia) or low readings (anemia) that are not due to
respiratory disturbances.78
Anemia would also tend to be
misread by overestimating respiratory-caused desaturations. Tissue
optics in very obese patients can cause the same effect.81
Herer et al82
found that oximetric data do not reliably
predict OSA in obese patients. Mower et al83
studied
SaO2 data from 12,096 patients at the
UCLA Emergency Medicine Center. They believed that no conclusions could
be drawn from the data due to high variations in respiratory rates
among the patients and the artifacts that this caused.83
Another type of limitation of pulse oximetry is due to the inability of
technology to detect other forms of sleep-disordered breathing where
oxygen desaturation does not occur. These disorders include upper
airway resistance syndrome or pure central sleep apnea in diseases like
Ondines curse. A normal minute ventilation in upper airway resistance
syndrome maintains normal oxygen levels, but high respiratory workload
causes arousals and daytime sleepiness. Understandably, pulse oximetry
would appear normal in this setting.24
84
The limitations of pulse oximetry might not have much impact in the
sleep laboratory, where several other parameters are monitored to aid
in the interpretation of the study. However, these limitations become
of major importance in the application of pulse oximetry alone as a
screening tool for breathing-disordered sleep.
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Cost-effectiveness
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Bennet and Kinnear10
call pulse oximetry "sleep on
the cheap" in their 1999 editorial because it generates a lot of data
at a very low cost. Perhaps the only competitor for cost-effectiveness
is a structured and validated questionnaire. In other fields of
medicine, the cost-effectiveness of pulse oximetry is more or less
accepted.85
In sleep medicine, the clinical value of
overnight pulse oximetry alone for the diagnosis of sleep apnea
syndrome has become controversial since NPSG has been widely available.
However, the recent advent of managed care and pressures for cost
reduction have stimulated a variety of
investigations22
86
87
88
89
that substantiate the economies of
overnight pulse oximetry at home as a screening test for
sleep-disordered breathing. Epstein and Dorlac22
state
that initial diagnosis with home-based overnight pulse oximetry would
save $4,290 per 100 patients vs diagnostic NPSG or split-night studies.
However, they showed that oximetry is not very sensitive for patients
with mild sleep apnea.22
Chiner et al89
subsequently analyzed how many NPSGs could be saved by overnight pulse
oximetry in the initial diagnosis for patients with differing severity
of OSA. They concluded that in 275 suspected cases, of which 216
patients were confirmed to have OSA, pulse oximetry could have saved
140 polysomnographic studies in the group with a respiratory
disturbance index (RDI)
5, 119 in the group with an RDI
10, and
10 in the group with an RDI
15.89
Because of
its low cost, there is almost no alternative to overnight pulse
oximetry as a sole diagnostic tool, except for patient history and
questionnaires.90
If the pressure for cost reduction
continues, proposals may arise to perform pulse oximetry with reusable
finger and ear probes, or validated questionnaires may become the sole
"procedure" of first choice in the diagnostic evaluation of sleep
disorders.91
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Conclusion
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Overnight pulse oximetry is a very useful tool for the diagnosis
of sleep-disordered breathing. Authoritatively establishing a final
diagnosis is very difficult without oximetry data. As a screening tool
for the diagnosis of OSA, pulse oximetry is cost-effective and shows
substantial accuracy. Sensitivity and specificity remain controversial,
however, and deserve further clarification through controlled studies.
Technical limitations, limited user knowledge, and the lack of
consensus on interpretation of data all play a role in diminishing the
value of pulse oximetry as a diagnostic tool. The authors suggest a
flow diagram to delineate the clinical use of overnight pulse oximetry
as a screening tool for sleep-disordered breathing (Fig 3
). The establishment of clinical practice guidelines that outline
technical requirements and strategies for interpretation, along with
improved automated analysis, may improve the clinical utility of pulse
oximetry in the future.

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Figure 3. Flow diagram for the use of overnight pulse
oximetry to screen for sleep-disordered breathing with a descending
progressive therapeutic approach for patients with an ODI > 15
desaturations per hour. PSG = polysomnography; CPAP = continuous
positive airway pressure.
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Footnotes
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Abbreviations: AHI = apnea-hypopnea index;
NPSG = nocturnal polysomnography; ODI = oxygen desaturation index;
OSA = obstructive sleep apnea; RDI = respiratory disturbance index;
SaO2 = arterial oxygen saturation
Received for publication October 11, 2000.
Accepted for publication February 1, 2001.
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