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Fundamentals of Sleep Medicine Expert Consult Online
and Print 1 Har/Psc Edition Richard B. Berry Md Digital
Instant Download
Author(s): Richard B. Berry MD
ISBN(s): 9781437703269, 1437703267
Edition: 1 Har/Psc
File Details: PDF, 14.36 MB
Year: 2011
Language: english
FUNDAMENTALS of
Sleep Medicine
FUNDAMENTALS of
Sleep Medicine
Richard B. Berry, MD
Professor of Medicine
University of Florida, Gainesville
Medical Director
University of Florida and Shands Sleep Disorder Center
Gainesville, Florida
1600 John F. Kennedy Blvd.
Ste 1800
Philadelphia, PA 19103-2899
All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any
means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval
system, without permission in writing from the publisher. Details on how to seek permission, further
information about the Publisher’s permissions policies and our arrangements with organizations such as the
Copyright Clearance Center and the Copyright Licensing Agency, can be found at our website: www.elsevier.
com/permissions.
This book and the individual contributions contained in it are protected under copyright by the Publisher
(other than as may be noted herein).
Notices
Knowledge and best practice in this field are constantly changing. As new research and experience broaden
our understanding, changes in research methods, professional practices, or medical treatment may become
necessary.
Practitioners and researchers must always rely on their own experience and knowledge in evaluating
and using any information, methods, compounds, or experiments described herein. In using such
information or methods they should be mindful of their own safety and the safety of others, including
parties for whom they have a professional responsibility.
With respect to any drug or pharmaceutical products identified, readers are advised to check the most
current information provided (i) on procedures featured or (ii) by the manufacturer of each product to be
administered, to verify the recommended dose or formula, the method and duration of administration,
and contraindications. It is the responsibility of practitioners, relying on their own experience and
knowledge of their patients, to make diagnoses, to determine dosages and the best treatment for each
individual patient, and to take all appropriate safety precautions.
To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors, assume
any liability for any injury and/or damage to persons or property as a matter of products liability,
negligence or otherwise, or from any use or operation of any methods, products, instructions, or ideas
contained in the material herein.
The goal of this book is to provide the reader with a core of fundamental knowledge about
sleep medicine and polysomnography. I have tried to write the book so that a person
without training in sleep medicine can start reading chapter one and progress until the end
of the book. With the publication of the International Classification of Sleep Disorders,
Second Edition, and the American Academy of Sleep Medicine scoring manual, there is a
need for an up-to-date text using current terminology and diagnostic criteria. A single text
cannot hope to cover all aspects of sleep medicine and sleep physiology. Therefore, I have
tried to focus on information that I feel is the most clinically useful. The field of sleep
medicine is changing so rapidly that any text is “out-of-date” before it is even published.
To this end, there will be an associated website to allow for updates, corrections, review
questions, illustrative case studies, and some video clips of parasomnias.
My inspiration for writing this book has come in part from the satisfaction and appre-
ciation that I received from writing the text Sleep Medicine Pearls. Sleep Medicine Pearls
had short fundamentals chapters mixed with cases and was heavy on graphics and illustra-
tive sleep tracings. I have tried to amplify the fundamentals sections to provide what I hope
is a concise and useful introduction to the entire spectrum of sleep disorders. In particular,
I have tried to cover aspects of the technology of sleep monitoring and interpreting sleep
studies that many new to the sleep field find difficult. The challenging but enjoyable experi-
ence of teaching sleep fellows and residents about sleep medicine has also prompted me to
write a book covering the fundamentals both to serve as an introductory text and to assist
those physicians actively taking care of sleep patients.
Richard B. Berry, MD
vii
viii Chapter 21
Acknowledgments
I would like to express my gratitude for the support and encouragement of the University
of Florida sleep physicians, including Dr. Abby Wagner, co-director of the University of
Florida Sleep Medicine Fellowship, Dr. Stephan Eisenschenk, and Dr. Craig Foster. It is a
pleasure to work with such a dedicated and talented group of individuals. I would also like
to thank Dr. Klark Turpen for her assistance in editing the book chapters. The patience and
assistance of the Elsevier editorial staff is also greatly appreciated. Jessica Pritchard helped
assemble the chapters and many figures. Dolores Meloni, Senior Acquisitions Editor, was
instrumental in developing the concept for the book and provided critical support in the
planning stages. Julie Goolsby, Associate Acquisitions Editor, provided encouragement
during the final stages of book preparation. I am also grateful for the patience and diligence
of Berta Steiner of Bermedica Production, Ltd. during the production process.
viii
Chapter 1
movement; R&K = Rechtschaffen and Kales A1; REM = rapid eye movement;
stages 3 and 4 are combined into stage N3.
F3 Fz F4
20%
C3 Cz C4
M1 M2
20%
O1 O2
20% Oz
10%
Inion
10% 20%
10%
10% O2 10% Nasion
Inion Preauricular F4 F3
M2 Fpz
point
Fp2 Fp1
O1 Oz O2
Inion
TABLE 1–4
Alternative Electroencephalographic Derivations with Backup Derivations
ALTERNATIVE DERIVATIONS FZ FAILS CZ FAILS OZ FAILS C4 OR M1 FAILS
Fz-Cz Fpz-Cz Fpz-C3 Fz-Cz Fz-Cz
Cz-Oz Cz-Oz C3-Oz Cz-O1 Cz-Oz
C4-M1 C4-M1 C4-M1 C4-M1 C3-M2
TABLE 1–5
Characteristics of Alpha Rhythm and Sleep Spindles
ALPHA RHYTHM SLEEP SPINDLES
• 8–13 Hz. • 11–16 Hz (classically 12–14 Hz).
• Most prominent over the occipital areas. • Duration ≥ 0.5 sec (0.5–1.5 sec).
• Activity increased by eye closure. • Maximal over central areas.
• Activity suppressed by eye opening. • One of the defining characteristics of stage N2.
• Predominate EEG activity in drowsy, eyes closed stage W. • Thalamocortical oscillations (reticular thalamic
• Common in REM sleep (1–2 Hz slower than during stage W or N1). nucleus).
• Can occur with arousals (brief awakenings). • Can be seen in stage N3 sleep.
• 10% of persons do not produce alpha rhythm with eye closure. • Drug spindles (benzodiazepines) may be slightly faster.
EEG = electroencephalographic; REM = rapid eye movement.
TABLE 1–6
Characteristics of K Complex and Slow Wave Activity
K COMPLEX SLOW WAVE ACTIVITY
• High amplitude–biphasic deflection. • Frequency 0.5–2 Hz and > 75 µV peak to peak in the
• A well-delineated negative sharp wave (upward) followed by a frontal derivations.
positive (downward) slow wave. • Used to define stage N3 sleep.
• Stands out from the lower voltage background. • Stage N2 < 20% SWA (<6 sec).
• Duration ≥ 0.5 sec. • Stage N3 ≥ 20% SWA (≥6 sec).
• Characteristic of stage N2 sleep. • SWA is usually transmitted to eye derivations.
• Maximal over frontal areas (frontal > central > occipital).
• K complex–associated arousal requires arousal to start no more
than 1 second after K complex termination.
SWA = slow wave activity.
TABLE 1–7
Characteristics of Vertex Sharp and Saw-Tooth Waves
VERTEX SHARP WAVES SAW-TOOTH WAVES
• Sharply contoured waves • Trains of triangular waves, often serrated
• Duration < 0.5 sec • 2–6 Hz waves
• Maximal over the central region (derivations containing C3, C4, Cz) • Maximal in amplitude in central derivations
and distinguishable from the background activity (higher amplitude). • Often, but not always, preceding a burst of REMs
• Occurs in stage N1 often near transition to stage N2 • Characteristic of stage R but not required for
scoring stage R
REMs = rapid eye movements.
followed by a slow wave (Fig. 1–4). A burst of spindle activity complex. An arousal during sleep stages N1, N2, and N3 is
is often superimposed on a K complex. A K complex stands scored if there is an abrupt shift of EEG frequency including
out from the lower voltage background. K complex activity alpha, theta, and/or frequencies greater than 16 Hz (but not
is greatest in frontal derivations (also central > occipital). A spindles) that lasts at least 3 seconds, with at least 10 seconds
K complex is said to be associated with an arousal if the of stable sleep preceding the change. Arousals are discussed
arousal commences no more than 1 second after the K in more detail in Chapter 3.
Chapter 1 Sleep Stages and Basic Sleep Monitoring 5
30 second
window
(as viewed)
1 sec
10 second
window
(as viewed)
1 sec
TABLE 1–8
Summary of Important Wave Form Characteristics
ALPHA SLEEP VERTEX SLOW WAVE SAW-TOOTH
RHYTHM SPINDLE K COMPLEX SHARP WAVE ACTIVITY WAVES
Frequency (Hz) 8–13 11–16 N/A N/A 0.5–2 2–6
Amplitude/ Oscillation Spindle- High amplitude Sharp wave High-amplitude Triangular,
shape shaped (usually > 100 µV) broad wave serrated
oscillation Stands out against >75 µV peak to
EEG background peak
Biphasic-negative
sharp wave
followed by positive
component
Duration Variable ≥0.5 >0.5 sec <500 msec 0.5–2 sec Variable
Location of Occipital Central Frontal Central Frontal Central
highest (vertex)
amplitude
Associated Stage W Stage N2 Stage N2 Stage N1 Stage N2 Stage R
sleep stages/ Stage N1 Stage N3 Stage N3 Stage N3
events Stage R
Arousals
EEG = electroencephalogram; N/A = not applicable.
100 µV
1 sec
V
F4-M1
C4-M1
O2-M1
E1-M2
E2-M2
Chin EMG
Alpha waves Sleep spindle K complex Vertex sharp Slow waves Saw-tooth waves
wave
FIGURE 1–4 Important EEG patterns for sleep staging. The grid lines are 1 second apart. V = position of the vertex sharp wave.
75 µV
1 sec
F4-M1
C4-M1
O2-M1
E1-M2
E2-M2
Chin1-Chin2
FIGURE 1–5 A K complex associated with an arousal. An abrupt shift in EEG frequency immediately follows the K complex that lasts greater than 3 seconds. To be
considered associated with a K complex, an arousal must commence no later than 1 second after K complex termination.
a peak-to-peak amplitude of greater than 75 µV in the meeting amplitude criteria) using the AASM scoring manual
frontal derivations (see Fig. 1–4). SWA has the greatest definition2 (frontal derivations) compared with the R&K
amplitude over frontal areas. In the R&K definitions, only definition (using central derivations).
central derivations were utilized. Because slow wave ampli- Vertex sharp waves (see Fig. 1–4) are narrow-duration
tude is higher over the frontal areas, a given epoch of EEG waves (<500 msec according to the AASM scoring manual2)
activity would potentially have greater SWA (longer duration prominent in derivations containing electrodes near the
Chapter 1 Sleep Stages and Basic Sleep Monitoring 7
1 cm 1 cm 1 cm
LOC
E1 E2 E1
vertex (Cz, C3, C4). They are often seen near the transition E2
Look Look
between stage N1 and stage N2 sleep. Saw-tooth waves (see left right
Fig. 1–4) occur during REM sleep, although they are not
always present during this sleep stage. They are triangular
waves of 2 to 6 Hz of highest amplitude in the central deriva- E1
tions. The presence of saw-tooth waves is not required to
score stage R. However, the presence of saw-tooth waves is E1-M2
very helpful when they occur.
EOG MONITORING FOR SLEEP E2-M2
Recording of eye movements is possible because a potential
difference exists across the eyeball with the front/cornea E1 positive to M2, E1 negative to M2,
positive (+) and back/retina negative (–). Eye movements are deflection down deflection up
detected by EOG recording of voltage changes associated E2 negative to M2, E2 positive to M2,
with eye movement. deflection up deflection down
The recommended EOG electrodes in the AASM scoring FIGURE 1–7 Schematic shows deflections in E1-M2 and E2-M2 from eye movements.
manual2 are illustrated in Figure 1–6. E1 and E2 refer to the
left and right eye electrodes, respectively. Previously eye
electrodes were named right outer canthus (ROC) and left In the recommended EOG derivations, eye movements
outer canthus (LOC). For comparison, the positions of the result in out-of-phase deflections. This is because eye move-
ROC and LOC electrodes are also shown. Please note that ments are conjugate, and when both eyes move laterally or
E1 is placed below the LOC and E2 is placed above the ROC, vertically, they both move toward one EOG electrode and
whereas LOC and ROC were placed lateral to the respective away from the other EOG electrode. The polarity of the eye
outer canthus. Because E1 is below and E2 above the eyes, electrodes determines the net voltage difference of the EOG
vertical as well as horizontal movement can be detected. derivations because the electrodes are much closer to the
Alternate eye electrode positions were also recommended eyes than M2. The schematic in Figure 1–7 illustrates eye
for use with alternate eye movement derivations (see movements and the resulting deflections (this assumes that
Fig. 1–6). The AASM scoring manual recommends the both eye derivation tracings have negative polarity upward
EOG derivations E1-M2 and E2-M2 (see Table 1–8). Note which is standard).
that both eye derivations use the right mastoid (M2) as the Note that when the alternate EOG derivations E1-Fpz and
reference electrode. Previous ROC and LOC derivations E2-Fpz are used, both E1 and E2 are 1 cm below and 1 cm lateral
varied between sleep centers, and these electrodes were ref- to the LOC and ROC, respectively. In this scheme, vertical
erenced either to the same mastoid or to the opposite eye movements result in in-phase deflections and lateral eye
mastoid. The AASM scoring manual also specified the alter- movements result in out-of-phase deflections (Fig. 1–8). The
native eye movement derivations (E1-Fpz and E2-Fpz). If these advantages of the alternative EOG derivations are that verti-
eye movement derivations are used, both E1 and E2 are cal deflections tend to produce larger deflections (blinks are
below and lateral to the LOC and ROC, respectively (see more prominent) and one can distinguish vertical (in-phase)
Fig. 1–6). from horizontal (out-of-phase) eye movements. In addition,
When the eyes move toward an electrode, a positive it is easy to remember that downward eye movements result
voltage is recorded (Fig. 1–7). Recall that in EEG recording, in downward deflections in the eye derivations and upward
by polarity convention, if an eye electrode is negative com- eye movements result in upward deflections. Alternatively,
pared with the reference electrode, the signal has an upward the recommended eye derivations make it easier to recognize
deflection. Thus, eye movement (cornea +) toward an elec- artifacts or EEG activity transmitted to the eye derivations
trode referenced to another electrode further away from the because these cause in-phase deflections while eye move-
eyes results in a downward deflection. ments cause out-of-phase deflections (Fig. 1–9).
8 Chapter 1 Sleep Stages and Basic Sleep Monitoring
TABLE 1–10
Fpz Look Look Eye Movements Pattern Definitions
up down • Eye blinks: Conjugate vertical eye movements at a
frequency of 0.5–2 Hz present in wakefulness with the
eyes open or closed.
E2 E1 • Reading eye movements: Trains of conjugate eye
E1-Fpz movements consisting of a slow phase followed by a
rapid phase in the opposite direction as the subject reads.
• Slow eye movements: Conjugate, fairly regular,
E2-Fpz sinusoidal eye movements with an initial deflection
lasting > 500 msec.
• Rapid eye movements (REMs): Conjugate, irregular,
FIGURE 1–8 Schematic shows deflections in E1-Fpz and E2-Fpz due to horizontal and
sharply peaked eye movements with an initial deflection
vertical eye movements. Note that, using these derivations, vertical eye movements
usually lasting < 500 msec. Whereas rapid eye movements
result in in-phase deflections whereas lateral eye movements result in out-of-phase
are characteristic of stage R sleep, they may also be seen in
deflections. In addition, downward eye movements result in downward deflections.
wakefulness with eyes open (as patients look around the
room)
Adapted from Iber C, Ancoli-Israel S, Chesson A, Quan SF for the American
Academy of Sleep Medicine: The AASM Manual for the Scoring of Sleep and
Associated Events: Rules, Terminology and Technical Specifications, 1st ed.
Westchester, IL: American Academy of Sleep Medicine, 2007.
F4-M1
C4-M1
O2-M1
E1-M1
E2-M2
Chin EMG
K complex REM
FIGURE 1–9 Using the recommended electro-oculographic (EOG) derivations, the K complex results in deflections that are in phase and the rapid eye
movement (REM) results in out-of-phase deflections. The vertical lines are 1 second apart. EMG = electromyography.
Chapter 1 Sleep Stages and Basic Sleep Monitoring 9
100 µV
1 sec
Reading eye
E1-M2
movements
E2-M2
E1-M2
Blinks
E2-M2
FIGURE 1–10 Eye movement patterns. The grid lines are 1 second apart.
but can occur with any of the SSRIs (see Chapter 4). Reading THREE ELECTRODES ARE RECOMMENDED
eye movements are due to a slow scan of the written page TO RECORD THE CHIN EMG
(left to right) followed by a rapid return to the left. This
results in a slowly increasing downward deflection in E2-M2
followed by a rapid upward deflection. In E1-M2, there is a
slow upward deflection followed by a rapid downward
deflection (see Fig. 1–10). Chin1
B
F4-M1
C4-M1
O2-M1
E1-M2
C
E2-M2
Chin EMG
A
FIGURE 1–12 A 30-second tracing shows a reduction in the chin EMG on transition to stage R sleep (A). Note saw-tooth waves (B) and REMs (C).
3. D. Sleep spindles have a frequency of 11–16 Hz and rep- of Sleep and Associated Events: Rules, Terminology and Tech-
resent thalamocortical oscillations generated by the retic- nical Specifications, 1st ed. Westchester, IL: American Academy
of Sleep Medicine, 2007.
ular nucleus of the thalamus. Sleep spindles are most
3. International Federation of Societies for Electroencephalogra-
prominent in central derivations. phy and Clinical Neurophysiology: Ten twenty electrode
system. EEG Clin Neurophysiol 1958;10:371–375.
4. B. SWA is characterized by a minimum amplitude peak 4. Williams RL, Karacan I, Hursch CJ: Electroencephalography of
to peak of > 75 µV in the frontal derivations with a fre- Human Sleep: Clinical Applications. New York: John Wiley &
quency of 0.5 to 2 Hz. Sons, 1974.
5. West P, Kryger MH: Sleep and respiration: terminology and
5. A. In the recommended derivations, eye movements methodology. Clin Chest Med 1985;6:691–712.
6. Caraskadon MA, Rechschaffen A: Monitoring and staging
cause out-of-phase deflections. Because the cornea is
human sleep. In Kryger MH, Roth T, Dement WC (eds): Prin-
positive with respect to the retina, a rightward gaze results ciples and Practice of Sleep Medicine. Philadelphia: Elsevier
in E2 being positive with respect to M2 (E2 is closer to the Saunders, 2005, pp. 1359–1377.
cornea) and this results in a downward deflection. With 7. DeGennaro L, Ferrara M: Sleep spindles: an overview. Sleep
a rightward gaze, E1 is negative with respect to M2 (upward Med Rev 2003;7:423–440.
8. McCormick L, Nielsen T, Nicolas A, et al: Topographical dis-
deflection).
tribution of spindles and K complexes in normal subjects. Sleep
1997;20:939–941.
6. A. SEMs can occur during wake (eyes closed drowsy 9. Silber MH, Ancoli-Israel S, Bonnet MH, et al: The visual
wake) or stage N1 and are sinusoidal out-of-phase scoring of sleep in adults. J Clin Sleep Med 2007;15:121–131.
movements. 10. Schenck CH, Mahowlad MW, Kim SW, et al. Prominent eye
movements during NREM sleep and REM sleep behavior dis-
REFERENCES order associated with fluoxetine treatment of obsessive-
compulsive disorder. Sleep 1992;15:226–235.
1. Rechtschaffen A, Kales A (eds): A Manual of Standardized 11. Armitage R, Trivedi M, Rush AJ: Fluoxetine and oculomotor
Terminology, Techniques and Scoring System for Sleep Stages activity during sleep in depressed patients. Neuropsychophar-
of Human Sleep. Los Angeles: Brain Information Service/Brain macology 1995;12:159–165.
Research Institute, UCLA, 1968.
2. Iber C, Ancoli-Israel S, Chesson A, Quan SF for the American
Academy of Sleep Medicine: The AASM Manual for the Scoring
Chapter 2
It should be noted that a localized EEG transient (e.g., and abdomen), leg EMG inputs, and electrocardiographic
sharp wave) that is located midway between two electrodes (ECG) inputs.
will produce an equal signal in both sides of the differential In referential recording, multiple electrodes are recorded
AC amplifier that will cancel out (output approximately against a common electrical reference (often a single or two
zero). This cancellation effect will alter the overall EEG signal linked electrodes placed near the vertex). A display of any
amplitude less if electrodes are further apart. Thus, a greater derivation using two referentially recorded electrodes is then
distance between two electrode inputs will increase the obtained by digital subtraction [(electrode A − reference) −
amplitude of the recorded signal (less cancellation). This is (electrode B − reference) = electrode A − electrode B] either
one reason the recommended EEG derivations use contra- during live recording or during review (see Fig. 2–3). The
lateral mastoid references (C4-M1, not C4-M2). digital subtraction for display does NOT change the recorded
data. For example, if the sleep technologist failed to observe
REFERENTIAL AND BIPOLAR RECORDING that the electrode F4 went bad during the recording, the
reviewer can change the viewed frontal derivation to F3-M1
Most digital recording systems use a combintation of refer- or F3-M2 (the recommended alternative) (Fig. 2–4). For this
ential, true bipolar, and DC recording (Table 2–1).2 In true reason, both F3 and F4 are recorded (against the reference
bipolar recording, each amplifier records the difference electrode) even though only F4-M1 may be displayed in the
between two electrodes of interest (A–B, C–D). Before the default montage. Of note, if the reference electrode is faulty,
digital era, paper recording was performed using a selector all referential signals are affected (Fig. 2–5). In Figure 2–5,
panel and dedicated individual differential amplifiers. Using note that the true bipolar channels are not affected by a faulty
this approach, it is possible to change the electrodes (deriva- reference electrode. In most digital PSG systems, the EEG,
tion) that are recorded with a given amplifier (Fig. 2–3). EOG, mastoid, and chin EMG electrodes are recorded refer-
However, changing the derivation once the signal is recorded entially (see Table 2–1). DC recording is used for nasal pres-
(changing from A–B to A–D) is not possible. Today, selector sure, pulse oximetry, and other DC signals such as those
panels are rarely used in digital sleep recording. However,
true bipolar recording is still used for inputs that one would
not desire to change in review—for example, the two inputs TABLE 2–1
of the thermal flow sensor, respiratory effort bands (thorax Types of Recording
Referential EEG: F4, F3, C4, C3, O2, O1, M1, M2
recording EOG: E1, E2, M1, M2
IF G1 IS NEGATIVE TO G2,
DERIVATION G1-G2 THE DEFLECTION IS UPWARD Chin1, Chin2, Chin3
Reference
30 µV
True bipolar ECG, thermal flow, thorax and
Differential amplifier 20 µV
(two inputs abdominal sensors, right and left
each) anterior tibial EMG
G1
DC Nasal pressure, SpO2, positive airway
G2 0 pressure device (flow, leak, pressure),
end-tidal or transcutaneous PCO2
10 µV
Ground ECG = electrocardiography; EEG = electroencephalography;
EMG = electromyography; EOG = electro-oculography; PCO2 = partial
FIGURE 2–1 Differential amplifier. The difference between the two inputs is amplified
pressure of carbon dioxide; SpO2 = pulse oximetry.
(for simplicity, the amplification factor = 1).
DETAILS
DIFFERENTIAL AMPLIFIER
80 µV Common mode rejection Input 1
60 µV
Input 1 Output
20 µV
Output 1 Ground
0
Ground
Input 2
Input 2
FIGURE 2–2 Common mode rejection by a differential amplifier (for simplicity, the amplification factor = 1).
Chapter 2 The Technology of Sleep Monitoring 15
BIPOLAR RECORDING REFERENTIAL RECORDING FIGURE 2–3 The difference between true bipolar
recording and referential recording. In referential
C4 C4-M1 C4
Amplifier 1
recording, each electrode is recorded against a common
C3 C3 reference. Specific derivations are then displayed by
C3-M2 Reference (Ref) digital subtraction (during acquisition or review).
M1 Amplifier 2 M1
M2 M2
Selector box
DISPLAY BIPOLAR VIEWS
F4-M1
F3-M1
C4-M1
O2-M1
E1-M2
E2-M2
Chin EMG
FIGURE 2–4 In the F4-M1, derivation 60-Hz artifact is present. The F4 electrode is at fault because other derivations containing M1 are not affected.
The displayed derivation is then changed to F3-M1, allowing an artifact-free frontal derivation to be viewed. Viewing a derivation using any two of the
referentially recorded electrodes is possible. The recommended derivation when the F4 electrode is faulty is actually F3-M2, but the use of F3-M1 is shown
for illustration. EMG = electromyography.
E1-M2
E2-M2
F4-M1
C4-M1
O2-M1
Chin1-Chin3
ECG
R, L legs
Airflow
Chest
Abdomen
SpO2
A B
FIGURE 2–5 A, The reference electrode is faulty. All referentially recorded electrodes show artifact. The true bipolar channels and DC
channels are not affected. In B, the reference electrode was repaired. SpO2 = pulse oximetry.
16 Chapter 2 The Technology of Sleep Monitoring
000000000011
1250 000000000100
used, the signal can be very distorted and the addition of 000000000101
000000000110
frequencies lower than the original signal sampled may be
introduced (Fig. 2–6). For this reason, signals with a fre-
quency higher than half the sampling rate must be filtered Etc,
out because they can cause aliasing distortion.2,4,5 For Input at
example, if the sampling rate is 200 samples/sec, the ampli- A/D board
fied signal must be processed by a high frequency filter with Resolution 0.97 µV per bit
a cutoff frequency of 100 Hz or lower before being sampled
(A/D converter). The required sampling rate depends on the FIGURE 2–7 Dynamic range and resolution of an analog-to-digital (A/D) converter.
frequency of the signal to be recorded. Slower varying signals
require a lower sampling rate. In Table 2–2, the sampling range. A typical A/D converter might have a dynamic range
rates recommended by the American Academy of Sleep for the amplified signal of 5 V (±2.5 V). Commonly, a set
Medicine (AASM) scoring manual6 are illustrated. Some amplification is applied to all AC signals before A/D conver-
digital PSG systems have the ability to record different signals sion (e.g., a gain of 1250). If one assumes an amplification of
at different sampling rates. Ultimately, the computer program 1250, then the dynamic range (peak to peak) of an A/D
uses only a small portion of the data for the display because converter with an amplified voltage range of 5 V expressed
monitor resolution (in pixels per displayed time duration) is as the unamplified signal would be approximately 4000 µV
usually much less than the sampling rate.5 (4000 µV × 1250 = 5,000,000 µV = 5.0 V). If a 12-bit A/D
A/D conversion is also characterized by the dynamic converter is used, this would result in a resolution of 0.97 µV/
range (the range of voltages accepted by the A/D converter) bit (4000 µV/4096 digital values) (Fig. 2–7).
and the resolution. The dynamic range may be expressed as
the amplified or unamplified signal range. The resolution
Monitor Resolution
depends on the A/D converter as well as the dynamic range.
A 12-bit DC converter produces 212 = 4096 digital values An important limitation on the accuracy of signal recording
(bits) or a 16-bit converter = 65,536 values across the dynamic and display is introduced by the fact that the monitor
Chapter 2 The Technology of Sleep Monitoring 17
Respiratory event
100%
95%
SpO2 90%
85%
80%
75%
Desaturation
Left
Right
Position Prone
Supine
Sitting
Wake
REM
Stage 1
2
3
Epoch
Time
FIGURE 2–8 An overview of the entire night of the recording shows respiratory events, pulse oximetry (SpO2), desaturation events, body position, and sleep stage
(hypnogram). REM = rapid eye movement.
resolution is usually much lower than the data sampling rate. an all-night condensed view with graphs of the hypnogram
Because the sampling rate used for most digital systems is (representation of sleep stages), arterial oxygen saturation
200 samples/sec or higher, the resolution of the monitor is (SpO2 tracing), continuous positive airway pressure (CPAP)
often the limiting factor in the accuracy of signal display. The levels, respiratory events, and body position (Fig. 2–8). This
minimum monitor resolution recommended by the AASM allows a useful overview of the entire recording. One can
scoring manual is 1600 × 1200. Assuming 1600 pixels hori- usually select a time point (double click) on a given position
zontally, the visual sampling rate for displays of a 30- or in the summary view and be taken to that time point in the
10-second window of data corresponds to a sampling rate of more detailed tracings.
approximately 50 and 150 samples/sec if the entire monitor
display consists of waveforms. Then according to the Nyquist FILTERS (LOW-FREQUENCY, HIGH-
theorem, frequencies of 25 or 75 Hz or greater would be
FREQUENCY, AND NOTCH FILTERS)
prone to aliasing. A monitor-induced aliasing distortion of
data can sometimes be noted if switching from a 30-second Any signal of interest can be contaminated by unwanted
to a 10-second view significantly changes the shape of the low- or high-frequency signals or 50- to 60-Hz artifact (from
activity being visualized.5 nearby AC power lines). Filters allow these components to
be diminished. For example, a low-frequency filter (high-
pass filter) attenuates the amplitude of low-frequency signals.
Time Window for Display
A high-frequency filter (low-pass filter) attenuates the ampli-
During traditional paper-ink recording for sleep, the paper tude of high-frequency signals.1 The amount of signal reduc-
speed was 10 mm/sec, which produced 30-second pages (30- tion due to a given analog or digital filter is given in decibels.
cm-wide paper). A faster speed was used for clinical EEG The amount of signal reduction in decibels (dB) is given by
(30 mm/sec). However, such a fast paper speed would the formula 20 log (voltage-out/voltage-in), where voltage-
produce a very large amount of paper for each sleep study. out and voltage-in are the amplitude of the signal entering
In digital recording, one can choose various time windows and leaving the filter, respectively. A signal reduction of 30%
during either acquisition or review. A 30-second window and 50% (voltage-out/voltage-in ratios of ∼ 0.7 and 0.5,
(equivalent to a paper speed of 10 mm/sec) is used for sleep respectively) corresponds to 3 dB and 6 dB reductions. Dif-
staging and for scoring arousals. Time windows of 60 to 240 ferent filter settings (e.g., 0.3, 1) are named by the “cutoff
seconds may be used to view and score respiratory events frequency,” which is the frequency of the signal that is reduced
and leg movements. Alternatively, viewing data in a by 3 or 6 dB depending on the terminology and the type of
10-second window (equivalent to 30 mm/sec) is the usual filter the manufacturer uses. Therefore, a filter setting of “X
method for clinical EEG recording. This allows better visu- Hz” means that the amplitude of a signal with a frequency
alization of very brief events (sharp waves and spikes) and of X is diminished by 30% or 50% depending on whether the
interictal or epileptiform activity. The 10-second window 3 dB or 6 dB cutoff frequency is used to name the filter.
can also be useful for measuring the frequency of a group of
oscillations or viewing the ECG result. The traditional ECG
Low-Frequency Filter
speed is 25 mm/sec, which is quite close to 30 mm/sec. Some
systems allow split screens with different time windows in A 1-Hz low-frequency filter (3 dB) attenuates a 1-Hz signal
each screen. All digital sleep monitoring systems also provide by 30% (or to 70% of the original signal). Similarly, a 6 dB
18 Chapter 2 The Technology of Sleep Monitoring
filter would attenuate a 1-Hz signal by 50%. Signal strength circuits. In RC circuits, an increase in step voltage produces
of frequencies below 1 Hz would be attenuated even more an abrupt increase in voltage across the resistor, then an
(Figs. 2–9 and 2–10). It is important to realize that frequen- exponential fall in voltage to 1/e (0.37) of the maximum
cies slightly above the low-frequency filter setting of 1 Hz voltage in one time constant (TC). In a simple, low-frequency
will also be attenuated by a 1-Hz low-frequency filter, filter RC circuit, the frequency (fc) at which the output
although to a lesser degree. Figure 2–10 illustrates the effect voltage across the resistor is attenuated to 0.37% of the input
of various low-frequency filters (denoted by their 3 dB cutoff voltage is related to the TC by the formula fc = 1/(2π/TC).
frequency) on low-frequency signals. A range of possible In RC circuits, the TC = RC, where R is the resistance and
low-frequency filter settings (off, 0.01, 0.03, 0.1, 0.3, 1, 3, and C the capacitance of the circuit. Even if digital filters are
10) is commonly provided. used, the relationship between the TC and the 3 dB fre-
Sometimes low-frequency filter settings are specified as a quency is given by Equation 2–1:
time constant rather than as a cutoff frequency (Fig. 2–11).
Traditional analog filters used resistance-capacitance (RC) TC = 1/(2π × filter frequency ) Equation 2–1
Percent amplitude
3 less than 50%
the horizonal axis uses a logarithmic scale and 75 75
Filter setting of 1
the vertical axis is linear. 50 10 50 reduces signal with
frequency of 1 Hz
25 25 by 50%
Filter settings 1.0
0 0 Lower frequency
0.1 0.2 0.5 1 2 5 10 0.1 0.2 0.5 1 2 5 10
attenuated more
Signal frequency Signal frequency than 50%
LF 0.3
LF 1 70
LF 3 100 µV
1 second
Chapter 2 The Technology of Sleep Monitoring 19
Vin input
voltage LF = 0.3 Hz TC = 0.53
LF = 1 Hz TC = 0.16
Voltage 37%
across R
37% LF = 5 Hz TC = 0.03
TC
1 sec
30 Hz high filter FIGURE 2–12 The effects of a high-frequency filter. A 6 dB 30-Hz filter
0.3 Hz low filter Frequency slightly attenuates a 30-Hz signal by 50%. Signals less than 30 Hz are attenuated
lower than 30 Hz less (low pass). Signals with a frequency higher than 30 Hz are attenuated
100 attenuated slightly much more. The gray shows a frequency range that is attenuated less
Percent amplitude
For example, a 0.3-Hz low-frequency filter has a TC of Using the combination of a low-frequency and a high-
approximately 0.53 second. Of note, the actual TC after a frequency filter, a range of frequencies is amplified. Alterna-
step increase in voltage may vary depending on the high- tively, if digital filters are applied to raw digital data, a range
frequency filter setting as well. The lower the cutoff fre- of frequencies is displayed. The range of signal displayed or
quency, the longer the time constant (see Fig. 2–11). If amplified is called the bandwidth.
amplifiers are calibrated by step (square wave) voltage
change, the actual TC can be noted from the time it takes 60-Hz or Notch Filters
for the deflection to return to 0.37 of the maximum Most amplifiers (digital PSG systems) provide optional notch
deflection. filters to significantly attenuate a narrow range of frequency
associated with power line signal contamination (e.g., 50 or
60 Hz). The notch filter can be added or removed. If the
notch filter is turned on, it is applied to the signal in addition
High-Frequency Filters
to the low-frequency and high-frequency filters. The routine
A 35-Hz high-frequency filter attenuates a signal of 35 Hz use of a notch filter is usually not recommended. The sudden
by 50% (6 dB filter), and frequencies above 35 Hz would appearance of increased 60-Hz activity in a derivation is a
be attenuated more. In addition, frequencies slightly below clue that one or more electrodes is faulty. However, as previ-
the high-frequency filter setting will also be slightly attenu- ously mentioned, use of a high-frequency filter of 35 Hz
ated. Figure 2–12 illustrates the effects of a 6 dB 30 Hz (commonly used for EEG and EOG derivations) already
filter. A range of high-frequency filter settings is typically substantially attenuates a 60-Hz signal (much the same as
provided (off, 3, 15, 35, 70, and 100 Hz). Note that using a turning on the 60-Hz filter)
30-Hz high-frequency filter (see Fig. 2–12) significantly Turning on and off the 60-Hz (notch) filter can be useful
attenuates 60-Hz signals. Therefore, the addition of a 60-Hz in determining the degree of signal contamination by 60-Hz
notch filter adds little if a 30- to 35-Hz filter is already interference. If turning off the notch filter dramatically
being used. increases signal amplitude, this suggests considerable 60-Hz
20 Chapter 2 The Technology of Sleep Monitoring
signal contamination (Fig. 2–13). One would expect switch- TABLE 2–3
ing on and off the 60-Hz filter to have more effect if a high- Recommended Filter Settings
frequency filter of 100 Hz was used (commonly used for
LOW FREQUENCY HIGH FREQUENCY
EMG derivations) compared with a high-frequency filter of
35 Hz (EEG and EOG derivations). For this reason, 60-Hz EEG 0.3 Hz 35 Hz
contamination is most frequently visualized in the chin and EOG 0.3 Hz 35 Hz
leg EMG derivations even if the 60-Hz filter is turned on.
Artifacts including 60-Hz artifact are discussed in more EMG 10 Hz 100 Hz
detail in Chapter 4. ECG 0.3 Hz 70 Hz
Respiration 0.1 Hz 15 Hz
AMPLIFIER FILTER SETTINGS FOR Snoring 10 Hz 100 Hz
DIGITAL SLEEP RECORDING ECG = electrocardiography; EEG = electroencephalography;
EMG = electromyography; EOG = electro-oculography.
Sleep recording with traditional dedicated bipolar AC ampli- From Iber C, Ancoli-Israel S, Chesson A, Quan SF for the American Academy
fiers used RC circuits (RC filters) as filters and the recorded of Sleep Medicine: The AASM Manual for the Scoring of Sleep and Associated
(on paper or computer) signal was filtered at the current Events: Rules, Terminology and Technical Specifications, 1st ed. Westchester,
IL: American Academy of Sleep Medicine, 2007.
amplif ier settings. Today, most amplifiers used for digital
recording (referential and true bipolar) record signals “wide
open,” that is, with default low-frequency filter (0.03–0.1)
and a high-frequency filter setting usually at or less than half
Clinical Example of the Effects of Filter Settings
the sampling rate (e.g., 100-Hz for a sampling rate of 200/
sec). Thus, “raw” signals are actually recorded over a wide As discussed in Chapter 7, monitoring nasal pressure pro-
frequency range or bandwidth (between default low and vides a more accurate estimate of airflow than thermal
high frequencies) but are viewed (displayed) after applica- sensors. During upper airway narrowing, the nasal pressure
tion of selected digital low-frequency and high-frequency signal shows a flattening (flow plateau) during inspiration.
filters. The digital filters alter the displayed signal but NOT Some sleep centers record nasal pressure with an AC ampli-
the recorded data. This allows multiple choices of filters if fier instead of acquiring the signal in the DC mode. However,
desired by the technologist or reviewer. The filter settings a low-frequency filter setting of 0.03 or less (or a long TC) is
recommended by the AASM scoring manual6,7 are shown in ideal to allow demonstration of a flow plateau in the nasal
Table 2–3. The filter settings are selected to include the fre- pressure signal (Fig. 2–14). To accurately record or display a
quencies of interest in sleep monitoring. For example, to very slowly varying signal, a sufficiently low cutoff frequency
detect slow waves and eye movements but avoid the effect of must be used for the low filter.
scalp DC voltage changes (very low frequency), a low- If the nasal pressure signal is unfiltered, vibration during
frequency filter of 0.3 Hz is selected. Setting the low- snoring is often visible. However, the ability to see snoring
frequency filter of the EEG or EOG channels higher would (high-frequency vibration) depends on the high-frequency
reduce slow wave and eye movement amplitude. For EMG filter settings. Use of a fairly low high-frequency filter setting
and ECG channels, a low-frequency filter of 10-Hz is used, will reduce high-frequency signals such as noted in the nasal
because the relevant activity is of a much higher frequency. pressure tracing during snoring (Fig. 2–15). Ideally, one
For EEG and EOG monitoring, selection of a 35-Hz high- would use a high-frequency filter setting of 70 to 100 Hz.
frequency filter removes unwanted higher frequencies but
attenuates the characteristic EEG patterns such as sleep spin-
DIGITIAL PSG SYSTEM OVERVIEW
dles (11–16 Hz) to a lesser degree. In contrast, the EMG
frequences of interest are much higher and a high-frequency The typical digital PSG system includes a headbox in which
filter of 100 Hz is usually selected. individual electrodes are attached to an amplifier. An
Chapter 2 The Technology of Sleep Monitoring 21
0.03
0.1
0.3
Nasal
pressure
Snore
Nasal
pressure
Snore
accessory box for DC channel inputs or dedicated input jacks derivations and processes the data with the selected digital
on the amplifier are also usually available. The amplifier is low-frequency and high-frequency filters. A display sensitiv-
then connected to the A/D converter. Today, the A/D con- ity is also chosen to determine the upper and lower limits
verter is often contained within the amplifier that sits at the of data to be displayed in the channel width (digital gain).
patient’s bedside. The digitized signal can then be sent over The changes in the display (specific derivations, digital
ethernet cables to the computer or sent in the wireless mode filters, digital gain) do not change the raw data that are
to a computer, which then records the digital data. This recorded by the computer. The entire process is summarized
arrangement avoids the difficulties that occur when an in Figure 2–16.
analog signal is sent over a long distance (60 Hz contamina-
tion or loss of signal strength). A schematic of a typical
Montages for Digital Recording
system is shown in Figure 2–16. A typical PSG amplifier
often has a fixed gain and default low- and high-frequency Digital systems allow the user to specify a number of user-
filter settings (e.g., 0.1 and 100 Hz). AC signals are recorded defined display montages with the ability to select the
over a wide frequency range (bandwidth). The A/D con- number of channels (traces) to be displayed, the derivations
verter samples the signal and raw digital data are stored in for each channel, the order in which the desired derivations
the computer. After the raw data are digitized and stored, are displayed (the inputs for each channel), as well as the
extensive manipulation is possible to produce the desired sensitivity (gain), low- and high-frequency filter settings,
signal display. During acquisition and review, the computer notch filter on or off, and the color of each tracing. A sample
program performs digital subtraction to display the desired montage (Table 2–4) is displayed in Figure 2–17. Typically,
22 Chapter 2 The Technology of Sleep Monitoring
Amplifier
Computer
Fixed
program Data
gain Raw
Electrode A/D display
LF 0.1 data Digital sensitivity
box converter
HF 100 stored Digital filters C4-M1
C4 -Ref (LF, HF)
M1 -Ref
FIGURE 2–16 Schematic of a digital polysomnography (PSG) system. In many systems, the A/D converter is within the same
unit housing the amplifier(s). Modern digital PSG systems usually perform a fixed amplification with default low (LF) and high
(HF) filters permitting a wide frequency range to be amplified. The digitized data are stored on media (hard drive in the
computer). The PSG software then scales the raw data, applies the selected low-frequency and high-frequency filters, and
provides a display (either during acquisition or at review).
TABLE 2–4
Montage 1: Diagnostic Adult
CHANNEL INPUT SENSITIVITY (P-P) LF HF NOTCH
(TRACING) TYPE INPUT 1 INPUT 2 µV UNLESS DC (HZ) (HZ) FILTER
1 Ref F4 M1 150 0.3 35 Off
2 Ref C4 M1 150 0.3 35 Off
3 Ref O2 M1 150 0.3 35 Off
4 Ref F3 M2 150 0.3 35 Off
5 Ref C3 M2 150 0.3 35 Off
6 Ref O1 M2 150 0.3 35 Off
7 Ref E1 M2 150 0.3 35 Off
8 Ref E2 M2 150 0.3 35 Off
9 Ref Chin1 Chin2 150 10 100 Off
10 BP ECG1 ECG2 1500 0.3 70 Off
11 DC Nasal pressure N/A −1 to +1 V †
DC 100 Off
*
12 BP NOTF—input 1 Input 2 750 0.1 15 Off
*
13 BP Snore—input 1 Input 2 750 10 100 Off
*
14 BP Thorax—input 2 Input 2 1500 0.1 15 Off
*
15 BP Abdomen—input 1 Input 2 1500 0.1 15 Off
16 DC SpO2 DC 0–1 V DC N/A Off
17 BP RAT—input 1 Input 2 150 10 100 Off
18 BP LAT—input 1 Input 2 150 10 100 Off
*The sensitivity settings for bipolar channels depend on the output range for a particular device.
†
Varies with transducer type.
BP = dedicated bipolar inputs (input-1, input-2); ECG = electrocardiography; HF = high frequency filter setting; LAT = left anterior tibial; LF = low frequency filter
setting; N/A = not applicable; NOTF = nasal-oral thermal flow sensor; P-P = peak to peak; RAT = right anterior tibial; Ref = referential input; SpO2 = pulse oximetry.
one montage is adapted for a diagnostic study and another gain), low-frequency and high-frequency filters, channel
for a positive-pressure titration. During review or acquisi- width, and inversion of signal. Default settings for each
tion, each individual channel may be altered if so desired or channel can be specified, so they do not have to be individu-
an entirely different montage may be displayed. ally set for each recording. Figure 2–17 illustrates typical
channel controls. Recall that changes in channel settings do
not change the recorded (and digitally stored) data.
Channel Settings/Montages
In sleep recording using paper, the EEG was usually
Each channel (tracing) display can be changed by the viewer recorded at a sensitivity of 50 µV/cm in adults. In children,
with respect to the inputs, sensitivity (sometimes called a lower sensitivity (100 µV/cm) was used because of the very
Chapter 2 The Technology of Sleep Monitoring 23
high amplitude EEG activity. The term “gain” rather than ultimate size of the channel width depends on the way the
sensitivity was also used. However, this implies an amplifica- computer program scales the signal for display. Some pro-
tion of signal. In digital recording, amplification actually grams have an option to allow signals either to overlap or to
occurs before the signal is digitized. The size of the display be cropped if they exceed the given channel width.
of a given signal is varied by the computer program that
scales the display based on the available channel width and Impedance Checking and Referential
the voltage limits or sensitivity. For example, if a channel
Display View
width of 100 pixels represents 100 µV peak to peak, a signal
of 50-µV peak to peak would vary between the 25th and the Traditionally, after electrodes were applied to the patient’s
75th pixel. The default digital displays for EEG often use 100 head, the impedance of each electrode was checked by plug-
or 150 µV peak to peak per channel width (200 for children). ging the electrodes into an impedance box that allowed com-
Figure 2–18 shows two methods of adjusting the display parison of any electrode referred to the ground electrode or
(gain/voltage per division or peak-to-peak sensitivity). The a combination of all the other electrodes. Most digital
systems can measure impedance on line using a signal from
the amplifier. The values can then be stored with other digital
Channel 5 data for later review. The AASM scoring manual recom-
mends a maximum electrode impedance of 5 KΩ (<10 KΩ
Input 1 Input 2 Low freq filter High freq filter
is acceptable). Another useful method of looking at the
C4 M2 0.3 Hz 35 Hz
quality of each individual electrode is to display all of
the unfiltered referentially recorded electrode against the
Notch filter On Off common reference (rather than the digital subtraction of two
Trace width
100 Sensitivity referentially recorded electrodes). Figure 2–19 displays a ref-
erential view with all high-frequency filters set to 100 Hz.
100 µV p-p Electrode impedance is also displayed. One can tell that F4,
Invert
Chin2, and Chin3 electrodes are faulty and should be
FIGURE 2–17 Example of typical controls for each display channel (tracing). Controls changed or fixed. As previously noted, if all tracings on the
allow selection of the derivation, low-frequency and high-frequency filters, notch filter referential view are bad, this suggests a problem with the
(on or off), and sensitivity. On most digital PSG systems, channel width and trace color reference electrode. However, a faulty reference electrode
can also be selected. p-p = peak to peak. does not affect the true bipolar channels (see Fig. 2–5).
1 second
One division
100 µV/division
50 µV/division
Channel width
FIGURE 2–18 Two methods of adjusting the sensitivity (digital gain) are shown. A 100-Hz peak-to-peak signal of 10 Hz is shown. The top panels
specify a voltage per division value. A larger channel width is needed to display a given signal if the actual division size remains constant when voltage per
division decreases. The bottom panel illustrates a method by which the peak-to-peak voltage of the entire channel width is specified. The actual
channel width will depend on the way the computer program scales the display.
24 Chapter 2 The Technology of Sleep Monitoring
Impedance
O1-REF 6.4 KΩ
O2-REF 6.3
C3-REF 5.6
C4-REF 2.5
E1-REF 3.5
E2-REF 4.4
M1-REF 4.8
M2-REF 4.3
Chin1-REF 3.8
Chin2-REF 19.2
Chin3-REF 10.3
F3-REF 6.7
F4-REF 30.2
FIGURE 2–19 A “referential display” with each electrode displayed against the common reference electrode. The electrode impedance is also displayed. One
can see that the Chin2, Chin3, and F4 electrodes should be replaced or repaired.
Reference
Patient
ground Circuit
ground Power
Chassis
ground Earth ground NH
Video-Audio PSG
sec). Simultaneous audio is also usually available and this is
Today, most digital systems allow for the simultaneous very useful for documenting teeth grinding (bruxism),
recording of video and audio signals. Ideally, the video talking during parasomnias, snoring, and other behaviors
should be synchronized with the recorded EEG and other during the recording.
signals. This will allow the reviewer to see patient movement
corresponding exactly to a given time point in the recorded
Grounds
PSG signals. For example, one could note facial twitching
during a particular EEG pattern. Video PSG is an important The terminology is confusing with three different grounds
development and allows the reviewer to confirm the patient being used in modern PSG recording (Fig. 2–20). These
position as well as document unusual behavior (e.g., para- include
somnias) during the night. Video files are often quite large
and are usually compressed (e.g., MPEG4). The size of the 1. The patient ground (iso-ground input on the electrode
file will depend on the quality of the video (10 or 25 frames/ box). This neutral electrode is usually connected to the
Chapter 2 The Technology of Sleep Monitoring 25
forehead. It is used to balance the inputs of all the differ- C. Decreases the amplitude of a 0.1-Hz signal more than
ential amplifiers (essential for common mode rejection). a 0.3-Hz signal.
2. Chassis ground (container ground). Because a metal D. A and B.
chassis is rarely used today, this would be the amplifier E. A and C.
circuit ground (or the ground of the nonisolated portion
of the amplifier). 6. If a sampling rate of 400 samples/sec is used, what is the
3. Earth ground. In the three-wire power line (three-prong highest frequency cutoff for the high filter that can be
plug) AC input, the three wires are designated “hot (H),” used and still avoid significant aliasing distortion?
“neutral (N),” and “earth” ground. Most amplifiers use an A. 400 Hz.
isolated medical-grade power supply that outputs low- B. 200 Hz.
level DC voltage to power the amplifiers. C. 100 Hz.
In modern systems, the patient ground is never directly D. 50 Hz.
connected to the earth ground. A current-limiting device
7. Signals X, Y, and Z are recorded against a reference
or isolation device is always placed between the patient
(referential) and W1 and W2 are acquired by bipolar
ground and the earth ground. A common method is to use
recording (W1-W2) using digital PSG. Which of the
optical isolation in which the signal is transmitted by light
following is NOT true?
within a small element of the circuit. Figure 2–20 illustrates
one method in which part of the amplifier is isolated from A. The derivation X-Y can be displayed.
the chassis and earth grounds. B. The derivation W1-X can be displayed.
C. If all derivations containing X, Y, and Z show artifact,
CLINICAL REVIEW QUESTIONS the reference electrode is probably faulty.
1. What (low, high) filter settings are recommended for D. The filter settings of the displayed derivation W1-W2
PSG recording (display) of EEG and EOG derivations? can be changed.
A. 0.5, 70 Hz. 8. What is the minimum recommended sampling rate to
B. 0.3, 35 Hz. record the oximetry signal?
C. 0.5, 70 Hz. A. 50 samples/sec
D. 0.5, 35 Hz. B. 25 samples/sec.
C. 10 samples/sec.
2. What are the recommended (low, high) filter settings for
D. 100 samples/sec.
display of EMG?
A. 1 Hz, 70 Hz. 9. What is the recommended electrode impedance less
B. 0.3 Hz, 35 Hz. than?
C. 10 Hz, 100 Hz. A. 10 KΩ.
D. 10 Hz, 70 Hz. B. 5 KΩ.
C. 20 KΩ.
3. What is the minimal recommended sampling rate for D. 1 KΩ.
recording EEG, EOG, EMG, and ECG signals?
A. 100 samples/sec. 10. What are the recommended (low, high) filter settings for
display of the ECG?
B. 200 samples/sec.
A. 10, 100 Hz.
C. 400 samples/sec.
B. 0.3, 35 Hz.
D. 500 samples/sec.
C. 10, 70 Hz.
4. What is the minimal recommended sampling rate for D. 0.3, 70 Hz.
airflow, rib cage and abdominal movements, and NP?
11. Using a high filter of 35 Hz for the EEG and EOG display
A. 10 samples/sec. (recording) reduces 60-Hz activity in the displayed
B. 25 samples/sec. signal.
C. 100 samples/sec. A. True
D. 200 samples/sec. B. False
5. Which of the following is true about the effect of a low 12. What are the recommended (low, high) filter settings for
filter setting of 0.3 Hz? display of the thermal airflow or chest and abdominal
A. Has minimal effect on a 10-Hz signal. RIP signals?
B. Does not affect the amplitude of slow wave activity A. 0.3, 35 Hz.
(0.5–2 Hz). B. 0.1, 15 Hz.
26 Chapter 2 The Technology of Sleep Monitoring
100 µV F -M
4 1
1 sec C4-M1
O2-M1
E1-M2
E2-M2
Chin EMG
FIGURE 3–1 Stage W. A 30-second epoch with eyes closed and then eyes open. More than 50% of the epoch has occipital alpha activity. EMG = electromyogram.
Epochs without visually discernible alpha rhythm (see Table chin EMG tone for REMs is because stage R (REM sleep) is
3–2, rule B) are scored as stage W if any of the following are characterized by REMs and low muscle tone.
present: Eye blinks of a frequency of 0.5 to 2 Hz, reading eye How should one score epochs that contain both portions
movements, or irregular conjugate REMs with normal or with alpha rhythm (but < 50% of the epoch) AND portions
high chin muscle tone. These eye movement patterns are with eye movements consistent with wake? The AASM
characteristic of stage W. The requirement of normal or high scoring manual did not specifically address this situation.
Chapter 3 Sleep Staging in Adults 29
However, one can modify stage W rule B to apply to the TABLE 3–3
portions of the epoch without alpha rhythm that contain eye Stage N1 Rules
movements consistent with wake (see Table 3–2, rule B). If
A. In subjects who generate alpha rhythm with eye
the portions of the epoch containing alpha rhythm AND the closure, score stage N1 if
portions of the epoch considered to be wake due to eye 1. EEG: Alpha rhythm is attenuated and replaced by
movements add up to more than 15 seconds (majority of the low-amplitude mixed-frequency (4–7 Hz) activity for
epoch), then the epoch is scored as stage W. more than 50% of the epoch (<50% of the epoch has
Of note, approximately 10% of subjects do not generate alpha rhythm).
alpha rhythm on eye closure and a further 10% may generate a. EEG: Vertex sharp waves may be present but are
limited alpha rhythm. In these subjects, the occipital EEG not required for scoring stage N1.
activity is similar during eye opening and eye closure. When 2. EOG: Slow eye movements may be present in N1, but
alpha rhythm is not generated with eye closure, the rules for these are not required for scoring N1.
3. Chin EMG: Variable amplitude, often lower than wake.
scoring stage W and stage N1 are somewhat different and
sleep onset is more difficult to define (Tables 3–3 and 3–4). B. In subjects who do NOT generate alpha rhythm with eye
In patients who do not generate alpha rhythm, epochs satis- closure, score stage N1 commencing with the earliest of
fying rule B in Table 3–2 are scored as stage W. Otherwise, any of the following phenomena:
epochs are scored as stage W if they do NOT meet criteria 1. The EEG shows 4- to 7-Hz activity with slowing of
for stages N1, N2, N3, or R. In contrast to patients generating background frequencies by 1 Hz or greater from those
of stage W.
alpha rhythm, the presence of SEMs is a criterion for scoring
2. Vertex sharp waves.
stage N1 in subjects who do not generate alpha rhythm (see 3. Slow eye movements.
Table 3–4).
Note: Because slow eye movements often commence before attenuation of
In Figure 3–1, a 30-second tracing shows the transition alpha rhythm, sleep latency may be slightly shorter for some individuals who
from eyes-closed stage W to eyes-open stage W. Slightly do not generate alpha rhythm than for those who do.
more than 50% of the epoch contains alpha activity. Alpha EEG = electroencephalogram; EMG = electromyogram;
EOG = electro-oculogram.
activity is attenuated with eye opening and REMs are noted. Adapted from Iber C, Ancoli-Israel S, Chesson A, Quan SF for the American
In Figure 3–2, portions of the epoch contain alpha rhythm Academy of Sleep Medicine: The AASM Manual for the Scoring of Sleep and
and other portions are considered stage W owing to the Associated Events: Rules, Terminology and Technical Specifications, 1st ed.
Westchester, IL: American Academy of Sleep Medicine, 2007.
presence of eye movements consistent with wakefulness
TABLE 3–4
Scoring Stage W and N1
EEG* EOG CHIN EMG
Alpha rhythm Stage W >50% of the epoch with alpha activity SEMs may be present Variable
on eye Eyes closed
closure Stage W Low-amplitude beta and alpha frequencies REMs Normal or high
Eyes open
Blinks Variable
Reading eye movements
Stage N1 >50% of epoch with alpha attenuation SEMs may be present Variable
and replacement with low-amplitude
mixed-frequency EEG
No alpha Stage W Low-amplitude beta and alpha frequencies REMs Normal or high
rhythm on
Eye blinks Variable
eye closure
Reading eye movements
SEMs absent
Stage N1 Vertex sharp wave Variable Variable
Slowing of 4 to 7 Hz, slowing of Variable Variable
frequency ≥ 1 Hz, compared to stage W
Low-amplitude beta and alpha frequencies SEMs appear Variable
Note: Bold text denotes essential features.
*The EEG is assumed not to contain sleep spindles or K complexes not associated with arousal.
EEG = electroencephalogram; EMG = electromyogram; EOG = electro-oculogram; REMs = rapid eye movements; SEMs = slow eye movements.
30 Chapter 3 Sleep Staging in Adults
100 µV F -M
4 1
C4-M1
O2-M1
E1-M2
E2-M2
Chin EMG
FIGURE 3–2 Stage W. A 30-second epoch containing rapid eye movements (REMs), high chin electromyographic (EMG) activity, and some alpha activity. The majority of the
epoch contains either alpha activity or eye movements consistent with wakefulness.
100 µV
F4-M1
1 sec
C4-M1
O2-M1
E1-M2
E2-M2
Chin EMG
FIGURE 3–3 Stage W. A 30-second epoch is shown containing REMs, blinks, relatively high chin electromyographic (EMG) activity, and the absence of discernible alpha activity.
100 µV
F4-M1
1 sec
C4-M1
O2-M1
E1-M2 SEM
E2-M2
Chin EMG
FIGURE 3–4 Stage W with the eyes closed. A 30-second epoch is shown. Note that alpha rhythm is more prominent in the occipital derivation and present for more than 50% of
the epoch. Slow eye movements (SEMs) are present in this epoch. Although characteristic, they are not a criterion for scoring stage W or N1 in patients producing alpha rhythm
with eye closure. The chin electromyography (EMG) has a low amplitude, but this is variable. In some patients, the chin EMG activity is higher in stage W than during sleep.
(see Table 3–2, stage W rule B). The majority of the epoch eyes-closed stage W. Here, greater than 50% of the epoch has
contains either alpha rhythm or eye movements consistent prominent alpha activity. SEMs are also present and the
with wakefulness, and hence, the epoch is scored as stage W. EMG activity is relatively decreased. It should be noted that
In Figure 3–3, the chin EMG activity is relatively high, REMs SEMs can be seen during both eyes-closed stage W and stage
and blinks are present, and there is no discernible alpha N1. If patients produce alpha rhythm with eye closure, SEMs
activity. The epoch is scored as stage W using stage W rule are not part of the criteria to score stage W (although they
B (see Table 3–2). Figure 3–4 illustrates an example of are characteristic during eyes-closed stage W).
Chapter 3 Sleep Staging in Adults 31
Stage N1 Stage N2
Low-amplitude mixed-frequency (LAMF) activity is defined Stage N2 is characterized by the presence of one or more
as a low-amplitude EEG pattern with predominantly 4- to nonarousal KCs (i.e., KCs NOT associated with an arousal)
7-Hz activity. Stage N1 is characterized by LAMF activity or one or more trains of SSs (Fig. 3–7). Arousal rules are
and the absence of sleep spindles (SSs) and K complexes discussed later in this chapter. During epochs of stage N2,
(KCs) not associated with arousal. SEMs may occur (see eye movements have usually ceased and the chin EMG is
Table 3–3). At the transition from stage N1 to stage N2, variable but usually at a level lower than that during wakeful-
vertex sharp waves may appear. In patients who produce ness. Recall that a KC is said to be associated with an arousal
alpha activity with eye closure (stage N1 rule A, see Table (KC+Ar) if the arousal commences no more than 1 second
3–3), the onset of stage N1 occurs when more than 50% of after the termination of the KC. Also note that the KC activ-
the epoch is marked by alpha attenuation (alpha activity in ity is seen in the recommended electro-oculographic (EOG)
< 50% of the epoch) and replacement with LAMF EEG (Fig. derivations (E1-M2 and E2-M2) as in-phase deflections in
3–5). In individuals who do not produce alpha activity with contrast to REMs (out-of-phase deflections). The rules for
eye closure (Fig. 3–6), the start of stage N1 occurs at the scoring stage N2 are listed in Table 3–5 and summarized in
earliest occurrence of SEMs, a slowing of the EEG by 1 Hz Table 3–6.
or more from that in stage W, or the presence of vertex sharp
waves (stage N1 rule B, see Table 3–3). Table 3–4 displays Start and Continuation of Stage N2
the characteristics of stage W and stage N1 for patients who According to the stage N2 rules (see Table 3–5, rule A), begin
do and do not produce alpha with eye closure. As noted in scoring stage N2 (see Fig. 3–7) when a KC (not associated
the AASM scoring manual, because SEMs may occur before with an arousal) or an SS occurs in the first half of the
alpha attenuation in subjects who have alpha activity with current epoch or the last half of the previous epoch. This
eye closure, the sleep onset may be scored somewhat earlier assumes that the epoch does not meet criteria for stage N3
in patients who do not produce alpha activity with eye (slow wave activity [SWA] present in ≥ 20% of the epoch,
closure. i.e., ≥6 sec). Recall that SWA is defined as EEG activity of
100 µV
F4-M1
1 sec
C4-M1
O2-M1
E1-M2
E2-M2
Chin1-Chin2
A
V
100 µV
F4-M1
1 sec
C4-M1
O2-M1
E1-M2
E2-M2
Chin EMG
FIGURE 3–5 A, Stage N1. A 30-second epoch in which no sleep spindles or K complexes are noted in the electroencephalogram (EEG). Less than 50% of the epoch has alpha rhythm.
The EEG shows alpha attenuation and low-amplitude mixed-frequency (4–7 Hz) activity for more than 50% of the epoch. Slow eye movements are present but not required. The
chin electromyogram (EMG) is often lower than stage W. B, Stage N1. A vertex sharp wave (V) is noted. No sleep spindles or K complexes are seen in the EEG. The chin EMG is relatively
high in this example.
Exploring the Variety of Random
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personages in the entourage of the Sultan. … The Porte,
however, protested, with the support of Germany, against the
appointment of Colonel Schaeffer, who appears to have been
suspected of English sympathies. Russia, too, it was said,
objected, insisting that the appointee must be of the Orthodox
Greek faith. Thus, on the question of selecting a
governor-general for Crete, the concert of the powers broke
down as it did at other points during the long crisis. At the
end of November the name of Prince Francis Joseph of
Battenberg was prominently mentioned as a prospective
candidate of favor. The Cretan assembly proposed, unless a
suitable governor were speedily chosen by the powers, to offer
the post to a candidate of its own selection."
Months went on, while the Powers still discussed the Cretan
situation and no agreement was reached. In January, 1898, the
Turkish government appointed Edhem Pasha governor of Candia;
but, in the face of the admirals of the blockading squadrons,
who exercised an undefined authority, he seems to have had
practically little power. Presently, a new attempt was made to
select a Christian Governor-general. France and Russia
proposed Prince George of Greece, but Austria and Turkey
opposed. In April, Austria and Germany withdrew from the
blockade and from the "Concert," leaving Great Britain,
Russia, France and Italy to deal with Cretan affairs alone.
The admirals of these Powers, acting under instructions, then
divided the Cretan coast among themselves, each directing the
administration of such government as could be conducted in his
own part. The British admiral had Candia, the capital town,
and there trouble arose which brought the whole Cretan
business to a crisis. He attempted to take possession of the
customs house (September 6), and landed for that purpose a
small force of 60 men. They were attacked by a Turkish mob,
with which they fought desperately for four hours, losing 12
killed and some 40 wounded, before they could make their
retreat to the shore and regain their ship. At the same time a
general massacre of Christians in the town was begun and some
800 perished before it was stopped. Edhem Pasha, with about
4,000 Turkish troops at his command, was said to have waited
long for the mob to do its work before he interfered.
{550}
Spectator (London),
December 2, 1899.
TURKEY: A. D. 1899-1901.
Impending outbreak in Macedonia.
TURKEY: A. D. 1900.
The Zionist movement of the Jews to colonize Palestine.
TURKEY: A. D. 1901.
The Cretan question.
"The Cretan Assembly meets at the end of next month, and its
probable attitude towards the question of union with Greece is
already the subject of speculation here. The decision of the
conference of Ambassadors at Rome is embodied in a memorandum
which has been handed to Prince George by the Consuls at
Canea, while a copy of the document has been unofficially
presented to King George 'à titre d'information.' The
Ambassadors express their opinion that any manifestation on
the part of the Cretans in favour of union with Greece would
be inopportune at the present moment, and they propose a
prolongation of the present provisional system of government
without assigning any definite term to the High Commissioner's
mandate.
"Whether Prince George, who is an enthusiastic advocate of
union with Greece, will accept the new arrangement
unconditionally remains to be seen. Meanwhile the islanders
are occupied with preparations for the elections.
{552}
TURKEY: A. D. 1901.
Order regulating the visit of Jews to Palestine.
----------TURKEY: End--------
TWAIN, Mark:
Description of scenes in the Austrian Reichsrath.
U.
UGANDA: A. D. 1897-1898.
Native insurrection and mutiny of Sudanese troops.
UITLANDERS.
"Section 4.
That to aid the public land States in the reclamation of the
desert lands therein, and the settlement, cultivation, and
sale thereof in small tracts to actual settlers, the Secretary
of the Interior with the approval of the President, be, and
hereby is, authorized and empowered, upon proper application
of the State to contract and agree, from time to time, with
each of the States in which there may be situated desert lands
as defined by the Act entitled 'An Act to provide for the sale
of desert land in certain States and Territories,' approved
March 3d, 1877, and the Act amendatory thereof, approved March
3d, 1891, binding the United States to donate, grant and
patent to the State free of cost for surveyor price such
desert lands, not exceeding one million acres in each State,
as the State may cause to be irrigated, reclaimed, occupied,
and not less than twenty acres of each one hundred and
sixty-acre tract cultivated by actual settlers, within ten
years next after the passage of this Act, as thoroughly as is
required of citizens who may enter under the said desert land
law.
"The court has reversed the decree of the Circuit Court and
remanded the case, with directions to enter a decree in favor
of complainant in respect only of the voluntary payment of the
tax on the rents and income of defendant's real estate and
that which it holds in trust, and on the income from the
municipal bonds owned or so held by it. While, therefore, the
two points above stated have been decided, there has been no
decision of the remaining questions regarding the
constitutionality of the act, and no judgment has been
announced authoritatively establishing any principle for
interpretation of the statute in those respects."
The re-hearing asked for was granted by the Court on the 6th
of May, when Justice Jackson was able to take his seat on the
bench, after which, on the 20th of May, by the opinion of five
members of the Court against four, the law was pronounced null,
so far as concerned the imposition of a tax on incomes. The
opinion of the majority was delivered by Chief Justice Fuller,
who said, in part:
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