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POLYSMNOGRAPHY

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POLYSMNOGRAPHY By Aida Mahmoud yousef Polysomnography (PSG) : Is a multi-parametric test used in the study of sleep and as a diagnostic tool in sleep Medicine. – PowerPoint PPT presentation

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Title: POLYSMNOGRAPHY


1
POLYSMNOGRAPHY
  • By
  • Aida Mahmoud yousef

2
  • Polysomnography (PSG)
  • Is a multi-parametric test used in the study of
    sleep and as a diagnostic tool in sleep
  • Medicine.
  • The test result is called a polysomnogram,

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  • Polysomnography is a comprehensive recording of
    the biophysiological changes that occur during
    sleep. It is usually performed at night, when
    most people sleep, but shift workers and people
    with circadian rhythm sleep disorders can do the
    test at other times of day.

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  • A single-night PSG is usually adequate. However,
    night-to-night variability may exist in patients
    who have a high probability but a low apnea
    index.
  • . So some authorities caution that more than one
    night of recording may be necessary so the
    patient can become comfortable with the
    surroundings and sleep more naturally.

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  • The PSG monitors many body functions including
    brain (EEG), eye movements (EOG), muscle activity
    or skeletal muscle activation (EMG) and heart
    rhythm (ECG) during sleep. After the
    identification of the sleep disorder sleep apnea
    in the 1970s, the breathing functions respiratory
    airflow and respiratory effort indicators were
    added along with peripheral pulse oximetry.

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Full Polysomnography
  • EEG EOG EMG ECG

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Indications
  • Polysomnography is used to diagnose, or rule out,
    many types of sleep disorders It is often ordered
    for patients with complaints of daytime fatigue
    or sleepiness that may be caused by interrupted
    sleep.

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Sleep Disorders
  • Obstructive
  • Central
  • Mixed
  • Upper airway resistance
  • Periodic Breathing
  • Narcolepsy
  • Insomnia
  • Periodic leg movement(PLM)
  • Restless legs
  • insomnia, sleep terrors

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  • Any combination of two or more of the following
    symptoms of sleep apnea a. through e.
  • Excessive daytime sleepiness as evidenced by
    inappropriate daytime napping (e.g., during
    driving, conversation, or eating) sleepiness
    that interferes with daily activities not
    explained by other conditions, e.g., poor sleep
    hygiene, medication, drugs, alcohol, psychiatric
    or psychological disorders, or an Epworth
    Sleepiness Scale score greater than 10  or
  • Persistent or frequent socially disruptive
    snoring or choking or gasping episodes associated
    with awakenings  or

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  • Symptoms suggesting narcolepsy, e.g., sleep
    paralysis, hypnagogic hallucinations, cataplexy
    OR
  • Violent or injurious behavior during sleep OR
  • Nocturnal oxygen desaturation with unexplained
    right heart failure, polycythemia, cardiac
    arrhythmias during sleep or pulmonary
    hypertension OR
  • Excessive daytime sleepiness together with
    witnessed periodic limb movements of sleep.
  • Unexplained hypertension or
  • Craniofacial or upper airway soft tissue
    abnormalities  OR
  • neck circumference
  • Obesity (BMI greater than 30 kg/m²) or
  • .Witnessed apnea during sleep greater than 10
    seconds in duration

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  • Individuals with moderate or severe congestive
    heart failure, stroke/TIA, coronary artery
    disease, or significant tachycardic or
    bradycardic arrythymias who have nocturnal
    symptoms suggestive of a sleep apnea.
  • Any other unexplained symptoms associated with
    disruption of normal sleeping patterns that have
    persisted for 6 to 12 months

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  •   The American Academy of Sleep Medicine (AASM)
    states that, "Adult patients with habitual
    snoring, excessive daytime sleepiness, a BMI
    greater than 35 and observed apneas are at high
    risk for OSA with at least a 75 likelihood of
    having an AHI (or RDI) equal to or greater than
    10." 
  • "Berlin Questionnaire" with three groups of
    questions one regarding snoring, the second
    regarding daytime sleepiness, and the third
    regarding the presence of hypertension or
    obesity. 

15
  • Repeat PSG for adults is considered medically
    necessary under the following circumstances
  • To re-evaluate an individual with failure of
    resolution of symptoms or recurrence of symptoms
    during treatment OR 
  • To evaluate the impact of uvulopalatopharyngoplast
    y (UPPP) or other corrective surgeries for
    obstructive sleep apnea (OSA)
  • To evaluate the impact of an oral appliance
  • To titrate continuous positive airway pressure
    (CPAP)

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  • using CPAP, if a significant weight loss has
    occurred since the initial study OR
  • To titrate CPAP prescription when half night or
    "split night" PSG with titration of CPAP
    performed in the second part of the study is not
    possible due to AHI or RDI less than 20 or when
    initial PSG was not diagnostic in time to allow
    for at least 3 hours of CPAP titration including
    both REM and non-REM sleep.

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Mechanism
  • A polysomnogram will typically record from eight
    to twelve channels requiring about 22 wire
    attachments to the patient. These channels vary
    in every lab and may be adapted to meet the
    doctor's requests.

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  • Wires for each channel of recorded data lead from
    the patient and converge into a central box,
    which in turn is connected to a computer system
    for recording, storing and displaying the data.
    During sleep the computer monitor can display
    multiple channels continuously. In addition, most
    labs have a small video camera in the room so the
    technician can observe the patient visually from
    an adjacent room

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(EEG)
  • The electroencephalogram (EEG) will generally use
    six "exploring" electrodes and two "reference"
    electrodes, unless a seizure disorder is
    suspected,
  • The exploring electrodes are usually attached to
    the scalp near the frontal, central (top) and
    occipital (back) portions of the brain via a
    paste that will conduct electrical signals
    originating from the neurons of the cortex.

23
  • One EEG channel (central channel with an ear
    reference provides the best amplitude) is used to
    monitor sleep stage. However, most laboratories
    use 2 central channels and 2 occipital channels,
    with ear references as an adjunct to help
    identify sleep latency and arousals. A 10- to
    20-electrode placement system is used to
    determine the location of these channels.
    Additional EEG channels can be used, particularly
    in patients with epilepsy (ie, a full 10-20
    montage).

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  • These electrodes will provide a readout of the
    brain activity that can be "scored" into
    different stages of sleep (N1, N2, N3 which
    combined are referred to as NREM sleep, and Stage
    R which is rapid eye movement sleep or REM, and
    Wakefulness).

29
EOG
  • The electrooculogram (EOG) uses two electrodes
    one that is placed 1 cm above the outer canthus
    of the right eye and one that is placed 1 cm
    below the outer canthus of the left eye. These
    electrodes pick up the activity of the eyes and
    the electropotential difference between the
    cornea and the retina (the cornea is positively
    charged relative to the retina). Evaluation of
    the eye movements is necessary for 2 reasons.
    First is for documentation of the onset of rapid
    eye movement (REM) sleep, and second is to note
    the presence of slow-rolling eye movements that
    usually accompany the onset of sleep.

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  • Eye blinks Conjugate vertical eye movements at a
    frequency of 0.52 Hz present in wakefulness.
  • Slow eye movements Conjugate, fairly regular,
    sinusoidal eye movements with an initial
    deflection lasting gt 500 msec. are typical of
    eyes closed drowsy, wakefulness, and stage N1
    sleep.
  • Rapid eye movements (REMs) Conjugate, irregular,
    sharply peaked eye movements with an initial
    deflection usually lasting lt 500 msec. Whereas
    rapid eye movements are characteristic of stage R
    sleep, they may also be seen in wakefulness with
    eyes open
  • Reading eye movements Trains of conjugate eye
    movements consisting of a slow phase followed by
    a rapid phase in the opposite direction as the
    subject reads. due to a slow scan of the written
    page (left to right) followed by a rapid return
    to the left.

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EMG
  • The electromyogram (EMG) typically uses four
    electrodes to measure muscle tension in the body
    as well as to monitor for an excessive amount of
    leg movements during sleep (which may be
    indicative of periodic limb movement disorder,
    PLMD).. This, like the EOG, helps determine when
    sleep occurs as well as REM sleep. Sleep
    generally includes relaxation and so a marked
    decrease in muscle tension occurs.

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  • in REM sleep. A person becomes partially
    paralyzed to make acting out of dreams
    impossible, although people that do not have this
    paralysis can suffer from REM behavior disorder.
  • Two or more leads are placed on the anterior
    tibialis of each leg to measure leg movements.
  • To assess bruxism, the EMG electrodes can be
    placed over the masseter.
  • the intercostal EMG is used as adjunctive help
    for determining effort during respiratory events.

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  • Though a typical electrocardiogram (ECG or EKG)
    would use ten electrodes, only two or three are
    used for a polysomnogram.. These can be analyzed
    for any abnormalities that might be indicative of
    an underlying heart pathology

41
  • Two channels are used for monitoring airflow. One
    thermistor channel (oral and/or nasal) is used to
    evaluate the presence or absence of airflow.
    Thermistor is the recommended channel for
    evaluation of apneas.
  • Nasal pressure transducer channel is a more
    sensitive measure of airflow restriction(
    hypopneas ,airflow resistance in upper airway
    resistance syndrome).

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  • Normal breathing has a rounded pattern, while
    resistance to airflow leads to a squaring off of
    the flow signal,This forces air in and out of the
    mouth while no air enters the airway and lungs.
    Thus, the pressure transducer and thermocouple
    will detect this diminished airflow and the
    respiratory event may be falsely identified as a
    hypopnea, or a period of reduced airflow, instead
    of an obstructive apnea.

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  • Other parameters that can be monitored in a sleep
    study include the following
  • Pulse oximetry
  • End tidal or transcutaneous CO2
  • Sound recordings to measure snoring
  • Continuous video monitoring
  • Sleep position

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  • Optional parameters that can be monitored in a
    sleep study include the following
  • Core body temperature
  • Pressure and pH at various esophageal levels

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  • Pulse oximetry determines changes in blood oxygen
    levels that often occur with sleep apnea and
    other respiratory problems. The pulse oximeter
    fits over a finger tip or an ear lobe.

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snoring
  • may be recorded with a sound probe over the neck,
    though more commonly the sleep technician will
    just note snoring as "mild", "moderate" or "loud"
    or give a numerical estimate on a scale of 1 to
    10.
  • Also, snoring indicates airflow and can be used
    during hypopneas to determine whether the
    hypopnea may be an obstructive apnea

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instructions
  • Maintain regular sleep-wake rhythm.
  • Alcohol and sleeping pills may alter the PSG
    results, but if they are part of the patient's
    normal routine, they should not be abruptly
    stopped.
  • Avoid stimulants, including medications for
    narcolepsy.
  • Avoid strenuous exercise on the day of the PSG.
  • Avoid naps on the day of the sleep study.

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  • Stimulant medications, nicotine, and caffeine can
    affect the mean sleep latency, and medications
    (especially selective serotonin reuptake
    inhibitors SSRIs) can affect sleep-onset rapid
    eye movement (REM) periods.3 In general, SSRIs
    and stimulants need to be discontinued at least 2
    weeks prior to the test. Small amounts of
    caffeine do not usually need to be discontinued.

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Procedure
  • For the standard test the patient comes to a
    sleep lab in the early evening, and over the next
    12 hours is introduced to the setting and "wired
    up" so that multiple channels of data can be
    recorded when he/she falls asleep. During the
    study, the technician observes sleep activity by
    looking at the video monitor and the computer
    screen that displays all the data second by
    second. In most labs the test is completed and
    the patient is discharged home by 7 a.m. unless a
    Multiple Sleep Latency Test (MSLT) is to be done
    during the day to test for excessive daytime
    sleepiness.

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  • High costs and long waiting lists have prompted
    the exploration of alternative methods of
    evaluation. Although the following studies may
    have usefulness in specific clinical situations,
    but their role compared with conventional sleep
    studies remains controversial.
  • Ambulatory monitoring with portable equipment
  • Daytime PSG
  • Simplified sleep studies with limited subsets of
    monitored parameters

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  • physicians may prescribe home studies to enhance
    patient comfort and reduce expense. The patient
    is given instructions after a screening tool is
    used, uses the equipment at home and returns it
    the next day. Most screening tools consist of an
    airflow measuring device (thermistor) and a blood
    oxygen monitoring device (pulse oximeter). The
    patient would sleep with the screening device for
    one to several days, then return the device to
    the physician

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Interpretation
  • After the test is completed analyzing the data
    by reviewing the study in 30 second "epochs
  • The score consists of the following
    informationOnset of sleep from time the lights
    were turned off this is called "sleep onset
    latency" and normally is less than 20 minutes.
    (Note that determining "sleep" and "awake" is
    based solely on the EEG. Patients sometimes feel
    they were awake when the EEG shows they were
    sleeping. This may be because of sleep state
    misperception, drug effects on brain waves, or
    individual differences in brain waves.)

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  • Sleep efficiency the number of minutes of sleep
    divided by the number of minutes in bed. Normal
    is approximately 85 to 90 or higher.
  • Sleep stages these are based on 3 sources of
    data coming from 7 channels EEG (4 channels
    usually), EOG (2) and chin EMG (1). From this
    information each 30-second epoch is scored as
    "awake" or one of 4 sleep stages 1, 2, 3, and
    REM or Rapid Eye Movement sleep. Stages 13 are
    together called non-REM sleep.

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  • Non-REM sleep is distinguished from REM sleep,
    which is altogether different. Within non-REM
    sleep, stage 3 is called "slow wave" sleep
    because of the relatively wide brain waves
    compared to other stages another name for stage
    3 is "deep sleep". By contrast, stage 1 and 2 are
    "light sleep". The figures show stage 3 sleep and
    REM sleep each figure is a 30-second epoch from
    an overnight PSG.

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  • The percentage of each sleep stage varies by age,
    with decreasing amounts of REM and deep sleep in
    older people. The majority of sleep at all ages
    (except infancy) is Stage 2. REM normally
    occupies about 20-25 of sleep time. Many factors
    besides age can affect both the amount and
    percentage of each sleep stage, including drugs
    (particularly anti-depressants and pain meds),
    alcohol taken before bed time, and sleep
    deprivation.)

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  • Any breathing irregularities mainly apneas and
    hypopneas. Apnea is a complete or near complete
    cessation of airflow for at least 10 seconds
    followed by an arousal and/or 3 oxygen
    desaturation hypopnea is a 50 decrease in
    airflow for at least 10 seconds followed by an
    arousal and/or 3 oxygen desaturation. (Medicare
    requires a 4 desaturation in order to include
    the event in the report.)

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  • Arousals" are sudden shifts in brain wave
    activity. They may be caused by numerous factors,
    including breathing abnormalities, leg movements,
    environmental noises, etc. An abnormal number of
    arousals indicates "interrupted sleep" and may
    explain a person's daytime symptoms of fatigue
    and/or sleepiness.
  • Cardiac rhythm abnormalities.
  • Leg movements.
  • Body position during sleep.
  • Oxygen saturation during sleep.

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CPAP Titration
  • The above report mentions CPAP as treatment for
    obstructive sleep apnea. CPAP is continuous
    positive airway pressure and is delivered via a
    mask to the patient's nose or the patient's nose
    and mouth. (Some masks cover one, some both).
    CPAP is typically prescribed after the diagnosis
    of OSA is made from a sleep study (i.e., after a
    PSG test). To determine the correct amount of
    pressure and the right mask type and size, and
    also to make sure the patient can tolerate this
    therapy, a "CPAP titration study" is recommended.
    This is the same as a "PSG", but with the
    addition of the mask applied, so the technician
    can increase the airway pressure inside the mask
    as needed, until all, or most, of the patient's
    airway obstructions are eliminated

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  • a CPAP titration study, which means a return to
    the lab for a second all-night PSG (this one with
    the mask applied). Often, however, when a patient
    manifests OSA in the first 2 or 3 hours of the
    initial PSG, the technician will interrupt the
    study and apply the mask right then and there
    the patient is awakened and fitted for a mask.
    The rest of the sleep study is then a "CPAP
    titration." When both the diagnostic PSG and a
    CPAP titration are done the same night, the
    entire study is called "Split Night".

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Split night" study
  • The split-night study has these advantages
  • The patient only has to come to the lab once, so
    it is less disruptive than is coming two
    different nights
  • It is "half as expensive" to whoever is paying
    for the study.

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  • The split-night study has these disadvantages
  • There is less time to make a diagnosis of OSA
    (Medicare requires a minimum of 2 hours of
    diagnosis time before the mask can be applied)
    and
  • There is less time to assure an adequate CPAP
    titration. If the titration begins with only a
    few hours of sleep left, the remaining time may
    not assure a proper CPAP titration, and the
    patient may still have to return to the lab.

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