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E series

Manufactured by Compumedics
Sourced in Australia

The E-Series is a line of laboratory equipment by Compumedics. It is designed for the measurement and analysis of various physiological signals. The E-Series provides reliable and accurate data collection capabilities for research and clinical applications.

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32 protocols using e series

1

Polysomnographic Assessment of Sleep Architecture

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Polysomnography (PSG) was utilised during the four study nights to assess sleep architecture [30 ,31 ]. PSG arrangement and recording began each night at 9:00 p.m. for both conditions. Standard PSG equipment (Compumedics E Series, Melbourne) was arranged as follows: EEG (Oz and Cz positions); EOG (outer canthi of each eye); EMG (masseter and facial muscles); the earth electrode on the right clavicle. All signals were recorded using gold Grass electrodes with initial impedances below 10 kΩ. The PSG recordings were scored according to standard criteria of AASM [32 ] in 30-s epochs. Each epoch was assigned a stage of sleep (Stages 1–3, REM) or wake by a blinded scorer using Profusion 3 software (Compumedics E Series, Melbourne, Australia). From each sleep period, participants’ total sleep time was calculated. Participants were continuously monitored throughout the study to ensure napping did not occur.
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2

Comprehensive Sleep Disorder Evaluation

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Each patient underwent standard PSG (E-Series, Compumedics Limited, Abbotsford, Australia) study. The sleep-related laryngeal stridor, sleep breath disturbance, and involuntary movements were recorded. Sleep scoring was carried out for 30-second epochs according to AASM scoring criteria 2012. Next, sleep structure, sleep efficiency (total sleep time/total time in bed ×100%), arousal, periodic limb movement in sleep (PLMS) indices (AI and PLMS-I) (number of arousals and PLMS per hour of sleep), and the calculated AHI (apnea + hypopnea index) were evaluated.
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3

Overnight Polysomnography for OSAS Diagnosis

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As detailed elsewhere [26 (link)], OSAS was detected using overnight PSG (Compumedics, E-series, Melbourne, VIC, Australia). Hypopnea was defined as a ≥30% reduction in nasal pressure for ≥10 s with ≥4% oxygen desaturation, or a ≥50% reduction in nasal pressure for ≥10 s with ≥3% oxygen desaturation or arousal. Apnea was defined as a ≥90% reduction in airflow for ≥10 s. These events were manually scored by experienced technicians based on the recommendation of Task Force of the American Sleep Disorders Association 2007 [27 ]. The total number of apneas plus hypopneas divided by the total sleep time (hour) was defined as the apnea-hypopnea index (AHI). An AHI < 30 was defined as normal to moderate OSAS, and an AHI ≥ 30 was defined as severe OSAS.
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4

Polysomnographic Analysis of Sleep Apneas

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Sleep apneas were confirmed by an overnight PSG (Compumedics, E-Series, Australia). Six EEG signals (C3-M2, C4-M1, F3-M2, F4-M1, O1-M2, and O2-M1), two channels of electrooculography (EOG) signals (E1-M2, E2-M2), chin EMG (EMG1-EMG2, EMG1-EMG3), electrocardiography (ECG), respiration (nasal pressure, airflow), oxygen saturation (SpO2), abdominal and chest movement, and leg movements were recorded according to the American Academy of Sleep Medicine (AASM) guidelines [13 (link), 14 (link)].
Sleep stage and respiratory events were analyzed according to the AASM 2.3 guidelines [13 (link), 14 (link)]. Sleep stages were divided into the NREM (N1, N2, and N3) sleep, rapid eye movement (REM) sleep, and wake stages.
Sleep-related parameters (total sleep time (TST), sleep efficiency (SE), sleep latency (SL), wake time after sleep onset (WASO), and the proportion of each sleep period to total sleep (N1/TST, N2/TST, N3/TST)) were calculated and reported in the PSG study report.
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5

Comprehensive Polysomnographic Assessments

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All patients underwent a night of standard vPSG (Compumedics-E series, Australia) monitoring in the sleep center. The basic recordings included electroencephalogram (F3-A2, F4-A1, C3-A2, C4-A1, O1-A2, and O2-A1), electrooculogram (EOG, LOC-A2, and ROC-A1), chin EMG, electrocardiogram, nasal-oral pressure transducer airflow, thermal oronasal airflow, thoracic and abdominal respiratory efforts, oxyhemoglobin saturation, snoring sound, and body position. All the vPSGs were manually scored by experienced technologists according to the American Academy of Sleep Medicine guidelines.
The following vPSG data were obtained and analyzed: awakenings; total sleep time (TST); sleep efficiency (SE); sleep latency (SL); REM sleep latency (REML); wake after sleep onset (WASO); percentage of sleep spent in non-REM sleep stage (NREM) 1, NREM2, NREM3, and REM sleep; arousal index; apnea-hypopnea index (AHI); minimal oxygen saturation (SaO2); mean SaO2; and the percentage of time spent at SaO2 <90% (time − [SaO2 <90%]).
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6

Overnight Polysomnography for OSA Diagnosis

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All patients underwent in-laboratory overnight PSG (Compumedics E series, Australia) examination. OSA was defined as an apnea-hypopnea index (AHI)≥5 events per hour; further, the severity of OSA was defined as follows: mild OSA (5≤AHI<15), moderate OSA (15≤AHI<30), and severe OSA (AHI≥30).
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7

Polysomnography Assessment of Sleep Disorders

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Polysomnography was performed using a computerized diagnostic system (E series; Compumedics) in the Sleep Laboratory. All participants received overnight PSG according to standardized criteria by an experienced sleep technician. PSG recordings included electroencephalography, electrooculography, electromyography of the submental muscles and of bilateral anterior tibialis muscles, electrocardiography, oxygen saturation, as well as oral and nasal airflow. The PSG recordings were scored based on the standard criteria of the American Academy of Sleep Medicine.25 Apnea was defined as continuous cessation of airflow for >10 s. Hypopnea was defined as a ≥30% decrease in airflow persisting for >10 s accompanied by oxygen desaturation of ≥4%. AHI was expressed as the total number of apnea plus hypopnea events per hour during sleep. The mean oxygen saturation (MSaO2) and lowest oxyhaemoglobin saturation (LSaO2) value were also recorded during sleep as parameters of nocturnal hypoxemia.
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8

Scoring Sleep Apnea Types by PSG

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All PSGs were digitally recorded on either a Network Concepts Incorporated (Middleton, Wisconsin) or an E-Series (Compumedics; Victoria, Australia) digital PSG acquisition system. All PSGs were scored for sleep stages and disordered breathing events according to AASM scoring guidelines (Iber et al., 2007 ). Sleep apnea was defined by the type (central/mixed/obstructive) and by the apnea-hypopnea index (AHI)≥5 by PSG. Accordingly, subjects were divided into 4 groups: 1) CSA 2) mixed apnea 3) no apnea and 4) obstructive sleep apnea.
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9

Comprehensive Sleep Apnea Assessment Protocol

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Body weight and height were measured in the morning, body mass index (BMI) was calculated as weight (kg)/height2 (link) (m). Waist circumference was measured at a level midway between the lower costal margin and the iliac crest. Blood pressure was measured on the right arm with the participants in a sitting position, using a mercury sphygmomanometer. PSG (E series, Compumedics, Australia) consisted of the following variables: oronasal airflow, snoring, thoracic and abdominal respiratory efforts, pulse oxygen saturation, body position, electroencephalography, electrooculography, electromyography, and electrocardiography. PSG records were staged in accordance with the criteria of the American Academy of Sleep Medicine (AASM).15 (link) Apnea hypopnea index (AHI) was defined as the number of apneas and hypopneas per hour of sleep. Oxygen desaturation index (ODI) was defined as the total number of episodes of oxygen desaturation ≥4% from the immediate baseline. Percentage of total sleep time spent with SaO2 < 90% and lowest oxygen saturation were also obtained. The severity of OSA was classified as simple snoring, mild, moderate, and severe by AHI <5, 5–14.9, 15–29.9, and ≥30 events/h, respectively. PSG was repeated during the CPAP titration.
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10

Polysomnographic Evaluation of Sleep Apnea

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Sleep apnea was confirmed by overnight PSG (Compumedics, E-Series, Australia). Six channels of EEG signals (C3-M2, C4-M1, F3-M2, F4-M1, O1-M2, and O2-M1), two channels of electrooculography signals (E1-M2 and E1-M2), and chin EMG (EMG1–EMG2, EMG1–EMG3), electrocardiography, respiration (nasal pressure, airflow), oxygen saturation, abdominal and chest movement, and leg movements were recorded according to the American Academy of Sleep Medicine (AASM) scoring manual (version 2.4) [14 (link)].
Sleep stage and respiratory events were analyzed according to the guidelines of the AASM [14 (link)]. Sleep stages were divided into N1, N2, N3, R, and W stages. Respiratory events were divided into obstructive apnea, central apnea, mixed apnea, and hypopnea. The apnea-hypopnea index (AHI) was defined and calculated as the sum of the number of apneas and hypopneas per hour.
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