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Embla n7000 system

Manufactured by Natus
Sourced in United States

The Embla N7000 system is a comprehensive sleep diagnostic platform designed for clinical and research applications. It offers high-quality data acquisition and analysis capabilities for sleep studies.

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4 protocols using embla n7000 system

1

Overnight Sleep Study Protocol for OSA

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Overnight PSG was performed using an Embla N7000 system (Natus Medical Incorporated, USA) from 10 PM to 6 AM in the sleep-disordered breathing laboratory of our hospital. The overall process and manual scoring were performed by skilled technicians who were supervised by experienced sleep physicians in accordance with the AASM manual 2.5.30 The AHI was defined as the total number of apnea and hypopnea events per hour of sleep. LSpO2 was defined as the lowest pulse oxygen saturation during sleep. The oxygen desaturation index (ODI) was defined as the frequency of instances when the blood oxygen levels decreased (desaturation) by 3% or more. T90 was defined as the percentage of time when the oxygen saturation was < 90% during the period of monitoring. An AHI ≥15 events/h was used as a cutoff to divide the patients into two groups: the control group featuring patients with an AHI <15 events/h and an OSA group of patients with an AHI ≥15 events/h based on the International Classification of Sleep Disorders (3rd Edition).31 (link) In addition, we classified patients with a T90 > 0 into a nocturnal hypoxemia (NH) group and those with a T90 = 0 as a no NH group.
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2

Polysomnographic Evaluation of Sleep Disorders

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The in-lab polysomnogram for the patients recruited from the sleep center included recordings of C3 and C4 electroencephalograms, right and left electrooculograms, and submental and bilateral anterior tibialis electromyograms. Sleep-stage scoring was performed in 30-second epochs. Respiration was monitored with a nasal pressure transducer, nose and mouth thermocouples, and thoracic and abdominal strain gauges. Recording of the oxyhemoglobin saturation (SpO2) was obtained with Biox 3700 pulse oximeter (Ohmeda, Englewood, CO) at 10 Hz and averaged over each 30-second epoch. Apneas were identified if airflow was absent in thermocouples and nasal cannula channels for at least 10 seconds. Hypopneas were identified if there was at least 30% reduction in airflow for at least 10 seconds accompanied with at least 4% oxyhemoglobin desaturation. AHI was determined as the frequency of apneas and hypopneas per hour of total sleep time. The in-lab polysomnography was conducted using the Embla N-7000 system (Natus Medical, Pleasanton, CA). Polysomnography for the community participants was performed at home, using the Compumedics P-series recording system (Compumedics, Abbotsford, Victoria, Australia).
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3

Full Polysomnography with Sleep Fragmentation

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The established 10–20 system [61 ] was used for full PSG including F3/F4, C3/C4, O1/O2, bilateral electro-oculogram (EOG) and submental electromyogram (EMG), electrocardiogram (EKG), abdominal and thoracic respiratory belts, an oral/nasal airflow thermistor, a snore sensor, a pulse oximeter, and leg EMG sensors. When the first night of screening indicated no sleep disorders, the participant continued in the study and the next two nights (baseline and sleep fragmentation) included a minimal montage of EEG, EOG, EMG, and EKG. High resolution video monitoring was used for behavioral observation and video recording. Recordings were made with the Embla N7000 system (Natus Neurology, Middleton, WI) and data were analyzed using Rembrandt software (Natus Neurology, Middleton, WI).
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4

Comprehensive Sleep Monitoring Protocol

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Sleep monitoring was performed to all participants with an Embla N7000 System (Natus Medical, Pleasanton, CA, USA). The monitoring sleep time is more than 7 hours with simultaneous recording of AHIs and lowest SaO2. They were banned from taking hypnosis, caffeine, concentrated tea, sedatives, and antihypertensive drugs before the day of polysomnogram monitoring.
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