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Somnoscreen plus

Manufactured by SOMNOmedics
Sourced in Germany

The SOMNOscreen plus is a compact and portable sleep diagnostic system designed for comprehensive sleep studies. It features high-quality signal recording and analysis capabilities to assist healthcare professionals in diagnosing sleep disorders.

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26 protocols using somnoscreen plus

1

Sleep Characterization via Portable EEG Monitoring

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Sleep was recorded using a portable EEG device (SOMNOscreenTM plus, SOMNOmedics GmbH, Randersacker, Germany). Fourteen Ag/AgCl electrodes were applied to the cleansed sites at the scalp, face and upper body of the participants, including Fz, C3, C4, Cz, Pz, Oz, A1, A2, Ground, Electrooculography (left and right), Electromyography (left and right upper chin and beneath chin), Electrocardiography (ECG) (Lead II: left lower rib cage and right clavicle), according to the AASM recommendations [38 ]. EEG recordings were referenced to Cz. All channels were sampled at 256 Hz. To ensure high quality, impedances were kept within a tolerable range (≤20 Ω). Sleep measures of the nap group resemble typical values of nap studies and are summarized in Table 1.

Descriptive sleep measures of the nap group.

Duration in minutes Mean (SEM)Percentage of total sleep time Mean (SEM)
Total sleep time71.95 (3.74)
NREM1 sleep7.38 (1.18)10.15 (1.41)
NREM2 sleep35.76 (2.76)51.25 (3.81)
NREM3 sleep16.14 (3.17)22.91 (4.49)
REM sleep6.57 (1.79)7.92 (2.17)
WASO6.0 (1.69)7.64 (2.10)

REM rapid eye movement sleep, NREM non REM sleep, WASO wake after sleep onset.

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2

Nocturnal Polysomnography for Obstructive Sleep Apnea Diagnosis

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All patients were subjected to nocturnal attended full polysomnography (PSG) (type I sleep study) (16 (link)) (SOMNOscreen TM Plus, SOMNOmedics GmbH, Germany). The PSG recording included electroencephalography (EEG), electrooculogram (EOG), electromyogram (EMG; chin and bilateral anterior tibialis), electrocardiogram (ECG), pulse oximetry, body position, airflow, and thoracic and abdominal movements using respiratory inductance plethysmography. Airflow was measured using both nasal thermistor and pressure transducer. Patients were monitored via camera throughout the study with video recording, and synchronized PSG video. The PSG studies were manually scored by one of the authors (MIM) using the American Academy of Sleep Medicine (AASM) scoring manual version 2.5 (17 (link)). Apnea hypopnea index (AHI) was calculated as the number of apneas and hypopneas per hour of sleep. The oxygen desaturation index (ODI) (number of 3% or more drops in the oxygen saturation per hour of sleep) as well as the percentage of the sleep time spent with oxygen saturation <90% (T90) were recorded. Those with an AHI > 5 events/hour with symptoms [symptoms were defined as presented in (17 (link))] or those with an AHI > 15 regardless of symptoms were considered to have OSA (17 (link)).
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3

Overnight Polysomnographic Sleep Assessment

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Overnight polysomnographic sleep recordings (PSG) were conducted in the homes of the participants with SOMNOscreen plus (SOMNOmedics GmbH, Germany). Electroencephalography (EEG) measurements were recorded with gold cup electrodes at 6 EEG locations (F3, F4, C3, C4, O1 and O2) and two derivations for the mastoids (A1, A2) according to the standardized 10/20 system. The electro-oculogram (EOG) and the electromyogram (EMG) were measured by using disposable adhesive electrodes (Ambu Neuroline 715, Ambu A/S, Denmark), two locations for EOG and three locations for EMG. In addition, an online reference Cz and a ground electrode in the middle of forehead were used. The sampling rate was 256 Hz (the hardware filters for SOMNOscreen plus are 0.2–35 Hz).
All signals were digitally offline filtered with pass band of 0.5–40 Hz (Hamming windowed sinc zero-phase FIR filter, cut-off (−6 dB) 0.25 Hz and 44.3 Hz respectively) and re-referenced to the average signal of A1 and A2 electrodes. Sleep stages from PSG data were scored manually with the DOMINO program (v2.7; SOMNOmedics GmbH, Germany) by three experienced researchers in 30-second epochs.
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4

Portable Polysomnography in Foals

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The polysomnograph used for the measurement was the portable SOMNOscreen-plus from SOMNOmedics GmbH (D-97236 Randersacker). Including the battery, the weight of the device was 220 g with a dimension of 140 × 70 × 22 mm. The polysomnograph was attached with a belt to the distal part of the foal’s neck. The data were stored simultaneously on a 2-GB high-speed compact flash card in the polysomnograph and on the hard disk of a Dell notebook. Data transfer to the notebook, which was placed outside the horse box, occurred with 16-bit resolution via a radio module attached to the SOMNOscreen-plus.
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5

Portable Polysomnographic Sleep Recordings

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Overnight polysomnographic sleep recordings were made for two consecutive nights at the participants’ home, using a 15-channel Somnoscreen plus (SOMNOmedics GmbH, Randersacker, Germany) portable device. Electroencephalography (EEG) measurements were recorded with gold cup electrodes at six EEG locations (F3, F4, C3, C4, O1, and O2) and were attached according to the American Academy of Sleep Medicine rules (Berry et al. 2015 (link)). See Supplementary Materials for further details on the sleep recordings.
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6

Portable PSG and Cuffless BP Monitoring

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Portable PSG devices (SOMNOscreen™ plus, SOMNOmedics GmbH, Randersacker, Germany) were used with 2 canal ECG at 512 samples/s, SpO2 and Cuffless Continuous Blood Pressure Measurement based on puls transit time. Additionally, the blood pressure was manually measured before and after each exposure.
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7

Synchronizing PSG and ICP Data

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As previously described [4 (link)], simultaneous recordings of PSG (SOMNOscreen™ plus, Somnomedics) and ICP (RAUMEDIC AG) were performed. Briefly, after manually scoring the PSG, all data were transferred to MATLAB 2020b (MathWorks®). We recorded data using two sensors: the Datalogger MPR1 and the PSG. Since these sensors collected data asynchronously, time alignment was necessary to eliminate delays. Furthermore, this also ensured the accuracy of absolute ICP values by avoiding drift of the ICP signal recorded by the PSG. We achieved this alignment by integrating the Datalogger MPR1 signal into the PSG signal using MATLAB. Specifically, we used the transferred ICP signal record by the PSG as a temporal reference, guiding the alignment process to ensure that each peak and pattern in the ICP signal matched. Subsequent ICP analyses exclusively utilized the synchronized ICP data from the Datalogger. Before conducting the ICP analysis, artifacts were identified and removed from the synchronized ICP signal.
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8

Sleep Patterns and Gut Health Study

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The Institutional Review Board of the Second Affiliated Hospital of Fujian Medical University (Quanzhou, China) approved this study (approval no. 2017–78). Patients with unexplained diarrhea, infection, or gastrointestinal diseases and who used antibiotics or probiotics approximately 1 month before recruitment began were excluded. In total, 72 subjects were recruited. They underwent a full night of PSG (SOMNOscreen plus; SOMNOmedics, Randersacker, Germany) conducted by technologists in a sleep laboratory. Fasting blood or fecal samples were collected on the following morning.
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9

Comprehensive Sleep Electrophysiology Assessment

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Sleep electrophysiology was measured each night using PSG. All electroencephalogram (EEG: Fpz, F3, F4, Cz, C3, C4, O1, O2, M1, M2), electrooculogram (EOG), electromyogram, and electrocardiogram electrode placements, electrical impedances, and sampling and filter frequencies followed recommendations of the American Academy of Sleep Medicine [40 ]. Data were recorded offline onto an ambulatory device (SOMNOscreen plus, Somnomedics, Germany) and downloaded each morning.
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10

Continuous Polysomnographic Monitoring in Patients

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A continuous 24 h polysomnographic recording included EEG; two channels of electrooculography (EOG), with the electrodes positioned 1 cm lateral and below and above to the outer canthi of both eyes; three channels of electromyography (EMG), with the electrodes placed on the chin; and video recording. Single cup EEG electrodes were attached at F3, F4, Fz, C3, C4, Cz, P3, P4, Pz, and both mastoids, referenced to Cz with the ground electrode at Fpz.
The data were recorded using a mobile polysomnography device (SomnoScreenplus, Somnomedics, Germany) with a 256-Hz sampling rate with 0.2-Hz high-pass and 35-Hz low-pass filters.
All recordings were performed in the patients’ wards on weekends when no rehabilitative treatments took place. During the recording, all patients (including control patients) had to be moved by nurse personnel to prevent decubitus. After each such intervention, the experimenter checked electrode impedance and renewed electrodes whenever the impedance exceeded 5 kΩ.
The individual medication intake had remained stable during at least 1 week before recording. Recordings started between around 10 am and 12 noon and ended at the same time on the next day.
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