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Alice diagnostic equipment

Manufactured by Philips
Sourced in United States

The Alice® diagnostic equipment is a medical device designed for sleep disorder diagnosis. It is used to record and analyze physiological data, such as brain activity, eye movements, and breathing patterns, during a patient's sleep. The device collects this data, which can then be reviewed by healthcare professionals to identify potential sleep disorders or other related conditions.

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Lab products found in correlation

5 protocols using alice diagnostic equipment

1

Polysomnographic Assessment of OSA Severity

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All participants had a standard diagnostic sleep study (Type 1).10 (link),23 The following sleep parameters were recorded during the study, standard electroencephalogram, cardiogram, respiratory flow and efforts, pulse oximeter, and leg and chin electromyogram via Alice® diagnostic equipment (Philips, Respironics Inc., Murrysville, PA, USA). Sleep studies and respiratory events were scored manually according to the American Academy of Sleep Medicine (AASM) scoring criteria and rechecked by certified staff.23
Hypopneas were scored when there was a decrement in nasal pressure signal by ≥50% for ≥10 seconds, resulting in arousal or a ≥3% drop in SpO2 from the pre-event baseline. The desaturation index was calculated as the number of desaturations (fall in SpO2 of ≥3%) divided by total sleep time in hours. OSA severity was assessed using the AHI (the number of obstructive apneas and hypopneas per hour of sleep).
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2

Evaluation of Sleep Apnea Severity

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All patients underwent a standard level I attended overnight sleep study with
neurological, cardiac and respiratory monitoring using Alice®diagnostic equipment (Philips, Respironics Inc., Murrysville, PA, USA). The
following parameters were monitored, four leads of electroencephalography (EEG:
C1-A4, C2-A3, O1-A4, O2-A3), electrooculography (EOG), chin electromyography
(EMG (lead II)), electrocardiography (EKG), oxygen saturation, chest and
abdominal wall movements, air flow (thermistor and nasal pressure). As per the
American Academy of Sleep Medicine Scoring Manual, a single channel Lead II
(right arm to left hip) was used for recording EKG12 . Scoring of sleep studies was performed
manually according to established scoring criteria12 . An apnea is defined as a complete cessation
of airflow for =10 seconds. A hypopnea is a =30% decrease in airflow from
baseline of more than or equal to 10 seconds associated with a 3% oxygen
desaturation or arousal. The desaturation index was defined as the number of
desaturation events (more than or equal to 3% decrease in oxygen saturation from
the pre-event baseline) per hour of sleep.
The apnea-hypopnea index (AHI) quantifies the number of apneas and hypopneas per
hour of sleep. Patients with AHI <5 were used as control (non-exposed).
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3

Polysomnography for Sleep-Disordered Breathing

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As part of the clinical work-up, all patients with sleep-disordered breathing underwent a standard overnight sleep study (Type 1). The type 1 sleep study includes collection of neurological, cardiac, respiratory, and muscular data using EEG, chin and leg EMG, ECG, pulse oximeter, end-tidal CO2, and respiratory monitoring. Alice® diagnostic equipment (Philips, Respironics Inc., Murrysville, PA, USA) was used to acquire sleep study data. The scoring of raw data was performed manually and rechecked by certified staff according to the latest American Academy of Sleep Medicine (AASM) scoring criteria.23 The severity of obstructive sleep-disordered breathing was assessed using the AHI, which quantifies the number of apneas and hypopneas (obstructive events) per hour of sleep.
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4

Scoring and Characterizing Sleep Apnea

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All patients underwent standard PSG in accordance with the American Academy of Sleep Medicine (AASM) recommendations,14 (link) with six leads for electroencephalography, electrooculography, electromyography for the chin and legs, electrocardiography, oxygen saturation (SPO2), thoracoabdominal movements, and airflow (thermistor and nasal pressure), using Alice® diagnostic equipment (Philips, Respironics Inc., Murrysville, PA, USA). Raw data were scored manually according to the AASM scoring criteria.14 (link) Hypopneas scoring criteria included a decrement in nasal pressure signal by ≥50% for at least ≥10 seconds, followed by a ≥3% desaturation from the pre-event baseline or arousal. The desaturation index was computed as the number of desaturations (drop in oxygen saturation of ≥3%) divided by total sleep time expressed in hours. Obstructive apneas and hypopneas were calculated during REM and NREM sleep and expressed as REM-AHI and NREM-AHI.
REM-predominant OSA was defined as an obstructive AHI of ≥5, with a REM-AHI that was two times the NREM-AHI (REM-AHI/NREM-AHI of more than 2), an NREM-AHI of less than 15 events/h, and a minimum of 15 min of REM sleep.5 (link) Patients with an obstructive AHI of more than 5 events/h but did not fulfill the criteria for REM-predominant OSA were considered as having a non-stage-specific OSA group (NSS).
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5

Diagnosing Sleep Breathing Disorders

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All referred patients with suspected SBD undertook a standard level I overnight attended polysomnography (PSG) using the Alice® diagnostic equipment (Philips, Respironics Inc., Murrysville, PA, USA). Manual scoring of the raw data was done following scoring criteria of the American Academy of Sleep Medicine.19 The adopted definition of the desaturation index was ≥3% decrease in oxygen saturation from the pre-event baseline. The scorers of the sleep studies were blind to the results of the thyroid function test.
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