Home Sleep Test (HST) Devices Comparison Guide

Home Sleep Test (HST) Devices Comparison Guide


Maximum Channels:12: SpO2, PPG, pulse rate (x2 from PPG and from sounds), activity (movement), heart sounds, respiration inhalation and exhalation patterns, airflow, respiratory effort (x2), respiratory rate, snoring, body position13: EEG, LEOG, REOG, EMG or ECG, forehead pulse, snoring (dB), head movement, head position; PSG2 adds wireless finger SpO2, pulse, nasal pressure airflow, optional abd, thx piezo or RIP belts5: plethysmogram, pulse rate, heart rate variability, oximetry, actigraphy12: snore, flow limitation, pressure flow, RIP chest effort, RIP abd Effort, SUM (RIP chest + RIP abd), SpO2, pulse rate, body position (internal), PPG, event marker, CPAP flow, CPAP pressure8: airflow, snore, SpO2, pulse rate, chest effort, body position, CPAP pressure, PPG13: Core: thoracic effort, pressure, snore (from cannula), SpO2, pulse rate, plethysmography, body position; Legacy: thoracic effort, abd effort, pressure, snore (from cannula), snore, SpO2, pulse rate, plethysmography, body position; TST: thoracic effort, abd effort, pressure, snore (from cannula), snore, SpO2, pulse rate, plethysmography, body position, ExG (3 channels)8: heart rate, SpO2, respiratory airflow (CPAP compatible), RIP belt, snore, body
position, auxiliary (second RIP, thermal airflow, or IDcheck), actigraphy10: EEG, EOG x 2, EMG, peripheral arterial tonometry, pulse rate, SpO2, snoring, movement, ambient light10: EEG, EOG x 2, EMG, peripheral arterial tonometry, pulse rate, SpO2, snoring, movement, ambient light9: EEG sleep staging, airflow (cannula or Bi/CPAP interface), Bi/CPAP pressure, respiratory effort (RIP), snore, SpO2, pulse rate, plethysmography, tri-axis body position9: oximetry, ECG, respiratory effort, snoring, body position, sleep staging, chest movement, activity, heart rate6: airflow, respiratory effort, pulse rate, SpO2, heart rate variability, photoplethysmogram19: pressure, sound, gravity (x/y/z), bipolar ExG, thermistor, thoracic effort (RIP), abd effort (RIP), DC (0-1V) battery, event button, SpO2, SpO2B-B, SpO2 quality, pulse rate, plesthymography, RD quality, PPG; + multiple derived channels. Optional proxies add up to 8 EEG, 2 EOG, 3 chin EMG, 2x leg EMG,1 ECG5: body position, ECG, derived-respiratory events, derived-staging, SpO213: 2x RIP, pressure
transducer, SpO2, pulse, plethysmography, body position, 2x ExG; 3x DC channels, luminosity sensor9: SpO2, pulse rate, pulse waveform, pressure transducer, snore, RIP, actigraphy, body position, poly24: (15 recorded, 9 derived) 2x bipolar channels: RIP, abd + thorax breathing effort, respiratory sound, audio volume, gravity, activity, body position, flow, snore, PWA; pulse, SpO2; 9 derived: heart rate; calibrated RIP flow, calibrated RIP sum, RIP flow, RIP sum, RIP phase, PTT, respiratory rate15: EEG right, EEG left, EOG right, EOG left, EMG right, EMG left, SpO2, respiratory effort (via bioimpedance), respiratory flow (via bioimpedance), respiratory flow (via nasal cannula), ECG, activity, body position, sound pressure level, EMG leg4: PPG, heart rate, oximetry, actigraphy4: SpO2, PPG, pulse rate, actigraphy6: SpO2, plethysmogram, actigraphy; calculated post-acquisition by SleepImage System: heart variability, respiration, pulse rate6: SpO2, plethysmogram, actigraphy; calculated post-acquisition by SleepImage System: heart variability, respiration, pulse rate7: respiratory airflow, chest effort, sound (snoring), SpO2, heart rate, optional: movement, body position15: 3x EEG, EOGl, EOGr, EMG, light, activity, body position, impedance, snore, SpO2, heart rate, plethysmogram, autonomic arousals11: respiratory airflow, snore, CPAP pressure, thorax breathing effort, SpO2, pulse rate, finger plethysmogram, body position, movement, patient marker, optional: abd breathing effort7: airflow, heart rate, oximetry, head position, actigraphy, 2x respiratory effort6: airflow, respiratory effort, pulse rate, SpO2, heart rate variability, photoplethysmogram15: body position, airflow, pressure, staging, snoring, effort (abd, thx), SpO2, heart rate, HRV, PPG, temperature (abd, thx), respiratory rate, movement7: PAT signal, pulse rate, oximetry, actigraphy, snoring, body position, chest motion7: PAT signal, pulse rate, oximetry, actigraphy, snoring, body position, chest motion
Features:Classification of obstructive and central events (using airflow and effort information).Scientifically-validated and editable autoscored full disclosure signals with forehead-based self-application. For multi-night evaluation of sleep architecture and sleep continuity in home or hospital, with auto-detection of sleep biomarkers associated with neurodegeneration. PSG2 upgrade enables auto-detection of apneas, hypopneas, RERAs, and REM-related SDB severity.No need for phone pairing or WiFi. The FDA 510(k) cleared ring & artificial intelligence system measures AHI, sleep stages, and autonomic nervous system response. The cradle allows multiple-night testing (~14 nights) & acts as a digital sleep diary. 7 sizes of changeable ring arms for fit and comfort.Constructed of smooth nylon/plastic with extra-strength LEMO connectors, the MediByte was designed for durability. Ideal for both adult and pediatric studies. Side wings attach the unit to the chest effort belt. Event push button. Auxiliary port for expanded recordings: sound, EMG, and EKG. Use the sensitive snore microphone for high frequency snoring analysis and a derived quantitative dB sound level.Local PC software or the BridgeBuilder Cloud Portal. SDB analysis including RERA, flow limitation, breath statistics, SpO2 perfusion. Carrying case, patient instructional video, USB cable. CPAP compatible, multiple nights, immediate report access, unlimited custom reports, locking connectors, stainless steel connector, LED study status indicator, all internal biosensors.Automatically download completed records. Add sleep time with ApneaTrak TST or EnsoData integration. Pre-programmed device start times help reduce failed studies. Compatible with non-proprietary respiratory belts. Connection to the PC (zero-click) automatically downloads completed recording, recharges the device, and prepares ApneaTrak for the next patient. Through CadCare, Cadwell is always there for you with education, support, and service plans.Web-based software offers access to studies, scoring, and reports from anywhere—facilitating collaboration between sleep labs and physician offices. Services are available for manual scoring and logistics for mail delivery to patient homes.Somfit is a lightweight, wireless device designed for patient comfort. It enables quick self-setup with a low failure rate. Study data is cloud hosted on the Nexus360 platform, where AI driven autoscoring provides a comprehensive report with full sleep-architecture, detailed hypnograms, respiratory indices at both 3% and 4%, a cortical arousal index, and NREM spindle density. Signals are accessible for manual review and overscoring. Nexus360 is capable of full HL7 integration of all reported Somfit study metrics and population data.Somfit-D is a lightweight, wireless device designed for patient comfort. It enables quick self-setup with a low failure rate. Study data is cloud hosted on the Nexus360 platform, where AI driven autoscoring provides a comprehensive report with full sleep-architecture, detailed hypnograms, respiratory indices at both 3% and 4%, a cortical arousal index, and NREM spindle density. Signals are accessible for manual review and overscoring. Nexus360 is capable of full HL7 integration of all reported Somfit study metrics and population data.A chest-worn device that combines single-channel EEG
sleep staging technology with
traditional respiratory channels to report an AHI based
on EEG-derived sleep time and body position (not just recording time). With one-touch controls, multinight
recordings, and a full-color LED interface, the Synergy is now PAP compatible and backed by a HIPAA-compliant cloud portal.Simplify sleep testing without compromising diagnostic insight and precision. Patients use a single patch with one-button setup—no phone apps needed—backed by 24/7 support to eliminate calls. Boost efficiency and control with a secure cloud portal that provides autoscored results and customizable, automated reporting. Diagnose with confidence using a test validated in 340 patients, demonstrating 91% correlation to PSG. Book a demo: huxleymed.com/#contact.Simple setup for patients (simple devices, intuitive mobile app). Up to 7 nights of consecutive testing available + 98% patient success rate when testing 2 nights. FDA cleared for diagnosing OSA total sleep time and 4 sleep stages. Detects central events, RERAs, arousals, RDI. Provides HRV and hypoxic burden.Scalable multinight recorder with auto or
timed start options; high
resolution screen with signal display; signal test features (including impedance measurement),
signal quality/status
information; disposable and reusable sensors
available; RemLogic or Natus SleepWorks for HST recordings included.It utilizes clinically validated ECG-based staging and scoring, and single cell can last up to 30 records.A compact type III and IV device powered by one AA battery, the HST Compass contains 2x AC bipolar channels, pressure transducer, integrated RIP interfaces, oximeter, integrated body position and DC channels—all embedded into a single module that will comfortably fit on the chest. Capability to see the traces and study information right on the screen.Integrated cellular capability, SmartStart (automatically initiates recording when valid signals are detected), valid data algorithm (automatically schedules an additional recording night if user-defined valid data is not met), can record up to three nights of data on a single AA battery, fully integrated with Polysmith DMS, integrated RIP driver and pulse oximeter.The Nox T3s has refined calibrated Nox RIP technology with 200 Hz sampling frequency, which can be used as a primary flow measurement; built-in sensors for snoring, ability to add two bipolar signals (EKG, EMG, or EEG), Bluetooth BLE 5.0 technology for multinight studies, analysis in Noxturnal Software with artificial intelligence. Indicated for use in patients >2 years old. Audio playback after recording. Built-in pressure transducer for diagnostic or therapeutic studies (with nasal cannula or PAP devices).Onera STS is a patch-based, wireless system that records 15 channels of direct signal data from four contact points delivering a gold standard PSG quality study while ensuring patient comfort and convenience. The device is self-applied within minutes, easy to use, and comfortable to wear. Raw data is available for editing and scoring on an easy-to-use cloud platform.Home sleep testing with instant, cloud-based access to auto-scored results. Report metrics include sleep, respiratory, oximetry data, and additional indices such as hypoxic burden, autonomic nervous system balance, and snoring statistics.A fully disposable, FDA-cleared HST that records up to 10 nights of sleep data with a simple, streamlined experience that delivers a highly accurate measurement of sleep health. Raw patient data is autoscored with an algorithm clinically validated against PSG. Automated and editable reports are available in the provider portal. Seamless integration with Somnoware software.Slip on, sync, and sleep. The SleepImage Fingertip is a wireless, single-patient, multi-use acquisition device for use with the SleepImage System, an FDA-cleared SaMD. Each purchase includes 3 reports. System analysis parameters include AHI, RDI, sAHIcentral, TST, SleepImage Sleep Quality Index, and sleep staging (stable vs unstable NREM and REM/W). Raw data is provided for review and manual edit.Slip on, sync, and Sseep. The SleepImage Ring is a wireless, multi-patient use acquisition device for use with the SleepImage System, an FDA-cleared SaMD. It is available in two sizes, Large and small (2+ yrs). System analysis parameters include AHI, RDI, sAHIcentral, TST, SleepImage Sleep Quality Index, and sleep staging (stable vs unstable NREM and REM/W). Raw data is provided for review and manual edit.Service includes manual scoring by RPSGT, with differentiation of obstructive and central events. Analyzed indices include count of apneas, count of hypopneas, AHI, RDI, REI, CI, ODI, and acoustical snoring analysis. Raw data is provided in standard format. Resumable recording and rechargeable battery allow easy multinight testing. Results based upon analyzed sleep time.Data straight away available in the cloud for analysis or several nights comparison (for instance, with and without therapy or as a cost-effective tool for sleep staging over several nights), Usage cases include insomnia, circadian rhythm, OSA screening, etc.Plug and play with Intelligent Connect sensors for easy application by the patient at home—programmed or manual start. Analysis and reporting software (1 license). Charging and data transfer simultaneously via USB. CPAP-compatible recordings. Auto-detection of sleep/wake. Additional abdominal belt available. Also available: SOMNOtouch RESP eco, a type III and IV HST.The device detects respiratory events such as obstructive and central apneas and hypopneas, respiratory event-related arousal and identifies sleep time, stages, micro-arousals, and position. The device generates sleep parameters, eg, AHI, RDI, oxygen desaturation index, REM/NREM sleep stages, total sleep time, arousal index, % of time spent increased respiratory effort and position.Integrated with Sleepifi’s feature robust HST management platform. Sleepifi generates a report within minutes and notifies staff or physician that it is ready for review and interpretation. Report includes AHI 3% and 4% (OSA & CSA), ODI, and sleep staging by TST, as well as sleep efficiency, latency, onset, duration, fragmentation, NREM and REM sleep, and WASO.Wesper goes beyond a simple HSAT. Featuring actionable metrics such as hypoxic burden analysis, giving a deeper, more clinically relevant view. Paired with multi-night, longitudinal monitoring, Wesper uncovers variability—meaning fewer false negatives and greater diagnostic accuracy, not to mention faster treatment titration. Built-in real-time data validation flags issues before they become wasted studies, while seamless EPIC and Cerner integration keeps everything flowing smoothly in your existing workflow. AI-powered autoscoring delivers 95% PSG correlation—plus the flexibility to overscore.WatchPAT 300 is simple, accurate, and reliable HSAT that has a smart design to streamline the workflow. It may also utilize screening, pre and post sleep questionnaires through a smartphone app. WatchPAT 300 provides a validated autoscored report and raw data for manual review and editing. The report differentiates obstructive and central events and provides AHI, AHIc, RDI, and ODI based upon TST, and sleep staging.WatchPAT ONE is a fully disposable HSAT that also utilizes screening, pre and post sleep questionnaires through a smartphone app. As soon as the study is completed, sleep data is available for interpretation. It provides a validated autoscored report and raw data for manual review and editing. The report differentiates obstructive and central events and provides an AHI, AHIc, RDI, and ODI based upon TST, and sleep staging.



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