ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
medimedia.ir

Sleep monitoring devices

Sleep monitoring devices
  Type 1 device
(Attended polysomnography)
Type 2 device
(Unattended polysomnography)
Type 3 device
(Portable HSAT)
Type 4 device
(Single or dual bioparameter recording)
        Example of a type 3 device*  
Minimal measurements
  • EEG
  • EOG
  • Chin EMG
  • ECG
  • Airflow
  • Respiratory effort
  • Oxygen saturation
  • EEG
  • EOG
  • Chin EMG
  • ECG
  • Airflow
  • Respiratory effort
  • Oxygen saturation
Minimum 4 parameters, typically:
  • Two ventilation parameters (eg, respiratory movement or airflow)
  • Heart rate or ECG
  • Oxygen saturation
(No EEG)
PAT, oximetry, heart rate, snoring actigraphy, body position Only 1 or 2 variables measured (typically oxygen saturation, airflow, chest movement)
Body position Measured or observed Possible but optional Possible Yes No
Sleep staging Yes Yes No No No
Sleep surrogate Not applicable Not applicable Possible Yes (PAT actigraphy) No
Leg movement Documented by EMG or motion sensor Possible but optional Possible but optional No No
Personnel Present Absent Absent Absent Absent
Interventions possible Yes No No No No
Respiratory event terminology (denominator) AHI (total sleep time) AHI (total sleep time) REI (total recording time) pAHI, pRDI (PAT algorithm) REI (total recording time)
Some Medicare administrative contractors only recognize AHI for PAP coverage. Clarification with local coverage determinator contractors may be required.
HSAT: home sleep apnea testing; EEG: electroencephalography; EOG: electrooculography; EMG: electromyography; ECG: electrocardiography; PAT: peripheral arterial tonometry; AHI: apnea hypopnea index; REI: respiratory event index; pAHI: PAT-determined apnea hypopnea index; pRDI: PAT-determined respiratory event index; PAP: positive airway pressure; AASM: American Academy of Sleep Medicine; CMS: Centers for Medicare and Medicaid Services.
* The classification of devices that include PAT is challenging. While many experts consider them as type 3 devices (per the original AASM classification), the CMS classify them as a type 4 device.
References:
  1. Ferber R, Millman R, Coppola M, et al. Portable recording in the assessment of obstructive sleep apnea. ASDA standards of practice. Sleep 1994; 17:378.
  2. Littner MR. Portable monitoring in the diagnosis of the obstructive sleep apnea syndrome. Semin Respir Crit Care Med 2005; 26:56.
Graphic 121906 Version 1.0

آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟