TY - JOUR
T1 - Significance of a screening device (Apnomonitor 5®) for sleep apnea syndrome
AU - Yagi, Hidehito
AU - Nakata, Seiichi
AU - Tsuge, Hayato
AU - Yasuma, Fumihiko
AU - Noda, Akiko
AU - Morinaga, Mami
AU - Tagaya, Mitsuhiko
AU - Nakashima, Tsutomu
PY - 2009/4
Y1 - 2009/4
N2 - Objectives: The objective was to evaluate the significance of a portable sleep-monitoring device (Apnomonitor 5®, Chest Co., Tokyo, Japan) to diagnose sleep apnea syndrome (SAS). Methods: The Apnomonitor 5® comprised an oronasal thermistor, a pulse oximeter, chest and abdominal belts to monitor the circumferences of the chest and abdomen, a microphone to monitor tracheal sound, a position detector, and an integrative unit. This screening device was commercially available and it had been used to diagnose SAS in our country. Twenty-two consecutive adults who attended Inazawa City Hospital who were suspected for SAS were prospectively enrolled and they undertook the standard polysomnography (PSG) and Apnomonitor 5® simultaneously. The designated polysomnographers analyzed the records of the PSG and Apnomonitor 5®. These sleep and respiratory parameters of the devices were compared, the results of which were double-checked by the designated sleep specialist. Results: The apnea-hypopnea index (AHI), apnea index, total number of apnea, and oxygen desaturation index obtained by the PSG and Apnomonitor 5® correlated significantly, whereas the averaged sleep time, total number of hypopnea, hypopnea index, and nadir oxygen saturation differed between the devices. The sensitivity of the Apnomonitor 5® versus PSG was 95% in the SAS patients with the AHI ≥ 15. Conclusions: The Apnomonitor 5® can be a sensitive and useful screening device for SAS especially in patients with the AHI ≥ 15.
AB - Objectives: The objective was to evaluate the significance of a portable sleep-monitoring device (Apnomonitor 5®, Chest Co., Tokyo, Japan) to diagnose sleep apnea syndrome (SAS). Methods: The Apnomonitor 5® comprised an oronasal thermistor, a pulse oximeter, chest and abdominal belts to monitor the circumferences of the chest and abdomen, a microphone to monitor tracheal sound, a position detector, and an integrative unit. This screening device was commercially available and it had been used to diagnose SAS in our country. Twenty-two consecutive adults who attended Inazawa City Hospital who were suspected for SAS were prospectively enrolled and they undertook the standard polysomnography (PSG) and Apnomonitor 5® simultaneously. The designated polysomnographers analyzed the records of the PSG and Apnomonitor 5®. These sleep and respiratory parameters of the devices were compared, the results of which were double-checked by the designated sleep specialist. Results: The apnea-hypopnea index (AHI), apnea index, total number of apnea, and oxygen desaturation index obtained by the PSG and Apnomonitor 5® correlated significantly, whereas the averaged sleep time, total number of hypopnea, hypopnea index, and nadir oxygen saturation differed between the devices. The sensitivity of the Apnomonitor 5® versus PSG was 95% in the SAS patients with the AHI ≥ 15. Conclusions: The Apnomonitor 5® can be a sensitive and useful screening device for SAS especially in patients with the AHI ≥ 15.
UR - http://www.scopus.com/inward/record.url?scp=59849113477&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=59849113477&partnerID=8YFLogxK
U2 - 10.1016/j.anl.2008.06.001
DO - 10.1016/j.anl.2008.06.001
M3 - Article
C2 - 18635324
AN - SCOPUS:59849113477
SN - 0385-8146
VL - 36
SP - 176
EP - 180
JO - Auris Nasus Larynx
JF - Auris Nasus Larynx
IS - 2
ER -