2017
DOI: 10.5664/jcsm.6464
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Validation of the System One RemStar Auto A-Flex for Obstructive Sleep Apnea Treatment and Detection of Residual Apnea-Hypopnea Index: A European Randomized Trial

Abstract: A commentary on this article appears in this issue on page 167.

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Cited by 27 publications
(14 citation statements)
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References 31 publications
(45 reference statements)
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“…In our study, visual analysis allowed us to identify and exclude pressure values related to those events. In addition, the rAHI value in this type of devices is reliable when < 10 events/hour is recorded, as compared to manual titration by PSG [27]. Our results, however, cannot be extrapolated to all available algorithms because of potential marked variations in the performance of each device.…”
Section: Discussionmentioning
confidence: 88%
“…In our study, visual analysis allowed us to identify and exclude pressure values related to those events. In addition, the rAHI value in this type of devices is reliable when < 10 events/hour is recorded, as compared to manual titration by PSG [27]. Our results, however, cannot be extrapolated to all available algorithms because of potential marked variations in the performance of each device.…”
Section: Discussionmentioning
confidence: 88%
“…Основными анализируемыми параметрами являлись: 1) среднее время СРАР-терапии за все дни использования (AU) (ч/ночь) -индекс, отражающий воспроизводимость СРАР-терапии при домашнем использовании; 2) среднее значение лечебного давления СРАРтерапии (CMP) (мбар) -индекс, отражающий уровень лечебного давления СРАР-терапии; 3) среднее значение коррекционного индекса апноэ-гипопноэ при проведении СРАР-терапии (AHI срар ) (соб./час)индекс, отражающий эффективность СРАР-терапии. По уровню использования ночной СРАР-терапии с функцией авто-адаптации к вдоху и выдоху пациента (A-Flex) пациенты разделялись: 1) <4 часов/ночьнизко комплаентные пациенты ОАС (группа «А»); 2) от 4 до 6 часов/ночь -средне комплаентные пациенты ОАС (группа «Б»); 3) >6 часов/ночь -высоко комплаентные пациенты ОАС (группа «В») [15].…”
Section: оценка комплаенса к срар-терапииunclassified
“…It measures changes in airflow by an internal pneumotachograph to identify respiratory events. If flow decreases by 40% to 80% for at least 10 sec, the event is labeled a hypopnea; a decrease in flow by more than 80% for at least 10 sec is labeled an apnea [9,10]. The device starts off at the minimum pressure set point for five minutes.…”
Section: Auto-cpap Studiesmentioning
confidence: 99%