A randomized crossover pilot study comparing the efficacy of an auto-demand oxygen delivery system with that of a conventional demand oxygen delivery system in patients with chronic respiratory failure. Issue 37 (17th September 2021)

• Record Type: Journal Article
• Authors: Otoshi, Takehiro; Nagano, Tatsuya; Murakami, Sae; Omori, Takashi; Hazama, Daisuke; Katsurada, Naoko; Yamamoto, Masatsugu; Tachihara, Motoko; Nishimura, Yoshihiro; Kobayashi, Kazuyuki
• Other Names: Fröhlich. Eleonore section editor.
• Is Part Of: Medicine. Volume 100:Issue 37(2021)
• Publication Date: 2021-09-17
• Subjects: chronic respiratory failure -- demand oxygen delivery system -- portable oxygen concentrator -- trigger sensitivity; Medicine -- Periodicals; Medicine -- Periodicals; Médecine -- Périodiques; Geneeskunde; Medicine; Periodicals; Periodicals; 610.5
• DOI: 10.1097/MD.0000000000027191
• Languages: English
• ISSNs: 0025-7974

Abstract

Abstract: Introduction: : When using portable oxygen, a demand oxygen delivery system (DODS), which senses the beginning of inhalation and delivers a bolus of oxygen, is often used. However, conventional DODS may not supply sufficient oxygen when reduced tidal flow fails to trigger the flow sensor. Recently, "auto-DODS, " which detects the negative pressure of inhalation and switches among 3 trigger sensitivity levels ( standard, high, and extra high ), has been developed to improve the efficacy of oxygenation. An auto-DODS can also supply pulsed-flow oxygen when it detects apnea, whereas a conventional DODS has only standard sensitivity. This randomized, open-label, crossover pilot study compared the performance of an auto-DODS with that of a conventional DODS. Methods: : We recruited patients with chronic obstructive pulmonary disease (COPD) or interstitial pneumonia receiving long-term oxygen therapy. Interventions were performed on 2 different days for each participant. On each day, an auto-DODS or a conventional DODS were tested at rest for 30 minutes and during the 6-minute walk test. The primary outcome was mean oxygen saturation (SpO2). Secondary outcomes were the ratios of time for each sensitivity level and pulsed-flow oxygen when using the auto-DODS, total time desaturated below SpO2 90%, percentage of time desaturated below SpO2 90%, minimum SpO2, mean and maximum pulse rate, six-minute walk distance, recovery time after 6-minute walk test, modified Borg scale, comfort, and discomfort index. Results: : When using the auto-DODS at rest, a high or extra high sensitivity level was observed in addition to standard sensitivity in 6 of 8 participants. During the 6-minute walk test, only standard sensitivity was observed in 6 participants. Mean SpO2 differences between the auto-DODS and conventional DODS at rest and during the 6-minute walk test were −0.6 [−4.5, 3.4] and 0.0 [−2.5, 2.5] ([95% confidence interval]), respectively, neither of which were significant ( P = .73 and P = .99). There were no significant differences in secondary outcomes. There were no adverse events when using the auto-DODS. Conclusions: : This study showed that the auto-DODS did not show superiority in oxygenation either at rest or during exercise compared to a conventional DODS. The auto-DODS was shown to supply oxygen safely and detect inhalations with various trigger sensitivities. Abstract : Supplemental Digital Content is available in the text