Abstract
BACKGROUND: Portable oxygen devices simplify and facilitate patient therapy. This study was designed to compare SpO2 and patient satisfaction with a portable oxygen concentrator or a combined system consisting of a fixed device with continuous-flow oxygen dispensation and a portable device with pulse dispensation for ambulation.
METHODS: This crossover trial assessed 25 subjects with COPD (92% men, mean age of 72.2 ± 7.4 y, mean FEV1 of 34.14 ± 12.51% of predicted) at 4 hospitals in Madrid. All subjects had previously used the combined system, consisting of a fixed oxygenation system and a portable system for ambulation, with 16 (64%) using stationary and portable concentrators and 9 (36%) using a stationary reservoir and portable liquid oxygen bag. Oxygenation settings at rest and while walking were determined at baseline. Subjects were maintained on the previous combined system for 1 week and then switched to the portable oxygen concentrator for 1 week. Mean SpO2 over 24 h was calculated using the software in the oximeter, and compliance was monitored (Visionox).
RESULTS: Low SpO2 (< 90%) was significantly more frequent during use of the portable concentrator alone than with the combined system (37.1% vs 18.4%, P < .05). The portable system alone was preferred by 43% of subjects, and the combined system was preferred by 36%, whereas 21% were not sure.
CONCLUSIONS: Subjects preferred using a single portable oxygenation system both at home and during ambulation. Portable systems alone, however, did not supply the same levels of oxygenation as the combination of fixed and portable systems. Before the widespread adoption of portable systems as a single device, additional studies are needed to determine best-practice protocols for adjustment of daytime and nighttime oxygenation settings. (ClinicalTrials.gov registration NCT02079753)
Footnotes
- Correspondence: Aina M Yáñez PhD, Instituto de Investigación Sanitaria de Palma (IdISPa), Carretera de Valldemossa 79, 07120 Palma de Mallorca, Islas Baleares, Spain. E-mail: ainam.yanez{at}ssib.es.
This study was supported by Linde Healthcare (Linde Médica, Madrid, Spain). The authors have disclosed no other conflicts of interest.
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