Long-term oxygen therapy 24 or 15 hours/day and outcomes: a multicenter, registry-based, randomized, clinical trialUppsala Clin Res Ctr, Uppsala, Sweden.
Northern Älvsborg Cty Hosp, Trollhättan, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Linköping Univ Hosp, Linköping, Sweden; Falun Cent Hosp, Falun, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Karolinska Univ Hosp, Stockholm, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Uppsala Univ, Uppsala, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Uppsala Univ, Uppsala, Sweden; Umeå Univ, Umeå, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Umeå Univ, Umeå, Sweden; Karolinska Univ, Stockholm, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Uppsala Univ, Uppsala, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Karolinska Univ, Stockholm, Sweden; Halland Hosp Halmstad, Halmstad, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Halland Hosp Halmstad, Halmstad, Sweden; Ängelholm Hosp, Ängelholm, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Sundsvall Härnösand Cty Hosp, Sundsvall, Sweden.
Sundsvall Härnösand Cty Hosp, Sundsvall, Sweden; Sunderby Cty Hosp, Sunderbyn, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Sunderby Cty Hosp, Sunderbyn, Sweden; Uppsala Clin Res Ctr, Uppsala, Sweden.
Uppsala Clin Res Ctr, Uppsala, Sweden.
Uppsala Clin Res Ctr, Uppsala, Sweden; Inst Breathing & Sleep, Melbourne Vic, Australia.
Uppsala Clin Res Ctr, Uppsala, Sweden; Univ Wollongong, Wollongong, Australia.
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2024 (English)In: European Respiratory Journal, ISSN 0903-1936, E-ISSN 1399-3003, Vol. 64, no Suppl. 68, article id OA4566Article in journal, Meeting abstract (Other academic) Published
Abstract [en]
Background: Long-term oxygen therapy (LTOT) improves survival in severe hypoxemia and is recommended 24h/day based on non-randomized data. However, LTOT 24h/day is burdensome and recent observational data indicate no difference in patient-related outcomes for 24 versus 15h/day. We tested the hypothesis that LTOT prescribed 24 versus 15h/day would not reduce risk of hospitalization or death at one year.
Methods: In this multicenter, registry-based, randomized, clinical trial using the Swedish Registry for Respiratory Failure, patients starting LTOT were randomized (in a 1:1 ratio) to LTOT 24 or 15h/day. Primary outcome was time to all-cause hospitalization or mortality at one year. Secondary outcomes were hospitalizations and mortality (all-causes, respiratory, or cardiac disease) at three and twelve months, in all patients and stratified according to severity of baseline hypoxemia and underlying condition (chronic obstructive pulmonary disease or other).
Results: Between May 2018 and April 2022, 241 patients were randomized to LTOT 24h/day (n=117) or 15h/day (n=124). No patient was lost to follow-up. Compared to LTOT 15h/day, LTOT 24h/day did not improve the primary outcome of hospitalization or death up to one year (hazard ratio, 0.99; 90% confidence interval, 0.76–1.29; non-superiority p=0.007), or any secondary outcomes overall or in any sub-group. Self-reported adherence to the randomized treatment was high (for 24h/day: median 24.0 [interquartile range, 21.0–24.0]; for 15h/day: median 15.0 [15.0–16.0] h/day) at twelve months.
Conclusion: LTOT prescribed for 24h/day compared with 15h/day did not decrease the risk of hospitalization or death up to one year.
Place, publisher, year, edition, pages
European Respiratory Society , 2024. Vol. 64, no Suppl. 68, article id OA4566
National Category
Respiratory Medicine and Allergy
Identifiers
URN: urn:nbn:se:oru:diva-117781DOI: 10.1183/13993003.congress-2024.OA4566ISI: 001357992300051OAI: oai:DiVA.org:oru-117781DiVA, id: diva2:1922890
Conference
European-Respiratory-Society Congress (ERS), Vienna, Austria, September 7-11, 2024
2024-12-192024-12-192024-12-20Bibliographically approved