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Abstract
Background
The efficacy of high flow nasal canula oxygen therapy (HFNO) to prevent invasive mechanical ventilation (IMV) is not well established in severe coronavirus disease 2019 (COVID-19). The aim of this study was to compare the risk of IMV between two strategies of oxygenation (conventional oxygenation and HFNO) in critically ill COVID 19 patients.
Methods
This was a bicenter retrospective study which took place in two intensive care units (ICU) of tertiary hospitals in the Paris region from March 11, to May 3, 2020. We enrolled consecutive patients hospitalized for COVID-19 and acute respiratory failure (ARF) who did not receive IMV at ICU admission. The primary outcome was the rate of IMV after ICU admission. Secondary outcomes were death at day 28 and day 60, length of ICU stay and ventilator-free days at day 28. Data from the HFNO group were compared with those from the standard oxygen therapy (SOT) group using weighted propensity score.
Results
Among 138 patients who met the inclusion criteria, 62 (45%) were treated with SOT alone, and 76 (55%) with HFNO. In HFNO group, 39/76 (51%) patients received IMV and 46/62 (74%) in SOT group (OR 0.37 [95% CI, 0.18–0.76] p = 0.007). After weighted propensity score, HFNO was still associated with a lower rate of IMV (OR 0.31 [95% CI, 0.14–0.66] p = 0.002). Length of ICU stay and mortality at day 28 and day 60 did not significantly differ between HFNO and SOT groups after weighted propensity score. Ventilator-free days at days 28 was higher in HNFO group (21 days vs 10 days, p = 0.005). In the HFNO group, predictive factors associated with IMV were SAPS2 score (OR 1.13 [95%CI, 1.06–1.20] p = 0.0002) and ROX index > 4.88 (OR 0.23 [95%CI, 0.008–0.64] p = 0.006).
Conclusions
High flow nasal canula oxygen for ARF due to COVID-19 is associated with a lower rate of invasive mechanical ventilation.
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1 CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Intensive Care Unit, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621); UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France (GRID:grid.11318.3a) (ISNI:0000000121496883)
2 Unité de Recherche Clinique, CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621)
3 Unité de Recherche Clinique, CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621); UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France (GRID:grid.11318.3a) (ISNI:0000000121496883)
4 Intensive Care Unit, Rambouillet, France (GRID:grid.11318.3a)
5 CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Intensive Care Unit, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621); Hypoxie Et Poumon, INSERM, Villetaneuse, France (GRID:grid.7429.8) (ISNI:0000000121866389)
6 CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Intensive Care Unit, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621)
7 Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Unité D’Hygiène Hospitalière, Service de Microbiologie, CHU Avicenne, Bobigny, France (GRID:grid.50550.35) (ISNI:0000 0001 2175 4109); UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France (GRID:grid.11318.3a) (ISNI:0000000121496883)
8 CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Intensive Care Unit, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621); UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France (GRID:grid.11318.3a) (ISNI:0000000121496883); Sorbonne Université, INSERM, Common and Rare Kidney Diseases, Paris, France (GRID:grid.11318.3a)
9 CHU Avicenne, Groupe Hospitalier Paris Seine Saint-Denis, AP-HP, Intensive Care Unit, Bobigny, France (GRID:grid.413780.9) (ISNI:0000 0000 8715 2621); UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France (GRID:grid.11318.3a) (ISNI:0000000121496883); INSERM, Paris, France (GRID:grid.7429.8) (ISNI:0000000121866389)