Background- Clinical effectiveness of high-flow nasal therapy (HFNT) over conventional oxygen therapy (COT) in patients with mild COVID-19-related acute hypoxaemic respiratory failure (AHRF) remains uncertain. The COVID-HIGH trial did not demonstrate statistically significant benefits of HFNT over COT. However, the trial was slightly underpowered, and the event rate lower-than-expected. Bayesian methods provide deeper insight by incorporating prior knowledge and quantifying uncertainty intuitively. This analysis aimed to quantify the probability of benefit or harm associated with HFNT, adopting a Bayesian approach. Methods- We performed a Bayesian reanalysis of the COVID-HIGH trial (NCT, which randomised 364 patients with PaO₂/FiO₂ between 200–300 mmHg to receive HFNT or COT. The primary outcome was escalation of respiratory support (continuous positive airway pressure, noninvasive ventilation or invasive mechanical ventilation) within 28 days. A key secondary outcome was clinical recovery at day 14. Bayesian logistic models with noninformative and informative priors were used to estimate the posterior probability of treatment effects. Results- Escalation of respiratory support occurred in 23.6% (HFNT) versus 30.2% (COT) (risk difference −6.6%, 95% CI −15.1 to 2.1; p=0.14). Across a wide range of priors, the posterior probability mass on the beneficial side remained high, generally >70%, while the proportion on the harm side remained consistently low at ≤6% for all models, underscoring a favourable benefit-risk profile. The acute respiratory failure meta-analysis model (OR 0.76, 95% CrI 0.60 - 0.97), the COVID-19 randomised evidence model (OR 0.76, 95% CrI 0.60 - 0.97), the COVID-19 observational evidence model (OR 0.60, 95% CrI 0.45 - 0.80), and the COVID-19 Bayesian meta-analysis mixed evidence model (OR 0.66, 95% CrI 0.52 - 0.86) showed posterior probability mass on the beneficial side of 70% - 94%. Clinical recovery at day 14 occurred in 61.5% (HFNT) versus 53.3% (COT), with 61-73% of posterior probability mass on the clinical benefit side. Conclusions- This Bayesian re-analysis of the COVID-HIGH trial suggests that HFNT likely reduces escalation of respiratory support and improves clinical recovery in patients with COVID-19 pneumonia and mild hypoxaemia, although the magnitude of benefit remains uncertain and sensitive to prior assumptions.
High Flow Nasal Therapy vs Conventional Oxygen Therapy in Mild COVID-19 Hypoxaemia: A Bayesian Reanalysis of the COVID-HIGH Trial / Crimi, Claudia; Sardo, Salvatore; Noto, Alberto; Madotto, Fabiana; Ippolito, Mariachiara; Nolasco, Santi; Campisi, Raffaele; Fiorentino, Giuseppe; Pantazopoulos, Ioannis; Chalkias, Athanasios; Mattei, Alessio; Scala, Raffaele; Clini, Enrico; Ergan, Begum; Lujan, Manel; Carlos Winck, João; Giarratano, Antonino; Carlucci, Annalisa; Gregoretti, Cesare; Groff, Paolo; Cortegiani, Andrea. - In: JOURNAL OF ANESTHESIA, ANALGESIA AND CRITICAL CARE. - ISSN 2731-3786. - 6:1(2026), pp. 1-15. [10.1186/s44158-026-00361-3]
High Flow Nasal Therapy vs Conventional Oxygen Therapy in Mild COVID-19 Hypoxaemia: A Bayesian Reanalysis of the COVID-HIGH Trial.
Enrico Clini;
2026
Abstract
Background- Clinical effectiveness of high-flow nasal therapy (HFNT) over conventional oxygen therapy (COT) in patients with mild COVID-19-related acute hypoxaemic respiratory failure (AHRF) remains uncertain. The COVID-HIGH trial did not demonstrate statistically significant benefits of HFNT over COT. However, the trial was slightly underpowered, and the event rate lower-than-expected. Bayesian methods provide deeper insight by incorporating prior knowledge and quantifying uncertainty intuitively. This analysis aimed to quantify the probability of benefit or harm associated with HFNT, adopting a Bayesian approach. Methods- We performed a Bayesian reanalysis of the COVID-HIGH trial (NCT, which randomised 364 patients with PaO₂/FiO₂ between 200–300 mmHg to receive HFNT or COT. The primary outcome was escalation of respiratory support (continuous positive airway pressure, noninvasive ventilation or invasive mechanical ventilation) within 28 days. A key secondary outcome was clinical recovery at day 14. Bayesian logistic models with noninformative and informative priors were used to estimate the posterior probability of treatment effects. Results- Escalation of respiratory support occurred in 23.6% (HFNT) versus 30.2% (COT) (risk difference −6.6%, 95% CI −15.1 to 2.1; p=0.14). Across a wide range of priors, the posterior probability mass on the beneficial side remained high, generally >70%, while the proportion on the harm side remained consistently low at ≤6% for all models, underscoring a favourable benefit-risk profile. The acute respiratory failure meta-analysis model (OR 0.76, 95% CrI 0.60 - 0.97), the COVID-19 randomised evidence model (OR 0.76, 95% CrI 0.60 - 0.97), the COVID-19 observational evidence model (OR 0.60, 95% CrI 0.45 - 0.80), and the COVID-19 Bayesian meta-analysis mixed evidence model (OR 0.66, 95% CrI 0.52 - 0.86) showed posterior probability mass on the beneficial side of 70% - 94%. Clinical recovery at day 14 occurred in 61.5% (HFNT) versus 53.3% (COT), with 61-73% of posterior probability mass on the clinical benefit side. Conclusions- This Bayesian re-analysis of the COVID-HIGH trial suggests that HFNT likely reduces escalation of respiratory support and improves clinical recovery in patients with COVID-19 pneumonia and mild hypoxaemia, although the magnitude of benefit remains uncertain and sensitive to prior assumptions.| File | Dimensione | Formato | |
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