Respiratory failure & ventilation

High-flow nasal oxygen therapy via a single-prong cannula interface during bronchoscopy in patients with acute respiratory failure: a two-center, open-label, randomized controlled trial

Ann Intensive CarePublished Randomised controlled trial

Authors' conclusion

In patients with ARF, HFNO-SPC significantly reduced the proportion of patients requiring respiratory support escalation within 24 h after FB compared with SOT.

Study context

Population
Patients with acute respiratory failure undergoing flexible bronchoscopyall in ITT analysis
Participants
160 patients
Comparison
HFNO-SPC vs standard oxygen therapy (SOT)
  • HFNO-SPCn = 80
  • SOTn = 80reference
Primary endpoint
Escalation of respiratory support (invasive mechanical ventilation (IMV), noninvasive ventilation (NIV) or HFNO, or increased support parameters without mode change)
Follow-up
Within 24 h after FB
Methodological detailstwo-center, open-label
  • Two-center
  • Open-label

Primary result

As reported in the abstract

Respiratory support escalation

P = 0.006

Secondary outcomes

Hierarchical composite of escalation events

P = 0.004

Intubation · within 24 h

P = 0.022

Hierarchical composite of escalation events

Supported the primary findings

Electrical impedance tomography (EIT): tidal impedance variation and end-expiratory lung impedance

Smaller tidal impedance variation (TIV) reductions during flexible bronchoscopy (FB) and less pronounced ΔEELI changes during and after FB with HFNO-SPC

Original publication

High-flow nasal oxygen therapy via a single-prong cannula interface during bronchoscopy in patients with acute respiratory failure: a two-center, open-label, randomized controlled trial. Ann Intensive Care. Published 12 May 2026. doi:10.1016/j.aicoj.2026.100081

Composed by AI from the published abstract and checked against it. How Briefs are made →

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