About this trial
This observational study aims to evaluate the relationship between clinical and physiological variables and the failure of non-invasive respiratory support (NIRS), including high-flow nasal oxygen (HFNO) and non-invasive ventilation (NIV), in patients with acute respiratory failure (ARF), both hypoxemic and/or hypercapnic. The study includes both retrospective and prospective components. Retrospective data will be collected from patient charts, while prospective data will be collected at defined time points during clinical care. The primary outcome is NIRS failure, defined as the need for orotracheal intubation. Secondary outcomes include in-hospital and 90-day mortality, ICU and hospital length of stay, and duration of non-invasive and invasive support.
Eligibility criteria
Qualifiers
Age ≥ 18 years
Hospitalization in the Respiratory Medicine Unit at AOU Policlinico di Modena
Acute respiratory failure (hypoxemic and/or hypercapnic) with PaO₂/FiO₂ < 300 mmHg
Undergoing treatment with HFNO or NIV
Disqualifiers
Immediate need for invasive ventilation upon admission
Known neuromuscular disease
Pregnancy
Lack of informed consent
Trial design
Treatments tested in this trial
- This is an observational study. Interventions are standard of care and include: High-flow nasal oxygen (HFNO) Non-invasive ventilation (NIV) Pnose monitoring