High-Flow Nasal Oxygenation Is Associated with Improved Respiratory Stability During Moderate Multimodal Analgosedation for Pars Plana Vitrectomy: A Randomized Controlled Trial

Background/Objectives: High-flow nasal oxygenation (HFNO) may improve respiratory stability during procedural sedation, but treatment-associated differences across patient risk categories remain uncertain. We compared HFNO with low-flow nasal oxygenation (LFNO) during moderate multimodal analgosedation (MMAS) for pars plana vitrectomy (PPV) in patients with ASA physical status I–III.

Methods

In this prospective, single-center randomized trial, 164 adults undergoing elective PPV under regional eye anesthesia with MMAS were randomized to HFNO (40 L·min−1, set FiO2 0.40) or LFNO (5 L·min−1, intended to approximate a nominal FiO2 of 0.40). Sedation depth was monitored using the Patient State Index and evaluated using the Ramsay Sedation Scale. The primary outcome was maintenance of target oxygenation (SpO2 94–98%) without hypoxemia (SpO2 < 90%), assessed by peripheral oxygen saturation (SpO2) at three predefined time points (T0, T1, and T2). Secondary outcomes included breathing frequency (BF), measured end-tidal CO2 (EtCO2), and clinically significant bradypnea (CSB), defined as ≥1 bradypnea episode (BF < 12 breaths·min−1 persisting ≥1 min) accompanied by SpO2 90–93%, EtCO2 > 45 mmHg, or both.