Clinical Performance of Sp o2 /F io2 and Pa o2 /F io2 Ratio in Mechanically Ventilated Acute Respiratory Distress Syndrome Patients: A Retrospective Study.

Coppola, Silvia; Pozzi, Tommaso; Catozzi, Giulia; Monte, Alessandro; Frascati, Enrico; Chiumello, Davide · Crit Care Med · 2025

retrospective_cohort · Level III

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Abstract

The present study aims to evaluate the severity classification of acute respiratory distress syndrome (ARDS) in mechanically ventilated patients according to peripheral oxygen saturation by pulse oximetry (Sp o2 )/F io2 ratio compared with Pa o2 /F io2 ratio and the relationship between Sp o2 /F io2 ratio and venous admixture. Retrospective observational study. Medical-surgical ICU. A cohort of 258 mechanically ventilated patients with ARDS already enrolled in previous studies. None. Gas exchange, Sp o2 , and respiratory mechanics were measured on ICU admission and during the positive end-expiratory pressure (PEEP) trial. Radiological data from CTs were used to compute lung recruitability and to assess different lung compartments. A nonlinear association was found between Sp o2 /F io2 and Pa o2 /F io2 . Considering the possible confounding factors of the pulse oximeter on the relationship between Sp o2 /F io2 and Pa o2 /F io2 ratio, arterial pH, and Pa co2 had no effect. Sp o2 /F io2 and Pa o2 /F io2 ratio demonstrated a moderate agreement in classifying ARDS severity (intraclass correlation coefficient = 0.63). Between the correspondent classes according to Sp o2 /F io2 vs. Pa o2 /F io2 ratio-derived severity classifications, there was no difference in terms of respiratory mechanics, gas exchange, lung radiological characteristics and mortality in ICU, and within two levels of PEEP. A Sp o2 /F io2 ratio less than 235 was able to detect 89% of patients with a venous admixture greater than 20%, similarly to a Pa o2 /F io2 ratio less than 200. Sp o2 /F io2 ratio can detect oxygenation impairment and classify ARDS severity similarly to Pa o2 /F io2 ratio in a more rapid and handy way, even during a PEEP trial. However, our results may not be applicable to different patient populations; in fact, the pulse oximeter is merely a monitoring device and the information should be personalized by the physician on the patient's characteristics and conditions.

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