Identification of focal ARDS using PF ratio: a cross-sectional study

In normal lungs, ventilation exceeds perfusion in lung areas above the heart while perfusion exceeds ventilation in lung areas below the heart (i.e., in the posterobasal lung areas when a person is supine) [1]. When the lung bases are diseased, perfusion exceeds ventilation more markedly, gas exchange within the affected alveoli gets diminished, the partial pressure of alveolar oxygen falls, and hypoxemia ensues. To mitigate this mismatch of perfusion and ventilation, hypoxic vasoconstriction occurs in areas of poorly ventilated lung. However, hypoxic vasoconstriction is impaired in acute respiratory distress syndrome (ARDS) [2, 3]. As such, if consolidation exists predominantly in the posterobasal lung regions (i.e., focal ARDS) [4], we can expect that greater ventilation-perfusion mismatch could reduce oxygenation more severely, as measured using the partial pressure of arterial oxygen divided by fraction of inspired oxygen (PF ratio). If an association between focal ARDS and PF ratio can be shown, PF ratio could then be used in place of thoracic imaging to identify focal ARDS. We therefore hypothesized that focal ARDS is associated with lower PF ratio and investigated this relationship. We included patients with ARDS fulfilling the Berlin Definition, who were admitted to our Medical Intensive Care Unit in 2014–2017, and who only received invasive mechanical ventilation. On admission, trained respiratory therapists performed a 12-point lung ultrasound using a 2–4 MHz phased array transducer and semi-quantitatively scored each region [5]. We identified focal ARDS on lung ultrasound [6], if the consolidated regions were only

In normal lungs, ventilation exceeds perfusion in lung areas above the heart while perfusion exceeds ventilation in lung areas below the heart (i.e., in the posterobasal lung areas when a person is supine) [1]. When the lung bases are diseased, perfusion exceeds ventilation more markedly, gas exchange within the affected alveoli gets diminished, the partial pressure of alveolar oxygen falls, and hypoxemia ensues. To mitigate this mismatch of perfusion and ventilation, hypoxic vasoconstriction occurs in areas of poorly ventilated lung.
However, hypoxic vasoconstriction is impaired in acute respiratory distress syndrome (ARDS) [2,3]. As such, if consolidation exists predominantly in the posterobasal lung regions (i.e., focal ARDS) [4], we can expect that greater ventilation-perfusion mismatch could reduce oxygenation more severely, as measured using the partial pressure of arterial oxygen divided by fraction of inspired oxygen (PF ratio). If an association between focal ARDS and PF ratio can be shown, PF ratio could then be used in place of thoracic imaging to identify focal ARDS. We therefore hypothesized that focal ARDS is associated with lower PF ratio and investigated this relationship.
We included patients with ARDS fulfilling the Berlin Definition, who were admitted to our Medical Intensive Care Unit in 2014-2017, and who only received invasive mechanical ventilation. On admission, trained respiratory therapists performed a 12-point lung ultrasound using a 2-4 MHz phased array transducer and semi-quantitatively scored each region [5]. We identified focal ARDS on lung ultrasound [6], if the consolidated regions were only present in the posterobasal regions (combination of lower lateral, upper posterior, and lower posterior regions) and absent in the anteroapical regions (combination of upper anterior, lower anterior, and upper lateral regions) [4].
The association of focal ARDS with PF ratio was analyzed using logistic regression and with PF ratio (taken at the time of the lung ultrasound scan) as a continuous variable. To check for any nonlinear relationship of focal ARDS with PF ratio, we fitted a logistic regression model using a restricted cubic spline with four knots and taking the PF ratio of the first knot as the reference level. Wald test for linearity was then done (P < 0.05 indicates nonlinearity).
We found that PF ratio was not associated with focal ARDS. A possible reason could be that the degree of oxygenation impairment is related to the extent of lung involvement in ARDS, rather than the distribution of lung involvement. To illustrate using data from our patients, for every 1 point increase in total lung ultrasound score, PF ratio decreased by 1.7 (95% CI − 3.3 to − 0.19, P = 0.028). In the light of our results, thoracic imaging remains a requirement for identification of focal ARDS. Admittedly, our study is limited by a single-center cohort involving medical patients and using ultrasound as the sole modality for detailed lung imaging. Our findings should therefore be validated in external cohorts, in non-medical patients, and with computed tomography.