Transpulmonary pressure: importance and limits

Transpulmonary pressure (P_L) is computed as the difference between airway pressure and pleural pressure and separates the pressure delivered to the lung from the one acting on chest wall and abdomen. Pleural pressure is measured as esophageal pressure (P_ES) through dedicated catheters provided with esophageal balloons. We discuss the role of PL in assessing the effects of mechanical ventilation in patients with acute respiratory distress syndrome (ARDS). In the supine position, directly measured P_L represents the pressure acting on the alveoli and airways. Because there is a pressure gradient in the pleural space from the non-dependent to the dependent zones, the pressure in the esophagus probably represents the pressure at a mid-level between sternal and vertebral regions. For this reason, it has been proposed to set the end-expiratory pressure in order to get a positive value of PL. This improves oxygenation and compliance. P_L can also be estimated from airway pressure plateau and the ratio of lung to respiratory elastance (elastance-derived method). Some data suggest that this latter calculation may better estimate P_L in the nondependent lung zones, at risk for hyperinflation. Elastance-derived P_L at end-inspiration (P_Lend-insp) may be a good surrogate of end-inspiratory lung stress for the “baby lung”, at least in non-obese patients. Limiting end-inspiratory PL to 20–25 cmH₂O appears physiologically sound to mitigate ventilator-induced lung injury (VILI). Last, lung driving pressure (∆P_L) reflects the tidal distending pressure. Changes in P_L may also be assessed during assisted breathing to take into account the additive effects of spontaneous breathing and mechanical breaths on lung distension. In summary, despite limitations, assessment of P_L allows a deeper understanding of the risk of VILI and may potentially help tailor ventilator settings.