Influence of Lung Recruitment Potential on PEEP Titration Strategies in ARDS Patients.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHospital Dr. Franco Ravera Zunino

About this trial

Acute Respiratory Distress Syndrome (ARDS) is characterized by severe hypoxemia and diffuse alveolar collapse, often requiring invasive mechanical ventilation. Non-individualized mechanical ventilation settings can cause ventilator-induced lung injury (VILI). Positive end-expiratory pressure (PEEP) prevents alveolar collapse, but its effect varies among individuals. The recruitment-to-inflation (R/I) ratio evaluates bedside lung recruitment potential. This pilot study aims to compare two individualized PEEP titration strategies-one guided by the best static respiratory compliance and another guided by transpulmonary pressure via an esophageal balloon-and evaluate how baseline lung recruitment potential alters the early physiological responses to these interventions. Both strategies are preceded by an identical, standardized pressure-controlled initial lung recruitment maneuver to establish a baseline recruitment state.

Eligibility criteria

Qualifiers

Diagnosis of moderate or severe Acute Respiratory Distress Syndrome (ARDS) according to the Berlin definition: acute onset, bilateral opacities not fully explained by heart failure or fluid overload, and PaO2/FiO2 <= 200 mmHg with PEEP >= 5 cmH2O.

ARDS duration < 36 hours since fully meeting Berlin consensus criteria.

Relative hemodynamic stability: absence of refractory shock, defined as norepinephrine dose <= 0.5 mcg/kg/min.

Disqualifiers

Evidence of active pulmonary air leaks (bronchopleural fistula, pneumothorax, pneumomediastinum).

Severe uncorrected hemodynamic instability (norepinephrine > 0.5 mcg/kg/min).

Contraindications for esophageal balloon placement (esophageal obstruction, known perforation, recent esophageal surgery, severe esophagitis).

Elevated intracranial pressure or conditions where hypercapnia-induced increases in intracranial pressure must be avoided (intracranial hemorrhage, cerebral contusion, cerebral edema, mass effect with midline shift on CT).

Trial design

Treatments tested in this trial

  • PEEP Titration guided by Static Compliance
  • PEEP Titration guided by Transpulmonary Pressure

Treatment groups

52 Participants
are divided into 2 treatment groups

Locations

This trial has no locations