CT for Personalized Mechanical Ventilation

Columbia University

Status: Active, not recruiting

Conditions: Sepsis Syndrome; Mechanical Ventilation Complication; Ventilator-Induced Lung Injury

Treatments: Procedure: PEEP (positive end-expiratory pressure) - maximum; Procedure: PEEP (positive end-expiratory pressure) - standard

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT05977153

AAAT8623

5R01HL121228-09 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this study is to compare two different ways of helping patients with a condition called sepsis who need help breathing using a machine called a ventilator. The investigators want to study which way of setting the ventilator is better for the lungs.

Here are the main questions the investigators want to answer:

1. How does the amount of air in the lungs and the way it moves differ between the two ways?
2. How does the way air spreads out in different parts of the lungs differ between the two ways? In this study, the investigators will take special pictures of the lungs using a machine called a CT scan. The pictures will show us how much the lungs stretch and how much air is in different parts of the lungs. The investigators will compare two different ways of using the ventilator: one personalized for each patient based on their breathing, and another way that is commonly used.

By comparing these two ways, the investigators hope to learn which one is better for helping patients with sepsis who need the ventilator. This information can help doctors make better decisions about how to care for these patients and improve their breathing.

Full description

Mechanical ventilation is a key life support method applied to millions of surgical and critically ill patients. Ventilator-induced lung injury (VILI) is a major factor for morbidity and mortality in patients with the acute respiratory distress syndrome (ARDS), the most severe form of respiratory dysfunction. Furthermore, mechanical ventilation settings also contribute to the risk for postoperative pulmonary complications (PPCs) in surgical patients and lung injury in critically ill patients with normal lungs at onset of ventilation. In summary, mitigation of VILI is critical to reduce perioperative and critical care morbidity and mortality, with major impact on outcomes and health care costs.

In this project, we propose to apply novel CT methods to assess spatial distributions of strain and aeration and establish measures of global lung mechanics best indicative of the PEEP leading to least injurious distributions and, thus, least VILI.

Enrollment: 7 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Following onset of mechanical ventilation and not longer than 5 days after intubation.

• Sepsis as defined by the most recent criteria:

  • Life-threatening organ dysfunction caused by a dysregulated host response to infection operationalized by presumed or documented infection and a Sequential [Sepsis-related] Organ Failure Assessment (SOFA) score >= 2 or a change by 2 from the baseline if baseline known to be different from 0;

Exclusion criteria

• Age < 18 years;
• Hemodynamic instability, defined as: systolic blood pressure (SBP) < 90 mmHg that is not adequately stabilized by vasopressors or inotropic agents. For these purposes, SBP will not be considered "adequately stabilized" if the dose of the vasopressor/inotrope has not been stable for at least one hour;
• Hypoxemia, defined as: PaO2 < 70 mmHg on an inspired oxygen fraction (FiO2) greater than or equal to 0.9;
• Hemodynamic and/or respiratory instability (as defined, in items 2 and 3) that develop when the patient is mobilized during routine nursing care such as repositioning/washing the patient or changing their bed linens;
• Hemodynamic and/or respiratory instability (as defined, in items 2 and 3) that develop when a 20 second respiratory pause is required to implement the study protocol. This will be tested by inducing such a pause prior to transporting the patient;
• Any acute or chronic condition which, in the opinion of the investigators, might confound the imaging measurements (such as, but not limited to, severe bronchospasm, pulmonary infection, and lung tumor);
• Any acute or chronic condition which, in the opinion of the investigators or managing critical care team, could prevent safe transport to the CT suite.
• "Air leaks" requiring tube thoracotomy (e.g., pneumothorax, bronchopleural fistula);
• Body mass index > 40 kg/m2;
• Pregnancy (since this is a study that would expose a fetus to radiation risk);
• Patients who have taken part in other research studies involving radiation exposure, or those patients for whom this research radiation history is unavailable at the time of consent.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

7 participants in 2 patient groups

Group 1: ARDSNet

Active Comparator group

Description:

Participants will receive standard ARDSNet low-stretch PEEP (positive end-expiratory pressure) protocol.

Treatment:

Procedure: PEEP (positive end-expiratory pressure) - standard

Group 2: Individualized PEEP (positive end expiratory pressure) Strategy

Experimental group

Description:

Participants will receive individualized PEEP (positive end-expiratory pressure).

Treatment:

Procedure: PEEP (positive end-expiratory pressure) - maximum