Lung Atelectasis Improvement Through Positive End Expiratory Pressure During Anesthetic Induction

Fudan University

Status: Completed

Conditions: Lung Injury, Acute

Treatments: Other: 10 PEEP; Other: ZEEP; Other: 5PEEP

Study type: Interventional

Funder types: Other

Identifiers

NCT06900426

2502-Exp148

Details and patient eligibility

About

Anesthetic induction could lead to lung atelectasis, increase intrapulmonary shunt, and potentially impair oxygenation. The study aimed to validate that a positive end-expiratory pressure (PEEP) of 10 cmH2O could reduce lung atelectasis, comparing to 0 or 5 cmH2O with limited overdistension.

Full description

General anesthesia may introduce lung atelectasis, which causes an increase in intrapulmonary shunt, and impairs oxygenation, even in the lung-healthy subjects. The magnitude of shunt is correlated with the formation of pulmonary atelectasis. The study aimed to validate that a positive end-expiratory pressure (PEEP) of 10 cmH2O could reduce lung atelectasis, comparing to 0 or 5 cmH2O with limited overdistension. Surgical patients with healthy lungs were randomly assigned to receive 0, 5 or 10 cmH2O PEEP (PEEP0, PEEP5 and PEEP10 groups). Anesthetic induction was performed by certified registered anesthesiologists, during which the patients were mechanically ventilated using the volume-controlled mode. Electrical impedance tomography (EIT) was used to dynamically assess the lung atelectasis during anesthetic induction (spontaneous, mask, and endotracheal intubation ventilation). The primary outcome was the dorsal change of end expiratory lung impedance (△EELI) after 2 mins anesthetic induction. The secondary outcome was driving pressure, EIT-derived ventilation homogeneity, hemodynamics and PaO2/FiO2.

Enrollment: 120 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• between 18 and 80 years
• scheduled for elective non-cardiothoracic cancer surgery
• general anesthesia.

Exclusion criteria

• acute or chronic respiratory disorders, such as chronic obstructive pulmonary disease (COPD) or asthma;
• a history of lung surgery
• a high risk of reflux and aspiration
• a requirement for awake intubation
• facial or thoracic deformities
• the presence of implants, such as cardiac pacemakers
• pregnant

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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120 participants in 3 patient groups

PEEP0

Other group

Description:

There is ZEEP during anesthetic induction

Treatment:

Other: ZEEP

PEEP5

Experimental group

Description:

There is 5 cmH2O PEEP during anesthetic induction.

Treatment:

Other: 5PEEP

PEEP10

Experimental group

Description:

There is 10 cmH2O PEEP during anesthetic induction.

Treatment:

Other: 10 PEEP