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Prevalence and Clinical Impact of Airway Opening Pressure in Post-Cardiac Surgery Patients

Prevalence and Clinical Impact of Airway Opening Pressure in Post-Cardiac Surgery Patients: A Prospective Observational Study

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07189026
Enrollment
196
Registered
2025-09-23
Start date
2025-06-27
Completion date
2027-06-30
Last updated
2025-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery, Mechanical Ventilation After Surgery

Brief summary

Airway opening pressure is a key parameter in assessing respiratory mechanics. Current practice primarily relies on indirect assessments of lung mechanics, but growing evidence suggests that direct airway opening pressure measurement could enhance individualized ventilatory strategies. Significant airway opening pressure suggests incomplete alveolar recruitment at end-expiration, which may contribute to ventilation-perfusion mismatch, increased respiratory effort, and postoperative pulmonary complications such as atelectasis and impaired gas exchange. Determining the prevalence and clinical relevance of significant airway opening pressure in post-cardiac surgery patients could contribute to more personalized respiratory strategies and improve postoperative care.

Interventions

DIAGNOSTIC_TESTAirway opening pressure

Airway opening pressure will be measured within one hour of intensive care unit admission (using a standardized low-flow insufflation maneuver flow 5-6 LPM). The inflection point on the pressure-time or pressure-volume waveform- depending on ventilator model-will define the airway opening pressure.

Sponsors

Laval University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Months to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (≥18 years) * Undergoing elective coronary artery bypass grafting (CABG) or valve surgery, or combined procedures with expected postoperative mechanical ventilation

Exclusion criteria

\- Patient receiving invasive mechanical ventilation prior to surgery

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of significant airway opening pressureup to 1 hour after intensive care admissionairway opening pressure ≥ 5 cmH₂O

Secondary

MeasureTime frameDescription
Airway opening pressure prevalence based on body mass indexup to 1 hourAirway opening pressure prevalence base on Obesity status (body mass index ≥30 vs. \<30 kg/m²)
Airway opening pressure prevalence based on cardiopulmonary bypass durationup to 1 hourAirway opening pressure prevalence based on cardiopulmonary bypass duration (minutes)
Airway opening pressure prevalence based on left ventricular dysfunctionup to 1 hourAirway opening pressure prevalence based on left ventricular dysfunction (Ieft ventricular ejection fraction \< 50 percent vs \> 50 percent)
Airway opening pressure prevalence based on inotropic supportup to 1 hourAirway opening pressure prevalence based on use of amines (\< 0.1 mcg/kg/min or norepinephrine equivalent vs \> 0.1 mcg/kg/min or norepinephrine equivalent)
Airway opening pressure prevalence based on ageup to 1 hourAirway opening pressure prevalence base on age
Airway opening pressure prevalence based on intraoperative fluid balanceup to 1 hourAirway opening pressure prevalence base on intraoperative fluid balance
Patient positionup to 1 hourComparison of airway opening pressure values in flat versus semi-recumbent (30-degree) positions
Positive end expiratory pressure levelup to 1 hourNumber of times Positive end expiratory pressure is set greater than measured airway opening pressure
ExtubationDay7Correlation between airway opening pressure and time to extubation
Hemodynamic tolerance base on blood pressure dropup to 15 minutesEvaluation of hemodynamic tolerance based on arterial pressure during positive end-expiratory pressure adjustment (if inotropic agents are required, an increase of more than 0.05 mcg/kg/min in norepinephrine equivalent is considered significant)
Hemodynamic tolerance base on pulse oxygen saturation dropup to 15 minutesEvaluation of hemodynamic tolerance based on pulse oxygen saturation. A decrease in pulse oxygen saturation of 5 percent from baseline or more is considered significant.
Non-interruptive airway opening pressure measurement methodup to 1 hourThe novel non-interruptive airway opening pressure measurement method will be validated
Feasibility of airway opening pressure measurementup to 1 hourproportion of patients in whom the maneuver is successfully completed

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026