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Optimal High CPAP Pressures in Preterm Neonates Post-extubation

Not Applicable
Conditions
Preterm Birth
Mechanical Ventilation Complication
Respiratory Distress Syndrome, Newborn
Interventions
Other: CPAP level
Registration Number
NCT05230485
Lead Sponsor
McMaster Children's Hospital
Brief Summary

Use of continuous positive airway pressure (CPAP) in preterm neonates has traditionally been limited to between 5-8 cmH2O. In recent years, use of CPAP pressures ≥9 cmH2O is becoming more common in neonates with evolving chronic lung disease, in lieu of other non-invasive modes or invasive mechanical ventilation. A particular knowledge gap in the current literature is the choice of the level of pressure level when using High CPAP as a post-extubation support mode. In this study, we will comparatively evaluate the short-term impact of two different high CPAP pressures when used as a post-extubation support mode in preterm neonates.

Detailed Description

Background: Use of continuous positive airway pressure (CPAP) in preterm neonates has traditionally been limited to between 5-8 cmH2O. In recent years, use of CPAP pressures ≥9 cmH2O is becoming more common in neonates with evolving chronic lung disease, in lieu of other non-invasive modes or invasive mechanical ventilation. However, there are limited data on the effectiveness and safety of this mode.

A particular knowledge gap in the current literature is the choice of the level of pressure level when using High CPAP as a post-extubation support mode. While it could be argued that the initial High CPAP pressure post-extubation should be somewhat higher than the pre-extubation mean airway pressure (Paw), there remain concerns of potential complications as well as uncertainty around degree of leak and resulting effectiveness. On the other hand, a suboptimal post-extubation High CPAP level may lead to atelectasis and contribute towards extubation failure, potentially prolonging invasive ventilation and associated risks. As such, research towards identification of the optimal High CPAP level post-extubation from high invasive ventilation pressures is warranted.

Objective: To comparatively evaluate the short-term impact of two different high CPAP pressures when used as a post-extubation support mode in preterm neonates.

Hypothesis: We hypothesize that babies extubated from invasive mechanical ventilation with a mean Paw between 9-15 cmH2O will demonstrate better physiological and clinical parameters when using High CPAP+2 cmH2O vs equivalent CPAP levels.

Methods: Design - This will be a prospective, single-centre, randomized cross-over study.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
26
Inclusion Criteria
  • Gestational age <29 weeks; chronological age >7 days; post-menstrual age <37 weeks; extubation from invasive ventilation with measured mean airway pressure 9-15 cmH2O
Exclusion Criteria
  • Any congenital or genetic/chromosomal abnormality

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Equivalent CPAPCPAP levelCPAP level will be equal to the pre-extubation measured mean airway pressure
Higher CPAPCPAP levelCPAP level will be 2 cmH2O higher than pre-extubation measured mean airway pressure
Primary Outcome Measures
NameTimeMethod
Peak Edi60 min following each CPAP level - assessed over 10 min

The peak electrical diaphragmatic activity - a surrogate for work of breathing to generate tidal volume

Secondary Outcome Measures
NameTimeMethod
Minimum EDi60 min following each CPAP level - assessed over 10 min

The minimum eelectrical diaphragmatic activity - a surrogate for work of breathing to maintain functional residual capacity

Regional cerebral perfusion60 min following each CPAP level - assessed over 10 min

The cerebral tissue extraction of oxygen - determined by near infra-red spectroscopy

Pressure level - Ventilator60 min following each CPAP level - assessed over 10 min

Pressure level as measured by the ventilator

Pressure level - Interface60 min following each CPAP level - assessed over 10 min

Pressure level at measured at the nasal interface used to deliver CPAP

Work of breathing scoreOver entire duration (70 min) at each CPAP level, assessed every 10 min

Using Silverman Scoring

Heart RateOver entire duration (70 min) at each CPAP level, assessed every 10 min

From cardiorespiratory monitoring

Respiratory RateOver entire duration (70 min) at each CPAP level, assessed every 10 min

From cardiorespiratory monitoring

Transcutaneous CO2 levelOver entire duration (70 min) at each CPAP level, assessed every 10 min

From bedside transcutaneous CO2 monitoring

FiO2 levelOver entire duration (70 min) at each CPAP level, assessed every 10 min

Fractional inspired oxygen level, as determined by clinical and inputted into ventilator

Number of bradycardic episodes <80 bpmOver entire duration (70 min) at each CPAP level

as above

Proportion of duration with SpO2 <90%Over entire duration (70 min) at each CPAP level

duration of time where the patient's SpO2 is less than 90%

Trial Locations

Locations (1)

McMaster Children's Hospital

🇨🇦

Hamilton, Ontario, Canada

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