search
Back to results

Assessment of Esophageal Pressure Reliability to Estimate Pleural Pressure in Critically Ill Children (APPLE)

Primary Purpose

Mechanical Ventilation

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
esophageal and pleural pressure measurement
Sponsored by
St. Justine's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Mechanical Ventilation focused on measuring Mechanical ventilation, Children, Esophageal Pressure, Pleural Pressure

Eligibility Criteria

1 Day - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children <18 years old, hospitalized in the pediatric intensive care unit;
  • Requiring invasive ventilation for more than 4 hours according to the prescription of the attending physician;
  • With at least one chest tube.

Exclusion Criteria:

  • Contraindications to the placement of a new nasogastric tube (e.g. bilateral phrenic paralysis, trauma or recent surgery in cervical or nasopharyngeal regions, severe coagulation disorder);
  • Hemodynamic instability, as defined by the treating team, and the absence of recent (<4 hours) increase in the flow of dopamine, epinephrine, norepinephrine, or dobutamine;
  • Respiratory instability defined as a severe respiratory failure requiring FiO2 > 60%, or PaCO2 > 80 mmHg on blood gas in the last hour;
  • Persistent pleural effusion or pneumothorax despite the chest-tube;
  • Bronchopleural fistula;
  • Recent (<12 hours) thoracic hemorrhage;
  • Delayed sternal closure at the time of study;
  • Significant pericardial effusion;
  • Absence of parental or tutor consent;
  • Patient for whom a limitation of life support treatments is discussed or decided.

Sites / Locations

  • St. Justine's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Patients

Arm Description

Patient baseline characteristics will be collected. Specific nasogastric tube installation: a specific nasogastric tube equipped with pressure transducers (Gaeltec® probe) will be installed. Connection of a pressure transducer to the existing chest-tube. Simultaneous recordings of PES (Gaeltec®), PPL, PAW, respiratory volume and flow (5 minutes). Removal of the Gaeltec® probe, and repositioning of the pre-existing nasogastric tube in the esophagus for PES measurement. Simultaneous recordings of PES (feeding tube), PPL, PAW, respiratory volume and flow (5 minutes). Repositioning of the nasogastric tube in the stomach, and disconnection of the different recording equipment.

Outcomes

Primary Outcome Measures

End-expiratory esophageal
End-expiratory PES and PL, calculated as the mean value of 10 consecutive breaths, during a stable period with no intervention or artifacts;
Pleural pressure
PPL, directly measured in the existing chest tubes, and calculated as the mean value of 10 consecutive breaths, during a stable period with no intervention or artifacts.
transpulmonary pressures

Secondary Outcome Measures

The Elastance-derived end-inspiratory transpulmonary pressure
The Elastance-derived end-inspiratory transpulmonary pressure, calculated as: PAW at end-inspiration x EL/ERS (EI and ERS being the respective elastances of the lung and the respiratory system, estimated on the esophageal and airway Pressure-Volume curves);

Full Information

First Posted
April 28, 2016
Last Updated
August 22, 2018
Sponsor
St. Justine's Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT02762279
Brief Title
Assessment of Esophageal Pressure Reliability to Estimate Pleural Pressure in Critically Ill Children
Acronym
APPLE
Official Title
Assessment of Esophageal Pressure Reliability to Estimate Pleural Pressure in Critically Ill Children
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
June 28, 2016 (Actual)
Primary Completion Date
October 1, 2017 (Actual)
Study Completion Date
October 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Justine's Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background During ventilatory assistance, optimization of settings is critical to allow a personalized support and avoid over- or under-assistance. But little data are available in clinical practice to guide the adjustment of the support. In adults, esophageal pressure (PES) has been shown to be a reliable surrogate of pleural pressure (PPL) and clinical studies suggest that PES may be useful to guide the management of mechanical ventilation. In children, the PES measurement could have similar potential benefits, but beforehand the reliability of PES to estimate PPL needs to be assessed. Objective The primary objective of this study is to validate the reliability of PES directly monitored using a miniature catheter tip pressure transducer (Gaeltec® system) to estimate PPL, when compared to a gold standard, i.e the direct PPL measurement in situ. Method This is a prospective single center study. Children <18 years old, hospitalized in the pediatric intensive care unit, requiring invasive ventilation and with at least one chest tube will be included. Protocol A pressure transducer will be connected to the existing chest-tube and PES (measured by Gaeltec® and feeding tube), PPL, PAW, respiratory volume and flow will be simultaneously recorded. Expected results We expect that the PES-based methods will provide an accurate estimation of PPL. Once this tool validated, PES could be helpful to optimize mechanical ventilation in children, and further interventional trials would be warranted to evaluate if its use could allow a reduction of the ventilation support duration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mechanical Ventilation
Keywords
Mechanical ventilation, Children, Esophageal Pressure, Pleural Pressure

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients
Arm Type
Experimental
Arm Description
Patient baseline characteristics will be collected. Specific nasogastric tube installation: a specific nasogastric tube equipped with pressure transducers (Gaeltec® probe) will be installed. Connection of a pressure transducer to the existing chest-tube. Simultaneous recordings of PES (Gaeltec®), PPL, PAW, respiratory volume and flow (5 minutes). Removal of the Gaeltec® probe, and repositioning of the pre-existing nasogastric tube in the esophagus for PES measurement. Simultaneous recordings of PES (feeding tube), PPL, PAW, respiratory volume and flow (5 minutes). Repositioning of the nasogastric tube in the stomach, and disconnection of the different recording equipment.
Intervention Type
Other
Intervention Name(s)
esophageal and pleural pressure measurement
Intervention Description
Esophageal pressure will be monitored by a dedicated catheter and pleural pressure will be measured into the chest tube already in place
Primary Outcome Measure Information:
Title
End-expiratory esophageal
Description
End-expiratory PES and PL, calculated as the mean value of 10 consecutive breaths, during a stable period with no intervention or artifacts;
Time Frame
Up to 2 hours from the beginning of the study
Title
Pleural pressure
Description
PPL, directly measured in the existing chest tubes, and calculated as the mean value of 10 consecutive breaths, during a stable period with no intervention or artifacts.
Time Frame
Up to 2 hours from the beginning of the study
Title
transpulmonary pressures
Time Frame
Up to 2 hours from the beginning of the study
Secondary Outcome Measure Information:
Title
The Elastance-derived end-inspiratory transpulmonary pressure
Description
The Elastance-derived end-inspiratory transpulmonary pressure, calculated as: PAW at end-inspiration x EL/ERS (EI and ERS being the respective elastances of the lung and the respiratory system, estimated on the esophageal and airway Pressure-Volume curves);
Time Frame
Up to 2 hours from the beginning of the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children <18 years old, hospitalized in the pediatric intensive care unit; Requiring invasive ventilation for more than 4 hours according to the prescription of the attending physician; With at least one chest tube. Exclusion Criteria: Contraindications to the placement of a new nasogastric tube (e.g. bilateral phrenic paralysis, trauma or recent surgery in cervical or nasopharyngeal regions, severe coagulation disorder); Hemodynamic instability, as defined by the treating team, and the absence of recent (<4 hours) increase in the flow of dopamine, epinephrine, norepinephrine, or dobutamine; Respiratory instability defined as a severe respiratory failure requiring FiO2 > 60%, or PaCO2 > 80 mmHg on blood gas in the last hour; Persistent pleural effusion or pneumothorax despite the chest-tube; Bronchopleural fistula; Recent (<12 hours) thoracic hemorrhage; Delayed sternal closure at the time of study; Significant pericardial effusion; Absence of parental or tutor consent; Patient for whom a limitation of life support treatments is discussed or decided.
Facility Information:
Facility Name
St. Justine's Hospital
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Assessment of Esophageal Pressure Reliability to Estimate Pleural Pressure in Critically Ill Children

We'll reach out to this number within 24 hrs