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Esophageal Balloon Guided Weaning of the Morbidly Obese Patient

Primary Purpose

Morbid Obesity

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Esophageal Balloon
Cstat
Sponsored by
East Carolina University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Morbid Obesity focused on measuring Transpulmonary pressure, Esophageal balloon, Esophageal pressure monitoring device, Cstat, Static effective compliance, Ventilator weaning, Morbidly Obese Ventilator Dependent Tracheotomized Patients

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Morbidly obese patients with BMI of 40 or greater
  • Ventilator dependent patients (defined as at least one prior failure at weaning)
  • Tracheotomized
  • No active underlying lung disease that would preclude ventilator weaning
  • Stable hemodynamics
  • Patient/ family able to give consent
  • No naso-facial abnormalities that would interfere with placement of an esophageal balloon
  • Fio2 <= 60%
  • Patient able to tolerate Pressure Support ventilation

Exclusion Criteria:

  • Lack of consent
  • Patient deemed not weanable from mechanical ventilation as per the clinical judgement of the pulmonary physician
  • Significant lung, heart or neuromuscular disease that would interfere with or preclude ventilator weaning, including an active ongoing lung infection.
  • Contraindications to placement of an esophageal pressure monitoring device - such as ulcerations, tumors, diverticulitis, uncontrolled bleeding varices, sinusitis, epistaxis or recent nasopharyngeal surgery

Sites / Locations

  • Vidant Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Esophageal balloon Arm

Cstat Arm

Historic Controls

Arm Description

Patients in this arm were randomly assigned to have their PEEP adjusted to maintain a positive transpulmonary pressure (0 to 10 cm H20).

Patients in this arm had their PEEP adjusted to achieve the best static effective compliance (CStat).

These were historic controls with similar patient characteristics weaned by traditional methods in the 2-year period prior to the start of the study.

Outcomes

Primary Outcome Measures

Number of patients weaned by day 30
A patient was considered successfully weaned and "ventilator independent" if they were spontaneously breathing without ventilator support for at least 24 hours, and remained off the ventilator by day 30. If ventilator support was subsequently required, the patient was returned to their original group and considered not weaned. The patients were considered to be weaned or not, after a period of thirty days.

Secondary Outcome Measures

Time to wean
The time to wean/ time to achieve ventilator independence was measured from the date of randomization to the date of final successful liberation from mechanical ventilation. If patient had an unsuccessful initial wean, he was not considered weaned. Only patients who were considered weaned by day 30 accrued "time to ventilator independence."

Full Information

First Posted
December 12, 2014
Last Updated
December 17, 2014
Sponsor
East Carolina University
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1. Study Identification

Unique Protocol Identification Number
NCT02323009
Brief Title
Esophageal Balloon Guided Weaning of the Morbidly Obese Patient
Official Title
Esophageal Balloon Guided Weaning of the Morbidly Obese Patient
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Terminated
Why Stopped
Minimal recruitment. very few patients available with eligibility criteria
Study Start Date
January 2011 (undefined)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
East Carolina University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a study to evaluate whether PEEP adjusted by use of an esophageal balloon to overcome negative transpulmonary pressure; or adjusted by use of "CStat" to achieve the best effective static compliance will have any effect on outcomes with respect to ventilator weaning in tracheotomized morbidly obese patients (BMI >=40) with at least one failed prior weaning attempt.
Detailed Description
Tracheotomized morbidly obese patients (BMI >= 40) who had failed an initial attempt at ventilator weaning (defined in the investigators study as ventilator dependent) were randomly assigned to one of two methods for setting Positive End Expiratory Pressure (PEEP). Patients randomized to the esophageal balloon arm (ESO group) had their PEEP adjusted to overcome negative transpulmonary pressure and maintain a positive transpulmonary pressure (Ptp) of 0 to 10 cm H20 - targeting as close to zero as possible. Patients randomized to the static effective compliance arm (CStat group) had their PEEP adjusted to achieve the best static effective compliance as automatically calculated and displayed on the graphic interphase of the hamilton G5 or Galileo ventilator. For this group, the PEEP was adjusted in increments of 3 cm H20 until there was a less than 5% observed improvement in the static effective compliance. the PEEP with the best Cstat was chosen. At the end of the intervention period, this intervention cohort (termed "PEEP intervention cohort") will be compared to a group of historical controls to compare the efficiency of a PEEP-based weaning protocol to traditional weaning methods. The investigators hypothesized that PEEP levels titrated by use of an esophageal balloon to maintain a positive transpulmonary pressure between 0 to 10 cm H20, would lead to improved outcomes with respect to ventilator weaning in this subset of patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morbid Obesity
Keywords
Transpulmonary pressure, Esophageal balloon, Esophageal pressure monitoring device, Cstat, Static effective compliance, Ventilator weaning, Morbidly Obese Ventilator Dependent Tracheotomized Patients

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Esophageal balloon Arm
Arm Type
Active Comparator
Arm Description
Patients in this arm were randomly assigned to have their PEEP adjusted to maintain a positive transpulmonary pressure (0 to 10 cm H20).
Arm Title
Cstat Arm
Arm Type
Active Comparator
Arm Description
Patients in this arm had their PEEP adjusted to achieve the best static effective compliance (CStat).
Arm Title
Historic Controls
Arm Type
No Intervention
Arm Description
These were historic controls with similar patient characteristics weaned by traditional methods in the 2-year period prior to the start of the study.
Intervention Type
Device
Intervention Name(s)
Esophageal Balloon
Intervention Description
Esophageal balloon was used to measure esophageal pressure (Paux) which was used as an estimate of pleural pressure. Transpulmonary pressure (Ptp) was calculated as the difference between airway pressure (Pao) and Paux. Applied PEEP was then adjusted to overcome negative Ptp which we maintained between 0 to 10 cm H20. All measurements were made at end-expiration.
Intervention Type
Other
Intervention Name(s)
Cstat
Intervention Description
PEEP was adjusted to achieve the best CStat in this group of patients
Primary Outcome Measure Information:
Title
Number of patients weaned by day 30
Description
A patient was considered successfully weaned and "ventilator independent" if they were spontaneously breathing without ventilator support for at least 24 hours, and remained off the ventilator by day 30. If ventilator support was subsequently required, the patient was returned to their original group and considered not weaned. The patients were considered to be weaned or not, after a period of thirty days.
Time Frame
30-days
Secondary Outcome Measure Information:
Title
Time to wean
Description
The time to wean/ time to achieve ventilator independence was measured from the date of randomization to the date of final successful liberation from mechanical ventilation. If patient had an unsuccessful initial wean, he was not considered weaned. Only patients who were considered weaned by day 30 accrued "time to ventilator independence."
Time Frame
30-days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Morbidly obese patients with BMI of 40 or greater Ventilator dependent patients (defined as at least one prior failure at weaning) Tracheotomized No active underlying lung disease that would preclude ventilator weaning Stable hemodynamics Patient/ family able to give consent No naso-facial abnormalities that would interfere with placement of an esophageal balloon Fio2 <= 60% Patient able to tolerate Pressure Support ventilation Exclusion Criteria: Lack of consent Patient deemed not weanable from mechanical ventilation as per the clinical judgement of the pulmonary physician Significant lung, heart or neuromuscular disease that would interfere with or preclude ventilator weaning, including an active ongoing lung infection. Contraindications to placement of an esophageal pressure monitoring device - such as ulcerations, tumors, diverticulitis, uncontrolled bleeding varices, sinusitis, epistaxis or recent nasopharyngeal surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Shaw, MD
Organizational Affiliation
East Carolina University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vidant Medical Center
City
Greenville
State/Province
North Carolina
ZIP/Postal Code
27834
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16540960
Citation
Talmor D, Sarge T, O'Donnell CR, Ritz R, Malhotra A, Lisbon A, Loring SH. Esophageal and transpulmonary pressures in acute respiratory failure. Crit Care Med. 2006 May;34(5):1389-94. doi: 10.1097/01.CCM.0000215515.49001.A2.
Results Reference
background
PubMed Identifier
19001507
Citation
Talmor D, Sarge T, Malhotra A, O'Donnell CR, Ritz R, Lisbon A, Novack V, Loring SH. Mechanical ventilation guided by esophageal pressure in acute lung injury. N Engl J Med. 2008 Nov 13;359(20):2095-104. doi: 10.1056/NEJMoa0708638. Epub 2008 Nov 11.
Results Reference
background
PubMed Identifier
20105342
Citation
Talmor DS, Fessler HE. Are esophageal pressure measurements important in clinical decision-making in mechanically ventilated patients? Respir Care. 2010 Feb;55(2):162-72; discussion 172-4.
Results Reference
background
PubMed Identifier
20890197
Citation
Loring SH, Pecchiari M, Della Valle P, Monaco A, Gentile G, D'Angelo E. Maintaining end-expiratory transpulmonary pressure prevents worsening of ventilator-induced lung injury caused by chest wall constriction in surfactant-depleted rats. Crit Care Med. 2010 Dec;38(12):2358-64. doi: 10.1097/CCM.0b013e3181fa02b8.
Results Reference
background
PubMed Identifier
20019160
Citation
Loring SH, O'Donnell CR, Behazin N, Malhotra A, Sarge T, Ritz R, Novack V, Talmor D. Esophageal pressures in acute lung injury: do they represent artifact or useful information about transpulmonary pressure, chest wall mechanics, and lung stress? J Appl Physiol (1985). 2010 Mar;108(3):515-22. doi: 10.1152/japplphysiol.00835.2009. Epub 2009 Dec 17.
Results Reference
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PubMed Identifier
22699701
Citation
Hedenstierna G. Esophageal pressure: benefit and limitations. Minerva Anestesiol. 2012 Aug;78(8):959-66. Epub 2012 Jun 14.
Results Reference
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PubMed Identifier
22695479
Citation
Owens RL, Campana LM, Hess L, Eckert DJ, Loring SH, Malhotra A. Sitting and supine esophageal pressures in overweight and obese subjects. Obesity (Silver Spring). 2012 Dec;20(12):2354-60. doi: 10.1038/oby.2012.120. Epub 2012 May 4.
Results Reference
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PubMed Identifier
13630830
Citation
MEAD J, GAENSLER EA. Esophageal and pleural pressures in man, upright and supine. J Appl Physiol. 1959 Jan;14(1):81-3. doi: 10.1152/jappl.1959.14.1.81. No abstract available.
Results Reference
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PubMed Identifier
21255501
Citation
Piraino T, Cook DJ. Optimal PEEP guided by esophageal balloon manometry. Respir Care. 2011 Apr;56(4):510-3. doi: 10.4187/respcare.00815. Epub 2011 Jan 21.
Results Reference
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PubMed Identifier
16306256
Citation
Washko GR, O'Donnell CR, Loring SH. Volume-related and volume-independent effects of posture on esophageal and transpulmonary pressures in healthy subjects. J Appl Physiol (1985). 2006 Mar;100(3):753-8. doi: 10.1152/japplphysiol.00697.2005. Epub 2005 Nov 23.
Results Reference
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PubMed Identifier
24283226
Citation
Slutsky AS, Ranieri VM. Ventilator-induced lung injury. N Engl J Med. 2013 Nov 28;369(22):2126-36. doi: 10.1056/NEJMra1208707. No abstract available. Erratum In: N Engl J Med. 2014 Apr 24;370(17):1668-9.
Results Reference
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PubMed Identifier
30245572
Citation
Obi ON, Mazer M, Bangley C, Kassabo Z, Saadah K, Trainor W, Stephens K, Rice PL, Shaw R. Obesity and Weaning from Mechanical Ventilation-An Exploratory Study. Clin Med Insights Circ Respir Pulm Med. 2018 Sep 18;12:1179548418801004. doi: 10.1177/1179548418801004. eCollection 2018.
Results Reference
derived

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Esophageal Balloon Guided Weaning of the Morbidly Obese Patient

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