Assessments of Diaphragm-pleural Mechanics During the Weaning From Prolonged Mechanical Ventilation

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03842280
Collaborator
(none)
200
1
35
5.7

Study Details

Study Description

Brief Summary

Weaning failure from mechanical ventilator is commonly seen in respiratory failure and increases duration of ventilator use, ICU stay, ventilator associated pneumonia and even mortality. The diaphragm serves as one of the most important respiratory mechanism and its function differs the weaning success rate. Since 1980s, ultrasonography assessment in diaphragm movement were developed and further discussion upon whether it serves as a predicting factor for extubation failure. The measurement includes difference of diaphragm thickness, diaphragm excursion or the movement of liver and spleen.

Multiple studies targeted intubated patients with different measurement methods and all resulted with good weaning prediction value.6 Of all the studies, only one study targeted tracheostomy tube patients. They reported diaphragm thickness fraction >36% as cutoff value is associated with successful spontaneous breathing trial (SBT), with a sensitivity of 0.82, specificity of 0.88. However, little comparison with traditional weaning parameters was mentioned in the study. We designed this prospective observational study to evaluate whether diaphragm movement under ultrasound serves as a predicting index of ventilator discontinuation in patients with tracheostomy. The diaphragm movement will also correlate with other parameters such as RSBI, Pi max, Pe max, Tv spont., WEANSNOW score(WS), VO2, APACHE II. Esophageal pressure is also provided as an option for our study population for more information such as pleural pressure, transdiaphragm pressure, etc.

The ultrasonography measurement of diaphragm movement will be performed within 6 hours before discontinuation of ventilator. The patient remains in semi-recumbent position with the convex probe selected for its good penetration. The probe is placed at a craniocaudal axis, 90 degrees to the skin at the lower intercostal spaces to right anterior axillary line (AAL) and left posterior axillary line (PAL), which allows a perpendicular ultrasound beam direction to the diaphragm movement. Liver (border or vascular structure), splenic (border or vascular structure) will be selected as target point and the marked distance of movement during quiet respiration cycle will be measured 10 times with a largest value calculated. Other echo measurements will also be attempted.

The study aims to investigate if the measurement of the diaphragm movement serves as a reliable predicting factor for weaning failure in respiratory care center patients.

Condition or Disease Intervention/Treatment Phase
  • Device: Diaphragm ultrasound assessment & Esophageal pressure measurement

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessments of Diaphragm-pleural Mechanics During the Weaning From Prolonged Mechanical Ventilation
Actual Study Start Date :
Feb 1, 2019
Anticipated Primary Completion Date :
Jun 30, 2021
Anticipated Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Prolonged mechanical ventilation

Prolonged mechanical ventilation with tracheostomy

Device: Diaphragm ultrasound assessment & Esophageal pressure measurement
Diaphragm ultrasound assessment and/or Esophageal pressure measurement before, during and after spontaneous breathing trial

Outcome Measures

Primary Outcome Measures

  1. Weaning success [1 month]

    Liberation from mechanical ventilation

Secondary Outcome Measures

  1. Ventilator free 30 days after liberation [30 days after liberation]

    No mechanical ventilation use in 30 days after liberation

  2. Ventilator free 60 days after liberation [60 days after liberation]

    No mechanical ventilation use in 30 days after liberation

  3. Ventilator free 90 days after liberation [90 days after liberation]

    No mechanical ventilation use in 90 days after liberation

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Prolonged mechanical ventilation with tracheostomy tube

  • Oxygen with a fraction of ≤ 0.4

  • Positive end expiratory pressure at ≤ 5 cm H2O

  • Pressure support at ≤ 8 cmH2O

Exclusion Criteria:
  • No spontaneous breathing

  • Unstable hemodynamic status,

  • History of peritonitis, intraabdominal operation, empyema, or pleurodesis.

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwan University Hospital Taipei Taiwan

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT03842280
Other Study ID Numbers:
  • 201811015RINA
First Posted:
Feb 15, 2019
Last Update Posted:
Mar 25, 2020
Last Verified:
Mar 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Taiwan University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 25, 2020