Echocardiographic Detection of Extravascular Lung Water Increase During Weaning From Mechanical Ventilation (ECHOBAG)

December 1, 2015 updated by: DEMOSTHENES MAKRIS, University of Thessaly

Switching from positive airway pressure ventilation to spontaneous ventilation during weaning from mechanical ventilation, pulmonary edema may occur and in this case, doppler echocardiographic (U/S) indices of cardiac dysfunction correlates with the concentration of fluid in interstitial space.

Forty consecutive mechanically ventilated critical ill patients who fulfill criteria for weaning from mechanical ventilation, will be included in this study. All patients will be evaluated daily and when the patients fulfill weaning criteria them they will undergo a 2-hour spontaneous breathing trial (SBT) through a T-piece.

Before and after SBT cardiopulmonary function will be assessed by thermodilution and echocardiography. In patients with preserved LV systolic function, an echocardiographic index of diastolic dysfunction (E/Em ratio) before preforming SBT may identify high risk patients for increasing extravascular water in weaning.

In addition, the investigators expect to find positive correlations (p<0.05) between pulmonary extravascular lung water and echocardiographic indices (such as E/Em ratio) during SBT.

Study Overview

Detailed Description

Pulmonary edema (PE) is an underestimated factor of weaning failure. The interruption of mechanical ventilation

  1. increases left ventricular (LV) afterload, sympathetic tone and may provoke myocardial schema, LV dysfunction and
  2. augments blood in-flow into the thorax and may cause right ventricular dilation and intraventricular septum left shift.

These events may impair LV compliance during weaning, increase intra-capillary pulmonary pressures and cause cardiogenic PE (CPE). The investigators have recently shown that LV diastolic dysfunction may predispose to weaning failure, while echocardiographic markers of CPE may provide further insight in weaning process. Notably, this could be especially true in chronic obstructive pulmonary disease patients where strategies aiming to manage heart failure (i.e. diuretics, nitroglycerin) has been shown to improve weaning outcomes.

In addition, vigorous inspiratory efforts against the endotracheal tube during spontaneous weaning trials may reduce excessively extracapillary pressures in pulmonary interstitial spaces, causing an intra-pulmonary fluid shift known as negative pressure PE (NPPE).

Primary aim: To study whether echocardiographic parameters of left and right ventricular function, and echocardiographic surrogates of cardiogenic PE (markers of elevated LV filling pressures, such as E/Em) are associated to weaning-induced alterations in extravascular lung water index (EVLWI).

Hypothesis A) Switching from positive airway pressure ventilation to spontaneous ventilation during weaning from mechanical ventilation, pulmonary edema may occur and in this case, doppler echocardiography (U/S) indices of cardiac dysfunction correlates with the concentration of fluid in interstitial space.

B) These events can be further provoked after Maximum Inspiratory Pressure (MIP) trials.

C) Pulmonary edema is a major cause of weaning failure in chronic obstructive pulmonary disease (COPD) patients, even in those without known cardiac disease.

SUBJECTS Thirty-five consecutive mechanically ventilated critical ill patients who fulfil criteria for weaning, will be included.

METHODS All patients will be evaluated daily for the aforementioned weaning criteria and when the patients fulfill them they will undergo A) a 2-hour spontaneous breathing trial (SBT) through a T-piece and B) MIP trial.

Before and after SBT and MIP trials cardiopulmonary function will be assessed by thermodilution and echocardiography.

Extravascular Lung Water Index (EVLWI) study. EVLWI will be assessed by transpulmonary thermodilution (PiCCO plus system, Pulsion Medical Systems and Philips Medical Systems, USA). Transpulmonary thermodilution measures left-side CO by injection of a cold injectate (15-20 ml,10C lower than blood temperature) via subclavian or internal jugular vein and by the detection of the change in temperature in the arterial system via femoral access. Analysis of the thermodilution curve in terms of mean transit time (MTt) and downslope time (DSt) will be used for determination of intra and extra vascular fluid volumes. EVLW correlates to the extravascular thermal volume in the lungs and it is evaluated through the MTt.

Principle parameters obtained by transpulmonary thermodilution are following

  • cardiac output (absolute/indexed parameters, CO/CI)
  • cardiac function index (CFI)
  • extravascular lung water (EVLW/EVLWI)
  • pulmonary vascular permeability index (PVPI)
  • global ejection fraction (GEF)

Echocardiographic study. Baseline Doppler echocardiographic measurements will be obtained before SBT initiation, while participants will be in pressure support ventilation (pre-SBT). Follow up measurements (end-SBT) in patients who succeeded in the trial, will be collected 120 minutes after SBT initiation. In those participants who fail the procedure, measurements will obtained before reconnection to the ventilator. Doppler echocardiography will be performed as previously described (Philips i33, U.S.A.). Mitral inflow pulsed-wave Doppler signals [peak velocities of early (E) and late (A) LV diastolic filling, E-wave deceleration time (DTE)], Tissue Doppler Imaging(TDI)-derived peak systolic (Sm)/early diastolic (Em)/late diastolic (Am) velocities at the lateral/septal mitral annulus and lateral tricuspid annulus, and color M-mode Doppler velocity of propagation (Vp) will be obtained from the apical 4-chamber view. Analysis will be also performed for "conventional" (E/A ratio) and "advanced" (E/Em, ) echocardiographic indices of LV filling pressures.

Expected Results Recruitment period: three months Analysis of results: three months Based on a previous study contacted by the investigators, echocardiographic variables of LV diastolic dysfunction is expected to be found associated with direct measurements of pulmonary edema (EVLWI). In participants with preserved LV systolic function, an E/Em ratio>7.8 before preforming SBT may identify high risk patients for increasing extravascular water in weaning.

Based on preliminary findings EVLWI values measured in critical patients by the investigators were 2-11 ml/Kg.

The investigators expect to find positive correlations (p<0.05) between EVLWI and E/Em during SBT and MIP trials.

Implications:

The findings of the study will provide further insights in the pathophysiology of weaning. This could be especially true in COPD patients where failure rates are high.

Diagnosis of weaning failure and identification of those patients who are prone to develop LV dysfunction during weaning and weaning outcomes may improve with the application of strategies aiming to manage heart failure (i.e diuretics, nitroglycerin).

EVLW measurements and DE indices will be use as an aid to diagnose and to determine the etiology of pulmonary edema in critical care patients.

These indices may retain the predictive value even in the subset of patients who initially pass SBT; therefore, E/Em pre-SBT could identify patients who will probably fail to remain in SBT.

The relationship between DE indices and EVLWI could be advantageous compared to EVLWI measurement alone, for the quantification of lung edema and the guidance of therapy.

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Larissa, Greece
        • University Hospital Larissa

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • adequate oxygenation (pressure of oxygen in arterial blood (PaO2)>60mmHg with fraction of inspired oxygen (FiO2)<40%, PEEP<5-10cmH2O, PaO2/FIO2>150-300)
  • stable cardiovascular system (Heart rate<140/min, stable blood pressure, without or very minimal vasopressors)
  • absence of sepsis and temperature <38 degree of Celcius
  • no respiratory acidosis
  • adequate hemoglobin (Hb > 8-10g/dL)
  • sufficient (adequate mentation ) arousable Glasgow coma scale >13/15, no continuous sedative infusions
  • Ramsay score<3
  • stable metabolic status (acceptable levels of electrolytes )
  • subjective clinical assessments such as resolution of the acute phase of disease and adequate cough.

Exclusion Criteria:

  • atrial fibrillation or other arrhythmias
  • insufficiency of tricuspidal valve ( +++),
  • continuous venous-venous hemodialysis

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: patients who undergo weaning from mechanical ventilation
consecutive mechanically ventilated critical ill patients who fulfil criteria for weaning will be included

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Extravascular water increase during weaning from mechanical ventilation measured by echocardiography and thermodilution method
Time Frame: 24 hours
24 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2015

Primary Completion (Actual)

December 1, 2015

Study Registration Dates

First Submitted

March 27, 2015

First Submitted That Met QC Criteria

April 8, 2015

First Posted (Estimate)

April 9, 2015

Study Record Updates

Last Update Posted (Estimate)

December 2, 2015

Last Update Submitted That Met QC Criteria

December 1, 2015

Last Verified

December 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 273/2015

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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