Respiratory Weaning Following Cardiac Surgery.

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-31

Study Completion Date

2019-01-31

Brief Summary

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Respiratory weaning failure worsens prognostic of patients following on-pump cardiac surgery. There are increasing evidences that pulmonary, diaphragmatic or cardiologic echographies are useful in order to improve this critical medical status.

Based both on a previous study conducted in the critical care unit of Purpan and on literature we hypothesize that a combined thoracic echography score could be of interest. We make the hypothesis that the use of a score based on thoracic combined echography (ETC = cardiac, pulmonary and diaphragmatic) allows to predict the failure of respiratory weaning in cardiac surgery and allows to improve the characterization of the causes of this failure

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Detailed Description

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Conditions

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Respiratory Insufficiency

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patient with mechanical ventilation

Patient will be followed with combined Thoracic Echography Record

Combined Thoracic Echography Record

Intervention Type OTHER

This examination will be done to do the longitudinal follow-up of the patient

Interventions

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Combined Thoracic Echography Record

This examination will be done to do the longitudinal follow-up of the patient

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adult (\> 18 years old) beneficiating of mechanical ventilation following cardiac surgery
* Weaning test period
* Patient insured under the French social security system

Exclusion Criteria

* Tracheostomy
* Neurological disorders
* Need for prophylactic non invasive ventilation.
* Global obstructive lung disease with a forced expiratory volume \< 50%.
* Judicial protection
* Patient already included in a trial still running.
* Pregnancy

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No