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Clinical Trials/NCT03660592
NCT03660592CompletedNot Applicable

Contribution LUS and Reproducibility of Lung Ultrasound in the Diagnosis of Acute Heart Failure in the Emergency Department (ED)

University of Monastir0 sites1,024 target enrollmentStarted: October 1, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,024
Primary Endpoint
the reproductibility of LUS in the diagnosis of heart failure

Study Overview

Brief Summary

Discrimination between cardiac and non-cardiac causes of dyspnea can be challenging, causing excessive delay before adequate therapy. In clinical practice lung ultrasound (LUS) is becoming an easy and reliable noninvasive tool for the evaluation of dyspnea and can shorten the time to diagnosis .However the reproductibility of this test was not extensively studied.

Detailed Description

Dyspnea is one of the most distressing situations for the patient . Emergency cases do not always present in conditions that are ideal for immediate diagnosis, which sometimes compromises outcome. Physical examination, laboratory findings and radiography are imperfect, resulting in a need for sophisticated test results that delay management.

Lung ultrasonography is becoming a standard tool in critical cases in the ED.

the investigators aim to perform ultrasonography on consecutive patients admitted to the ICU with dyspnea, comparing lung ultrasonography results on initial presentation with the final diagnosis by the ICU team.

Three items were assessed: artifacts (horizontal A lines or vertical B lines indicating interstitial syndrome), lung sliding, and alveolar consolidation and/or pleural effusion, these items were grouped to assess ultrasound profiles.

This study assesses the potential of lung ultrasonography to diagnose heart failure.The second aim of this study was to evaluate the inter-observer reproducibility of LUS performed by ED residents in the evaluation of cardiac causes of acute dyspnea.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • non traumatic dyspnea with the final diagnosis of heart failure

Exclusion Criteria

  • impossibility to give consent to participate in the study
  • post traumatic dyspnea
  • pregnant women
  • need for endotracheal intubation or inotropic drugs
  • patients who were deemed too unstable for sonography by the treating team

Outcomes

Primary Outcomes

the reproductibility of LUS in the diagnosis of heart failure

Time Frame: 0 days

the reproductibility of the LUS in the diagnosis of heart failure between two different operators (using the Kappa and the agreement index)

the accuracy of LUS in the diagnosis of heart failure the accuracy of LUS in the diagnosis of heart failure measured by sensitivity ,specificity, and area under the roc curve

Time Frame: 0 days

the accuracy of LUS in the diagnosis of heart failure measured by sensitivity ,specificity, and area under the roc curve

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Pr. Semir Nouira

Pr Nouira Semir

University of Monastir

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