Feasibility and Accuracy of an Ultrasound Algorithm for Acute Dyspnea Diagnosis in the Emergency Department (EMERALD-US)

Evaluation of the Feasibility and Accuracy of an Ultrasound Algorithm for Acute Dyspnea Diagnosis in the Emergency Department

The management of chest pain has revolutionized its prognosis, primarily by improving urgent diagnosis of myocardial infarction. Currently, acute dyspnea is twice as frequent as chest pain and its associated mortality is much higher (16% of acute dyspnea admitted to emergency departments (ED) ).

Inappropriate treatment of acute dyspnea in the ED is frequent (30%) and is associated with a tripling of intra-hospital mortality after adjustment for confounding factors (2.83, IC 1.48 to 5.41, p=0.002). Other elements have also highlighted the importance of a quick and appropriate acute dyspnea diagnosis:

• The 2015 European Guidelines on acute heart failure emphasize the need for appropriate treatment within 90 minutes after the first medical contact.
• Inadequate treatment of chronic bronchitis decompensation is associated with a doubling of intra-hospital mortality.
• An initiation of antibiotic treatment within 4 hours of admission for pneumonia is recommended.
• 30% of pulmonary embolisms are not diagnosed during the initial emergency department visit, whereas their mortality in the absence of treatment is 25%.

Lung, venous and (simplified) cardiac ultrasound is associated with improved diagnostic performance in ED. However, no ultrasound algorithm dedicated to emergency physicians has been formally validated. The Blue Protocol (Lichtenstein et al., Chest 2008) has been validated in intensive care patients with very different phenotypes than those admitted to the ED. Pivetta et al. (Chest 2015) proposed an algorithm focused solely for the diagnosis of heart failure, thus not providing a diagnosis for all the other causes of dyspnea in ED. Finally, Zanbonetti et al. (Chest 2017) proposed an "unguided" ultrasound use, notably integrating inferior vena cava evaluation. However, measuring the inferior vena cava is difficult at the start of ED management when patients are in acute respiratory distress.

Study Overview

• Status: Recruiting
• Conditions: Dyspnea
• Intervention / Treatment: Procedure: Ultrasound algorithm (EMERALD-US)

Detailed Description

The investigators aim to assess the feasibility and accuracy of a new pragmatic and original ultrasound algorithm adapted for acute dyspnea diagnosis in the emergency department.

This primary objective of this prospective multicenter study is to assess the diagnostic accuracy of an ultrasound algorithm (EMERALD-US) dedicated to emergencies using lung, cardiac and vascular ultrasound for the 3 main dyspnea causes (heart failure, pneumonia and obstructive pulmonary disease exacerbation) in patients with acute non-traumatic dyspnea managed in the emergency department. Ultrasound exams will be blindly read by a centralized core laboratory after the standardized acquisition of all exams by a physician not involved in the care of patients in the ED. The main discharge diagnosis from initial hospitalization (heart failure, pneumonia and obstructive pulmonary disease exacerbation) will be adjudicated by a college of 3 senior physicians (emergency physician, cardiologist and internist) blinded to the use of ultrasound in the ED.

The secondary objectives of the study are to:

A/ Assess the feasibility of the ultrasound algorithm (EMERALD-US) in emergency departments.

B/ Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional (laboratory and radiological exams.

C/ Assess the diagnostic accuracy of the ultrasound algorithm (EMERALD-US) for less frequent dyspnea causes (pulmonary embolism, pleural effusion).

D/ Assess, the diagnostic accuracy of clinical (including BREST and PREDICA score), laboratory and radiological variables.

E/ Assess, the improvement in diagnosis accuracy with the ultrasound algorithm (EMERALD-US) on top of the diagnostic accuracy of clinical, laboratory and radiological exams.

F/ Assess the association between misdiagnosis (without using ultrasound) and survival at D30.

• Study Type: Interventional
• Enrollment (Anticipated): 225
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Tahar CHOUIHED, MD; Phone Number: +33 (0)3 83 85 14 96; Email: t.chouihed@chru-nancy.fr
• Study Contact Backup: Name: Nicolas GIRERD, MD PhD; Email: n.girerd@chru-nancy.fr

Study Locations

• France
  • Châlons-en-Champagne, France, 51000
    • Recruiting
    • Ch de Chalons En Champagne
    • Contact: Alice PENINE, MD
    • Principal Investigator: Alice PENINE, MD
  • Nancy, France, 54500
    • Recruiting
    • CHRU Nancy
    • Contact: Tahar CHOUIHED, MD
  • Paris, France
    • Recruiting
    • AP-HP - Hôpital Cochin
    • Contact: Jérôme BOKOBZA, MD
  • Paris, France
    • Recruiting
    • AP-HP - Hôpital Lariboisière
    • Contact: Anthony CHAUVIN, MD
  • Sarreguemines, France, 57200
    • Recruiting
    • CH de Sarreguemines
    • Contact: Emmanuelle SERIS, MD
    • Principal Investigator: Emmanuelle SERIS, MD
  • Strasbourg, France
    • Recruiting
    • CHRU de Strasbourg, Hôpital de Hautepierre
    • Contact: Pierrick Le Borgne, Dr
    • Principal Investigator: Pierrick Le Borgne, Dr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 50 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Men and women ≥ 50 years old
• Patients with non-traumatic acute dyspnea managed in the emergency department
• Patients affiliated with a social security system

Exclusion Criteria:

• Patients in cardiac arrest
• Patients in persistent shock
• Patients with impaired consciousness (Glasgow Score<9)
• Patients with a history of thoracic surgery or pulmonary fibrosis
• Dementia
• Patients with Acute Coronary Syndrome with ST elevation
• Known current pregnancy
• Patients under guardianship, trusteeship or legal protection

Study Plan

How is the study designed?

Design Details

• Primary Purpose: DIAGNOSTIC
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

OTHER: Acute non-traumatic dyspnea patients; Patients with acute non-traumatic dyspnea managed in the emergency department to assess the diagnostic accuracy of an ultrasound algorithm (EMERALD-US) dedicated to emergencies using lung, cardiac and vascular ultrasound for the 3 main dyspnea causes (heart failure, pneumonia and obstructive pulmonary disease exacerbation)

Procedure: Ultrasound algorithm (EMERALD-US); Ultrasound algorithm EMERALD-US is an dedicated to emergencies using lung, cardiac and vascular ultrasound for the 3 main dyspnea causes (heart failure, pneumonia and obstructive pulmonary disease exacerbation) in patients with acute non-traumatic dyspnea managed in the emergency department. The ultrasounds will be performed within first hour after first medical contact in emergency department by another emergency physician not in charge of the patient. The ultrasound results will be not shared with the emergency physician in charge of the patient.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Main discharge diagnosis (heart failure, pneumonia and obstructive pulmonary disease exacerbation)	Main discharge diagnosis (heart failure, pneumonia and obstructive pulmonary disease exacerbation) adjudicated by a college of 3 senior physicians (emergency physician, cardiologist and internist) blinded to the use of ultrasound in the emergency department	an average of 2 weeks (from date of admission in the emergency department until the date of hospitalization discharge)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Duration of the ultrasound examination	Duration of the ultrasound examination is defined by the delay between the first and last contact between the ultrasound probe and the patient	up to 30 minutes
Proportion of complete realization of the ultrasound algorithm	Proportion of complete realization of the ultrasound algorithm through study completion	up to 30 minutes
Diagnosis given by the algorithm after core-lab reading of the blinded ultrasound compared to the diagnosis provided by the emergency physician based on the EMERALD algorithm in the emergency department	Diagnosis given by the algorithm after core-lab reading of the blinded ultrasound compared to the diagnosis provided by the emergency physician based on the EMERALD algorithm in the emergency department	At baseline
Patient management time in the emergency department	Patient management time in the emergency department is defined by the time between the time of entry to the emergency department and the time of discharge specified in the patient's medical report.	An average of 24 hours (Time between the time of entry to the emergency department and the time of discharge).
Brain Natriuretic Peptide (BNP) or N-terminal pro-brain natriuretic peptide concentration	Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional laboratory exams. NT pro BNP will be measured from the biobanking.	At admission in the emergency department
C Reactive protein and procalcitonin concentration,	Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local laboratory exams	At admission in the emergency department
D-dimer concentration,	Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local laboratory exams	At admission in the emergency department
Radiological diagnosis (chest X-ray or chest CT).	Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local radiological exams	At admission in the emergency department
Main discharge diagnosis including combined diagnosis (e.g. heart failure and pneumonia) from initial hospitalization adjudicated by a college of 3 senior physicians	Main discharge diagnosis including combined diagnosis (e.g. heart failure and pneumonia) from initial hospitalization adjudicated by a college of 3 senior physicians	An average of 2 weeks (from date of admission in the emergency department until the date of discharge)
All-cause mortality at D30.	Assess the association between misdiagnosis (without using ultrasound) and survival at D30	At Day 30

Collaborators and Investigators

• Sponsor: CHOUIHED Tahar
• Investigators: Principal Investigator: Tahar CHOUIHED, MD, Central Hospital, CHRU de Nancy, France; Study Chair: Nicolas GIRERD, MD PhD, CHRU de Nancy, France; Study Chair: Patrick ROSSIGNOL, MD PhD, CHRU de Nancy, France

Study record dates

Study Major Dates

• Study Start (ACTUAL): December 14, 2020
• Primary Completion (ANTICIPATED): March 14, 2024
• Study Completion (ANTICIPATED): April 14, 2024

Study Registration Dates

• First Submitted: September 20, 2018
• First Submitted That Met QC Criteria: September 28, 2018
• First Posted (ACTUAL): October 2, 2018

Study Record Updates

• Last Update Posted (ACTUAL): March 7, 2022
• Last Update Submitted That Met QC Criteria: March 4, 2022
• Last Verified: March 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Respiratory Tract Diseases; Respiration Disorders; Disease Attributes; Signs and Symptoms, Respiratory; Emergencies; Dyspnea
• Other Study ID Numbers: 2018-A02136-49

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No