Feasibility and Accuracy of an Ultrasound Algorithm for Acute Dyspnea Diagnosis in the Emergency Department (EMERALD-US)
Primary Purpose
Dyspnea
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Ultrasound algorithm (EMERALD-US)
Sponsored by
About this trial
This is an interventional diagnostic trial for Dyspnea
Eligibility Criteria
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
Sites / Locations
- CH de Chalons en ChampagneRecruiting
- CHRU NancyRecruiting
- AP-HP - Hôpital CochinRecruiting
- AP-HP - Hôpital LariboisièreRecruiting
- CH de SarregueminesRecruiting
- CHRU de Strasbourg, Hôpital de HautepierreRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Acute non-traumatic dyspnea patients
Arm Description
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)
Outcomes
Primary Outcome Measures
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
Secondary Outcome Measures
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
Proportion of complete realization of the ultrasound algorithm
Proportion of complete realization of the ultrasound algorithm through study completion
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
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.
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.
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
D-dimer concentration,
Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local laboratory exams
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
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
All-cause mortality at D30.
Assess the association between misdiagnosis (without using ultrasound) and survival at D30
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03691857
Brief Title
Feasibility and Accuracy of an Ultrasound Algorithm for Acute Dyspnea Diagnosis in the Emergency Department
Acronym
EMERALD-US
Official Title
Evaluation of the Feasibility and Accuracy of an Ultrasound Algorithm for Acute Dyspnea Diagnosis in the Emergency Department
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 14, 2020 (Actual)
Primary Completion Date
March 14, 2024 (Anticipated)
Study Completion Date
April 14, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
CHOUIHED Tahar
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyspnea
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
225 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Acute non-traumatic dyspnea patients
Arm Type
Other
Arm Description
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)
Intervention Type
Procedure
Intervention Name(s)
Ultrasound algorithm (EMERALD-US)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Main discharge diagnosis (heart failure, pneumonia and obstructive pulmonary disease exacerbation)
Description
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
Time Frame
an average of 2 weeks (from date of admission in the emergency department until the date of hospitalization discharge)
Secondary Outcome Measure Information:
Title
Duration of the ultrasound examination
Description
Duration of the ultrasound examination is defined by the delay between the first and last contact between the ultrasound probe and the patient
Time Frame
up to 30 minutes
Title
Proportion of complete realization of the ultrasound algorithm
Description
Proportion of complete realization of the ultrasound algorithm through study completion
Time Frame
up to 30 minutes
Title
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
Description
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
Time Frame
At baseline
Title
Patient management time in the emergency department
Description
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.
Time Frame
An average of 24 hours (Time between the time of entry to the emergency department and the time of discharge).
Title
Brain Natriuretic Peptide (BNP) or N-terminal pro-brain natriuretic peptide concentration
Description
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.
Time Frame
At admission in the emergency department
Title
C Reactive protein and procalcitonin concentration,
Description
Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local laboratory exams
Time Frame
At admission in the emergency department
Title
D-dimer concentration,
Description
Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local laboratory exams
Time Frame
At admission in the emergency department
Title
Radiological diagnosis (chest X-ray or chest CT).
Description
Assess the association between the diagnosis obtained from the ultrasound algorithm (EMERALD-US) and the results of additional local radiological exams
Time Frame
At admission in the emergency department
Title
Main discharge diagnosis including combined diagnosis (e.g. heart failure and pneumonia) from initial hospitalization adjudicated by a college of 3 senior physicians
Description
Main discharge diagnosis including combined diagnosis (e.g. heart failure and pneumonia) from initial hospitalization adjudicated by a college of 3 senior physicians
Time Frame
An average of 2 weeks (from date of admission in the emergency department until the date of discharge)
Title
All-cause mortality at D30.
Description
Assess the association between misdiagnosis (without using ultrasound) and survival at D30
Time Frame
At Day 30
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tahar CHOUIHED, MD
Phone
(0)3 83 85 14 96
Ext
+33
Email
t.chouihed@chru-nancy.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Nicolas GIRERD, MD PhD
Email
n.girerd@chru-nancy.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tahar CHOUIHED, MD
Organizational Affiliation
Central Hospital, CHRU de Nancy, France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nicolas GIRERD, MD PhD
Organizational Affiliation
CHRU de Nancy, France
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Patrick ROSSIGNOL, MD PhD
Organizational Affiliation
CHRU de Nancy, France
Official's Role
Study Chair
Facility Information:
Facility Name
CH de Chalons en Champagne
City
Châlons-en-Champagne
ZIP/Postal Code
51000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alice PENINE, MD
First Name & Middle Initial & Last Name & Degree
Alice PENINE, MD
Facility Name
CHRU Nancy
City
Nancy
ZIP/Postal Code
54500
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tahar CHOUIHED, MD
First Name & Middle Initial & Last Name & Degree
Tahar CHOUIHED, MD
Facility Name
AP-HP - Hôpital Cochin
City
Paris
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jérôme BOKOBZA, MD
First Name & Middle Initial & Last Name & Degree
Jérôme BOKOBZA, MD
Facility Name
AP-HP - Hôpital Lariboisière
City
Paris
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anthony CHAUVIN, MD
First Name & Middle Initial & Last Name & Degree
Anthony CHAUVIN, MD
Facility Name
CH de Sarreguemines
City
Sarreguemines
ZIP/Postal Code
57200
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emmanuelle SERIS, MD
First Name & Middle Initial & Last Name & Degree
Emmanuelle SERIS, MD
Facility Name
CHRU de Strasbourg, Hôpital de Hautepierre
City
Strasbourg
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierrick Le Borgne, Dr
First Name & Middle Initial & Last Name & Degree
Pierrick Le Borgne, Dr
12. IPD Sharing Statement
Learn more about this trial
Feasibility and Accuracy of an Ultrasound Algorithm for Acute Dyspnea Diagnosis in the Emergency Department
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