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Enhanced FoCUS in Patients With Shortness of Breath

Completed
Conditions
Shortness of Breath
Acute Respiratory Failure
Interventions
Diagnostic Test: Diagnostic test
Registration Number
NCT05403619
Lead Sponsor
Nantes University Hospital
Brief Summary

Retrospective observational study performed in a internal medicine ward of a French university hospital. Included patients were hospitalized for acute shortness of breath who have benefited from a eFOCUS which was defined as a focused cardiac Ultrasound with utilization of Doppler measurements.

The objectives were the therapeutic and diagnosis changes induced by eFoCUS. The primary endpoint was defined by the pooled introduction or discontinuation of diuretics, antibiotics or anticoagulants associated with eFoCUS results.

Detailed Description

It was a retrospective observational study performed in a internal medicine ward of a French University Hospital. Patients were identified in the hospital database, pertinent features and eFoCUS findings were extracted and anonymized.

Inclusion criteria:

* Adult patients admitted to an internal medicine ward from the ED for acute shortness of breath.

* Realization of an eFoCUS prescribed by the physician in charge of the patient

Exclusion criteria:

• Comprehensive echocardiography already performed Methods For each identified patient, pertinent data (demography, initial diagnosis and treatment (diuretics, antibiotics, anticoagulants)) and eFoCUS findings were extracted from the hospital files, anonymized and entered in a LibreOffice spreadsheet. Extracted diagnosis were gathered into the following categories: Community-acquired pneumonia (CAP), Acute cardiogenic pulmonary edema (ACPE), Pulmonary embolism (PE), Chronic Obstructive Pulmonary Disease (COPD) and other (OTHER).

Objectives and endpoints

* The main objective was the therapeutic change induced by eFoCUS. The primary endpoint was defined by the pooled introduction or discontinuation of diuretics, antibiotics or anticoagulants associated with eFoCUS results.

* The secondary objectives were diagnosis modifications induced by eFoCUS. Data analysis

* Numerical data were presented as mean ± SD or as median with interquartile range depending on the normality. The paired Student's t-test was used to compare normally distributed data. The chi-square test was used for the comparison of noncontinuous variables expressed as proportions. A p-value \<0.05 was considered significant. All p-values were two-sided. Statistical analysis was realized with R (4.03.3) in the Rstudio® environment.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
119
Inclusion Criteria
  • Adult patients admitted to a internal medicine ward from the ED for acute shortness of breath.
  • Realization of an eFoCUS prescribed by the physician in charge of the patient
Exclusion Criteria
  • Comprehensive echocardiography already performed

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
PatientsDiagnostic testPatients hospitalized for shortness of breath with realization of an enhanced FoCUS
Primary Outcome Measures
NameTimeMethod
Pooled introduction or discontinuation of diuretics, antibiotics or anticoagulantsup to 24 hours after eFoCUS

Number of patients for whom there was an introduction or discontinuation of diuretics, antibiotics or anticoagulants associated with Focused cardiac ultrasound

Secondary Outcome Measures
NameTimeMethod
Changes of diagnostic categories associated with eFOCUSup to 24 hours after eFoCUS

Number of patients for whom the diagnostic category (pneumonia, acute cardiac failure, pulmonary embolism, COPD, other) was modified after Focused cardiac ultrasound

Trial Locations

Locations (1)

Nantes University Hospital

🇫🇷

Nantes, France

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