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Lung Ultrasound for Acute Dyspnea in Emergency Department

Lung Ultrasound for Acute Dyspnea in Emergency Department - Prospective Multicenter Study on Accuracy, Reproducibility, and Diagnostic Impact of Lung Ultrasound in the Evaluation of Patients With Dyspnea in the Emergency Department

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01287429
Enrollment
1005
Registered
2011-02-01
Start date
2010-10-31
Completion date
2012-10-31
Last updated
2012-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congestive Heart Failure, Dyspnea

Keywords

Ultrasonography

Brief summary

Dyspnea is a frequent symptom in patients admitted to the Emergency Department (ED); discriminating between cardiogenic and non-cardiogenic dyspnea is a common clinical dilemma. The initial diagnostic work-out is often not very accurate in defining the etiology and the underlying pathophysiology. In the last years, lung ultrasound (US) has emerged as a useful real-time bedside diagnostic tool in the critical patient. The aim of this study was to evaluate the accuracy, reproducibility, and diagnostic impact of pleural and lung US, performed by emergency physicians at the time of patient first presentation to the ED, in identifying cardiac causes of acute dyspnea.

Interventions

OTHERlung and pleural ultrasound

After the initial diagnostic work-out (medical history, physical examination, EKG, arterious blood gas), the emergency physician will classify dyspnoea in cardiogenic or respiratory dyspnoea and write it down in a specific form (clinical form). Immediately after this, lung and pleural ultrasound will be performed: the physician will describe it and evaluate the etiology again (integrated evaluation form). Then a chest X-ray evaluation will be performed for each patient.

Sponsors

Azienda Ospedaliera San Giovanni Battista
CollaboratorOTHER
San Luigi Gonzaga Hospital
CollaboratorOTHER
Agnelli Hospital, Italy
CollaboratorOTHER
Azienda Ospedaliera Ordine Mauriziano di Torino
CollaboratorOTHER
Martini Hospital, Turin, Italy
CollaboratorOTHER
Ospedale Cardinal Massaia
CollaboratorOTHER
Ospedale Santa Croce-Carle Cuneo
CollaboratorOTHER
University of Turin, Italy
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients had to present to the ED with a principal complaint of shortness of breath, defined as either the sudden onset of dyspnea with no history of chronic dyspnea or an increase in the severity of chronic dyspnea in the last 48 hours; * Presence of an emergency physician with lung US experience at the time of enrollment; * US examination within 30 minutes after the start of the clinical evaluation.

Exclusion criteria

* Dyspnea cases clearly due to neither cardiogenic nor respiratory etiology will considered not eligible.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026