This is a prospective, observational study conducted in the emergency department. Adult patients presenting with dyspnea will be enrolled, and study data will be collected from routine clinical assessments, including medical history, physical examination, laboratory tests, and echocardiography results, as well as non-invasive cardiovascular measurements obtained using the CardioStory device.
Age ≥ 18 years
Recent onset dyspnea (less than 7 days)
Informed consent obtained
Age inferior to 18 years,
Severe comorbidity, hemodynamic compromise or immediate need for mechanical ventilation were exclusion criteria.
Dyspnea clearly of traumatic or allergic origin
CardioStory INC
Lead sponsor
Eshmoun Clinical Research Center
Collaborator
Sahloul Hospital of Sousse
Collaborator
University Hospital Monastir, Tunis
Collaborator