Longitudinal Observational Study for mIddle Term Follow-up Patients Admitted for Acute Dyspnea in TunIsia (SIDI)

S Form Pharma

Status: Unknown

Conditions: Longitudinal Observational Study With 6 Months Follow-up

Study type: Observational

Funder types: Industry

Identifiers

NCT04947358

AD201801

Details and patient eligibility

About

The purpose of the SIDI study is to follow, few months after discharge from the hospital, the patients admitted to the 3 emergency departments in Tunisia for acute dyspnea and to determine the proportion and the factors favoring rehospitalization and death.

Enrollment: 180 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients admitted for unexpected respiratory difficulty
• Patient admitted to the emergency department
• One of the following 3 criteria have to be present at admission to the ER:
• O2 < or = 95%
• Respiratory rate RR > or = 20
• Suffocation sensation

Exclusion criteria

• Patients <18 years old and> 85 years' old
• Pregnancy
• History of allergic asthma at early age
• Diagnosis retained of pulmonary embolism
• Patients with heart failure (HF) with left ventricular ejection fraction LVEF <40% are known beforehand or discovered at admission to ER
• known Allergy for Polyamide; Polyester; Elastane; Silicone; Silver; Synthetic material Cardiorespiratory disorders which may be aggravated by the slight compression of the thorax Open wound on the skin, at the level of the trunk