Analysis of the Availability of the Treatments for ACE-I and ARB-induced Angioedema

Civil Hospices of Lyon

Status: Completed

Conditions: ACE-I and ARB-induced Angioedema.

Study type: Observational

Funder types: Other

Identifiers

NCT02826356

69HCL16_0430

Details and patient eligibility

About

Specific treatments for angiotensin-converting-enzyme inhibitor (ACE-I) and angiotensin-receptor-blocker (ARB)-induced angioedema exist. Early access to these treatments is challenging because they are expensive and have short shelf lives making it illusory that all emergency department (ED) stock them. The aim of this retrospective study was to define, for each patient with a confirmed ACE-I or ARB-induced angioedema, at which step of the care, the specific treatment was administered. The second objective was to analyse the availability of these treatment in the area around Lyon, France and the factors that may influence it.

Enrollment: 38 patients

Sex

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Every patient followed for the first time in our reference center for severe confirmed ACE-I or ARB-induced angioedema. Data were analyzed from patients attended either in a specialized angioedema consultation or during a hospitalization in our intensive care unit.
• Severe attack was defined either by its localization over the shoulder or by an severe abdominal attack.

Exclusion criteria

• Patients which received no specific treatment (icatibant, C1-inhibitor concentrate) were excluded.