Universal Access to On-Demand Treatment of Patients with Hereditary Angioedema, the Chilean Experience

Pediatr Allergy Immunol Pulmonol. 2023 Dec;36(4):130-132. doi: 10.1089/ped.2023.0083. Epub 2023 Nov 2.

Abstract

Background: In Chile, patients with hereditary angioedema (HAE) type I and type II are protected under Ley Ricarte Soto (LRS), which guarantees access to on demand plasma-derived C1-INH (pdC1-INH) since 2018. We aimed to analyze the first 3 years of LRS. Methods: Review of the LRS database between 2018 and 2021. Results: During the study period, 154 patients were covered by LRS, with an estimated prevalence of HAE in Chile at 0.8:100,000 inhabitants. A delay in diagnosis of 22 years was noted, 50 patients received epinephrine during an attack before the diagnosis of HAE. Mean number of attacks per year was 8, with 50% of adults and 42% of children experiencing more than 1 attack per month. Conclusion: Disease awareness must improve to reduce the diagnostic delay of HAE. Long-term prophylactic medications should be included in LRS to treat patients with high attack rates and control the costs of frequent on-demand treatment with pdC1-INH.

Keywords: angioedema; epidemiology; plasma derived C1 inhibitor.

MeSH terms

  • Adult
  • Angioedemas, Hereditary* / diagnosis
  • Angioedemas, Hereditary* / drug therapy
  • Angioedemas, Hereditary* / epidemiology
  • Child
  • Chile / epidemiology
  • Delayed Diagnosis
  • Humans
  • Plasma
  • Treatment Outcome