Hereditary angioedema attacks resolve faster and are shorter after early icatibant treatment

PLoS One. 2013;8(2):e53773. doi: 10.1371/journal.pone.0053773. Epub 2013 Feb 4.

Abstract

Background: Attacks of hereditary angioedema (HAE) are unpredictable and, if affecting the upper airway, can be lethal. Icatibant is used for physician- or patient self-administered symptomatic treatment of HAE attacks in adults. Its mode of action includes disruption of the bradykinin pathway via blockade of the bradykinin B(2) receptor. Early treatment is believed to shorten attack duration and prevent severe outcomes; however, evidence to support these benefits is lacking.

Objective: To examine the impact of timing of icatibant administration on the duration and resolution of HAE type I and II attacks.

Methods: The Icatibant Outcome Survey is an international, prospective, observational study for patients treated with icatibant. Data on timings and outcomes of icatibant treatment for HAE attacks were collected between July 2009-February 2012. A mixed-model of repeated measures was performed for 426 attacks in 136 HAE type I and II patients.

Results: Attack duration was significantly shorter in patients treated <1 hour of attack onset compared with those treated ≥ 1 hour (6.1 hours versus 16.8 hours [p<0.001]). Similar significant effects were observed for <2 hours versus ≥ 2 hours (7.2 hours versus 20.2 hours [p<0.001]) and <5 hours versus ≥ 5 hours (8.0 hours versus 23.5 hours [p<0.001]). Treatment within 1 hour of attack onset also significantly reduced time to attack resolution (5.8 hours versus 8.8 hours [p<0.05]). Self-administrators were more likely to treat early and experience shorter attacks than those treated by a healthcare professional.

Conclusion: Early blockade of the bradykinin B(2) receptor with icatibant, particularly within the first hour of attack onset, significantly reduced attack duration and time to attack resolution.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Adrenergic beta-Antagonists / therapeutic use*
  • Adult
  • Bradykinin / analogs & derivatives*
  • Bradykinin / pharmacology
  • Bradykinin / therapeutic use
  • Bradykinin B2 Receptor Antagonists
  • Drug Administration Schedule
  • Female
  • Hereditary Angioedema Types I and II / drug therapy*
  • Hereditary Angioedema Types I and II / metabolism
  • Hereditary Angioedema Types I and II / physiopathology
  • Humans
  • Male
  • Prospective Studies
  • Self Administration
  • Time Factors
  • Treatment Outcome

Substances

  • Adrenergic beta-Antagonists
  • Bradykinin B2 Receptor Antagonists
  • icatibant
  • Bradykinin

Grants and funding

The Icatibant Outcome Survey is funded and supported by Shire Human Genetic Therapies (HGT), Eysins, Switzerland. The funders, HGT, were involved in the study design and analysis and provided funding support for medical writing services to aid the preparation of this manuscript. The listed authors were responsible for the decision to publish and have been fully involved with the preparation of this manuscript. The following listed authors comprise the Icatibant Outcome Survey (IOS) Executive Committee: Marcus Maurer (Chair), Werner Aberer, Laurence Bouillet, Teresa Caballero, Gisèle Kanny, Hilary Longhurst and Andrea Zanichelli. These authors were responsible for data collection and analysis.