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Guideline for hereditary angioedema (HAE) 2010 by the Japanese Association for Complement Research - secondary

Takahiko Horiuchi1, Hiroyuki Ohi, Isao Ohsawa

  • 1Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan. horiuchi@intmed1.med.kyushu−u.ac.jp

Allergology International : Official Journal of the Japanese Society of Allergology
|October 25, 2012
PubMed

Insights

This guideline helps clinicians accurately diagnose and promptly treat hereditary angioedema (HAE) in Japan. It is a 2010 version, awaiting updates for medical advancements.

Area of Science:

  • Immunology
  • Clinical Medicine

Background:

  • Hereditary angioedema (HAE) is a rare genetic disorder.
  • Accurate diagnosis and timely treatment are crucial for HAE patients.

Purpose of the Study:

  • To provide a clinical guideline for HAE diagnosis and treatment in Japan.
  • To support clinicians in managing HAE patients effectively.

Main Methods:

  • Guideline development by the Japanese Association for Complement Research.
  • Targeting clinicians for practical application.

Main Results:

  • Established diagnostic criteria for HAE.
  • Recommended treatment protocols for HAE management.

Conclusions:

  • The guideline aims to improve HAE patient outcomes in Japan.
  • This 2010 version requires updates based on future medical advancements.

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