TY - JOUR
T1 - International Guideline on the Diagnosis and Management of Pediatric Patients With Hereditary Angioedema
AU - the Hereditary Angioedema Working Group (HAWK Group)
AU - Farkas, Henriette
AU - Martinez-Saguer, Inmaculada
AU - Bork, Konrad
AU - Germenis, Anastasios E.
AU - Grumach, Anete S.
AU - Horváth, Hanga Réka
AU - Luczay, Andrea
AU - Zanichelli, Andrea
AU - Magerl, Markus
AU - Betschel, Stephen
AU - Aygören-Pürsün, Emel
AU - Bernstein, Jonathan A.
AU - Boccon-Gibod, Isabelle
AU - Caballero, Teresa
AU - Cancian, Mauro
AU - Christiansen, Sandra
AU - Cohn, Danny M.
AU - Contreras, Francisco
AU - Craig, Sansanee
AU - Isaic, Camelia
AU - Jindal, Ankur
AU - Katelaris, Constance H.
AU - Longhurst, Hilary J.
AU - MacGinnitie, Andrew
AU - Peter, Jonny
AU - Porebski, Grzegorz
AU - Reshef, Avner
AU - Van Nguyen, Dinh
AU - Zuraw, Bruce
AU - Castaldo, Anthony J.
AU - Boysen, Henrik Balle
AU - Craig, Timothy
AU - Adatia, Adil
AU - Adrianzen, Fiorella
AU - Andarawewa, Shimalee
AU - Andrejevic, Sladjana
AU - Arce-Estrada, Gabriel Emmanuel
AU - Ay, Ecem
AU - Bahadir, Adil
AU - Bara, Noemi Anna
AU - Barešić, Marko
AU - Baynova, Krasimira
AU - Benor, Shira
AU - Besson, Juliette
AU - Bhattarai, Dharmagat
AU - Bigas, Patricia
AU - Bocquet, Alexis
AU - Bouillet, Laurence
AU - Brodszki, Nicholas
AU - Buttgereit, Thomas
N1 - Publisher Copyright:
© 2026 The Author(s). Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.
PY - 2026
Y1 - 2026
N2 - Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families. Clinical symptoms of HAE are not specific, which may cause difficulties in differential diagnosis. Additionally, if not appropriately treated, HAE attacks can be life-threatening. The international HAE guidelines published so far have focused mainly on adults. A guideline that refers to the age-specific characteristics of pediatric patients, both in terms of diagnosis and management, was therefore needed. The International Steering Committee and Taskforce developed recommendations and provided evidence-based grading based on expert opinion and strength of evidence. Recommendations were presented to, discussed, and electronically voted by healthcare professionals during the 14th C1 Inhibitor Deficiency and Angioedema Workshop in Budapest, Hungary, 2025. This international guideline will ensure early diagnosis, standardized and up-to-date treatment, and promote the availability of effective therapies for all pediatric patients affected with this rare disease. It also draws attention to the importance of establishing HAE centers and registries, which solicit specialist care and research of the disease.
AB - Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families. Clinical symptoms of HAE are not specific, which may cause difficulties in differential diagnosis. Additionally, if not appropriately treated, HAE attacks can be life-threatening. The international HAE guidelines published so far have focused mainly on adults. A guideline that refers to the age-specific characteristics of pediatric patients, both in terms of diagnosis and management, was therefore needed. The International Steering Committee and Taskforce developed recommendations and provided evidence-based grading based on expert opinion and strength of evidence. Recommendations were presented to, discussed, and electronically voted by healthcare professionals during the 14th C1 Inhibitor Deficiency and Angioedema Workshop in Budapest, Hungary, 2025. This international guideline will ensure early diagnosis, standardized and up-to-date treatment, and promote the availability of effective therapies for all pediatric patients affected with this rare disease. It also draws attention to the importance of establishing HAE centers and registries, which solicit specialist care and research of the disease.
UR - https://www.scopus.com/pages/publications/105030291603
UR - https://www.scopus.com/pages/publications/105030291603#tab=citedBy
U2 - 10.1111/all.70207
DO - 10.1111/all.70207
M3 - Review article
C2 - 41618059
AN - SCOPUS:105030291603
SN - 0105-4538
JO - Allergy: European Journal of Allergy and Clinical Immunology
JF - Allergy: European Journal of Allergy and Clinical Immunology
ER -