Allergologie select, Volume 10 (2026) - 1st issue (1 - 10)

Achieving a normal life in hereditary angioedema: Quality of life and treatment gaps among German HAE patients
Markus Magerl1,2, Thomas Buttgereit1,2, Inmaculada Martinez-Saguer3, Petra Staubach-Renz4, Jens Greve5, Emel Aygören-Pürsün6, Lucia Schauf7, Kathrin Schön1,2,7
1 Institute of Allergology, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 2 Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin, 3 HZRM Haemophilia Center Rhein Main, Frankfurt am Main, 4 University Medical Center, Mainz, 5 Department of Otorhinolaryngology, Head and Neck Surgery, Ulm University Medical Center, Ulm, 6 University Hospital Frankfurt, Department for Children and Adolescents, Frankfurt, and 7 HAE Vereinigung e.V., Germany

   

 

DOI 10.5414/ALX02603E

Abstract

Background: Hereditary angioedema (HAE) is a rare genetic disease characterized by recurrent swelling attacks. Current guidelines for HAE management emphasize achieving complete disease control to normalize patients’ lives. Quality of life (QoL) differences between patients with 0 attacks and those with persistent attacks remain to be explored. Materials and methods: The German patient organization for individuals affected by hereditary angioedema, HAE Vereinigung e.V. conducted an online survey with 122 HAE patients in Germany in 2024. Participants were categorized according to their therapy – long-term prophylaxis (LTP) or on-demand therapy (ODT) – and according to their attack frequency over the last 6 months. Patient-reported outcomes for functional, emotional, and social impacts were analyzed to evaluate QoL. Results: Although 83% of patients expressed satisfaction with their treatment, 59% of patients still had attacks. Patients on LTP reported significantly fewer attacks (p < 0.001) and higher QoL compared to those on ODT (p < 0.001). Patients with 0 attacks consistently showed significantly better outcomes across all QoL domains than those with 1 or more attacks (p < 0.001). Conclusion: The findings highlight that even minimal residual disease activity can meaningfully reduce QoL. Achieving complete attack freedom, rather than partial control, is necessary to restore normalcy for patients with HAE. Hence, regular adjustments of the HAE management plans based on patient-reported outcomes are crucial to ensure that treatment strategies address both medical and QoL needs.

Author Details

Authors

Departments

  • 1 Institute of Allergology, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin,
  • 2 Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin,
  • 3 HZRM Haemophilia Center Rhein Main, Frankfurt am Main,
  • 4 University Medical Center, Mainz,
  • 5 Department of Otorhinolaryngology, Head and Neck Surgery, Ulm University Medical Center, Ulm,
  • 6 University Hospital Frankfurt, Department for Children and Adolescents, Frankfurt, and
  • 7 HAE Vereinigung e.V., Germany

Address

Thomas Buttgereit, MD, Charité – Universitätsmedizin Berlin, Institute of Allergology, Hindenburgdamm 30, 12203 Berlin, Germany
Email: [email protected]

Citation

Markus Magerl, Thomas Buttgereit, Inmaculada Martinez-Saguer, Petra Staubach-Renz, Jens Greve, Emel Aygören-Pürsün, Lucia Schauf, and Kathrin Schön.Achieving a normal life in hereditary angioedema: Quality of life and treatment gaps among German HAE patients. Allergologie select. 2026; 10: 1-10. doi: 10.5414/ALX02603E.

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