Evidence map›Paper›PMID 40949786›Full record

ArticleThe World Allergy Organization journal2025

Real-world treatment patterns and burden-of-disease of sub-optimally controlled hereditary angioedema.

Henriette Farkas, Emel Aygören-Pürsün, Didier G Ebo, Noemi Bara, Fotis Psarros, Francois Gavini, Nawal Bent-Ennakhil, Laura Sayegh, Irmgard Andresen

Registry-linked trialAbstract read
In one paragraph

Article in The World Allergy Organization journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04957641 (A Retrospective Observational Chart Review Study Evaluating the Burden of Illness and Treatment Patterns in Hereditary Angioedema Type I and II), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04957641 completednot on this map

A Retrospective Observational Chart Review Study Evaluating the Burden of Illness and Treatment Patterns in Hereditary Angioedema Type I and II

TypeobservationalSponsorTakedaRan2022 to 2023Enrolled221ConditionsHereditary Angioedema
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Henriette FarkasSemmelweis University, Budapest, Hungary.
Emel Aygören-PürsünUniversity Hospital Frankfurt, Pediatric Clinic, Goethe University, Frankfurt, Germany.
Didier G EboDept Immunology Allergology Rheumatology Antwerp University Hospital and Antwerp University, Belgium.
Noemi BaraMediQuest Clinical Research Center, Sangiorgiu de Mures, Romania.
Fotis PsarrosNavy Hospital of Athens, Athens, Greece.
Francois GaviniEUCAN Medical Affairs, Takeda Pharmaceuticals International AG, Zürich, Switzerland.
Nawal Bent-EnnakhilEUCAN Medical Affairs, Takeda Pharmaceuticals International AG, Zürich, Switzerland.
Laura SayeghReal-World Evidence, PPD, Part of Thermo Fisher Scientific, Montreal, Quebec, Canada.
Irmgard AndresenEUCAN Medical Affairs, Takeda Pharmaceuticals International AG, Zürich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hereditary angioedema (HAE) is a rare disease characterized by unpredictable, recurrent subcutaneous or submucosal swelling that negatively impacts patients' health-related quality of life (HRQoL). Despite treatment goals aimed at achieving complete control of the disease and normalizing patients' lives, the disease remains poorly controlled for some patients. Objectives: To describe the demographic, clinical and treatment characteristics, as well as the HRQoL impairment of patients with sub-optimally controlled HAE type I/II per treating physician's judgment, focusing on understanding the factors influencing the burden of illness. Methods: A chart review was conducted at 32 HAE care centers across 18 European countries, Canada, and Israel between April 2022 and January 2023 in 214 patients aged ≥12 years with HAE type I/II sub-optimally controlled with on-demand treatment (ODT) and/or long-term prophylaxis (LTP). Patients receiving lanadelumab were excluded, as it was not yet widely available during the eligibility period. A cross-sectional survey at patient enrollment included the Angioedema Quality of Life (AE-QoL) and EQ-5D-5L questionnaires to assess the impact of HAE on HRQoL. Results: Patients with uncontrolled HAE had a mean (standard deviation [SD]) of 9.9 (13) attacks per year, with a mean (SD) duration of 1.9 (1) days per attack. During the one-year observation period, 50.5% of patients were on ODT only, 36.0% used LTP and ODT concurrently, 6.5% used LTP without ODT, and 7.0% were untreated. Attenuated androgens (AA; stanozolol and danazol) in LTP were used by 24.7% of patients, while tranexamic acid (TA) and C1-esterase inhibitor (C1-INH) replacement products were used for LTP by 9.8% and 6.5%, respectively. The mean (SD) AE-QoL total score was 44.4 (24.0), indicating a moderate level of impairment, with women experiencing worse HRQoL (total score of 50.9 [SD 24] vs 37.3 [SD 23] in men) [where the minimal clinically important difference is 6 points] [1]. HRQoL worsened with increasing attack rates, from 41.4 (SD 24.0) among patients with one to 5 attacks/year, still indicating moderate impairment in HRQoL, to 73.0 (SD 27.0) for patients with >40 attacks/year. Conclusions: Suboptimal disease control in HAE was associated with the use of ODT only, as well as LTP mainly with AA/TA. It imposes a substantial burden on patients' HRQoL, more particularly, but not exclusively, for those with frequent attacks and for women. The results suggest a need for improved HAE management.ClinicalTrial.gov study identifier NCT04957641.

Indexed as

Burden of illnessDisease managementHereditary angioedema

Identifiers

PMID40949786
PMCPMC12423343

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.