Evidence map›Paper›PMID 41715164›Full record

ArticleOrphanet journal of rare diseases2026

Burden of disease in adult patients with hereditary angioedema: results from a multinational survey.

Maureen Watt, Inmaculada Martinez-Saguer, Angela Simon, Ryan Murphy, Marie De La Cruz, Ricardo Zwiener, Mauricio Sarrazola, Anete S Grumach

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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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

8 authors.

Maureen WattTakeda Development Center Americas, Inc., 500 Kendall Street, Lexington, Cambridge, MA, 02142, USA. maureen.watt@takeda.com.ORCID http://orcid.org/0000-0002-7868-2625
Inmaculada Martinez-SaguerHZRM Hemophilia Center Rhine Main, Frankfurt/Main, Germany.
Angela SimonTakeda Development Center Americas, Inc., 500 Kendall Street, Lexington, Cambridge, MA, 02142, USA.
Ryan MurphyICON, Raleigh, NC, USA.
Marie De La CruzICON, Raleigh, NC, USA.
Ricardo ZwienerServicio de Alergia e Inmunología Clínica, Hospital Universitario Austral, Pilar, Buenos Aires, Argentina.
Mauricio SarrazolaDepartamento de Medicina, Grupo GIPPAM, Universidad de Pamplona, Cúcuta, Colombia.
Anete S GrumachClinical Immunology, Faculdade de Medicina, Centro Universitario Faculdade de Medicina ABC (CEUFMABC), Santo Andre, Brazil.

Funding

Takeda Development Center Americas, Inc. NA
6 · The paper itself

Abstract

backgroundHereditary angioedema (HAE) is a rare genetic disease manifesting as recurrent painful, burdensome, and potentially life-threatening swelling attacks. This noninterventional, cross-sectional, web-based survey of adult (aged ≥ 18 years) participants with HAE from Argentina, Brazil, Colombia, Croatia, Denmark, Germany, Hungary, Ireland, Norway, Poland, Portugal, Romania, and Sweden sought to deepen the understanding of HAE burden. Individuals were eligible if they had a self-reported physician diagnosis of HAE, ≥ 1 HAE attack or prodromal symptom within the last year, and received HAE medications within the last 2 years. Data were collected on participant demographics, clinical characteristics, and patient-reported outcomes using validated questionnaires; these included disease control (Angioedema Control Test [AECT]), health-related quality of life (HRQoL; Angioedema Quality of Life [AE-QoL]), general health status (12-Item Short Form Survey [SF-12 v2]), anxiety and depression (Hospital Anxiety and Depression Scale [HADS]), and work productivity impairment (Work Productivity and Activity Impairment: General Health [WPAI:GH]).

resultsOverall, 260 participants were included; age (mean ± SD) was 43.3 ± 13.5 years; 72.7% of participants were female, 89.6% had HAE due to C1 inhibitor deficiency, and 78.5% reported family history of HAE. Participants reported 11.5 ± 14.2 (mean ± SD) HAE attacks in the 6 months before the survey, with 68.5% reporting their most recent attack occurring within the last 4 weeks. Of 260 participants, 153 (58.8%) reported currently using any medication for long-term prophylaxis, but only 56/153 (36.6%) reported using a first-line LTP option per international guidelines. Patient-reported disease burden included, on average, moderate to large HRQoL impairment (AE-QoL total score [mean ± SD] 42.9 ± 23.2), poor disease control (AECT score [mean ± SD] 7.4 ± 3.1), and work productivity impairment (WPAI:GH overall work productivity loss score [mean ± SD] 26.9% ± 32.2). Participants with a lower versus higher number of HAE attacks in the past 6 months reported better disease control, less HRQoL impairment, and less work productivity loss.

conclusionResults of this large multinational survey highlight that patients included in this study, most of whom were not using first-line LTP, reported being burdened by their disease, including frequent HAE attacks, HRQoL impairment, poor disease control, and work productivity impairment.

Indexed as

Angioedemas, HereditaryCost of IllnessGlobal Burden of DiseaseAdultComplement C1 Inhibitor ProteinCross-Sectional StudiesFemaleHealth StatusHumansMaleMiddle AgedQuality of LifeSurveys and QuestionnairesYoung AdultComplement C1 Inhibitor ProteinSERPING1 protein, humanHereditary angioedemaPatient-reported outcomesQuality of lifeSurvey

Identifiers

PMID41715164
PMCPMC12922389

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Registered trials

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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.