Evidence map›Paper›PMID 41857746›Full record

ArticleOrphanet journal of rare diseases2026

Health-related quality of life in adults with epidermolysis bullosa: a cross-sectional study in seven European countries using EQ-5D-5L.

Renata Linertová, Márta Péntek, Benjamín Rodríguez-Díaz, Christine Bodemer, Vinzenz Hübl, May El Hachem, Gudrun Salamon, Verónica Alonso-Ferreira, Georgi Stefanov, Ritu Jain and 3 more

Abstract read
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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. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Renata LinertováFundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC), Santa Cruz de Tenerife, Spain. renata.linertova@sescs.es.ORCID http://orcid.org/0000-0002-0138-9252
Márta PéntekHealth Economics Research Center (HECON), University Research and Innovation Center, Obuda University, Budapest, Hungary.
Benjamín Rodríguez-DíazFundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC), Santa Cruz de Tenerife, Spain.
Christine BodemerPediatric Dermatology Department and National Expert Centre for Genodermatoses (MAGEC-Necker), Necker Enfants Malades Hospital, APHP, University Paris Cité, Paris, France.
Vinzenz HüblDepartment of Dermatology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
May El HachemDermatology Unit and Genodermatosis Research Unit, Translational Paediatrics and Clinical Genetics Research Area, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Gudrun SalamonHEALTH Lab | Competence Center for Medical and Health Psychology, Sigmund Freud University, Vienna, Austria.
Verónica Alonso-FerreiraInstitute of Rare Diseases Research (IIER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Georgi StefanovBulgarian Association of Promotion of Education and Science (BAPES), Institute for Rare Diseases, Plovdiv, Bulgaria.
Ritu JainDEBRA International, Vienna, Austria.
Yolanda Ramallo-FariñaFundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC), Santa Cruz de Tenerife, Spain.
Lidia García-PérezFundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC), Santa Cruz de Tenerife, Spain.
BUR-EB Study Group

Funding

DEBRA Austria DEBRA AustriaEuropean Joint Programme for Rare Diseases EJP RD COFUND-EJP Nº 825575Instituto de Salud Carlos III AC21_2/00011National Research, Development and Innovation Fund of Hungary 2019-2.1.7-ERA-NET
6 · The paper itself

Abstract

backgroundEpidermolysis bullosa (EB) is a rare genetic disorder that causes extreme skin fragility, chronic pain, and functional impairment, with major psychosocial and economic consequences. Health-related quality of life (HRQoL) data is critical to capture the full burden of EB. Health utilities derived from preference-based generic instruments such as the EQ-5D-5L provide standardized health status utility values that enable cross-disease comparisons and provide input data for cost-utility analyses to inform resource allocation. There is a notable lack of multinational, up-to-date utility data for EB. This cross-sectional study aimed to assess HRQoL in adults with EB across seven European countries (Austria, Bulgaria, Germany, Hungary, Italy, France, and Spain) using the EQ-5D-5L.

resultsA total of 328 adults with EB participated in the survey, 61% were female, 37% were between 18 and 30 years old and 46% had dystrophic EB. Based on self-reported symptoms, 58% were classified as severe EB. Pain/discomfort was the most affected EQ-5D-5L dimension (92% reporting problems; 27% severe or extreme). The mean EQ-5D value (health utility) was 0.63 (SD 0.32), ranging from 0.57 in Spain to 0.71 in Bulgaria. Patients with severe EB reported significantly lower utilities than non-severe cases (0.52 vs. 0.78, p < 0.001). Mean EQ VAS score was 60 (SD 23.2). Compared to general population norms, EB patients in all countries had markedly lower HRQoL (p < 0.005), with large effect sizes for the EQ-5D value (Cohen's d ≥ 0.8). Symptomatic burden and functional deterioration were the primary drivers of HRQoL impairments.

conclusionsThis multinational study provides the most extensive and current health utility data for adults with EB in Europe. Findings reveal the profound HRQoL impairment in EB, particularly in severe cases. These standardized utility values fill a major evidence gap, supporting their use in health economic evaluations, cross-disease comparisons, and policy development.

Indexed as

Epidermolysis BullosaQuality of LifeAdolescentAdultCross-Sectional StudiesEuropeFemaleHumansMaleMiddle AgedSurveys and QuestionnairesYoung AdultEpidermolysis bullosaEQ-5D-5LHealth-related quality of lifeHealth utilitiesPatient reported outcomes

Identifiers

PMID41857746
PMCPMC13122926

What OpenQuestion holds

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LicenceCC BY
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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.