Evidence map›Paper›PMID 41808205›Full record

ArticleOrphanet journal of rare diseases2026

Identifying quality of life domains and facets affected in relapsing polychondritis: a qualitative analysis for the development of a disease-specific health-related quality of life instrument.

Philippe Mertz, Oliver Sander, Raquel Faria, Francesca Crisafulli, Sofia Silva-Ribeiro, Lou Kawka, Cedric Sztejkowski, Christina Düsing, Thomas Rose, Antonio Lamas and 12 more

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

22 authors.

Philippe MertzSorbonne université, Hôpital Tenon, DMU3ID APHP, ERN RITA, Paris, France.
Oliver SanderDepartment for Rheumatology and Hiller Research Centre for Rheumatology, University Hospital, Düsseldorf, Germany.
Raquel FariaUnidade de Imunologia Clínica, Hospital de Santo António, Unidade Local de Saúde Santo António, Porto, Portugal.
Francesca CrisafulliRheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
Sofia Silva-RibeiroInstituto Universitário de Lisboa, Lisboa, Portugal.
Lou KawkaDepartment of Rheumatology, National Reference Center for Rare Autoimmune Diseases (RESO), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Cedric SztejkowskiDepartment of Rheumatology, National Reference Center for Rare Autoimmune Diseases (RESO), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Christina DüsingDepartment for Rheumatology and Hiller Research Centre for Rheumatology, University Hospital, Düsseldorf, Germany.
Thomas RoseKlinik für Rheumatologie und Klinische Immunologie, Charité Universitätsmedizin Berlin, Charité Platz 1, 10117, Berlin, Germany.
Antonio LamasUnidade de Imunologia Clínica, Hospital de Santo António, Unidade Local de Saúde Santo António, Porto, Portugal.
Carlos VasconcelosUnidade de Imunologia Clínica, Hospital de Santo António, Unidade Local de Saúde Santo António, Porto, Portugal.
Giulia FontanaRheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
Paolo SemeraroRheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
Teodora NeaguDepartment of Rheumatology, Emergency County Teaching Hospital, University of Medicine and Pharmacy Iuliu Hatieganu, Cluj-Napoca, Romania.
Mihaela ResteuDepartment of Rheumatology, Emergency County Teaching Hospital, University of Medicine and Pharmacy Iuliu Hatieganu, Cluj-Napoca, Romania.
Laura DamianDepartment of Rheumatology, Emergency County Teaching Hospital, University of Medicine and Pharmacy Iuliu Hatieganu, Cluj-Napoca, Romania.
Cristina PamfilDepartment of Rheumatology, Emergency County Teaching Hospital, University of Medicine and Pharmacy Iuliu Hatieganu, Cluj-Napoca, Romania.
Camelia BucsaASPOR Association of Romanian Relapsing Polychondritis Patients & Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Lisa J MatthewsRelapsing Polychondritis Awareness & Support, (relapsingpolychondritis.org), Worcester, UK.
Hervé DevilliersInternal Medicine and Systemic Diseases Unit, University Hospital Centre Dijon, Dijon, France.
Simona RednicDepartment of Rheumatology, Emergency County Teaching Hospital, University of Medicine and Pharmacy Iuliu Hatieganu, Cluj-Napoca, Romania.
Laurent ArnaudDepartment of Rheumatology, National Reference Center for Rare Autoimmune Diseases (RESO), Hôpitaux Universitaires de Strasbourg, Strasbourg, France. Laurent.arnaud@chru-strasbourg.fr.ORCID http://orcid.org/0000-0002-8077-8394

Funding

European Commission 101157143
6 · The paper itself

Abstract

introductionRelapsing polychondritis (RP) is a rare inflammatory disease characterized by recurrent inflammation of cartilaginous structures and a broad spectrum of systemic features. To date, no Health-related Quality of life (QoL) data are available in RP, and generic measures may not fully capture the unique burden faced by patients, given the specific nature of RP symptoms. This study aimed to identify QoL facets relevant for further inclusion in a disease-specific QoL instrument, the RP-QoL.

methodsAn international study was conducted within the framework of the European Reference Network ReCONNET, using an online interview script designed by nine physicians, a clinical psychologist, and two patient representatives. The survey was cross-culturally adapted into five languages. Thematic analysis was performed by native speakers of each language and further aggregated to characterize QoL in RP.

resultsA total of 274 patients (median age: 54yo, 86% women) from 22 countries completed the interview. The most affected QoL facets were ‘personal relationships’ (58.8%), ‘work capacity’ (51.8%), and ‘daily activities’ (47.8%). Additional concerns included mainly fatigue, pain, cognition, mental health and social life. A total of 67 patients (24.5%) identified 20 specific issues not fully captured by generic QoL instruments, such as difficulties for planning, verbal communication, vision impairment, as well as not being considered seriously by those around them.

conclusionThis study highlights the profound burden of RP and emphasizes the need for the development of a disease-specific health-related QoL instrument, as a way to improve patient-centered care and disease management.

Indexed as

Polychondritis, RelapsingQuality of LifeAdultAgedFemaleHumansMaleMiddle AgedSurveys and QuestionnairesBurden of diseaseQuality of lifeRelapsing polychondritis

Identifiers

PMID41808205
PMCPMC13088433

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.