Evidence map›Paper›PMID 42054259›Full record

ArticleDermatology (Basel, Switzerland)2026

Patient Perspectives on Treatment Outcomes and Priorities in Autoimmune Bullous Diseases: An Exploratory Survey among Dutch Patients.

Marjolein A J Hiel, Eva W H Korte, Maria C Bolling, Joost M Meijer, Barbara Horváth

Abstract read
In one paragraph

Article in Dermatology (Basel, Switzerland), 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

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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Marjolein A J HielDepartment of Dermatology, Center of Expertise for Blistering Diseases, European Reference Network for Rare Skin Diseases (ERN SKIN), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands, m.a.j.hiel@umcg.nl.
Eva W H KorteDepartment of Dermatology, Center of Expertise for Blistering Diseases, European Reference Network for Rare Skin Diseases (ERN SKIN), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Maria C BollingDepartment of Dermatology, Center of Expertise for Blistering Diseases, European Reference Network for Rare Skin Diseases (ERN SKIN), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Joost M MeijerDepartment of Dermatology, Center of Expertise for Blistering Diseases, European Reference Network for Rare Skin Diseases (ERN SKIN), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Barbara HorváthDepartment of Dermatology, Center of Expertise for Blistering Diseases, European Reference Network for Rare Skin Diseases (ERN SKIN), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAutoimmune bullous diseases (AIBDs), comprising pemphigoid and pemphigus diseases, have seen limited therapeutic advances beyond rituximab for pemphigus vulgaris. As novel therapies are evaluated in clinical trials, well-defined, uniform, and relevant outcomes with patient involvement are essential. To date, however, patient-reported outcomes remain underrepresented, leaving uncertainty about whether trial results genuinely reflect patients' expectations. This study examines perspectives of patients with AIBD on treatment outcomes and priorities to ensure that future research focuses on what matters most to them.

methodsA cross-sectional study was conducted among Dutch patients with AIBD between October 2023 and January 2024, using a self-developed questionnaire with both closed- and open-ended questions to assess patient perspectives on treatment outcomes and priorities, key factors in choosing a treatment, and indicators of treatment success.

resultsRegarding skin and/or mucous membrane complaints, "the formation of new blisters and wounds" emerged as the most important complaint a treatment should address for both pemphigoid (43%) and pemphigus (86%) patients. In open-ended questions, patients with pemphigoid most frequently prioritized "pruritus" (44%), while patients with pemphigus emphasized "pain" (39%). Most important concerns regarding physical and daily functioning were "vision problems" (20%), "sleep disturbances" (20%), and "self-care difficulties" (23%) for patients with pemphigoid, whereas patients with pemphigus most commonly cited "eating and/or swallowing difficulties" (57%) and "daily activity limitations" (41%). Regarding emotional/psychological functioning, both subgroups prioritized "anxiety and/or worry" as most important concern (pemphigoid: 28%, pemphigus: 43%). Side effects were identified as the most important factor in choosing a treatment (pemphigoid: 41%, pemphigus: 39%). The absence of one or more symptoms and clinical signs (i.e., "no blisters") was mentioned as the most important indicator of treatment success (pemphigoid: 88%, pemphigus: 91%), although minimal clinical signs (i.e., "minimal blisters") were also considered acceptable (pemphigoid: 25%, pemphigus: 13%).

conclusionPatients with pemphigoid and pemphigus exhibit some distinct treatment priorities, reflecting their distinct pathomechanisms. Nonetheless, both subgroups consistently prioritize not only the resolution of disease-specific clinical signs but also preservation of physical and psychological well-being, underscoring the need for more holistic and patient-centered outcome measurement to ensure the establishment of meaningful, AIBD subgroup specific treatment outcomes.

Indexed as

Autoimmune bullous diseaseImmunobullous diseasePatient perspectivesTreatment outcomesTreatment priorities

Identifiers

PMID42054259
PMCPMC13313618

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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 Socratic graph.