Evidence map›Paper›PMID 35841105›Full record

ArticleOrphanet journal of rare diseases2022

A global, cross-sectional survey of patient-reported outcomes, disease burden, and quality of life in epidermolysis bullosa simplex.

Jodi Y So, Shivali Fulchand, Christine Y Wong, Shufeng Li, Jaron Nazaroff, Emily S Gorell, Mark P de Souza, Dedee F Murrell, Joyce M Teng, Albert S Chiou and 1 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 16% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

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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

11 authors at 5 institutions in 2 countries.

Jodi Y SoDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Shivali FulchandDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Christine Y WongDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Shufeng LiDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Jaron NazaroffDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Emily S GorellDepartment of Dermatology, University of Cincinnati, College of Medicine, Cincinnati, OH, USA.
Mark P de SouzaPhoenix Tissue Repair, Inc., Boston, MA, USA.
Dedee F MurrellDepartment of Dermatology, University of New South Wales, Sydney, NSW, Australia.
Joyce M TengDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Albert S ChiouDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Jean Y TangDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA. tangy@stanford.edu.ORCID 0000-0002-5510-6502
Stanford University · USAdvanced Tissue (United States) · USStanford Medicine · USUniversity of Cincinnati Medical Center · USUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpidermolysis bullosa simplex (EBS) comprises a group of rare, blistering genodermatoses. Prior work has been limited by small sample sizes, and much remains unexplored about the disease burden and health-related quality of life (QOL) of patients with EBS. The aim of this study was to characterize the most common patient-reported clinical manifestations and the health-related impact of QOL in EBS, and to examine differences in disease burden by age.

methodsPatients with a diagnosis of epidermolysis bullosa (EB) or their caregivers completed a one-time online survey administered by EBCare, an international online EB registry. Survey data from respondents self-reporting a diagnosis of EBS were analyzed for clinical and wound manifestations, medication use, and QOL (using Quality of Life in Epidermolysis Bullosa [QOLEB] scores). Differences across age groups were assessed using Kruskal-Wallis and Fisher's exact tests.

resultsThere were 214 survey respondents with EBS. The mean age was 32.8 years (standard deviation = 19.2). Many respondents reported blisters (93%), recurrent wounds (89%), pain (74%), chronic wounds (59%), itch (55%), and difficulty walking (44%). Mean QOLEB score was 14.7 (standard deviation = 7.5) indicating a "moderate" impact on QOL, and 12% of respondents required regular use of opiates. Findings were consistent in subgroup analyses restricted to respondents with diagnostic confirmation via genetic testing or skin biopsy (n = 63 of 214). Age-stratified analyses revealed differences in disease burden: younger respondents were more likely to self-report severe disease (24% vs. 19% vs. 5% for respondents aged 0-9 vs. 10-17 vs. 18 + , p = 0.001), failure to thrive (9% vs. 15% vs. 3%, p = 0.02), and use of gastrostomy tubes (15% vs. 12% vs. 1%, p < 0.001) and topical antibiotics (67% vs. 69% vs. 34%, p < 0.001), while older respondents were more likely to be overweight or obese (6% vs. 0% vs. 51%, p < 0.001) and have difficulty walking (24% vs. 46% vs. 48%, p = 0.04).

conclusionsIn the largest international cross-sectional survey of EBS patients conducted, respondents reported extensive disease burden including significant wounding, pain, itch, difficulty walking, and impact on QOL. Age stratified disease manifestations. These findings suggest significant unmet need, and treatment and counseling for EBS patients should consider age-specific differences.

Indexed as

Epidermolysis BullosaEpidermolysis Bullosa SimplexAdultCost of IllnessCross-Sectional StudiesHumansMobility LimitationPainPatient Reported Outcome MeasuresQuality of LifeBullous dermatosesEpidermolysis bullosaEpidermolysis bullosa simplexGenodermatosesPatient-reported outcomesQuality of life

Identifiers

PMID35841105
PMCPMC9287948
OpenAlexW4285492218

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.