Evidence map›Paper›PMID 39921830›Full record

ArticleDermatology and therapy2025

Implementation Science to Improve the Diagnosis and Management of Hidradenitis Suppurativa: HELyx Study Design Overview.

John R Ingram, Georgios Kokolakis, Barry M McGrath, Marco Romanelli, Falk G Bechara, Antonio Martorell, Mona Biermann, Yvonne Geissbühler, Benjamin M Haeberle, Mahrukh Zahid and 4 more

Abstract read
In one paragraph

Article in Dermatology and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

John R IngramDivision of Infection and Immunity, Cardiff University, Cardiff, UK. ingramjr@cardiff.ac.uk.ORCID http://orcid.org/0000-0002-5257-1142
Georgios KokolakisPsoriasis Research and Treatment Center, Department of Dermatology, Venereology and Allergology, Charité Universitätsmedizin Berlin, Berlin, Germany.
Barry M McGrathHS Ireland, Hidradenitis Suppurativa Association, County Clare, Ireland.
Marco RomanelliDepartment of Dermatology, University of Pisa, Pisa, Toscana, Italy.
Falk G BecharaInternational Center for Hidradenitis Suppurativa/Acne Inversa (ICH), Department of Dermatology, Venereology and Allergology, Ruhr-University Bochum, Bochum, Germany.
Antonio MartorellDepartment of Dermatology, Hospital de Manises, Valencia, Spain.
Mona BiermannNovartis Pharma GmbH, Nuremberg, Germany.
Yvonne GeissbühlerNovartis Pharma AG, Basel, Switzerland.
Benjamin M HaeberleNovartis Pharma GmbH, Nuremberg, Germany.
Mahrukh ZahidNovartis Pharma AG, Basel, Switzerland.
Michael FritzNovartis Pharma GmbH, Nuremberg, Germany.
Erhard Quebe-FehlingNovartis Pharma AG, Basel, Switzerland.
Craig RichardsonNovartis Pharma AG, Basel, Switzerland.
Pierre-André BecherelDepartment of Dermatology, Venereology and Allergology, Antony Private Hospital, Antony, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHidradenitis suppurativa (HS) is a chronic, inflammatory skin disease associated with a high disease burden and substantial impact on patients' quality of life. Limited therapeutic options are available, with an unmet medical need for earlier diagnosis and treatment and more effective treatment options. Low awareness of HS amongst healthcare professionals (HCPs) leads to delayed diagnosis and a prolonged patient journey to HS-specific treatment. This article aims to describe the design of HELyx, an implementation science study in Germany, which aims to evaluate the effectiveness of an implementation strategy to improve screening and diagnosis of HS among HCPs (dermatologists and non-dermatologists) and timely referral to HS-treating dermatologists.

methodsHELyx is a hybrid, effectiveness-implementation science study with a pre-post design involving HCPs and is guided by the Consolidated Framework for Implementation Research. HELyx is being conducted in Germany over four consecutive phases (context analysis, pre-implementation, implementation, and post-implementation) in a sequential manner. A similar implementation science study is also being conducted in the United Arab Emirates (UAE) and Spain. HELyx aims to identify key unmet medical needs in the HS patient journey, to develop and implement a tailored medical education program, and to measure the effectiveness of the implementation. PLANNED OUTCOMES: The primary endpoint is the change in the proportion of HCPs who used a diagnostic screening tool to identify patients with suspected HS during the 24 weeks of the post-implementation phase (assessed at Week 24) compared to the 24 weeks before implementation (assessed at baseline). Secondary endpoints include assessment of the use of HS disease severity assessment and patient-reported outcome tools and HCP referral behaviours.

Indexed as

DermatologistsDiagnosisGeneral practitionersGynaecologistsHidradenitis suppurativaImplementation scienceReferralScreeningSurgeons

Identifiers

PMID39921830
PMCPMC11833011

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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.