Evidence map›Paper›PMID 41992712›Full record

ReviewActa dermato-venereologica2026

Exploring the Impact of Fatigue and Sleep Disturbance in Hidradenitis Suppurativa: Perspectives from Patients and Healthcare Professionals.

Barry M McGrath, Donna Atherton, Phil Brady, Marie-France Bru-Daprés, Jennifer L Hsiao, Silvia Lobo, Latoya Palmer, Giuseppina Pintori, Jacek C Szepietowski, Mei Go and 2 more

Abstract readReview
In one paragraph

Review in Acta dermato-venereologica, 2026. 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

12 authors.

Barry M McGrathHS Ireland - Hidradenitis Suppurativa Association, Gortatogher, Ireland. barry@hsireland.ie.ORCID 0000-0001-6995-7714
Donna AthertonInternational Association of Hidradenitis Suppurativa Network, Boston, MA, United States.
Phil BradyBritish Skin Foundation, London, United Kingdom.
Marie-France Bru-DaprésAssociation Française pour la Recherche sur l'Hidrosadénite, Saint-Benoît, France.
Jennifer L HsiaoDepartment of Dermatology, Keck Medicine of University of Southern California, Los Angeles, CA, United States.
Silvia LoboAsociación de Enfermos de Hidrosadenitis - ASENDHI, Madrid, Spain.
Latoya PalmerHidradenitis and Me Support Group, Brampton, Ontario, Canada.
Giuseppina PintoriPassion People, Cagliari, Italy.
Jacek C SzepietowskiDivision of Dermatology, Venereology and Clinical Immunology, Faculty of Medicine, Wroclaw University of Science and Technology, Wroclaw, Poland; Department of Dermato-Venereology, 4th Military Hospital, Wroclaw, Poland.
Mei GoNovartis Pharma AG, Basel, Switzerland.
Ivette AlarconNovartis Pharma AG, Basel, Switzerland.
John R IngramDepartment of Dermatology & Academic Wound Healing, Division of Infection and Immunity, Cardiff University, Cardiff, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease that affects physical, social and emotional aspects of life for people living with HS (plwHS). Although many plwHS consider pain the most bothersome symptom, fatigue and sleep disturbance are underexplored in research and rarely discussed in clinical practice. This article shares perspectives from plwHS and people working with patients, including healthcare professionals (HCPs), from Europe and North America, on the impact of HS-related fatigue and sleep disturbance on quality of life (QoL). Fatigue was described as a debilitating symptom affecting QoL, with HCPs often noting that plwHS were unaware of the full impact of fatigue until treatment improved their HS symptoms. Sleep disturbance was mainly attributed to HS-related pain, pruritus and lesion drainage, with sleep deficits accumulating over time. The strain of HS impacted personal relationships, with plwHS expressing less interest in social interactions or intimate relationships, leading to feelings of guilt, failure, isolation and reduced self-esteem. Fatigue and sleep disturbance also affected work productivity, and consequently, career progression and financial stability. Recognizing the multifaceted HS symptoms, providing reasonable adjustments in the workplace, encouraging open dialogue with HCPs and measuring fatigue with a validated instrument could help improve QoL of plwHS.

Indexed as

Attitude of Health PersonnelFatigueHidradenitis SuppurativaQuality of LifeSleepSleep QualitySleep Wake DisordersCost of IllnessHumansSelf ConceptSymptom Burden

Identifiers

PMID41992712
PMCPMC13086963

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.