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Balato A, Venturini M, Scalvenzi M, Foti C, Maifredi G, Creazzola SS, Antonacci S, Tonelli A, Valsecchi D, Vassellatti D, Cipelli R, Ori A, Casoli L. Management and Burden of Hidradenitis Suppurativa: An Italian Hybrid Real-World Study. Dermatol Ther (Heidelb) 2025; 15:1771-1785. [PMID: 40343666 DOI: 10.1007/s13555-025-01407-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/20/2024] [Accepted: 03/31/2025] [Indexed: 05/11/2025] Open
Abstract
INTRODUCTION Hidradenitis suppurativa (HS) is a chronic, inflammatory skin disease that severely impacts quality of life and carries a substantial economic burden. METHODS This multicenter observational study generated real-world evidence on HS in Italy, focusing on clinical profiles, management, and costs. Data were collected from 50 adults at four specialized centers, combining primary data with retrospective administrative data. RESULTS Patients with moderate-to-severe disease had longer diagnostic delays (median 1.8 versus 0.7 years), lower symptom control (40.7% versus 95.2%), and worse quality of life (Dermatology Life Quality Index: 11.8 versus 8.0) than those with mild disease. Furthermore, HS was associated with higher costs in moderate-to-severe cases, including greater direct (€2214 versus €873) and indirect expenses (€2435 versus €262). CONCLUSIONS The findings highlight the social and economic burden of HS and emphasize the need for increased healthcare awareness for earlier diagnosis and better management.
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Affiliation(s)
- Anna Balato
- Unit of Dermatology, University of Campania Luigi Vanvitelli, Naples, Italy
| | - Marina Venturini
- Dermatology Clinic, ASST-Spedali Civili Hospital and University of Brescia, Brescia, Italy
| | | | - Caterina Foti
- Dermatology and Venereology Unit, University A.O.U. Consorziale Policlinico, Bari, Italy
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Tzellos T. Conventional treatment of hidradenitis suppurativa: serving the "window of opportunity" concept. Clin Dermatol 2025:S0738-081X(25)00157-9. [PMID: 40373947 DOI: 10.1016/j.clindermatol.2025.05.015] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/17/2025]
Abstract
Hidradenitis suppurativa (HS) is a chronic, systemic, inflammatory skin disease characterized by inflammatory nodules, painful abscesses, and draining tunnels. It is associated with significant comorbidities, including inflammatory bowel disease, arthritis, pain, and a reduced quality of life. Unlike psoriasis or atopic dermatitis, it can progress from an inflammatory state to a nonreversible scaring component if not treated early enough and in an evidence-based manner. Until recently, adalimumab has been the only approved treatment for HS. Many conventional systemic treatments are currently used and have an appropriate role in HS therapy, provided they are used correctly in suitable patients. Unfortunately, many therapies, including antimicrobials, are used empirically, leading to continuous cycles of incorrect and inefficient treatment, disease progression, and reduced quality of life. Contributing to the problem is the delay in diagnosis which may be as long as seven years and insufficient or inappropriate intervention.. Capturing the "window of opportunity" is essential for a disease such as HS.
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Affiliation(s)
- T Tzellos
- European Hidradenitis Suppurativa Foundation e.V., Dessau, Germany; Department of Dermatology, Nordland Hospital Trust, Bodø, Norway.
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3
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Perković DT, Marinović B, Tešanović M, Mokos ZB. Biologic therapies and small molecules in the treatment of hidradenitis suppurativa. Clin Dermatol 2025:S0738-081X(25)00146-4. [PMID: 40373949 DOI: 10.1016/j.clindermatol.2025.05.004] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/17/2025]
Abstract
Hidradenitis suppurativa (HS) is a debilitating chronic skin condition challenging to manage. Treatment options range from topical and systemic medications to various surgical procedures. With the expanding knowledge of cytokine signaling pathways, systemic treatment for hidradenitis suppurativa is entering an exciting phase, offering new opportunities to address imbalanced immune responses. The primary categories of treatment include biologics and small molecules. Currently, the only three approved biologics for HS are the anti-TNF-α antibody adalimumab, the anti-IL-17A secukinumab and the anti-IL-17A/17F, bimekizumab. While studies indicate moderate effectiveness of all three drugs, achieving adequate disease control remains challenging for many patients. Research in the field of HS is rapidly evolving, with a wide range of treatments being developed that leverage various mechanisms of action. Drugs targeting the IL-17 and Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathways show promise in ongoing and completed phase 3 studies, offering the potential for more comprehensive treatment responses.
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Affiliation(s)
| | - Branka Marinović
- University Hospital Centre Zagreb, Department of Dermatology and Venereology, European Reference Network (ERN) - Skin Reference Centre, Zagreb, Croatia; University of Zagreb School of Medicine, Zagreb, Croatia
| | - Mara Tešanović
- Dubrovnik General Hospital, Department of Gynecology and Obstetrics, Dubrovnik, Croatia
| | - Zrinka Bukvić Mokos
- University Hospital Centre Zagreb, Department of Dermatology and Venereology, European Reference Network (ERN) - Skin Reference Centre, Zagreb, Croatia; University of Zagreb School of Medicine, Zagreb, Croatia.
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Orehovec SS, Mijatović D, Gatin L, Brkić L. Surgical treatment of hidradenitis suppurativa. Clin Dermatol 2025:S0738-081X(25)00150-6. [PMID: 40360032 DOI: 10.1016/j.clindermatol.2025.05.008] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/15/2025]
Abstract
The treatment of HS is multimodal, even though it begins with a dermatologic examination and therapy prescribed by the dermatologist. A multidisciplinary approach is necessary to achieve the best results and to optimize the treatment. Surgical treatment must be individualized according to the degree of the disease. Adequate preoperative preparation of the patient and the wound is necessary. Surgical treatment alone does not give a 100% safe outcome, and remissions are possible regardless of the treatment method. We present current surgical treatment modalities available for HS treatment. The methods are divided into local and radical procedures. Recent advancements and findings are also discussed.
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Affiliation(s)
- Sanda Smuđ Orehovec
- University of Zagreb School of Medicine, 10000 Zagreb, Croatia; Division of Plastic and Reconstructive Surgery and Breast Surgery, Department of Surgery, University Hospital Centre Zagreb, 10000 Zagreb, Croatia.
| | - Davor Mijatović
- University of Zagreb School of Medicine, 10000 Zagreb, Croatia; Division of Plastic and Reconstructive Surgery and Breast Surgery, Department of Surgery, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
| | - Lucija Gatin
- Division of Plastic and Reconstructive Surgery and Breast Surgery, Department of Surgery, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
| | - Lucija Brkić
- University of Zagreb School of Medicine, 10000 Zagreb, Croatia; Division of Abdominal Surgery, Department of Surgery, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
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Soto-Moreno A, Delgado-Moya N, Sánchez-Díaz M, Arias-Santiago S, Molina-Leyva A. Skin Homeostasis is Impaired in Hidradenitis Suppurativa Lesions: A Comparative Study. ACTAS DERMO-SIFILIOGRAFICAS 2025; 116:449-454. [PMID: 39067573 DOI: 10.1016/j.ad.2024.05.027] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/14/2024] [Revised: 04/28/2024] [Accepted: 05/17/2024] [Indexed: 07/30/2024] Open
Abstract
INTRODUCTION Hidradenitis suppurativa (HS) is a chronic skin disease whose impact on skin homeostasis has not been adequately studied at present. Knowledge about how skin function changes in these patients, and could be of interest not only to improve the topical management of the disease, but also as an objective measure of disease activity. The aim of this study was to compare skin homeostasis and the epidermal barrier function in lesional and healthy skin areas of patients with HS. METHODS We conducted a cross-sectional study. Skin homeostasis and the epidermal barrier function of lesions were assessed in HS patients using validated tools. A healthy perilesional skin control was assigned to each lesion to compare skin homeostasis parameters. RESULTS A total of 43 patients were included: 22 nodules, 10 abscesses and 25 draining tunnels were measured. The male-to-female ratio was 20:23, and the mean age, 35.95 years (SD, 14.82). Increased transepidermal water loss (TEWL) and erythema were found in nodules, abscesses and draining tunnel vs healthy skin. A direct association was observed between inflammatory nodules TEWL and IHS4 stage. In draining tunnels, a direct association was observed between TEWL and smoking. A trend of increasing TEWL values was observed as a function of Hurley stage. CONCLUSION HS lesions exhibit epidermal barrier dysfunction that depends on the severity of inflammatory activity. These results could be useful to develop objective classification systems for the severity and degree of involvement of HS or help in the development of vehicles for specific drugs, antiseptics and dressings for the management of this disease.
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Affiliation(s)
- A Soto-Moreno
- Dermatology Unit, Hospital Universitario Virgen de las Nieves Instituto de Investigación Biosanitaria IBS, Granada, Spain
| | - N Delgado-Moya
- Dermatology Unit, Hospital Universitario Virgen de las Nieves Instituto de Investigación Biosanitaria IBS, Granada, Spain
| | - M Sánchez-Díaz
- Dermatology Unit, Hospital Universitario Virgen de las Nieves Instituto de Investigación Biosanitaria IBS, Granada, Spain; Hidradenitis Suppurativa Clinic, Dermatology Unit, Hospital Universitario Virgen de las Nieves, Granada, Spain
| | - S Arias-Santiago
- Hidradenitis Suppurativa Clinic, Dermatology Unit, Hospital Universitario Virgen de las Nieves, Granada, Spain; School of Medicine, University of Granada, Granada, Spain.
| | - A Molina-Leyva
- Hidradenitis Suppurativa Clinic, Dermatology Unit, Hospital Universitario Virgen de las Nieves, Granada, Spain; School of Medicine, University of Granada, Granada, Spain
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6
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Zouboulis CC, Bechara FG, Benhadou F, Bettoli V, Bukvić Mokos Z, Del Marmol V, Dolenc‐Voljč M, Giamarellos‐Bourboulis EJ, Grimstad Ø, Guillem P, Horváth B, Hunger RE, Ingram JR, Ioannidis D, Just E, Kemény L, Kirby B, Liakou AI, McGrath BM, Marzano AV, Matusiak Ł, Molina‐Leyva A, Nassif A, Podda M, Prens EP, Prignano F, Raynal H, Romanelli M, Saunte DML, Szegedi A, Szepietowski JC, Tzellos T, Valiukevičienė S, van der Zee HH, van Straalen KR, Villumsen B, Jemec GBE. European S2k guidelines for hidradenitis suppurativa/acne inversa part 2: Treatment. J Eur Acad Dermatol Venereol 2025; 39:899-941. [PMID: 39699926 PMCID: PMC12023723 DOI: 10.1111/jdv.20472] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/11/2024] [Accepted: 10/30/2024] [Indexed: 12/20/2024]
Abstract
INTRODUCTION This second part of the S2k guidelines is an update of the 2015 S1 European guidelines. OBJECTIVE These guidelines aim to provide an accepted decision aid for the selection, implementation and assessment of appropriate and sufficient therapy for patients with hidradenitis suppurativa/acne inversa (HS). METHODS The chapters have been selected after a Delphi procedure among the experts/authors. Certain passages have been adopted without changes from the previous version. Potential treatment complications are not included, being beyond the scope of these guidelines. RESULTS Since the S1 guidelines publication, validation of new therapeutic approaches has almost completely overhauled the knowledge in the field of HS treatment. Inflammatory nodules/abscesses/draining tunnels are the primary lesions, which enable the classification of the disease severity by new validated tools. In relation to the degree of detectable inflammation, HS is classified into the inflammatory and the predominantly non-inflammatory forms. While the intensity of the inflammatory form can be subdivided by the IHS4 classification in mild, moderate and severe HS and is treated by medication accordingly, the decision on surgical treatment of the predominantly non-inflammatory form is based on the Hurley stage of the affected localization. The effectiveness of oral tetracyclines as an alternative to the oral combination of clindamycin/rifampicin should be noted. The duration of systemic antibiotic therapy can be shortened by a 5-day intravenous clindamycin treatment. Adalimumab, secukinumab and bimekizumab subcutaneous administration has been approved by the EMA for the treatment of moderate-to-severe HS. Various surgical procedures are available for the predominantly non-inflammatory form of the disease. The combination of a medical therapy to reduce inflammation with a surgical procedure to remove irreversible tissue damage is currently considered a holistic therapeutic approach. CONCLUSIONS Suitable therapeutic options while considering HS severity in the therapeutic algorithm according to standardized criteria are aimed at ensuring a proper therapy.
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Affiliation(s)
- C. C. Zouboulis
- Departments of Dermatology, Venereology, Allergology and Immunology, Staedtisches Klinikum DessauBrandenburg Medical School Theodor Fontane and Faculty of Health Sciences BrandenburgDessauGermany
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
| | - F. G. Bechara
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology, Venereology and Allergology, International Centre for Hidradenitis Suppurativa/Acne Inversa (ICH)Ruhr‐University BochumBochumGermany
| | - F. Benhadou
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Dermatology Unit, Hôpitaux Unviversitaires de BruxellesUniversité Libre de BruxellesBrusselsBelgium
| | - V. Bettoli
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- HS Clinic, O.U. of DermatologyAzienda Ospedaliera – University of FerraraFerraraItaly
| | - Z. Bukvić Mokos
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- University of Zagreb School of MedicineZagrebCroatia
- Department of Dermatology and VenereologyUniversity Hospital Centre ZagrebZagrebCroatia
| | - V. Del Marmol
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Dermatology Unit, Hôpitaux Unviversitaires de BruxellesUniversité Libre de BruxellesBrusselsBelgium
| | - M. Dolenc‐Voljč
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatovenereology, Faculty of MedicineUniversity of LjubljanaLjubljanaSlovenia
- Department of DermatovenereologyUniversity Medical Centre LjubljanaLjubljanaSlovenia
| | - E. J. Giamarellos‐Bourboulis
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- 4th Department of Internal MedicineNational and Kapodistrian University of AthensAthensGreece
| | - Ø. Grimstad
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Clinical MedicineUiT ‐ The Arctic University of NorwayTromsøNorway
- Department of DermatologyUniversity Hospital of North NorwayTromsøNorway
| | - P. Guillem
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of SurgeryClinique du Val d'OuestLyonFrance
| | - B. Horváth
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology, Center for Blistering DiseasesUniversity Medical Center GroningenGroningenThe Netherlands
| | - R. E. Hunger
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology, Inselspital, Bern University HospitalUniversity of BernBernSwitzerland
| | - J. R. Ingram
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Division of Infection and Immunity, Dermatology DepartmentCardiff UniversityCardiffUK
| | - D. Ioannidis
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- 1st Department of Dermatology‐VenereologyAristotle University Medical SchoolThessalonikiGreece
| | - E. Just
- Deutsche Akne Inversa PatientenvereinigungCoesfeldGermany
| | - L. Kemény
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology and AllergologyUniversity of SzegedSzegedHungary
| | - B. Kirby
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Charles Department of Dermatology, St Vincent's University Hospital and Charles Institute of DermatologyUniversity College DublinDublinIreland
| | - A. I. Liakou
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- 1st Department of Dermatology‐Venereology, “Andreas Sygros” Hospital for Venereal and Cutaneous DiseasesNational and Kapodistrian University of Athens Medical SchoolAthensGreece
| | - B. M. McGrath
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- HS IrelandHidradenitis Suppurativa AssociationCounty ClareIreland
| | - A. V. Marzano
- Dermatology UnitFondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoMilanItaly
- Department of Pathophysiology and TransplantationUniversità Degli Studi di MilanoMilanItaly
| | - Ł. Matusiak
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Faculty of MedicineWroclaw University of Science and TechnologyWroclawPoland
| | - A. Molina‐Leyva
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology and VenereologyHospital Universitario Virgen de las Nieves – Ibs GranadaGranadaSpain
| | - A. Nassif
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Centre d'Infectiologie Necker‐Pasteur, Institut PasteurCentre Médical and Université Paris‐CitéParisFrance
| | - M. Podda
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology, Medical Center Klinikum DarmstadtTeaching Hospital Goethe‐University FrankfurtDarmstadtGermany
| | - E. P. Prens
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of DermatologyErasmus University Medical CenterRotterdamThe Netherlands
| | - F. Prignano
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Section of Dermatology, Department of Health SciencesUniversity of FlorenceFlorenceItaly
| | - H. Raynal
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Solidarité VerneuilLyonFrance
| | - M. Romanelli
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of DermatologyUniversity of PisaPisaItaly
| | - D. M. L. Saunte
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology and AllergyCopenhagen University Hospital ‐ Herlev‐Gentofte HospitalHellerupDenmark
- Department of DermatologyZealand University HospitalRoskildeDenmark
- Department of Clinical Medicine, Faculty of Health and Medical SciencesUniversity of CopenhagenCopenhagenDenmark
| | - A. Szegedi
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Dermatology, Faculty of Medicine and Clinical CenterUniversity of DebrecenDebrecenHungary
| | - J. C. Szepietowski
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Faculty of MedicineWroclaw University of Science and TechnologyWroclawPoland
| | - T. Tzellos
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Clinical MedicineUiT ‐ The Arctic University of NorwayTromsøNorway
- Department of DermatologyUniversity Hospital of North NorwayTromsøNorway
| | - S. Valiukevičienė
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of Skin and Venereal DiseasesThe Lithuanian University of Health SciencesKaunasLithuania
- Department of Skin and Venereal DiseasesThe Hospital of Lithuanian University of Health Sciences Kauno klinikosKaunasLithuania
| | - H. H. van der Zee
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of DermatologyErasmus University Medical CenterRotterdamThe Netherlands
| | - K. R. van Straalen
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of DermatologyErasmus University Medical CenterRotterdamThe Netherlands
| | - B. Villumsen
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Danish HS Patients' AssociationSoborgDenmark
| | - G. B. E. Jemec
- European Hidradenitis Suppurativa Foundation e.V.DessauGermany
- Department of DermatologyZealand University HospitalRoskildeDenmark
- Department of Clinical Medicine, Faculty of Health and Medical SciencesUniversity of CopenhagenCopenhagenDenmark
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Soto-Moreno A, Delgado-Moya N, Sánchez-Díaz M, Arias-Santiago S, Molina-Leyva A. Skin Homeostasis is Impaired in Hidradenitis Suppurativa Lesions: A Comparative Study. ACTAS DERMO-SIFILIOGRAFICAS 2025; 116:T449-T454. [PMID: 39988201 DOI: 10.1016/j.ad.2025.02.019] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/14/2024] [Revised: 04/28/2024] [Accepted: 05/17/2024] [Indexed: 02/25/2025] Open
Abstract
INTRODUCTION Hidradenitis suppurativa (HS) is a chronic skin disease whose impact on skin homeostasis has not been adequately studied at present. Knowledge about how skin function changes in these patients, and could be of interest not only to improve the topical management of the disease, but also as an objective measure of disease activity. The aim of this study was to compare skin homeostasis and the epidermal barrier function in lesional and healthy skin areas of patients with HS. METHODS We conducted a cross-sectional study. Skin homeostasis and the epidermal barrier function of lesions were assessed in HS patients using validated tools. A healthy perilesional skin control was assigned to each lesion to compare skin homeostasis parameters. RESULTS A total of 43 patients were included: 22 nodules, 10 abscesses and 25 draining tunnels were measured. The male-to-female ratio was 20:23, and the mean age, 35.95 years (SD, 14.82). Increased transepidermal water loss (TEWL) and erythema were found in nodules, abscesses and draining tunnel vs healthy skin. A direct association was observed between inflammatory nodules TEWL and IHS4 stage. In draining tunnels, a direct association was observed between TEWL and smoking. A trend of increasing TEWL values was observed as a function of Hurley stage. CONCLUSION HS lesions exhibit epidermal barrier dysfunction that depends on the severity of inflammatory activity. These results could be useful to develop objective classification systems for the severity and degree of involvement of HS or help in the development of vehicles for specific drugs, antiseptics and dressings for the management of this disease.
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Affiliation(s)
- A Soto-Moreno
- Dermatology Unit, Hospital Universitario Virgen de las Nieves Instituto de Investigación Biosanitaria IBS, Granada, España
| | - N Delgado-Moya
- Dermatology Unit, Hospital Universitario Virgen de las Nieves Instituto de Investigación Biosanitaria IBS, Granada, España
| | - M Sánchez-Díaz
- Dermatology Unit, Hospital Universitario Virgen de las Nieves Instituto de Investigación Biosanitaria IBS, Granada, España; Hidradenitis Suppurativa Clinic, Dermatology Unit, Hospital Universitario Virgen de las Nieves, Granada, España
| | - S Arias-Santiago
- Hidradenitis Suppurativa Clinic, Dermatology Unit, Hospital Universitario Virgen de las Nieves, Granada, España; School of Medicine, University of Granada, Granada, España.
| | - A Molina-Leyva
- Hidradenitis Suppurativa Clinic, Dermatology Unit, Hospital Universitario Virgen de las Nieves, Granada, España; School of Medicine, University of Granada, Granada, España
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Piętowska-Marczak Z, Krefft-Trzciniecka K, Pakiet A, Nowicka D. The Role of Sex in Body Composition Differences in Hidradenitis Suppurativa: Insights from Bioelectrical Impedance Analysis. J Clin Med 2025; 14:2760. [PMID: 40283590 PMCID: PMC12028129 DOI: 10.3390/jcm14082760] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/30/2025] [Revised: 03/30/2025] [Accepted: 04/10/2025] [Indexed: 04/29/2025] Open
Abstract
Background: Hidradenitis suppurativa (HS) is a rare, debilitating, chronic inflammatory skin disease. This study aimed to investigate differences in body composition between patients with hidradenitis suppurativa (HS) and healthy controls, with a particular focus on sex-specific disparities, while also exploring secondary associations with muscle health and quality of life. Methods: Body composition was measured using a bioanalyzer and compared between HS individuals (n = 53) and controls (n = 50). Results: The mean BMI was significantly higher in the HS group than in the controls (median 29.6 vs. median 22.1; p < 0.001, effect size -0.581). The patients with HS had a significantly higher fat mass (mean 26.2 ± 22.7 vs. 16.3 ± 6.0; p < 0.001, effect size -0.400), level of visceral fat (median 9 vs. 2; p < 0.001, effect size -0.473), percentage of total body water (mean 45.9 ± 12.3 vs. 31.9 ± 14.3; p < 0.001, effect size -0.508), skeletal muscle index (median 8.9 vs. 7.3; p < 0.001, effect size -0.445), and bone mass (median 3.2 vs. 2.5; p < 0.001, effect size -0.421); at the same time, they had a significantly lower predicted muscle mass (median 19.8 vs. 47.3; p < 0.001, effect size -0.740) and percentage of skeletal muscle mass (mean 38.2 ± 7.8 vs. 42.3 ± 5.5; p = 0.008, effect size -0.263) in comparison to the controls. The HS group was also characterized by a higher metabolic age (median 65 vs. 21 years; p < 0.001, effect size -0.760) and basal metabolic rate (median 1927 vs. 1489 kcal; p < 0.001, effect size -0.444). Conclusions: Patients with HS exhibit a distinctive pattern in body composition parameters when compared to healthy controls, which may hold significant potential for enhancing diagnostic accuracy and monitoring disease progression. This study highlighted sex-specific differences in body composition, emphasizing the need to consider biological sex in the pathophysiology and clinical evaluation of HS. Further research is needed to explore the clinical utility of body composition analysis in disease progression, therapeutic response, and personalized management.
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Affiliation(s)
- Zuzanna Piętowska-Marczak
- Department of Aesthetic Dermatology and Regenerative Skin Medicine, Wrocław Medical University, 50-556 Wrocław, Poland; (Z.P.-M.)
| | | | - Alicja Pakiet
- Department of Aesthetic Dermatology and Regenerative Skin Medicine, Wrocław Medical University, 50-556 Wrocław, Poland; (Z.P.-M.)
| | - Danuta Nowicka
- Department of Aesthetic Dermatology and Regenerative Skin Medicine, Wrocław Medical University, 50-556 Wrocław, Poland; (Z.P.-M.)
- Faculty of Physiotherapy, Wroclaw University of Health and Sport Sciences, 51-612 Wrocław, Poland
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9
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Cucu CI, Giurcăneanu C, Poenaru E, Popa LG, Popa MI, Chifiriuc MC, Lazăr V, Holban AM, Gheorghe-Barbu I, Muntean AA, Caracoti CȘ, Mihai MM. Phenotypic and Genotypic Bacterial Virulence and Resistance Profiles in Hidradenitis Suppurativa. Int J Mol Sci 2025; 26:3502. [PMID: 40331997 PMCID: PMC12026681 DOI: 10.3390/ijms26083502] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/15/2025] [Revised: 03/13/2025] [Accepted: 03/24/2025] [Indexed: 05/08/2025] Open
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory skin condition, primarily affecting young individuals, with a significant impact on their quality of life due to recurrent, painful nodules, abscesses, and oozing sinus tracts, primarily affecting intertriginous areas. The pathogenesis of HS is multifactorial, involving a complex interplay between genetic predisposition, immune dysregulation, microbial, and environmental factors. While it is known that cutaneous and gut microbiome contribute to innate immune dysregulation in HS, their precise involvement in disease pathogenesis remains unclear. Despite several studies investigating the microbiome of HS lesions, either by culture-dependent or independent methods, there is no data available on the interplay between bacterial virulence profiles, clinical manifestations, and the host immune response. This study aimed to explore the phenotypic and genotypic resistance and virulence profiles of microorganisms isolated from HS lesions (including the expression of soluble virulence factors and the ability to develop biofilms), with a special focus on Staphylococcus aureus (S. aureus), one of the most frequent infectious agents of HS. A total of 92 bacterial strains, belonging to 20 different bacterial species, were isolated from the HS lesions of 23 patients. The strains of Staphylococcus, Corynebacterium, and Enterococcus expressed the highest levels of soluble virulence factors, such as hemolysins, lecithinase, and lipase, which are involved in bacterial persistence, local invasivity, and tissue damage. Moreover, a significant variation among bacterial species was noted regarding the capacity to develop biofilms, with a potential impact on disease chronicization, bacterial tolerance to antibiotics, and immune defense mechanisms. The genetic characterization of methicillin-resistant staphylococci revealed the presence of adhesins, hemolysin and enterotoxin genes as well as methicillin and macrolides resistance genes. Our findings highlight the critical role of virulence determinants, including bacterial biofilms, in HS pathogenesis, emphasizing the need for targeted therapeutic strategies to disrupt biofilms and mitigate infection severity.
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Affiliation(s)
- Corina Ioana Cucu
- Department of Oncologic Dermatology, “Elias” Emergency University Hospital, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (C.I.C.); (C.G.); (L.G.P.); (M.M.M.)
| | - Călin Giurcăneanu
- Department of Oncologic Dermatology, “Elias” Emergency University Hospital, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (C.I.C.); (C.G.); (L.G.P.); (M.M.M.)
| | - Elena Poenaru
- Department of Medical Informatics and Biostatistics, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania
| | - Liliana Gabriela Popa
- Department of Oncologic Dermatology, “Elias” Emergency University Hospital, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (C.I.C.); (C.G.); (L.G.P.); (M.M.M.)
| | - Mircea Ioan Popa
- Department of Microbiology II, “Cantacuzino” Institute, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (M.I.P.); (C.Ș.C.)
| | - Mariana Carmen Chifiriuc
- Research Institute of the University of Bucharest-ICUB, University of Bucharest, 050663 Bucharest, Romania (V.L.); (I.G.-B.)
| | - Veronica Lazăr
- Research Institute of the University of Bucharest-ICUB, University of Bucharest, 050663 Bucharest, Romania (V.L.); (I.G.-B.)
| | - Alina Maria Holban
- Research Institute of the University of Bucharest-ICUB, University of Bucharest, 050663 Bucharest, Romania (V.L.); (I.G.-B.)
| | - Irina Gheorghe-Barbu
- Research Institute of the University of Bucharest-ICUB, University of Bucharest, 050663 Bucharest, Romania (V.L.); (I.G.-B.)
| | - Andrei-Alexandru Muntean
- Department of Microbiology II, “Cantacuzino” Institute, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (M.I.P.); (C.Ș.C.)
| | - Costin Ștefan Caracoti
- Department of Microbiology II, “Cantacuzino” Institute, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (M.I.P.); (C.Ș.C.)
| | - Mara Mădălina Mihai
- Department of Oncologic Dermatology, “Elias” Emergency University Hospital, “Carol Davila” University of Medicine and Pharmacy, 020021 Bucharest, Romania; (C.I.C.); (C.G.); (L.G.P.); (M.M.M.)
- Research Institute of the University of Bucharest-ICUB, University of Bucharest, 050663 Bucharest, Romania (V.L.); (I.G.-B.)
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10
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Mateu-Arrom L, Puig L, Vilarrasa E. Surgical Approach to Hidradenitis Suppurativa. ACTAS DERMO-SIFILIOGRAFICAS 2025:S0001-7310(25)00219-4. [PMID: 40185225 DOI: 10.1016/j.ad.2025.04.003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/30/2024] [Revised: 09/01/2024] [Accepted: 10/20/2024] [Indexed: 04/07/2025] Open
Abstract
Hidradenitis suppurativa is a chronic inflammatory skin condition characterized by painful nodules, abscesses, and sinus tracts that may lead to irreversible scarring complications. Therapeutic options include antibiotics, biologic therapies, and surgical procedures. Current management of hidradenitis suppurativa favors early surgical intervention along with medical therapy to promote healing and minimize scars and complications in a disease characterized by a therapeutic window of opportunity. Surgical techniques range from incision and drainage to wide excision, with varying recurrence rates mainly based on the extent of procedures. Reconstruction techniques would vary primarily based on the extent of the defect and the area involved. In all cases, a good preoperative planning and delimitation with imaging modalities, preferably intra- or perioperative facilitates complete removal of involved tissue, preserving the integrity and function of healthy skin and minimizing recurrences.
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Affiliation(s)
- L Mateu-Arrom
- Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Universitat Autònoma de Barcelona, Barcelona, España.
| | - L Puig
- Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Universitat Autònoma de Barcelona, Barcelona, España
| | - E Vilarrasa
- Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Universitat Autònoma de Barcelona, Barcelona, España
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11
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Pulminskas A, Hojjatie R, Karatas TB, Li YH, Orenstein LAV. Hidradenitis Suppurativa Symptom Relief: Pain and Itch. Dermatol Clin 2025; 43:247-260. [PMID: 40023625 DOI: 10.1016/j.det.2024.12.009] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/04/2025]
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory skin condition that may cause debilitating pain and itch. Given their physical and psychological burden, recognition and treatment of HS-associated symptoms are critical for supporting patients with HS. The complex nature of HS pain, encompassing acute and chronic timing as well as nociceptive, neuropathic, and nociplastic character, requires a tailored treatment approach. Itch in HS, although less studied, is also a prevalent and distressing symptom. The aim of this narrative review is to apply current knowledge of HS pain and pruritus to develop a practical approach for symptomatic management in the dermatology office.
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Affiliation(s)
- Anna Pulminskas
- Department of Dermatology, Emory University School of Medicine, Atlanta, GA 30322, USA
| | - Roxana Hojjatie
- Department of Dermatology, Emory University School of Medicine, Atlanta, GA 30322, USA
| | - Turkan Banu Karatas
- Department of Dermatology, Emory University School of Medicine, Atlanta, GA 30322, USA
| | - Yiwen H Li
- Department of Dermatology, Emory University School of Medicine, Atlanta, GA 30322, USA
| | - Lauren A V Orenstein
- Department of Dermatology, Emory University School of Medicine, Atlanta, GA 30322, USA.
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12
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Knecht-Gurwin K, Matusiak L, Szepietowski JC. The preclinical discovery and development of secukinumab for the treatment of moderate-to-severe hidradenitis suppurativa. Expert Opin Drug Discov 2025; 20:405-417. [PMID: 40106842 DOI: 10.1080/17460441.2025.2482058] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/18/2024] [Accepted: 03/17/2025] [Indexed: 03/22/2025]
Abstract
INTRODUCTION Hidradenitis suppurativa (HS) is a chronic skin condition with a significant impact on patient quality of life, highlighting the need for innovative therapeutic approaches. HS is characterized by its chronicity; it presents in the form of painful nodules, abscesses, and sinus tracts or fistulas, typically localized in intertriginous areas, emerging in early adulthood and in predominantly the female population. AREAS COVERED In this review, the authors discuss the preclinical discovery and development of secukinumab for HS, highlighting target identification, validation, and compound selection. Methodologies such as high-content screening, chemoinformatics, and animal models that validate the IL-17 pathway's role in HS are explored. The transition from preclinical to clinical development, including pharmacokinetics (PK), pharmacodynamics (PD), and ADME-Tox studies, is elaborated. The literature search was conducted using PubMed, Web of Science, Scopus, UpToDate, Cochrane Library, Embase, and Google Scholar, covering relevant studies published up to December 2024. EXPERT OPINION The integration of secukinumab into HS treatment highlights the critical role of targeting the IL-17A pathway. Although efficacious and safe in trials, understanding secukinumab's long-term effects and optimal treatment placement remains challenging. Future research should prioritize the development of tailored therapeutic strategies that align with individual disease phenotypes and immune profiles to enhance treatment outcomes in HS management.
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Affiliation(s)
- Klaudia Knecht-Gurwin
- University Centre of General Dermatology and Oncodermatology, Wroclaw Medical University, Wroclaw, Poland
| | - Lukasz Matusiak
- Department of Dermato-Venereology, 4th Military Hospital, Wroclaw, Poland
- Faculty of Medicine, Wroclaw University of Science and Technology, Wroclaw, Poland
| | - Jacek C Szepietowski
- Department of Dermato-Venereology, 4th Military Hospital, Wroclaw, Poland
- Faculty of Medicine, Wroclaw University of Science and Technology, Wroclaw, Poland
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13
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Kimball AB, Bechara FG, Badat A, Giamarellos-Bourboulis EJ, Gottlieb AB, Jemec GBE, Reguiai Z, Villani AP, Alarcon I, Bansal A, Gasperoni F, Martin R, Paguet B, Uhlmann L, Zouater H, Ravichandran S, Alavi A. Long-term efficacy and safety of secukinumab in patients with moderate-to-severe hidradenitis suppurativa: week 104 results from the SUNSHINE and SUNRISE extension trial. Br J Dermatol 2025; 192:629-640. [PMID: 39611771 DOI: 10.1093/bjd/ljae469] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/25/2024] [Revised: 11/26/2024] [Accepted: 11/26/2024] [Indexed: 11/30/2024]
Abstract
BACKGROUND The SUNSHINE and SUNRISE phase III trials demonstrated sustained clinical efficacy of secukinumab in patients with moderate-to-severe hidradenitis suppurativa (HS) through 52 weeks. Patients completing the core trials could enter a 4-year extension trial. OBJECTIVES To evaluate the long-term efficacy, safety/tolerability and maintenance of clinical response to secukinumab through week 104 in the extension trial. METHODS Patients with a hidradenitis suppurativa (HS) clinical response (HiSCR) at week 52 of the core trials (extension trial baseline visit) entered a randomized withdrawal period. HiSCR responders receiving subcutaneous secukinumab 300 mg every 2 or 4 weeks (SECQ2W/SECQ4W) through week 52 in the core trials were randomized 2 : 1 to continue secukinumab (SECQ2W-R-Q2W or SECQ4W-R-Q4W) or receive placebo (SECQ2W-R-PBO or SECQ4W-R-PBO) through week 104. The primary endpoint was time to loss of response (LOR; newly defined for this trial) through week 104 in week 52 HiSCR responders (SECQ2W-R-Q2W vs. SECQ2W-R-PBO and SECQ4W-R-Q4W vs. SECQ4W-R-PBO). Time to LOR was tested at 1.25% (one-sided) for each comparison (one-sided familywise alpha of 2.5%) through week 104. If LOR was met, patients could remain in the trial on open-label secukinumab treatment. Additional endpoints included safety and HiSCR. The trial was registered with ClinicalTrials.gov (NCT04179175). RESULTS Overall, 84.3% of patients who completed the core trials entered the extension trial; 55.9% were week 52 HiSCR responders. The primary endpoint was not met for either secukinumab dosing regimen. The estimated risk reduction for LOR was 13% (SECQ2W-R-Q2W vs. SECQ2W-R-PBO; one-sided P = 0.25) and 30% (SECQ4W-R-Q4W vs. SECQ4W-R-PBO; one-sided P = 0.04). The median time to LOR was numerically longer in the secukinumab arms vs. placebo {SECQ2W-R-Q2W [283 days; 95% confidence interval (CI) 176, -] vs. SECQ2W-R-PBO [239 days; 95% CI 120, -]; SECQ4W-R-Q4W [365 days 95% CI 225, -] vs. SECQ4W-R-PBO [171 days; 95% CI 113-337]}. In week 52 HiSCR responders reporting LOR, 44% (SECQ2W-R-Q2W), 58% (SECQ2W-R-PBO), 40% (SECQ4W-R-Q4W) and 34% (SECQ4W-R-PBO) were achieving HiSCR at the time of LOR. Overall, the safety of secukinumab was consistent with the core trials. CONCLUSIONS The primary endpoint of this trial was not met. HiSCR was maintained in many patients at the time of LOR. The safety of secukinumab was consistent with the previously characterized safety profile in the core trials.
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Affiliation(s)
- Alexa B Kimball
- Harvard Medical School and Clinical Laboratory for Epidemiology and Applied Research in Skin (CLEARS), Department of Dermatology, Beth Israel Deaconess Medical Center, Boston, MA, USA
| | - Falk G Bechara
- International Centre for Hidradenitis Suppurativa/Acne Inversa (ICH), Department of Dermatology, Venereology and Allergology, Ruhr-University Bochum, Bochum, Germany
| | - Aysha Badat
- Chris Hani Baragwanath Academic Hospital, Soweto, Gauteng, South Africa
| | | | - Alice B Gottlieb
- Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York City, NY, USA
| | - Gregor B E Jemec
- Department of Dermatology, Zealand University Hospital, Roskilde, Denmark
| | - Ziad Reguiai
- Dermatology Department, Polyclinique Courlancy-Bezannes, Reims, France
| | - Axel P Villani
- Department of Dermatology, Edouard Herriot Hospital, Hospices Civils de Lyon, Claude Bernard Lyon I University, Lyon, France
| | | | | | | | - Ruvie Martin
- Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA
| | | | | | | | | | - Afsaneh Alavi
- Department of Dermatology, Mayo Clinic, Rochester, MN, USA
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14
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Rao S, Sharma A, Kumaran MS, Narang T, Sinha A, Dogra S. Disease severity assessment in hidradenitis suppurativa: A single-centre cross-sectional study utilising clinical evaluation, high-resolution ultrasound and colour doppler. Indian J Dermatol Venereol Leprol 2025; 91:145-151. [PMID: 39912177 DOI: 10.25259/ijdvl_542_2024] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/15/2024] [Accepted: 08/02/2024] [Indexed: 02/07/2025]
Abstract
Background Hidradenitis suppurativa (HS) is a chronic inflammatory skin disorder characterised by recurrent painful nodules, abscesses, and sinus tract formation in intertriginous areas. Accurate staging of this disorder is crucial for appropriate management and prognosis. The role of imaging in the staging of HS is still evolving. Objectives To assess the correlation between clinical disease severity staging and high-resolution ultrasonography and colour doppler (HRUS-CD) staging in HS patients. Methods This was a cross-sectional, single-centre study in patients above 18 years of age with the clinical diagnosis of HS. All patients underwent clinical examination and high-resolution ultrasonography and colour doppler study with high-frequency linear probe (L+ 8-24 MHz). Correlations between clinical Hurley staging and the various ultrasonographic parameters i.e. SOS-HS (sonographic staging of severity of HS), degree of vascularisation, fibrotic scarring and oedema were explored and analysed. Spearman's correlation coefficient was applied to study the correlations and p<0.05 was considered significant. Results A total of 46 patients with HS who met the inclusion criteria were included. The majority of patients were clinically in Hurley stages 1 (32.6%; n=15) and 2 (56.5%; n=26) (41 in all). However, on the basis of ultrasonographic findings, significant numbers of patients had greater severity of staging on SOS-HS (58.5%; n=24/41), higher vascularity on colour doppler (26.8%; n=11), more severe grading of fibrous scarring (43.9%; n=18) and oedema (68.2%; n=28) in comparison to the clinical Hurley staging. Limitations Limitations of our study include a small sample size and cross-sectional design. Conclusion The results of the study indicate that the majority of the patients were under-staged and under-treated clinically, hence emphasising the role of high-resolution ultrasonography and colour doppler study in the accurate determination of HS severity. Future research should focus on standardised protocols and larger, prospective studies to establish the role of these imaging modalities in routine clinical practice.
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Affiliation(s)
- Sophia Rao
- Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
| | - Apoorva Sharma
- Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
| | - Muthu Sendhil Kumaran
- Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
| | - Tarun Narang
- Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
| | - Anindita Sinha
- Department of Radiodiagnosis and Imaging, Postgraduate Institute of Medical Education and Research, Chandigarh, India
| | - Sunil Dogra
- Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
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15
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Tafica A, Fida M, Bardhi B, Toçi E, Vasili E. Hidradenitis suppurativa: A prospective epidemiologic study in Albania. J Eur Acad Dermatol Venereol 2025; 39:e239-e241. [PMID: 38994731 DOI: 10.1111/jdv.20240] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/29/2024] [Accepted: 06/23/2024] [Indexed: 07/13/2024]
Affiliation(s)
- A Tafica
- Department of Dermatology, University Hospital Center "Mother Teresa", Tirana, Albania
| | - M Fida
- Department of Dermatology, University Hospital Center "Mother Teresa", Tirana, Albania
- Dermatology Department, Faculty of Medicine, University of Medicine of Tirana, Tirana, Albania
| | - B Bardhi
- Outpatient Clinic Nr.3, Tirana, Albania
| | - E Toçi
- Department of Public Health, Faculty of Medicine, University of Medicine of Tirana, Tirana, Albania
| | - E Vasili
- Department of Dermatology, University Hospital Center "Mother Teresa", Tirana, Albania
- Dermatology Department, Faculty of Medicine, University of Medicine of Tirana, Tirana, Albania
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16
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Frew J, Smith A, Penas PF, Ellis E, Foley P, Rubel D, McMeniman E, Marshman G, Saunders H, Veysey E, Nicolopolous J, Spelman L, Gebauer K. Australasian hidradenitis suppurativa management guidelines. Australas J Dermatol 2025; 66:75-89. [PMID: 39578415 PMCID: PMC11898165 DOI: 10.1111/ajd.14388] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/11/2024] [Revised: 08/22/2024] [Accepted: 11/13/2024] [Indexed: 11/24/2024]
Abstract
Hidradenitis Suppurativa is a burdensome inflammatory skin disease with significant quality of life impact. These management guidelines were developed to direct appropriate clinical management in the Australasian context. A systematic review was used for the basis of the consensus guidelines. Thirteen clinical experts were involved in a modified Delphi consensus process to develop the guidelines and treatment algorithms. Overall management strategies include appropriate severity assessment of disease and comorbidities, multimodal therapy with systemic and local treatments, and evidence-based progression along the therapeutic ladder in the event of inadequate response. Sequential monotherapy with antibiotics and/or single agent therapy is discouraged and aggressive treatment of moderate to severe disease to capture the window of opportunity is highly emphasised. Specific considerations in the setting of disease comorbidities, pregnancy and breastfeeding are also addressed. Overall, the complex nature of HS requires a complex and multimodal therapeutic response with medical, physical and surgical therapies to achieve best patient outcomes.
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Affiliation(s)
- John Frew
- The Skin HospitalSydneyNew South WalesAustralia
- Department of Dermatology, Liverpool HospitalSydneyNew South WalesAustralia
- University of New South WalesSydneyNew South WalesAustralia
| | - Annika Smith
- The Skin HospitalSydneyNew South WalesAustralia
- Department of Dermatology, Westmead HospitalSydneyNew South WalesAustralia
- University of SydneySydneyNew South WalesAustralia
| | - Pablo Fernandez Penas
- Department of Dermatology, Westmead HospitalSydneyNew South WalesAustralia
- University of SydneySydneyNew South WalesAustralia
| | | | - Peter Foley
- Skin Health Institute MelbourneMelbourneVictoriaAustralia
- St Vincent's HospitalMelbourneVictoriaAustralia
| | - Diana Rubel
- Canberra HospitalCanberraAustralian Capital TerritoryAustralia
| | | | - Gillian Marshman
- Flinders Medical CentreAdelaideSouth AustraliaAustralia
- Flinders UniversityAdelaideSouth AustraliaAustralia
| | | | - Emma Veysey
- St Vincent's HospitalMelbourneVictoriaAustralia
| | | | - Linda Spelman
- Queensland Institute of DermatologyBrisbaneQueenslandAustralia
| | - Kurt Gebauer
- Fremantle DermatologyFremantleWestern AustraliaAustralia
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Haselgruber S, Muñoz‐Barba D, Leon‐Pérez FJ, Cuenca‐Barrales C, Arias‐Santiago S, Molina‐Leyva A. Therapeutic burden in hidradenitis suppurativa: a cross-sectional study of 557 patients. Int J Dermatol 2025; 64:539-545. [PMID: 39407357 PMCID: PMC11840222 DOI: 10.1111/ijd.17517] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/14/2024] [Revised: 08/23/2024] [Accepted: 09/28/2024] [Indexed: 02/21/2025]
Abstract
INTRODUCTION Therapeutic burden (TB) has been identified as a potential predictor of response to biologic therapy in hidradenitis suppurativa (HS). We aim to analyze the determinants of TB in real-world clinical settings among HS patients to explain this concept and its utility as an additional tool for guiding therapeutic decision-making. METHODS We conducted a cross-sectional study including all consecutive HS patients attending a specialized HS clinic between 2017 and 2024. The primary variable was TB, defined as the cumulative sum of prior systemic treatment cycles and surgical interventions for HS. We analyzed whether sociodemographic or clinical factors were associated with a higher TB. RESULTS We included 557 HS patients. Of these, 50.81% were women, and the mean age was 41.87 (14.19) years. Most patients (62.30%) were referred from general dermatology consultations. The mean disease duration was 17.52 (11.51) years. Regarding disease severity, 46.50% presented with Hurley II, and 42.19% had an IHS-4 score between 4 and 10. Before their baseline visit, 9.70% of patients had received biological therapy, mostly adalimumab (88.89%). The mean TB was 2.42 (2.25) systemic medical and/or surgical interventions. Referral from general dermatology or other hospital departments, older age, longer disease duration, greater HS severity, presence of pilonidal sinus, and prior biological therapy were significantly associated with higher TB. CONCLUSIONS Our findings suggest that TB comprehensively captures HS severity and progression factors. This metric could prove valuable in aiding decision-making for HS patients by indicating when a change in therapy might be necessary.
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Affiliation(s)
- Sofía Haselgruber
- Hospital Universitario Virgen de las NievesServicio de DermatologíaGranadaSpain
- Instituto de Investigación Biosanitaria ibs.GRANADAGranadaSpain
- European Hidradenitis Suppurativa Foundation e.VDessauGermany
| | - Daniel Muñoz‐Barba
- Hospital Universitario Virgen de las NievesServicio de DermatologíaGranadaSpain
- Instituto de Investigación Biosanitaria ibs.GRANADAGranadaSpain
| | - Francisco Javier Leon‐Pérez
- Hospital Universitario Virgen de las NievesServicio de DermatologíaGranadaSpain
- Instituto de Investigación Biosanitaria ibs.GRANADAGranadaSpain
| | - Carlos Cuenca‐Barrales
- Hospital Universitario Virgen de las NievesServicio de DermatologíaGranadaSpain
- Instituto de Investigación Biosanitaria ibs.GRANADAGranadaSpain
| | - Salvador Arias‐Santiago
- Hospital Universitario Virgen de las NievesServicio de DermatologíaGranadaSpain
- Instituto de Investigación Biosanitaria ibs.GRANADAGranadaSpain
- Facultad de MedicinaUniversidad de GranadaGranadaSpain
| | - Alejandro Molina‐Leyva
- Hospital Universitario Virgen de las NievesServicio de DermatologíaGranadaSpain
- Instituto de Investigación Biosanitaria ibs.GRANADAGranadaSpain
- European Hidradenitis Suppurativa Foundation e.VDessauGermany
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18
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Marzano AV, Bartoletti M, Bettoli V, Bianchi L, Chiricozzi A, Clerici M, Dapavo P, Dini V, Foti C, Magnoni C, Megna M, Micali G, Molinelli E, Prignano F. Hidradenitis suppurativa, from basic science to surgery and a new era of tailored targeted therapy: An expert opinion paper. Arch Dermatol Res 2025; 317:511. [PMID: 40021535 PMCID: PMC11870890 DOI: 10.1007/s00403-025-04016-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/23/2025] [Revised: 01/23/2025] [Accepted: 02/12/2025] [Indexed: 03/03/2025]
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory disease characterised by an aberrant activation of innate immunity and increased production of pro-inflammatory mediators such as interleukin 17 (IL-17). IL-17 has been shown to play a key role in the pathogenesis of HS and evidence highlights the potential of IL-17-targeted therapies. The fully human IgG/κ monoclonal antibody secukinumab, which specifically targets IL-17A and inhibits interaction with its receptor, has recently been approved for the treatment of moderate-to-severe HS. Secukinumab offers patients an efficacious and well-tolerated treatment option in terms of sustained response by rapidly improving signs and symptoms, and preventing disease progression in the absence of loss of response. Being a challenging disease, HS is associated with a delay to diagnosis of 3-10 years and, consequently, late implementation of appropriate treatment, leading to disease progression. Misdiagnosis due to flawed understanding and lack of awareness among medical providers and patients is considered an important factor contributing to the delayed diagnosis. Thus, serious efforts must be made on a large scale to urgently reduce the delay in HS diagnosis and reduce the disease burden in patients, including raising awareness, implementation of education programmes at medical and specialisation schools, as well as continuous education of healthcare providers at different levels for the early detection of HS and initiation of appropriate treatment. Here, we present the main critical unmet needs in the diagnosis and treatment of patients affected by HS, address how disease awareness and comprehensive multidisciplinary management (offering both medical and surgical care) can benefit patients, and suggest therapeutic options, based on clinical characterisation and early identification and intervention (window of opportunity), to be adopted for a timely and better management of disease progression and to fill current gaps.
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Affiliation(s)
- Angelo Valerio Marzano
- Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
- Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.
| | - Michele Bartoletti
- Department of Biomedical Sciences, Humanitas University, Milan, Italy
- Infectious Disease Unit, IRCCS Humanitas Research Hospital, Rozzano, Italy
| | - Vincenzo Bettoli
- O.U. Of Dermatology, Department of Medical Sciences, University of Ferrara, Ferrara, Italy
| | - Luca Bianchi
- Dermatology, Fondazione Policlinico Tor Vergata, Department of Systems Medicine, Tor Vergata University, Rome, Italy
| | - Andrea Chiricozzi
- Dermatologia, Dipartimento Universitario di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome, Italy
- U.O.C. Dermatologia, Dipartimento di Scienze Mediche e Chirurgiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy
| | - Mario Clerici
- Università Degli Studi Di Milano, Milan, Italy
- Don C Gnocchi Foundation IRCCS, Milan, Italy
| | - Paolo Dapavo
- Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino, Turin, Italy
| | | | | | - Cristina Magnoni
- Surgical, Medical and Dental Department of Morphological Sciences Related to Transplant, Oncology and Regenerative Medicine, University of Modena and Reggio Emilia, Modena, Italy
| | - Matteo Megna
- Section of Dermatology, Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy
| | | | - Elisa Molinelli
- Department of Clinical and Molecular Science, Dermatologic Clinic, Azienda Ospedaliero Universitaria delle Marche, Ancona, Italy
| | - Francesca Prignano
- Department of Health Sciences, Dermatology Section, Università degli Studi di Firenze, Florence, Italy
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19
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Klufas DM, Ojute F, Shochat G, Naik HB. Diagnosis and management of hidradenitis suppurativa: a review for the emergency clinician. Emerg Med J 2025; 42:202-208. [PMID: 39251339 DOI: 10.1136/emermed-2024-213949] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/24/2024] [Accepted: 07/26/2024] [Indexed: 09/11/2024]
Abstract
Hidradenitis suppurativa (HS) is a complex, chronic skin disease characterised by painful inflammatory nodules, abscesses, dermal tunnels, sinus tracts and fistulae with a predilection for intertriginous skin. HS carries a substantial disease burden due to its prevalence, associated comorbidities and quality of life impacts and is associated with high healthcare resource utilisation. Clarity regarding the prevalence and pathogenesis of HS has led to improved therapies and more patients seeking care in both outpatient and acute care settings, including the emergency department. Emergency medicine providers play a critical role in HS diagnosis, management of acute flares and connection of HS patients with long-term dermatologic care, which can in turn help manage utilisation of acute care resources.
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Affiliation(s)
- Daniel M Klufas
- Dermatology, University of California San Francisco, San Francisco, California, USA
| | - Feyisayo Ojute
- School of Medicine, University of California San Francisco, San Francisco, California, USA
| | - Guy Shochat
- Emergency Medicine, University of California San Francisco, San Francisco, California, USA
| | - Haley B Naik
- Dermatology, University of California San Francisco, San Francisco, California, USA
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20
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Mateu-Arrom L, Puig L, Vilarrasa E. Surgical Approach to Hidradenitis Suppurativa. ACTAS DERMO-SIFILIOGRAFICAS 2025:S0001-7310(25)00094-8. [PMID: 39961528 DOI: 10.1016/j.ad.2024.10.061] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/30/2024] [Revised: 09/01/2024] [Accepted: 10/20/2024] [Indexed: 03/08/2025] Open
Abstract
Hidradenitis suppurativa is a chronic inflammatory skin condition characterized by painful nodules, abscesses, and sinus tracts that may lead to irreversible scarring complications. Therapeutic options include antibiotics, biologic therapies, and surgical procedures. Current management of hidradenitis suppurativa favors early surgical intervention along with medical therapy to promote healing and minimize scars and complications in a disease characterized by a therapeutic window of opportunity. Surgical techniques range from incision and drainage to wide excision, with varying recurrence rates mainly based on the extent of procedures. Reconstruction techniques would vary primarily based on the extent of the defect and the area involved. In all cases, a good preoperative planning and delimitation with imaging modalities, preferably intra- or perioperative facilitates complete removal of involved tissue, preserving the integrity and function of healthy skin and minimizing recurrences.
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Affiliation(s)
- L Mateu-Arrom
- Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.
| | - L Puig
- Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain
| | - E Vilarrasa
- Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain
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21
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Ingram JR, Marzano AV, Prens E, Schneider-Burrus S, Warren RB, Keal A, Jha R, Hernandez Daly AC, Kimball AB. Hidradenitis suppurativa with and without draining tunnels: A real-world study characterizing differences in treatment and disease burden. J Eur Acad Dermatol Venereol 2025. [PMID: 39903577 DOI: 10.1111/jdv.20550] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/15/2024] [Accepted: 01/03/2025] [Indexed: 02/06/2025]
Abstract
BACKGROUND Hidradenitis suppurativa (HS) is a chronic, inflammatory, neutrophilic skin disease associated with a considerable clinical burden. In more severe disease, subepidermal draining tunnels may form. OBJECTIVES To characterize the clinical profile of patients with moderate-severe HS with and without draining tunnels, and the clinical and health-related quality of life (HR-QoL) burden of draining tunnels. METHODS Data were drawn from the Adelphi HS Disease Specific Programme™, a cross-sectional survey with retrospective data collection, across the United States, France, Germany, Italy, Spain and the United Kingdom between November 2020 and April 2021. Patients were aged ≥10 years and had HS. Clinical outcomes, recorded by physicians, comprised patient demographics and HS characteristics, symptoms and treatment. HR-QoL measures included patient and physician survey questions, and validated HR-QoL instruments. RESULTS Of the 580 patients with moderate-severe HS, 46% had draining tunnels. Patients with draining tunnels had more abscesses, inflammatory nodules and scarring than those without. Patients with draining tunnels were significantly (p < 0.05) more likely to be treated with biologics (41% vs. 27%), but often patients with tunnels who were eligible for biologics had not received them. Patients with draining tunnels experienced significantly more inflammation/redness (73% vs. 63%), drainage from lesions (62% vs. 40%) and pain on sitting (48% vs. 37%) than those without (p < 0.05). Draining tunnels were also significantly associated with low mood/depression (30% vs. 18%), sleep disturbance (28% vs. 19%) and fatigue (28% vs. 18%) versus no tunnels (p < 0.05). Physicians agreed that patients with draining tunnels experienced a negative impact of disease compared to those without. This was reflected in patient-reported surveys and HR-QoL instruments. CONCLUSIONS Patients with moderate-severe HS and draining tunnels experience greater clinical and HR-QoL burden than those without, emphasizing the importance of tunnels in disease impact.
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Affiliation(s)
- J R Ingram
- Division of Infection and Immunity, Cardiff University, University Hospital of Wales, Cardiff, UK
| | - A V Marzano
- Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy
- Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy
| | - E Prens
- Department of Dermatology, Erasmus University Medical Center, Rotterdam, The Netherlands
| | | | - R B Warren
- Dermatology Centre, Northern Care Alliance NHS Foundation Trust, Manchester, UK
- NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK
| | - A Keal
- Adelphi Real World, Bollington, UK
| | - R Jha
- Boehringer Ingelheim International GmbH, Ingelheim Am Rhein, Germany
| | | | - A B Kimball
- Harvard Medical School and Clinical Laboratory for Epidemiology and Applied Research in Skin, Department of Dermatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
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22
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Esme P, Botsali A, Caliskan E. Interruption versus continuation of adalimumab during hidradenitis surgery: secondary wound healing and postoperative complications. J Wound Care 2025; 34:112-118. [PMID: 39928475 DOI: 10.12968/jowc.2021.0365] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 02/12/2025]
Abstract
OBJECTIVE The combination of adalimumab and surgical interventions plays a crucial role in managing severe hidradenitis suppurativa (HS). However, there is still limited scientific evidence regarding administering adalimumab during the perioperative period. This study aimed to evaluate whether adalimumab could adversely affect postoperative complications and the total time of wound closure (TTWC) in patients undergoing cutaneous surgery for HS. METHOD In this single-centre cohort study, patients with HS were allocated to two groups. Group 1 (biological cohort) consisted of patients with HS who had continuously received adalimumab for at least three months before the procedure. Group 2 (non-biological cohort) patients underwent cutaneous surgery after only four weeks of anti-inflammatory medication. All patients were left to secondary wound healing. RESULTS A total of 30 surgical sites in 20 patients were included in the study (Group 1: 15 surgical sites/nine patients; Group 2: 15 surgical sites/11 patients). Disease severity and excised skin areas were significantly higher in Group 1 (p<0.001 and p=0.042, respectively) than in Group 2. While the median TTWC was longer in Group 1 than in Group 2 (p=0.004), multivariate regression analysis showed that TTWC was associated with the excised skin area (p=0.016) and Hurley stage (p=0.032), but was not affected by the use of adalimumab (p=0.076). CONCLUSION In this study, the use of adalimumab around surgery was not associated with an increased risk of postoperative complications or a prolonged course of wound closure. The results in this patient cohort suggest that adalimumab should not be discontinued during the perioperative period of HS surgery.
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Affiliation(s)
- Pelin Esme
- University of Health Sciences, Gulhane Training and Research Hospital, Department of Dermatology and Venereology, Ankara, Turkey
| | - Aysenur Botsali
- University of Health Sciences, Gulhane Training and Research Hospital, Department of Dermatology and Venereology, Ankara, Turkey
| | - Ercan Caliskan
- University of Health Sciences, Gulhane Training and Research Hospital, Department of Dermatology and Venereology, Ankara, Turkey
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23
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Miskinyte S, Duchatelet S, Delage M, Ungeheuer MN, Auffret N, Binois R, Guillem P, Join-Lambert O, Nassif A, Hovnanian A. Clinical characteristics and genetic analysis of 14 patients affected with acne (A) fulminans and hidradenitis suppurativa (SH): ASH syndrome, a new phenotypic entity. J Am Acad Dermatol 2025; 92:332-334. [PMID: 39401609 DOI: 10.1016/j.jaad.2024.07.1533] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/30/2023] [Revised: 07/12/2024] [Accepted: 07/31/2024] [Indexed: 11/10/2024]
Affiliation(s)
- Snaigune Miskinyte
- INSERM UMR1163, Laboratory of Genetic Skin Diseases, Imagine Institute, Paris, France; University Paris Cité, Paris, France
| | - Sabine Duchatelet
- INSERM UMR1163, Laboratory of Genetic Skin Diseases, Imagine Institute, Paris, France; University Paris Cité, Paris, France
| | - Maïa Delage
- University Paris Cité, Paris, France; Institut Pasteur, Centre Médical de l'Institut Pasteur, Paris, France
| | | | | | | | | | - Olivier Join-Lambert
- CHU de Caen, Laboratoire de Microbiologie, Caen, France; Normandy University, Rouen, France
| | - Aude Nassif
- University Paris Cité, Paris, France; Institut Pasteur, Centre Médical de l'Institut Pasteur, Paris, France.
| | - Alain Hovnanian
- INSERM UMR1163, Laboratory of Genetic Skin Diseases, Imagine Institute, Paris, France; University Paris Cité, Paris, France; Department of Genomic Medicine of Rare Diseases, Hôpital Necker Enfants Malades, AP-HP, Paris, France
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24
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Özbek L, Güldan M, Alpsoy E, Vural S. Hidradenitis Suppurativa Treatment During Pregnancy and Lactation: Navigating Challenges. Int J Dermatol 2025. [PMID: 39887706 DOI: 10.1111/ijd.17672] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 10/31/2024] [Revised: 11/22/2024] [Accepted: 01/16/2025] [Indexed: 02/01/2025]
Abstract
Hidradenitis suppurativa (HS), or acne inversa, is a chronic inflammatory skin condition primarily affecting skin folds such as the axilla, groins, and the inframammary, perineal, and perianal regions. It is characterized by painful abscesses, sinus tracts, and scarring. Predominantly affecting young adults, particularly females, HS often emerges during reproductive age, and flares are widely reported during pregnancy and postpartum, underscoring the need to consider management strategies tailored to pregnant or lactating individuals. Moreover, the chronic and relapsing nature of HS, along with challenges related to the safety and compliance of medication use during pregnancy and lactation, as well as various comorbidities and psychological distress, significantly complicate its management in pregnant or lactating women. Treatment options, including topical clindamycin, oral clindamycin-rifampicin, adalimumab, metformin, antiseptic washes, and certolizumab pegol, have accumulated evidence supporting their relative safety in pregnant and lactating women. While certolizumab pegol has shown promising safety data among biologics, it requires more efficacy data in HS. Conversely, while newly approved HS medications such as secukinumab and bimekizumab show promise for the general population, further research is necessary to evaluate their safety profiles in pregnant and breastfeeding individuals. The scant research available on HS in pregnant and lactating women, also shown by our systematic literature review, highlights the need for a comprehensive investigation into the safety, efficacy, and suitability of management strategies.
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Affiliation(s)
- Laşin Özbek
- School of Medicine, Koç University, Istanbul, Turkey
| | | | - Erkan Alpsoy
- Department of Dermatology and Venereology, Akdeniz University School of Medicine, Antalya, Turkey
| | - Seçil Vural
- Department of Dermatology and Venereology, Koç University School of Medicine, Istanbul, Turkey
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25
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Caliezi A, Rabufetti A, Hunger R, Wolf R, Seyed Jafari SM. Impact of Hidradenitis Suppurativa on Sexual Quality of Life. J Clin Med 2025; 14:910. [PMID: 39941581 PMCID: PMC11818454 DOI: 10.3390/jcm14030910] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/08/2025] [Revised: 01/24/2025] [Accepted: 01/24/2025] [Indexed: 02/16/2025] Open
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory skin condition that affects about 1% of the world's population. It is characterized by round, painful nodules, abscesses or sinuses, often in the genital area. HS has the worst impact on quality of life (QoL) of any dermatological condition. Methods: The aim of this systematic review is to analyze how HS affects patients' sexual quality of life (SQoL), herein defined as a person's evaluation of their sexual relationships, including physical and mental aspects, and their response to this evaluation. Results: The systematic search yielded 41 primary results. After screening, 6 studies were selected for this review. Men with HS suffer from lower SQoL than male controls and sexual dysfunction is more common in both male and female patients than in controls. Sexual dysfunction is worse in all HS patients than in controls, and worse in female patients than in male patients. Disease severity is not related to any of the sexual concepts analysed. Conclusions: HS has a strong impact on SQoL, as patients suffer from sexual dysfunction and sexual distress more often than healthy controls, and feel that their relationships are negatively affected by the disease. Therefore, the impact of HS on SQoL should be further investigated, especially the psychological aspect of SQoL.
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26
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Gisondi P, Montalto E, Curic T, Danese E, Bellinato F, Girolomoni G. Certolizumab pegol in severe hidradenitis suppurativa in pregnancy: A case report. SAGE Open Med Case Rep 2025; 13:2050313X241311374. [PMID: 39803378 PMCID: PMC11724419 DOI: 10.1177/2050313x241311374] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/07/2024] [Accepted: 11/18/2024] [Indexed: 01/16/2025] Open
Abstract
Hidradenitis suppurativa is a chronic inflammatory disease of the skin with a suppurative-cicatricial outcome affecting the infundibular component of the pilo-sebaceous unit. The lesions are typically localized in the intertriginous and apocrine gland-rich areas. Hidradenitis suppurativa mainly affects patients at a young age and is very often refractory to conventional medical treatment. During pregnancy, the management of hidradenitis suppurativa becomes demanding due to the need of safety therapies. Certolizumab pegol is a pegylated monoclonal TNF-α inhibitor that lacks the fragment crystallizable region preventing active placental transfer and could be used in pregnancy and lactation if clinically needed and is label for chronic plaque psoriasis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease. Herein, we describe a case of a 32-year-old pregnant woman with Hurley stage III hidradenitis suppurativa successfully treated with certolizumab pegol.
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Affiliation(s)
- Paolo Gisondi
- Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy
| | - Elena Montalto
- Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy
| | - Tea Curic
- Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy
| | - Elisabetta Danese
- Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy
| | - Francesco Bellinato
- Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy
| | - Giampiero Girolomoni
- Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy
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27
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Kaya G, Özgen FP, Kelahmetoğlu O, Su Küçük Ö, Onsun N. Demographic features, clinical characteristics, and comorbid relation in hidradenitis suppurativa: a population-based study. Front Med (Lausanne) 2025; 11:1499509. [PMID: 39850102 PMCID: PMC11755345 DOI: 10.3389/fmed.2024.1499509] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/20/2024] [Accepted: 12/16/2024] [Indexed: 01/25/2025] Open
Abstract
Background/objective Hidradenitis suppurativa (HS) is a chronic inflammatory disease affecting apocrine gland areas, characterized by painful nodules and abscesses that may result in sinus tracts and scarring. The global prevalence of HS is increasing due to heightened awareness, improved diagnostic methods, rising obesity rates, and higher smoking prevalence. This study aimed to describe the epidemiological, clinical, and comorbid characteristics of HS patients. Methodology This retrospective descriptive cross-sectional study included 193 outpatients aged between 15 and 73 years who visited a tertiary HS clinic between 2017 and 2022. Demographic, clinical, and comorbid characteristics were recorded and analyzed using chi-square and ordinal regression methods. Results The mean age was 34.5 ± 12.1 years, with a mean disease duration of 5.9 ± 6.7 years. According to the Hurley classification, 61.1, 24.4, and 14.5% were stages I, II, and III, respectively. Comorbidities were present in 48.2% of patients, with psychiatric disorders (19.2%), diabetes mellitus (14%), and hypertension (9.3%) being most common. Disease duration, smoking, male gender, and atypical localization were associated with increased disease severity. Conclusion Geographic and cultural factors influence the prevalence, severity, and management of HS, necessitating tailored treatment. Effective management requires multidisciplinary screening for early detection and prevention of comorbidities, including psychiatric disorders, cardiovascular conditions, and metabolic syndrome.
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Affiliation(s)
- Gökhan Kaya
- Ministry of Health Nizip State Hospital, Department of Dermatology, Gaziantep, Türkiye
| | | | - Osman Kelahmetoğlu
- Istanbul Okan University, Department of Plastic, Reconstructive, and Aesthetic Surgery, Istanbul, Türkiye
| | - Özlem Su Küçük
- Department of Dermatology, Faculty of Medicine, Bezmialem Vakif University, Istanbul, Türkiye
| | - Nahide Onsun
- Department of Dermatology, Biruni University, İstanbul, Türkiye
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28
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Chiang N, Alhusayen R. Hidradenitis Suppurativa: A Review of the Biologic and Small Molecule Immunomodulatory Treatments. J Cutan Med Surg 2025; 29:NP1-NP20. [PMID: 39604305 PMCID: PMC11829511 DOI: 10.1177/12034754241300292] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/29/2024]
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease that presents as painful, deep-seated nodules, sinus tracts, and abscesses in about 1% of the population. Although the pathogenesis of HS is not perfectly understood, it is generally recognized to be caused by a combination of genetic, endocrine, environmental, and microbiological factors. The treatment principles of HS focus on decreasing the microbial load with antibiotics and/or modulating the host immune response to reduce inflammation. The treatment of adults with moderate-to-severe HS has significantly changed recently with the development of new biological medications and immunomodulators. While previously the mainstay of treatment of moderate-to-severe HS was adalimumab, a biologic tumour necrosis factor α inhibitor, the evidence for the use of other treatment classes such as interleukin (IL)-17 inhibitors, IL-1 inhibitors, and Janus kinase inhibitors has been growing. The goal of this review article is to review the available evidence that supports the efficacy and safety of biologics and small molecule immunomodulator treatments to treat adults with moderate-to-severe HS.
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Affiliation(s)
- Nicholas Chiang
- Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada
| | - Raed Alhusayen
- Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada
- Department of Dermatology, Sunnybrook Health Sciences Centre, Toronto, ON, Canada
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29
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McCarthy S. Hidradenitis Suppurativa. Annu Rev Med 2025; 76:69-80. [PMID: 39869430 DOI: 10.1146/annurev-med-051223-031234] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/29/2025]
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease characterized by the formation of nodules, abscesses, and fistulae at intertriginous sites. Pain, pruritus, malodor, and suppuration have a significant impact on quality of life for HS patients. Prevalence figures vary greatly in the literature from 0.05% to 4.1%, and HS is more common in females. The current understanding of the etiology and pathogenesis of HS is incomplete; numerous hypotheses concern the interplay of lifestyle factors, skin microbiota, genetics, and a dysregulated immune system. Due to its phenotypic heterogeneity and multifactorial pathogenesis, HS is a complex disease that can prove challenging to manage. Two approved biologic therapies for the management of HS have led to clinical response in approximately 50% of treated patients. New therapies targeting the interleukin (IL)-1, IL-17, IL-36, and Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathways are in ongoing clinical trials, and preliminary data offer hope for greater clinical efficacy in HS in the future.
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Affiliation(s)
- S McCarthy
- Division of Dermatology, University College Cork, The National University of Ireland, Cork, Ireland;
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30
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Garbayo-Salmons P, Vilarrasa E, Bassas-Vila J, Mora-Fernández V, Fuertes I, Luque-Luna M, Fornons-Servent R, Martin-Ezquerra G, Aguayo-Ortiz RS, Ceravalls J, Mollet J, Gómez Tomás Á, Masferrer E, Corral-Magaña O, Matas-Nadal C, Del Estal J, Fuertes Bailón D, Calvet J, Romaní J. Real-world adalimumab survival and discontinuation factors in hidradenitis suppurativa. J Eur Acad Dermatol Venereol 2025; 39:221-229. [PMID: 38687278 DOI: 10.1111/jdv.20044] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/08/2024] [Accepted: 03/11/2024] [Indexed: 05/02/2024]
Abstract
BACKGROUND AND OBJECTIVES Survival analyses can provide valuable insights into effectiveness and safety as perceived by prescribers. Here, we aimed to evaluate adalimumab (ADA) survival and the interruption risk factors in a multicentre cohort of patients with hidradenitis suppurativa (HS). Moreover, we performed a subanalysis considering the periods before and after the onset of the COVID-19 pandemic. METHODS We conducted a retrospective study including 539 adult patients with HS who received ADA from 1 May 2015 to 31 December 2022. Overall drug survival was analysed using Kaplan-Meier survival curves and compared between the subgroups via stratified log-rank test. Possible predictors for overall drug survival and reasons for discontinuation were assessed using univariate and multivariate Cox regression. RESULTS Overall, 50.1% were females with a mean age of 43.5 ± 1 years and a mean BMI of 29.5 ± 6.7. At the start of ADA, 95.29% were biologic-naïve and 24.63% had undergone surgical treatment. During follow-up, 9.46% of patients required dose escalation, while 39.92% interrupted ADA. Concomitant therapy was used in 64.89% of cases. A subanalyses comparing pre- and post-pandemic periods revealed a tendency to initiate ADA treatment at a younger age, among patient with higher BMI and at a lower HS stage after COVID-19 pandemic. Interestingly, ADA demonstrated extended survival compared to previous studies, with a median overall drug survival of 56.2 months (95% CI 51.2 to 80.3). The primary causes for discontinuation were inefficacy (51.69%), followed by adverse effects (21.35%). Female sex, longer delay in HS diagnosis, higher baseline IHS4 score and concomitant spondyloarthritis were associated with poorer ADA survival or increased risk of discontinuation. CONCLUSIONS ADA demonstrated prolonged survival (median 56.2 months). While addition of antibiotics did not have a positive effect on survival rate, basal IHS4 proved useful in predicting ADA survival.
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Affiliation(s)
- Patricia Garbayo-Salmons
- Dermatology Department, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, Spain
- Departament de Medicina, Universitat Autònoma de Barcelona, Sabadell, Spain
| | - Eva Vilarrasa
- Dermatology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
| | - Julio Bassas-Vila
- Dermatology Department, Hospital Germans Trias i Pujol, Barcelona, Spain
| | | | - Irene Fuertes
- Dermatology Department, Hospital Clínic de Barcelona, Barcelona, Spain
| | - Mar Luque-Luna
- Dermatology Department, Hospital Clínic de Barcelona, Barcelona, Spain
| | | | | | | | - Joan Ceravalls
- Dermatology Department, Hospital Universitari Sagrat Cor, Grupo Quirónsalud, Barcelona, Spain
| | - Jordi Mollet
- Dermatology Department, Hospital Vall d'Hebrón, Barcelona, Spain
| | | | - Emili Masferrer
- Dermatology Department, Hospital Universitari Mútua Terrassa, Terrassa, Spain
| | - Oriol Corral-Magaña
- Dermatology Department, Hospital Universitari Mútua Terrassa, Terrassa, Spain
| | - Clara Matas-Nadal
- Dermatology Department, Hospital de Santa Caterina de Girona, Girona, Spain
| | - Jorge Del Estal
- Pharmacy Department, Parc Taulí Hospital Universitari, Universitat Autònoma de Barcelona, Sabadell, Spain
| | - Diana Fuertes Bailón
- Research Support Unit, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain
| | - Joan Calvet
- Departament de Medicina, Universitat Autònoma de Barcelona, Sabadell, Spain
- Rheumatology Department, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, Spain
| | - Jorge Romaní
- Dermatology Department, Hospital General de Granollers, Granollers, Spain
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Zahid JA, Henning MAS, Bouazzi D, Jemec GBE. Questionnaire-Based Global Prevalence of Hidradenitis Suppurativa: A Systematic Review and Meta-Analysis. Dermatology 2024:1-10. [PMID: 39715604 DOI: 10.1159/000537920] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/03/2024] [Accepted: 01/31/2024] [Indexed: 12/25/2024] Open
Abstract
BACKGROUND Hidradenitis suppurativa (HS), a chronic inflammatory skin disease affecting intertriginous areas, presents a recurring and debilitating challenge. Even though recent efforts have been made to estimate the overall HS prevalence, variations in screening modalities and missing data from the Global South warrant further investigation. Understanding the HS prevalence is crucial for treatment approaches and pathogenesis. Thus, we aimed to estimate a global HS prevalence based on studies using homogeneous validated questions. METHODS This systematic review was prospectively registered on PROSPERO and adhered to Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. Searches in PubMed, Embase, and CINAHL were performed on August 9, 2023. Original reports assessing the HS prevalence in adults using the following two questions were included: "Do you have recurrent boils of the skin?" and "Have you for the past 6 months had 2 or more boils/abscesses in any of the below locations: in the axilla, in the groin, around your genitals, on the buttocks, several locations i.e., first the buttocks then the axilla, etc.?" A pooled prevalence with 95% confidence interval (CI) was calculated with a random-effects model. RESULTS Eight studies qualified for inclusion, of which the prevalence estimate ranged from 0.7% to 6.4%. The meta-analysis encompassing 49,971 participants revealed a global HS prevalence of 2.5% (95% CI, 1.8-3.5%). CONCLUSION This meta-analysis suggests a global HS prevalence of 2.5% using a validated questionnaire. Due to heterogeneity and sparse data from the Global South, this estimate should be interpreted with caution.
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Affiliation(s)
- Jawad Ahmad Zahid
- Department of Surgery, Center for Surgical Science, Zealand University Hospital, University of Copenhagen, Copenhagen, Denmark
- Department of Dermatology, Zealand University Hospital, Roskilde, Denmark
| | | | - Dorra Bouazzi
- Department of Dermatology, Zealand University Hospital, Roskilde, Denmark
| | - Gregor B E Jemec
- Department of Dermatology, Zealand University Hospital, Roskilde, Denmark
- Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
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Eshmawi MT, Yousef Al-Mudaiheem H, Fatani M, Binamer Y, Alajlan M, Alharithy R, Alotaibi H, Almohanna HM, Alsantali A, Madani A, Al-Faraidy N, Bechara FG, Hamden Al-Jedaie A. Expert consensus on unmet needs, referral criteria and treatment goals for hidradenitis suppurativa in Saudi Arabia. J DERMATOL TREAT 2024; 35:2353693. [PMID: 38862417 DOI: 10.1080/09546634.2024.2353693] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/17/2023] [Accepted: 05/01/2024] [Indexed: 06/13/2024]
Abstract
Purpose: There is limited information about the diagnosis and treatment of hidradenitis suppurativa (HS) in the Kingdom of Saudi Arabia (KSA). This Delphi consensus study was conducted to develop recommendations for the management of HS in the KSA.Methods: The expert panel including 12 dermatologists with extensive experience treating HS patients provided nine consensus statements and recommendations on diagnosis and assessment, management, comorbidities and multidisciplinary approach, and education. The experts also developed clinical questions pertaining to the management of HS and rolled out as a survey to 119 dermatologists practising in the KSA.Results: The topics covered included: referring physicians' awareness of HS; referral criteria for HS; definition of moderate-to-severe HS; treatment goals; definition of treatment success; treatment and biologic initiation; comorbidities and multidisciplinary approach; patient education and awareness of HS. Full consensus (100%) from the expert dermatologists was received on all the topics except referring physicians' awareness of HS, definition of treatment success, and treatment and biologic initiation. The survey results resonated with the expert opinion.Conclusion: As HS is a chronic disease with negative impact on quality-of-life, timely diagnosis and treatment, early identification of comorbid conditions and a multidisciplinary care approach are crucial for effective management of HS.
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Affiliation(s)
- Maysa T Eshmawi
- College of Medicine, Imam Mohammad Ibn Saud Islamic University, Riyadh, Saudi Arabia
- King Abdullah Medical Complex Jeddah, MOH, Saudi Arabia
| | | | - Mohammed Fatani
- Department of Dermatology, Hera General Hospital, Makkah, Saudi Arabia
| | - Yousef Binamer
- Department of Dermatology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
- Alfaisal University, Riyadh, Saudi Arabia
| | - Mohammed Alajlan
- Department of Dermatology, King Fahad Medical City, Riyadh, Saudi Arabia
| | - Ru'aa Alharithy
- Department of Dermatology, Security Forces Hospital, Riyadh, Saudi Arabia
| | - Hend Alotaibi
- Department of Dermatology, King Saud University, Riyadh, Saudi Arabia
| | - Hind M Almohanna
- Department of Dermatology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia
| | - Adel Alsantali
- Department of Dermatology, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia
| | - Abdulaziz Madani
- Department of Dermatology, College of medicine, King Saud University, Riyadh, Saudi Arabia
| | - Nadya Al-Faraidy
- Department of Medicine, King Fahad Specialist Hospital, Dammam, Saudi Arabia
| | - Falk G Bechara
- Department of Dermatology, Venereology and Allergology, Ruhr-University, Bochum, Germany
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Jaleel T, Mitchell B, Burge R, Cohee A, Wallinger H, Truman I, Keal A, Middleton‐Dalby C, Barlow S, Patel D. Exploring racial and ethnic disparities in the hidradenitis suppurativa patient disease journey: Results from a real-world study in Europe and the USA. J Dermatol 2024; 51:1547-1558. [PMID: 39400427 PMCID: PMC11624158 DOI: 10.1111/1346-8138.17386] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/01/2024] [Revised: 06/05/2024] [Accepted: 07/03/2024] [Indexed: 10/15/2024]
Abstract
Hidradenitis suppurativa (HS) is an inflammatory skin disease associated with high morbidity and disability that has limited treatment options. People from racial and ethnic minority groups may experience greater disease severity and delay to diagnosis. This study assessed the impact of race/ethnicity on HS diagnosis and management in real-world clinical settings. Data were derived from the Adelphi Real World Hidradenitis Suppurativa Disease Specific Programme, a survey of dermatologists and their consulting HS patients in five European countries and the USA in 2020/2021. Dermatologists returned demographic and clinical data, and treatment goals and satisfaction for their next five to seven consulting patients. Patients completed a questionnaire on disease history and diagnosis, disease burden, and treatment satisfaction. Groups were compared with bivariate tests. In total, 312 physicians returned data on 1787 patients; 57.6% were female and 77.7% White. People from racial and ethnic minority groups were younger than White patients (32.9 ± 11.6 vs. 34.9 ± 12.4, mean ± standard deviation) and reported symptoms at a younger age (23.3 ± 10.8 vs. 26.2 ± 11.1), but their time to first consultation was longer than for White patients (2.6 ± 5.7 vs. 1.2 ± 2.5 years). People from racial and ethnic minority groups took longer to receive a correct diagnosis following first consultation (2.7 ± 5.3 vs. 1.5 ± 4.1 years) and were more likely to be misdiagnosed with boils (73.5% vs. 40.4%). People from racial and ethnic minority groups had a greater disease awareness at diagnosis and reported wanting greater support. People from racial and ethnic minority groups reported a greater impact on life, more severe pain, and a greater level of activity impairment in the Work Productivity and Activity Impairment: General Health (27.0 ± 25.2 vs. 20.0 ± 20.6). All P values were ≤0.05. These data show evidence of delayed diagnosis and higher HS symptom burden amongst people from racial and ethnic minority groups, highlighting health disparities in HS.
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Affiliation(s)
| | - Beth Mitchell
- Eli Lilly and CompanyValue Evidence & OutcomesIndianapolisIndianaUSA
| | - Russel Burge
- Eli Lilly and CompanyValue Evidence & OutcomesIndianapolisIndianaUSA
- Division of Pharmaceutical Sciences, Winkle College of PharmacyUniversity of CincinnatiCincinnatiOhioUSA
| | - Andrea Cohee
- Eli Lilly and CompanyValue Evidence & OutcomesIndianapolisIndianaUSA
| | | | | | | | | | | | - Dipak Patel
- Eli Lilly and CompanyValue Evidence & OutcomesIndianapolisIndianaUSA
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Surapaneni V, Milosavljevic MV, Orenstein LAV. Pain management in hidradenitis suppurativa. J Am Acad Dermatol 2024; 91:S52-S63. [PMID: 39627001 DOI: 10.1016/j.jaad.2024.09.006] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/16/2024] [Revised: 09/03/2024] [Accepted: 09/05/2024] [Indexed: 12/31/2024]
Abstract
Pain is the most impactful symptom in hidradenitis suppurativa (HS), contributing to physical limitations, worsened mental health, and impaired social relationships. Some HS-directed therapies ameliorate HS pain; however, these medications provide insufficient relief for many people living with HS. This article reviews what is currently known about HS pain phenotypes and pathophysiology, the effectiveness of HS treatments for pain, and practical suggestions for dermatologists to help patients manage the symptoms of acute and chronic HS pain.
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35
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Liao YH, Chu CB, Hui CYR, Li CY, Lin SY, Tseng HC, Wang YJ, Wu J, Yu WW, Chao SC. Taiwanese Dermatological Association (TDA) consensus recommendations for the definition, classification, diagnosis, and management of hidradenitis suppurativa. J Formos Med Assoc 2024; 123:1228-1238. [PMID: 38160191 DOI: 10.1016/j.jfma.2023.12.012] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/08/2023] [Revised: 11/12/2023] [Accepted: 12/17/2023] [Indexed: 01/03/2024] Open
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory follicular disease characterized by painful, recurrent, inflamed lesions most commonly occurring in the axillary, inguinal, and anogenital regions. HS can inflict immense physical and psychological impact on patients who suffer from this distressing disease. Management of HS generally requires combining various medical and procedural treatment modalities; however, the disease is often recalcitrant to conventional treatments. In light of recent evidence supporting the effectiveness of biologic agents in the treatment of HS, the Taiwanese Dermatological Association established an expert panel of nine dermatologists to develop consensus statements aimed to provide up-to-date evidence-based guidance in optimizing HS patient management in Taiwan. The recommendations described in the statements were summarized in a management algorithm in terms of general care, topical treatment, systemic treatment, and procedural treatment.
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Affiliation(s)
- Yi-Hua Liao
- Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan; College of Medicine, National Taiwan University, Taipei, Taiwan
| | - Chia-Bao Chu
- Department of Dermatology, College of Medicine, National Cheng Kung University, Tainan, Taiwan
| | | | - Cheng-Yuan Li
- Department of Dermatology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Dermatology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan
| | - Sheng-Yao Lin
- Department of Dermatology, Kaohsiung Medical University, Kaohsiung, Taiwan
| | - Han-Chi Tseng
- Department of Dermatology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; Graduate Institute of Clinical Medicine, Chang Gung University, Taoyuan, Taiwan
| | - Yen-Jen Wang
- Department of Dermatology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Cosmetic Applications and Management, MacKay Junior College of Medicine, Nursing, and Management, New Taipei City, Taiwan
| | - Jennifer Wu
- Department of Dermatology, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan; College of Medicine, Chang Gung University, Taoyuan, Taiwan
| | - Wei-Wen Yu
- Department of Dermatology, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan
| | - Sheau-Chiou Chao
- Department of Dermatology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
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Murray N, Truman I, Milligan G, Modi H, Adlard N. Equity and Outcome Events in Hidradenitis Suppurativa: Exploring Effect Modifiers Associated with Diagnostic Delay in the Real World. Dermatol Ther (Heidelb) 2024; 14:3211-3227. [PMID: 39487935 PMCID: PMC11604871 DOI: 10.1007/s13555-024-01291-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/06/2024] [Accepted: 10/02/2024] [Indexed: 11/04/2024] Open
Abstract
INTRODUCTION Patients with hidradenitis suppurativa (HS) experience significantly delayed diagnoses of 7-10 years from symptom onset on average, but the reasons for this remain largely unknown. This study investigated drivers of diagnostic delay from the perspective of healthcare system equity. METHODS A literature review was performed to identify published factors associated with delayed HS diagnosis to inform data analysis. Clinical and demographic data from the Adelphi HS Disease Specific Programme (DSP)™, a real-world cross-sectional survey of dermatologists and their consulting patients in France, Germany, Italy, Spain, the UK and the USA in 2020/2021, were used to model factors influencing delay to diagnosis from onset of symptoms and first consultation. RESULTS Factors influencing delay to HS diagnosis in the literature with the most available evidence were misdiagnosis, delay in specialist referral and patient embarrassment. Data analysis revealed that increasing age was associated with reduced diagnostic delay after symptom onset. Patients with HS who were White or in Germany were also more likely to receive a faster diagnosis. Smokers, patients with concomitant conditions, or a family history of HS were slower to be diagnosed. When time to diagnosis following first consultation was assessed, increasing age was associated with quicker diagnosis. Moreover, patients with a family history of HS were diagnosed quicker, whereas those with high body mass index, more concomitant conditions, in employment, managed by multiple physicians or European were more delayed. CONCLUSION On the basis of a thorough analysis of real-world data, multiple factors that potentially influenced the timely diagnosis of HS have been identified. For the first time, this study quantifies the relative impact of these modifiers, providing valuable insights into areas that require attention for faster diagnoses and improved disease outcomes.
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Vu D, Park M, Alhusayen R. Response to Chawla et al, "Response to Vu et al's "Efficacy of moxifloxacin as a mono-antibiotic therapy for hidradenitis suppurativa: A retrospective cohort study"". J Am Acad Dermatol 2024; 91:e177-e178. [PMID: 39154745 DOI: 10.1016/j.jaad.2024.08.013] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/24/2024] [Accepted: 08/08/2024] [Indexed: 08/20/2024]
Affiliation(s)
- Don Vu
- Division of Dermatology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
| | - Megan Park
- Division of Dermatology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada
| | - Raed Alhusayen
- Division of Dermatology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada
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Lai PT, Tseng HC. Adopting adalimumab combined surgery in the management of moderate to severe hidradenitis suppurativa: Experience from a single medical center in southern Taiwan. J Dermatol 2024; 51:1615-1621. [PMID: 39032108 DOI: 10.1111/1346-8138.17375] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/13/2024] [Revised: 06/05/2024] [Accepted: 06/21/2024] [Indexed: 07/22/2024]
Abstract
Hidradenitis suppurativa (HS) is a chronic inflammatory disorder primarily affecting the intertriginous and anogenital regions. Guidelines recommend various treatments for HS, including biologic agents like adalimumab for moderate to severe cases. Adalimumab is a type of human monoclonal IgG1 antibody designed to target tumor necrosis factor α. Recent studies have shown the effectiveness of adalimumab, either alone or combined with surgery, in managing HS. We retrospectively analyzed the medical chart of HS patients in a southern Taiwan medical center from 2019 to 2022 and investigated clinical features and treatment response. The institutional review board at Chang Gung Medical Foundation granted approval for the study. We primarily focused on moderate to severely affected patients. One hundred and two clinically diagnosed HS patients participated, with a male-to-female ratio of 2:1 and an average age of 31.8 at diagnosis. Among them, 41.2% were in Hurley stage III and 32.4% in stage II. Nineteen patients received excision with pre-surgical adalimumab; their average age at diagnosis was 31.1, with a gender ratio of 5.3:1. Surgery was most common on the buttocks (68%), axillae (21%), and groin (10%). Excision patients were primarily in advanced stages (Hurley III 94.7%, II 5.3%) with high body mass index. Adalimumab and surgery combined yielded a 68.4% improvement rate, while 15.8% remained stable and 15.8% did not respond as expected. In addition, smoking and obesity were prevalent among patients. Adalimumab showed promising results in moderate to severe HS, with significant improvement observed in our cases. The combination of adalimumab and surgery appeared effective in advanced HS patients with larger involved areas and more tunnels. No severe adverse events were reported. However, our study was limited by its retrospective nature and the lack of a control group. Despite these limitations, our study revealed the benefits of integrating adalimumab with suitable surgical procedures in managing patients experiencing moderate to severe HS in real-world scenarios.
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Affiliation(s)
- Po-Ta Lai
- Department of Dermatology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan, ROC
| | - Han-Chi Tseng
- Department of Dermatology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan, ROC
- Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan, ROC
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Franceschin L, Guidotti A, Mazzetto R, Tartaglia J, Ciolfi C, Alaibac M, Sernicola A. Repurposing Historic Drugs for Neutrophil-Mediated Inflammation in Skin Disorders. Biomolecules 2024; 14:1515. [PMID: 39766222 PMCID: PMC11673839 DOI: 10.3390/biom14121515] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/01/2024] [Revised: 11/23/2024] [Accepted: 11/26/2024] [Indexed: 01/11/2025] Open
Abstract
Neutrophil-mediated inflammation is a key feature of immune-mediated chronic skin disorders, but the mechanistic understanding of neutrophil involvement in these conditions remains incomplete. Dapsone, colchicine, and tetracyclines are established drugs within the dermatologist's therapeutic armamentarium that are credited with potent anti-neutrophilic effects. Anti-neutrophilic drugs have established themselves as versatile agents in the treatment of a wide range of dermatological conditions. Some of these agents are approved for the management of specific dermatologic conditions, but most of their current uses are off-label and only supported by isolated reports or case series. Their anti-inflammatory and immunomodulatory properties make them particularly valuable in managing auto-immune bullous diseases, neutrophilic dermatoses, eosinophilic dermatoses, interface dermatitis, and granulomatous diseases that are the focus of this review. By inhibiting inflammatory pathways, reducing cytokine production, and modulating immune responses, they contribute significantly to the treatment and management of these complex skin conditions. Their use continues to evolve as our understanding of these diseases deepens, and they remain a cornerstone of dermatological therapy.
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Affiliation(s)
| | | | - Roberto Mazzetto
- Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padova, Italy; (L.F.); (A.G.); (J.T.); (C.C.); (M.A.)
| | | | | | | | - Alvise Sernicola
- Dermatology Unit, Department of Medicine (DIMED), University of Padua, 35121 Padova, Italy; (L.F.); (A.G.); (J.T.); (C.C.); (M.A.)
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Alpsoy E, Fettahlıoglu Karaman B, Demirseren DD, Cınar SL, Kacar N, Türel Ermertcan A, Bulbul Baskan E, Ucmak D, Mammadli K, Kılınc F, Yazici S, Temiz SA, Özkök Akbulut T, Ataseven A, Şikar Aktürk A, Sarıcaoğlu H, Türkmen M, Gülbaşaran F, Engin B, Kaya Özden H, Durmaz K, Güler Özden M, Özdemir H, Çevirgen Cemil B, Sarıkaya Solak S, Bilgili SG, Yavuz İH, Özaydın Yavuz G, Güven M, Polat Ekinci A, Atcı T, Didar Balci D, Oztürk A, Kıvanç Altunay İ, Özkur E, Ugurer E, Karadag AS, Kalkan G, Kılıc S, Erdoğan B, Yayli S, Baykal Selçuk L, Dönmez L, Bilgic A. Clinical Features and Natural Course of Hidradenitis Suppurativa in Turkey: A Multicenter Study. Dermatology 2024; 241:162-172. [PMID: 39571540 DOI: 10.1159/000542670] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/03/2023] [Accepted: 11/11/2024] [Indexed: 01/16/2025] Open
Abstract
INTRODUCTION The natural history, the progression of a disease process in an individual over time, has not yet been fully elucidated in hidradenitis suppurativa (HS). In this large multicenter study, we aimed to investigate the natural history of HS and its gender differences. METHODS This cross-sectional study included 827 patients. The chronological order of the clinical manifestations for each patient was recorded retrospectively. Sociodemographic characteristics, triggering factors, clinical, treatment, and prognostic features were also evaluated. RESULTS The mean age of disease onset was significantly younger in women than in men (22.42 ± 9.28 vs. 27.06 ± 20.56, p < 0.001) and those with a family history (p < 0.0001). The mean disease duration was 91.17 ± 83.64 months. The most common symptom was purulent discharge (81%). The mean duration of abscess was shorter in women than in men (3.11 ± 2.65 vs. 3.75 ± 3.75, p = 0.01). The axilla was the most common onset area followed by the inguinal and gluteal regions. The disease ran a more severe course in men. Abscess/inflammatory nodule was defined in the last 6 months in 88.6% of the patients; however, the first 5 years of the disease were the most active disease period in 67.5% of the patients. Multivariate analysis revealed being male, older age, family history, involvement of the axillary, inguinal, and perianal regions independently associated with HS severity. While antibiotic use was the most important factor in improving the disease symptoms, stress was the most common aggravating factor. Biological therapy in men, laser epilation and pregnancy in women were significant alleviating factors, whereas weight gain was a more common aggravating factor for women. CONCLUSION HS shows a relentlessly progressive course with inflammatory attacks, but the first years of the disease are the most active period. This study confirms that environmental and hormonal factors may play an important role in the disease course, probably with other endogenous or exogenous factors.
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Affiliation(s)
- Erkan Alpsoy
- Department of Dermatology and Venereology, Faculty of Medicine, Akdeniz University, Antalya, Turkey
| | | | - Duriye Deniz Demirseren
- Department of Dermatology and Venerology, Ankara Bilkent City Hospital, University of Health Sciences, Ankara, Turkey
| | - S Levent Cınar
- Department of Dermatology and Venereology, Faculty of Medicine, Erciyes University, Kayseri, Turkey
| | - Nida Kacar
- Department of Dermatology and Venereology, Faculty of Medicine, Pamukkale University, Denizli, Turkey
| | - Aylin Türel Ermertcan
- Department of Dermatology and Venereology, Faculty of Medicine, Celal Bayar University, Manisa, Turkey
| | - Emel Bulbul Baskan
- Department of Dermatology and Venereology, Faculty of Medicine, Uludağ University, Bursa, Turkey
| | - Derya Ucmak
- Department of Dermatology and Venereology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey
| | - Kifayet Mammadli
- Department of Dermatology and Venereology, Faculty of Medicine, Akdeniz University, Antalya, Turkey
| | - Fadime Kılınc
- Department of Dermatology and Venerology, Ankara Bilkent City Hospital, University of Health Sciences, Ankara, Turkey
| | - Serkan Yazici
- Department of Dermatology and Venereology, Faculty of Medicine, Uludağ University, Bursa, Turkey
| | - Selami Aykut Temiz
- Department of Dermatology and Venereology, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey
| | - Tugba Özkök Akbulut
- Department of Dermatology and Venereology, Haseki Training and Research Hospital, University of Health Sciences, İstanbul, Turkey
| | - Arzu Ataseven
- Department of Dermatology and Venereology, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey
| | - Aysun Şikar Aktürk
- Department of Dermatology and Venereology, Faculty of Medicine, Kocaeli University, İzmir, Turkey
| | - Hayriye Sarıcaoğlu
- Department of Dermatology and Venereology, Faculty of Medicine, Uludağ University, Bursa, Turkey
| | - Meltem Türkmen
- Department of Dermatology and Venereology, İzmir Bozyaka Training and Research Hospital, University of Health Sciences, İzmir, Turkey
| | - Fatmagül Gülbaşaran
- Department of Dermatology and Venereology, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey
| | - Burhan Engin
- Department of Dermatology and Venereology, Cerrahpaşa Faculty of Medicine, İstanbul University-Cerrahpaşa, İstanbul, Turkey
| | - Hatice Kaya Özden
- Department of Dermatology and Venereology, Kocaeli Derince Training and Research Hospital, İzmit, Turkey
| | - Koray Durmaz
- Department of Dermatology and Venereology, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey
| | - Müge Güler Özden
- Department of Dermatology and Venereology, Faculty of Medicine, Ondokuzmayıs University, Samsun, Turkey
| | - Hilal Özdemir
- Department of Dermatology and Venereology, Faculty of Medicine, Ondokuzmayıs University, Samsun, Turkey
| | - Bengü Çevirgen Cemil
- Department of Dermatology and Venereology, Dış Kapı Yıldırım Beyazıt Training and Research Hospital, Ankara, Turkey
| | - Sezgi Sarıkaya Solak
- Department of Dermatology and Venereology, Faculty of Medicine, Trakya University, Edirne, Turkey
| | - Serap Günes Bilgili
- Department of Dermatology and Venereology, Faculty of Medicine, Van Yüzüncü Yıl University, Van, Turkey
| | - İbrahim Halil Yavuz
- Department of Dermatology and Venereology, Faculty of Medicine, Van Yüzüncü Yıl University, Van, Turkey
| | - Göknur Özaydın Yavuz
- Department of Dermatology and Venereology, Faculty of Medicine, Van Yüzüncü Yıl University, Van, Turkey
| | - Münevver Güven
- Department of Dermatology and Venereology, Faculty of Medicine, Aydın Adnan Menderes University, Aydın, Turkey
| | - Algün Polat Ekinci
- Department of Dermatology and Venereology, Istanbul Faculty of Medicine, Istanbul University, İstanbul, Turkey
| | - Tuğba Atcı
- Department of Dermatology and Venereology, Istanbul Faculty of Medicine, Istanbul University, İstanbul, Turkey
| | - Didem Didar Balci
- Department of Dermatology and Venereology, Tepecik Training and Research Hospital, İzmir, Turkey
| | - Aylin Oztürk
- Department of Dermatology and Venereology, Tepecik Training and Research Hospital, İzmir, Turkey
| | - İlknur Kıvanç Altunay
- Department of Dermatology and Venereology, Sisli Etfal Training and Research Hospital, İstanbul, Turkey
| | - Ezgi Özkur
- Department of Dermatology and Venereology, Sisli Etfal Training and Research Hospital, İstanbul, Turkey
| | - Ece Ugurer
- Department of Dermatology and Venereology, Sisli Etfal Training and Research Hospital, İstanbul, Turkey
| | - Ayse Serap Karadag
- Department of Dermatology and Venereology, Faculty of Medicine, İstanbul Medeniyet University, İstanbul, Turkey
| | - Göknur Kalkan
- Department of Dermatology and Venereology, Faculty of Medicine, Ankara Yıldırım Beyazıt University, Ankara, Turkey
| | - Sevilay Kılıc
- Department of Dermatology and Venereology, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey
| | - Bilgen Erdoğan
- Department of Dermatology and Venereology, İstanbul Başakşehir Çam ve Sakura State Hospital, University of Health Sciences, İstanbul, Turkey
| | - Savas Yayli
- Department of Dermatology and Venereology, School of Medicine, Koç University, Istanbul, Turkey
| | - Leyla Baykal Selçuk
- Department of Dermatology and Venereology, Faculty of Medicine, Karadeniz Teknik University, Trabzon, Turkey
| | - Levent Dönmez
- Department of Public Health, Faculty of Medicine, Akdeniz University, Antalya, Turkey
| | - Aslı Bilgic
- Department of Dermatology and Venereology, Faculty of Medicine, Akdeniz University, Antalya, Turkey,
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Samela T, Raimondi G, Pintori G, Pupa MB, Cordella G, Antinone V, Melo Salcedo N, Fusari R, Pallotta S, Sampogna F, Fania L, Ciccone D, Pellacani G, Abeni D. Clinically mild hidradenitis suppurativa: mild for whom? Br J Dermatol 2024; 191:1026-1027. [PMID: 39183702 DOI: 10.1093/bjd/ljae310] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/19/2024] [Revised: 05/30/2024] [Accepted: 08/01/2024] [Indexed: 08/27/2024]
Abstract
Severe levels of illness, measured through patient-reported outcomes, are frequent among patients with hidradenitis suppurativa classified as having mild disease according to the International Hidradenitis Suppurativa Score System. The systematic use in clinical practice of patient-centred outcome measures, capable of accurately detecting and portraying the true severity of the impact of skin conditions, may help improve patient care.
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Affiliation(s)
- Tonia Samela
- Clinical Epidemiology Unit, IDI-IRCCS, Rome, Italy
- Clinical Psychology Unit, IDI-IRCCS, Rome, Italy
| | | | - Giusi Pintori
- Patient association 'Passion People', Cagliari, Italy
| | | | | | | | | | | | | | | | - Luca Fania
- Dermatology Unit, IDI-IRCCS, Rome, Italy
| | | | - Giovanni Pellacani
- UOC of Dermatology, Policlinico Umberto I Hospital, Sapienza Medical School of Rome, Rome, Italy
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Ingram JR, Bettoli V, Espy JI, Kokolakis G, Martorell A, Villani AP, Wallinger H, Truman I, Coak E, Kasparek T, Muscianisi E, Richardson C, Kimball AB. Treatment Satisfaction in Patients with Hidradenitis Suppurativa: A Real-World Survey from the EU5 and USA. Dermatology 2024; 241:149-161. [PMID: 39500291 PMCID: PMC11965843 DOI: 10.1159/000542343] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/16/2023] [Accepted: 10/19/2024] [Indexed: 01/21/2025] Open
Abstract
INTRODUCTION Hidradenitis suppurativa (HS) is a debilitating, inflammatory skin disorder. Treatment strategies in patients with HS are challenging; real-world evidence in a HS population is warranted for greater disease understanding. The objective of this analysis was to describe real-world treatment patterns and treatment satisfaction in patients with HS. METHODS This was a cross-sectional market research survey with retrospective data collection in patients with HS from the USA and five European countries (France, Germany, Italy, Spain, and the UK) between November 2020 and April 2021, using physician- and patient-reported surveys. Eligible physicians were general dermatologists actively managing patients with HS; dermatologists were required to have consulted with ≥2 patients with HS in the previous 12 months. Adult (≥18 years) and adolescent (10-17 years) HS patients visiting a participating dermatologist were included. Outcomes included treatment patterns, flare status, treatments prescribed in response to flares, previous surgeries, barriers to biologics, and patient- and physician-reported satisfaction with the disease control provided by treatment. RESULTS Survey data from 1,787 patients were collected from 312 dermatologists. The most frequently prescribed treatments were topicals, oral antibiotics, and antiseptic washes/creams at diagnosis and sampling. At sampling, biologics were more frequently prescribed in patients with more severe disease (prescribed in 26.6%, 31.0%, and 52.4% of patients with mild, moderate, and severe disease, respectively); oral antibiotics (48.8%), topicals (37.4%), and biologics (34.3%) were the most frequently prescribed treatment classes in response to a flare. Of patients currently not receiving a biologic, dermatologists reported that 18.9% of patients' condition warranted their use. Approximately one quarter of dermatologists (24.5%) and patients (27.4%) were not satisfied with current treatment; of patients who were dissatisfied, 12.8% reported they would never raise their dissatisfaction with their doctor. CONCLUSION These real-world data suggest a high disease burden and potential undertreatment in patients with HS. Patients received multiple treatments, and a notable proportion underwent surgery. Robustly integrating the patient voice in HS treatment decisions may lead to better outcomes and improved treatment satisfaction. INTRODUCTION Hidradenitis suppurativa (HS) is a debilitating, inflammatory skin disorder. Treatment strategies in patients with HS are challenging; real-world evidence in a HS population is warranted for greater disease understanding. The objective of this analysis was to describe real-world treatment patterns and treatment satisfaction in patients with HS. METHODS This was a cross-sectional market research survey with retrospective data collection in patients with HS from the USA and five European countries (France, Germany, Italy, Spain, and the UK) between November 2020 and April 2021, using physician- and patient-reported surveys. Eligible physicians were general dermatologists actively managing patients with HS; dermatologists were required to have consulted with ≥2 patients with HS in the previous 12 months. Adult (≥18 years) and adolescent (10-17 years) HS patients visiting a participating dermatologist were included. Outcomes included treatment patterns, flare status, treatments prescribed in response to flares, previous surgeries, barriers to biologics, and patient- and physician-reported satisfaction with the disease control provided by treatment. RESULTS Survey data from 1,787 patients were collected from 312 dermatologists. The most frequently prescribed treatments were topicals, oral antibiotics, and antiseptic washes/creams at diagnosis and sampling. At sampling, biologics were more frequently prescribed in patients with more severe disease (prescribed in 26.6%, 31.0%, and 52.4% of patients with mild, moderate, and severe disease, respectively); oral antibiotics (48.8%), topicals (37.4%), and biologics (34.3%) were the most frequently prescribed treatment classes in response to a flare. Of patients currently not receiving a biologic, dermatologists reported that 18.9% of patients' condition warranted their use. Approximately one quarter of dermatologists (24.5%) and patients (27.4%) were not satisfied with current treatment; of patients who were dissatisfied, 12.8% reported they would never raise their dissatisfaction with their doctor. CONCLUSION These real-world data suggest a high disease burden and potential undertreatment in patients with HS. Patients received multiple treatments, and a notable proportion underwent surgery. Robustly integrating the patient voice in HS treatment decisions may lead to better outcomes and improved treatment satisfaction.
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Affiliation(s)
- John R. Ingram
- Department of Dermatology & Academic Wound Healing, Division of Infection and Immunity, Cardiff University, Cardiff, UK
| | - Vincenzo Bettoli
- Department of Oncology and Specialistic Medicine, O.U. of Dermatology, Azienda Ospedaliera - University of Ferrara, Ferrara, Italy
| | - Jasmine I. Espy
- Hidradenitis Suppurativa Patient Advocate, Multimedia Journalist, and Filmmaker, Los Angeles, CL, USA
- The Association of Hidradenitis Suppurativa and Inflammatory Diseases, Detroit, MI, USA
| | - Georgios Kokolakis
- Psoriasis Research and Treatment Center, Department of Dermatology, Venereology and Allergology Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany
| | | | - Axel P. Villani
- Hospices Civils de Lyon, Claude Bernard Lyon I University, Department of Dermatology – Edouard Herriot Hospital, Lyon, France
| | | | | | | | | | | | | | - Alexa B. Kimball
- Department of Dermatology, Beth Israel Deaconess Medical Center, Harvard Medical School and Clinical Laboratory for Epidemiology and Applied Research in Skin (CLEARS), Boston, MA, USA
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Holgersen N, Nielsen VW, Rosenø NAL, Ring HC, Holm Nielsen S, Maul JT, Thyssen JP, Egeberg A, Thomsen SF. The Copenhagen Hidradenitis Suppurativa Cohort: Insights from the First 8 Years. Dermatology 2024; 240:917-921. [PMID: 39476814 DOI: 10.1159/000541612] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/10/2024] [Accepted: 09/20/2024] [Indexed: 11/20/2024] Open
Affiliation(s)
| | | | | | | | | | - Julia-Tatjana Maul
- Faculty of Medicine, University of Zürich, Zürich, Switzerland
- Department of Dermatology, University Hospital Zürich, Zürich, Switzerland
| | - Jacob P Thyssen
- Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark
- Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
| | - Alexander Egeberg
- Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark
- Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
| | - Simon Francis Thomsen
- Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark
- Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark
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Özdemir AK, Tamer E. 808 nm diode laser in the treatment of Hidradenitis Suppurativa: a retrospective study. Arch Dermatol Res 2024; 316:708. [PMID: 39528770 DOI: 10.1007/s00403-024-03472-5] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/04/2024] [Revised: 10/02/2024] [Accepted: 10/16/2024] [Indexed: 11/16/2024]
Abstract
Hidradenitis suppurativa (HS) is a chronic, recurrent inflammatory disease characterized by painful lesions such as nodules, abscesses, and sinus tracts, primarily affecting intertriginous areas. Traditional treatments range from antibiotics and hormonal therapies to biologics and surgical options. Recently, lasers and light-based treatments has gained attention as a non-systemic treatment for HS, targeting hair follicles to potentially alleviate symptoms and improve quality of life. This study evaluated the efficacy of 808 nm Diode laser therapy in managing HS by retrospectively reviewing data from 16 patients (13 men, 3 women) aged 23-61 who underwent between two and four sessions. Patients had not received systemic treatment in the three months preceding or during the therapy. Key outcome measures included the Modified Hidradenitis Suppurativa Score (MHSS), Hidradenitis Suppurativa Physician's Global Assessment (HS-PGA), Hidradenitis Suppurativa Clinical Response (HiSCR), and Dermatology Life Quality Index (DLQI). Results indicated a significant reduction in MHSS from a median of 20.0 before treatment to 9.0 at six months (p = 0.001). The HS-PGA score also significantly decreased from a median of 3.0 to 2.0 (p = 0.012). Of the 10 patients evaluated for HiSCR, 8 showed a positive response. DLQI scores improved from a median of 4.5 to 1.0 (p = 0.002). The treatment was well-tolerated, with only mild pain reported and no severe adverse effects. In conclusion, 808 nm Diode laser therapy appears to be an effective modality for reducing disease severity and enhancing quality of life in HS patients, likely due to its anti-inflammatory effects. These findings suggest that Diode laser therapy could be a valuable addition to current HS management strategies, with further research needed to explore its long-term efficacy.
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Affiliation(s)
- Ahmet Kağan Özdemir
- Department of Dermatology, Sincan Training and Research Hospital, Ankara, Turkey.
| | - Emine Tamer
- Ankara City Hospital Department of Dermatology, Health Sciences University, Ankara, Turkey
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Ingram JR, Geissbühler Y, Darcy J, Foley S, Gaffney A, McConnon A, Richardson C, Garg A. Comprehensive Codified Algorithms to Identify the Underestimated Burden of Hidradenitis Suppurativa in the United States. Dermatol Ther (Heidelb) 2024; 14:2859-2876. [PMID: 39316357 PMCID: PMC11480298 DOI: 10.1007/s13555-024-01259-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/06/2024] [Accepted: 08/13/2024] [Indexed: 09/25/2024] Open
Abstract
INTRODUCTION Hidradenitis suppurativa (HS) is a painful, inflammatory skin disease associated with a high disease burden and long diagnostic delay. Prevalence estimates of HS vary widely in the literature owing to differing estimation methodologies. This study aimed to apply stepwise algorithms to estimate the prevalence of possible/diagnosed cases of HS in the US. METHODS This was a retrospective cohort study in adult and pediatric patients with HS which utilized data from four US databases (MarketScan [Medicare and Medicaid] and Optum [electronic health record (EHR) and Clinformatics Data Mart (CDM)]). Patients with possible/diagnosed HS were identified using two algorithms (termed Algorithm 1 and Algorithm 2), which assessed symptoms such as multiple skin boils in site-specific areas based on international classification of disease (ICD) codes. Patients with diagnosed HS were defined as having ≥ 2 outpatient or ≥ 1 inpatient diagnosis codes of HS. In each database, patients with continuous medical and pharmacy benefits in the 365 days pre-index and 0-365 days post-index periods were eligible for inclusion. RESULTS Across all databases, Algorithm 2 (MarketScan Medicare [N = 309,916]; MarketScan Medicaid [N = 188,783]; Optum EHR [N = 366,158]; Optum CDM [N = 173,812]) identified more patients with possible/diagnosed HS than Algorithm 1 (MarketScan Medicare [N = 194,353]; MarketScan Medicaid [N = 99,276]; Optum EHR [N = 177,957]; Optum CDM [N = 112,244]). Based on ICD-9/10 codes, the 5-year period prevalence of HS ranged from 0.06% to 0.12% across all databases, while for Algorithm 1 and Algorithm 2, this ranged from 0.27% to 0.41% and 0.49% to 0.78%, respectively. Adults and females generally had a higher 5-year period prevalence versus pediatric patients and males, respectively. CONCLUSION This real-world study highlights that HS diagnosis codes alone may be insufficient to estimate the prevalence of HS, demonstrating the value of employing algorithms in practice which assess for parameters such as multiple skin boils in site-specific areas. Integrating robust methods to identify the prevalence of HS may improve the diagnostic delay observed in HS and improve treatment outcomes.
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Affiliation(s)
- John R Ingram
- Department of Dermatology and Academic Wound Healing, Division of Infection and Immunity, Cardiff University, Cardiff, UK.
| | | | - John Darcy
- Novartis Pharmaceuticals Corporation, East Hanover, NJ, US
| | | | | | | | | | - Amit Garg
- Northwell Health, New Hyde Park, NY, US
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Sugiura K, Fujita H, Komine M, Yamanaka K, Akiyama M. The role of interleukin-36 in health and disease states. J Eur Acad Dermatol Venereol 2024; 38:1910-1925. [PMID: 38779986 DOI: 10.1111/jdv.19935] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/03/2023] [Accepted: 01/29/2024] [Indexed: 05/25/2024]
Abstract
The interleukin (IL)-1 superfamily upregulates immune responses and maintains homeostasis between the innate and adaptive immune systems. Within the IL-1 superfamily, IL-36 plays a pivotal role in both innate and adaptive immune responses. Of the four IL-36 isoforms, three have agonist activity (IL-36α, IL-36β, IL-36γ) and the fourth has antagonist activity (IL-36 receptor antagonist [IL-36Ra]). All IL-36 isoforms bind to the IL-36 receptor (IL-36R). Binding of IL-36α/β/γ to the IL-36R recruits the IL-1 receptor accessory protein (IL-1RAcP) and activates downstream signalling pathways mediated by nuclear transcription factor kappa B and mitogen-activated protein kinase signalling pathways. Antagonist binding of IL-36Ra to IL-36R inhibits recruitment of IL-1RAcP, blocking downstream signalling pathways. Changes in the balance within the IL-36 cytokine family can lead to uncontrolled inflammatory responses throughout the body. As such, IL-36 has been implicated in numerous inflammatory diseases, notably a type of pustular psoriasis called generalized pustular psoriasis (GPP), a chronic, rare, potentially life-threatening, multisystemic skin disease characterised by recurrent fever and extensive sterile pustules. In GPP, IL-36 is central to disease pathogenesis, and the prevention of IL-36-mediated signalling can improve clinical outcomes. In this review, we summarize the literature describing the biological functions of the IL-36 pathway. We also consider the evidence for uncontrolled activation of the IL-36 pathway in a wide range of skin (e.g., plaque psoriasis, pustular psoriasis, hidradenitis suppurativa, acne, Netherton syndrome, atopic dermatitis and pyoderma gangrenosum), lung (e.g., idiopathic pulmonary fibrosis), gut (e.g., intestinal fibrosis, inflammatory bowel disease and Hirschsprung's disease), kidney (e.g., renal tubulointerstitial lesions) and infectious diseases caused by a variety of pathogens (e.g., COVID-19; Mycobacterium tuberculosis, Pseudomonas aeruginosa, Streptococcus pneumoniae infections), as well as in cancer. We also consider how targeting the IL-36 signalling pathway could be used in treating inflammatory disease states.
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Affiliation(s)
- Kazumitsu Sugiura
- Department of Dermatology, Fujita Health University School of Medicine, Toyoake, Japan
| | - Hideki Fujita
- Department of Dermatology, Nihon University School of Medicine, Tokyo, Japan
| | - Mayumi Komine
- Department of Dermatology, Faculty of Medicine, Jichi Medical University, Tochigi, Japan
| | - Keiichi Yamanaka
- Department of Dermatology, Graduate School of Medicine, Mie University, Tsu, Japan
| | - Masashi Akiyama
- Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
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Ezanno AC, Texier G, Marchi J, Fougerousse AC. Factors Affecting Wound Healing after the Wide Surgical Excision of Hidradenitis Suppurativa Lesions. J Clin Med 2024; 13:5598. [PMID: 39337085 PMCID: PMC11433379 DOI: 10.3390/jcm13185598] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/02/2024] [Revised: 09/18/2024] [Accepted: 09/18/2024] [Indexed: 09/30/2024] Open
Abstract
Background: Hidradenitis suppurativa (HS) is a chronic and inflammatory disease. Its management depends on the stage and extent of the disease. Surgery plays an important role in treatment options. This study explores the factors influencing healing after wide excision. Methods: This study analyzed data from patients who underwent wide excision for HS between 2016 and 2021. Results: A total of 160 patients (64.4% women) were included, with surgeries performed in the axillae (70), inguinal-ano-genital (73), and other locations (17, including gluteal). The mean TTWC was 74 ± 6 days, varying from 11 to 445 days. Factors negatively influencing TTWC included axillary localization (p < 0.001) and the presence of another inflammatory disease (p = 0.017). Factors positively influencing healing were smoking (<0.001) and previous or ongoing medical treatment (antibiotherapy or biologics) (p = 0.011). Obesity or being overweight did not impact the TTWC in multivariate analysis, although overweight was significant in univariate analysis. Conclusions: While smoking cessation remains important in the management of HS, it does not appear to be a prerequisite for successful surgical treatment. Conversely, patients with an inflammatory disease or those undergoing surgery for an axillary lesion exhibit slower healing and should be informed of potential healing delays before surgery.
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Affiliation(s)
- Anne-Cecile Ezanno
- Department of Digestive Surgery, Begin Military Teaching Hospital, 94160 Saint-Mandé, France
| | - Gaëtan Texier
- Armed Forces Epidemiology and Public Health Center, 13014 Marseille, France
- VITROME, IHU-Méditerranée Infection, Aix Marseille University, 13005 Marseille, France
| | - Joffrey Marchi
- Armed Forces Epidemiology and Public Health Center, 13014 Marseille, France
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Alavi A, Prens EP, Kimball AB, Frew JW, Krueger JG, Mukhopadhyay S, Gao H, Ranganathan U, Ivanoff NB, Hernandez Daly AC, Zouboulis CC. Proof-of-concept study exploring the effect of spesolimab in patients with moderate-to-severe hidradenitis suppurativa: a randomized double-blind placebo-controlled clinical trial. Br J Dermatol 2024; 191:508-518. [PMID: 38576350 DOI: 10.1093/bjd/ljae144] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/12/2024] [Revised: 03/26/2024] [Accepted: 03/28/2024] [Indexed: 04/06/2024]
Abstract
BACKGROUND Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease with a considerable disease burden. Existing treatment options are limited and often suboptimal; a high unmet need exists for effective targeted therapies. OBJECTIVES To explore the effects of spesolimab treatment in patients with HS. METHODS This randomized double-blind placebo-controlled proof-of-clinical-concept (PoCC) study was conducted at 25 centres across 12 countries from 3 May 2021 to 21 April 2022. Patients had moderate-to-severe HS for ≥ 1 year before enrolment. Patients were randomized (2 : 1) to receive a loading dose of 3600-mg intravenous spesolimab (1200 mg at weeks 0, 1 and 2) or matching placebo, followed by maintenance with either 1200-mg subcutaneous spesolimab every 2 weeks from weeks 4 to 10 or matching placebo. The primary endpoint was the percentage change from baseline in total abscess and inflammatory nodule (AN) count at week 12. Secondary endpoints were the absolute change from baseline in the International Hidradenitis Suppurativa Severity Score System (IHS4), percentage change from baseline in draining tunnel (dT) count, the proportion of patients achieving a dT count of 0, absolute change from baseline in the revised Hidradenitis Suppurativa Area and Severity Index (HASI-R), the proportion of patients achieving Hidradenitis Suppurativa Clinical Response (HiSCR50), the proportion of patients with ≥ 1 flare (all at week 12) and patient-reported outcomes. RESULTS In this completed trial, randomized patients (n = 52) received spesolimab (n = 35) or placebo (n = 17). The difference vs. placebo in least squares mean is reported. At week 12, the percentage change in total AN count was similar between treatment arms: -4.1% [95% confidence interval (CI) -31.7 to 23.4]. There was greater numerical improvement in the spesolimab arm, as measured by IHS4 (13.9, 95% CI -25.6 to -2.3); percentage change from baseline in dT count (-96.6%, 95% CI -154.5 to -38.8); and the proportion of patients achieving a dT count of 0 (18.3%, 95% CI -7.9 to 37.5). Spesolimab treatment also improved HASI-R and HiSCR50 vs. placebo. Spesolimab demonstrated a favourable safety profile, similar to that observed in trials in other diseases. CONCLUSIONS This exploratory PoCC study supports the development of spesolimab as a new therapeutic option in HS.
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Affiliation(s)
- Afsaneh Alavi
- Department of Dermatology, Mayo Clinic, Rochester, MN, USA
| | - Errol P Prens
- Department of Dermatology, Erasmus University Medical Center, Rotterdam, the Netherlands
| | | | - John W Frew
- School of Clinical Medicine, UNSW Medicine and Health, Sydney, NSW, Australia
| | - James G Krueger
- Laboratory for Investigative Dermatology, The Rockefeller University, New York, NY, USA
| | | | - Heli Gao
- Boehringer Ingelheim Shanghai Pharmaceuticals Co. Ltd, Shanghai, China
| | - Usha Ranganathan
- Boehringer Ingelheim International GmbH, Ingelheim Am Rhein, Germany
| | | | | | - Christos C Zouboulis
- Departments of Dermatology, Venereology, Allergology and Immunology, Staedtisches Klinikum Dessau, Brandenburg Medical School Theodor Fontane and Faculty of Health Sciences Brandenburg, Dessau, Germany
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49
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Merchant SA, Shah SFH. The impact of hidradenitis suppurativa on work productivity and performance: a systematic review and meta-analysis. Clin Exp Dermatol 2024; 49:1156-1163. [PMID: 38589980 DOI: 10.1093/ced/llae120] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/03/2024] [Accepted: 03/28/2024] [Indexed: 04/10/2024]
Abstract
BACKGROUND Hidradenitis suppurativa (HS) is a chronic inflammatory skin disorder affecting the skinfold regions. There is growing appreciation of the need for socioeconomic factors to be included in multidisciplinary assessments of HS. However, knowledge regarding HS and workplace function is limited. OBJECTIVES To assess the relationship between HS and workplace function. METHODS CINAHL, Embase, MEDLINE, PsycINFO and PubMed were systematically searched to collect data from studies in which validated surveys of workplace function were administered to patients with HS. RESULTS Of 1932 publications, 12 studies were included in this review and 7 reported sufficient data for meta-analysis. The studies included in this review encompassed 5187 patients with HS and no controls. All studies used the Work Productivity and Activity Impairment questionnaire, reporting percentage scores for absenteeism, presenteeism, total work productivity impairment (TWPI) and total activity impairment (TAI). The pooled mean scores for HS were calculated as 10.17% [95% confidence interval (CI) 8.68-11.66] for absenteeism, 31.13% (95% CI 25.02-37.23) for presenteeism, 34.25% (95% CI 29.37-39.14) for TWPI and 42.23% (95% CI 38.56-45.89) for TAI. Significant heterogeneity was identified; most studies were of 'poor' to 'fair' quality. CONCLUSIONS Current evidence suggests considerable impairment of workplace functioning in patients with HS. Our findings point to a significant unmet treatment need with respect to improving working capability in HS. The existing literature is inadequate to reliably assess the mechanisms underlying this effect or to comparatively assess the capabilities of HS therapies to improve workplace function.
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Affiliation(s)
- Serena A Merchant
- Tunbridge Wells Hospital, Maidstone and Tunbridge Wells NHS Foundation Trust, Tunbridge Wells, UK
| | - Syed F H Shah
- John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
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50
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Raudonis T, Šakaitytė A, Vileikis TP, Černel V, Gancevičiene R, Zouboulis CC. Demographic Data, Risk Factors, and Disease Burden of HS Patients in Lithuania at a Reference Center. Healthcare (Basel) 2024; 12:1849. [PMID: 39337190 PMCID: PMC11431364 DOI: 10.3390/healthcare12181849] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/26/2024] [Revised: 09/08/2024] [Accepted: 09/12/2024] [Indexed: 09/30/2024] Open
Abstract
BACKGROUND Hidradenitis suppurativa (HS) diagnosis often faces a global delay of 7.2 years due to factors like lack of recognition, stigma, and socioeconomic barriers. Limited effective therapies and frequent exacerbations impact patients' quality of life, posing a significant burden on healthcare systems. METHODS HS patients were assessed according to European Hidradenitis Suppurativa Foundation (EHSF) Registry questionnaire guidelines at various stages of the disease and treatment. RESULTS The study included 49 patients; 57.14% (n = 28) of them were male. The average age of the subjects was 39.91 ± 13.665 years; the average BMI was 27.84 ± 7.362. A total of 59.18% (n = 29) were active or previous smokers. There were statistically more male smokers than female (p < 0.01). Average disease onset was 25.71 ± 13.743 years; the mean time to diagnosis was 5.2 ± 7.607 years. A total of 70.2% (n = 33) were previously misdiagnosed. Subjects had 6.17 ± 6.98 painful days over the preceding 4 weeks. The average intensity of pain according to the visual analogue scale (VAS) was 5.60 ± 3.36 points. The mean dermatology life quality index (DLQI) at baseline was 8.9 ± 7.436. CONCLUSIONS The research revealed delayed diagnoses, especially for females. Smoking was linked to higher Hurley stages, with a prevalence among male smokers, and HS had a substantial impact on patients' quality of life.
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Affiliation(s)
- Tadas Raudonis
- Clinic of Infectious Disease and Dermatovenereology, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, M. K. Čiurlionio g. 21, 03101 Vilnius, Lithuania; (A.Š.); (T.P.V.); (R.G.)
- European Hidradenitis Suppurativa Foundation e.V., 06847 Dessau, Germany;
| | - Austėja Šakaitytė
- Clinic of Infectious Disease and Dermatovenereology, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, M. K. Čiurlionio g. 21, 03101 Vilnius, Lithuania; (A.Š.); (T.P.V.); (R.G.)
| | - Tomas Petras Vileikis
- Clinic of Infectious Disease and Dermatovenereology, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, M. K. Čiurlionio g. 21, 03101 Vilnius, Lithuania; (A.Š.); (T.P.V.); (R.G.)
| | - Vitalij Černel
- Faculty of Medicine, Vilnius University, M. K. Čiurlionio g. 21, 03101 Vilnius, Lithuania;
| | - Rūta Gancevičiene
- Clinic of Infectious Disease and Dermatovenereology, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, M. K. Čiurlionio g. 21, 03101 Vilnius, Lithuania; (A.Š.); (T.P.V.); (R.G.)
- European Hidradenitis Suppurativa Foundation e.V., 06847 Dessau, Germany;
| | - Christos C. Zouboulis
- European Hidradenitis Suppurativa Foundation e.V., 06847 Dessau, Germany;
- Departments of Dermatology, Venereology, Allergology and Immunology, Dessau Medical Center, Brandenburg Medical School Theodor Fontane and Faculty of Health Sciences Brandenburg, 06847 Dessau, Germany
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