Evidence-based approach to the treatment of hidradenitis suppurativa/acne inversa, based on the European guidelines for hidradenitis suppurativa
- PMID: 26831295
- PMCID: PMC5156664
- DOI: 10.1007/s11154-016-9328-5
Evidence-based approach to the treatment of hidradenitis suppurativa/acne inversa, based on the European guidelines for hidradenitis suppurativa
Abstract
Hidradenitis suppurativa/acne inversa (HS) is a chronic inflammatory skin disease characterized by painful, recurrent nodules and abscesses that rupture and lead to sinus tracts and scarring. To date, an evidence-based therapeutic approach has not been the standard of care and this is likely due to the lack of evidence based treatment guidelines. The purpose of this study was to promote a holistic evidence-based approach which implemented Level of Evidence and Strength of Recommendation for the treatment of HS. Based upon the European Dermatology Forumguidelines for the management of HS, evidence-based approach was explored for the treatment of HS. The diagnosis of HS should be made by a dermatologist or other healthcare professional with expert knowledge in HS. All patients should be offered adjuvant therapy as needed (pain management, weight loss, tobacco cessation, treatment of super infections, and application of appropriate dressings). The treating physician should be familiar with disease severity scores, especially Hurley staging, physician global assessment and others. The routine use of patient'reported outcomesincluding DLQI, itch and pain assessment (Visual Analogue Scale) is strongly recommended. The need for surgical intervention should be assessed in all patients depending upon type and extent of scarring, and an evidence-based surgical approach should be implemented. Evidence-based medical treatment of mild disease consists of topical Clindamycin 1 % solution/gel b.i.d. for 12 weeks or Tetracycline 500 p.o. b.i.d. for 4 months (LOE IIb, SOR B), for more widespread disease. If patient fails to exhibit response to treatment or for a PGA of moderate-to-severe disease, Clindamycin 300 p.o. b.i.d. with Rifampicin 600 p.o. o.d. for 10 weeks (LOE III, SOR C) should be considered. If patient is not improved, then Adalimumab 160 mg at week 0, 80 mg at week 2; then 40 mg subcutaneously weekly should be administered (LOE Ib, SOR A). If improvement occurs then therapy should be maintained as long as HS lesions are present. If the patient fails to exhibit response, then consideration of second or third line therapy is required. A growing body of evidence is being published to guide the treatment of HS. HS therapy should be based upon the evaluation of the inflammatory components as well as the scarring and should be directed by evidence-based guidelines. Treatment should include surgery as well as medical treatment. Future studies should include benefit risk ratio analysis and long term assessment of efficacy and safety, in order to facilitate long term evidence based treatment and rational pharmacotherapy.
Keywords: Evidence-based dermatology; Guidelines; Hidradenitis suppurativa; Medical therapy; Surgical therapy.
Conflict of interest statement
W Gulliver has received honoraria from AbbVie, Amgen, Celgene, Cipher, Eli Lilly, Galderma, Janssen, Leo, Novartis, Pfizer, Roche, Valeant for participation on advisory boards, consultant services, and speaker engagements. He has also received Grant/Research Support/Clinical Trials from AbbVie, Amgen, Astellas, Celgene, Lilly, Novartis, Pfizer and Regeneron. CC Zouboulis has received honoraria from AbbVie for participation on ad boards, as a consultant, investigator, and speaker; his department received grants from AbbVie and Novartis for his participation as an investigator. E Prens has received honoraria from AbbVie, Amgen, Celgene, Janssen, Galderma, Novartis and Pfizer for participation as a speaker, as member of advisory boards and he received investigator-initiated grants (paid to the Erasmus MC) from AbbVie, AstraZeneca, Janssen, and Pfizer. GBE Jemec has received honoraria from AbbVie, MSD, and Pfizer for participation on advisory boards, and grants from Abbvie, Actelion, Janssen-Cilag, Leo Pharma, and Novartis for participation as an investigator, and received speaker honoraria from AbbVie, Galderma, Leo Pharma, and MSD. He has furthermore received unrestricted research grants from AbbVie and Leo Pharma. T Tzellos has been reimbursed for travel expenses and hotel accommodation to attend dermatologic congresses by Janssen-Cilag, by MSD, and by Novartis. T. Tzellos also participates at the hidradenitis suppurativa advisory board of Abbvie.
References
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- Zouboulis CC, Desai N, Emtestam L, et al. European S1 guideline for the treatment of hidradenitis suppurativa/acne inversa. J Eur Acad Dermatol Venereol. 2015 - PubMed
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