Development of a Skin-Directed Scoring System for Stevens-Johnson Syndrome and Epidermal Necrolysis: A Delphi Consensus Exercise. Academic Article uri icon

Overview

abstract

  • IMPORTANCE: Scoring systems for Stevens-Johnson syndrome and epidermal necrolysis (EN) only estimate patient prognosis and are weighted toward comorbidities and systemic features; morphologic terminology for EN lesions is inconsistent. OBJECTIVES: To establish consensus among expert dermatologists on EN terminology, morphologic progression, and most-affected sites, and to build a framework for developing a skin-directed scoring system for EN. EVIDENCE REVIEW: A Delphi consensus using the RAND/UCLA appropriateness criteria was initiated with a core group from the Society of Dermatology Hospitalists to establish agreement on the optimal design for an EN cutaneous scoring instrument, terminology, morphologic traits, and sites of involvement. FINDINGS: In round 1, the 54 participating dermatology hospitalists reached consensus on all 49 statements (30 appropriate, 3 inappropriate, 16 uncertain). In round 2, they agreed on another 15 statements (8 appropriate, 7 uncertain). There was consistent agreement on the need for a skin-specific instrument; on the most-often affected skin sites (head and neck, chest, upper back, ocular mucosa, oral mucosa); and that blanching erythema, dusky erythema, targetoid erythema, vesicles/bullae, desquamation, and erosions comprise the morphologic traits of EN and can be consistently differentiated. CONCLUSIONS AND RELEVANCE: This consensus exercise confirmed the need for an EN skin-directed scoring system, nomenclature, and differentiation of specific morphologic traits, and identified the sites most affected. It also established a baseline consensus for a standardized EN instrument with consistent terminology.

authors

  • Waters, Margo
  • Dobry, Allison
  • Le, Stephanie T
  • Shinkai, Kanade
  • Beachkofsky, Thomas M
  • Davis, Mark D P
  • Dominguez, Arturo R
  • Kroshinsky, Daniela
  • Markova, Alina
  • Micheletti, Robert G
  • Mostaghimi, Arash
  • Pasieka, Helena B
  • Rosenbach, Misha
  • Seminario-Vidal, Lucia
  • Trinidad, John
  • Albrecht, Joerg
  • Altman, Emily M
  • Arakaki, Ryan
  • Arden-Jones, Michael
  • Bridges, Alina G
  • Cardones, Adela R
  • Chadha, Angad A
  • Chen, Jennifer K
  • Chen, Steven T
  • Cheng, Kyle
  • Daveluy, Steven
  • DeNiro, Katherine L
  • Harp, Joanna
  • Keller, Jesse J
  • King, Brett
  • Korman, Abraham M
  • Lowenstein, Eve J
  • Luxenberg, Erin
  • Mancuso, Jennifer Brescoll
  • Mauskar, Melissa M
  • Milam, Philip
  • Motaparthi, Kiran
  • Nelson, Caroline A
  • Nguyen, Cuong V
  • Nutan, Fnu
  • Ortega-Loayza, Alex G
  • Patel, Tejesh
  • Rahnama-Moghadam, Sahand
  • Rekhtman, Sergey
  • Rojek, Nathan W
  • Sarihan, Mansi
  • Shaigany, Sheila
  • Sharma, Timmie R
  • Shearer, Sabrina M
  • Shields, Bridget E
  • Strowd, Lindsay C
  • Tartar, Danielle M
  • Thomas, Cristina
  • Wanat, Karolyn A
  • Walls, Andrew C
  • Zaba, Lisa C
  • Ziemer, Carolyn M
  • Maverakis, Emanual
  • Kaffenberger, Benjamin H

publication date

  • May 31, 2023

Research

keywords

  • Stevens-Johnson Syndrome

Identity

Digital Object Identifier (DOI)

  • 10.1001/jamadermatol.2023.1347

PubMed ID

  • 37256599