Drug reaction with eosinophilia and systemic symptoms (DRESS): an original multisystem adverse drug reaction. Results from the prospective RegiSCAR study

S. H. Kardaun*, P. Sekula, L. Valeyrie-Allanore, Y. Liss, C. Y. Chu, D. Creamer, A. Sidoroff, L. Naldi, M. Mockenhaupt, J. C. Roujeau, RegiSCAR Study Grp

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    679 Citations (Scopus)

    Abstract

    BackgroundCases of severe drug hypersensitivity, demonstrating a variable spectrum of cutaneous and systemic involvement, are reported under various names, especially drug reaction with eosinophilia and systemic symptoms (DRESS). Case definition and overlap with other severe cutaneous adverse reactions (SCAR) are debated.

    ObjectivesTo analyse the spectrum of signs and symptoms of DRESS and distribution of causative drugs in a large multicentre series.

    Patients and methodsRegiSCAR, a multinational registry of SCAR, prospectively enrolled 201 potential cases from 2003 to mid-2009. Using a standardized scoring system, 117 cases were validated as showing probable or definite DRESS.

    ResultsThe male/female ratio was 080; females were borderline significantly younger than males. Next to the ubiquitous exanthema, the main features were eosinophilia (95%), visceral involvement (91%), high fever (90%), atypical lymphocytes (67%), mild mucosal involvement (56%) and lymphadenopathy (54%). The reaction was protracted in all but two patients; two patients died during the acute phase. Drug causality was plausible in 88% of cases. Antiepileptic drugs were involved in 35%, allopurinol in 18%, antimicrobial sulfonamides and dapsone in 12% and other antibiotics in 11%. The median time interval after drug intake was 22days (interquartile range 17-31) for all drugs with (very) probable causality, with differences between drugs.

    ConclusionThis prospective observational study supports the hypothesis that DRESS is an original phenotype among SCAR in terms of clinical and biological characteristics, causative drugs, and time relation. The diversity of causative drugs was rather limited, and mortality was lower than that suggested by prior publications.

    Original languageEnglish
    Pages (from-to)1071-1080
    Number of pages10
    JournalBritish Journal of Dermatology
    Volume169
    Issue number5
    DOIs
    Publication statusPublished - Nov-2013

    Keywords

    • STEVENS-JOHNSON-SYNDROME
    • TOXIC EPIDERMAL NECROLYSIS
    • GENERALIZED EXANTHEMATOUS PUSTULOSIS
    • INDUCED HYPERSENSITIVITY SYNDROME
    • HERPESVIRUS 6 INFECTION
    • HUMAN-HERPESVIRUS-6 REACTIVATION
    • INDUCED PSEUDOLYMPHOMA
    • CLINICAL-FEATURES
    • RISK-FACTORS
    • RASH

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