4.6 Article

The role of prior corticosteroid use on the clinical course of Stevens-Johnson syndrome and toxic epidermal necrolysis: a case-control analysis of patients selected from the multinational EuroSCAR and RegiSCAR studies

期刊

BRITISH JOURNAL OF DERMATOLOGY
卷 167, 期 3, 页码 555-562

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1365-2133.2012.11074.x

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资金

  1. ADIR Cie
  2. Bayer Pharma/AG/Vital
  3. Boehringer Ingelheim
  4. Cassenne
  5. Ciba Geigy/Novartis
  6. Cilag GmbH
  7. Dr Willmar Schwabe
  8. Goedecke Parke Davis
  9. Glaxo Wellcome/GlaxoSmithKline
  10. Hoechst AG/Hoechst Marion Roussel/Aventis
  11. Hoffmann-La Roche
  12. IRIS Servier
  13. Jouveinal Lab
  14. LEO
  15. Lilly
  16. MSD Sharp Dohme
  17. Pfizer
  18. Rhone Poulenc Rorer
  19. Sanofi Winthrop/Sanofi Synthelabo GmbH
  20. Schering AG
  21. INSERM (Institut National de la Sante et de la Recherche Medicale)
  22. French Ministry of Health [PHRC AOM 98027]
  23. European Commission [QLRT-2002-01738]
  24. GIS-Institut des Maladies Rares
  25. INSERM in France [4CH09G]
  26. Bayer Vital
  27. Boehringer-Ingelheim
  28. Cephalon
  29. GlaxoSmithKline
  30. MSD Sharp and Dohme
  31. Merck
  32. Novartis
  33. Roche
  34. Sanofi-Aventis
  35. Servier
  36. Tibotec
  37. Else Kroner-Fresenius Foundation

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Background Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are immunologically mediated, severe cutaneous adverse reactions involving cytotoxic T cells, natural killer cells and various mediators. In large studies, up to 15% of SJS/TEN occurred in patients with chronic corticosteroid use. It is unclear if this prior exposure to corticosteroids modified the disease course. Objectives To evaluate whether systemic corticosteroid usage prior to the onset of SJS/TEN modified the clinical course and outcome. If a disease-modifying effect is present, information from such an analysis may have implications on the therapeutic use of corticosteroids in SJS/TEN. Methods This is a case-control study based on data collected in the EuroSCAR and RegiSCAR studies. Ninety-two cases of SJS/TEN with exposure to corticosteroids prior to the onset of disease, and 321 randomly selected SJS/TEN patients without prior exposure were included. Primary outcomes included progression of disease, disease severity and mortality. A secondary analysis of latency between the beginning of drug use and the onset of disease, based on exposure to a single high-risk drug, was also performed. Results On multivariate analysis, cases with prior exposure to corticosteroids had a longer progression of disease by 2.2 days [95% confidence interval (CI) 1.1-1-3.2]. The disease severity and mortality outcome were unaffected. In addition, there is evidence that corticosteroids delayed the onset of SJS/TEN in patients with exposure to high-risk drugs by 7.1 days (CI) 0.2 to 14.5). Conclusions The prior use of corticosteroids prolonged the period of disease progression without influencing the disease severity or mortality. In addition, when SJS/TEN is preceded by use of a single high-risk drug, the latency between the drug intake and the onset of SJS/TEN may also be increased. These findings suggest that corticosteroids have a mild impact on the course of SJS/TEN, and further studies are required to clarify any potential therapeutic effects.

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