Cyclosporine Treatment of Drug-Induced Hypersensitivity Syndrome
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Published on: November 8, 2015
Mark G Kirchhof1, Aaron Wong2, Jan P Dutz3
1Department of Dermatology and Skin Science, University of British Columbia, Vancouver, British Columbia, Canada2Division of Dermatology, Department of Medicine, Queen's University, Kingston, Ontario, Canada.
Importance:
Drug-induced hypersensitivity syndrome (DIHS), also known as drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome, is a potentially life-threatening reaction to medications with a mortality rate up to 10%. Standard therapy involves the use of systemic corticosteroids with tapering doses extending up to 9 months after the initial reaction. Alternative treatments for DIHS are needed, especially for patients for whom systemic corticosteroids are contraindicated.
Objective:
To assess a short course of cyclosporine as first-line therapy for DIHS.
Design, Setting, And Participants:
In this case series, 2 patients referred to the dermatology service of an academic tertiary care hospital and subsequently diagnosed as having DIHS were studied from December 1, 2013, through July 31, 2014.
Interventions:
Short course (3-7 days) of cyclosporine.
Main Outcomes And Measures:
Clinical and laboratory indicators were examined to determine the timing and efficacy of cyclosporine treatment.
Results:
Two cases are reported of drug hypersensitivity reaction that were treated with cyclosporine, resulting in rapid and significant clinical improvement. The first case involved a woman in her 40s who developed DIHS after treatment with carbamazepine. A 7-day course of cyclosporine resulted in clinical resolution of the DIHS. The second case was that of a man in his 30s with minocycline-induced DIHS. A 3-day course of cyclosporine resulted in rapid and sustained clinical improvement.
Conclusions And Relevance:
A short course of cyclosporine was of therapeutic benefit in the treatment of 2 patients with DIHS. Short courses of cyclosporine in the acute care setting may be an alternative to longer courses of systemic corticosteroids in the treatment of DIHS.
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