Original articleRetrospective review of Stevens-Johnson syndrome/toxic epidermal necrolysis treatment comparing intravenous immunoglobulin with cyclosporine
Section snippets
Methods
The procedures and protocols of this study were reviewed and approved by the Clinical Research Ethics Board of the University of British Columbia. Using the International Classification of Diseases Version 9 codes for SJS/TEN, we were able to identify 62 patients admitted from January 2001 to December 2011 to Vancouver General Hospital, British Columbia, Canada, for SJS/TEN. Vancouver General Hospital serves as a referral center for the majority of SJS/TEN cases in the province as it has a
Results
We identified 71 patients admitted with a possible diagnosis of SJS/TEN between January 2001 and December 2011 (Fig 1). After chart review, 7 patients were excluded from further evaluation because of an alternate diagnosis. The 64 remaining patient charts were classified according to the systemic treatment received, either IVIg or cyclosporine or supportive measures only. It should be noted that none of the patients received glucocorticoids after evaluation by the dermatology service, however a
Discussion
The systemic treatment of SJS/TEN remains controversial. To date, much of the information regarding IVIg and cyclosporine use has come from case reports, case series, or small open prospective trials. In this retrospective study of IVIg versus cyclosporine, we show a mortality benefit to cyclosporine use and possible increased mortality with IVIg use.
One of the major points of contention between studies examining IVIg has been the discrepancy between low-dose IVIg (0.2-0.5 g/kg) and high-dose
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Funding sources: None.
Conflicts of interest: None declared.