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Year : 2008  |  Volume : 74  |  Issue : 5  |  Page : 494-495

Authors' reply

Department of Dermatology, All India Institute of Medical Sciences, New Delhi-110 029, India

Correspondence Address:
Vinod K Sharma
Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi
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Source of Support: None, Conflict of Interest: None

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How to cite this article:
Sharma VK, Sethuraman G. Authors' reply. Indian J Dermatol Venereol Leprol 2008;74:494-5

How to cite this URL:
Sharma VK, Sethuraman G. Authors' reply. Indian J Dermatol Venereol Leprol [serial online] 2008 [cited 2020 Nov 29];74:494-5. Available from:

We thank Dr. Pasricha for his interest in our paper and his comments about the use of steroids in  Stevens-Johnson syndrome More Details (SJS) and toxic epidermal necrolysis (TEN). It is apparent from the title that our paper was focused mainly on the etiological agents and outcome of SJS and TEN. [1] The role of steroids in the treatment of SJS-TEN generates a lot of discussion and the recommendation has recently been published in the IADVL therapeutic guidelines. [2] In our report we have used systemic steroids in all except one. [1]

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe adverse cutaneous drug reactions characterized by massive keratinocyte apoptosis. It has been shown that the apoptosis is mediated by the drug specific cytotoxic T cells through the activation of the Fas receptor by increased Fas ligand expression, via the perforin / granzyme pathway. Several cytokines produced by the T cells, macrophages,and keratinocytes, upregulate the adhesion molecules and enhance the expression of Fas and FasL on keratinocytes. [3],[4] Hence there are enough reasons to start immunosuppressive therapy such as steroids in the early evolving stage of the disease. The exact mode of action of steroids in SJS/TEN is not known. But they have a plethora of immunomodulating / immunosuppressive and anti-apoptotic effects which will hamper the events leading to apoptosis.

There are many reports of better outcomes with the use of steroids in SJS/TEN. [5],[6] In a report of 52 cases of SJS and 65 cases (2000-2006) of TEN from Japan, the authors have used methyl prednisolone pulse (125-1000 mg/day) for 3 days. They have concluded that the mortality rates for patients with SJS and TEN were 1.9% and 6.2% respectively which has decreased from 21.6% (58/269) during previous 17 years (1981-1997) in which period steroids were rarely used. [7] Tripathi et al in their report of 67 cases with SJS, 66 cases recovered with steroid therapy. [8] In a recent report of 12 cases of SJS/TEN, from Netherlands, the authors have used dexamethasone pulse therapy, 11 patients recovered and only one died due to brain metastasis while his skin had healed. [9]

There are some conflicting views on steroid usage in SJS/TEN. It is reported that systemic corticosteroids can prolong wound healing, increase the risk of infection, mask early signs of sepsis, and may precipitate gastrointestinal bleeding, thus increasing mortality. [3] What we believe from our experience is that use of steroids in a fully developed case of SJS/TEN or prolonged use of steroids, might be detrimental and predispose to sepsis and other complications.

The fatality in SJS/TEN is largely caused by sepsis, thrombocytopenia, leucopenia, electrolyte imbalance, total body surface area involvement, renal involvement, and delay in referral to special burns centre. TEN itself predisposes to sepsis due to loss of skin barrier, hospitalization and nosocomial infection and use of empirical antibiotics. Sepsis is one of the most important causes of death in TEN (Odds Ratio 304). [10] The mortality rate varies from 20-60%. [10] In a retrospective review of 56 patients with TEN over a period of 13 years, the mortality was 35.7%, which was not associated with steroid use. [10] Most of the deaths occur in patients with TEN as is evident in our study. [1] The proportion of SJS, TEN and SJS-TEN overlap in different series contributes to varied mortality rates.

Intravenous immune globulin (IVIG) is also found to be useful in SJS/TEN. [11],[12],[13],[14],[15] It interferes with Fas-FasL interactions. The recommended dose is 1g/kg/day for 3 days. In a multicenter retrospective study involving 14 European and American centers, IVIG was used in 48 TEN patients and the survival rate was 88%. [11] However some data show no benefit on mortality or progression. [16],[17] In one of the recent report by Faye and Roujeau, nine different series published in indexed journals were analyzed. Among the 156 patients of SJS or TEN treated with IVIG, 32 patients died. When the analysis was restricted to 5 series that included some comparison with the expected deaths, the mortality was 27% versus an expected rate of 30%. [18] This clearly shows that the use of IVIG in SJS/TEN is questionable. The additional limiting factor of IVIG is the high cost.

Overall from our personal experience and also from the literature search, it seems that steroids or other immunosuppressive drugs have definite role in SJS/TEN.

We agree with Dr. Pasricha that 1) Steroids should be used in SJS/TEN as immune mechanisms are involved in the massive keratinocyte necrosis. 2) Steroids should be used in early and evolving disease preferably within the first 72 hours of onset (to prevent widespread involvement) or during reappearance of erythema and/or necrosis on newly regenerated skin. However, we feel that once a large area of skin is uncovered, i.e. >20% of BSA, the advantages of the treatment would be far outweighed by its drawbacks. Dose and duration of steroid therapy is to be individualized. Oral prednisolone 1-2 mg/kg per day or parenteral steroid, either dexamethasone 8-16 mg or equivalent hydrocortisone, is started and continued for 3-5 days followed by rapid tapering. Further, steroids have limited or no role in fully established cases of SJS/TEN with no new lesions. These cases should be managed with supportive and barrier nursing care.

  References Top

1.Sharma VK, Sethuraman G, Minz A. Stevens Johnson syndrome, toxic epidermal necrolysis and SJS-TEN overlap: A retrospective study of causative drugs and clinical outcome. Indian J Dermatol Venereol Leprol 2008;74:238-40.  Back to cited text no. 1  [PUBMED]  Medknow Journal
2.Sharma VK. Guidelines for Stevens Johnson syndrome and Toxic epidermal Necrolysis, and Psoriasis. Delhi: Therapeutic Guidelines Committee IADVL; 2007. p. 7-19.  Back to cited text no. 2    
3.Chave TA, Mortimer NJ, Sladden MJ, Hall AP, Hutchinson PE. Toxic epidermal necrolysis: Current evidence, practical management and future directions. Br J Dermatol 2005;153:241-53.  Back to cited text no. 3  [PUBMED]  [FULLTEXT]
4.Borchers AT, Lee JL, Naguwa SM, Cheema GS, Gershwin ME. Stevens-Johnson syndrome and toxic epidermal necrolysis. Autoimmun Rev 2008;7:598-605.   Back to cited text no. 4  [PUBMED]  [FULLTEXT]
5.Pasricha JS. Management of toxic epidermal necrolysis. Indian J Dermatol Venereol Leprol 1990;50:458-9.  Back to cited text no. 5    
6.Pasricha JS, Khaitan BK, Shantharaman R, Mittal A, Girdhar M. Toxic epidermal necrolysis. Int J Dermatol 1996;35:523-7.  Back to cited text no. 6    
7.Yamane Y, Aihara M, Ikezawa Z. Analysis of Stevens-Johnson syndrome and toxic epidermal necrolysis in Japan from 2000 to 2006. Allergol Int 2007;56:419-25.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]
8.Tripathi A, Ditto AM, Grammer LC, Greenberger PA, McGrath KG, Zeiss CR, et al . Corticosteroid therapy in an additional 13 cases of Stevens-Johnson syndrome: A total series of 67 cases. Allergy Asthma Proc 2000;21:101-5.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]
9.Kardaun SH, Jonkman MF. Dexamethasone pulse therapy for Stevens-Johnson syndrome/toxic epidermal necrolysis. Acta Derm Venereol 2007;87:144-8.  Back to cited text no. 9  [PUBMED]  [FULLTEXT]
10.Ducic I, Shalom A, Rising W, Nagamoto K, Munster AM. Outcome of patients with toxic epidermal necrolysis syndrome revisited. Plast Reconstr Surg 2002;110:768-73  Back to cited text no. 10  [PUBMED]  [FULLTEXT]
11.Prins C, Kerdel FA, Padilla RS, Hunziker T, Chimenti S, Viard I, et al . TEN-IVIG Study Group. Toxic epidermal necrolysis-intravenous immunoglobulin. Treatment of toxic epidermal necrolysis with high-dose intravenous immunoglobulins: Multicenter retrospective analysis of 48 consecutive cases. Arch Dermatol 2003;139:26-32.  Back to cited text no. 11    
12.Trent JT, Kirsner RS, Romanelli P, Kerdel FA. Analysis of intravenous immunoglobulin for the treatment of toxic epidermal necrolysis using SCORTEN: The University of Miami Experience. Arch Dermatol 2003;139:39-43.  Back to cited text no. 12  [PUBMED]  [FULLTEXT]
13.Al-Mutairi N, Arun J, Osama NE, Amr Z, Mazen AS, Ibtesam el-A. Prospective, noncomparative open study from Kuwait of the role of intravenous immunoglobulin in the treatment of toxic epidermal necrolysis. Nazeha el-B. Int J Dermatol 2004;43:847-51.  Back to cited text no. 13    
14.Tristani-Firouzi P, Petersen MJ, Saffle JR, Morris SE, Zone JJ. Treatment of toxic epidermal necrolysis with intravenous immunoglobulin in children. J Am Acad Dermatol 2002;47:548-52.   Back to cited text no. 14  [PUBMED]  [FULLTEXT]
15.Prins C, Vittorio C, Padilla RS, Hunziker T, Itin P, Fφrster J, et al . Effect of high-dose intravenous immunoglobulin therapy in Stevens-Johnson syndrome: A retrospective, multicenter study. Dermatology 2003;207:96-9.  Back to cited text no. 15    
16.Bachot N, Revuz J, Roujeau JC. Intravenous immunoglobulin treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis: A prospective noncomparative study showing no benefit on mortality or progression. Arch Dermatol 2003;139:33-6.  Back to cited text no. 16  [PUBMED]  [FULLTEXT]
17.Shortt R, Gomez M, Mittman N, Cartotto R.Intravenous immunoglobulin does not improve outcome in toxic epidermal necrolysis. J Burn Care Rehabil 2004;25:246-55.  Back to cited text no. 17  [PUBMED]  [FULLTEXT]
18.Faye O, Roujeau JC. Treatment of epidermal necrolysis with high-dose intravenous immunoglobulins (IV Ig): Clinical experience to date. Drugs 2005;65:2085-90.  Back to cited text no. 18  [PUBMED]  


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