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BRIEF REPORT
Year : 2008  |  Volume : 74  |  Issue : 3  |  Page : 238-240

Stevens Johnson syndrome, toxic epidermal necrolysis and SJS-TEN overlap: A retrospective study of causative drugs and clinical outcome


Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India

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


DOI: 10.4103/0378-6323.41369

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  Abstract 

Background and Aims: Stevens Johnson syndrome (SJS), toxic epidermal necrolysis (TEN) and SJS-TEN overlap are serious adverse cutaneous drug reactions. Drugs are often implicated in these reactions. Methods: A retrospective analysis of inpatients' data with these dermatological diagnoses were carried out for three years, to study the causative drugs, clinical outcome, and mortality in these conditions. Results: Thirty patients (15 TEN, nine SJS-TEN overlap, and six SJS) were admitted. In 21 cases, multiple drugs were implicated whereas single drugs were responsible in nine. Anticonvulsants (35.08%) were the most commonly implicated drugs followed by antibiotics (33.33%) and NSAIDS (24.56%). Twenty-five patients recovered whereas five died (four TEN, one SJS-TEN overlap). Conclusion: Anticonvulsants, antibiotics and NSAIDs were the most frequently implicated drugs. TEN causes higher mortality than both SJS and SJS-TEN overlap.


Keywords: Anticonvulsants, SJS-TEN overlap, Stevens Johnson syndrome, toxic epidermal necrolysis


How to cite this article:
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

How to cite this URL:
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 [serial online] 2008 [cited 2019 Jul 22];74:238-40. Available from: http://www.ijdvl.com/text.asp?2008/74/3/238/41369



  Introduction Top


Cutaneous drug eruptions are one of the most frequent manifestations of adverse drug reactions. [1] Adverse cutaneous drug reactions are found to affect 2-3% of hospitalized patients. [2] The reported percentage of "potentially serious" adverse drug reactions varies greatly and is estimated to be above 2%. [2] Some of the serious reactions include Stevens Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and the overlap category of SJS and TEN. SJS is a serious mucocutaneous illness with systemic symptoms characterized by the presence of flat, atypical target lesions and the epidermal detachment is < 10% of the total body surface area (BSA). Two or more mucosal sites are usually affected. [3] TEN is a life-threatening serious illness characterized by high fever and confluent erythema followed by necrolysis. [3] The epidermal detachment is > 30% of the total BSA. Flat, atypical target lesions may also be seen (TEN with spots) and sometimes, extensive necrolysis can occur without target lesions (TEN without spots). [3] In the SJS-TEN overlap category, the epidermal detachment is 10-30% of the total BSA. [3] Drugs are implicated in most of these serious adverse drug reactions. [2] These reactions are often associated with significant mortality. [3]

In this retrospective study, we present data on the causative drugs, clinical outcome and mortality of our patients with SJS, TEN or the SJS-TEN overlap category.


  Methods Top


Analysis was performed of the inpatient records of all patients hospitalized between July 2003 and September 2006 with the diagnosis of SJS, TEN or the SJS-TEN overlap category. The following details were recorded: the duration of the rash, drug intake, the time period between the drug intake and the appearance of the rash, systemic symptoms, the types of target lesions, extent of epidermal necrosis or detachment, mucosal involvement, and systemic evaluations. The diagnosis of SJS, TEN and the SJS-TEN overlap were made as per the criteria laid down by Bastuji et al . [3] Drug(s) that have been taken within four weeks preceding the onset of symptoms were considered as "culprit drugs". If the patient had taken more than one drug, all of them were considered as culprit drugs.

All the patients were given barrier nursing care including regular monitoring of vitals, fluid and electrolyte balance, strict asepsis, and nutrition. Prophylactic antibiotics were administered to address infections due to gram negative and/or gram positive organisms. All except one patient were given short (2-14 days) courses of tapering doses of systemic steroids-inj. dexamethasone dose ranging from 4-8 mg or an equivalent corticosteroid.


  Results Top


A total of 30 patients were admitted during the study period, of which 17 were females and 13 were males in the age range of 4-65 years (mean age = 22.3 ± 15.4 years). The duration of cutaneous eruption was 1-40 days (mean duration = 7.04 ± 7.89 days). The mean period between the intake of the drug and the onset of eruption was 24.4 ± 37.0 days. Twenty-six patients had prodromal symptoms in the form of fever, cough, sore throat and headache. Nine patients had underlying seizure disorder while two patients had intracranial pathologies. Two cases had systemic lupus erythematosus. Six patients were classified as SJS, nine as SJS-TEN overlap and 15 as TEN. The duration of hospital stay was 1-41 days (mean = 20.2 ± 15.1 days).

Multiple drugs were implicated in 21 cases while single drug was responsible for the reactions in the remaining nine patients. Fifty-seven drugs have been implicated in the observed adverse events, out of which anticonvulsants were the most common category (35.08%), followed by antibiotics (33.33%) and nonsteroidal antiinflammatory drugs (24.56%). Among the anticonvulsants, phenytoin (45%) and carbamazepine (30%) were the more common drugs. Cephalosporins (26%) were the most common group of antibiotics that caused the adverse reaction. Among the nine patients who reacted to a single drug as the culprit, anticonvulsants (phenytoin in four and carbamazepine in three) were implicated in seven cases. The detailed list of drugs causing adverse reactions is shown in [Table 1].

Systemic complications were observed more frequently among the TEN group [Table 2]. Twenty-five patients recovered completely while five patients died (four with TEN, one with SJS-TEN).


  Discussion Top


In agreement with other reports, we observed a female preponderance (56% females vs 44% males). [4],[5] The maximum number of cases were seen to be in their 2 nd decade of life. In contrast, Roujeau et al. reported the occurrence of these reactions in TEN cases in their 5 th decade of life. [5] The mean age in our study was 22.3 ± 15.4 years as compared to 63 and 25 years in TEN and SJS patients respectively, in a report from Germany. [5]

All patients in our study gave a history of drug intake prior to the onset of the reactions. However, Roujeau et al. [4] and Schopf et al . [5] reported a small number of patients (4.5 and 3%, respectively) with TEN who did not have any history of drug intake preceding the onset. Single drug was found to cause adverse cutaneous reactions in 60, 39 and 14.6% of the patients in our series, a report from Germany [5] and in a series studied by Roujeau et al, respectively. [4] The mean numbers of drugs causing the reactions in our study and in a series reported by Roujeau et al. were 3.36 ± 2.3 and 4.4 ± 3.4, respectively. [4]

In our 30 cases, of the 57 drugs implicated, the three most common groups of drugs were anticonvulsants, antibiotics and NSAIDS. Anticonvulsant drugs were also the drugs most frequently implicated in SJS-TEN in a six-year series examining drug reactions in 500 patients from Chandigarh, North India. [6] In another survey of the clinical spectrum of drug rashes due to antiepileptics, a significant number of patients had serious rashes of SJS and TEN and these were mostly due to phenytoin and carbamazepine. [7] Carbamazepine was the culprit in all the five cases of SJS and phenytoin in two of the six cases of TEN in a study of adverse cutaneous reactions in children and adolescents. [8] Kamalaiah et al. in their report of EM, SJS and TEN in North East Malaysia, also confirm that anticonvulsants were the most commonly implicated group of drugs. [9] In contrast to the Indian and Asian series, antimicrobial drugs were the most common group of drugs resulting in these serious reactions in many of the reports from developed countries. [10],[11],[12] In a French Survey, NSAIDS were most commonly involved as culprits causing adverse cutaneous reactions. [4]

The reported mortality rates in the largest series of patients with TEN was found to be 28.6% (10-70%). [13] In our series, the mortality rate was 26 and 9% in the TEN group and SJS-TEN overlap category, respectively. The role of systemic steroids in SJS and TEN is controversial although they may be used in patients with early active disease or with the reappearance of erythema in recovering cases. We have used dexamethasone in most of our patients and the observed mortality rate was comparable with that reported in many series in the literature. [13]

In conclusion, serious adverse reactions such as SJS, TEN and the overlap category of SJS-TEN are mostly caused by anticonvulsants, especially carbamazepine and phenytoin, and also by antibiotics and NSAIDS.

 
  References Top

1.Sharma VK, Sethuraman G, Kumar B. Cutaneous adverse drug reaction patterns to antimicrobial drugs in North India. J Assoc Physicians India 1998;46:1012-5.  Back to cited text no. 1    
2.Sharma VK, Sethuraman G. Adverse cutaneous reactions to drugs: An overview. J Postgrad Med 1998;42:15-22.  Back to cited text no. 2    
3.Bastuji-Garin S, Rzany B, Stern RS, Shear NH, Naldi L, Roujeau JC. Clinical classification of cases of toxic epidermal necrolysis, Stevens Johnson Syndrome and erythema multiforme. Arch Dermatol 1993;129:92-6.  Back to cited text no. 3  [PUBMED]  
4.Roujeau JC, Guillaume JC, Fabre JP, Penso Dominique P, Flechet ML, Girre JP. Toxic epidermal necrolysis (lyell Syndrome). Arch Dermatol 1990;126:37-42.  Back to cited text no. 4    
5.Schopf E, Stuhmer A, Rzany B, Victor N, Zentgraft R, Kapp JF. Toxic epidermal necrolysis and Stevens Johnson Syndrome: An epidemiologic study from West Germany. Arch Dermatol 1991;127:839-42.  Back to cited text no. 5    
6.Sharma VK, Sethuraman G, Kumar B. Cutaneous adverse drug reactions: Clinical pattern and causative agents: A 6 year series from Chandigarh, India. J Postgrad Med 2001;47:95-9.  Back to cited text no. 6    
7.Sharma VK, Vatve M, Sawhney IMS, Kumar B. Clinical spectrum of drug rashes due to antiepileptics. J Assoc Physicians India 1998;46:595-7.  Back to cited text no. 7    
8.Sharma VK, Dhar S. Clinical pattern of cutaneous drug eruption among children and adolescents in North India. Pediatr Dermatol 1995;12:178-83.   Back to cited text no. 8  [PUBMED]  
9.Kamaliah MD, Zaimal D, Mokhtar N, Nazmi N. Erythema multiforme, Steven Johnson Syndrome and toxic epidermal necrolysis in North East Malaysia. Int J Dermatol 1998;37:520-3.  Back to cited text no. 9    
10.Alanko K, Stubb S, Kauppinen K. Cutaneous drug reactions: Clinical types and causative agents. Acts Derm Venereol (Stockh) 1989;69:223-6.  Back to cited text no. 10    
11.Kauppinen K, Stubb S. Drug eruptions: Causative agents and clinical types. Acta Dermal Venereol (Stock) 1984;64:320-4.   Back to cited text no. 11    
12.Wong KC, Kennedy PJ, Lee S. Clinical manifestations and outcomes in 17 cases of Stevens Johnson Syndrome and toxic epidermal necrolysis. Australas J Dermatol 1999;40:131-4.   Back to cited text no. 12  [PUBMED]  [FULLTEXT]
13.Guillaume JC, Roujeau JC, Revuz J, Pensol D, Touraine R. The culprit drugs in 87 cases of toxic epidermal necrolysis (Lyell's Syndrome). Arch Dermatol 1987;123:1166-70.  Back to cited text no. 13    



 
 
    Tables

  [Table 1], [Table 2]

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