Abstract

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), severe drug reactions, are often misdiagnosed due to their rarity and lack of information on differential diagnosis. The objective of the study was to develop an electronic medical record (EMR)-based algorithm to identify patients with SJS/TEN for future application in database studies. From the EMRs of a university hospital, two dermatologists identified all 13 patients with SJS/TEN seen at the Department of Dermatology as the case group. Another 1472 patients who visited the Department of Dermatology were identified using the ICD-10 codes for diseases requiring differentiation from SJS/TEN. One hundred of these patients were then randomly sampled as controls. Based on clinical guidelines for SJS/TEN and the experience of the dermatologists, we tested 128 algorithms based on the use of ICD-10 codes, clinical courses for SJS/TEN, medical encounters for mucocutaneous lesions from SJS/TEN, and items to exclude paraneoplastic pemphigus. The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and diagnostic odds ratio (DOR) of each algorithm were calculated, and the optimal algorithm was defined as that with high PPV and maximal sensitivity and specificity. One algorithm, consisting of a combination of clinical course for SJS/TEN, medical encounters for mucocutaneous lesions from SJS/TEN, and items to exclude paraneoplastic pemphigus, but not ICD-10 codes, showed a sensitivity of 76.9%, specificity of 99.0%, PPV of 40.5%, NPV of 99.8%, and DOR of 330.00. We developed a potentially optimized algorithm for identifying SJS/TEN based on clinical practice records. The almost perfect specificity of this algorithm will prevent bias in estimating relative risks of SJS/TEN in database studies. Considering the small sample size, this algorithm should be further tested in different settings.

Highlights

  • Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare life-threatening diseases characterized by epidermal detachment and mucosal lesions, and are mainly induced by medications [1]

  • We developed four electronic medical record (EMR)-based algorithm sets, A to D, with four domains: Domain 1 included diagnosis of SJS/TEN at the Department of Dermatology; Domain 2 included items related to the clinical course of SJS/TEN; Domain 3 included items related to medical encounters for mucocutaneous lesions from SJS/TEN; and Domain 4 included items to exclude the differential diagnosis of paraneoplastic pemphigus (PNP) (Table 1)

  • The distribution of ICD-10 codes in the case and control patients is shown in S9 and S10 Tables

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Summary

Introduction

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare life-threatening diseases characterized by epidermal detachment and mucosal lesions, and are mainly induced by medications [1]. SJS and TEN are considered one disease entity, and differ in the percentage of body surface area affected: in Japan, SJS is defined as

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