Pediatric Stevens-Johnson syndrome and toxic epidermal necrolysis in the United States
- PMID: 28285784
- PMCID: PMC5502094
- DOI: 10.1016/j.jaad.2016.12.024
Pediatric Stevens-Johnson syndrome and toxic epidermal necrolysis in the United States
Abstract
Background: Little is known about the epidemiology of Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) in children.
Objective: We sought to determine the morbidity, mortality, and comorbid health conditions of SJS and TEN in US children.
Methods: This was a cross-sectional study of the 2009 to 2012 Nationwide Inpatient Sample, which contains a representative 20% sample of all US hospitalizations. Sociodemographics, inflation-adjusted cost, length of stay, comorbidities, and mortality were analyzed using descriptive statistics and multivariate regression analyses.
Results: The incidences of SJS, SJS-TEN, and TEN were a mean 5.3, 0.8, and 0.4 cases per million children per year in the US, respectively. Prolonged length of stay and higher costs of care (SJS: 9.4 ± 0.6 days, $24,947 ± $3171; SJS-TEN: 15.7 ± 1.5 days, $63,787 ± $8014; TEN: 20.4 ± 6.3 days, $102,243 ± $37,588) were observed compared with all other admissions (4.6 ± 0.1 days, $10,496 ± $424). Mortality was 0% for SJS, 4% for SJS-TEN, and 16% for TEN. In regression models, predictors of mortality included renal failure (adjusted OR [aOR] 300.28, 95% confidence interval [CI] 48.59->999.99), malignancy (aOR 54.33, 95% CI 9.40-314.22), septicemia (aOR 30.45, 95% CI 7.91-117.19), bacterial infection (aOR 20.38, 95% CI 5.44-76.36), and epilepsy (aOR 5.56, 95% CI 1.37-26.2).
Limitations: Data regarding treatment were not available. Date of diagnosis of comorbidities was not present, precluding temporal analysis.
Conclusions: Pediatric SJS/TEN poses a substantial health burden in the United States.
Keywords: Stevens-Johnson syndrome; burden of disease; children; epidemiology; hospitalization; pediatric; toxic epidermal necrolysis.
Copyright © 2016 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflicts of interest: The authors have no conflicts of interest relevant to this article to disclose.
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Comment in
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Prognosis and management of Stevens-Johnson syndrome and toxic epidermal necrolysis.J Am Acad Dermatol. 2017 Oct;77(4):e117. doi: 10.1016/j.jaad.2017.05.057. J Am Acad Dermatol. 2017. PMID: 28917480 No abstract available.
References
-
- 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. Archives of dermatology. 1993;129:92–6. - PubMed
-
- Rzany B, Mockenhaupt M, Baur S, Schroder W, Stocker U, Mueller J, et al. Epidemiology of erythema exsudativum multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis in Germany (1990–1992): structure and results of a population-based registry. Journal of clinical epidemiology. 1996;49:769–73. - PubMed
-
- Schopf E, Stuhmer A, Rzany B, Victor N, Zentgraf R, Kapp JF. Toxic epidermal necrolysis and Stevens-Johnson syndrome. An epidemiologic study from West Germany. Archives of dermatology. 1991;127:839–42. - PubMed
-
- Strom BL, Carson JL, Halpern AC, Schinnar R, Snyder ES, Shaw M, et al. A population-based study of Stevens-Johnson syndrome. Incidence and antecedent drug exposures. Archives of dermatology. 1991;127:831–8. - PubMed
-
- Roujeau JC, Guillaume JC, Fabre JP, Penso D, Flechet ML, Girre JP. Toxic epidermal necrolysis (Lyell syndrome). Incidence and drug etiology in France, 1981–1985. Archives of dermatology. 1990;126:37–42. - PubMed
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