Clinical characteristics of drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis: A single-center study.

IF 1.6 Q3 ALLERGY
Hye Won Yoo, Hye-Young Kim, Kihyuk Shin, Seong Heon Kim
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引用次数: 2

Abstract

Background: Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe adverse cutaneous reactions, most commonly triggered by medications, characterized by extensive necrosis and detachment of the epidermis.

Objective: We investigated the differences in clinical characteristics of drug-induced SJS/TEN depending on the type of drug in a single center.

Methods: The relevance of sex, age, culprit drugs, clinical features, courses, treatment options, and follow-up results were retrospectively evaluated in patients diagnosed with drug-induced SJS/TEN at Pusan National University Hospital between 2008 and 2019.

Results: Ninety-two patients with a mean age of 58.7 ± 20.2 years (range, 10-93 years) were included in the study. Those aged 60-80 years accounted for the largest number of patients (42.4%). Patients with drug-induced SJS/TEN comprised 40 women (43.5%) and 52 men (56.5%). We categorized drug-induced SJS/TEN cases by culprit drugs into 6 groups: antibiotics, allopurinol, antiepileptic (AED), nonsteroidal anti-inflammatory drugs (NSAIDs), acetaminophen, and other drugs. The rate of NSAID-induced disease significantly increased from SJS to TEN (p = 0.016). Among the patients in the NSAID group, the proportion of TEN (40%) was higher than that in the other groups (p = 0.021). The mean body surface area was significantly lower in the AED group than in the non-AED groups (7.1 ± 9.8 vs. 23.1 ± 27.3, p = 0.020) and higher in the NSAID group than in the non-NSAID groups (47.5 ± 39.5 vs. 15.7 ± 20.0, p = 0.010).

Conclusion: This study showed that the clinical characteristics of each causative drug group may be different in drug-induced SJS/TEN. Our findings may help clinicians better understand drug-induced SJS/TEN.

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药物性Stevens-Johnson综合征和中毒性表皮坏死松解的临床特征:一项单中心研究。
背景:Stevens-Johnson综合征(SJS)和中毒性表皮坏死松解症(TEN)是严重的皮肤不良反应,最常由药物引发,以表皮广泛坏死和脱离为特征。目的:探讨单中心药物性SJS/TEN在不同药物类型下的临床特征差异。方法:回顾性评价2008 - 2019年釜山国立大学医院诊断为药物性SJS/TEN患者的性别、年龄、罪魁祸首药物、临床特征、病程、治疗方案和随访结果的相关性。结果:92例患者纳入研究,平均年龄58.7±20.2岁(范围10-93岁)。60 ~ 80岁患者占比最大(42.4%)。药物性SJS/TEN患者中女性40例(43.5%),男性52例(56.5%)。我们将药物性SJS/TEN病例按罪魁祸首药物分为抗生素、别嘌呤醇、抗癫痫药(AED)、非甾体抗炎药(NSAIDs)、对乙酰氨基酚和其他药物6组。从SJS到TEN,非甾体抗炎药引起的疾病发生率显著增加(p = 0.016)。在NSAID组患者中,TEN的比例(40%)高于其他组(p = 0.021)。AED组的平均体表面积显著低于非AED组(7.1±9.8比23.1±27.3,p = 0.020), NSAID组的平均体表面积显著高于非NSAID组(47.5±39.5比15.7±20.0,p = 0.010)。结论:本研究显示药物性SJS/TEN各致药组的临床特征可能不同。我们的发现可能有助于临床医生更好地理解药物诱导的SJS/TEN。
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来源期刊
CiteScore
2.50
自引率
5.90%
发文量
33
期刊介绍: Asia Pacific Allergy (AP Allergy) is the official journal of the Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI). Although the primary aim of the journal is to promote communication between Asia Pacific scientists who are interested in allergy, asthma, and clinical immunology including immunodeficiency, the journal is intended to be available worldwide. To enable scientists and clinicians from emerging societies appreciate the scope and intent of the journal, early issues will contain more educational review material. For better communication and understanding, it will include rational concepts related to the diagnosis and management of asthma and other immunological conditions. Over time, the journal will increase the number of original research papers to become the foremost citation journal for allergy and clinical immunology information of the Asia Pacific in the future.
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