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史蒂文斯-约翰逊综合征和中毒性表皮坏死松解症:烧伤科 10 年经验。

Stevens-Johnson syndrome and toxic epidermal necrolysis: a 10-year experience in a burns unit.

机构信息

Department of Dermatology and Allergology, University Hospital RWTH Aachen, Germany.

Department of Plastic and Hand Surgery, Burn Unit, Trauma Center Bergmannstrost Halle, Halle, Germany.

出版信息

J Wound Care. 2021 Jun 2;30(6):492-496. doi: 10.12968/jowc.2021.30.6.492.

Abstract

OBJECTIVE

Stevens-Johnson syndrome (SJS) and its more severe counterpart, toxic epidermal necrolysis (TEN), are skin hypersensitivity reactions defined by epidermal blistering and necrosis. The exact pathophysiology of SJS/TEN is yet to be deciphered, but a number of risk factors have been identified including adverse drug reactions. The diagnosis of SJS/TEN is made on a clinical basis, and treatment consists of supportive care and occasionally immunosuppressants, such as cyclosporin, high-dose intravenous immunoglobulins and/or corticosteroids. Mortality rates can reach 20-25% in adults but are reduced with early intervention. To identify optimal treatment regimens, to better understand the patient cohort affected, and to help identify key risk factors for mortality, we report our experience with the treatment and management of SJS/TEN patients.

METHODS

A retrospective review of consecutive patients with SJS and/or TEN admitted to a single burns centre in Germany, between 2008 and 2018, was conducted. The primary outcomes of demographics, clinical course, treatment and patient-reported outcomes were recorded and compared with a control group of patients with burns without a diagnosis of SJS/TEN.

RESULTS

A total of 23 patients with SJS/TEN met the inclusion criteria: 17 (74%) with TEN; four (17%) with SJS/TEN overlap; and two (9%) with SJS. Of the patients, 14 (61%) were female and nine (39%) were male. Patient age ranged from 32-78 years (mean: 52 years). A matched cohort of 23 patients with burns served as the control group. All patients received standard of care with a multidisciplinary team. Compared with the control group, SJS/TEN patients had higher mortality rates (n=6, 26% versus n=8, 35%, respectively). The average age of death was 69 years in SJS/TEN patients versus 63 years in control group patients. Age and SCORTEN scores were significant predictors of mortality.

CONCLUSIONS

SJS and TEN are rare but extreme reactions of the skin and mucosa, associated with high disease mortality rates. This 10-year single-centre retrospective review contributes to the bank of information for reviews evaluating the management of SJS/TEN patients.

摘要

目的

史蒂文斯-约翰逊综合征(SJS)及其更严重的毒性表皮坏死松解症(TEN)是由表皮水疱和坏死定义的皮肤超敏反应。SJS/TEN 的确切病理生理学尚未被破解,但已确定了许多危险因素,包括药物不良反应。SJS/TEN 的诊断基于临床,治疗包括支持性护理和偶尔使用免疫抑制剂,如环孢素、高剂量静脉内免疫球蛋白和/或皮质类固醇。在成年人中,死亡率可达到 20-25%,但早期干预可降低死亡率。为了确定最佳治疗方案,更好地了解受影响的患者群体,并帮助确定死亡率的关键危险因素,我们报告了我们在 SJS/TEN 患者的治疗和管理方面的经验。

方法

对 2008 年至 2018 年间在德国一家烧伤中心连续收治的 SJS 和/或 TEN 患者进行回顾性分析。记录人口统计学、临床病程、治疗和患者报告结局的主要结局,并与无 SJS/TEN 诊断的烧伤患者的对照组进行比较。

结果

共有 23 例 SJS/TEN 患者符合纳入标准:17 例(74%)为 TEN;4 例(17%)为 SJS/TEN 重叠;2 例(9%)为 SJS。患者中,14 例(61%)为女性,9 例(39%)为男性。患者年龄为 32-78 岁(平均:52 岁)。烧伤患者的匹配对照组有 23 例。所有患者均接受了多学科团队的标准治疗。与对照组相比,SJS/TEN 患者的死亡率更高(n=6,26%与 n=8,35%,分别)。SJS/TEN 患者的平均死亡年龄为 69 岁,对照组患者为 63 岁。年龄和 SCORTEN 评分是死亡率的显著预测因素。

结论

SJS 和 TEN 是罕见但严重的皮肤和黏膜反应,与高疾病死亡率相关。这项为期 10 年的单中心回顾性研究为评估 SJS/TEN 患者管理的综述提供了信息。

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