Fei Weiqiang, Shen Jun, Cai Hui
College of Nursing, Hangzhou Vocational & Technical College, Hangzhou, Zhejiang Province, People's Republic of China.
Nursing Department, Sir Run Run Shaw Hospital Affiliated to Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, People's Republic of China.
Clin Cosmet Investig Dermatol. 2023 Aug 16;16:2249-2257. doi: 10.2147/CCID.S422928. eCollection 2023.
The purpose of the study is to analyze FAERS data to identify drugs associated with Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), determine demographics, drug classes involved, most likely resulted in death, and highlight emerging trends in SJS/TEN reactions.
We reviewed the publicly available FAERS database from 2004-2021. Using search terms "Stevens-Johnson syndrome" or "Toxic epidermal necrolysis", we identified the reports of SJS/TEN or SJS/TEN followed by death that might associated with specific drugs. Then the amounts and trends were counted analyzed.
During the study period of 2004-2021, the Food and Drug Administration (FDA) received a total of 14,363,139 reports of adverse reactions, among which 24,976 were linked to SJS or TEN. After excluding the cases with incomplete or insufficient information on age, gender, or country of origin, the median median age of patients was 53.82 (IQR = 57.52), the females accounted for 56.59% (12,827 cases) and 8,507 (38.34%) originated in the United States. The top 50 drugs were associated with 15,149 cases (60.65%). The subsequent fatal outcome occurring in 4878 out of 24,976 cases (19.53%). Top 3 drug classes associated with SJS/TEN in FAERS were antiepileptics, non-steroidal anti-inflammatory drugs (NSAIDs) and others. Top drug classes associated with SJS/TEN deaths were antineoplastic agents and cephalosporins. Linear regression showed that the annual percentage of monoclonal antibody-related SJS/TEN reactions increased at an average rate of 0.25% (95% confidence interval: 0.18, 0.32) from 0.00% in 2004 to 4.79% in 2021, faster than any other drug class except antigout drug (allopurinol).
By using the publicly available FAERS data, we have identified some important themes and trends in drug-related SJS/TEN reactions. Monoclonal antibodies and proton pump inhibitors are drugs with emerging trends causing SJS/TEN. Additionally, cephalosporin antibiotics have a higher mortality rate following SJS/TEN.
本研究旨在分析美国食品药品监督管理局不良事件报告系统(FAERS)的数据,以确定与史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)相关的药物,确定人口统计学特征、涉及的药物类别、最可能导致死亡的药物,并突出SJS/TEN反应的新趋势。
我们回顾了2004年至2021年公开可用的FAERS数据库。使用搜索词“史蒂文斯-约翰逊综合征”或“中毒性表皮坏死松解症”,我们确定了可能与特定药物相关的SJS/TEN报告或SJS/TEN后死亡的报告。然后对数量和趋势进行统计分析。
在2004年至2021年的研究期间,美国食品药品监督管理局共收到14363139份不良反应报告,其中24976份与SJS或TEN有关。在排除年龄、性别或原籍国信息不完整或不足的病例后,患者的中位年龄为53.82岁(四分位距=57.52),女性占56.59%(12827例),8507例(38.34%)来自美国。前50种药物与15149例(60.65%)病例相关。在24976例病例中,有4878例(19.53%)随后出现致命结局。FAERS中与SJS/TEN相关的前三大药物类别是抗癫痫药、非甾体抗炎药(NSAIDs)和其他药物。与SJS/TEN死亡相关的前几大药物类别是抗肿瘤药和头孢菌素。线性回归显示,单克隆抗体相关的SJS/TEN反应的年度百分比从2004年的0.00%以平均0.25%的速率增加(95%置信区间:0.18,0.32)至2021年的4.79%,增速快于除抗痛风药物(别嘌醇)外的任何其他药物类别。
通过使用公开可用的FAERS数据,我们确定了药物相关SJS/TEN反应中的一些重要主题和趋势。单克隆抗体和质子泵抑制剂是导致SJS/TEN的具有新趋势的药物。此外,头孢菌素类抗生素在SJS/TEN后具有较高的死亡率。