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视神经脊髓炎谱系疾病患者接受 Satralizumab 治疗的尿脓毒症风险。

Urosepsis Risk in Neuromyelitis Optica Spectrum Disorder Patients Administered Satralizumab.

机构信息

Department of Neurology, Kansai Medical University Medical Center, Japan.

Department of Neurology, Kyoto University Graduate School of Medicine, Japan.

出版信息

Intern Med. 2023 Nov 15;62(22):3317-3320. doi: 10.2169/internalmedicine.1642-23. Epub 2023 Apr 7.

DOI:10.2169/internalmedicine.1642-23
PMID:37032080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10713369/
Abstract

Objective The interleukin-6 (IL-6) inhibitor satralizumab is an established treatment for neuromyelitis optica spectrum disorder (NMOSD). Although IL-6 inhibitors are generally well-tolerated, serious infections, including sepsis, can occur. In this study, we compared the sepsis characteristics in NMOSD patients administered satralizumab (NMOSD-satralizumab) to those in rheumatoid arthritis patients administered tocilizumab (RA-tocilizumab), another IL-6 inhibitor. Methods We examined adverse event reports from the Japanese Pharmaceuticals and Medical Devices Agency regarding NMOSD-satralizumab from August 2020 to March 2022 and RA-tocilizumab from April 2008 to November 2019 (term 1) and to March 2022 (term 2). Results We identified 6 sepsis cases in NMOSD-satralizumab, of which 5 (83%) developed from urinary tract infections (UTIs). Although data were unavailable for two patients, three cases had urologic complications in addition to recognized risk factors for serious infections, such as an older age, corticosteroid use, obesity, diabetes mellitus and motor disability. Urosepsis was relatively infrequent in RA-tocilizumab (term 1: 24.2%, term 2: 20.1%). Conclusion Safe satralizumab use requires risk factor assessment to minimize the incidence of severe infections. Management of UTIs is also recommended.

摘要

目的

白细胞介素-6(IL-6)抑制剂 satralizumab 是视神经脊髓炎谱系疾病(NMOSD)的一种既定治疗方法。虽然 IL-6 抑制剂通常具有良好的耐受性,但仍可能发生严重感染,包括败血症。在这项研究中,我们比较了接受 satralizumab(NMOSD-satralizumab)治疗的 NMOSD 患者和接受另一种 IL-6 抑制剂 tocilizumab(RA-tocilizumab)治疗的类风湿关节炎患者的败血症特征。

方法

我们检查了日本药品和医疗器械管理局关于 NMOSD-satralizumab 的不良事件报告,该报告时间为 2020 年 8 月至 2022 年 3 月,以及关于 RA-tocilizumab 的报告,该报告时间为 2008 年 4 月至 2019 年 11 月(第 1 期)和 2022 年 3 月(第 2 期)。

结果

我们在 NMOSD-satralizumab 中发现了 6 例败血症病例,其中 5 例(83%)由尿路感染(UTIs)引起。尽管有两名患者的数据不可用,但除了严重感染的已知危险因素(如年龄较大、使用皮质类固醇、肥胖、糖尿病和运动障碍)外,还有三个病例存在泌尿系统并发症。RA-tocilizumab 中败血症相对较少见(第 1 期:24.2%,第 2 期:20.1%)。

结论

安全使用 satralizumab 需要评估危险因素,以尽量减少严重感染的发生率。还建议管理尿路感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbf2/10713369/c616390eb68b/1349-7235-62-3317-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbf2/10713369/c616390eb68b/1349-7235-62-3317-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbf2/10713369/c616390eb68b/1349-7235-62-3317-g001.jpg

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