Pharmacy Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Pharmacy Department. Hospital, Universitario "12 de Octubre", Research Institute 12 de Octubre (i+12, Madrid, Spain.
J Clin Pharm Ther. 2021 Aug;46(4):1062-1070. doi: 10.1111/jcpt.13394. Epub 2021 Feb 26.
Tocilizumab is an IL-6 receptor inhibitor agent which has been proposed as a candidate to stop the inflammatory phase of infection by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). However, safety data of tocilizumab in pregnant women and their newborn are scarce. We aimed to describe maternal and neonatal safety outcomes associated with tocilizumab treatment in pregnant women with severe COVID-19.
This is a retrospective study of severe COVID-19 pregnant women, treated with tocilizumab in two Spanish hospitals between 1 March and 31 April 2020. Demographics, medical history, clinical and radiologic findings, treatment information and laboratory data of mothers and their newborns were collected from electronic medical records.
A total of 12 pregnant women were identified to have received tocilizumab during pregnancy in the two hospitals. Median gestational age at admission was 27.7 weeks (interquartile range, 18.0-36.4). Most of them received lopinavir/ritonavir, azithromycin and hydroxychloroquine, two patients received corticosteroids and one received interferon beta 1B. All 12 pregnancies resulted in live births. Somatometric values were normal for all newborns, and evolution at 14 and 28 days was favourable for all of them. Hepatotoxicity was observed in 2 patients, which improved or resolved at discharge. Cytomegalovirus reactivation was detected in another patient who had also received corticosteroids for 15 days, causing a congenital infection in her newborn. Both hepatotoxicity and viral reactivation adverse events were classified as possibly related to tocilizumab administration according to Naranjo's causality algorithm.
It does not appear that tocilizumab has detrimental effects for the mother and newborn. Close monitoring of infections should be considered, especially if other immunosuppressive agents are used.
托珠单抗是一种白细胞介素-6(IL-6)受体抑制剂,被认为是阻止严重急性呼吸综合征冠状病毒-2(SARS-CoV-2)感染炎症期的候选药物。然而,托珠单抗在孕妇及其新生儿中的安全性数据仍然很少。我们旨在描述托珠单抗治疗严重 COVID-19 孕妇的母婴安全性结局。
这是一项对 2020 年 3 月 1 日至 4 月 31 日期间在西班牙的两家医院接受托珠单抗治疗的严重 COVID-19 孕妇的回顾性研究。从电子病历中收集母亲及其新生儿的人口统计学、病史、临床和影像学发现、治疗信息和实验室数据。
在这两家医院中,共发现 12 例孕妇在怀孕期间接受了托珠单抗治疗。入院时的中位孕龄为 27.7 周(四分位距,18.0-36.4)。大多数患者接受洛匹那韦/利托那韦、阿奇霉素和羟氯喹治疗,2 例患者接受皮质类固醇治疗,1 例患者接受干扰素β 1B 治疗。所有 12 例妊娠均导致活产。所有新生儿的体尺值均正常,他们在第 14 天和第 28 天的发育情况均良好。2 例患者出现肝毒性,出院时已改善或缓解。另一名患者还接受了 15 天的皮质类固醇治疗,导致其新生儿发生先天性感染,检测到巨细胞病毒再激活。根据 Naranjo 因果关系算法,这两种肝毒性和病毒再激活不良事件均被归类为可能与托珠单抗给药相关。
托珠单抗似乎对母亲和新生儿没有不良影响。应考虑密切监测感染情况,特别是如果使用其他免疫抑制剂。