Sharma Priyanka, Gupta Priyanka, Virmani Rashmi, Pandey Anil, Sharma Jagadish C, Sarkar Avir
Obstetrics and Gynecology, Employees' State Insurance Corporation (ESIC) Medical College and Hospital, Faridabad, Faridabad, IND.
Pediatrics, Employees' State Insurance Corporation (ESIC) Medical College and Hospital, Faridabad, Faridabad, IND.
Cureus. 2023 Aug 17;15(8):e43671. doi: 10.7759/cureus.43671. eCollection 2023 Aug.
Pregnancy is associated with immunological changes that could render an individual vulnerable to the severe coronavirus disease 2019 (COVID-19) disease. Even as we witnessed the third and most widespread pandemic wave, a conclusively advantageous treatment option still remained elusive. Remdesivir was one of the front-running therapeutic options that received emergency use authorization (EUA) and subsequent approval for the management of moderate to severe COVID-19 infections. Here, we report a series of moderate to severe COVID-19-infected pregnancies and the experience of remdesivir use on a compassionate basis. Four cases of pregnancy complicated with moderate to severe COVID-19 infections where remdesivir was administered were recruited into the study, and their outcome was assessed objectively. Of these cases, three women received remdesivir in addition to standard SARS-CoV-2 treatment in the antenatal period. One woman received remdesivir after delivery. One woman received tocilizumab in addition to remdesivir and standard SARS-CoV-2 care. Two women survived and were subsequently discharged to home care. Two succumbed to the disease. One baby who was exposed to remdesivir in utero is doing well at six months post-delivery. Remdesivir had been granted EUA for the treatment of suspected or laboratory-confirmed COVID-19 infection in adults and children who were hospitalized with severe disease or requiring supplemental oxygen and mechanical ventilation or extracorporeal membrane oxygenation (ECMO) in May 2020. This issuance allowed the use of the same dosing regimen in pregnant and parturient women as in the general adult population. Thus, this series of cases tried to assess the outcome of this drug among COVID-19-infected pregnant women. Early initiation of remdesivir in pregnancy in the viremic phase seems to provide some advantages in the survival outcome. Its use may be associated with transient elevation in hepatic transaminases in some cases. No detrimental effects on the ongoing pregnancies, fetuses, or neonates have been observed. Further large-scale studies may provide more conclusive evidence.
怀孕与免疫变化相关,这些变化可能使个体易患严重的2019冠状病毒病(COVID-19)。即便我们见证了第三波也是最广泛传播的疫情浪潮,但一种具有决定性优势的治疗方案仍然难以捉摸。瑞德西韦是领先的治疗选择之一,它获得了紧急使用授权(EUA),随后被批准用于治疗中度至重度COVID-19感染。在此,我们报告一系列中度至重度COVID-19感染的孕妇以及基于同情使用瑞德西韦的经验。本研究纳入了4例接受瑞德西韦治疗的中度至重度COVID-19感染合并妊娠的病例,并对其结局进行了客观评估。在这些病例中,3名女性在孕期除接受标准的SARS-CoV-2治疗外还接受了瑞德西韦治疗。1名女性在产后接受了瑞德西韦治疗。1名女性除接受瑞德西韦和标准的SARS-CoV-2治疗外还接受了托珠单抗治疗。2名女性存活,随后出院接受家庭护理。2名女性死于该疾病。1名在子宫内接触过瑞德西韦的婴儿在出生后6个月情况良好。2020年5月,瑞德西韦已被授予EUA,用于治疗因严重疾病住院或需要补充氧气、机械通气或体外膜肺氧合(ECMO)的疑似或实验室确诊的成人和儿童COVID-19感染。这一授权允许在孕妇和产妇中使用与普通成年人群相同的给药方案。因此,这一系列病例试图评估该药物在COVID-19感染孕妇中的结局。在病毒血症期早期开始在孕期使用瑞德西韦似乎在生存结局方面具有一些优势。在某些情况下,其使用可能与肝转氨酶短暂升高有关。未观察到对正在进行的妊娠、胎儿或新生儿有不利影响。进一步的大规模研究可能会提供更确凿的证据。