Remdesevir Antiviral Therapy in Pregnant Women with COVID-19

IF 0.5 Q4 INFECTIOUS DISEASES
G. Shaimerdenova, G. Abuova, Serikbayeva Saltanat, Saltanat Baimbetova, Atabay Aidana
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引用次数: 0

Abstract

Background: Coronavirus disease 2019 (COVID-19) is difficult to treat in pregnant women due to pregnancy itself and the lack of standard treatment for the disease. As of August 2021, the etiotropic drug remdesivir has been added to the prescription list for women during gestation. There are few publications in the global scientific community regarding the use of this antiviral drug in pregnant women. Moreover, there are only sporadic scientific studies in Kazakhstan, so the question remains open. Objectives: This study aimed to evaluate the efficacy of remdesivir in pregnant women with probable or confirmed COVID-19. Methods: The study comprehensively examined 120 pregnant women with severe to very severe COVID-19, who were divided into two groups of patients. The study group consisted of women who received remdesivir and standard therapy. The control group included patients who received standard therapy per the protocol. Results: Statistically significant age differences were observed between the main and control groups (P = 0.019). The differences detected were due to a higher frequency in the age group of 33 and 42 years in patients taking remdesivir than in the control group (P = 0.036). Women in the main group (Median = 9.00; Q1 - Q3 = 8.00 - 11.0) had longer hospital stays than the control group (Me = 8.00; Q1 - Q3 = 7.00 - 10.0). This was due to the more severe condition of the patients in this group. There were statistically significant differences in amniotic fluid changes according to ultrasound between the control and main groups (P = 0.013). When comparing the groups in pairs, amniotic fluid was more common in women who received remdesivir (P = 0.316) than in the control group. Our study found that a decrease in temperature to normal levels occurred earlier in the control group (68%) than in the main group. Further SpO2 increases of more than 95% were seen on days 3 - 4 in the main group (71%) and days 1 - 2 in the control group (43%). After three days, there was an improvement in respiratory rate (41.6%) and a reduction in subjective dyspnea (66.6%) in the main group. Conclusions: The study found that repeat mothers have a more severe course of COVID-19. The older age group and the third trimester of pregnancy are risk factors for progression to severe disease.
瑞德西韦抗病毒治疗COVID-19孕妇
背景:2019冠状病毒病(COVID-19)由于妊娠本身和缺乏标准治疗方法,在孕妇中难以治疗。截至2021年8月,致病因药物remdesivir已被添加到妊娠期妇女的处方清单中。全球科学界关于孕妇使用这种抗病毒药物的出版物很少。此外,在哈萨克斯坦只有零星的科学研究,因此这个问题仍然悬而未决。目的:本研究旨在评估瑞德西韦对可能或确诊的COVID-19孕妇的疗效。方法:对120例重度至极重度新冠肺炎孕妇进行综合检查,将其分为两组。研究组由接受瑞德西韦和标准治疗的妇女组成。对照组包括按照方案接受标准治疗的患者。结果:两组患者年龄差异有统计学意义(P = 0.019)。检测到的差异是由于服用瑞德西韦的患者在33岁和42岁年龄组中的频率高于对照组(P = 0.036)。主组女性(中位数= 9.00;Q1 - Q3 = 8.00 - 11.0)的住院时间比对照组长(Me = 8.00;Q1 - q3 = 7.00 - 10.0)。这是由于该组患者的病情更为严重。超声检查羊水变化与对照组比较,差异有统计学意义(P = 0.013)。当对两组进行比较时,接受瑞德西韦治疗的妇女羊水比对照组更常见(P = 0.316)。我们的研究发现,对照组体温降至正常水平的时间比主组早(68%)。在第3 - 4天,主组(71%)和对照组(43%)的SpO2进一步升高95%以上。3天后,主组呼吸频率改善(41.6%),主观呼吸困难减少(66.6%)。结论:研究发现,重复母亲的COVID-19病程更严重。年龄较大的年龄组和妊娠晚期是发展为严重疾病的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
46
期刊介绍: Archives of Clinical Infectious Diseases is a peer-reviewed multi-disciplinary medical publication, scheduled to appear quarterly serving as a means for scientific information exchange in the international medical forum. The journal particularly welcomes contributions relevant to the Middle-East region and publishes biomedical experiences and clinical investigations on prevalent infectious diseases in the region as well as analysis of factors that may modulate the incidence, course, and management of infectious diseases and pertinent medical problems in the Middle East.
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