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孕早期接种mRNA新冠疫苗后,自然流产风险并未增加。

The Risk of Spontaneous Abortion Does Not Increase Following First Trimester mRNA COVID-19 Vaccination.

作者信息

Citu Ioana Mihaela, Citu Cosmin, Gorun Florin, Sas Ioan, Bratosin Felix, Motoc Andrei, Burlea Bogdan, Rosca Ovidiu, Malita Daniel, Gorun Oana Maria

机构信息

Department of Internal Medicine I, Victor Babes University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square 2, 300041 Timisoara, Romania.

Department of Obstetrics and Gynecology, Victor Babes University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square 2, 300041 Timisoara, Romania.

出版信息

J Clin Med. 2022 Mar 18;11(6):1698. doi: 10.3390/jcm11061698.

Abstract

Clinical trials for COVID-19 vaccines initially excluded pregnant women due to safety concerns, and when the vaccines were authorized for emergency use, they were not recommended for this population. However, observational studies discovered that pregnant women infected with COVID-19 have higher risks of negative pregnancy and delivery outcomes compared to non-pregnant women, raising the question of the risks-benefits of administering COVID-19 vaccines to pregnant women. By mid-2021, there was general consensus on the relative safety of COVID-19 vaccination during pregnancy; therefore, it is critical to investigate the safety issues related to these vaccines, considering the increasing acceptance among pregnant women. To address these concerns, we developed a research project to study the short-term effects and outcomes of COVID-19 vaccination during the first trimester of pregnancy. Our research followed an observational retrospective design for 12 months from the beginning of the vaccination campaign, and included 124 cases of spontaneous abortions and 927 ongoing pregnancies. The odds of spontaneous abortion were non-significant for both versions of the mRNA vaccine (Pfizer BNT162b2 AOR = 1.04, CI = 0.91-1.12; Moderna mRNA-1273 AOR = 1.02, CI = 0.89-1.08). Overall, our data indicated that the risk of spontaneous abortion after mRNA COVID-19 immunization during the first trimester of pregnancy is commensurate with the predicted risk in non-vaccinated pregnant women. These findings contribute to the growing body of information regarding the safety of mRNA COVID-19 vaccination during pregnancy.

摘要

由于安全担忧,新冠疫苗的临床试验最初将孕妇排除在外,并且当这些疫苗被批准用于紧急使用时,也不建议该人群接种。然而,观察性研究发现,与未感染新冠病毒的孕妇相比,感染新冠病毒的孕妇出现不良妊娠和分娩结局的风险更高,这就引发了向孕妇接种新冠疫苗的风险效益问题。到2021年年中,人们对孕期接种新冠疫苗的相对安全性已达成普遍共识;因此,鉴于孕妇对疫苗的接受度不断提高,调查与这些疫苗相关的安全问题至关重要。为了解决这些担忧,我们开展了一项研究项目,以研究孕期头三个月接种新冠疫苗的短期影响和结局。我们的研究采用观察性回顾性设计,自疫苗接种活动开始起为期12个月,包括124例自然流产病例和927例持续妊娠病例。两种mRNA疫苗(辉瑞BNT162b2,调整后比值比[AOR]=1.04,可信区间[CI]=0.91-1.12;莫德纳mRNA-1273,AOR=1.02,CI=0.89-1.08)导致自然流产的几率均无统计学意义。总体而言,我们的数据表明,孕期头三个月接种新冠mRNA疫苗后自然流产的风险与未接种疫苗的孕妇的预测风险相当。这些发现为有关孕期接种新冠mRNA疫苗安全性的信息库增添了内容。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ced/8955378/0f0a0fba45e4/jcm-11-01698-g001.jpg

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