Pregistry, London, Cheshire, UK.
, Chicago, IL, USA.
Drug Saf. 2023 Mar;46(3):297-308. doi: 10.1007/s40264-022-01271-3. Epub 2023 Jan 22.
The advent of the coronavirus disease 2019 (COVID-19) pandemic has led to the development of vaccines against severe acute respiratory syndrome coronavirus 2. Prospective evidence regarding safety for pregnant people and their developing fetuses is lacking. The aim of the COVID-19 Vaccines International Pregnancy Exposure Registry (C-VIPER) is to estimate the relative risk of obstetric, neonatal, and infant outcomes by comparing participants vaccinated against COVID-19 during pregnancy to a reference group of people enrolled in the Pregistry International Pregnancy Exposure Registry (PIPER) who remained unvaccinated during pregnancy.
The C-VIPER and the PIPER are international, non-interventional, real-world cohort studies. Participants receiving a COVID-19 vaccine during pregnancy will be matched in the analyses by country and gestational age at enrollment to unvaccinated individuals. Self-enrolled and self-consented participants complete online questionnaires at enrollment, during pregnancy, and for 12 months after the delivery of a live infant. Where possible, outcomes are verified by medical records. The study aims to recruit at least 500 pregnancies for each approved or authorized vaccine and will last for 5 years for each product.
By collecting data for each vaccine brand, the C-VIPER will be able to determine individual safety profiles. The study design allows for analysis of the effects of exposure to COVID-19 vaccines during specific etiologically relevant periods of gestation. Although the sample size may be too small to detect associations with rare outcomes, the study will be used to generate hypotheses for future research. Ultimately, the C-VIPER should provide data that will allow pregnant people and their healthcare providers to make informed decisions about COVID-19 vaccination.
ClinicalTrials.gov NCT04705116. Registered on 12 January, 2021. EU PAS EUPAS39096. Registered on 20 January, 2021.
2019 年冠状病毒病(COVID-19)大流行的出现导致了针对严重急性呼吸综合征冠状病毒 2 的疫苗的发展。缺乏针对孕妇及其胎儿发育的安全性的前瞻性证据。COVID-19 疫苗国际妊娠暴露登记(C-VIPER)的目的是通过比较怀孕期间接种 COVID-19 疫苗的参与者与未接种疫苗的 Pregistry 国际妊娠暴露登记(PIPER)中的参考组参与者,来估计产科、新生儿和婴儿结局的相对风险。
C-VIPER 和 PIPER 是国际性的、非干预性的、真实世界的队列研究。在分析中,根据国家和妊娠登记时的孕龄,对接受 COVID-19 疫苗接种的参与者与未接种疫苗的个体进行匹配。自我注册和自我同意的参与者在登记时、怀孕期间以及活产婴儿出生后 12 个月完成在线问卷。在可能的情况下,通过病历验证结果。该研究旨在为每种批准或授权的疫苗招募至少 500 例妊娠,并为每种产品持续 5 年。
通过收集每种疫苗品牌的数据,C-VIPER 将能够确定个体安全性概况。该研究设计允许分析在特定病因相关的妊娠时期暴露于 COVID-19 疫苗的影响。虽然可能太小而无法检测到罕见结局的关联,但该研究将用于为未来的研究生成假设。最终,C-VIPER 应提供数据,使孕妇及其医疗保健提供者能够就 COVID-19 疫苗接种做出明智的决策。
ClinicalTrials.gov NCT04705116. 于 2021 年 1 月 12 日注册。EU PAS EUPAS39096. 于 2021 年 1 月 20 日注册。