孕妇和哺乳期妇女COVID-19疫苗的安全性和不良反应

Q1 Medicine
Nguyen Thi Minh Thanh, Le Thi Hang, Mai Trong Hung, Tran Hoa Phuong, Nguyen Thi Phuong Lan, Mac Dang Tuan, Nguyen Xuan Bach, Nguyen Duy Anh
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引用次数: 0

摘要

目的:本研究旨在评估孕妇和哺乳期妇女COVID-19疫苗不良反应的发生率,并确定相关的人口统计学和临床因素。方法:于2021年11月至2022年3月在越南河内的一家医院进行横断面研究。通过方便抽样,共招募了1204名参与者,其中包括991名怀孕13周以上的孕妇和213名母乳喂养妇女。数据收集采用自行填写的问卷,旨在获取人口统计信息和疫苗接种后7至28天内发生的不良反应。统计学分析采用Stata 16.0进行,包括卡方检验、Fisher精确检验和逻辑回归,显著性设置为p < 0.05。结果:最常见的不良反应为注射部位局部疼痛(26.2%)、头晕乏力(19.2%)、发热低于39℃(29.1%)。严重的不良反应,如喉咙紧绷、昏迷和早产,是罕见的。多变量分析确定了与不良反应相关的重要因素,包括年龄(36-40岁参与者的aOR = 2.04)、职业(农民和商业专业人员的aOR较低)、城市居住(aOR = 0.64)和过敏史(aOR = 1.59)。受教育程度、子女数量和胎龄与不良事件无显著相关。结论:研究结果支持COVID-19疫苗对孕妇和哺乳期妇女的安全性,大多数不良反应轻微且具有自限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety of and Adverse Reactions to the COVID-19 Vaccine Among Pregnant and Breastfeeding Women.

Objectives: This study aimed to evaluate the incidence of adverse reactions to the COVID-19 vaccine among pregnant and breastfeeding women and identify associated demographic and clinical factors.

Methods: A cross-sectional study was conducted at a hospital in Hanoi, Vietnam, from November 2021 to March 2022. A total of 1204 participants, including 991 pregnant women beyond 13 weeks of gestation and 213 breastfeeding women, were recruited through convenience sampling. Data were collected using a self-administered questionnaire designed to capture demographic information and adverse reactions occurring within seven to 28 days post-vaccination. Statistical analyses, including chi-square tests, Fisher's exact tests, and logistic regression, were performed using Stata 16.0, with the significance set at p < 0.05.

Results: The most common adverse reactions were localized pain at the injection site (26.2%), dizziness and fatigue (19.2%), and fever below 39 °C (29.1%). Severe adverse reactions, such as a tight throat, coma, and premature birth, were rare. A multivariate analysis identified the significant factors associated with the adverse reactions, including age (aOR = 2.04 for participants aged 36-40 years), occupation (lower odds for farmers and business professionals), urban residency (aOR = 0.64), and a history of allergies (aOR = 1.59). Education level, number of children, and gestational age were not significantly associated with adverse events.

Conclusions: The findings support the safety of the COVID-19 vaccine in pregnant and breastfeeding women, with most of the adverse reactions being mild and self-limiting.

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