首页> 外文期刊>American Journal of Epidemiology >Risk of Preterm or Small-for-Gestational-Age Birth After Influenza Vaccination During Pregnancy: Caveats When Conducting Retrospective Observational Studies
【24h】

Risk of Preterm or Small-for-Gestational-Age Birth After Influenza Vaccination During Pregnancy: Caveats When Conducting Retrospective Observational Studies

机译:怀孕期间接种流感疫苗后早产或小胎龄的风险:进行回顾性观察研究时的警告

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Vaccines are increasingly targeted toward women of reproductive age, and vaccines to prevent influenza and pertussis are recommended during pregnancy. Prelicensure clinical trials typically have not included pregnant women, and when they are included, trials cannot detect rare events. Thus, postmarketing vaccine safety assessments are necessary. However, analysis of observational data requires detailed assessment of potential biases. Using data from 8 Vaccine Safety Datalink sites in the United States, we analyzed the association of monovalent H1N1 influenza vaccine (MIV) during pregnancy with preterm birth (< 37 weeks) and small-for-gestational-age birth (birth weight < 10th percentile). The cohort included 46,549 pregnancies during 2009-2010 (40% of participants received the MIV). We found potential biases in the vaccine-birth outcome association that might occur due to variable access to vaccines, the time-dependent nature of exposure to vaccination within pregnancy (immortal time bias), and confounding from baseline differences between vaccinated and unvaccinated women. We found a strong protective effect of vaccination on preterm birth (relative risk = 0.79, 95% confidence interval: 0.74, 0.85) when we ignored potential biases and no effect when accounted for them (relative risk = 0.91; 95% confidence interval: 0.83, 1.0). In contrast, we found no important biases in the association of MIV with small-for-gestational-age birth. Investigators conducting studies to evaluate birth outcomes after maternal vaccination should use statistical approaches to minimize potential biases.
机译:疫苗越来越多地针对育龄妇女,建议在怀孕期间预防流感和百日咳的疫苗。准确诊临床试验通常不包括孕妇,如果包括孕妇,则试验无法检测到罕见事件。因此,上市后疫苗安全性评估是必要的。但是,对观测数据的分析需要对潜在偏差进行详细评估。使用来自美国8个疫苗安全数据链接站点的数据,我们分析了妊娠期单价H1N1流感疫苗(MIV)与早产(<37周)和小胎龄婴儿(出生体重<10%)的关联)。该队列包括2009-2010年期间的46,549例怀孕(40%的参与者接受了MIV)。我们发现疫苗与出生结局之间的潜在偏差可能是由于疫苗的获取途径不同,怀孕期间暴露于疫苗的时间依赖性(永生时间偏差)以及已接种疫苗和未接种疫苗的女性之间的基线差异而引起的。当我们忽略潜在偏倚时,我们发现疫苗对早产具有很强的保护作用(相对风险= 0.79,95%置信区间:0.74、0.85),而考虑到它们时则没有影响(相对风险= 0.91; 95%置信区间:0.83) ,1.0)。相比之下,我们发现MIV与小胎龄出生之间没有重要的偏差。进行研究以评估产妇接种疫苗后的出生结局的研究人员应使用统计方法以最大程度地减少潜在偏见。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号