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Risk of adverse fetal outcomes following administration of a pandemic influenza A(H1N1) vaccine during pregnancy

机译:怀孕期间接种大流行性A(H1N1)流感疫苗后胎儿不良结局的风险

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Context: Assessment of the fetal safety of vaccination against influenza A(H1N1) pdm09 in pregnancy has been limited. Objective: Toinvestigate whether exposure toanadjuvanted influenzaA(H1N1)pdm09 vaccine during pregnancy was associated with increased risk of adverse fetal outcomes. Design, Setting, and Participants: Registry-based cohort study based on all live-born singleton infants in Denmark, delivered between November 2, 2009, and September 30, 2010. In propensity score-matched analyses, we estimated prevalence odds ratios (PORs) of adverse fetal outcomes, comparing infants exposed and unexposed to an AS03-adjuvanted influenza A(H1N1)pdm09 vaccine during pregnancy. Main Outcome Measures: Major birth defects, preterm birth, and small size for gestational age. Results: From a cohort of 53 432 infants (6989 [13.1%] exposed to the influenza A[H1N1]pdm09 vaccine during pregnancy [345 in the first trimester and 6644 in the second or third trimester]), 660 (330 exposed) were included in propensity score-matched analyses of adverse fetal outcomes associated with first-trimester exposure. For analysis of small size for gestational age after second- or third-trimester exposure, 13 284 (6642 exposed) were included; for analyses of preterm birth, 12 909 (6543 exposed) were included. A major birth defect was diagnosed in 18 of 330 infants (5.5%) exposed to the vaccine in the first trimester, compared with 15 of 330 unexposed infants (4.5%) (POR, 1.21; 95% CI, 0.60-2.45). Preterm birth occurred in 31 of 330 infants (9.4%) exposed in the first trimester, compared with 24 of 330 unexposed infants (7.3%) (POR, 1.32; 95% CI, 0.76-2.31), and in 302 of 6543 infants (4.6%) with second-or third-trimester exposure, compared with 295 of 6366 unexposed infants (4.6%) (POR, 1.00; 95% CI, 0.84-1.17). Small size for gestational age was observed in 25 of 330 infants (7.6%) with first-trimester exposure compared with 31 of 330 unexposed infants (9.4%) (POR, 0.79; 95% CI, 0.46-1.37), and in 641 of 6642 infants (9.7%) with second- or third-trimester exposure, compared with 657 of 6642 unexposed infants (9.9%) (POR, 0.97; 95% CI, 0.87-1.09). Conclusions: In this Danish cohort, exposure to an adjuvanted influenza A(H1N1) pdm09 vaccine during pregnancy was not associated with a significantly increased risk of major birth defects, preterm birth, or fetal growth restriction.
机译:背景:在孕妇中,针对A型流感(H1N1)pdm09疫苗接种的胎儿安全性评估有限。目的:探讨怀孕期间暴露于辅助性流感A(H1N1)pdm09疫苗是否与胎儿不良结局风险增加有关。设计,背景和参与者:基于注册表的队列研究基于丹麦所有活产单身婴儿,研究于2009年11月2日至2010年9月30日进行。在倾向得分匹配分析中,我们估算了患病几率(POR) )对胎儿不利的结局,比较了在怀孕期间接触和未接触AS03辅助的A型流感H1N1pdm09疫苗的婴儿。主要结果指标:主要的出生缺陷,早产和较小的胎龄。结果:从队列中的53 432名婴儿(6989 [13.1%]的孕妇在怀孕期间暴露[A3H1N1] pdm09疫苗[孕早期为345例,孕中期或孕中期为6644例])中,有660例(暴露了330例)包括与孕早期妊娠相关的不良胎儿结局倾向得分匹配分析中的内容。为了分析孕中期或孕晚期的小胎龄,纳入了13 284(6642暴露)。为了分析早产,纳入了12 909(暴露的6543)。在头三个月中,接触疫苗的330名婴儿中有18名被诊断出严重的出生缺陷,而330名未暴露的婴儿中有15名(4.5%)被诊断为重大出生缺陷(POR,1.21; 95%CI,0.60-2.45)。早孕期的330名婴儿中有31名早产(9.4%),而未孕的330名婴儿中有24名(7.3%)(POR,1.32; 95%CI,0.76-2.31),以及6543名婴儿中的302名( 4.36%的孕妇在第二或第三学期暴露,而6366名未暴露婴儿中有295人(4.6%)(POR,1.00; 95%CI,0.84-1.17)。在330名初孕期婴儿中,有25名胎龄较小(7.6%),而330名未暴露婴儿中的31名(9.4%)(POR,0.79; 95%CI,0.46-1.37)和641名婴儿中6642名婴儿(妊娠中期或中晚期)(9.7%),而6642名未暴露婴儿中的657名(9.9%)(POR,0.97; 95%CI,0.87-1.09)。结论:在这个丹麦队列中,在怀孕期间暴露于辅助性甲型H1N1流感pdm09疫苗与重大出生缺陷,早产或胎儿生长受限的风险显着增加无关。

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