Kaiser Permanente Vaccine Study Center and Division of Research, Kaiser Permanente Northern California, Oakland, CA, United States.
Kaiser Permanente Vaccine Study Center and Division of Research, Kaiser Permanente Northern California, Oakland, CA, United States.
Vaccine. 2018 May 3;36(19):2733-2739. doi: 10.1016/j.vaccine.2017.08.080. Epub 2017 Sep 13.
Following the H1N1 influenza pandemic in 2009, pregnant women were recommended to receive both seasonal (TIV) and H1N1 influenza vaccines. This study presents incidence of adverse birth and pregnancy outcomes among a population of pregnant women immunized with TIV and H1N1 vaccines at Kaiser Permanente Northern California during 2009-2010.
We telephone surveyed pregnant Kaiser Permanente Northern California members to assess non-medically-attended reactions following H1N1, TIV or both vaccines during 2009-2010 (n=5365) in a separate study. Here we assessed preterm birth (<37weeks), very preterm birth (<32weeks), low birth weight (<2500 g, LBW), very low birth weight (<1500g), small for gestational age, spontaneous abortions, stillbirths and congenital anomalies among this cohort by comparing incidence and 95% confidence intervals between the following immunization groups: TIV only, H1N1 only, H1N1 prior to TIV immunization, TIV prior to H1N1 and both immunizations given at the same time.
Results did not vary significantly between groups. Comparing H1N1 with TIV, incidence were similar for preterm births (6.37vs 6.28/100 births), very preterm births (5.30vs 8.29/1000 births), LBW (4.19vs 2.90/100 births), very LBW (4.54vs 5.52/1000 births), small for gestational age (9.99vs 9.24/1000 births), spontaneous abortion (7.10vs 6.83/1000 pregnancies), stillbirths (7.10vs 4.57/1000 pregnancies), and congenital anomalies (2.66vs 2.43/100 births).
Although constrained by small sample size, complex vaccine groups, and differential vaccine availability during 2009-2010, this study found no difference in adverse birth outcomes between H1N1 vaccine and TIV.
2009 年 H1N1 流感大流行后,建议孕妇接种季节性(TIV)和 H1N1 流感疫苗。本研究报告了在 2009-2010 年期间,Kaiser Permanente 北加州的孕妇群体接种 TIV 和 H1N1 疫苗后的不良出生和妊娠结局的发生率。
我们通过电话调查了 Kaiser Permanente 北加州的孕妇会员,以评估 2009-2010 年期间(n=5365)接种 H1N1、TIV 或两者疫苗后的非医疗相关反应。在这里,我们通过比较以下免疫接种组之间的发生率和 95%置信区间,评估了早产(<37 周)、极早产(<32 周)、低出生体重(<2500 克,LBW)、极低出生体重(<1500 克)、小于胎龄儿、自然流产、死产和先天性异常:仅接种 TIV、仅接种 H1N1、在接种 TIV 免疫接种之前接种 H1N1、在接种 H1N1 免疫接种之前接种 TIV 以及同时接种两种疫苗。
结果在组间没有显著差异。与 TIV 相比,H1N1 的早产发生率(6.37 与 6.28/100 出生)、极早产发生率(5.30 与 8.29/1000 出生)、LBW 发生率(4.19 与 2.90/100 出生)、极低 LBW 发生率(4.54 与 5.52/1000 出生)、小于胎龄儿发生率(9.99 与 9.24/1000 出生)、自然流产发生率(7.10 与 6.83/1000 妊娠)、死产发生率(7.10 与 4.57/1000 妊娠)和先天性异常发生率(2.66 与 2.43/100 出生)相似。
尽管受到小样本量、复杂疫苗组和 2009-2010 年期间疫苗供应差异的限制,但本研究未发现 H1N1 疫苗与 TIV 之间不良出生结局存在差异。