National Vaccine Program Office, Office of the Assistant Secretary for Health, Department of Health and Human Services, Washington, DC, USA.
Lancet. 2013 Apr 27;381(9876):1461-8. doi: 10.1016/S0140-6736(12)62189-8. Epub 2013 Mar 13.
The influenza A (H1N1) 2009 monovalent vaccination programme was the largest mass vaccination initiative in recent US history. Commensurate with the size and scope of the vaccination programme, a project to monitor vaccine adverse events was undertaken, the most comprehensive safety surveillance agenda in the USA to date. The adverse event monitoring project identified an increased risk of Guillain-Barré syndrome after vaccination; however, some individual variability in results was noted. Guillain-Barré syndrome is a rare but serious health disorder in which a person's own immune system damages their nerve cells, causing muscle weakness, sometimes paralysis, and infrequently death. We did a meta-analysis of data from the adverse event monitoring project to ascertain whether influenza A (H1N1) 2009 monovalent inactivated vaccines used in the USA increased the risk of Guillain-Barré syndrome.
Data were obtained from six adverse event monitoring systems. About 23 million vaccinated people were included in the analysis. The primary analysis entailed calculation of incidence rate ratios and attributable risks of excess cases of Guillain-Barré syndrome per million vaccinations. We used a self-controlled risk-interval design.
Influenza A (H1N1) 2009 monovalent inactivated vaccines were associated with a small increased risk of Guillain-Barré syndrome (incidence rate ratio 2·35, 95% CI 1·42-4·01, p=0·0003). This finding translated to about 1·6 excess cases of Guillain-Barré syndrome per million people vaccinated.
The modest risk of Guillain-Barré syndrome attributed to vaccination is consistent with previous estimates of the disorder after seasonal influenza vaccination. A risk of this small magnitude would be difficult to capture during routine seasonal influenza vaccine programmes, which have extensive, but comparatively less, safety monitoring. In view of the morbidity and mortality caused by 2009 H1N1 influenza and the effectiveness of the vaccine, clinicians, policy makers, and those eligible for vaccination should be assured that the benefits of inactivated pandemic vaccines greatly outweigh the risks.
US Federal Government.
甲型 H1N1 流感 2009 单价疫苗接种计划是美国近代史上最大规模的大众疫苗接种计划。与疫苗接种计划的规模和范围相称,美国开展了一项监测疫苗不良事件的项目,这是迄今为止美国最全面的安全监测计划。不良事件监测项目发现接种疫苗后发生格林-巴利综合征的风险增加;然而,一些结果存在个体差异。格林-巴利综合征是一种罕见但严重的健康疾病,人体自身免疫系统会损害其神经细胞,导致肌肉无力,有时甚至瘫痪,极少数情况下会导致死亡。我们对不良事件监测项目的数据进行了荟萃分析,以确定美国使用的甲型 H1N1 2009 单价灭活疫苗是否会增加患格林-巴利综合征的风险。
数据来自六个不良事件监测系统。约 2300 万接种者纳入分析。主要分析包括计算每百万接种者中格林-巴利综合征超额病例的发病率比和归因风险。我们使用了自我对照风险间隔设计。
甲型 H1N1 2009 单价灭活疫苗与格林-巴利综合征的风险略有增加相关(发病率比 2.35,95%CI 1.42-4.01,p=0.0003)。这一发现相当于每百万人接种疫苗后约有 1.6 例格林-巴利综合征的超额病例。
接种疫苗导致的格林-巴利综合征的适度风险与季节性流感疫苗接种后对该疾病的先前估计一致。这种微小风险的程度很难在常规季节性流感疫苗接种计划中发现,因为这些计划的安全性监测范围广泛,但相对较少。考虑到 2009 年 H1N1 流感的发病率和死亡率以及疫苗的有效性,临床医生、政策制定者和符合接种条件的人应该确信,灭活大流行疫苗的益处大大超过风险。
美国联邦政府。