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Absence of associations between influenza vaccines and increased risks of seizures, Guillain-Barré syndrome, encephalitis, or anaphylaxis in the 2012-2013 season

机译:在2012-2013赛季中,流感疫苗与癫痫发作,格林-巴利综合征,脑炎或过敏反应的风险增加之间没有关联

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Purpose: We conducted weekly surveillance for pre-specified adverse events following receipt of the 2012-2013 influenza vaccines in the Vaccine Safety Datalink (VSD). Methods: For each outcome, risk intervals (i.e., period after vaccination with a potentially increased risk) were defined on the basis of biologic plausibility and prior literature. Seizures following inactivated influenza vaccine (IIV) were monitored in children in three age groups (6-23months, 24-59months, and 5-17years) using a self-controlled risk interval design. We also monitored for Guillain-Barré syndrome, encephalitis, and anaphylaxis following IIV in patients ≥6months of age using a cohort design with historical controls. In the risk intervals following live attenuated influenza vaccine (LAIV), we collected weekly counts of Guillain-Barré syndrome, encephalitis, and anaphylaxis in patients ages 2-49. Among LAIV vaccinees, numbers of expected events based on rates in historical controls were calculated, adjusted for age and site. Results: At the end of surveillance, approximately 3.6 million first doses of IIV and 250000 first doses of LAIV had been administered in the VSD. No elevated risks were identified in risk intervals following 2012-2013 IIV, as compared with a self-matched control interval or to historical controls. For each outcome, fewer than three events occurred in the risk interval following 2012-2013 LAIV, and we thus were unable to estimate measures of relative risks. Conclusions: No increased risk was identified for any of the pre-specified outcomes following 2012-2013 influenza vaccinations in the VSD.
机译:目的:在疫苗安全数据链(VSD)中收到2012-2013年流感疫苗后,我们每周进行针对预定不良事件的监视。方法:对于每种结局,根据生物学上的合理性和现有文献确定风险间隔(即接种后可能增加风险的时间)。使用自我控制的风险间隔设计,对三个年龄段(6-23个月,24-59个月和5-17岁)的儿童进行了灭活流感疫苗(IIV)发作的监测。我们还采用队列设计和历史对照对IIV后≥6个月的患者进行了格林-巴利综合征,脑炎和过敏反应的监测。在减毒活疫苗(LAIV)接种后的风险间隔中,我们收集了2-49岁患者的吉兰-巴雷综合征,脑炎和过敏反应的每周计数。在LAIV疫苗中,根据历史对照的发生率计算了预期事件的数量,并根据年龄和地点进行了调整。结果:在监视结束时,已在VSD中进行了大约360万次IIV初次给药和250000次LAIV初次给药。与自我匹配的控制间隔或历史控制相比,在2012-2013 IIV之后的风险间隔中未发现升高的风险。对于每个结果,在2012-2013年LAIV之后的风险间隔内发生的事件少于三个,因此我们无法估计相对风险的度量。结论:2012-2013年在VSD中接种流感疫苗后,未发现任何预先指定结果的风险增加。

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