McNeil Michael M, Weintraub Eric S, Duffy Jonathan, Sukumaran Lakshmi, Jacobsen Steven J, Klein Nicola P, Hambidge Simon J, Lee Grace M, Jackson Lisa A, Irving Stephanie A, King Jennifer P, Kharbanda Elyse O, Bednarczyk Robert A, DeStefano Frank
Immunization Safety Office, Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Ga.
Immunization Safety Office, Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Ga.
J Allergy Clin Immunol. 2016 Mar;137(3):868-78. doi: 10.1016/j.jaci.2015.07.048. Epub 2015 Oct 6.
Anaphylaxis is a potentially life-threatening allergic reaction. The risk of anaphylaxis after vaccination has not been well described in adults or with newer vaccines in children.
We sought to estimate the incidence of anaphylaxis after vaccines and describe the demographic and clinical characteristics of confirmed cases of anaphylaxis.
Using health care data from the Vaccine Safety Datalink, we determined rates of anaphylaxis after vaccination in children and adults. We first identified all patients with a vaccination record from January 2009 through December 2011 and used diagnostic and procedure codes to identify potential anaphylaxis cases. Medical records of potential cases were reviewed. Confirmed cases met the Brighton Collaboration definition for anaphylaxis and had to be determined to be vaccine triggered. We calculated the incidence of anaphylaxis after all vaccines combined and for selected individual vaccines.
We identified 33 confirmed vaccine-triggered anaphylaxis cases that occurred after 25,173,965 vaccine doses. The rate of anaphylaxis was 1.31 (95% CI, 0.90-1.84) per million vaccine doses. The incidence did not vary significantly by age, and there was a nonsignificant female predominance. Vaccine-specific rates included 1.35 (95% CI, 0.65-2.47) per million doses for inactivated trivalent influenza vaccine (10 cases, 7,434,628 doses given alone) and 1.83 (95% CI, 0.22-6.63) per million doses for inactivated monovalent influenza vaccine (2 cases, 1,090,279 doses given alone). The onset of symptoms among cases was within 30 minutes (8 cases), 30 to less than 120 minutes (8 cases), 2 to less than 4 hours (10 cases), 4 to 8 hours (2 cases), the next day (1 case), and not documented (4 cases).
Anaphylaxis after vaccination is rare in all age groups. Despite its rarity, anaphylaxis is a potentially life-threatening medical emergency that vaccine providers need to be prepared to treat.
过敏反应是一种可能危及生命的过敏反应。成人接种疫苗后发生过敏反应的风险以及儿童接种新型疫苗后的过敏反应风险尚未得到充分描述。
我们试图估计疫苗接种后过敏反应的发生率,并描述确诊过敏反应病例的人口统计学和临床特征。
利用疫苗安全数据链中的医疗保健数据,我们确定了儿童和成人接种疫苗后过敏反应的发生率。我们首先识别出2009年1月至2011年12月期间所有有疫苗接种记录的患者,并使用诊断和操作代码来识别潜在的过敏反应病例。对潜在病例的医疗记录进行了审查。确诊病例符合布莱顿协作组织对过敏反应的定义,并且必须被确定为由疫苗引发。我们计算了所有疫苗联合接种后以及选定的个别疫苗接种后过敏反应的发生率。
我们识别出25173965剂疫苗接种后发生的33例确诊的疫苗引发的过敏反应病例。过敏反应发生率为每百万剂疫苗1.31例(95%可信区间,0.90 - 1.84)。发生率在不同年龄组之间无显著差异,女性略占优势但无统计学意义。特定疫苗的发生率包括:灭活三价流感疫苗每百万剂1.35例(95%可信区间,0.65 - 2.47)(10例,单独接种7434628剂),灭活单价流感疫苗每百万剂1.83例(95%可信区间,0.22 - 6.63)(2例,单独接种1090279剂)。病例中症状出现时间在30分钟内(8例)、30至不到120分钟(8例)、2至不到4小时(10例)、4至8小时(2例)、第二天(1例)以及未记录(4例)。
接种疫苗后发生过敏反应在所有年龄组中都很罕见。尽管罕见,但过敏反应是一种可能危及生命的医疗紧急情况,疫苗接种提供者需要做好治疗准备。