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Adverse events following immunization in Ontario's female school-based HPV program

机译:安大略省女性学校HPV计划免疫后的不良事件

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Background: In September 2007, a school-based human papillomavirus (HPV) vaccination program targeting grade 8 girls (approximately 13 years old) and delivered by public health was implemented in Ontario, Canada. We assessed reports of adverse events following immunization (AEFI) from the school-based program as part of quadrivalent HPV (HPV4) vaccine safety surveillance and to contribute to a comprehensive HPV vaccine program evaluation. Methods: AEFIs following HPV4 vaccine (Gardasil (R)) administered between September 1, 2007 and December 31, 2011 were extracted from the province's reportable disease system. Confirmed AEFI reports among females 12-15 years old (i.e. assumed to have received vaccine through the program) were included. Events were grouped according to provincial AEFI case definitions. Rates were calculated using doses distributed as the denominator. Results: Between 2007 and 2011, 133 confirmed AEFIs were reported while 691,994 HPV4 vaccine doses were distributed in the school-based program. The overall reporting rate was 19.2 HPV4 AEFI per 100,000 doses distributed. Annual reporting rates decreased from 30.0 to 18.3 per 100,000 doses distributed. Frequently reported events included 'allergic reaction dermatologic/mucosa' (25%), 'rash' (22%), and 'local/injection site reaction' (20%); 26% of reports had a non-specific event of 'other severe/unusual events' selected. Ten serious AEFIs were reported (7.5% of reports) including 2 anaphylaxis, 2 seizures, 1 thrombocytopenia and 1 death. Further review found that the reports of anaphylaxis did not meet the Brighton anaphylaxis definition and the death was attributed to a preexisting cardiac condition. Conclusions: Overall these findings are consistent with the safety profile of HPV4 vaccine from prelicensure clinical trials and post-marketing surveillance reports and importantly, no new safety signals were identified, especially no reports of VTE in this younger female population. Continued assessment of HPV4 AEFI surveillance data may be important to detect and investigate safety signals
机译:背景:2007年9月,在加拿大安大略省实施了一项针对学校的人乳头瘤病毒(HPV)疫苗接种计划,该计划针对8岁女孩(大约13岁)并由公共卫生部门实施。我们评估了基于学校的计划中的免疫接种后不良事件的报告(AEFI),作为四价HPV(HPV4)疫苗安全性监视的一部分,并为全面的HPV疫苗计划评估做出了贡献。方法:从省报告的疾病系统中提取2007年9月1日至2011年12月31日间注射HPV4疫苗(Gardasil(R))后的AEFI。包括12至15岁女性(即假定已通过该计划接种疫苗)的确诊AEFI报告。根据省级AEFI案例定义对事件进行了分组。使用分配的剂量作为分母计算比率。结果:在2007年至2011年之间,报告了133例确诊的AEFI,同时在基于学校的计划中分配了691,994株HPV4疫苗剂量。总体报告率为每分配100,000剂19.2 HPV4 AEFI。年度报告率从每10万剂30.0降至18.3。经常报告的事件包括“皮肤/粘膜过敏反应”(25%),“皮疹”(22%)和“局部/注射部位反应”(20%); 26%的报告选择了“其他严重/异常事件”的非特定事件。据报道有十种严重的AEFI(占报告总数的7.5%),包括2种过敏反应,2次癫痫发作,1例血小板减少症和1例死亡。进一步的审查发现,过敏反应的报告不符合布莱顿过敏反应的定义,死亡归因于先前存在的心脏病。结论:总体而言,这些发现与许可前临床试验和上市后监测报告中的HPV4疫苗的安全性相一致,重要的是,未发现新的安全性信号,尤其是在这一年轻女性人群中未发现VTE的报告。持续评估HPV4 AEFI监视数据对于检测和调查安全信号可能很重要

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