Patricia Wodi A, Marquez Paige, Mba-Jonas Adamma, Barash Faith, Nguon Kosal, Moro Pedro L
Immunization Safety Office, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Immunization Safety Office, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Vaccine. 2023 Feb 24;41(9):1616-1622. doi: 10.1016/j.vaccine.2022.12.038. Epub 2023 Jan 31.
Since 2012, reports of primary ovarian insufficiency (POI) temporally associated with receipt of human papillomavirus (HPV) vaccine have been published leading to questions about a potential causal association. A Vaccine Safety Datalink study did not find an increased risk for POI after vaccination. We reviewed the Vaccine Adverse Event Reporting System (VAERS) to describe POI reports.
We searched VAERS, a U.S. passive surveillance system, for domestic POI reports received from 01/01/1990 to 12/31/2017 after any vaccination. The search used both Medical Dictionary for Regulatory Activity Preferred Terms and a text-based search for POI and its symptoms. All reports were reviewed, and the American College of Obstetricians and Gynecologists (ACOG) guidelines for POI diagnosis were applied. Data mining for disproportionate reporting was conducted.
Six hundred fifty-two reports met the search criteria and clinical review identified 19 POI reports. Most reports (n = 16) were received between 2013 and 2017. The median age at vaccination was 14.5 years (range 10-25 years) and the median interval between first dose of vaccination and reporting the event to VAERS was 43 months (range 4-132 months; mean 59.6 months). Four reports met ACOG diagnostic criteria; one with an underlying cause (47XXX chromosomal abnormality) reported. Eleven reports documented menstrual irregularity ≥ 3 months; 5 had ≥ 1 laboratory test result used to diagnose POI. Eighteen of 19 reports described receipt of HPV vaccine with or without other vaccines. Other vaccines reported were meningococcal conjugate vaccine, hepatitis A, varicella and tetanus toxoid, reduced diphtheria toxoid and acellular pertussis. Disproportionate reporting was found for three relevant coding terms after HPV vaccination.
POI is rarely reported to VAERS. Most reports contained limited diagnostic information and were submitted after published cases of POI following HPV vaccination. Results of our review do not suggest a safety concern.
自2012年以来,陆续有关于原发性卵巢功能不全(POI)与接种人乳头瘤病毒(HPV)疫苗存在时间关联的报告发布,这引发了人们对两者潜在因果关系的质疑。一项疫苗安全数据链研究未发现接种疫苗后POI风险增加。我们对疫苗不良事件报告系统(VAERS)进行了回顾,以描述POI报告情况。
我们在VAERS(美国一个被动监测系统)中搜索了1990年1月1日至2017年12月31日期间接种任何疫苗后收到的国内POI报告。搜索使用了《监管活动医学词典》首选术语以及基于文本的POI及其症状搜索。对所有报告进行了审查,并应用了美国妇产科医师学会(ACOG)的POI诊断指南。进行了不成比例报告的数据挖掘。
652份报告符合搜索标准,临床审查确定了19份POI报告。大多数报告(n = 16)是在2013年至2017年期间收到的。接种疫苗的中位年龄为14.5岁(范围10 - 25岁),首次接种疫苗与向VAERS报告事件之间的中位间隔为43个月(范围4 - 132个月;平均59.6个月)。4份报告符合ACOG诊断标准;报告了1例有潜在病因(47XXX染色体异常)的病例。11份报告记录月经不规律≥3个月;5份有≥1项用于诊断POI的实验室检查结果。19份报告中的18份描述了接种HPV疫苗的情况,有或没有接种其他疫苗。报告的其他疫苗有脑膜炎球菌结合疫苗、甲型肝炎疫苗、水痘疫苗以及破伤风类毒素、无细胞百日咳和白喉类毒素。HPV疫苗接种后发现三个相关编码术语存在不成比例报告情况。
向VAERS报告POI的情况很少见。大多数报告包含的诊断信息有限,且是在HPV疫苗接种后POI病例公布之后提交的。我们的审查结果未表明存在安全问题。