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Postlicensure safety surveillance for varicella vaccine.

机译:水痘疫苗的上市后安全监督。

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CONTEXT: Since its licensure in 1995, the extensive use of varicella vaccine and close surveillance of the associated anecdotal reports of suspected adverse effects provide the opportunity to detect potential risks not observed before licensure because of the relatively small sample size and other limitations of clinical trials. OBJECTIVES: To detect potential hazards, including rare events, associated with varicella vaccine, and to assess case reports for clinical and epidemiological implications. DESIGN AND SETTING: Postlicensure case-series study of suspected vaccine adverse events reported to the US Vaccine Adverse Event Reporting System (VAERS) from March 17, 1995, through July 25, 1998. MAIN OUTCOME MEASURES: Numbers of reported adverse events, proportions, and reporting rates (reports per 100,000 doses distributed). RESULTS: VAERS received 6574 case reports of adverse events in recipients of varicella vaccine, a rate of 67.5 reports per 100,000 doses sold. Approximately 4% of reports described serious adverse events, including 14 deaths. The most frequently reported adverse events were rashes, possible vaccine failures, and injection site reactions. Misinterpretation of varicella serology after vaccination appeared to account for 17% of reports of possible vaccine failures. Among 251 patients with herpes zoster, 14 had the vaccine strain of varicella zoster virus (VZV), while 12 had the wild-type virus. None of 30 anaphylaxis cases was fatal. An immunodeficient patient with pneumonia had the vaccine strain of VZV in a lung biopsy. Pregnant women occasionally received varicella vaccine through confusion with varicella zoster immunoglobulin. Although the role of varicella vaccine remained unproven in most serious adverse event reports, there were a few positive rechallenge reports and consistency of many cases with syndromes recognized as complications of natural varicella. CONCLUSION: Most of the reported adverse events associated with varicella vaccine are minor, and serious risks appear to be rare. We could not confirm a vaccine etiology for most of the reported serious events; several will require further study to clarify whether varicella vaccine plays a role. Education is needed to ensure appropriate use of varicella serologic assays and to eliminate confusion between varicella vaccine and varicella zoster immunoglobulin. JAMA. 2000;284:1271-1279
机译:上下文:自1995年获得许可以来,水痘疫苗的广泛使用以及对相关可疑副作用的轶事报道的密切监视,为发现许可前未发现的潜在风险提供了机会,因为样本量相对较小且临床试验存在其他局限性。目的:检测与水痘疫苗有关的潜在危害,包括罕见事件,并评估病例报告的临床和流行病学意义。设计与地点:从1995年3月17日至1998年7月25日,向美国疫苗不良事件报告系统(VAERS)报告的可疑疫苗不良事件的上市后病例系列研究。主要观察指标:报告的不良事件数量,比例,和报告率(每100,000剂剂量的报告分布)。结果:VAERS收到了6574例水痘疫苗接种者不良事件的病例报告,每销售100,000剂67.5例报告。大约4%的报告描述了严重的不良事件,包括14例死亡。最常见的不良事件是皮疹,可能的疫苗失败和注射部位反应。接种疫苗后对水痘血清学的误解似乎占疫苗可能失败报告的17%。在251例带状疱疹患者中,有14例具有水痘带状疱疹病毒(VZV)疫苗株,而12例具有野生型病毒。 30例过敏反应无一例是致命的。一名免疫缺陷性肺炎患者在肺活检中接种了VZV疫苗株。孕妇偶尔会因与水痘带状疱疹免疫球蛋白混淆而接受水痘疫苗。尽管在大多数严重不良事件报告中水痘疫苗的作用尚未得到证实,但仍有一些积极的再挑战报告,并且许多综合症病例被认为是自然水痘并发症,因此具有一致性。结论:大多数报道的与水痘疫苗有关的不良事件是轻微的,严重的风险似乎很少。对于大多数报道的严重事​​件,我们无法确定疫苗的病因。一些将需要进一步研究以阐明水痘疫苗是否起作用。需要进行教育,以确保正确使用水痘血清学检测方法,并消除水痘疫苗和水痘带状疱疹免疫球蛋白之间的混淆。贾玛2000; 284:1271-1279

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