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首页> 外文期刊>Journal of Clinical Epidemiology >Development of case definitions for acute encephalopathy, encephalitis, and multiple sclerosis reports to the Vaccine Adverse Event Reporting System.
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Development of case definitions for acute encephalopathy, encephalitis, and multiple sclerosis reports to the Vaccine Adverse Event Reporting System.

机译:向疫苗不良事件报告系统报告急性脑病,脑炎和多发性硬化症的病例定义。

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The Vaccine Adverse Event Reporting System (VAERS), administered by the FDA and CDC, is the U.S. system for surveillance of vaccine adverse events (AE). Acute encephalopathy age <18 months (EO < 18), age >/=18 months (EO >/= 18), encephalitis (EI), and multiple sclerosis (MS) after vaccination have been reported to VAERS, but reports often contain insufficient information to validate diagnoses. Standardized case definitions would enhance the utility of VAERS reports for AE surveillance. We developed practical case definitions for classification of VAERS reports, and three neurologists independently applied the definitions to reports submitted in 1993. Inter-observer agreement was assessed, and non-concordant classifications were reviewed in a follow-up conference call. Reports of EO < 18 (n = 8), EO >/= 18 (n = 20), EI (n = 15), and MS (n = 16) were classified as "definite" in 7% to 30% of the cases, while 26% to 51% of reports were thought to have insufficient information to make a classification. Agreement among reviewers was good to excellent, (kappa: 0.65 to 0.85) except for EO < 18 m for which it was marginal (kappa: 0.37). It is possible to develop reproducible case definitions for acute encephalopathy, encephalitis, and multiple sclerosis using a standardized approach. Application of standardized case definitions to VAERS reports documents the limited information in many reports, specifies data for supplemental collection, and indicates that VAERS reports should be cautiously interpreted. Development and application of case definitions for other adverse events reported after vaccination should enhance the value of vaccine safety databases. Published by Elsevier Science Inc.
机译:由FDA和CDC管理的疫苗不良事件报告系统(VAERS)是用于监视疫苗不良事件(AE)的美国系统。 VAERS已经报告了疫苗接种后<18个月的急性脑病(EO <18),> / = 18个月的年龄(EO> / = 18),脑炎(EI)和多发性硬化症(MS),但报告通常包含不足用于验证诊断的信息。标准化的病例定义将增强VAERS报告在AE监测中的效用。我们开发了用于VAERS报告分类的实际案例定义,并且三位神经科医师将这些定义独立地应用于1993年提交的报告。评估了观察者之间的协议,并在后续电话会议中审查了不一致的分类。 EO <18(n = 8),EO> / = 18(n = 20),EI(n = 15)和MS(n = 16)的报告在7%至30%的报告中被定为“确定”。案例中,有26%至51%的报告被认为没有足够的信息进行分类。评审员之间的一致性好到极好(kappa:0.65至0.85),但EO <18 m的边缘性(kappa:0.37)除外。使用标准方法可以为急性脑病,脑炎和多发性硬化症制定可重复的病例定义。将标准化案例定义应用于VAERS报告可记录许多报告中的有限信息,指定用于补充收集的数据,并指示应谨慎解释VAERS报告。疫苗接种后报告的其他不良事件的病例定义的开发和应用应能提高疫苗安全性数据库的价值。由Elsevier Science Inc.发布

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