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带状疱疹重组疫苗的广泛安全性评估。

A Broad Safety Assessment of the Recombinant Herpes Zoster Vaccine.

出版信息

Am J Epidemiol. 2022 Mar 24;191(5):957-964. doi: 10.1093/aje/kwac030.

Abstract

The recombinant herpes zoster vaccine (RZV), approved as a 2-dose series in the United States in October 2017, has proven highly effective and generally safe. However, a small risk of Guillain-Barré syndrome after vaccination was identified after approval, and questions remain about other possible adverse events. This data-mining study assessed RZV safety in the United States using the self-controlled tree-temporal scan statistic, scanning data on thousands of diagnoses recorded during follow-up to detect any statistically unusual temporal clustering of cases within a large hierarchy of diagnoses. IBM MarketScan data on commercially insured persons at least 50 years of age receiving RZV between January 1, 2018, and May 5, 2020, were used, including 56 days of follow-up; 1,014,329 doses were included. Statistically significant clustering was found within a few days of vaccination for unspecified adverse effects, complications, or reactions to immunization or other medical substances/care; fever; unspecified allergy; syncope/collapse; cellulitis; myalgia; and dizziness/giddiness. These findings are consistent with the known safety profile of this and other injected vaccines. No cluster of Guillain-Barré syndrome was detected, possibly due to insufficient sample size. This signal-detection method has now been applied to 5 vaccines, with consistently plausible results, and seems a promising addition to vaccine-safety evaluation methods.

摘要

在美国,重组带状疱疹疫苗(RZV)于 2017 年 10 月获得批准,作为两剂系列疫苗使用,其已被证明具有高度有效性和总体安全性。然而,在批准后发现疫苗接种后发生格林-巴利综合征的风险较小,并且对于其他可能的不良事件仍存在疑问。本数据挖掘研究使用自对照树时间扫描统计量在美国评估了 RZV 的安全性,扫描了数千项在随访期间记录的诊断数据,以检测在大型诊断层次结构内病例的任何统计学上不寻常的时间聚集。使用了 IBM MarketScan 中 2018 年 1 月 1 日至 2020 年 5 月 5 日期间接受 RZV 的至少 50 岁商业保险人员的数据,包括 56 天的随访;共包括 1014329 剂。在接种疫苗后几天内,发现未指定的不良反应、并发症或对免疫接种或其他医疗物质/护理的反应、发热、未指定的过敏、晕厥/昏倒、蜂窝织炎、肌痛和头晕/头晕等情况存在统计学上显著的聚集。这些发现与该疫苗和其他注射疫苗的已知安全性概况一致。未检测到格林-巴利综合征的聚集,可能是由于样本量不足。该信号检测方法现已应用于 5 种疫苗,结果均具有合理的可信度,似乎是疫苗安全性评估方法的一个有希望的补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2919/9071519/0c7aa0fcd81d/kwac030f1.jpg

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