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带状疱疹预防研究中的带状疱疹疫苗安全性:一项随机试验。

Safety of herpes zoster vaccine in the shingles prevention study: a randomized trial.

机构信息

New York University School of Medicine, New York, USA.

出版信息

Ann Intern Med. 2010 May 4;152(9):545-54. doi: 10.7326/0003-4819-152-9-201005040-00004.

Abstract

BACKGROUND

The herpes zoster vaccine is effective in preventing herpes zoster and postherpetic neuralgia in immunocompetent older adults. However, its safety has not been described in depth.

OBJECTIVE

To describe local adverse effects and short- and long-term safety profiles of herpes zoster vaccine in immunocompetent older adults.

DESIGN

Randomized, placebo-controlled trial with enrollment from November 1998 to September 2001 and follow-up through April 2004 (mean, 3.4 years). A Veterans Affairs Coordinating Center generated the permutated block randomization scheme, which was stratified by site and age. Participants and follow-up study personnel were blinded to treatment assignments. (ClinicalTrials.gov registration number: NCT00007501)

SETTING

22 U.S. academic centers.

PARTICIPANTS

38 546 immunocompetent adults 60 years or older, including 6616 who participated in an adverse events substudy.

INTERVENTION

Single dose of herpes zoster vaccine or placebo.

MEASUREMENTS

Serious adverse events and rashes in all participants and inoculation-site events in substudy participants during the first 42 days after inoculation. Thereafter, vaccination-related serious adverse events and deaths were monitored in all participants, and hospitalizations were monitored in substudy participants.

RESULTS

After inoculation, 255 (1.4%) vaccine recipients and 254 (1.4%) placebo recipients reported serious adverse events. Local inoculation-site side effects were reported by 1604 (48%) vaccine recipients and 539 (16%) placebo recipients in the substudy. A total of 977 (56.6%) of the vaccine recipients reporting local side effects were aged 60 to 69 years, and 627 (39.2%) were older than 70 years. After inoculation, herpes zoster occurred in 7 vaccine recipients versus 24 placebo recipients. Long-term follow-up (mean, 3.39 years) showed that rates of hospitalization or death did not differ between vaccine and placebo recipients.

LIMITATIONS

Participants in the substudy were not randomly selected. Confirmation of reported serious adverse events with medical record data was not always obtained.

CONCLUSION

Herpes zoster vaccine is well tolerated in older, immunocompetent adults.

PRIMARY FUNDING SOURCE

Cooperative Studies Program, Department of Veterans Affairs, Office of Research and Development; grants from Merck to the Veterans Affairs Cooperative Studies Program; and the James R. and Jesse V. Scott Fund for Shingles Research.

摘要

背景

带状疱疹疫苗在免疫功能正常的老年人中能有效预防带状疱疹和带状疱疹后神经痛。然而,其安全性尚未得到深入描述。

目的

描述免疫功能正常的老年人中带状疱疹疫苗的局部不良反应和短期及长期安全性概况。

设计

这是一项随机、安慰剂对照试验,纳入对象为 1998 年 11 月至 2001 年 9 月,随访至 2004 年 4 月(平均 3.4 年)。退伍军人事务协调中心生成了置换块随机化方案,方案按地点和年龄分层。参与者和随访研究人员对治疗分配情况不知情。(临床试验.gov 注册号:NCT00007501)

地点

美国 22 个学术中心。

参与者

38546 名免疫功能正常的 60 岁及以上成年人,其中 6616 人参加了不良事件亚研究。

干预措施

单次接种带状疱疹疫苗或安慰剂。

测量

所有参与者在接种后 42 天内的严重不良事件和皮疹,以及亚研究参与者的接种部位事件。此后,所有参与者监测与疫苗接种相关的严重不良事件和死亡,亚研究参与者监测住院情况。

结果

接种后,255 名(1.4%)疫苗接种者和 254 名(1.4%)安慰剂接种者报告了严重不良事件。在亚研究中,1604 名(48%)疫苗接种者和 539 名(16%)安慰剂接种者报告了局部接种部位副作用。报告局部副作用的疫苗接种者中,977 名(56.6%)年龄在 60 至 69 岁之间,627 名(39.2%)年龄大于 70 岁。接种后,7 名疫苗接种者出现带状疱疹,24 名安慰剂接种者出现带状疱疹。长期随访(平均 3.39 年)显示,疫苗接种者和安慰剂接种者的住院或死亡发生率无差异。

局限性

亚研究参与者并非随机选择。并非总是通过医疗记录数据确认报告的严重不良事件。

结论

带状疱疹疫苗在免疫功能正常的老年人群中具有良好的耐受性。

主要资金来源

退伍军人事务部合作研究计划、研究与发展办公室;默克公司向退伍军人事务合作研究计划提供的赠款;以及詹姆斯·R 和杰西·V·斯科特带状疱疹研究基金。

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