首页> 美国卫生研究院文献>Public Health Ethics >An Ethical Justification for Expanding the Notion of Effectiveness in Vaccine Post-Market Monitoring: Insights from the HPV Vaccine in Canada
【2h】

An Ethical Justification for Expanding the Notion of Effectiveness in Vaccine Post-Market Monitoring: Insights from the HPV Vaccine in Canada

机译:扩大疫苗上市后监测有效性概念的道德依据:加拿大HPV疫苗的见解

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Health regulators must carefully monitor the real-world safety and effectiveness of marketed vaccines through post-market monitoring in order to protect the public’s health and promote those vaccines that best achieve public health goals. Yet, despite the fact that vaccines used in collective immunization programmes should be assessed in the context of a public health response, post-market effectiveness monitoring is often limited to assessing immunogenicity or limited programmatic features, rather than assessing effectiveness across populations. We argue that post-market monitoring ought to be expanded in two ways to reflect a ‘public health notion of post-market effectiveness’, which incorporates normative public health considerations: (i) effectiveness monitoring should yield higher quality data and grant special attention to underrepresented and vulnerable populations; and (ii) the scope of effectiveness should be expanded to include a consideration of the various social factors that maximize (and minimize) a vaccine’s effectiveness at the population level, paying particular attention to how immunization programmes impact related health gradients. We use the case of the human papillomavirus vaccine in Canada to elucidate how expanding post-market effectiveness monitoring is necessary to close the gap between clinical practice and public health, and to ensure that vaccines are effective in a morally relevant sense.
机译:卫生监管机构必须通过上市后监测来仔细监测市售疫苗的现实安全性和有效性,以保护公众健康并推广最能实现公共卫生目标的疫苗。然而,尽管事实上应该在公共卫生应对措施中评估集体免疫计划中使用的疫苗,但是上市后有效性监测通常仅限于评估免疫原性或有限的程序特征,而不是评估跨人群的有效性。我们认为,应当以两种方式扩展售后监测,以反映“售后有效性的公共卫生概念”,其中纳入了规范性的公共卫生考虑因素:(i)有效性监测应产生更高质量的数据,并应特别关注代表性不足和脆弱的人群; (ii)应该扩大有效性的范围,包括考虑各种社会因素,以在人群水平上最大化(或最小化)疫苗的有效性,并特别注意免疫方案如何影响相关的健康梯度。我们以加拿大的人乳头瘤病毒疫苗为例,阐明如何有必要扩大上市后有效性监测,以缩小临床实践与公共卫生之间的差距,并确保疫苗在道德上有意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号