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全球疫苗安全体系的能力:国家监管机构的观点。

Capacity for a global vaccine safety system: the perspective of national regulatory authorities.

机构信息

Technoscience and Regulation Research Unit, Department of Pediatrics (Infectious Diseases), Faculty of Medicine, Dalhousie University, NS, Canada.

出版信息

Vaccine. 2012 Jul 13;30(33):4953-9. doi: 10.1016/j.vaccine.2012.05.045. Epub 2012 May 30.

DOI:10.1016/j.vaccine.2012.05.045
PMID:22658930
Abstract

Confidence in vaccine safety is critical to national immunization strategies and to global public health. To meet the Millenium Development Goals, and buoyed by the success of new vaccines produced in developing countries, the World Health Organization has been developing a strategy to establish a global system for effective vaccine pharmacovigilance in all countries. This paper reports the findings of a qualitative survey, conducted for the WHO Global Vaccine Safety Blueprint project, on the perspectives of national regulatory authorities responsible for vaccine safety in manufacturing and procuring countries. Capacity and capabilities of detecting, reporting and responding to adverse events following immunization (AEFI), and expectations of minimum capacity necessary for vaccine pharmacovigilance were explored. Key barriers to establishing a functional national vaccine safety system in developing countries were identified. The lack of infrastructure, information technology for stable communications and data exchange, and human resources affect vaccine safety monitoring in developing countries. A persistent "fear of reporting" in several low and middle income countries due to insufficient training and insecure employment underlies a perceived lack of political will in many governments for vaccine pharmacovigilance. Regulators recommended standardized and internationally harmonized safety reporting forms, improved surveillance mechanisms, and a global network for access and exchange of safety data independent of industry.

摘要

疫苗安全性的信心对于国家免疫策略和全球公共卫生至关重要。为了实现千年发展目标,并受到发展中国家生产的新疫苗成功的鼓舞,世界卫生组织一直在制定一项战略,以在所有国家建立一个有效的疫苗药物警戒全球系统。本文报告了为世界卫生组织全球疫苗安全蓝图项目进行的一项定性调查的结果,该调查涉及负责制造和采购国家疫苗安全的国家监管机构的观点。调查探讨了发现、报告和应对疫苗接种后不良反应(AEFI)的能力和能力,以及对疫苗药物警戒所需的最低能力的期望。确定了在发展中国家建立功能齐全的国家疫苗安全系统的主要障碍。缺乏基础设施、用于稳定通信和数据交换的信息技术以及人力资源,影响了发展中国家的疫苗安全监测。由于培训不足和就业不安全,在几个中低收入国家中存在持续的“报告恐惧”,这是许多政府对疫苗药物警戒缺乏政治意愿的根源。监管机构建议采用标准化和国际协调一致的安全报告表格,改进监测机制,以及一个独立于行业的安全数据获取和交流的全球网络。