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脑膜炎球菌 A 群结合疫苗引入前脑膜炎监测评估-布基纳法索和马里。

Evaluation of meningitis surveillance before introduction of serogroup a meningococcal conjugate vaccine - Burkina Faso and Mali.

出版信息

MMWR Morb Mortal Wkly Rep. 2012 Dec 21;61(50):1025-8.

Abstract

Each year, 450 million persons in a region of sub-Saharan Africa known as the "meningitis belt" are at risk for death and disability from epidemic meningitis caused by serogroup A Neisseria meningitidis. In 2009, the first serogroup A meningococcal conjugate vaccine (PsA-TT) developed solely for Africa (MenAfriVac, Serum Institute of India, Ltd.), was licensed for persons aged 1-29 years. During 2010-2011, the vaccine was introduced in the hyperendemic countries of Burkina Faso, Mali, and Niger through mass campaigns. Strong meningitis surveillance is critical for evaluating the impact of PsA-TT because it was licensed based on safety and immunogenicity data without field effectiveness trials. Case-based surveillance, which includes the collection of epidemiologic and laboratory data on individual cases year-round, is recommended for countries that aim to evaluate the vaccine's impact. A key component of case-based surveillance is expansion of laboratory confirmation to include every case of bacterial meningitis because multiple meningococcal serogroups and different pathogens such as Haemophilus influenzae type b and Streptococcus pneumoniae cause meningitis that is clinically indistinguishable from that caused by serogroup A Neisseria meningitidis. Before the introduction of PsA-TT, evaluations of the existing meningitis surveillance in Burkina Faso and Mali were conducted to assess the capacity for case-based surveillance. This report describes the results of those evaluations, which found that surveillance infrastructures were strong but opportunities existed for improving data management, handling of specimens shipped to reference laboratories, and laboratory capacity for confirming cases. These findings underscore the need to evaluate surveillance before vaccine introduction so that activities to strengthen surveillance are tailored to a country's needs and capacities.

摘要

在被称为“脑膜炎带”的撒哈拉以南非洲地区,每年有 4.5 亿人面临由 A 群脑膜炎奈瑟菌引起的流行性脑膜炎导致死亡和残疾的风险。2009 年,第一个专为非洲开发的 A 群脑膜炎球菌结合疫苗(PsA-TT,印度血清研究所)获得许可,可用于 1-29 岁人群。在 2010-2011 年期间,该疫苗通过大规模运动在布基纳法索、马里和尼日尔等高度流行国家推出。强有力的脑膜炎监测对于评估 PsA-TT 的影响至关重要,因为它是根据安全性和免疫原性数据获得许可的,而没有进行现场有效性试验。基于病例的监测,包括全年收集有关个体病例的流行病学和实验室数据,是那些旨在评估疫苗影响的国家推荐使用的方法。基于病例的监测的一个关键组成部分是扩大实验室确认范围,包括每一例细菌性脑膜炎病例,因为多种脑膜炎奈瑟菌血清群和不同的病原体,如乙型流感嗜血杆菌和肺炎链球菌,引起的脑膜炎在临床上与 A 群脑膜炎奈瑟菌引起的脑膜炎无法区分。在推出 PsA-TT 之前,对布基纳法索和马里现有的脑膜炎监测进行了评估,以评估基于病例的监测能力。本报告介绍了这些评估的结果,发现监测基础设施强大,但在数据管理、运往参考实验室的标本处理以及确认病例的实验室能力方面存在改进空间。这些发现强调了在疫苗推出前评估监测的必要性,以便根据国家的需求和能力调整加强监测的活动。

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