National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Centre Hospitalier Universitaire Pédiatrique Charles De Gaulle, Ouagadougou, Burkina Faso.
J Infect Dis. 2019 Oct 31;220(220 Suppl 4):S253-S262. doi: 10.1093/infdis/jiz301.
In 2013, Burkina Faso introduced 13-valent pneumococcal conjugate vaccine (PCV13) into the routine childhood immunization program, to be administered to children at 8, 12, and 16 weeks of age. We evaluated the impact of PCV13 on pneumococcal meningitis.
Using nationwide surveillance, we gathered demographic/clinical information and cerebrospinal fluid (CSF) results for meningitis cases. Pneumococcal cases were confirmed by culture, polymerase chain reaction (PCR), or latex agglutination; strains were serotyped using PCR. We compared annual incidence (cases per 100 000) 4 years after PCV13's introduction (2017) to average pre-PCV13 incidence (2011-2013). We adjusted incidence for age and proportion of cases with CSF tested at national laboratories.
In 2017, pneumococcal meningitis incidence was 2.7 overall and 10.5 (<1 year), 3.8 (1-4 years), 3.5 (5-14 years), and 1.4 (≥15 years) by age group. Compared to 2011-2013, PCV13-serotype incidence was significantly lower among all age groups, with the greatest decline among children aged <1 year (77%; 95% confidence interval [CI], 65%-84%). Among all ages, the drop in incidence was larger for PCV13 serotypes excluding serotype 1 (79%; 95% CI, 72%-84%) than for serotype 1 (52%; 95% CI, 44%-59%); incidence of non-PCV13 serotypes also declined (53%; 95% CI, 37%-65%). In 2017, 45% of serotyped cases among all ages were serotype 1 and 12% were other PCV13 serotypes.
In Burkina Faso, meningitis caused by PCV13 serotypes continues to decrease, especially among young children. However, the concurrent decline in non-PCV13 serotypes and short pre-PCV13 observation period complicate evaluation of PCV13's impact. Efforts to improve control of serotype 1, such as switching from a 3 + 0 schedule to a 2 + 1 schedule, may improve overall control of pneumococcal meningitis in this setting.
2013 年,布基纳法索将 13 价肺炎球菌结合疫苗(PCV13)纳入常规儿童免疫计划,在儿童 8、12 和 16 周龄时接种。我们评估了 PCV13 对肺炎球菌性脑膜炎的影响。
我们利用全国性监测,收集了脑膜炎病例的人口统计学/临床信息和脑脊液(CSF)结果。通过培养、聚合酶链反应(PCR)或乳胶凝集试验确认肺炎球菌病例;使用 PCR 对菌株进行血清分型。我们将 PCV13 引入后的第 4 年(2017 年)的年度发病率(每 100000 人发病数)与 PCV13 引入前的平均发病率(2011-2013 年)进行了比较。我们根据年龄和在国家实验室检测的 CSF 病例比例对发病率进行了调整。
2017 年,各年龄组肺炎球菌性脑膜炎的总发病率为 2.7/100000,其中<1 岁为 10.5/100000,1-4 岁为 3.8/100000,5-14 岁为 3.5/100000,≥15 岁为 1.4/100000。与 2011-2013 年相比,所有年龄组 PCV13 血清型的发病率均显著下降,<1 岁儿童的降幅最大(77%;95%置信区间[CI],65%-84%)。在所有年龄段中,除血清型 1 以外的 PCV13 血清型的发病率下降幅度大于血清型 1(79%;95% CI,72%-84%);非 PCV13 血清型的发病率也有所下降(53%;95% CI,37%-65%)。2017 年,所有年龄组中经血清分型的病例中,45%为血清型 1,12%为其他 PCV13 血清型。
在布基纳法索,PCV13 血清型引起的脑膜炎继续减少,尤其是在幼儿中。然而,非 PCV13 血清型的同时下降和 PCV13 观察期较短,使对 PCV13 影响的评估变得复杂。为改善对血清型 1 的控制而做出的努力,例如从 3+0 计划改为 2+1 计划,可能会改善该环境中对肺炎球菌性脑膜炎的整体控制。