Department of Paediatrics and Child Health, University of Zimbabwe, Harare, Zimbabwe.
Harare Central Hospital, Harare, Zimbabwe.
Clin Infect Dis. 2019 Sep 5;69(Suppl 2):S72-S80. doi: 10.1093/cid/ciz462.
Streptococcus pneumoniae is a leading cause of pneumonia and meningitis in children aged <5 years. Zimbabwe introduced 13-valent pneumococcal conjugate vaccine (PCV13) in 2012 using a 3-dose infant schedule with no booster dose or catch-up campaign. We evaluated the impact of PCV13 on pediatric pneumonia and meningitis.
We examined annual changes in the proportion of hospitalizations due to pneumonia and meningitis among children aged <5 years at Harare Central Hospital (HCH) pre-PCV13 (January 2010-June 2012) and post-PCV13 (July 2013-December 2016) using a negative binomial regression model, adjusting for seasonality. We also evaluated post-PCV13 changes in serotype distribution among children with confirmed pneumococcal meningitis at HCH and acute respiratory infection (ARI) trends using Ministry of Health outpatient data.
Pneumonia hospitalizations among children aged <5 years steadily declined pre-PCV13; no significant change in annual decline was observed post-PCV13. Post-PCV13 introduction, meningitis hospitalization decreased 30% annually (95% confidence interval [CI], -42, -14) among children aged 12-59 months, and no change was observed among children aged 0-11 months. Pneumococcal meningitis caused by PCV13 serotypes decreased from 100% in 2011 to 50% in 2016. Annual severe and moderate outpatient ARI decreased by 30% (95% CI, -33, -26) and 7% (95% CI, -11, -2), respectively, post-PCV13 introduction.
We observed declines in pediatric meningitis hospitalizations, PCV13-type pneumococcal meningitis, and severe and moderate ARI outpatient visits post-PCV13 introduction. Low specificity of discharge codes, changes in referral patterns, and improvements in human immunodeficiency virus care may have contributed to the lack of additional declines in pneumonia hospitalizations post-PCV13 introduction.
肺炎球菌是 5 岁以下儿童患肺炎和脑膜炎的主要原因。津巴布韦于 2012 年引入了 13 价肺炎球菌结合疫苗(PCV13),采用 3 剂婴儿免疫程序,无加强针或补种运动。我们评估了 PCV13 对儿科肺炎和脑膜炎的影响。
我们使用负二项回归模型,调整季节性因素,检查哈拉雷中央医院(HCH) 5 岁以下儿童肺炎和脑膜炎住院比例在 PCV13 接种前(2010 年 1 月至 2012 年 6 月)和 PCV13 接种后(2013 年 7 月至 2016 年 12 月)的年度变化。我们还评估了 HCH 确诊肺炎球菌脑膜炎患儿的血清型分布变化以及卫生部门诊数据中急性呼吸道感染(ARI)趋势。
5 岁以下儿童肺炎住院率在 PCV13 接种前稳步下降;PCV13 接种后,年度下降幅度无显著变化。PCV13 引入后,12-59 月龄儿童脑膜炎住院率每年下降 30%(95%置信区间[CI],-42,-14),0-11 月龄儿童无变化。PCV13 血清型引起的肺炎球菌脑膜炎从 2011 年的 100%下降到 2016 年的 50%。PCV13 引入后,严重和中度门诊 ARI 分别下降了 30%(95%CI,-33,-26)和 7%(95%CI,-11,-2)。
我们观察到 PCV13 引入后,儿科脑膜炎住院率、PCV13 型肺炎球菌脑膜炎和严重及中度门诊 ARI 有所下降。出院代码特异性低、转诊模式改变以及艾滋病毒治疗的改善可能导致 PCV13 引入后肺炎住院率没有进一步下降。