Centre for Global Health Research, Kenya Medical Research Institute, Kisumu.
Academic Medical Centre, University of Amsterdam, The Netherlands.
Clin Infect Dis. 2019 Nov 27;69(12):2177-2184. doi: 10.1093/cid/ciz139.
Data on pneumococcal conjugate vaccine (PCV) indirect effects in low-income countries with high human immunodeficiency virus (HIV) burden are limited. We examined adult pneumococcal pneumonia incidence before and after PCV introduction in Kenya in 2011.
From 1 January 2008 to 31 December 2016, we conducted surveillance for acute respiratory infection (ARI) among ~12 000 adults (≥18 years) in western Kenya, where HIV prevalence is ~17%. ARI cases (cough or difficulty breathing or chest pain, plus temperature ≥38.0°C or oxygen saturation <90%) presenting to a clinic underwent blood culture and pneumococcal urine antigen testing (UAT). We calculated ARI incidence and adjusted for healthcare seeking. The proportion of ARI cases with pneumococcus detected among those with complete testing (blood culture and UAT) was multiplied by adjusted ARI incidence to estimate pneumococcal pneumonia incidence.
Pre-PCV (2008-2010) crude and adjusted ARI incidences were 3.14 and 5.30/100 person-years-observation (pyo), respectively. Among ARI cases, 39.0% (340/872) had both blood culture and UAT; 21.2% (72/340) had pneumococcus detected, yielding a baseline pneumococcal pneumonia incidence of 1.12/100 pyo (95% confidence interval [CI]: 1.0-1.3). In each post-PCV year (2012-2016), the incidence was significantly lower than baseline; with incidence rate ratios (IRRs) of 0.53 (95% CI: 0.31-0.61) in 2012 and 0.13 (95% CI: 0.09-0.17) in 2016. Similar declines were observed in HIV-infected (IRR: 0.13; 95% CI: 0.08-0.22) and HIV-uninfected (IRR: 0.10; 95% CI: 0.05-0.20) adults.
Adult pneumococcal pneumonia declined in western Kenya following PCV introduction, likely reflecting vaccine indirect effects. Evidence of herd protection is critical for guiding PCV policy decisions in resource-constrained areas.
在艾滋病毒(HIV)负担较高的低收入国家,关于肺炎球菌结合疫苗(PCV)间接效应的数据有限。我们研究了 2011 年肯尼亚引入 PCV 前后成人肺炎球菌性肺炎的发病率。
从 2008 年 1 月 1 日至 2016 年 12 月 31 日,我们对西部肯尼亚约 12000 名成年人(≥18 岁)进行急性呼吸道感染(ARI)监测,该地区 HIV 流行率约为 17%。出现咳嗽或呼吸困难或胸痛、体温≥38.0°C 或血氧饱和度<90%的 ARI 病例在诊所接受血培养和肺炎球菌尿液抗原检测(UAT)。我们计算了 ARI 发病率,并进行了医疗寻求调整。在接受了完整检测(血培养和 UAT)的 ARI 病例中,检测出肺炎球菌的比例乘以调整后的 ARI 发病率,以估计肺炎球菌性肺炎的发病率。
PCV 前(2008-2010 年)粗发病率和调整发病率分别为 3.14/100 人年观察(pyo)和 5.30/100 pyo。在 ARI 病例中,39.0%(340/872)同时进行了血培养和 UAT;21.2%(72/340)检测到肺炎球菌,基线肺炎球菌性肺炎发病率为 1.12/100 pyo(95%置信区间[CI]:1.0-1.3)。在每个 PCV 后年份(2012-2016 年),发病率均明显低于基线;2012 年发病率比值比(IRR)为 0.53(95%CI:0.31-0.61),2016 年为 0.13(95%CI:0.09-0.17)。在 HIV 感染者(IRR:0.13;95%CI:0.08-0.22)和未感染者(IRR:0.10;95%CI:0.05-0.20)中也观察到类似的下降。
PCV 引入后,肯尼亚西部成人肺炎球菌性肺炎的发病率下降,这可能反映了疫苗的间接效应。群体保护的证据对于指导资源有限地区的 PCV 政策决策至关重要。