International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
INCLEN Trust International, New Delhi, India.
Lancet Glob Health. 2019 Jun;7(6):e735-e747. doi: 10.1016/S2214-109X(19)30081-6.
India accounts for a disproportionate burden of global childhood illnesses. To inform policies and measure progress towards achieving child health targets, we estimated the annual national and state-specific childhood mortality and morbidity attributable to Streptococcus pneumoniae and Haemophilus influenzae type b (Hib) between 2000 and 2015.
In this modelling study, we used vaccine clinical trial data to estimate the proportion of pneumonia deaths attributable to pneumococcus and Hib. The proportion of meningitis deaths attributable to each pathogen was derived from pathogen-specific meningitis case fatality and bacterial meningitis case data from surveillance studies. We applied these proportions to modelled state-specific pneumonia and meningitis deaths from 2000 to 2015 prepared by the WHO Maternal and Child Epidemiology Estimation collaboration (WHO/MCEE) on the basis of verbal autopsy studies from India. The burden of clinical and severe pneumonia cases attributable to pneumococcus and Hib was ascertained with vaccine clinical trial data and state-specific all-cause pneumonia case estimates prepared by WHO/MCEE by use of risk factor prevalence data from India. Pathogen-specific meningitis cases were derived from state-level modelled pathogen-specific meningitis deaths and state-level meningitis case fatality estimates. Pneumococcal and Hib morbidity due to non-pneumonia, non-meningitis (NPNM) invasive syndromes were derived by applying the ratio of pathogen-specific NPNM cases to pathogen-specific meningitis cases to the state-level pathogen-specific meningitis cases. Mortality due to pathogen-specific NPNM was calculated with the ratio of pneumococcal and Hib meningitis case fatality to pneumococcal and Hib meningitis NPNM case fatality. Census data from India provided the population at risk.
Between 2000 and 2015, estimates of pneumococcal deaths in Indian children aged 1-59 months fell from 166 000 (uncertainty range [UR] 110 000-198 000) to 68 700 (44 600-86 000), while Hib deaths fell from 82 600 (52 300-112 000) to 15 600 (9800-21 500), representing a 58% (UR 22-78) decline in pneumococcal deaths and an 81% (59-91) decline in Hib deaths. In 2015, national mortality rates in children aged 1-59 months were 56 (UR 37-71) per 100 000 for pneumococcal infection and 13 (UR 8-18) per 100 000 for Hib. Uttar Pradesh (18 900 [UR 12 300-23 600]) and Bihar (8600 [5600-10 700]) had the highest numbers of pneumococcal deaths in 2015. Uttar Pradesh (9300 [UR 5900-12 700]) and Odisha (1100 [700-1500]) had the highest numbers of Hib deaths in 2015. Less conservative assumptions related to the proportion of pneumonia deaths attributable to pneumococcus indicate that as many as 118 000 (UR 69 000-140 000) total pneumococcal deaths could have occurred in 2015 in India.
Pneumococcal and Hib mortality have declined in children aged 1-59 months in India since 2000, even before nationwide implementation of conjugate vaccines. Introduction of the Hib vaccine in several states corresponded with a more rapid reduction in morbidity and mortality associated with Hib infection. Rapid scale-up and widespread use of the pneumococcal conjugate vaccine and sustained use of the Hib vaccine could help accelerate achievement of child survival targets in India.
Bill & Melinda Gates Foundation.
印度在全球儿童疾病方面负担过重。为了为政策提供信息并衡量实现儿童健康目标的进展,我们估算了 2000 年至 2015 年期间由肺炎链球菌和乙型流感嗜血杆菌(Hib)引起的印度全国和各邦的儿童死亡率和发病率。
在这项建模研究中,我们使用疫苗临床试验数据来估算肺炎死亡归因于肺炎球菌和 Hib 的比例。从监测研究中特定病原体脑膜炎病例病死率和细菌性脑膜炎病例数据中得出每种病原体引起的脑膜炎死亡比例。我们将这些比例应用于 2000 年至 2015 年期间由世卫组织母婴和儿童流行病学估算合作组织(世卫组织/MCEE)根据来自印度的验尸研究准备的州特异性肺炎和脑膜炎死亡模型。使用来自印度的风险因素流行数据,通过疫苗临床试验数据和世卫组织/MCEE 制定的州特异性所有原因肺炎病例估计,确定肺炎球菌和 Hib 引起的临床和严重肺炎病例负担。通过应用特定病原体非肺炎、非脑膜炎(NPNM)侵袭性综合征病例与特定病原体脑膜炎病例的比例,确定非肺炎、非脑膜炎(NPNM)侵袭性综合征病例。根据州特异性特定病原体脑膜炎死亡和州特异性脑膜炎病死率估计,确定特定病原体脑膜炎病例。通过应用肺炎球菌和 Hib 脑膜炎病死率与肺炎球菌和 Hib 脑膜炎 NPNM 病死率的比例,计算 NPNM 病原体特定的病死率。印度的人口普查数据提供了受威胁人口。
2000 年至 2015 年间,印度 1-59 月龄儿童肺炎球菌死亡人数从 16.6 万(不确定范围[UR]11 万至 19.8 万)下降到 6.87 万(4.46 万至 8.6 万),而 Hib 死亡人数从 8.26 万(5.23 万至 11.2 万)下降到 1.56 万(9800 至 2.15 万),表示肺炎球菌死亡人数下降了 58%(UR 22%-78%),Hib 死亡人数下降了 81%(59%-91%)。2015 年,1-59 月龄儿童全国死亡率为肺炎感染 56 例(UR 37-71)/100 万,Hib 为 13 例(UR 8-18)/100 万。2015 年,北方邦(18900 [UR 12300-23600])和比哈尔邦(8600 [5600-10700])的肺炎球菌死亡人数最多。2015 年,北方邦(9300 [UR 5900-12700])和奥里萨邦(1100 [700-1500])的 Hib 死亡人数最多。与肺炎球菌死亡归因于肺炎球菌的比例相关的不太保守的假设表明,2015 年印度可能有多达 11.8 万(UR 6.9 万至 14 万)例肺炎球菌总死亡人数。
自 2000 年以来,印度 1-59 月龄儿童的肺炎球菌和 Hib 死亡率有所下降,甚至在全国范围内实施结合疫苗之前。几个邦引入 Hib 疫苗对应着与 Hib 感染相关的发病率和死亡率的更快下降。肺炎球菌结合疫苗的快速扩大和广泛使用以及 Hib 疫苗的持续使用将有助于加快实现印度儿童生存目标。
比尔及梅琳达·盖茨基金会。