The impact of measles immunization campaigns in India using a nationally representative sample of 27,000 child deaths
Abstract
India comprises much of the persisting global childhood measles mortality. India implemented a mass second-dose measles immunization campaign in 2010. We used interrupted time series and multilevel regression to quantify the campaign’s impact on measles mortality using the nationally representative Million Death Study (including 27,000 child deaths in 1.3 million households surveyed from 2005 to 2013). 1–59 month measles mortality rates fell more in the campaign states following launch (27%) versus non-campaign states (11%). Declines were steeper in girls than boys and were specific to measles deaths. Measles mortality risk was lower for children living in a campaign district (OR 0.6, 99% CI 0.4–0.8) or born in 2009 or later (OR 0.8, 99% CI 0.7–0.9). The campaign averted up to 41,000–56,000 deaths during 2010–13, or 39–57% of the expected deaths nationally. Elimination of measles deaths in India is feasible.
https://doi.org/10.7554/eLife.43290.001eLife digest
The introduction of the measles vaccine in the 1960s led to large reductions in measles deaths in many countries. Yet, measles remains a major killer of children younger than age five worldwide, particularly among children living in Africa and Asia, where fewer children are immunized. India has been particularly hard hit, with annual child measles deaths exceeding 60,000 in 2005.
In the 1990s, India’s national vaccination program made one dose of the measles vaccine part of routine vaccinations through much of the country to help reduce the numbers of measles deaths. However, it was one of the last countries to add a second dose of measles vaccine as recommended by the World Health Organization, which has been shown to prevent infection and death in 90-95% of vaccinated children.
In 2008, the Indian government announced it would introduce a second dose of measles vaccine to its routine vaccine schedule for children from 2010 onwards. Prior to the introduction of a second-dose measles vaccine, campaigns were launched to increase immunization rates in regions where few children were being vaccinated. But how many young children’s lives were saved by these campaigns was unknown.
Now, Wong et al. show that India’s measles immunization campaigns saved the lives of 41,000 to 56,000 children between 2010 and 2013. This averted between 39-57% of the expected measles deaths nationally during that time period. Wong et al. used data from the Million Death Study, which used household surveys to capture information on the cause of 27,000 child deaths in India between 2005 and 2013, to assess the affects of the state vaccination campaigns on measles deaths. Changes in measles deaths were compared to changes in unrelated child deaths to make sure any differences were related to the vaccination campaigns and not other improvements in children’s health care.
Indian states with measles immunization campaigns saw larger decreases in measles deaths among children younger than five than states without such a campaign (27% vs 11%). Similar decreases were not seen in child deaths from other causes. Girls, who are disproportionately affected by measles in India, benefited from larger reductions in deaths than boys in states with immunization campaigns. The success of two-dose measles vaccination campaigns at reducing young children’s deaths in India may help to boost vaccination rates and help combat parents’ hesitance to immunize their children.
https://doi.org/10.7554/eLife.43290.002Introduction
Measles remains an important cause of death among under-five children (Moss, 2017). Much of this persisting global burden of measles is located in Africa and Asia, notably in India (Black et al., 2010; Dabbagh et al., 2017). Direct estimation of cause-specific mortality documented a 90% decline in 1–59 month measles mortality rates in India from 2000 to 2015 (Fadel et al., 2017).
The role of national intervention strategies in explaining the decline in measles deaths in India is unknown. In 2005, the Government of India launched the National Rural Health Mission – a program geared towards improving public health infrastructure and reducing child mortality in priority states (Ministry of Health and Family Welfare, 2005). In 2008, the Government of India announced a policy change to introduce second-dose measles vaccine through the routine immunization (Ministry of Health and Family Welfare, 2010). District-level mass immunization campaigns (termed supplementary immunization activities) for second-dose measles vaccine were launched in 2010 in 14 target states where first-dose measles vaccination coverage was below 80% (hereafter referred to as campaign states). The campaign prioritized immunization of children aged 9 months to 10 years in the 14 campaign states, after which second-dose measles vaccine was provided through routine immunization. The remaining 21 states with higher coverage added only second-dose measles vaccine through routine immunization (Gupta et al., 2011).
The ideal method of evaluation, a randomized trial, was not practical in the rollout of the national campaign. Mathematical models estimate an 84% decline in measles deaths globally during 2000–2016, but are unable to evaluate the effectiveness of interventions (Dabbagh et al., 2017; Jha, 2014). In these scenarios, interrupted time series is considered a robust quasi-experimental evaluation method (Cochrane Effective Practice and Organisation of Care, 2017). Here, we apply interrupted time series supplemented with multilevel regression analysis to provide the first direct quantification of the impact of the national mass measles immunization campaign on childhood measles mortality in India. These analyses have the additional advantage of using the Million Death Study (MDS), a nationally representative sample of all deaths in India, including 27,000 child deaths from 1.3 million households surveyed from 2005 to 2013 (Fadel et al., 2017; Gomes et al., 2017).
Results
Characteristics of subjects
From 2005 to 2013, the MDS captured deaths for 13,490 girls and 13,007 boys aged 1–59 months after excluding children missing cause of death (2.8%). Of the 1,638 measles deaths using the definition of one or more physician coding or the family reported a measles history for the deceased, 79% occurred in rural areas, 73% in campaign states, 59% at ages 12–59 months, and 57% in girls (Table 1). 76% of families reporting a measles death noted the child to have a history of measles (using the local language term), but only 39% of the deceased children received at least one dose of measles vaccine. The proportion of measles deaths at 1–59 months in campaign states reporting at least one dose of measles vaccine rose modestly (34% to 47%) from 2005–2009 to 2010–2013, but was mostly unchanged in non-campaign states (48% to 51%). Despite inherent misclassification that can be expected from verbal autopsies, we observed that the proportion vaccinated against measles did not differ across case definitions, suggesting that physician assignment of deaths was not unduly biased by a history of measles vaccination (Table 1—source data 1).
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Table 1—source data 1
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Annual measles deaths at ages 1–59 months fell from 62,000 to 24,000 from 2005 to 2013 (Figure 1). Prior to campaign launch, 76% of measles deaths were concentrated in campaign states, 55% of which were in the states of Uttar Pradesh (18%), Madhya Pradesh (15%), Rajasthan (11%), and Bihar (11%). Following campaign launch, 59% of measles deaths were in campaign states, with 38% in the above four states (Figure 1—figure supplement 1). The age distributions did not differ greatly between pre-campaign and post-campaign periods (Figure 1—figure supplement 2). The 1–59 month measles mortality rate per thousand live births declined substantially during this period. The average annual rate reduction (AARR) in measles mortality over the full study period was 12% but accelerated to 22% following campaign launch. Post-campaign declines in measles mortality were faster in the campaign states (27%) versus non-campaign states (11%). The AARR declined most notably in campaign states (15%) and in the states of Madhya Pradesh (20%), Uttar Pradesh (19%), Rajasthan (17%), Chhattisgarh (17%), and Gujarat (14%) (Table 2).
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Figure 1—source data 1
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Table 2—source data 1
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Interrupted time series analysis
Measles mortality rates among 1–59 month-old children in campaign states declined significantly following campaign launch (Figure 2) when compared to control deaths from injuries, congenital anomalies, and non-communicable diseases of the same ages. There were no other mass public health interventions targeting this age group during the study period. The choice of control deaths is unbiased as these conditions are unaffected by measles vaccination and provide pre-intervention trends comparable to trends of measles deaths from 2005 to 2009. As well, cases and controls deaths were sampled with the same method and assigned a cause of death by two independent physicians. We noted a temporary increase in measles mortality in 2009. This might reflect increased reporting as this was also the period when measles surveillance expanded. Thus, we used 2009 as the intervention year to account for the increased reporting.
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Figure 2—source data 1
- https://doi.org/10.7554/eLife.43290.013
The interrupted time series analyzes changes in the slope of six-month measles mortality rate per thousand live births and changes in the level (which were few). Prior to campaign launch, the slope of measles mortality in campaign states remained unchanged at –0.004 deaths per thousand live births (95% CI –0.065, 0.056; Table 3). The control deaths also remained unchanged with an analogous slope of 0.003 (95% CI –0.054, 0.062). Following campaign launch, the slope of measles mortality in campaign states fell significantly to –0.164 (95% CI –0.320, –0.008, p=0.040), whereas the slope for the control deaths remained unchanged. Declines in measles mortality in India overall were similar to declines in campaign states (–0.132, 95% CI –0.252, –0.011, p=0.034; Figure 3). In comparison, non-campaign states saw no significant change in measles mortality rates following campaign launch. Notably, the rate ratio of 1–59 month measles mortality between campaign states and non-campaign states fell from 3.1 to 1.8 during 2005–2013. The declines were specific to measles deaths, as we observed no significant changes in slope for pneumonia and diarrhoea deaths following campaign launch.
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Figure 3—source data 1
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Following campaign launch, we observed sharper declines in measles mortality rates among campaign states compared to non-campaign states (Figure 3). Girls residing in campaign states saw steeper declines in measles mortality relative to boys, even though the direction of effect was similar in both sexes. Additional stratified analyses yielded generally similar results. In campaign states, the decline in measles mortality was significant at 12–59 months but not significant at 1–11 months. At ages 1–59 months, alternative definitions of measles cases, using one or both physicians assigning measles as the underlying cause of death, also yielded similar results (Figure 4). We observed a significant change in slope and level in campaign states when two physicians agreed immediately or when one physician assigned measles as the cause of death (both definitions excluded a family reported history of measles which might have been affected by publicity for the campaign). Moving the intervention year forward to 2010 resulted in the slope of measles mortality following campaign launch becoming non-significant (–0.01, 95% CI –0.08, 0.05). However, we observed a significant decrease in level of measles mortality following campaign launch (–1.05, 95% CI –1.50, –0.61). In all other stratified analyses, we observed no significant change in level (Table 3).
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Figure 4—source data 1
- https://doi.org/10.7554/eLife.43290.018
Coverage of measles immunization and related health indicators
National measles immunization coverage (defined as the percentage of children aged 12 to 23 months receiving any dose of measles vaccine from routine immunization) improved from 2002 to 2014, particularly in campaign states (Figure 5). In difference-in-difference analysis, we observed a significant increase in measles vaccination coverage in the campaign states relative to non-campaign states, concurrent with campaign launch (difference-in-difference estimate 16.9%, p=0.0000009). Other coverage indicators, such as vitamin A supplementation, pneumonia treatment-seeking, oral rehydration, maternal literacy, and diarrhoea treatment-seeking showed significant increases over time, but these increases did not differ significantly between campaign and other states (Figure 5).
Multilevel logistic regression analysis
Among 26,505 overall child deaths at 1–59 months for the whole of India from 2005 to 2013, the odds of measles mortality were higher at 12–59 months (OR 1.5, 99% CI 1.3–1.7) than at ages 1–11 months, after adjusting for covariates identified in the above difference-in-difference analyses (Figure 6). Children born in 2009 or later were at lower odds of measles mortality compared with earlier births (OR 0.8, 99% CI 0.7–0.9). Children living in districts within campaign states had lower odds of measles mortality (OR 0.6, 99% CI 0.4–0.8) than children living in non-campaign states. Girls had higher odds of measles mortality (OR 1.3, 99% CI 1.1–1.5) than boys. Consistent with this finding, girls had higher excess measles mortality risk relative to all-cause mortality in campaign states than boys, and the excess risk was distributed far more widely in girls than boys in these states (Figure 7).
Mortality impact
Conservatively, we estimate that the national campaign averted 41,000 to 56,000 (median 48,500) child deaths in India during 2010–2013 (Table 4). The majority of deaths averted were in campaign states (median 41,000) with a similar number of deaths averted among girls (median 18,500) and boys (median 22,500) in these states. For India as a whole, the averted measles deaths comprise 39–57% of the expected measles deaths during 2010–2013.
Discussion
The measles vaccine has high efficacy, preventing infection and death in 90–95% of children who receive two doses (Guerra et al., 2017; Moss, 2017). However, evidence for vaccine effectiveness in low- and middle-income countries is more limited. Evidence of effectiveness at the population level is particularly required to counter scientific skepticism and waning public confidence in government immunization programs in India (Francis et al., 2018; Larson et al., 2011; Larson et al., 2010). Our first ever quantification of the impact of national mass measles immunization campaign in a high-burden country using direct cause-specific data finds high effectiveness of measles vaccination programs in reducing child measles deaths in India.
Our direct estimates of 41,000–56,000 measles deaths averted are consistent with modeled estimates documenting approximately 66,000 under-five child deaths averted (Verguet et al., 2017). However, direct data are a far more robust form of evidence. We document 24,000 measles deaths in 2013 using a broad case definition that included family reporting of history of measles. WHO estimated 49,000 measles deaths in 2015 using a definition of either clinician-suspected measles infection or a diagnosis of fever with rash and cough, runny nose, or red eyes (World Health Organization, 2018a; World Health Organization, 2016). The addition of possible measles deaths with rash and fever to our original case definition raised the estimate of measles deaths in 2013 from 24,000 to 46,000. At our observed rate of decline, we would expect 35,000 deaths in 2015 using the WHO definition. Further investigation of the reasons for these differences in total deaths from measles, particularly at the subnational level, is required. Fadel et al. (2017) documented 7,000 measles deaths in 2015 using a narrower case definition that excluded a history of measles and where all deaths were so assigned by dual physician coding with final adjudication by a third senior physician if needed. Thus, substantial downward revisions of WHO modeled estimates are likely needed. The relationship between measles cases and deaths in India is also uncertain, given that WHO incidence estimates are inconsistent with documented case fatality rates in India which range from 0.8–1.4% (Sudfeld and Halsey, 2009; Verguet et al., 2017; Wolfson et al., 2009; World Health Organization, 2016; World Health Organization, 2018b; Murhekar et al., 2014). Our direct data should help to redefine current estimates of measles mortality and number of infections in India.
Could measles transmission or, at a minimum, measles deaths be eliminated in India? Drastic declines in child measles mortality suggest that elimination of measles deaths in India is feasible, albeit difficult. Measles elimination is challenging due to its high infectivity – each infected child can infect an additional 4–26 children in South-east Asia (Guerra et al., 2017; Holzmann et al., 2016). The WHO estimated the coverage of first-dose vaccine in South-east Asia (which includes India) to be below the levels that would achieve herd immunity (85% in 2012) and stagnation of coverage in the past decade (Dabbagh et al., 2017; Moss, 2017). Documented measles outbreaks indicate that India remains endemic to measles given suboptimal coverage, with about 3 million infants not receiving first-dose measles vaccination in 2013 (Dabbagh et al., 2017; Jamir et al., 2016; Singh and Garg, 2017; Vaidya et al., 2016). India’s Integrated Disease Surveillance Program reported a decline in annual measles outbreaks during 2011–2013 but gradual increases since (Ministry of Health and Family Welfare, 2018). The Global Vaccine Action Plan for 2012–2020 and the Government of India recommend second-dose measles vaccine to achieve herd immunity at 95% coverage to eliminate measles transmission (Dabbagh et al., 2017). Supplementary immunization activities must be regularly scheduled to reach herd immunity and to combat resurgence (Verguet et al., 2017). Though herd immunity may be difficult to achieve, efforts to improve vaccine coverage will curtail mortality, as evident by our findings. The observed reduction in under-five measles mortality may show herd immunity in cohorts born within nine months of the campaign launch. Since 2013, 11 states in India have implemented laboratory-confirmed measles surveillance. This infrastructure provides sero-epidemiological data to facilitate diagnoses of measles, detect suspected cases, and sequence circulating measles genotypes (Bose et al., 2014; Vaidya, 2015; Vaidya and Chowdhury, 2017). High quality measles surveillance through case-based detection and direct mortality statistics such as the MDS provide valuable data to monitor measles elimination programs (Bose et al., 2014; Vaidya, 2015).
The measles campaign was particularly successful for girls, which saw greater absolute declines in measles mortality than boys. Though the girl-boy gap in measles mortality rates narrowed, mortality remains higher in girls, as is the case for other infectious causes of death at ages 1–59 months (Fadel et al., 2017). Persisting higher mortality rates among girls than boys may be due to lower vaccination coverage, social preference for boys, and lower levels of breastfeeding and health care access (Alkema et al., 2014; Corsi et al., 2009; Fadel et al., 2017; Guilmoto et al., 2018; Jha et al., 2006b; Ram et al., 2013).
The interrupted time series design addresses potential confounding by the effects of different policies occurring at the same time as the measles campaign launch. Given that the majority of child causes of death were declining from 2000 onward, we selected unbiased control deaths comparable with the pre-intervention trends of measles, pneumonia, and diarrhoea deaths. The addition of control deaths allows for evaluation of post-intervention differences rather than single-group mean or slope differences. In stratified analysis, we tested alternate intervention time points and measles case definitions, all of which reported a consistent effect. We did not observe a change in slope when moving the intervention forward to 2010, likely due to fewer time points in the post-intervention trend. The observed decreased in level of measles mortality when using 2010 as the intervention year might reflect greater actual vaccine delivery.
The MDS verbal autopsy form is designed to identify all major causes of death in children with low levels of misclassification (Aleksandrowicz et al., 2014; Fadel et al., 2017). The verbal autopsy form contains specific questions relating to measles (e.g. presence of rash, cough, whether the respondent reported history of measles) but cannot ascertain exposure and timing of symptoms. Thus, we tested alternate case definitions, one including family-reporting of a history of measles to capture measles-associated deaths of pneumonia or diarrhoea, and the other using only physician coding of measles deaths. We observed declines specific to the campaign, in each case definition, as opposed to no additional declines in pneumonia or diarrhoea deaths. The lack of effect in pneumonia deaths may be due to measles contributing a smaller etiologic fraction than other viral, bacterial, or fungal agents (Farrar et al., submitted). The success of the measles campaign is the increase in vaccination in campaign states to levels comparable with non-campaign states. Though the effect was smaller in non-campaign states, the introduction of second-dose measles through routine immunization in these non-campaign states also contributed to the declines in measles mortality nationally. Continued diligence in mass immunization and direct mortality monitoring are both needed to achieve elimination of measles deaths in India.
Materials and methods
Study design
Request a detailed protocolMost deaths in India as in most low- and middle-income countries occur at home and without medical attention, precluding complete death registration and certification (Registrar General of India, 2016). Starting in 2001, the Registrar General of India (RGI) and the Centre for Global Health Research implemented the MDS in 1.3 million households within its Sample Registration System (SRS), an ongoing demographic surveillance system. Following each census, the RGI partitions India into 1 million small areas comprising 150–300 homes in either rural villages or urban census enumeration blocks. Over the ensuing decade, the SRS randomly selects and monitors several thousand units within these areas, capturing approximately 140,000 births and 46,000 deaths annually. This MDS relies on 14,268 units drawn from the 1991 and 2001 censuses (Registrar General of India, 2016). Approximately 900 trained non-medical RGI surveyors conduct two semi-annual rounds of interviews of household members or close associates of those who died in the preceding round. The interview uses a modified version of the 2011 WHO verbal autopsy questionnaire to capture death events and their chronology through structured checklist questions about key symptoms and a local language narrative. Each field report is randomly assigned to two of 404 trained physicians (Jha et al., 2008), who classify the underlying causes of death according to the International Classification of Diseases, Tenth Revision (ICD-10; Table 5) (Jha et al., 2006a; World Health Organization, 1992). Coding differences are resolved by both physicians who anonymously receive the other’s case notes. One of 40 senior physicians adjudicates persisting differences (Aleksandrowicz et al., 2014). Details of the quality assurance checks have been published earlier (Aleksandrowicz et al., 2014; Fadel et al., 2017; Jha et al., 2006a; Jha et al., 2008; Registrar General of India, 2016; Bassani et al., 2010). Ethics approval for the MDS was obtained from the Post Graduate Institute of Medical Research, St. John’s Research Institute and St. Michael’s Hospital, Toronto, Ontario, Canada. Consent procedures have been published earlier (Gomes et al., 2017; Jha et al., 2006a; Registrar General of India, 2016).
Mortality rate calculations
Request a detailed protocolThe main outcome was 1–59 month measles mortality using a case definition that required at least one physician reviewer of the verbal autopsy to code measles (ICD-10 codes B01 or B05) as the cause of death or that the living respondent reporting a measles death noted a history of measles (using the local language term) (Table 5). Though the campaign targeted children from 9 months to 10 years of age, our analysis focuses on children aged 1–59 months who comprised 84% (1638/1958) of these deaths. We applied proportions of measles deaths to all-causes among 1–59 month children and calculated three-year moving averages weighted by SRS sampling probabilities for the 35 Indian states or territories. We applied these weighted proportions to live births and deaths for India at the national and state level (derived from SRS vital statistics and census data) and adjusted to match the national birth totals from the UN Population Division and death totals from UN Population Division’s Inter-agency Group for Child Mortality Estimation (Fadel et al., 2017). We calculated rates for each six-month period as death counts were too low to separate into monthly data as semi-annual rates correspond to the frequency of survey collection conducted in the MDS.
Interrupted time series analysis
Request a detailed protocolWe conducted a multiple-group interrupted time series to assess the impact of measles campaign on 1–59 month measles mortality reduction. We arranged the data in a time series and divided the sample into time periods before and after campaign launch (Ministry of Health and Family Welfare, 2010). We used log transformed rates to account for potential nonlinearity. We calculated the average annual rate of reduction by India and by state using the linear association between log rate and time (UNICEF, 2007). We fitted the data using ordinary least squares linear segmented regression (Linden, 2015). As control deaths, we used injuries, congenital anomalies, and non-communicable diseases, each having ICD-10 code groupings as detailed in Table 5 (Fadel et al., 2017). We selected various control groups by comparing their pre-intervention trends to that of measles, pneumonia, and diarrhoea (Linden, 2015). Control selection used a matching framework to match control deaths to our measles, pneumonia, or diarrhoea deaths based on balancing of the pre-intervention trend characteristics (Linden, 2018). The pre-intervention trends excluding 2009 deaths did not differ from control deaths (p=0.9). We assessed model validity by visual inspection of autocorrelation/partial autocorrelation functions and residuals. We stratified models by age groups, sex, and campaign states. In sensitivity analysis, we fitted additional models using alternate case definitions and intervention time points.
Multilevel logistic regression analysis
Request a detailed protocolWe used multilevel logistic regression to examine characteristics of health-seeking behavior associated with measles mortality (Larsen and Merlo, 2005). We organized the data into a three-level hierarchical structure consisting of children (first level) nested within districts (second level) nested within states (third level). We fitted random intercepts at the district and state level to account for regional variation. The predictors considered were: age at death, sex, year of birth, and residence in a measles campaign district. We also adjusted for state-level coverage estimates of measles vaccination (defined in the National Family Health Survey and the District Level Household and Facility Survey as the percentage of children aged 12 to 23 months receiving any measles vaccine from routine immunization), vitamin A supplementation, oral rehydration supplementation, maternal literacy, and treatment-seeking for diarrhoea and pneumonia. We obtained the coverage data from Indian national surveys corresponding to our study period including the Government of India’s District Level Household Surveys (DLHS; 2002–2004, 2007–2008 and 2011–2012) and National Family Health Surveys (NFHS; 2005–2006, and 2013–2014). Using these coverage indicators, we conducted a difference-in-differences analysis assessing the change in coverage indicators before and after campaign launch in campaign states versus non-campaign states. We report measures of association as odds ratios (ORs; including 99% confidence intervals). We use area-level variances, median odds ratios, and intra-class correlations as measures of variation (Table 6) (Larsen and Merlo, 2005).
Geographical distribution of measles mortality risk
Request a detailed protocolWe constructed maps of 1–59 month measles mortality to determine the geographical distribution of measles mortality risk in India. We fitted the data using a generalized linear geostatistical model with integrated nested Laplace approximations. We adjusted for populations living in measles campaign districts and urban/rural residence. We used R version 3.5.1 for mapping.
Mortality impact
Request a detailed protocolTo estimate the magnitude of the intervention, we derived cumulative deaths differences using observed and expected measles mortality rates from the interrupted time series model. We extrapolated the expected rates using the pre-intervention trend from campaign launch to the end of the time series. We applied UN live births to their respective year and summed for the 2010–2013 period, then calculated deaths averted and percent averted between the observed deaths and the expected deaths. We report upper and lower bounds using the broad case definition, which captures one physician coding measles or family reporting of a history of measles, and the narrow case definitions, which captures only one physician coding measles. We used Stata version 15 for statistical analysis.
Data availability
Under legal agreement with the Registrar General of India, the MDS data cannot be redistributed outside of the Centre for Global Health Research. To request MDS data access procedures or to set up a data transfer agreement, please contact the Office of the Registrar General, RK Puram, New Delhi, India (rgoffice.rgi@nic.in). The public census reports can be found at http://www.censusindia.gov.in/vital_statistics/SRS_Statistical_Report.html. Source data files have been provided for Figures 1,2,3,4, Figure 1—figure supplement 1, and Table 2. National survey data (from Figure 5) can be obtained free of charge from the following websites: http://rchiips.org/nfhs/NFHS-4Report.shtml (NFHS-4); http://rchiips.org/nfhs/report.shtml (NFHS-3); http://rchiips.org/DLHS-4.html (DLHS-4); http://rchiips.org/prch-3.html (DLHS-3); and http://rchiips.org/state-report-rch2.html (DLHS-2).
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Article and author information
Author details
Funding
Canadian Institutes of Health Research (FDN154277)
- Prabhat Jha
Bill and Melinda Gates Foundation
- Prabhat Jha
National Institutes of Health (R01TW05991-01)
- Prabhat Jha
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Ethics
Human subjects: Ethics approval for the MDS was obtained from the Post Graduate Institute of Medical Research, St. John's Research Institute and St. Michael's Hospital, Toronto, Ontario, Canada. Consent procedures have been published earlier (Gomes et al., 2017; Jha et al., 2006a; Registrar General of India, 2016).
Copyright
© 2019, Wong et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
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Further reading
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Measles vaccination campaigns have saved the lives of about 50,000 Indian children in three years.
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- Epidemiology and Global Health
- Genetics and Genomics
Alzheimer’s disease (AD) is a complex degenerative disease of the central nervous system, and elucidating its pathogenesis remains challenging. In this study, we used the inverse-variance weighted (IVW) model as the major analysis method to perform hypothesis-free Mendelian randomization (MR) analysis on the data from MRC IEU OpenGWAS (18,097 exposure traits and 16 AD outcome traits), and conducted sensitivity analysis with six models, to assess the robustness of the IVW results, to identify various classes of risk or protective factors for AD, early-onset AD, and late-onset AD. We generated 400,274 data entries in total, among which the major analysis method of the IVW model consists of 73,129 records with 4840 exposure traits, which fall into 10 categories: Disease, Medical laboratory science, Imaging, Anthropometric, Treatment, Molecular trait, Gut microbiota, Past history, Family history, and Lifestyle trait. More importantly, a freely accessed online platform called MRAD (https://gwasmrad.com/mrad/) has been developed using the Shiny package with MR analysis results. Additionally, novel potential AD therapeutic targets (CD33, TBCA, VPS29, GNAI3, PSME1) are identified, among which CD33 was positively associated with the main outcome traits of AD, as well as with both EOAD and LOAD. TBCA and VPS29 were negatively associated with the main outcome traits of AD, as well as with both EOAD and LOAD. GNAI3 and PSME1 were negatively associated with the main outcome traits of AD, as well as with LOAD, but had no significant causal association with EOAD. The findings of our research advance our understanding of the etiology of AD.