In 2006, Brazil began routine immunization of infants <15 wk of age with a single-strain rotavirus vaccine. We evaluated whether the rotavirus vaccination program was associated with declines in childhood diarrhea deaths and hospital admissions by monitoring disease trends before and after vaccine introduction in all five regions of Brazil with varying disease burden and distinct socioeconomic and health indicators.
Methods and Findings
National data were analyzed with an interrupted time-series analysis that used diarrhea-related mortality or hospitalization rates as the main outcomes. Monthly mortality and admission rates estimated for the years after rotavirus vaccination (2007–2009) were compared with expected rates calculated from pre-vaccine years (2002–2005), adjusting for secular and seasonal trends. During the three years following rotavirus vaccination in Brazil, rates for diarrhea-related mortality and admissions among children <5 y of age were 22% (95% confidence interval 6%–44%) and 17% (95% confidence interval 5%–27%) lower than expected, respectively. A cumulative total of ∼1,500 fewer diarrhea deaths and 130,000 fewer admissions were observed among children <5 y during the three years after rotavirus vaccination. The largest reductions in deaths (22%–28%) and admissions (21%–25%) were among children younger than 2 y, who had the highest rates of vaccination. In contrast, lower reductions in deaths (4%) and admissions (7%) were noted among children two years of age and older, who were not age-eligible for vaccination during the study period.
After the introduction of rotavirus vaccination for infants, significant declines for three full years were observed in under-5-y diarrhea-related mortality and hospital admissions for diarrhea in Brazil. The largest reductions in diarrhea-related mortality and hospital admissions for diarrhea were among children younger than 2 y, who were eligible for vaccination as infants, which suggests that the reduced diarrhea burden in this age group was associated with introduction of the rotavirus vaccine. These real-world data are consistent with evidence obtained from clinical trials and strengthen the evidence base for the introduction of rotavirus vaccination as an effective measure for controlling severe and fatal childhood diarrhea.
Citation: do Carmo GMI, Yen C, Cortes J, Siqueira AA, de Oliveira WK, Cortez-Escalante JJ, et al. (2011) Decline in Diarrhea Mortality and Admissions after Routine Childhood Rotavirus Immunization in Brazil: A Time-Series Analysis. PLoS Med 8(4): e1001024. https://doi.org/10.1371/journal.pmed.1001024
Academic Editor: Lorenz von Seidlein, Menzies School of Health Research, Australia
Received: October 26, 2010; Accepted: March 10, 2011; Published: April 19, 2011
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Funding: No direct funding was received for this study. The authors were personally salaried by their institutions during the period of writing (though no specific salary was set aside or given for the writing of this paper). No funding bodies played any role in the design, writing or decision to publish this manuscript. Disclaimer: The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention (CDC).
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: CI, confidence interval; HDI, human development index; RR, relative reduction; SIH, Hospital Information System (Sistema de Informações Hospitalares); SIM, Mortality Information System (Sistema de Informações sobre Mortalidade); SUS, Sistema Unico de Saúde
Diarrheal disease, usually caused by infectious agents, is the second major cause of death in children aged under five years. As highlighted in a recent PLoS Medicine series, access to clean water and improved sanitation is the key to the primary prevention of diarrheal illnesses. Yet despite the targets of Millennium Development Goal 7 to half the number of people without access to clean water or improved sanitation by 2015, over one billion people worldwide do not currently have access to clean water and over two billion do not currently have access to improved sanitation.
Since enteric viruses are primarily transmitted directly from one person to another, they cannot be controlled completely by improvements in sanitation. Therefore, although not replacing the urgent need to provide access to clean water and improved sanitation for all, vaccination programs that protect young children against some infections that cause diarrhea, such as rotavirus, which accounts for one-third of all child deaths caused by diarrhea, are a pragmatic way forward. As large clinical trials have shown the safety and efficacy of rotavirus vaccines in population settings, in July 2009, the World Health Organization recommended including rotavirus vaccines into every country's national immunization programs.
Why Was This Study Done?
Although the protective effect of rotavirus vaccines has been assessed in various high-, middle-, and low-income settings, for reasons that remain unclear, the efficacy of live, oral rotavirus vaccines appears to be dependent on geographical location and correlated to the socioeconomic status of the population. Because of these concerns, evaluating the health impact of large-scale rotavirus vaccine programs and ensuring their equity in a real-world setting (rather than in clinical trial conditions) is important.
Therefore, the researchers addressed this issue by conducting this study to evaluate the effect of rotavirus vaccination on mortality and hospital admissions for diarrhea due to all causes among young children in the five regions of Brazil. The researchers chose to do this study in Brazil because of the high incidence of diarrhea-related deaths and hospital admissions and because five years ago, in July 2006, the Brazilian Ministry of Health introduced the single-strain rotavirus vaccine simultaneously in all 27 states through its national immunization program—allowing for “before” and “after” intervention analysis.
What Did the Researchers Do and Find?
The researchers obtained data on diarrheal deaths and hospital admissions in children aged under five years for the period 2002–2005 and 2007–2009 and data on rotavirus vaccination rates. The researchers got the data on diarrhea deaths from the Brazilian Mortality Information System—the national database of information collected from death certificates that covers 90% of all deaths in Brazil. The data on hospital admissions came from the electronic Hospital Information System of Brazil's Unified Health System (Sistema Unico de Saúde, SUS)—the publicly funded health-care system that covers roughly 70% of the hospitalizations and includes information on all admissions (from public hospitals and some private hospitals) authorized for payment by the Unified Health System. The researchers got regional rotavirus vaccination coverage estimates for 2007–2009 from the information department of the Ministry of Health, and estimated coverage of the two doses of oral rotavirus vaccine by taking the annual number of second doses administered divided by the number of infants in the region.
In 2007, an estimated 80% of infants received two doses of rotavirus vaccine, and by 2009, this proportion rose to 84% of children younger than one year of age. The researchers found that in the three years following the introduction of rotavirus vaccination, diarrhea-related mortality rates and admissions among children aged under five years were respectively 22% and 17% lower than expected, with a cumulative total of 1,500 fewer diarrhea deaths and 130,000 fewer admissions. Furthermore, the largest reductions in deaths and admissions were among children who had the highest rates of vaccination (less than two years of age), and the lowest reductions were among children who were not eligible for vaccination during the study period (aged 2–4 years).
What Do These Findings Mean?
These findings suggest that the introduction of rotavirus vaccination in all areas of Brazil is associated with reduced diarrhea-related deaths and hospital admissions in children aged under five years. These real-world impact data are consistent with the clinical trials and strengthen the evidence base for rotavirus vaccination as an effective measure for controlling severe and fatal childhood diarrhea.
These findings have important global policy implications. In middle-income countries, such as Brazil, that are not eligible for financial support from donors, the potential reductions in admissions and other health-care costs will be important for cost-effectiveness considerations to justify the purchase of these still relatively expensive vaccines.
Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.1001024
- PLoS Medicine has published a series on water and sanitation
- More information is available from the World Health Organization on diarrheal illness in children
- More information is available about rotavirus vaccines from the World Health Organization, the US Centers for Disease Control and Prevention, and the Rotavirus Vaccine Program
In July 2009, the World Health Organization recommended introduction of rotavirus vaccines into national immunization programs of all countries worldwide for controlling severe rotavirus disease, which accounts for approximately one-third of the 1.34 million diarrhea deaths and 9 million hospital admissions worldwide among children younger than 5 y of age –. Evaluating the health impact of large-scale programs, and ensuring their equity, is considered a top priority in global health for well-informed policy decisions –. This is particularly important for rotavirus vaccine programs because challenges remain concerning performance of the vaccine in regions with the highest morbidity and mortality ,.
The protective effect of rotavirus vaccines has been assessed in various high-, middle-, and low-income settings. For unclear reasons, efficacy of live, oral rotavirus vaccines is location-dependent, with a gradient in immune response and protective efficacy that correlates with the socioeconomic status of the population ,. In a clinical trial from Latin America, the single-strain human rotavirus vaccine Rotarix (GlaxoSmithKline Biologicals) showed a protective efficacy of 85% against severe rotavirus disease (i.e., hospital admissions) ,. Efficacy was lower in the middle-income settings of South Africa (77%) and El Salvador (76%) and the low-income setting of Malawi (49%) ,. A similar gradient in efficacy has also been shown for the pentavalent rotavirus vaccine RotaTeq (Merck) in clinical trials – and post-licensure evaluations –.
Although rotavirus vaccines have only recently been introduced, the population-level effect of vaccination has been assessed in various settings. A large reduction in national diarrhea hospital admissions after the introduction of pentavalent rotavirus vaccine has been shown in high-income settings –. While these data are promising, evaluations from middle- and low-income settings, most of which are using the single-strain vaccine , are limited. A recent study from Mexico demonstrated significant reductions in infant diarrhea mortality early after rotavirus vaccine introduction . Early evaluations of the impact of rotavirus vaccine in Brazil have shown a reduction in rotavirus and diarrhea hospitalizations during the first year after vaccine introduction –. However, Brazil is a large country with heterogeneous socioeconomic conditions and a high burden of diarrheal disease, where diarrhea deaths and admissions occur year-round and disease trends had been declining in recent years before vaccination . In such settings, accounting for secular declines and monitoring diarrhea trends for a longer duration after vaccine introduction are necessary to isolate the effect of vaccine from other concurrently implemented interventions or changes in practice. Thus, we conducted a comprehensive national evaluation quantifying the sustained effect of a vaccination program in Brazil on both relevant outcomes, diarrhea deaths and diarrhea admissions from all causes, using an interrupted time-series analysis.
In 2006, the Brazilian Ministry of Health introduced the single-strain rotavirus vaccine, Rotarix, simultaneously in all 27 states through its national immunization program in order to accelerate reaching the fourth Millennium Development Goal of reduced child mortality. The primary objective of this study was to evaluate the effect of rotavirus vaccination by analyzing trends in mortality and hospital admissions for diarrhea due to all causes among young children in the five regions of Brazil.
This evaluation involved analysis of existing, publicly available datasets. Because these are publicly available non-identifiable data, the Brazilian Ministry of Health and the United States Centers for Disease Control and Prevention human subjects' offices deemed that an ethics statement was not required for this work.
Setting and Design
Brazil is a middle-income Latin American country with an annual birth cohort of ∼3 million infants and a gross domestic product per capita of US$8,300. Brazil's 27 states are divided into five geographic regions (North, Northeast, Southeast, South, and Central-West) with distinct socioeconomic and health indicators (Table 1). The United Nations Development Program classifies countries with a human development index (HDI) below 0.90 as “developing” . In 2005, among 182 countries ranked in decreasing order of HDI, Brazil overall (HDI = 0.805) ranked 75th (for general comparison, Mexico [HDI = 0.844] ranked 53rd and the United Kingdom ranked 21st [HDI = 0.947]). The Northeast region of Brazil individually had an index (HDI = 0.720) below that of Bolivia (HDI = 0.722), a developing country that ranked 113th.
Brazil's national immunization program operates within the Sistema Unico de Saúde (SUS), Brazil's publicly funded health-care system, to provide universal access to recommended vaccines . The federal government purchases vaccines, which are distributed to state and local immunization programs and provided at no cost at public health facilities throughout the country. In April 2006, a rotavirus vaccine (Rotarix) was introduced into Brazil's national immunization program. Vaccination is recommended at 2 and 4 mo of age. The first dose can be administered at 6–14 wk, and the second dose at 14–24 wk of age.
Rotavirus vaccination coverage estimates for 2007 through 2009 among children under 1 y of age were obtained for each region from the information department of the Ministry of Health . Doses of rotavirus vaccine administered during the years 2007 through 2009, registered as a first or second dose, were recorded in a national electronic database by clinics providing immunization services. Coverage with two doses of oral rotavirus vaccine was estimated as the number of second doses administered divided by the population <1 y of age in the corresponding calendar year.
Diarrhea Admissions and Death Data
Data on diarrhea deaths were obtained from the Mortality Information System (Sistema de Informações sobre Mortalidade [SIM]) of the Brazilian Ministry of Health, the national database of information collected from death certificates . This system is estimated to capture 90% of all deaths that occur in Brazil, with lower percentages (∼80%) in the North and Northeast regions. Capture of neonatal deaths is lower, but neonatal deaths account for a small proportion (∼3%–4%) of diarrhea deaths in Latin America . Data on admissions were obtained from the electronic Hospital Information System (Sistema de Informações Hospitalares [SIH]) of SUS . This system includes information on all hospital admissions authorized for payment by SUS, which covers approximately 70% of hospitalizations in Brazil. The hospitalization data are from public hospitals and some private hospitals that are paid by the government to care for patients. No changes occurred during the study period in terms of the number of hospitals that reported to this system. Both the SIM and SIH use the International Classification of Diseases (ICD-10) for causes of death (SIM) or admission diagnosis (SIH). In this analysis, we included deaths and admissions with the principal cause coded as diarrheal disease of any cause (ICD-10 codes: A00–A03, A04, A05, A06.0–A06.3, A06.9, A07.0–A07.2, A07.9, A08–A09) among children younger than 5 y from January 2002 through December 2009.
Rates of all-cause diarrhea-related deaths and admissions among children younger than 5 y of age were examined before (2002 through 2005) and after (2007 through 2009) introduction of rotavirus vaccination using an interrupted time-series analysis. We excluded data from 2006, the year in which the vaccine was introduced. These rates were calculated from SIM and SIH figures for diarrhea-related events per month and population, using annual projections from the 2000 census .
For the regression analysis, a generalized linear model was fit to the time-series data, assuming that the diarrhea deaths and admissions were Poisson distributed. The standard error of the rate ratio was scaled to the Pearson chi-squared statistic divided by the residual degrees of freedom to account for over-dispersion of the monthly counts in the outcome data for all models . We first computed monthly rates of diarrhea-related deaths and admissions “expected” to occur in the absence of a rotavirus vaccination program by fitting the model to pre-vaccine data (2002 through 2005). We adjusted for seasonality by including an indicator variable for each calendar month and for secular trends by including calendar year in the model. The sequential year term captured the linear slope of decreasing secular trend; we assumed that this linear trend continued into the vaccine era (2007 through 2009). This model based on pre-vaccine data (including a constant and terms for month and year) was used to estimate expected values in the vaccine era. We then compared the absolute number of diarrhea-related deaths and admissions observed in the vaccine era with those expected in the absence of vaccination, as computed by the model, to assess the potential impact of vaccination. Finally, we calculated the rate ratio of diarrhea deaths and admissions in the vaccine era with the inclusion of an indicator variable for the period after rotavirus vaccine introduction; again, we controlled for seasonal and secular trends.
We investigated changes in rates of diarrhea deaths and admissions by age groups (under 1 y, 1 to <2 y, 2 to 4 y) because vaccine coverage during the early years of an immunization program and disease rates vary substantially by age. Separate models were also fitted for each region of Brazil in order to investigate differential impact of the vaccine program and to allow for different seasonality of rotavirus and secular trends. Results are presented as percent decline (1 − rate ratio) and 95% confidence interval (CI). Analyses were done with Stata (version 11).
In 2007, when an estimated 80% of children younger than 1 y of age received two doses of rotavirus vaccine, only 47% of those 1 to <2 y of age, and none of those 2 to 4 y of age had been completely immunized. By 2009, an estimated 84% of children younger than 1 y of age (Table 1) 81% of children 1 to <2 y of age, and 36% of children 2 to 4 y of age had received two doses of rotavirus vaccine.
From 2002 through 2005, an annual median of 2,700 diarrhea-related deaths occurred among children younger than 5 y at an average annual rate of 16 deaths per 100,000, accounting for 14% of the 19,000 post-neonatal deaths (i.e., 30 d to 5 y of age) in Brazil each year. Prior to rotavirus vaccine introduction, there was a trend of declining diarrhea-related mortality among children younger than 1 y (relative reduction [RR] = 0.87/y; 95% CI 0.83–0.94; p<0.001), 1 to <2 y of age (RR = 0.96/y; 95% CI 0.91–1.02; p = 0.23) and 2 to 4 y of age (RR = 0.93/y; 95% CI 0.87–1.00; p = 0.06) (Figure 1). Diarrhea mortality rates and seasonality differed significantly by region (Figure 2). A majority (73%) of diarrhea-related deaths occurred in the North and Northeast, where mortality rates were four to five times higher than those in the Central-West, South, and Southeast.
Each analysis examines trends from 2002–2009, by age, including comparison of observed events (blue dots) after rotavirus vaccination (2007 to 2009) in Brazil with expected events (solid line) and 95% CIs (gray shaded area) in the absence of vaccination. Expected number of events and 95% CIs are based on predictions from regression models fitted to historic data from each region (2002 to 2005).
Each analysis compares the monthly observed events among children under 5 y after rotavirus vaccination (2007 to 2009) with expected events in the absence of vaccination, by region. Expected number of events and 95% CIs are based on predictions from regression models fitted to historic data from each region (2002 to 2005).
Compared to expected rates based on pre-vaccine trends, diarrhea-associated mortality among children younger than 5 y of age was 22% (95% CI 6%–44%) lower during the three years after rotavirus vaccination (2007 through 2009; Table 2). Additionally, in the month-to-month comparison of observed versus expected diarrhea mortality, a decline occurred during most months of the post-vaccination period (Figure 2), with most prominent reductions during January through March. Similar declines in diarrhea deaths among children younger than 5 y of age were observed during each post-vaccination year, with a 21% reduction (95% CI 6%–34%) in 2007, a 24% reduction (95% CI 7%–38%) in 2008, and a 33% reduction (95% CI 14%–47%) in 2009.
Among all children younger than 5 y of age, observed mortality rates post-vaccination declined significantly in all regions, with largest absolute reductions occurring in high mortality regions of North and Northeast Brazil (Table 2). Among children younger than 1 y of age, observed rates were significantly lower than expected in all regions. Among 1- to <2-y-old children, the absolute declines in diarrhea-associated mortality in the North accounted for most of the overall declines in this age group. During each post-vaccination year, diarrhea-related mortality among children younger than 5 y of age was lower than expected in all but one region of Brazil (Figure 3). While a decline in mortality was not observed in the Central-West region (−2%; 95% CI −74% to 41%) in 2009 (Figure 3), overall diarrhea mortality during 2007–2009 for this region was non-significantly lower (22% decline; 95% CI −15% to 48%) than expected.
The maps depict the percent change in observed rates of diarrhea mortality and admission after rotavirus vaccination in Brazil compared to expected rates without a vaccination program, by year and region. Expected numbers of events are based on predictions from regression models fitted to historic data from each region (2002 to 2005). The percent declines are computed as one minus the RR of diarrhea events post-vaccine compared to the pre-vaccine era from Poisson regression models, adjusting for seasonality and secular trends.
In total, during 2007–2009, approximately 1,500 fewer diarrhea-related deaths were observed in Brazil compared to that expected without a vaccine program among children under 5 y of age.
During the pre-vaccine period, there were a total of ∼1,091,000 hospital admissions for diarrhea from all causes reported through the SUS among children younger than 5 y, giving an average annual rate of 1,593 per 100,000. Similar to diarrhea-related deaths, significant declining trends prior to vaccine introduction were also observed in diarrhea-related admissions among children younger than 1 y of age (RR = 0.93/y; 95% CI 0.90–0.97; p<0.001), but not in children 1 to <2 y of age (RR = 0.99/y; 95% CI 0.94–1.04; p = 0.66) or 2 to 4 y of age (RR = 0.98/y; 95% CI 0.94–1.03; p = 0.59) (Figure 1). Unlike diarrhea-related deaths, which were mostly concentrated in the poorest North and Northeast regions, diarrhea-related hospital admissions occurred throughout Brazil. However, the highest expected diarrhea admission rates (per 100,000) were in the less developed North (2,915) and Northeast (2,070) and the lowest rates in the more developed Southeast (666) and South (892) regions of Brazil (Table 3).
During the three years following vaccine introduction, the observed annual hospital admission rates for diarrhea among children younger than 1 y and children 1 to <2 y of age were 637 and 601 per 100,000 lower than the expected rates without vaccination (Table 3), reductions of 25% (95% CI 14%–34%) and 21% (95% CI 7%–33%; p<0.001), respectively. Reduction in diarrhea-related hospital admissions was most prominent during May to October (Figure 4). Countrywide observed diarrhea-related hospital admissions among children younger than 5 y of age were lower than expected during each post-vaccination year, with a 21% reduction (95% CI 9%–31%) in 2007, an 11% reduction (95% CI −5% to 24%) in 2008, and a 24% reduction (95% CI 8%–37%) in 2009. Compared to expected rates, significantly lower diarrhea-related hospital admission rates were observed in four out of five regions (Table 3). In the South, diarrhea-related hospital admissions were 12% (95% CI −8% to 29%) lower than expected in 2007 and 11% (95% CI −19% to 33%) lower than expected in 2009, but above the expected by 27% (95% CI 0%–62%) during 2008 (Figure 3).
Each analysis compares the monthly observed events among children under 5 y after rotavirus vaccination (2007 to 2009) with expected events in the absence of vaccination, by region. Expected number of events and 95% CIs are based on predictions from regression models fitted to historic data from each region (2002 to 2005).
Overall, during 2007–2009, a 17% (95% CI 5%–27%) reduction, or approximately 130,000 fewer diarrhea-related hospital admissions (∼42,480 per year), was observed compared to the number of admissions expected in the absence of vaccination among children under 5 y of age in Brazil.
The introduction of a single-strain rotavirus vaccine in the childhood immunization program in Brazil was associated with a significant nationwide decline in diarrhea-related deaths and hospital admissions among children younger than 5 y of age. Reductions in mortality are consistent with results from Mexico, where the single-strain rotavirus vaccine was introduced in the same year (2006) . However, Brazil is one of several countries in which substantial reductions in hospital admissions due to diarrhea have been shown following introduction of rotavirus vaccination into the national immunization program ,. Prevention of rotavirus-related admissions is particularly important for middle- and high-income countries in which nonfatal rotavirus diarrhea is a common cause of childhood morbidity. The results from Brazil suggest protection of rotavirus vaccination against both diarrhea deaths and diarrhea-related hospital admissions, adding to the strength of evidence supporting investment in rotavirus vaccination to curtail the 1.3 million deaths and 9 million hospital admissions related to diarrhea that occur annually worldwide.
In Brazil, we observed a reduction of approximately 40,000 admissions per year (i.e., nearly one in five diarrhea-related hospital admissions averted) among children under 5 y of age during 2007–2009. Declines in diarrhea-related hospital admissions were substantial both in the more developed South and Southeast regions, as well as in the poorest regions of Brazil (North and Northeast), where socioeconomic and health indicators approximate those of less developed countries. Because the baseline burden of diarrhea is three to five times greater in the North and Northeast than in other regions of Brazil, the absolute reduction in diarrhea-related deaths and diarrhea-related hospital admissions was much greater in this population. Lower rotavirus vaccine efficacy and immunogenicity have been observed in impoverished populations of Latin America, Asia, and Africa that have the highest risk of severe disease ,,. Significant reductions in diarrhea-associated mortality in the North of Brazil suggest that children living in areas with limited access to health care who are at highest risk of dying from diarrheal illnesses benefitted from vaccination.
Several pertinent findings support rotavirus vaccination as the most likely explanation for the reduction in diarrhea-related deaths and admissions. First, our estimates of decline were adjusted for seasonal fluctuations and secular declines in trends of diarrhea deaths and admissions. Second, the decline among vaccinated age groups was sustained on a national level for three full years after vaccine introduction. Third, the reduction in diarrhea-related hospital admissions was larger in children aged 1 y or less, who had high rates of vaccination, than in those 2 to 4 y of age, who were not eligible for rotavirus immunization during the study period.
Lastly, seasonal blunting in mortality and admissions was noted in several regions. Seasonality in rotavirus disease in Brazil varies by region and study –. In the South, Central-West, and Southeast regions of Brazil, previous surveillance indicated that seasonal peaks in rotavirus admissions occur during May to October, although year-round detection of the virus has also been reported ,. Our observation of the largest declines in diarrhea admissions during these months of peak rotavirus activity supports the contention that vaccination might have had a causal role. Data are sparse on the seasonality of rotavirus in the North and Northeast regions of Brazil, although one study suggests year-round detection of rotavirus , which is consistent with our finding of year-round decreases in diarrhea mortality in these regions.
We were intrigued by the increase in diarrhea-related hospital admissions during 2008 in the South despite high vaccination coverage, which contributed to an overall lower decline in diarrhea-related hospital admissions nationally during the same year. In 2007 and 2008, G2P was the predominant rotavirus strain circulating in Brazil, a strain fully heterotypic to the G1P vaccine used in Brazil, prompting a debate about whether vaccine pressure contributed to its emergence –. While emergence of this strain might explain the higher diarrhea-related hospital admission rates in the South during 2008, we think this is unlikely because the single-strain rotavirus vaccine provided good heterotypic cross-protection against G2P strains in Brazil , and a similar G2P strain predominated in the South as well as in other regions that had sustained declines in diarrhea-related disease. The possibility also exists that an accumulation of older susceptible children in 2008 who were unexposed to rotavirus during 2007 because of the large declines in rotavirus disease during that year might have contributed to an increase in the intensity of transmission during 2008 . However, we suspect this is also unlikely to fully explain the increase in the South because similar increases should have been observed across Brazil. One possible explanation for greater than expected diarrhea-related hospital admissions in 2008 in the South of Brazil is circulation of other enteric pathogens causing a regional epidemic of diarrhea.
Several factors could affect the interpretation of our findings, primarily relating to the ecological nature of our study. Ecological studies can be informative but have several shortcomings. Because these studies do not link an exposure to an outcome at an individual level, they may be prone to ecological fallacy (i.e., those unexposed get the disease). Confounding biases such as seasonal periodicity of disease, secular declines in trends, contribution of simultaneously implemented interventions, and changes in coding and health-care treatment patterns cannot be directly assessed with these studies because of the absence of a control group . Although we adjusted for seasonality and secular declines in diarrhea mortality and admissions, we cannot be fully confident that changes in coding or treatment practices did not occur during the study period. While we do not have evidence suggesting that reporting of diarrhea deaths changed over the study period, a decrease in reporting of deaths after rotavirus vaccine introduction could be misinterpreted as vaccine effectiveness. However, any changes in reporting would likely have affected all age groups, and led to decline of mortality or admissions in both older and younger children. The persistent reductions in diarrhea deaths and diarrhea-related hospital admissions across all regions, and the gradient in observed declines, with the lowest reduction in the oldest children, who were not immunized with the rotavirus vaccine, are consistent with vaccine-associated effects. Programmatic realities are such that diagnostic testing is typically not done for etiologic confirmation of diarrhea. Thus, we used all-cause diarrhea codes to assess vaccine impact. Although this may provide less precision with regard to vaccine effect on rotavirus disease, we suspect that measuring impact on all-cause diarrhea is more valuable to decision makers and the public health community because it provides an estimate of the preventable fraction of diarrhea deaths and admissions attributable to rotavirus.
In summary, this time-series analysis provides evidence of substantial reductions following the introduction of rotavirus vaccination of both diarrhea-related deaths and diarrhea-related hospital admissions from a large middle-income country in the Americas with both developing and developed regions. These findings have important global health policy implications. In low-income countries, the main impetus for introduction of rotavirus vaccines has been the potential to prevent rotavirus deaths: the consistency in findings of a sustained reduction in diarrhea mortality after rotavirus vaccination in Mexico  and Brazil suggests that rotavirus vaccination is an important tool for reducing the global burden of diarrhea deaths. In middle-income countries that are not eligible for financial support from donors, the potential reductions in diarrhea-related hospital admissions and other health-care costs will be important for cost-effectiveness considerations to justify the purchase of these relatively expensive vaccines. The reductions in diarrhea-related hospital admissions observed in Brazil, especially in low-mortality and higher income regions, are also relevant for decisions in higher income countries that have not yet introduced rotavirus vaccines into their routine immunization programs.
Conceived and designed the experiments: GMIdC CY JC AAS LHdO EHC. Analyzed the data: CY JC AAS WKdO JJC-E BL. Wrote the paper: GMIdC CY JC AAS WKdO JJC-E BL BF LHdO EHC MP. ICMJE criteria for authorship read and met: GMIdC CY JC AAS WKdO JJC-E BL BF LHdO EHC MP. Agree with the manuscript's results and conclusions: GMIdC CY JC AAS WKdO JJC-E BL BF LHdO EHC MP. Wrote the first draft: MP.
- 1. Black RE, Cousens S, Johnson HL, Lawn JE, Rudan I, et al. (2010) Global, regional, and national causes of child mortality in 2008: a systematic analysis. Lancet 375: 1969–1987.
- 2. Parashar UD, Burton A, Lanata C, Boschi-Pinto C, Shibuya K, et al. (2009) Global mortality associated with rotavirus disease among children in 2004. J Infect Dis 200: Suppl 1S9–S15.
- 3. World Health Organization (2009) Meeting of the Immunization Strategic Advisory Group of Experts, April 2009—conclusions and recommendations. Wkly Epidemiol Rec 84: 220–236.
- 4. [Anonymous] (2010) Evaluation: the top priority for global health. Lancet 375: 526.
- 5. Oxman AD, Bjorndal A, Becerra-Posada F, Gibson M, Block MA, et al. (2010) A framework for mandatory impact evaluation to ensure well informed public policy decisions. Lancet 375: 427–431.
- 6. Reidpath DD, Morel CM, Mecaskey JW, Allotey P (2009) The Millennium Development Goals fail poor children: the case for equity-adjusted measures. PLoS Med 6: e1000062.
- 7. Patel M, Shane AL, Parashar UD, Jiang B, Gentsch JR, et al. (2009) Oral rotavirus vaccines: how well will they work where they are needed most? J Infect Dis 200: Suppl 1S39–S48.
- 8. Patel MM, Parashar UD (2009) Assessing the effectiveness and public health impact of rotavirus vaccines after introduction in immunization programs. J Infect Dis 200: Suppl 1S291–S299.
- 9. Linhares AC, Velazquez FR, Perez-Schael I, Saez-Llorens X, Abate H, et al. (2008) Efficacy and safety of an oral live attenuated human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in Latin American infants: a randomised, double-blind, placebo-controlled phase III study. Lancet 371: 1181–1189.
- 10. Ruiz-Palacios GM, Perez-Schael I, Velazquez FR, Abate H, Breuer T, et al. (2006) Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. N Engl J Med 354: 11–22.
- 11. Madhi SA, Cunliffe NA, Steele D, Witte D, Kirsten M, et al. (2010) Effect of human rotavirus vaccine on severe diarrhea in African infants. N Engl J Med 362: 289–298.
- 12. de Palma O, Cruz L, Ramos H, de Baires A, Villatoro N, et al. (2010) Effectiveness of rotavirus vaccination against childhood diarrhoea in El Salvador: case-control study. BMJ 340: c2825.
- 13. Zaman K, Dang DA, Victor JC, Shin S, Yunus M, et al. (2010) Efficacy of pentavalent rotavirus vaccine against severe rotavirus gastroenteritis in infants in developing countries in Asia: a randomised, double-blind, placebo-controlled trial. Lancet 376: 615–623.
- 14. Vesikari T, Matson DO, Dennehy P, Van Damme P, Santosham M, et al. (2006) Safety and efficacy of a pentavalent human-bovine (WC3) reassortant rotavirus vaccine. N Engl J Med 354: 23–33.
- 15. Armah GE, Sow SO, Breiman RF, Dallas MJ, Tapia MD, et al. (2010) Efficacy of pentavalent rotavirus vaccine against severe rotavirus gastroenteritis in infants in developing countries in sub-Saharan Africa: a randomised, double-blind, placebo-controlled trial. Lancet 376: 606–614.
- 16. Boom JA, Tate JE, Sahni LC, Rench MA, Hull JJ, et al. (2010) Effectiveness of pentavalent rotavirus vaccine in a large urban population in the United States. Pediatrics 125: e199–e207.
- 17. Boom JA, Tate JE, Sahni LC, Rench MA, Quaye O, et al. (2010) Sustained protection from pentavalent rotavirus vaccination during the second year of life at a large, urban United States pediatric hospital. Pediatr Infect Dis J 29: 1133–1135.
- 18. Patel M, Pedreira C, De Oliveira LH, Tate J, Orozco M, et al. (2009) Association between pentavalent rotavirus vaccine and severe rotavirus diarrhea among children in Nicaragua. JAMA 301: 2243–2251.
- 19. Curns AT, Steiner CA, Barrett M, Hunter K, Wilson E, et al. (2010) Reduction in acute gastroenteritis hospitalizations among US children after introduction of rotavirus vaccine: analysis of hospital discharge data from 18 US states. J Infect Dis 201: 1617–1624.
- 20. Lambert SB, Faux CE, Hall L, Birrell FA, Peterson KV, et al. (2009) Early evidence for direct and indirect effects of the infant rotavirus vaccine program in Queensland. Med J Aust 191: 157–160.
- 21. Tate JE, Panozzo CA, Payne DC, Patel MM, Cortese MM, et al. (2009) Decline and change in seasonality of US rotavirus activity after the introduction of rotavirus vaccine. Pediatrics 124: 465–471.
- 22. Zeller M, Rahman M, Heylen E, De Coster S, De Vos S, et al. (2010) Rotavirus incidence and genotype distribution before and after national rotavirus vaccine introduction in Belgium. Vaccine 28: 7507–7513.
- 23. de Oliveira LH, Danovaro-Holliday MC, Matus CR, Andrus JK (2008) Rotavirus vaccine introduction in the Americas: progress and lessons learned. Expert Rev Vaccines 7: 345–353.
- 24. Richardson V, Hernandez-Pichardo J, Quintanar-Solares M, Esparza-Aguilar M, Johnson B, et al. (2010) Effect of rotavirus vaccination on death from childhood diarrhea in Mexico. N Engl J Med 362: 299–305.
- 25. Gurgel RG, Bohland AK, Vieira SC, Oliveira DM, Fontes PB, et al. (2009) Incidence of rotavirus and all-cause diarrhea in northeast Brazil following the introduction of a national vaccination program. Gastroenterology 137: 1970–1975.
- 26. Correia JB, Patel MM, Nakagomi O, Montenegro FM, Germano EM, et al. (2010) Effectiveness of monovalent rotavirus vaccine (Rotarix) against severe diarrhea caused by serotypically unrelated G2P strains in Brazil. J Infect Dis 201: 363–369.
- 27. Lanzieri TM, Costa I, Shafi FA, Cunha MH, Ortega-Barria E, et al. (2010) Trends in hospitalizations from all-cause gastroenteritis in children younger than 5 years of age in Brazil before and after human rotavirus vaccine introduction, 1998-2007. Pediatr Infect Dis J 29: 673–675.
- 28. Barros FC, Matijasevich A, Requejo JH, Giugliani E, Maranhao AG, et al. (2010) Recent trends in maternal, newborn, and child health in Brazil: progress toward Millennium Development Goals 4 and 5. Am J Public Health 100: 1877–1889.
United Nations Development Programme (2010) Human development report 2010. Available: http://hdr.undp.org/en/reports/global/hdr2010/. Accessed 19
- 30. Temporao JG (2003) [The private vaccines market in Brazil: privatization of public health.] Cad Saude Publica 19: 1323–1339.
Brazilian Ministry of Health (2011) Sistema de Informação do Programa Nacional de
Imunizações. Brasilia: Brazilian Ministry of Health. Available
Accessed 19 March 2011.
REDE Interagencial de Informação para a
Saúde (2008) Basic health indicators in Brazil: concepts and application,
2nd edition. Brasilia, Brazil: Pan American Health Organization. Available:
http://www.ripsa.org.br/php/index.php Accessed 19 March
Brazilian Institute of Geography and Statistics (2010) Population estimates. Available at: http://www.ibge.com.br/english/estatistica/populacao/estimativa2009/default.shtm
[Last accessed March 19, 2011].
McCullagh P, Nelder J (1989) Generalized linear models. London: Chapman and Hall.
- 35. Munford V, Gilio AE, de Souza EC, Cardoso DM, Cardoso DD, et al. (2009) Rotavirus gastroenteritis in children in 4 regions in Brazil: a hospital-based surveillance study. J Infect Dis 200: Suppl 1S106–S113.
- 36. Luz CR, Mascarenhas JD, Gabbay YB, Motta AR, Lima TV, et al. (2005) Rotavirus serotypes and electropherotypes identified among hospitalised children in Sao Luis, Maranhao, Brazil. Rev Inst Med Trop Sao Paulo 47: 287–293.
- 37. Linhares AC, Gabbay YB, Freitas RB, da Rosa ES, Mascarenhas JD, et al. (1989) Longitudinal study of rotavirus infections among children from Belem, Brazil. Epidemiol Infect 102: 129–145.
- 38. Gurgel RQ, Cuevas LE, Vieira SC, Barros VC, Fontes PB, et al. (2007) Predominance of rotavirus PG2 in a vaccinated population, Brazil. Emerg Infect Dis 13: 1571–1573.
- 39. Nakagomi T, Cuevas LE, Gurgel RG, Elrokhsi SH, Belkhir YA, et al. (2008) Apparent extinction of non-G2 rotavirus strains from circulation in Recife, Brazil, after the introduction of rotavirus vaccine. Arch Virol 153: 591–593.
- 40. Patel MM, de Oliveira LH, Bispo AM, Gentsch J, Parashar UD (2008) Rotavirus PG2 in a vaccinated population, Brazil. Emerg Infect Dis 14: 863–865.
- 41. United States Centers for Disease Control and Prevention (2009) Reduction in rotavirus after vaccine introduction—United States, 2000-2009. MMWR Morb Mortal Wkly Rep 58: 1146–1149.
World Health Organization (2008) Generic protocol for monitoring impact of rotavirus vaccination on
rotavirus disease burden and viral strains. Document WHO/IVB/08.16
Accessed 16 March 2011. Geneva: World Health Organization.