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Diarrhea and health inequity among Indigenous children in Brazil: results from the First National Survey of Indigenous People’s Health and Nutrition

BMC Public Health volume 15, Article number: 191 (2015) Cite this article

Abstract

Background

Globally, diarrhea is the second leading cause of death among children under five. In Brazil, mortality due to diarrhea underwent a significant reduction in recent decades principally due to expansion of the primary healthcare network, use of oral rehydration therapy, reduced child undernutrition, and improved access to safe drinking water. The First National Survey of Indigenous People’s Health and Nutrition in Brazil, conducted in 2008–2009, was the first survey based on a nationwide representative sample to study the prevalence of diarrhea and associated factors among Indigenous children in the country.

Methods

The survey assessed the health and nutritional status of Indigenous children < 5 years of age based on a representative sample of major Brazilian geopolitical regions. A stratified probabilistic sampling was carried out for Indigenous villages. Within villages, children < 5 years of age in sampled households were included in the study. Interviews were based on a seven day recall period. Prevalence rates of acute diarrhea were calculated for independent variables and hierarchical multivariable analyses were conducted to assess associations.

Results

Information on diarrhea was obtained for 5,828 children (95.1% of the total sample). The overall prevalence of diarrhea was 23.5%. Regional differences were observed, with the highest rate being in the North (38.1%). Higher risk of diarrhea was observed among younger children and those who had less maternal schooling, lower household socioeconomic status, undernutrition (weight-for-age deficit), presence of another child with diarrhea in the household, and occurrence of upper respiratory infection.

Conclusions

According to results of the First National Survey of Indigenous People’s Health and Nutrition, almost a quarter of Indigenous children throughout the country had diarrhea during the previous week. This prevalence is substantially higher than that documented in 2006 for Brazilian children < 5 years generally (9.4%). Due to its exceedingly multicausal nature, the set of associated variables that remained associated with child diarrhea in the final multivariable model provide an excellent reflection of the diverse social and health inequities faced by Indigenous peoples in contemporary Brazil.

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Background

Among infectious and parasitic diseases, diarrhea contributes importantly to overall disease burden, especially in settings marked by socioeconomic inequality, poor sanitation, and inadequate public health services coverage. Globally, diarrheal disease is the second leading cause of death among children under five and every year approximately 800,000 deaths are related to diarrhea in this age group [1-3].

In Brazil, mortality due to diarrhea underwent a significant reduction during the last three decades principally due to expansion of the primary healthcare network, widespread use of oral rehydration therapy, reduced child undernutrition, and improved sanitation conditions largely associated with improved access to safe drinking water [4-7]. Among children under one year, the mortality rate fell about 90%, from 11.7 deaths per 1,000 live births in 1980 to 1.5 in 2005 [6].

Despite the progress achieved nationally with regard to child health generally, important differences persist between different population segments with respect to conditions affecting vulnerability to diarrhea [8]. For example, basic health and sanitation services coverage have improved for the general population, but Indigenous peoples in Brazil suffer from significant accumulated deficits in access to services such as clean water, sewage treatment, and primary healthcare as compared to the non-Indigenous population [9-11]. Studies carried out in different regions of Brazil have reported that infectious and parasitic diseases are responsible for 20 to 40% of hospital admissions among Indigenous children under five years of age and diarrhea may account for up to 90% of total reported admissions in this group depending on region and ethnicity [12-15].

Numerous studies globally have pointed to the persistence of large health disparities between Indigenous and non-Indigenous peoples even in countries, such as Australia, the United States, and Canada, which experienced significant social advances and health indicator improvements long before Brazil. Despite differences in scale, being Indigenous in these countries is also accompanied by poorer socioeconomic and health indicators [16-18]. In the case of Indigenous peoples in Brazil and other Latin American countries, infectious diseases, such as diarrhea, that are preventable by means of basic health measures predominate in peoples’ experiences of illness and deaths in diverse communities. Therefore, its confrontation by means of adequate political policy formulation and better healthcare services coverage and quality is imperative.

The aim of this paper is to analyze the prevalence of reported diarrhea and associated factors among Indigenous children under 5 years of age in Brazil, based on data from the First National Survey of the Health and Nutrition of Indigenous Peoples in Brazil (henceforth, “National Survey”), conducted in 2008–2009. This was the first study of its kind to include a nationwide representative sample of Indigenous peoples and aims at contributing to the understanding of the contemporary health profile of the nation’s Indigenous population in terms of diverse demographic, socioeconomic, and environmental factors.

Methods

The National Survey assessed the health and nutritional status of Indigenous children < 5 years and women 14 to 49 years in Brazil. A representative sample of villages located in federally recognized Indigenous reserves was obtained by multi-stage probabilistic sampling stratified by geopolitical region, as previously reported [10]. The final sample included 123 villages distributed between the following regions: North (65 villages), Central-West (14), Northeast (23), and South/Southeast (21). Households in selected villages were investigated by either census or sample depending on estimated village population. In selected households, mothers, fathers, or other relatives of all children < 5 years of age were interviewed [10]. The respondent was asked whether the child had acute diarrhea during the seven days prior to the interview [19]. If the answer was affirmative, the respondent was also asked if the child received homemade or commercial oral rehydration therapy. The National Survey methodology also included a specific set of questions on feeding of children ≤ 24 months. Additional information about variables employed and construction of nutrition, morbidity, sanitation, and socioeconomic indicators are available elsewhere [10,20,21].

In initial data analysis, prevalence rates of diarrhea were calculated according to independent variables (region, demographic and socioeconomic variables, characteristics of the household environment, and maternal and child characteristics). Measures of associations were expressed as prevalence ratios (PR) and their corresponding 95% confidence intervals. Chi-square tests for heterogeneity and Student’s t-tests for linear trend were used to evaluate differences in proportions. Estimates were corrected for the complex sampling design of the study in order to obtain a stratified probabilistic sample whose primary selection unit was village and the weights of each participant were based on the relative size of each stratum and the proportion of women and children in the target population.

The multivariable analysis employed Poisson regression with robust adjustment of variance with presence of diarrhea during the previous week as the outcome variable. This analysis included only variables collected for all children < 5 years of age. Thus, variables related to feeding practices were not included because they were collected only for children < 24 months. Independent variables entered the analysis according to hierarchical level in the model [22,23]. All estimates were adjusted by region. The first and most distal level of the model included sociodemographic characteristics of the child (sex and age), a household goods index, presence of regular income, and maternal schooling. The second hierarchical level comprised variables related to household physical conditions (type of flooring, walls and roofing), household size and composition, and sanitation conditions (source of drinking water, location used to defecate, and presence of garbage collection in the village). The third level included maternal characteristics (age and parity). The fourth level encompassed child variables (place of delivery, birth weight, and nutritional status). Finally, the fifth and most proximal level included child’s hospitalization due to diarrhea during the preceding 12 months, presence of another child in the household with diarrhea in the prior week, and child’s acute lower respiratory infection in the preceding week.

Vaccination status against rotavirus was evaluated for inclusion in the model differently than other variables because the anti-rotavirus vaccine was only introduced in the Brazilian public health system in 2006 and, consequently, children 4 to 5 years of age in the sample had not had the opportunity to receive it during their first 6 months of age. The National Immunization Program of the Brazilian Ministry of Health stipulates that children receive the first dose at two months and the second at four months. Thus, diarrhea prevalence rates were compared for the subset of children 6 to 24 months according to vaccination status.

Multivariable analysis was conducted employing a backward selection procedure with p < 0.20 for initial selection at each level, controlling for region and variables retained in previous levels, and p < 0.05 for retention in the final model. This multivariable analysis procedure has been described in previous studies reporting on the National Survey [20,21]. All analyses were conducted using STATA 10.0 (College Station, Texas, USA).

This study was approved by the National Committee on Research Ethics (Comissão Nacional de Ética em Pesquisa – CONEP) and the National Indian Foundation (Fundação Nacional do Índio – FUNAI). Upon arrival at each community, the research team held meetings with leaders and other community members, during which the objectives and procedures of the study were clearly presented. A Free and Informed Collective Consent form was presented and signed by leaders, as well as other community representatives. Any village, household, or guardian could decline to participate at any moment.

Results

Information on diarrhea was obtained for 5,828 children (95.1% of the total sample). The seven-day prevalence of reported diarrhea was 23.5%. Regionally, the highest unadjusted prevalence rate was recorded in the North (38.1%), followed by the Central-West (21.2%), Northeast (19.5%), and South/Southeast (17.9%) (Table 1). Only the North region presented a rate (PR 2.12, CI95% 1.56–2.88) which was different from that in the reference region (South/Southeast). Prevalence rates of diarrhea were higher among children 6 to 23 (PR 2.07, CI95% 1.67–2.55) and 24 to 35 months of age (PR 1.43, CI95% 1.16–1.75). Diarrhea was more frequent among children whose mothers had no schooling (PR 1.37, CI95% 1.04–1.80) and 1 to 4 years of schooling (PR 1.41, CI95% 1.16–1.72), as well as those living in households in the lower strata of the household goods index: 1st tertile (PR 1.55, CI95% 1.25–1.93) and 2nd tertile (PR 1.39, CI95% 1.15–1.68).

Table 1 Prevalence rates of reported diarrhea during the previous week among Indigenous children < 5 years of age, with prevalence ratios and confidence intervals, according to sociodemographic (first level) characteristics
Full size table

Breastfeeding was practically universal in the sample, having been reported for 97.5% (CI95% 96.5–98.2) of children < 24 months (results not presented in table). Among children 6 to 23 months, only 34.0% (CI95% 29.6–38.7) were exclusively breastfed during the first six months of life. Among children < 6 months who were reported to have breastfed, 28.1% (CI95% 23.1–33.6) were also fed by bottle. In all regions of the country, the unadjusted frequencies of children < 24 months who had breastfed were over 95%. Whereas in the North region 43.8% (CI95% 37.1–50.9) of children between 6 and 23 months were exclusively breastfed until 6 months of age, this rate was consistently lower in the other regions [28.5% (CI95% 21.6–36.5) in the Central-West, 31.6% (CI95% 23.7–40.8) in the Northeast, and 32.5% (CI95% 24.2–42.1) in the South/Southeast].

Among children 6 to 23 months, the subset of our sample for whom the anti-retrovirus vaccine was made available by the national health system, only 45.2% (CI95% 38.2–52.5) had received both doses, with wide variation between regions, from 22.5% (CI95% 15.0–32.4) in the North to 60.7% (CI95% 50.0–70.5) in the Central-West (results not presented in table). Bivariate analysis of diarrhea according to vaccination status revealed no significant differences between groups. For this reason, this variable was not included in the multivariable model below.

Among children < 5 years with diarrhea, only 55.9% (CI95% 50.9–60.8) were reported to have received oral rehydration therapy, varying from 46.3% (CI95% 36.5–56.3) in the Northeast to 65.1% (CI95% 52.1–76.1) in the Central-West region (results not presented in table).

Table 2 presents unadjusted diarrhea prevalence rates according to household and environmental characteristics. The crude risk of diarrhea was higher among children living in houses with wood (PR 1.51, CI95% 1.21–1.89) and dirt (PR 1.70, CI95% 1.31–2.20) flooring, walls made of wood (PR 1.62, CI95% 1.27–2.06) and thatch or clay (PR 1.64, CI95% 1.30–2.06), and roofing made of concrete or corrugated zinc/asbestos sheets (PR 1.42, CI95% 1.15–1.74). It was also observed that diarrhea was less frequent among children in houses with canvas, plastic, or other roofing (PR 0.76, CI95% 0.57–0.99). Children living in larger households, both those with 5 to 8 (PR 1.18, CI95% 1.03–1.37) and ≥ 9 residents (PR 1.60, CI95% 1.38–1.87), and with more resident children < 5 years of age, including 2 to 3 (PR 1.26, CI95% 1.12–1.43), and ≥ 4 (PR 1.73, 1.37–2.17) children, also presented greater risk of diarrhea. Sanitation conditions such as absence of a faucet in the house, non-availability of filtered drinking water, and less adequate treatment of human and household waste were shown to increase occurrence of diarrhea (PR and CI95% are shown in Table 2).

Table 2 Prevalence rates of reported diarrhea during the previous week among Indigenous children < 5 years of age, with prevalence ratios and confidence intervals, according to household and environmental (second level) characteristics
Full size table

As shown in Table 3, whereas mother parity was not associated with occurrence of diarrhea, children of mothers < 20 years of age presented higher crude risk of diarrhea (PR 1.50, CI95% 1.15–1.95).

Table 3 Prevalence rates of reported diarrhea during the previous week among Indigenous children < 5 years of age, with prevalence ratios and confidence intervals, according to maternal (third level) characteristics
Full size table

Children born in villages presented higher risk of diarrhea (PR 1.58, CI95% 1.37–1.82) than those born at hospitals and other health facilities (Table 4). No association was observed for birthweight. Also more likely to present diarrhea were children with weight-for-age z-score < −1 (PR 1.56, CI95% 1.35–1.81), weight-for-height z-score < −1 (PR 1.44, CI95% 1.17–1.77), and height-for-age z-scores < 0 and ≥ −1 (PR 1.24, CI95% 1.01–1.53) and < −1 (PR 1.46, CI95% 1.20–1.78).

Table 4 Prevalence rates of reported diarrhea during the previous week among Indigenous children < 5 years of age, with prevalence ratios and confidence intervals, according to child’s health and nutritional (forth level) characteristics
Full size table

Several variables related to child health status were shown to be associated with diarrhea, including hospitalization due to diarrhea (PR 1.21, CI95% 1.00–1.46) or to any other cause (PR 1.20, CI95% 1.05–1.37) in the previous year (Table 5). Also, children with anemia (PR 1.62, CI95% 1.41–1.85), with lower respiratory tract infection in the previous week (PR 2.01, CI95% 1.74–2.38), and living with another child with diarrhea (PR 2.03, CI95% 1.74–2.38) were more likely to present diarrhea.

Table 5 Prevalence rates of reported diarrhea during the previous week among Indigenous children < 5 years of age, with prevalence ratios and confidence intervals, according to proximal child health (fifth level) characteristics
Full size table

In the multivariable hierarchical analysis, variables from all levels remained associated with the occurrence of diarrhea in the final model: region, child’s age, household goods index, maternal schooling, number of household residents, maternal age, weight-for-age deficit, presence of another child with diarrhea in the household, and occurrence of upper respiratory infections (Figure 1).

Figure 1
figure1

Hierarchical model for diarrhea among children < 5 years of age, First National Survey of Indigenous People’s Health and Nutrition, Brazil, 2008–2009. Values represent adjusted prevalence ratios with confidence intervals in parentheses. Geopolitical region was included as a control at all levels.

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Discussion

In 2006, the prevalence of diarrhea among Brazilian children < 5 years, as reported by caregivers for a 15-day recall period, was 9.4% [24]. Contrasting this figure with the seven-day prevalence of the present study highlights the importance of diarrhea in the health profiles of Indigenous peoples in Brazil. According to results of the First National Survey of Indigenous People’s Health and Nutrition, almost a quarter of Indigenous children throughout the country had diarrhea during the previous week. This rate reached 38.1% in the North region. The degree of health inequity between Indigenous and non-Indigenous children is even more apparent when viewed diachronically. The prevalence of diarrhea among Indigenous children in 2008–2009 was still vastly higher than it was for the national population over a decade before (14.8% in 1996) [8]. In addition to this elevated frequency, analyses show that a wide range of demographic, socioeconomic, and heath variables were associated with the occurrence of diarrhea among Indigenous children.

The most vulnerable age group with respect to diarrhea was children between 6 and 23 months, who presented 101% greater chance of having had diarrhea during the previous week than infants < 6 months. This chance fell to 40% in the group of children between 24 and 35 months. The relatively lower chance of diarrhea among children < 6 months may be closely related to the protective effect of breastfeeding for infectious diseases in general and diarrhea in particular [25]. In culturally differentiated populations, such as Indigenous peoples, breastfeeding practices may differ from the national populations to which they pertain.

There are no epidemiological or systematic anthropological studies of breastfeeding practices among the Indigenous peoples of Brazil. However, among the diverse ethnographic accounts of these societies are indications that the practice is ubiquitous [26-28], which supports the National Survey results reported here. Nevertheless, although the practice appears to be nearly universal, several of its specificities as reported in the literature should be considered. Among these are observations that breastfeeding in many Indigenous societies in Brazil does not necessarily follow international health agency recommendations, including exclusive breastfeeding during the first six months of life, to reduce risk of disease and death due to diarrhea [25]. Many reports suggest that Indigenous children in Brazil may, during the first months of life, when they are also breastfeeding, receive solid foods, often premasticated, such as nuts, roasted corn, and pieces of meat, fruit, or bread. Among the Xavante, for example, Maybury-Lewis [29] noted that crying infants “…may be fed slops from the mouth of one of the women present. Grandmothers are particularly fond of feeding their tiny grandchildren in this way…” (p. 67). Similarly, Crocker [30] reported that among the Canela, “…depending on a mother’s attitude, she feeds her [2 to 4 month] baby mashes of foods, such as bananas, manioc, sweet potatoes, rice, and even brown sugar” (p. 158). Murphy and Murphy [31] observed similar baby feeding behavior among the Munduruku: “After the age of about four months, the child is fed gruels of tapioca and yam and somewhat later he is given meat, premasticated by the mother” (p. 194). The very act of breastfeeding also may be distinctive, since among many ethnic groups children may be breastfed by other lactating women in the family, such as their aunts and grandmothers [29,30].

Another practice that substantially interferes in child feeding is the use of bottles. The National Survey showed bottle feeding to be frequent and to occur early. Among Indigenous children < 6 months, 29.9% were bottle fed independently of whether or not they also breastfed at the same time. This finding is worrying since it occurs precisely during the most critical period of life – the first six months, when exclusive breastfeeding is indicated. The National Survey results do not permit identification of the liquids they receive by bottle, whether cow’s milk, baby formula, juice, or plain water. However, from the point of diarrhea transmission, administrating other foods during this critical phase of life not only compromises the child’s nutritional status and immune system development, but also favors the transmission of infectious agents by means of contaminated foods or liquids [32,33].

Diverse socioeconomic factors may be associated with risk of disease and death from diarrhea. In the case of the National Survey, maternal education and socioeconomic status remained statistically significant in the multivariable model, which finds ample support in several studies in Brazil and other countries showing these to be indicators of material resources availability and child care knowledge, especially with regard to diarrhea [34-37].

The results of the National Survey show a significant inverse association between the occurrence of diarrhea and maternal age, indicating a protective effect, particularly from the age of 40. Similar findings, widely reported in epidemiological studies in Brazil and elsewhere, are interpreted as reflecting the greater experience of older women in child care [38,39].

With respect to socioeconomic status, it is notable that diverse variables indicative of sanitation conditions and widely recognized as important in diarrhea control [36,40-43] were associated in the descriptive analyses with the occurrence of the disease among Indigenous children but were not retained in the final multivariable model. For example, children in households with a faucet, a toilet connected to a sewage system, drinking water that was filtered or derived from a public supply, or garbage collection service, were showed significantly less likely to have diarrhea. These variables were excluded from the model because they are highly correlated with the household goods socioeconomic index. Therefore, after controlling for socioeconomic condition, no association was observed for sanitation variables.

Undernutrition is among the most important health challenges for Indigenous children in Brazil, as amply demonstrated in several recent studies of specific communities and ethnic groups, as well as by the National Survey [20,44-49]. In the present study, results indicate that children with low weight-for-age showed over 20% higher risk of having diarrhea in the previous week. This finding is consistent with other research in which diarrhea figures among the infectious diseases that most affect growth and development of children < 5 years [50].

The interaction between diarrhea and undernutrition also severely compromises child immune functions, not only favoring the occurrence of new episodes of the illness, but also contributing to increased risk of other infectious diseases, such as pneumonia [50,51]. According to the National Survey, the risk of an Indigenous child having diarrhea in the previous week was 60% higher if he or she was also reported to have had pneumonia. There are several pathways that may explain the amplification of risks arising from the interaction between undernutrition, diarrhea, and acute respiratory disease. For example, a child may start with diarrhea and evolve towards acute malnutrition, finally contracting pneumonia, or, conversely, begin with a respiratory infection that worsens with an acute episode of diarrhea [51-55]. Whether occurring simultaneously (i.e., comorbidity) or as sequential infections, the interaction between diarrhea and pneumonia, aggravated by malnutrition, seriously endangers the lives of young children and contributes to the maintenance of high infant mortality rates in regions of the world marked by poverty, lack of access to basic public services, and food insecurity.

Another important aspect of diarrhea determination among Indigenous children was the association with number of household residents. Indigenous children living in households with ≥ 9 residents had 27% higher risk of contracting diarrhea than those in households with ≤ 4 inhabitants. At the same time, the risk of a child having diarrhea during the previous week increased 66% if another child in the house was also reported to have the disease during the same period. Although there is no consensus in the literature regarding the association between households with large numbers of inhabitants (overcrowding) and increased risk of diarrhea and pneumonia in children under five years, there is strong evidence pointing in this direction based on studies conducted in different context [56-58]. This potential association may derive from cosleeping practices among Indigenous peoples, which often differ from larger national populations.

Among the Bororo and Terena of Central Brazil, for example, practically all children < 2 years and about 80% of those under 10 cosleep with other family members [59,60]. According to Cohen [61], among the Kayapó-Xikrín, “…in an ideal arrangement, a toddler sleeps with her mother, while her brothers up to about 10 years sleep with their grandparents; older children sleep alone” (p. 69). Although it is not possible to generalize about the internal organization of Indigenous households nationally, child cosleeping is widespread. The anthropological literature on Indigenous peoples in Brazil is replete with references to houses lacking internal divisions and children sleeping together and with adults on the same bed or mat, as well as sharing hammocks [62,63]. Sleeping together in the same room or sharing the sleeping surface is an important cultural practice among numerous ethnic groups and is consistent with the associations observed in this study between number of residents and diarrhea risk. This point is based on the idea that pathogenic microorganisms are more easily transmitted to others in the same house, especially children, if living in close proximity to one another and under conditions of poor ventilation, dampness, and precarious sanitation installations.

In Brazil, diarrhea prevention and care for children are available through the public primary healthcare network and involve administration of anti-rotavirus vaccine and dispensation of oral rehydration therapy. Because the rotavirus vaccine was first made available through the Brazilian public health system in 2006, only children < 24 months in our sample were expected to have received the vaccine. In the age group 6 to 24 months, only 37.8% of Indigenous children nationally had received two doses of the vaccine. In the North, this proportion fell to 21.6%. The National Survey data show that at the time of fieldwork the proportion of Indigenous children who had received two doses of vaccine, as prescribed by the Health Ministry, was low and no protective effect was observed. Considering the importance of rotavirus in the determination of diarrhea among Indigenous children in Brazil [64-66] and positive evaluations of the vaccine reducing the incidence of diarrhea in the general Brazilian population [67,68], additional studies are necessary to evaluate its impact on diarrhea morbidity and mortality among Indigenous children.

The Brazilian Health Ministry adopted oral rehydration therapy for diarrhea management in 1982. Since then, its availability through the public health system has been a major factor responsible for the continued decline in infant mortality observed in recent decades [5,69]. The National Survey revealed that among Indigenous children reported as having had diarrhea in the previous week, 55.1% made use of oral rehydration therapy, whether homemade or industrialized. In the Northeast region, the frequency of use of oral rehydration therapy was lower (48.6%) than in the rest of the country, despite being the region in which Indigenous mothers had the highest number of years of schooling [10].

This study does not explain the low use of oral rehydration therapy in the management of diarrhea among Indigenous children. In addition to known deficiencies in healthcare services available to the Indigenous population in Brazil, including low coverage and quality [9,10,70], the potential influence of sociocultural factors in child diarrhea treatment also require attention. As described in several anthropological studies, the therapeutic program for any disease usually starts in the home and directly depends on interpretation of severity by family members, based on the patient’s exhibited signs and symptoms. The choice to initiate a child’s diarrhea treatment with homemade remedies or to seek rehydration salts through local health services depends on multiple factors, the analysis of which is beyond the scope of this study but certainly deserves to be investigated further [71-75].

This study has potential limitations that should be discussed. Analyses were based on data obtained through interviews with mothers, fathers, or other caregivers of Indigenous children under five years. Therefore, responses may have been influenced by local concepts and perceptions about diarrhea signs and symptoms, which vary among the country’s diverse ethnic groups [73,75,76]. Additionally, some non-parent relatives and other respondents may have lacked direct knowledge of information requested in interview questions. Although recall bias may have influenced responses, methodological studies have shown the quality of information on child diarrhea occurrence reported for a seven-day recall period to be adequate [19,77,78]. Also, the study design included only Indigenous peoples residing in federally recognized Indigenous reserves. This limitation deserves special note because many Indigenous peoples not contemplated, such as those living along roadsides, in makeshift camps, and in urban outskirts and slums, may live under even more precarious sanitation conditions. Finally, the cross-sectional design of this study does not allow conclusions about causality.

Conclusion

The National Survey results reported here demonstrate that diarrhea weighs heavily in the epidemiology of Indigenous children in Brazil and highlight the magnitude of health inequity that persists in the country. The numerous variables found to be involved in the epidemiology of diarrhea reinforce the marginal position of this population segment within the national setting and reveal the broad linkages between social inequities deriving from a long history of political, social, and economic neglect, as well as impeded access to the marked infrastructural, health, socioeconomic, and educational improvements observed nationally in recent decades. These advances, coupled with expansion of the public healthcare network, have been widely recognized as responsible for the significant reductions in infectious and parasitic diseases, chronic malnutrition, and infant mortality observed among children nationally [6,7,34]. It should also be emphasized that improvements in basic sanitation and availability of safe drinking water in Indigenous villages, as well as the training of health workers are of fundamental importance in reducing the prevalence of diarrhea among Indigenous children in Brazil. Due to its exceedingly multicausal nature, the set of associated variables that remained associated with child diarrhea in the final multivariable model provide an excellent reflection of the diverse social and health inequities faced by Indigenous peoples in contemporary Brazil.

Abbreviations

ABRASCO:

Associação Brasileira de Saúde Coletiva

CONEP:

Comissão Nacional de Ética em Pesquisa

CI:

Confidence interval

PR:

Prevalence ratio

FUNAI:

Fundação Nacional do Índio

FUNASA:

Fundação Nacional de Saúde

References

  1. 1.

    Boschi-Pinto C, Lanata CF, Black RE. The Global Burden of Childhood Diarrhea. In: Ehriri J, editor. Maternal and Child Health: Global Challenges, Programs, and Policies. New York: Springer; 2009. p. 225–44.

    Chapter  Google Scholar 

  2. 2.

    Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet. 2012;379:2151–61.

    Article  PubMed  Google Scholar 

  3. 3.

    The United Nations Children’s Fund (UNICEF) and World Health Organization (WHO). Diarrhoea: Why Children are Still Dying and What Can be Done. New York and Geneve: UNICEF and WHO Press; 2009.

    Google Scholar 

  4. 4.

    Rasella D, Aquino R, Barreto ML. Reducing childhood mortality from diarrhea and lower respiratory tract infections in Brazil. Pediatrics. 2010;126:e534–40.

    Article  PubMed  Google Scholar 

  5. 5.

    Victora CG. Diarrhea mortality: what can the world learn from Brazil? J Pediatr (Rio J). 2009;85:3–5.

    Google Scholar 

  6. 6.

    Barreto ML, Teixeira MG, Bastos FI, Ximenes RAA, Barata RB, Rodrigues LC. Successes and failures in the control of infectious diseases in Brazil: social and environmental context, policies, interventions, and research needs. Lancet. 2011;377:1877–89.

    Article  PubMed  Google Scholar 

  7. 7.

    Barros FC, Matijasevich A, Requejo JH, Giugliani E, Maranhão AG, Monteiro CA, et al. Recent trends in maternal, newborn, and child health in Brazil: Progress toward Millennium Development Goals 4 and 5. Am J Public Health. 2010;100:1877–89.

    Article  PubMed  PubMed Central  Google Scholar 

  8. 8.

    Sastry N, Burgard S. The prevalence of diarrheal disease among Brazilian children: Trends and differentials from 1986 to 1996. Soc Sci Med. 2005;60:923–5.

    Article  PubMed  Google Scholar 

  9. 9.

    Garnelo L, Macedo G, Brandão LC. Os Povos Indígenas e a Construção das Políticas de Saúde no Brasil. Brasília: Organização Pan-Americana de Saúde; 2003.

    Google Scholar 

  10. 10.

    Coimbra Jr CEA, Cardoso AM, Welch JR, Souza MC, Rassi E, Follér M-L, et al. The First National Survey of Indigenous People’s Health and Nutrition in Brazil: Rationale, methodology, and overview of results. BMC Public Health. 2013;13:52.

    Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Pena JL, Heller L. Saneamento e saúde indígena: uma avaliação na população Xakriabá, Minas Gerais. Engenharia Sanitária e Ambiental. 2008;13:63–72.

    Google Scholar 

  12. 12.

    Escobar AL, Rodrigues AF, Alves CLM, Orellana JDY, Santos RV, Coimbra Jr CEA. Causas de internação hospitalar indígena em Rondônia. O Distrito Sanitário Especial Indígena Porto Velho (1998–2001). In: Coimbra Jr CEA, Santos RV, Escobar AL, editors. Epidemiologia e Saúde dos Povos Indígenas no Brasil. Rio de Janeiro: Editora Fiocruz; 2003. p. 127–47.

    Google Scholar 

  13. 13.

    Lunardi R, Santos RV, Coimbra Jr CEA. Morbidade hospitalar de indígenas Xavante, Mato Grosso, Brasil (2000–2002). Rev Brasil Epidemiol. 2007;10:441–52.

    Article  Google Scholar 

  14. 14.

    Orellana JDY, Basta PC, Santos RV, Coimbra Jr CEA. Morbidade hospitalar em crianças indígenas Suruí menores de dez anos, Rondônia, Brasil: 2000 a 2004. Revista Brasileira de Saúde Materno Infantil. 2007;7:281–7.

    Article  Google Scholar 

  15. 15.

    Cardoso AM, Coimbra Jr CEA, Tavares FG. Morbidade hospitalar indígena Guarani no Sul e Sudeste do Brasil. Rev Brasil Epidemiol. 2010;13:21–34.

    Article  Google Scholar 

  16. 16.

    Brenneman GR, Handler AO, Kaufman SF, Rhoades ER. Health status and clinical indicators. In: Rhoades ER, editor. American Indian Health: Health Care, Promotion, and Policy. Baltimore: Johns Hopkins University Press; 2000. p. 103–21.

    Google Scholar 

  17. 17.

    Carson B, Dunbar T, Chenhall RD, Bailie R. Social Determinants of Indigenous Health. Crows Nest: Allen & Unwin; 2007.

    Google Scholar 

  18. 18.

    Waldram JB, Herring DA, Young TK. Aboriginal Health in Canada: Historical, Cultural, and Epidemiological Perspectives. 2nd ed. Toronto: University of Toronto Press; 2006.

    Google Scholar 

  19. 19.

    Schmidt W-P, Arnold BF, Boisson S, Genser B, Luby SP, Barreto ML, et al. Epidemiological methods in diarrhoea studies. An update. Int J Epidemiol. 2011;40:1678–92.

    Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Horta BL, Santos RV, Welch JR, Cardoso AM, Santos JV, Assis AMO, et al. Nutritional status of indigenous children < 5 years of age: Findings from the First National Survey of the Health and Nutrition of Indigenous Peoples in Brazil. Int J Equity Health. 2013;12:23.

    Article  PubMed  PubMed Central  Google Scholar 

  21. 21.

    Leite MS, Cardoso AM, Coimbra Jr CEA, Welch JR, Gugelmin SA, Lira PC, et al. Prevalence of anemia and associated factors among Indigenous children in Brazil: Results from the First National Survey of Indigenous People’s Health and Nutrition. Nutr J. 2013;12:69.

    Article  PubMed  PubMed Central  Google Scholar 

  22. 22.

    Victora CG, Huttly SR, Fuchs SC, Olinto MTA. The role of conceptual frameworks in epidemiological analysis: A hierarchical approach. Int J Epidemiol. 1997;26:224–7.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Barros AJ, Hirakata V. Alternatives for logistic regression in cross-sectional studies: An empirical comparison of models that directly estimate the prevalence ratio. BMC Med Res Methodol. 2003;3:21.

    Article  PubMed  PubMed Central  Google Scholar 

  24. 24.

    Cunha EMGP, Barison EM. Saúde das crianças. In: Ministério da Saúde, editor. Pesquisa Nacional de Demografia e Saúde da Criança e da Mulher – PNDS 2006: Dimensões do Processo Reprodutivo e da Saúde da Criança. Brasília: Ministério da Saúde; 2009. p. 171–94.

    Google Scholar 

  25. 25.

    Lamberti LM, Fischer Walker CL, Noiman A, Victora CG, Black RE. Breastfeeding and the risk for diarrhea morbidity and mortality. BMC Public Health. 2011;11 Suppl 3:15.

    Article  Google Scholar 

  26. 26.

    Rissardo LK, Moliterno ACM, Borghi AC, Carreira L. Práticas de cuidado ao recém-nascido: Percepção de famílias Kaingang. Ciência, Cuidado e Saúde. 2011;10:634–41.

    Google Scholar 

  27. 27.

    Mattos A, Morais MB, Rodrigues DA, Baruzzi RG. Nutritional status and dietary habits of Indian children from Alto Xingu (Central Brazil) according to age. J Am Coll Nutr. 1999;18:88–94.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Cohn C. Crescendo como um Xikrin: Uma análise da infância e do desenvolvimento infantil entre os Kayapó-Xikrin do Bacajá. Revista de Antropologia (São Paulo). 2000;43:195–222.

    Google Scholar 

  29. 29.

    Maybury-Lewis D. Akwê-Shavante Society. Oxford: Claredon Press; 1967.

    Google Scholar 

  30. 30.

    Crocker WH. The Canela (Eastern Timbira), I: An Ethnographic Introduction. Washington, D.C.: Smithonian Institution Press; 1990.

    Google Scholar 

  31. 31.

    Murphy Y, Murphy R. Women of the Forest. 30 Anniversary Editionth ed. New York: Columbia University Press; 2004.

    Google Scholar 

  32. 32.

    Victora CG, Smith PG, Vaughan JP, Nobre LC, Lombardi C, Teixeira AMB, et al. Infant feeding and deaths due to diarrhea: A case–control study. Am J Epidemiol. 1989;129:1032–41.

    CAS  PubMed  Google Scholar 

  33. 33.

    Popkin BM, Adair L, Akin JS, Black R, Briscoe J, Flieger W. Breast-feeding and diarrheal morbidity. Pediatrics. 1990;86:874–82.

    CAS  PubMed  Google Scholar 

  34. 34.

    Victora CG, Adair L, Fall C, Hallal PC, Martorell R, Richter L, et al. Maternal and child undernutrition: Consequences for adult health and human capital. Lancet. 2008;371:340–57.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Brockerhoff M, Hewett P. Inequality of child mortality among ethnic groups in sub-Saharan Africa. Bull World Health Organ. 2000;78:30–41.

    CAS  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Mihrete TS, Alemie GA, Teferra AS. Determinants of childhood diarrhea among underfive children in Benishangul Gumuz Regional State, North West Ethiopia. BMC Pediatr. 2014;14:102.

    Article  Google Scholar 

  37. 37.

    Desai S, Alva S. Maternal education and child health: Is there a strong causal relationship? Demography. 1998;35:71–81.

    CAS  Article  PubMed  Google Scholar 

  38. 38.

    Mock NB, Sellers TA, Abdoh AA, Franklin RR. Socioeconomic, environmental, demographic and behavioral factors associated with occurrence of diarrhea in young children in the Republic of Congo. Soc Sci Med. 1993;36:807–16.

    CAS  Article  PubMed  Google Scholar 

  39. 39.

    Finlay JE, Ozaltin E, Canning D. The association of maternal age with infant mortality, child anthropometric failure, diarrhoea and anaemia for first births: evidence from 55 low- and middle-income countries. BMJ Open. 2011;1:e000226.

    Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Fewtrell L, Kaufmann RB, Kay D, Enanoria W, Haller L, Colford Jr JM. Water, sanitation, and hygiene interventions to reduce diarrhoea in less developed countries: A systematic review and meta-analysis. Lancet Infect Dis. 2005;5:42–52.

    Article  PubMed  Google Scholar 

  41. 41.

    Barreto ML, Genser B, Strina A, Teixeira MG, Assis AMO, Rego RF, et al. Effect of city-wide sanitation programme on reduction in rate of childhood diarrhoea in northeast Brazil: Assessment by two cohort studies. Lancet. 2007;370:1622–8.

    Article  PubMed  PubMed Central  Google Scholar 

  42. 42.

    Daniels D, Cousens S, Makoae L. A case–control study of the impact of improved sanitation on diarrhea morbidity in Lesotho. Bull World Health Organ. 1990;68:455–63.

    CAS  PubMed  PubMed Central  Google Scholar 

  43. 43.

    Checkley W, Gilman RH, Black RE, Epstein LD, Cabrera L, Sterling CR, et al. Effect of water and sanitation on childhood health in a poor Peruvian peri-urban community. Lancet. 2004;363:112–8.

    Article  PubMed  Google Scholar 

  44. 44.

    Ferreira AA, Welch JR, Santos RV, Gugelmin SA, Coimbra Jr CEA. Nutritional status and growth of indigenous Xavante children, Central Brazil. Nutr J. 2012;11:3.

    Article  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Orellana JDY, Coimbra Jr CEA, Lourenço AEP, Santos RV. Estado nutricional e anemia em crianças Suruí, Amazônia. Brasil J Pediatr (Rio J). 2006;82:383–8.

    Article  Google Scholar 

  46. 46.

    Escobar AL, Santos RV, Coimbra Jr CEA. Avaliação nutricional de crianças indígenas Pakaánova (Wari’), Rondônia, Brasil. Revista Brasileira de Saúde Materno Infantil. 2003;3:457–61.

    Article  Google Scholar 

  47. 47.

    Barreto CTG, Cardoso AM, Coimbra Jr CEA. Estado nutricional de crianças indígenas Guarani nos estados do Rio de Janeiro e São Paulo, Brasil. Cad Saude Publica. 2014;30:657–62.

    Article  PubMed  Google Scholar 

  48. 48.

    Menegolla IA, Drachler ML, Rodrigues IH, Schwingel LR, Scapinello E, Pedroso MB, et al. Estado nutricional e fatores associados à estatura de crianças da Terra Indígena Guarita, Sul do Brasil. Cad Saude Publica. 2006;22:395–406.

    Article  PubMed  Google Scholar 

  49. 49.

    Morais MB, Fagundes-Neto U, Mattos AP, Baruzzi RG. Estado nutricional de crianças índias do Alto Xingu em 1980 e 1992 e evolução pondero-estatural entre o primeiro e o quarto anos de vida. Cad Saude Publica. 2003;19:543–50.

    Article  PubMed  Google Scholar 

  50. 50.

    Black RE, Walker CLF, Lanata CF. Diarrheal disease. In: Nelson KE, Williams CM, editors. Infectious Disease Epidemiology: Theory and Practice. 3rd ed. Burlington, MA: Jones & Bartlett Learning; 2014. p. 613–34.

    Google Scholar 

  51. 51.

    Baqui AH, Black RE, Sack RB, Chowdhury HR, Yunus M, Siddique AK. Malnutrition, cell-mediated immune deficiency, and diarrhea: A community-based longitudinal study in rural Bangladeshi children. Am J Epidemiol. 1993;137:355–65.

    CAS  PubMed  Google Scholar 

  52. 52.

    Ashraf S, Huque MH, Kenah E, Agboatwalla M, Luby SP. Effect of recent diarrhoeal episodes on risk of pneumonia in children under the age of 5 years in Karachi, Pakistan. Int J Epidemiol. 2013;42:194–200.

    Article  PubMed  PubMed Central  Google Scholar 

  53. 53.

    Schmidt W-P, Cairncross S, Barreto ML, Clasen T, Genser B. Recent diarrhoeal illness and risk of lower respiratory infections in children under the age of 5 years. Int J Epidemiol. 2009;38:766–72.

    Article  PubMed  PubMed Central  Google Scholar 

  54. 54.

    Fischer Walker CL, Perin J, Liu JL, Katz J, Tielsch JM, Black R. Does comorbidity increase the risk of mortality among children under 3 years of age? BMJ Open. 2013;3:e003457.

    Article  PubMed  PubMed Central  Google Scholar 

  55. 55.

    Coles CL, Fraser D, Givon-Lavi N, Greenberg D, Gorodischer R, Bar-Ziv J, et al. Nutritional status and diarrheal illness as independent risk factors for alveolar pneumonia. Am J Epidemiol. 2005;162:999–1007.

    Article  PubMed  Google Scholar 

  56. 56.

    Ngale KMA, Santos IS, González-Chica DA, Barros AJD, Matijasevich A. Bed-sharing and risk of hospitalisation due to pneumonia and diarrhoea in infancy: the 2004 Pelotas Birth Cohort. J Epidemiol Comm Health. 2004;2013(67):245–9.

    Google Scholar 

  57. 57.

    Cardoso MRA, Cousens SN, Siqueira LFG, Alves FM, D’Angelo LAV. Crowding: Risk factor or protective factor for lower respiratory disease in young children? BMC Public Health. 2004;4:19.

    Article  PubMed  PubMed Central  Google Scholar 

  58. 58.

    Blake PA, Ramos S, MacDonald KL, Rassi V, Gomes TAT, Ivey C, et al. Pathogen-specific risk factors and protective factors for acute diarrheal disease in urban Brazilian infants. J Infect Dis. 1993;167:627–32.

    CAS  Article  PubMed  Google Scholar 

  59. 59.

    Reimão R, Souza JCRP, Gaudioso CEV. Sleep habits in native Brazilian Bororo children. Arq Neuropsiquiatr. 1999;57:14–7.

    Article  PubMed  Google Scholar 

  60. 60.

    Reimão R, Souza JCRP, Medeiros MM, Almirão RI. Sleep habits in native Brazilian Terena children in the state of Mato Grosso do Sul, Brazil. Arq Neuropsiquiatria. 1998;56:703–7.

    Article  Google Scholar 

  61. 61.

    Cohn C. A Criança Indígena: A Concepção Xikrin de Infância e Aprendizado. M.A. Thesis (Anthropology). São Paulo: Universidade de São Paulo; 2000.

    Google Scholar 

  62. 62.

    Novaes SC, editor. Habitações Indígenas. São Paulo: Livraria Nobel e Editora da Universidade de São Paulo; 1986.

    Google Scholar 

  63. 63.

    Costa MHF, Malhano HB. Habitação indígena brasileira. In: Ribeiro BG, editor. Suma Etnológica Brasileira 2: Tecnologia Indígena. Petrópolis: Vozes; 1986. p. 27–108.

    Google Scholar 

  64. 64.

    Linhares AC, Pinheiro FP, Freitas RB, Gabbay YB, Shirley JA, Beards GM. An outbreak of rotavirus diarrhea among a nonimmune, isolated South American Indian community. Am J Epidemiol. 1981;113:703–10.

    CAS  PubMed  Google Scholar 

  65. 65.

    Linhares AC, Salbé EV, Gabbay YB, Rees N. Prevalence of rotavirus antibody among isolated South American Indian communities. Am J Epidemiol. 1986;123:699–709.

    CAS  PubMed  Google Scholar 

  66. 66.

    Santos RV, Linhares AC, Coimbra Jr CEA. Estudos epidemiológicos entre grupos indígenas de Rondônia. IV. Inquérito sorológico para rotavírus entre os Suruí e Karitiána. Rev Saude Publica. 1991;25:230–2.

    CAS  PubMed  Google Scholar 

  67. 67.

    Carmo GMI, Yen C, Cortes J, Siqueira AA, Oliveira WK, Cortez-Escalante JJ, et al. Decline in diarrhea mortality and admissions after routine childhood rotavirus immunization in Brazil: A time-series analysis. PLoS Med. 2011;8:e1001024.

    Article  PubMed  PubMed Central  Google Scholar 

  68. 68.

    Lanzieria TM, Linhares AC, Costa I, Kolhed DA, Cunha MH, Ortega-Barria E, et al. Impact of rotavirus vaccination on childhood deaths from diarrhea in Brazil. Int J Infec Dis. 2011;15:e206–10.

    Article  Google Scholar 

  69. 69.

    Sastry N, Burgard S. Changes in diarrheal disease and treatment among Brazilian children from 1986 to 1996. Pop Res Policy Rev. 2011;30:81–100.

    Article  Google Scholar 

  70. 70.

    Coimbra Jr CEA, Santos RV. Emerging health needs and epidemiological research in indigenous peoples in Brazil. In: Salzano FM, Hurtado AM, editors. Lost Paradises and the Ethics of Research and Publication. Oxford: Oxford University Press; 2004. p. 89–109.

    Google Scholar 

  71. 71.

    Mwabu GM. Health care decisions at the household level: Results of a rural health survey in Kenya. Soc Sci Med. 1986;22:315–9.

    CAS  Article  PubMed  Google Scholar 

  72. 72.

    Nations MK, Rebhun LA. Mystification of a simple solution: Oral rehydration therapy in Northeast Brazil. Soc Sci Med. 1988;27:25–38.

    CAS  Article  PubMed  Google Scholar 

  73. 73.

    Pereira PPG. Variations around water: Bodies, encounters and translation processes. Vibrant: Virtual Brazilian Anthropology. 2012;9:154–80.

    Google Scholar 

  74. 74.

    Haverroth M. O Contexto Cultural das Doenças Diarréicas entre os Wari’, Estado de Rondônia, Brasil: Interfaces entre Antropologia e Saúde Pública. Ph.D. Dissertation (Public Health). Rio de Janeiro: Fundação Oswaldo Cruz; 2004.

    Google Scholar 

  75. 75.

    Yoder PS. Examining ethnomedical diagnoses and treatment choices for diarrheal disorders in Lubumbashi Swahili. Med Anthropol. 1994;16:211–47.

    Article  Google Scholar 

  76. 76.

    Garnelo L, Wright R. Doença, cura e serviços de saúde: Representações, práticas e demandas Baníwa. Cad Saude Publica. 2001;17:273–84.

    CAS  Article  PubMed  Google Scholar 

  77. 77.

    Lee G, Cama V, Gilman RH, Cabrera L, Saito M, Checkley W. Comparison of two types of epidemiological surveys aimed at collecting daily clinical symptoms in community-based longitudinal studies. Ann Epidemiol. 2010;20:151–8.

    Article  PubMed  PubMed Central  Google Scholar 

  78. 78.

    Byass P, Hanlon P. Daily morbidity records: Recall and reliability. Int J Epidemiol. 1994;23:757–63.

    CAS  Article  PubMed  Google Scholar 

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Acknowledgements

The Brazilian Ministry of Health and the World Bank provided financial support through the Vigisus II project. Support and assistance were offered by Indigenous leaders and community members in all of the villages surveyed, the project’s team members and research assistants, and the staff at local Fundação Nacional de Saúde (FUNASA) and Fundação Nacional do Índio (FUNAI) offices.

Author information

Affiliations

  1. Departamento de Medicina, Universidade Federal de Rondônia, Rodovia BR-364 Km 9.5, Porto Velho, RO, 76801-059, Brazil

    Ana Lúcia Escobar

  2. Escola Nacional de Saúde Pública, Fundação Oswaldo Cruz, Rua Leopoldo Bulhões 1480, Rio de Janeiro, RJ, 21041-210, Brazil

    Carlos EA Coimbra Jr, James R Welch, Ricardo Ventura Santos & Andrey M Cardoso

  3. Programa de Pós-Graduação em Epidemiologia, Universidade Federal de Pelotas, Rua Marechal Deodoro 1160, Pelotas, RS, 96020-220, Brazil

    Bernardo L Horta

  4. Departamento de Antropologia, Museu Nacional, Universidade Federal do Rio de Janeiro, Quinta da Boa Vista s/n, Rio de Janeiro, RJ, 20940-040, Brazil

    Ricardo Ventura Santos

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  1. Ana Lúcia Escobar
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  2. Carlos EA Coimbra Jr
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  3. James R Welch
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  4. Bernardo L Horta
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Correspondence to Carlos EA Coimbra Jr.

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The authors declare that they have no competing interests.

Authors’ contributions

ALE, CEAC, JRW, BLH, RVS, and AMC participated in the conception of the study and data collection. ALE and RVS performed data analysis. ALE, CEAC, JRW, and RVS drafted the paper. All authors participated in data interpretation, manuscript revision, and approved the version submitted for publication.

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Escobar, A.L., Coimbra, C.E., Welch, J.R. et al. Diarrhea and health inequity among Indigenous children in Brazil: results from the First National Survey of Indigenous People’s Health and Nutrition. BMC Public Health 15, 191 (2015). https://doi.org/10.1186/s12889-015-1534-7

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Keywords

  • Brazil
  • Indigenous peoples
  • Health surveys
  • Diarrhea
  • Social determinants
  • Child health

BMC Public Health

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