Abstract
This study aimed to explore the association between water, sanitation, and the prevalence of schistosomiasis mansoni in students aged 7 to 17 years from all 27 federative units in Brazil. It was a cross-sectional study conducted based on data on the prevalence of schistosomiasis mansoni referring to 197,567 students from 521 Brazilian municipalities, who participated in the National Survey on the Prevalence of Schistosomiasis Mansoni and Soil-transmitted Helminth Infections (2011-2015). Univariable and multivariable generalized linear models of the negative binomial type were adjusted using 25 and 5% significance levels, respectively, considering municipalities as the unit of analysis. While a protective association was found between access to filtered water in schools and schistosomiasis mansoni prevalence, sanitation in schools was indicated as a risk factor. The collection of wastewater through a network is not universal in Brazil, and even when present, it is not necessarily carried out by the treatment of collected effluents, thus often resulting in the direct discharge of raw sewage into water resources. Regarding septic tanks, only the presence of infrastructure alone does not guarantee its correct use by the population.
Keywords: Drinking water; Sanitation; Schistosoma mansoni; Brazil
Resumo
O presente trabalho teve como objetivo explorar a associação entre água, saneamento e a prevalência de esquistossomose mansoni em estudantes de 7 a 17 anos de todas as 27 unidades federativas do Brasil. Tratou-se de um estudo transversal, conduzido com base nos dados de prevalência de esquistossomose mansoni referentes a 197.567 estudantes de 521 municípios brasileiros que participaram do Inquérito Nacional da Prevalência de Esquistossomose Mansoni e Geo-helmintoses (2011-2015). Modelos lineares generalizados do tipo binomial negativo, univariável e multivariável foram construídos considerando níveis de significância de 25% e 5%, respectivamente, e os municípios como unidade de análise. Embora os resultados tenham indicado associação protetora entre o acesso à água filtrada nas escolas e a prevalência de esquistossomose mansoni, o acesso ao saneamento nas escolas foi apontado como um fator de risco. A coleta de águas residuais por rede não é universal no Brasil e, mesmo quando presente, não é necessariamente procedida pelo tratamento dos efluentes coletados, resultando, muitas vezes, no lançamento direto do esgoto bruto em matrizes aquosas. Com relação a soluções individuais como fossa sépticas, a presença da infraestrutura por si só não garante o seu uso correto pela população.
Palavras-chave: Água potável; Saneamento; Schistosoma mansoni; Brasil
Introduction
Faced with a dilemma of a country in the midst of a series of illnesses, doctor Miguel Pereira in 1916 declared that “Brazil is an enormous hospital”1. More than a century after his testimony, the country still faces difficulties in changing this reality.
According to data published by the World Health Organization (WHO)2, in 2016, Brazil was the country in Latin America with the highest number of people requiring interventions against Neglected Tropical Diseases (NTDs). It was estimated that in the same year, NTDs accounted for 475,410 Disability Adjusted Life Years (DALYs) in the country, with schistosomiasis being the second-largest contributor3. Still, according to the WHO data4, in 2018, 1,535,838 Brazilians required preventive chemotherapy for schistosomiasis. This last estimate, however, was based on the stipulated number of people at risk of infection and did not take into account national parasitological surveys.
Hitherto, Brazil faced a lack of statistical data showing the real national prevalence of schistosomiasis mansoni. From 1949 to 1978, only two nationwide surveys on the prevalence of schistosomiasis mansoni in school-aged children were conducted in Brazil, and none of them covered all Brazilian Federation Units5. After this period, all the studies conducted in Brazil regarding the prevalence of schistosomiasis mansoni were local studies (community, cities, villages). Bearing that in mind, the first National Survey on the Prevalence of Schistosomiasis mansoni and Soil-transmitted helminth infections (2011-2015) in Brazil was carried out covering all the 27 Brazilian Federation Units5. It was a school-based cross-sectional study with the objective of determining the current prevalence of schistosomiasis mansoni, trichuriasis, hookworm, and ascariasis, in schoolchildren from 7 to 17 years old. It was also intended to verify whether the prevalence of schistosomiasis mansoni in endemic areas was lower than that observed in the two previous surveys. For this purpose, 197,564 school-aged children living in 521 municipalities distributed in all five geographical regions of the country were examined5.
Compared with previous surveys, the results of this research, published in 2018, showed a significant reduction in the schistosomiasis mansoni prevalence. However, high rates of schistosomiasis positive results were still found in the municipalities of the Northeast and Southeast regions of the country5. The improvement of the access to water, sanitation, and hygiene (WASH) that occurred in the last decades in Brazil, was one of the conjectures to explain the new epidemiological profile of the country.
Although studies have already reported the protective effect of access to WASH against schistosomiasis mansoni6-9, the relationship between these determinants and the occurrence of the disease is not entirely clear. The effectiveness of WASH relies on its combination with other factors, such as social, cultural, educational aspects and the particular way in which solutions are designed and implemented.
Therefore, in order to better understand the role that WASH has played in the control of schistosomiasis mansoni infection in the recent decades in Brazil, as indicated by the data of the third National Survey, the present study aimed to assess the existence of association between water, sanitation and the prevalence of schistosomiasis mansoni in schoolchildren from 7 to 17 years old, in the 27 Brazilian Federation Units.
Methods
Study design
The current epidemiological study can be classified as ecological, explanatory, observational, and non-directional (cross-sectional).
Database
Prevalence of schistosomiasis mansion was used as the outcome variable and municipalities as the geographical unit of analysis. Data were retrieved by the National Survey on the Prevalence of Schistosomiasis mansoni and Soil-transmitted helminth infections (2011-2015)5. They are anonymous and available for research purposes by the Brazilian government. Moreover, The National Survey was approved by the Ethics and Research Committee of the René Rachou Research Center - Oswaldo Cruz Foundation and the National Research Ethics Commission - CONEP. Informed consent for participation was obtained from the students’ parents.
The National Survey was a school-based cross-sectional study conducted by the Oswaldo Cruz Foundation (FIOCRUZ) in 521 municipalities distributed in all five regions of the country, with the objective of assessing the current prevalence of schistosomiasis mansoni and STH in schoolchildren aged 7-17 years. Although it was the third national survey of schistosomiasis mansoni carried out in the country, it was the first to cover all Brazilian states. Each municipality was surveyed only once. Details about the survey, including its sample strategy, are presented in Portuguese5 and English language10.
Fifteen explanatory variables were examined, namely: (1) seven main explanatory variables expressing the water and sanitary conditions in households as well as in schools; (2) six confounding variables and; (3) two sampling variables related to the National Survey’s sampling strategy inserted in order to minimize possible sampling bias (Table 1).
Statistical analysis
The Generalized Linear Model (GLM) with the negative binomial distribution was used to evaluate the statistical association between outcome and explanatory variables.
In the univariable statistical analyses, explanatory variables with a significance level (p-value) less or equal to 0.25 were maintained to compose the multivariable model as suggested by Hosmer and Lemeshow11 and Dohoo et al., 200912. Adopting a liberal p-value is recommended to prevent an important predictor from being excluded if its effect is masked by another variable.The stepwise procedure was then implemented to select the possible variables to compose the final model. All selected variables were statistically significant at 5%. In addition, variables that were not significant in the univariable analysis were then introduced into the final model, one by one separately and also together, in order to evaluate if any could add some significant contribution when combined with the variables already selected by the stepwise procedure11. Data were analyzed using the Stata software, version 14 (Stata Corporation, College Station, TX, USA).
The goodness-of-fit analysis of the models was performed using the following statistics: Pearson’s deviance, natural logarithm of the likelihood function (log-likelihood), Akaike (AIC), and Bayesian (BIC) information criteria, the adjusted generalized variance inflation factors (AGVIF) and residuals correlation12,13. Possible outliers were identified by graphical analysis of Pearson residuals from the models and the Cook’s distance criterion12. As suggested in Stata manuals, any point with Cook’s distance greater than 4/n, where n is the number of observations, was examined14. Zero-inflated negative binomial model13 was also fitted to assess the overdispersion induced by the number of zeros in the outcome variable. Logistic distribution was used to adjust for the excess of zero. The statistically significant variables were the same in the inflated and non-inflated models. A comparison of the goodness-of-fit indicated that the non-inflated negative binomial model was preferable.
Results
Database description
The minimum of the prevalence estimates was 0%, reaching a maximum of 50%. The average and the standard deviations were 0.81% and 3.48%, respectively. The estimated prevalence was low in most municipalities as shown by the first, second, and third quartiles (0, 0 and 0.12%, respectively), and also by the high frequency of zero (384 out of 521 municipalities, representing 73.70%).
Most municipalities were small or medium-sized, with 41.65% comprising a population between 20,000 and 150,000 inhabitants, followed by 39.92% below 20,000 inhabitants, 12.09% between 150,000 and 500,000 inhabitants and 6.33% above 500,000 inhabitants. The majority of the municipalities were located in the Northeast region (43.38%) of the country, followed by Southeast (22.27%), North (15.74%), South (10.17%), Midwest (8.25%), and Federal District (0.19%). Regarding the endemic level, 28.60% of the municipalities were in endemic areas (16.32% in low and 12.28 % in high endemic). Approximately half of the sampled municipalities had historical records of the presence of one or more species of the genus Biomphalaria. Descriptive statistics of the other variables can be found in Poague et al.9.
Univariable analysis
The results of the adjusted univariable statistical models are presented in Table 2. Among the water and sanitation variables,”% Population served with adequate water supply at home”, “% Population served with adequate sanitation at home” and “% Schools served with adequate water supply” were not statistically significant at a significance level of 25%.
Multivariable analysis
Table 3 presents the results of the multivariable analysis. The significant explanatory variables (at 5% level) were: “Endemic Level”, “Natural log of Population in 2010”, “Presence of Snail”, “% Schools with filtered water”, “% Schools served with adequate sanitation”, “% Municipality’s urbanization”, “% Population served by primary health care services” and “Municipal Human Development Index: Education Component”. No interaction variable was statistically significant to be included in the model.
The variables “Endemic Level”, “Presence of Snail”, “% Schools served with adequate sanitation”, “% Municipality’s urbanization” and, “% Population served by primary health care services” presented Rate Ratio (RR) values greater than 1. These results indicate that low and high endemic levels and the presence of snails, compared to non-endemic levels and the absence of snails, lead to the increase of the prevalence average of schistosomiasis mansoni. For the continuous variables, these results indicate that the increase of these variables leads to the increase of the prevalence average of schistosomiasis mansoni. The AGVIF values were smaller than 2, indicating no presence of multicollinearity. The residuals were not correlated.
Discussion
The results from the multivariable statistical model suggest that adequate sanitation in schools (sewage disposal into a public sewerage system or septic tank) is related to S. mansoni infections as a risk factor. Particularly in Brazil, the collection of sewage does not necessarily imply its subsequent treatment and adequate disposal. Sewage collection by networks reaches 61.4% of the Brazilian urban population15, but the percentage served with wastewater treatment represents only 42.6% of the urban population. In other words, 30.6% of the sewage collected in urban areas by networks is not sent to sewage treatment plants. It is discharged somewhere else, as in water collections or on the soil. Besides releasing the S. mansoni eggs into the water bodies, the discharge of the untreated wastewater also provides nutrients (nitrogen and phosphorus), which favors the multiplication of phytoplankton, food for mollusks, which leads to a marked proliferation of snails16.
In addition, the presence of sanitary infrastructure alone does not guarantee the proper use of the facilities. For instance, a study using survey data from school-aged children in Burkina Faso, Mali, and Ghana (2003-2008) showed a positive association between having toilets in homes and an increased risk of S. mansoni infections17. The authors attributed this result to the “incorrect disposal of human excreta, even in the presence of adequate toilet facilities”16. Chimbari et al.18 also showed that young children might, for example, avoid the use of latrines due to fear of falling inside the toilet. People can also choose not to use the facilities, either because they are not convinced of their benefits or because of ingrained social behaviour19.
In Barreto20, it was pointed out that although most of the houses in the municipality of Santo Antonio de Jesus (Bahia, Brazil) were equipped with a sewage disposal system, there was a high percentage of snails infected with S. mansoni, suggesting persistent environmental contamination. The author concluded that there was no guarantee that some of the existing cesspits were safe enough to prevent fecal contamination of the environment.
Furthermore, some studies performed to explore the impact of the presence or absence of sanitary facilities on the occurrence of schistosomiasis mansoni have shown mixed results due, partly, to the difference among the indicators used to describe the concept of “adequate sanitation”21. Most of the epidemiological studies that identified adequate sanitation as a protective factor for S. mansoni infection used the presence of a latrine, toilet, and septic tank as indicators of “adequate sanitation”, without an accurate capacity to discriminate between safe and unsafe facilities7. Few studies included the collection of sanitary effluents by network indicator, as presented in this paper. Regarding septic tanks, the misclassification of this type of individual sanitation solution is well-known, leading to the inclusion of well-built and well-operated facilities together with very precarious ones, which could have been the case of our study.
Results may also vary between surveys due to the heterogeneity of the study participants’ ages, location of water source, the study setting, the presence or absence of intermediate snail hosts, reasons for water contact, the input of miracidia into the water, and the absence of socioeconomic confounding variables7. Soares Magalhães et al.17 also acknowledge that the lack of consideration of some confounding variables, such as community participation in the planning, construction, maintenance, and financing of infrastructures, may lead to different results.
In addition, it is necessary to consider that epidemiological studies usually take into account the relationship between exposure and health outcome at the individual level, and therefore, have a low capacity to capture the complex links between sanitation and schistosomiasis, which occur in the aquatic environment and not in the household. People without access to adequate infrastructure and sanitation services in their homes may remain uninfected due to the lack of the intermediate host in the locality, and, conversely, people with adequate sanitation can be infected when they have contact with snails in the aquatic environment, even far from their homes.
Among the other sanitary variables, a protective association was found between “% Schools with filtered water” and schistosomiasis mansoni prevalence. Pieces of evidence suggest that a safe water supply, at the household or school level, is an efficient way to avoid contact with contaminated water sources, whether at domestic, recreational, or occupational activities, lowering the chances of contracting the disease6 ,922- 25. As the longevity of cercaria usually varies between 36 and 48 hours16, reaching up to 100 hours depending on the environmental conditions26,27, water storage represents a possible transmission route. The existence of filters in schools or houses, often supplied by piped water, might have two positive effects: (i) the availability of water reducing the need to collect it elsewhere, and therefore, the contact with possible contaminated watercourses; (ii) the efficiency of filters in removing large pathogens, such as Schistosomosa cercaria.
Access to a safe water supply also prevents freshwater contamination by S. mansoni eggs through the hygienic washing route. Despite sanitation and hygiene measures, eggs of S. mansoni can remain on the perianal folds, being able to survive for a long time due to the moisture of the environment, and so providing a transmission risk19,28-30. Without water and sanitation infrastructure for hygiene practices after defecation (such as sinks and showers), people get used to hygienic washing in streams. In this process, eggs of S. mansoni can be transferred through bathing, hand washing, and perianal cleaning.
The set of the statistically significant variables in the final multivariable model of the current study reflects that improvements must be addressed both in infrastructure and in social determinants with regard to schistosomiasis mansoni. As pointed out by Grimes et al.6 the counterintuitive results, such as those found in Soares Magalhães et al.17 and also in this current research, perhaps reflect that sociocultural factors are as strong predictors of S. mansoni infection as WASH. On the other hand, although health education has been reportedly successful in promoting behavioral changes, its impact on worm prevalence and intensity is limited to access to adequate sanitary infrastructure19,9,31.
Likewise, promoting adequate water and sanitation solutions, while critical, is only part of a complex chain of interventions to control or eliminate the disease. Regardless of the implementation of safely managed sanitation, as promoted by the Sustainable Development Goals, occupational and leisure activities related to contaminated water bodies may persist due to cultural and socioeconomic norms, and therefore additional preventive measures are needed to address these forms of exposure8. As suggested by the latest WHO Guideline on control and elimination of human schistosomiasis32, WASH interventions are strongly recommended as a complementary measure to reduce the prevalence of schistosomiasis. They should be implemented in integration with other measures (such as behavioural change interventions) and always take into account the local context32.
The results found for the water and sanitation variables debated above are of major concern considering the implementation of the new Brazilian law that regulates the sanitation sector in the country (Law nº 14.026/2020)33, known in Brazil as the “novo marco regulatório do saneamento”. The new regulation aims for the universalization of water and sanitation services in the country, with goals of serving 99% and 90% of the Brazilian population with drinking water and sewage collection, respectively, by the end of 203333. The law also includes a series of mechanisms to expand the role of the private sector in water and sanitation services33. In the haste of achieving the established goals, if the water and sanitation services are not provided with quality and safety, we might witness an increase in the prevalence of schistosomiasis mansoni and other health-related outcomes as well.
Moreover, schistosomiasis is known to affect the poorest and most vulnerable communities, which are less likely to be able to afford the costs related to water and sanitation services32. If private companies decide to marginalize those that have the inability to pay for the services, inequalities will increase leading to the aggravation of not only schistosomiasis mansoni transmission but also on multiple infectious diseases.
Furthermore, the promotion of successful health education activities carried out by the Unified Health System (SUS), the Brazilian health public system, as pointed out by the literature, faces a series of obstacles: (i) current educational activities are based on the expository method, not integrating the common sense and concrete experiences of the local community served34, an educational strategy that has already proved to be inefficient35; (ii) lack of scientific rigor of educational materials, with some even presenting incorrect information about the parasite cycle and the transmission pathways36;(iii) the information provided about infectious diseases is offered in a single block, prompting people’s mind to mix elements of each disease34. In the case of schistosomiasis, the population tends to consider that, as with other worm infections, the disease is transmitted by ingestion of contaminated water. Sousa37 argues that these failures do not originate in the SUS, but rather in the curricula of health courses that prioritize the teaching of other specialties, marginalizing primary health care and preventive medicine. Activities to combat parasite infections require cross-sector collaborations19. Therefore, the responsibility to address a complex health issue, such as schistosomiasis, should not be only a role of a single sector.
The results of the present study also suggest that S.mansoni is now reaching the urban dimension of public health. The increased prevalence in urban districts can be a reflection of the under-reporting of the infection in rural areas. Although the National Survey was carried out with schoolchildren from rural and urban areas, most of them were students from schools located in urban areas. Access to and use of health services in Brazil is greater in urban than in rural areas38. In addition, as a result of the decentralization of the Schistosomiasis Control Program (SCP) and its integration process into the primary health care system, which started in the 1990s, health-seeking behavior changed, and the access to diagnosis and treatment was weakened in some rural areas38.
Limitations
Finally, some limitations of the current study have to be highlighted. In addition to the limitations pointed out by Poague et al.10, which also apply to this research, in the present study, the prevalence rate was adopted as the outcome variable rather than measures of infection intensity, which are widely recognized as better indicators of transmission and public health impact than just prevalence. Even though the Kato-Katz technique has become the standard for studies on intestinal schistosomiasis, it has serious sensitivity limitations depending on aspects such as the faecal consistency, number and frequency of sample collection, number of slides examined etc., which might lead to the possibility of underestimation of prevalence in areas with low intensity of infection. Moreover, although schistosomiasis mansoni typically occurs with focal transmission, the current study assessed the relationship among variables at the municipality level. Some aspects of the association between WASH and schistosomiasis mansoni, therefore, may not have been observed due to this difference in spatial scale. Furthermore, approximately 88% of the municipalities that were part of the National Survey on the Prevalence of Schistosomiasis mansoni and Soil-transmitted helminth infections (2011-2015) were located in non-endemic areas or in areas with low endemic level for schistosomiasis mansoni, which means that the National Survey might have underestimated the real prevalence of schistosomiasis mansoni. This possibility is reinforced by the fact that approximately half of the sampled municipalities had no historical records of the presence of one or more species of the genus Biomphalaria. In addition, variables that express hygiene practices and sociocultural factors, such as the migratory flow of people, frequency of domestic and leisure activities in water bodies, number of water bodies in the territory of each municipality and their distance from the population nearby, irrigation areas, construction of dams, among others were absent. Variables of this type should be included in future works.
Conclusion
Although there is evidence in the literature that water and sanitation have positive effects in preventing schistosomiasis mansoni, the results found in our study suggest that, in Brazil, while access to filtered water in schools is a protective factor, sanitation in schools is a risk factor. Wastewater collection by sewerage is not universal in Brazil, and when present, it is not necessarily proceeded treatment, often leading to direct discharge into water resources, with potential intensification of disease occurrence. With regard to septic tanks, the presence of infrastructure alone does not guarantee their correct use by the population.
Our findings support that the human right to water and sanitation should be provided with quality. Otherwise, poor sanitation can intensify disease transmission. Special attention should be given to improving water and sanitation services in schools, not just in households.
The results also suggest that, even though schistosomiasis is classically described as a rural disease, it is now reaching the urban dimension of public health, and, therefore, control and elimination strategies also need to be adapted to combat parasite and snails spread in suburban environments. Finally, the set of significant explanatory variables in the multivariable model reflects the importance of combining structural measures and actions for water and sanitation in the control of schistosomiasis mansoni, in particular, promoting the improvement of general and health education and the universalization of the primary health care services available in the country.
Acknowledgments
We are thankful to the Fundação Oswaldo Cruz for providing the database of the National Survey of Prevalence of Schistosomiasis Mansoni and Soil-transmitted Helminth Infections and the Brazilian Federal Research Funding Agency CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior), which supported the scholarship of the first author.
References
- 1 SÁ DM. A voz do Brasil: Miguel Pereira e o discurso sobre o "imenso hospital". Hist Ciênc Saúde - Manguinhos 2009; 16 (Supl.1):333-348.
- 2 World Health Organization (WHO). World Health Statistics 2018: monitoring health for the SDGs, sustainable development goal. [cited 2020 mar 21]. Geneva: WHO; 2018. Available from: http://apps.who.int/iris/bitstream/handle/10665/272596/9789241565585-eng.pdf?ua=1
- 3 Martins-Melo FR, Carneiro M, Ramos AN, Heukelbach J, Ribeiro ALP, Werneck GL. The burden of neglected tropical diseases in Brazil, 1990-2016: a subnational analysis from the Global Burden of Disease Study 2016. PloS Negl Trop Dis 2018; 12(6):e0006559.
-
4 World Health Organization (WHO). Neglected tropical diseases - PTC databank. [cited 2020 feb 7]. Available from: http://www.who.int/neglected_diseases/preventive_chemotherapy/sth/en/
» http://www.who.int/neglected_diseases/preventive_chemotherapy/sth/en - 5 Katz N. Inquérito Nacional de Prevalência da Esquitossomose Mansoni e Geo-helmintoses. Belo Horizonte: CPqRR; 2018.
- 6 Sady H, Al-Mekhlafi HM, Mahdy MAK, Lim YAL, Mahmud R, Surin J. Prevalence and associated factors of schistosomiasis among children in Yemen: implications for an effective control programme. PLoS Negl Trop Dis 2013; 7(8):e2377.
- 7 Grimes JET, Croll D, Harrison WE, Utzinger J, Freeman MC, Templeton MR. The relationship between water, sanitation and schistosomiasis: a systematic review and meta-analysis. PLoS Negl Trop Dis 2014; 8(12):e3296.
- 8 Braun L, Grimes JET, Templeton MR. The effectiveness of water treatment processes against schistosome cercariae: a systematic review. PLoS Negl Trop Dis 2018; 12(4):e0006364.
- 9 Takeuchi R, Njenga SM, Ichinose Y, Kaneko S, Estrada CA, Kobayashi J. Is there a gap between health education content and practice toward schistosomiasis prevention among schoolchildren along the shores of Lake Victoria in Kenya? PLoS Negl Trop Dis 2019; 13(8):e0007572.
- 10 Poague KIHM, Mingoti SA, Heller L. Association between water and sanitation and soil-transmitted helminthiases: analysis of the Brazilian National Survey of Prevalence (2011-2015). Arch Public Health 2021; 79(1):83.
- 11 Hosmer DW, Lemeshow S, Sturdivant RX. Applied logistic regression. New York: John Wiley & Sons; 2013.
- 12 Dohoo I, Martin; W, Stryhn H. Veterinary epidemiologic research. Charlottetown: VER Inc; 2009.
- 13 Hilbe JM. Negative binomial regression. Cambridge: Cambridge University Press; 2011
- 14 Bollen K, Jackman R. Regression diagnostics: an expository treatment of outliers and influential cases. Mod Methods Data Anal 1985; 13(5):510-542.
- 15 Brasil. Ministério das Cidades (MC). Agência Nacional das Águas. Atlas esgotos: despoluição de bacias hidrográficas. Brasília: MC; 2017.
- 16 Melo AL, Coelho PMZ. Schistosoma mansoni e a doença. In: Neves DP, organizador. Parasitologia humana. São Paulo: Atheneu; 2011. p. 231-240.
- 17 Soares Magalhães RJ, Barnett AG, Clements ACA. Geographical analysis of the role of water supply and sanitation in the risk of helminth infections of children in West Africa. Proc Natl Acad Sci USA 2011; 108(50):20084-20089.
- 18 Chimbari M, Ndlela B, Nyati Z, Thomson A, Chandiwana SK, Bolton P. Bilharzia in a small irrigation community: an assessment of water and toilet usage. Cent Afr J Med 1992; 38(12):451-458.
- 19 Rollinson D, Knopp S, Levitz S, Stothard JR, Tchuem Tchuenté LA, Garba A, Mohammed KA, Schur N, Person B, Colley DG, Utzinger J. Time to set the agenda for schistosomiasis elimination. Acta Trop 2013; 128(2):423-440.
- 20 Barreto ML. Geographical and socioeconomic factors relating to the distribution of Schistosoma mansoni infection in an urban area of north-east Brazil. Bull World Health Organ 1991; 69(1):93-102.
- 21 Aagaard-hansen J, Mwanga JR, Bruun B.. Social science perspectives on schistosomiasis control in Africa: past trends and future directions. Parasitology 2009; 136(13):1747-1758.
- 22 Coura-Filho P, Farah MWC, Rezende DF, Lamartine SS, Carvalho OS, Katz N. Determinantes ambientais e sociais da esquistossomose mansoni em Ravena, Minas Gerais, Brasil. Cad Saude Publica 1995; 11(2):254-265.
- 23 Coura-Filho P, Rocha RS, Farah MW, Silva GC, Katz N. Identification of factors and groups at risk of infection with Schistosoma mansoni: a strategy for the implementation of control measures? Rev Inst Med Trop Sao Paulo 1994; 36(3):245-253.
- 24 Vasconcelos CH, Cardoso PCM, Quirino WC, Massara CL, Amaral GL, Cordeiro R, Carvalho OS. Avaliação de medidas de controle da esquistossomose mansoni no Município de Sabará, Minas Gerais, Brasil, 1980-2007. Cad Saude Publica 2009; 25(5):997-1006.
- 25 Baptista AB, Ramos LDS, Santos HAG. Prevalência de enteroparasitos e aspesctosepidemiologicos de crianças e jovens do municipio de Altamira - PA. Rev Pesqui Saude 2013; 14(2):77-80.
- 26 Cheng Y, Chen X, Song W, Kong Z, Li P, Liu Y. Contribution of silver ions to the inhibition of infectivity of Schistosoma japonicum cercariae caused by silver nanoparticles. Parasitology 2013; 140(5):617-625.
- 27 Colley DG, Bustinduy AL, Secor WE, King CH. Human schistosomiasis. Lancet 2014; 383(9936):2253-2264.
- 28 Sow S, Polman K, Vereecken K, Vercruysse J, Gryseels B, de Vlas SJ. The role of hygienic bathing after defecation in the transmission of Schistosoma mansoni. Trans R Soc Trop Med Hyg 2008; 102(6):542-547.
- 29 Stothard JR, Campbell SJ, Osei-atweneboana MY, Durant T, Stanton MC, Biritwum N, Rollinson D, Ombede DRE. Towards interruption of schistosomiasis transmission in sub-Saharan Africa: developing an appropriate environmental surveillance framework to guide and to support 'end game' interventions. Infect Dis Poverty 2017; 6(1):10.
-
30 Boissier J, Mouahid G, Moné H. Schistosoma spp. In: Rose JB, Jiménez-Cisneros B, editors. Global Water Pathogen Project [Internet]. 2019. [cited 2020 feb 7]. Available from: http://www.waterpathogens.org/book/schistosom
» http://www.waterpathogens.org/book/schistosom - 31 Sturrock R. Schistosomiasis epidemiology and control: how did we get here and where should we go? Mem Inst Oswaldo Cruz 2001; 96(Suppl.):17-27.
- 32 World Health Organization (WHO). WHO Guideline on control and elimination of human schistosomiasis. Geneva: WHO; 2022.
- 33 Brasil. Lei nº 14.026, de 15 de julho de 2020; Diário Oficial da União 2020; 15 jul.
- 34 Rozemberg B. O saber local e os dilemas relacionados à validação e aplicabilidade do conhecimento científico em áreas rurais. Cad Saude Publica 2007; 23(Suppl. 1):S97-S105.
- 35 Quites HFO, Abreu MNS, Matoso LF, Gazzinelli A, Quites HFO, Abreu MNS, Matoso LF, Gazzinelli A. Avaliação das ações de controle da esquistossomose na Estratégia de Saúde da Família em municípios do Vale do Jequitinhonha em Minas Gerais. Rev Bras Epidemiol 2016; 19(2):375-389.
- 36 Massara CL, Murta FLG, Enk MJ, Araújo AD, Modena CM, Carvalho OS. Caracterização de materiais educativos impressos sobre esquistossomose, utilizados para educação em saúde em áreas endêmicas no Brasil. Epidemiol Serv Saude 2016; 25(3):575-584.
- 37 Sousa MRC. Esquistossomose no Brasil: ensinar versus educar. Rev Bras Educ Med 2009; 33(1):144-147.
- 38 Reis DC, Kloos H, King C, Quites HFO, Matoso LF, Coelho KR, Gazzinelli A. Accessibility to and utilisation of schistosomiasis-related health services in a rural area of state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz 2010; 105(4):587-597.
Publication Dates
-
Publication in this collection
16 Jan 2023 -
Date of issue
Feb 2023
History
-
Received
14 Nov 2021 -
Accepted
23 July 2022 -
Published
25 July 2022