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. 2019 Dec 26;13:1178630219896804. doi: 10.1177/1178630219896804

Socioeconomic Predictors of Intestinal Parasitic Infections Among Under-Five Children in Rural Dembiya, Northwest Ethiopia: A Community-Based Cross-sectional Study

Zemichael Gizaw 1,, Ayenew Addisu 2, Mulat Gebrehiwot 1
PMCID: PMC6935767  PMID: 31908472

Abstract

Background:

Soil-transmitted helminths and protozoan parasitic infections are endemic throughout the world. The problem of intestinal parasitic infection is higher among developing countries where children are the most vulnerable groups. Although health information related to parasitic infections is available globally, it is often limited in rural setups in least developed countries. This study was, therefore, conducted to assess socioeconomic predictors of intestinal parasitic infections among under-five children in rural Dembiya, Northwest Ethiopia.

Methods:

This cross-sectional study was conducted among 224 randomly selected households with under-five children. We used questionnaire to collect data and direct stool examination to identify intestinal parasitic infections. Adjusted odds ratio (AOR) with 95% confidence interval (CI) and P < .05 was used to identify socioeconomic predictors of parasitic infections.

Results:

We found that 25.4% (95% CI = [20.2, 31.1]) under-five children had intestinal parasitic infection. Ascaris lumbricoides was the leading infection, which accounted 44 of 224 (19.6%). The prevalence of childhood intestinal parasitic infections was higher among households with no members whose education level is secondary and above (AOR = 3.36, 95% CI = [1.23, 9.17]). Similarly, intestinal parasitic infections were statistically associated with presence of 2 under-five children in a household (AOR = 3.56, 95% CI = [1.29, 9.82]), absence of frequent health supervision (AOR = 3.49, 95% CI = [1.72, 7.09]), larger family size (AOR = 2.30, 95% CI = [1.09, 4.85]), and poor household economic status (AOR = 2.58, 95% CI = [1.23, 5.41]).

Conclusions:

Significant proportion of children was infected with intestinal parasitic infection in rural Dembiya. Educational status of family members, number of under-five children in a household, health supervision, family size, and wealth index were statistically associated with parasitic infections. Provision of anthelmintic drugs, health supervision, and health education targeted with transmission and prevention of infections are recommended.

Keywords: Intestinal parasitic infections, socioeconomic predictors, under-five children, rural Dembiya

Background

Helminth and protozoan parasites cause health problems in human. Twenty-five percent of the known human infections are caused by the helminth/protozoan group.1 The burden of disease caused by infection with soil-transmitted helminths (STH) remains enormous. Helminth/protozoan infections represented greater than 40% of the burden caused by all tropical diseases.2 Intestinal parasitic infections are associated with a disability-adjusted life year (DALY) loss of 5 266 000 globally.3

Intestinal parasitic infections are common in the world. However, the problem is higher in developing countries. In 2010, at least 1.3 billion people were estimated to be infected with STH.4 A global-level estimate indicated that greater than 0.8 billion people had ascariasis in 2010,5 around 0.45 billion people had hookworm,5 and at least 0.23 billion people are estimated to have schistosomiasis,6-8 in which the most of the cases are children. In 2010, an estimated 9 million life years lost due to the major worm infections of children.9,10

The burden of intestinal parasitic infections is higher in Sub-Saharan Africa (SSA).1,5,7,8 More than 90% of schistosomiasis cases occurred in SSA, with the largest number in Nigeria, Ethiopia, and Democratic Republic of Congo.11,12 In Ethiopia, a 2005 estimate showed that 4882 children were infected with Hookworm, 1956 with ascariasis, 1983 with trichiurasis, and 7357 with other STHs.12

The parasitic relation of worms with human has been influenced by global changes in the human sociocultural spectrum.13,14 Socioeconomic factors, like income or poverty,8,15-18 occupation especially farming and fishing,8,18-20 number of siblings,16,20 age of children,19,21,22 family size,19,20 households educational status,19,23 and health supervision or provision of health education24,25 are contributing for persistent transmission of the parasitic disease.

Although health information related to parasitic infections is available globally, health information often limited in rural setups in least developed countries including Ethiopia. This study was, therefore, done to investigate socioeconomic predictors of intestinal parasitic infections in under-five children in rural Dembiya, Northwest Ethiopia.

Materials and Methods

Study design and description of study settings

A cross-sectional survey, which is community-based, was conducted in rural Dembiya during May 2017. The study setting is described elsewhere.26

Sample size determination and sampling procedures

This study is part of the baseline survey for Dembiya Water, sanitation and hygiene—neglected tropical diseases (Dembiya WASH-NTDs) project. The project was implemented to prevent intestinal parasitic infections through improved WASH. In this project, single population proportion formula was used to calculate sample size. The assumptions we used to calculate sample size were presented elsewhere.26 A total of 225 children aged 6 to 59 months were selected from 5 rural kebeles (the lowest administrative units in Ethiopia). The study subjects were selected by systematic random sampling technique.

Data collection tools

We used pretested and structured questionnaire to collect sociodemographic information. Direct stool examination technique was used to identify parasitic infections in children. We used standardized procedures as presented in World Health Organization’s training manual on diagnosis on intestinal parasitic infections.27

Wealth index of households, one of the socioeconomic predictors of intestinal parasitic infections, was determined by principal component analysis (PCA). Asset information was gathered based on the list of assets in health and demographic surveys and other related studies to determine wealth index.28-30 Variables were selected based on eigenvalues greater than 1, and variables whose components greater than 0.4 in the component matrix were considered to compute wealth index. Finally, wealth index of households was classified into poor and rich.

Data analysis

Frequencies, percentages, mean or/and median, standard deviation (SD) or/and interquartile range (IQR) were used to present data. Socioeconomic predictors were selected by univariable binary logistic regression analysis on the basis of P < .2 and then analyzed by multivariable binary logistic regression for controlling the possible effect of confounders, and finally, the variables which had significant association were identified on the basis of adjusted odds ratio (AOR) with 95% confidence interval (CI) and P < .05. Hosmer and Lemeshow test was used to test the model goodness of fitness.

Results

Socioeconomic information

Two hundred twenty-five children were participated in this study. However, the data set for 1 child is incomplete for some variables and so that we considered 224 children in the analysis. Out of 224 children, 118 (52.7%) of them were women, and 166 (74.1%) of the study subjects were 24 to 59 months old. The median age was 42 months, and the IQR was 24 to 48 months. More than half 134 (59.8%) of the mothers were ⩽30 years old. The minimum age of mothers participated in this study was 18 years and the maximum was 47 years. The median age was 30 years and the IQR was 25 to 35 years. One hundred seventy-nine (79.9%) of mothers did not attend formal education and 50 (22.3%) of the households had at least 1 member whose education level is secondary and above. Two hundred thirteen (95.1%) of the mothers were married at the time of the survey and 221 (98.7%) of the mothers were farmer by their occupation. One hundred twenty-six (56.3%) of the households had more than 5 family members, and 139 (57.6%) households were economically poor (Table 1).

Table 1.

Sociodemographic information of households with children aged 6 to 59 months (225) in rural Dembiya, Northwest Ethiopia, May 2017.

Variables Frequency Percent
Sex of children
 Male 106 47.3
 Female 118 52.7
Age of children
 Under 2 years 58 25.9
 2 and above years 166 74.1
Mothers age
 ⩽30 years 134 59.8
 >30 years 90 40.2
Maternal education
 No formal education 179 79.9
 Have formal education 45 20.1
The household has at least 1 member whose education is secondary and above
 Yes 50 22.3
 No 174 77.7
Mother’s marital status
 Married 213 95.1
 Not married 11 4.9
Maternal occupation
 Farmer 221 98.7
 Merchant 3 1.3
Family size
 ⩽5 126 56.3
 >5 98 43.8
Wealth index
 Poor 129 57.6
 Rich 95 42.4

Health information of rural households

One hundred forty-one (62.9%) of the households reported that they were frequently supervised by health professionals. One hundred sixteen (51.8%) households reported as they received health messages 1 week before the time of the survey and the commonest source of information was government health workers, which accounted 112 (96.6%). One hundred thirty-eight (61.6%) households reported as they exchanged health information within the family weekly at regular basis (Table 2).

Table 2.

Health information of households with children aged 6 to 59 months (n = 225) in rural Dembiya, Northwest Ethiopia, May 2017.

Variables Frequency Percent
Health professional frequently visit the household
 Yes 141 62.9
 No 83 37.1
The household received health messages last week prior to the survey
 Yes 116 51.8
 No 108 48.2
Source of health messages
 Government health workers 112 96.6
 School children 26 22.4
 Church leaders 5 4.3
 Radio 3 2.6
 Community discussion 2 1.7
Households exchange health information at regular basis
 Yes 138 61.6
 No 86 38.4

Prevalence of intestinal parasitic infections

This study reported that 57 of 224 (25.4%; 95% CI = [20.2, 31.1]) of under-five children had intestinal parasitic infection. Ascaris lumbricoides (44 of 224), hookworm (6 of 224), Hymenolepis nana (3 of 224), Enterobius vermicularis (2 of 224), Schistosoma mansoni (1 of 224), and Giardia lamblia (1 of 224) were identified.

Socioeconomic factors associated with parasitic infections

Childhood intestinal parasitic infections were statistically associated with educational status of family members, number of under-five children in a household, health supervision, family size, and wealth index. Age of children and age of mothers did not show statistically significant association with parasitic infections (Table 3). Occupational and educational status of mothers did not pass the chi-square assumption.

Table 3.

Sociodemographic factors affecting parasitic infection among children aged 6 to 59 months (n = 225) in rural Dembiya, Northwest Ethiopia, May 2017.

Variables Parasitic infection
COR with 95% CI AOR with 95% CI
Yes No
The family has 1 or more members whose education level is secondary and above
 Yes 6 44 1
 No 51 123 3.04 [1.22, 7.58] 3.36 [1.23, 9.17]*
Age of children
 Under 2 years 20 38 1
 2 years and above 37 129 0.55 [0.28, 1.05] 0.62 [0.30, 1.32]
Mothers age
 ⩽35 years 27 107 1
 >35 years 30 60 1.98 [1.09, 3.64] 1.55 [0.73, 3.28]
Number of under-five children
 1 47 154 1
 2 10 13 2.52 [1.04, 6.12] 3.56 [1.29, 9.82]*
Health professional frequently visit households
 Yes 24 117 1
 No 33 50 3.23 [1.73, 5.99] 3.49 [1.72, 7.09]**
Family size
 ⩽5 22 104 1
 >5 35 63 2.63 [1.42, 4.87] 2.30 [1.09, 4.85]*
Wealth index
 Poor 43 86 2.89 [1.47, 5.68] 2.58 [1.23, 5.41]*
 Rich 14 81 1

Abbreviations: COR, crude odds ratio; CI, confidence interval; AOR, adjusted odds ratio.

Hosmer and Lemeshow test = 0.376.

*

Statistically significant at P < .05.

**

Statistically significant at P < .001.

This study revealed that childhood parasitic infections were associated with educational status of family members. The odds of childhood parasitic infections were 3.36 times more likely to be higher among households who had no members whose education status is secondary and above (AOR = 3.36, 95% CI = [1.23, 9.17]). The presence of 2 under-five children in a household was statistically associated with intestinal parasitic infections. Childhood parasitic infections were more prevalent among households having 2 under-five children compared with their counterparts (AOR = 3.56, 95% CI = [1.29, 9.82]). Intestinal parasitic infections were statistically associated with absence of health supervision. The prevalence of childhood parasitic infections was 3.49 times to be higher among households who had not been frequently supervised by health professionals (AOR = 3.49, 95% CI = [1.72, 7.09]). Children who live in households whose family size is greater than 5 had more odds to have parasitic infections (AOR = 2.30, 95% CI = [1.09, 4.85]). Households’ economic status was also identified as a contributing factor for the occurrence of parasitic infections in children. Children from the poor families had 2.58 more chance to have parasitic infections (AOR = 2.58, 95% CI = [1.23, 5.41]).

Discussion

This study reported that 57 of 224 (25.4%; 95% CI = [20.2, 31.1]) children had intestinal parasitic infection, which was lower than the findings of studies in Wondo Genet (85.1%),31 Hawassa Zuria District (51.3%),32 Southern Ethiopia (41.9%),33 and Chuahit (35.2 %).34 The prevalence reported by this study was similar to the findings in Wonji Shoa Sugar Estate (24.3%)35 and Butajira town (23.3%)36; Sudan (24.9%)37; Bogota (26.4%)20; and Diamantina, Brazil (27.5%).18 The current prevalence is also higher than the finding of a study in Nigeria (13.7%).38 The prevalence of intestinal parasitic infections in children was higher in rural Dembiya. This may be due to the fact that the population in the area had poor access to sanitation. During June 2017, clean water and latrine coverage was 26.6% and 55%, respectively.10 Moreover, as depicted by this study, significant proportion of the households lack WASH information. In this study, 37.1% of households reported that they were not frequently supervised by health professionals.

This study showed that educational status of family members was associated with intestinal parasitic infections in children. Childhood parasitic infections were higher among households who had no members whose education status is secondary and above. This may be due to the fact that educated households may have awareness about the transmission and prevention methods of infectious diseases. Education encourages changes in healthy behaviors at the household level. Other similar studies also reported the relation of education with occurrence of parasitic infections.19,23,39,40

Childhood intestinal parasitic infections were associated family size and number of under-five children in a household. Childhood intestinal parasitic infections were more prevalent among households having higher family size and 2 under-five children. Other studies also identified the relationship between number of under-five children and parasitic infections.16,19,20 This can be justified that children in larger families may be exposed to infections because the quality of care and attention from parents decreases as mothers may become unable to care children and less effort is available for each individual child. Moreover, high family size affects mothers or caregivers health seeking and hygienic behaviors.40-43

This study depicted that intestinal parasitic infections were associated with health supervision or health education. The prevalence of intestinal parasitic infections was higher among households who had not been frequently supervised by health professionals. Other studies also reported the association of health supervision or health education and intestinal parasitic infections.24,25,44,45 This fact can be justified that health education promotes health behaviors toward hygiene and sanitation practices. Health education increases knowledge and acceptability of interventions within the community. It also sustains integrated control of the infection.45-50

Childhood parasitic infections were significantly associated with households’ economic status. Children from the poor families had more chance to have parasitic infections. The finding of this study is in line with findings of other similar studies.8,15,16,19,39 This may be due to the fact that rich families may have greater opportunity to healthy measures like soap, household water treatment, toilets and other facilities, and lower income families could not afford these facilities.17,40,51

As a limitation, in this research, we did not use floatation techniques/McMaster technique to detect hookworm because the McMaster chamber was not available in the country. We used standardized wet mount preparation. We examined each specimen within 1 hour of sampling time to effectively detect hookworm. Moreover, the 95% CI for some predictor variables is wide due to small sample size.

Conclusions

Significant proportion of children was infected with intestinal parasitic infection in rural Dembiya. Educational status of family members, number of under-five children in a household, health supervision, family size, and wealth index were statistically associated with parasitic infections. Provision of anthelmintic drugs, health supervision, and health education targeted with transmission and prevention of infections are recommended.

Acknowledgments

The authors acknowledged NALA foundation, data collectors, field supervisors, and study participants for their contributions to this study.

Footnotes

Funding:The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The study was funded by NALA foundation.

Declaration of Conflicting Interests:The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Author Contributions: All the authors actively participated during development of a research proposal, data collection, analysis and interpretation, and writing various parts of the research report. ZG prepared the manuscript. All of the authors read and approved the final manuscript.

Availability of Data and Material: Data will be made available on requesting the primary author.

Ethics Approval and Consent to Participate: The Institutional Review Board of the University of Gondar approved the ethical aspects of this study. There were no risks due to participation in this research. Confidentiality and privacy were maintained. Verbal informed consent was obtained from the mothers and participation was on voluntary basis. Appropriate anthelmintic drugs were given for infected children. Moreover, the researchers provided health education for mothers or caregivers.

Consent for Publication: This manuscript does not contain any individual person’s data.

ORCID iD: Zemichael Gizaw Inline graphic https://orcid.org/0000-0002-6713-1975

References

  • 1. Cleaveland S, Laurenson M, Taylor L. Diseases of humans and their domestic mammals: pathogen characteristics, host range and the risk of emergence. Philos Trans R Soc Lond B Biol Sci. 2001;356:991-999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. World Health Organization (WHO). Neglected tropical diseases: PCT databank: schistosomiasis. http://www.who.int/neglected_diseases/preventive_chemotherapy/sch/en/. Updated 2015. Accessed December 20, 2017.
  • 3. World Health Organization (WHO). Global Health Estimates (GHE). Geneva: WHO; 2016. http://www.who.int/healthinfo/global_burden_disease/en/. Accessed December 28, 2017. [Google Scholar]
  • 4. Global Atlas of Helminth Infection (GAHI). Soil-transmitted helminths. http://www.thiswormyworld.org/maps/soil-transmitted-helminths. Accessed December 21, 2017.
  • 5. Pullan RL, Smith JL, Jasrasaria R, Brooker SJ. Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasit Vectors. 2014;7:37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Colley DG, Bustinduy AL, Secor WE, King CH. Human schistosomiasis. Lancet. 2014;383(9936):2253-2264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Knowles SC, Webster BL, Garba A, et al. Epidemiological interactions between urogenital and intestinal human schistosomiasis in the context of praziquantel treatment across three West African countries. PLoS Negl Trop Dis. 2015;9: e0004019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Adenowo AF, Oyinloye BE, Ogunyinka BI, Kappo AP. Impact of human schistosomiasis in Sub-Saharan Africa. Braz J Infect Dis. 2015;19:196-205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Murray CJ, Vos T, Lozano R, et al. Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2013;380:2197-2223. [DOI] [PubMed] [Google Scholar]
  • 10. Hotez PJ, Alvarado M, Basanez MG, et al. The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases. PLoS Negl Trop Dis. 2014;8:e2865. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. World Health Organization (WHO). Schistosomiasis: number of people receiving preventive chemotherapy in 2012= Schistosomiase: nombre de personnes ayant bénéficié d’une chimioprévention en 2012. Wkly Epidemiol Rec. 2014;89: 21-28. [PubMed] [Google Scholar]
  • 12. Brooker S, Clements AC, Bundy DA. Global epidemiology, ecology and control of soil-transmitted helminth infections. Adv Parasitol. 2006;62:221-261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Alum A, Rubino JR, Ijaz MK. The global war against intestinal parasites—should we use a holistic approach. Int J Infect Dis. 2010;14:e732-e738. [DOI] [PubMed] [Google Scholar]
  • 14. WHO/WER. Schistosomiasis and soil-transmitted helminthes infections: preliminary estimates of the number of children treated with albendazole or mebendazole. Wkly Epidemiol Rec. 2006;81:145-164. www.who.int/wer/2006/wer8116.pdf. Accessed December 28, 2017. [PubMed] [Google Scholar]
  • 15. Ngui R, Ishak S, Chuen CS, Mahmud R, Lim YA. Prevalence and risk factors of intestinal parasitism in rural and remote West Malaysia. PLoS Negl Trop Dis. 2011;5:e974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. El-Masry H, Ahmed Y, Hassan A, et al. Prevalence, risk factors and impacts of schistosomal and intestinal parasitic infections among rural school children in Sohag Governorate. Egypt J Hosp Med. 2007;29:616-630. [Google Scholar]
  • 17. De Silva NR, Brooker S, Hotez PJ, Montresor A, Engels D, Savioli L. Soil-transmitted helminth infections: updating the global picture. Trends Parasitol. 2003;19:547-551. [DOI] [PubMed] [Google Scholar]
  • 18. Nobre LN, Silva RV, Macedo MS, Teixeira RA, Lamounier JA, Franceschini SC. Risk factors for intestinal parasitic infections in preschoolers in a low socio-economic area, Diamantina, Brazil. Pathog Glob Health. 2013;107:103-106. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Al-Mohammed HI, Amin TT, Aboulmagd E, Hablus HR, Zaza BO. Prevalence of intestinal parasitic infections and its relationship with socio-demographics and hygienic habits among male primary schoolchildren in Al-Ahsa, Saudi Arabia. Asian Pac J Trop Med. 2010;3:906-912. [Google Scholar]
  • 20. Bouwmans MC, Gaona MA, Chenault MN, Zuluaga C, Pinzón-Rondon ÁM. Prevalence of intestinal parasitic infections in preschool-children from vulnerable neighborhoods in Bogotá. Rev Univ Ind Santander Salud. 2016;48:178-187. [Google Scholar]
  • 21. Okpala H, Josiah S, Oranekwulu M, Ovie E. Prevalence of intestinal parasites among children in day care centres in Esan West Local Government Area, Edo State, Nigeria. Asian J. Med. Sci. 2014;6:34-39. [Google Scholar]
  • 22. Jacobsen KH, Ribeiro PS, Quist BK, Rydbeck BV. Prevalence of intestinal parasites in young Quichua children in the highlands of rural Ecuador. J Health Popul Nutr. 2007;25:399-405. [PMC free article] [PubMed] [Google Scholar]
  • 23. Heidari A, Rokni M. Prevalence of intestinal parasites among children in day-care centers in Damghan-Iran. Iranian J Publ Health. 2003;32:31-34. [Google Scholar]
  • 24. Fouamno Kamga HL, Shey Nsagha D, Suh Atanga MB, et al. The impact of health education on the prevalence of faecal-orally transmitted parasitic infections among school children in a rural community in Cameroon. Pan Afr Med J. 2011;8:38. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Kanoa B, George E, Abed Y, Al-Hindi A. Evaluation of the relationship between intestinal parasitic infection and health education among school children in Gaza city, Beit-lahia village and Jabalia refugee camp, Gaza strip, Palestine. Islamic Univ J. 2006;14:39-49. [Google Scholar]
  • 26. Gizaw Z, Adane T, Azanaw J, Addisu A, Haile D. Childhood intestinal parasitic infection and sanitation predictors in rural Dembiya, Northwest Ethiopia. Environ Health Prev Med. 2018;23:26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. World Health Organization (WHO). Training manual on diagnosis of intestinal parasites based on the WHO bench aids for the diagnosis of intestinal parasites, district laboratory practice in tropical countries (WHO/CTD/SIP/98.2 CD-Rom). http://usaf.phsource.us/PH/PDF/HELM/trainingmanual_sip98–2.pdf. Updated 2004. Accessed November 1, 2017.
  • 28. Rutstein SO. The DHS Wealth Index: Approaches for rural and urban areas. Calverton, MD: Macro International; https://dhsprogram.com/pubs/pdf/WP60/WP60.pdf. Accessed October 23, 2017. [Google Scholar]
  • 29. Córdova A. Methodological note: measuring relative wealth using household asset indicators (Series No. 06). AmericasBarometer Insights. https://www.vanderbilt.edu/lapop/insights/I0806en_v2.pdf. Updated 2009. Accessed October 21, 2017.
  • 30. Kolenikov S, Angeles G. Socioeconomic status measurement with discrete proxy variables: is principal component analysis a reliable answer? Rev Income Wealth. 2009;55:128-165. [Google Scholar]
  • 31. Nyantekyi LA, Legesse M, Belay M, et al. Intestinal parasitic infections among under-five children and maternal awareness about the infections in Shesha Kekele, Wondo Genet, Southern Ethiopia. Ethiop J Health Dev. 2010;24: 185-190. [Google Scholar]
  • 32. Kabeta A, Assefa S, Hailu D, Berhanu G. Intestinal parasitic infections and nutritional status of pre-school children in Hawassa Zuria District, South Ethiopia. Afr J Microbiol Res. 2017;11:1243-1251. [Google Scholar]
  • 33. Unasho A. An investigation of intestinal parasitic infections among the asymptomatic children in, Southern Ethiopia. Int J Child Health Nutr. 2013;2:212-222. [Google Scholar]
  • 34. Alemu A, Tegegne Y, Damte D, Melku M. Schistosoma mansoni and soil-transmitted helminths among preschool-aged children in Chuahit, Dembia district, Northwest Ethiopia: prevalence, intensity of infection and associated risk factors. BMC Public Health. 2016;16:422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. G/hiwot Y, Degarege A, Erko B. Prevalence of intestinal parasitic infections among children under five years of age with emphasis on Schistosoma mansoni in Wonji Shoa Sugar Estate, Ethiopia. PLoS ONE. 2014;9:e109793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Shumbej T, Belay T, Mekonnen Z, Tefera T, Zemene E. Soil-transmitted helminths and associated factors among pre-school children in Butajira Town, South-Central Ethiopia: a community-based cross-sectional study. PLoS ONE. 2015;10:e0136342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Sun C. Prevalence and associated risk factors of Intestinal Helminths infections among pre-school children (1 to 5 years old) in IDPs settlements of Khartoum state, Sudan. J Global Health. https://www.ghjournal.org/prevalence-and-associated-risk-factors-of-intestinal-helminths-infections-among-pre-school-children-1-to-5-years-old-in-idps-settlements-of-khartoum-state-sudan/. Accessed November 13, 2017.
  • 38. Achi E, Njoku O, Nnachi A, et al. Prevalence of intestinal parasitic infections among under five children in Abakaliki local government area of Ebonyi state. Ejpmr. 2017;4:218-222. [Google Scholar]
  • 39. Quihui L, Valencia ME, Crompton DW, et al. Role of the employment status and education of mothers in the prevalence of intestinal parasitic infections in Mexican rural schoolchildren. BMC Public Health. 2006;6:225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Woldu W, Bitew BD, Gizaw Z. Socioeconomic factors associated with diarrheal diseases among under-five children of the nomadic population in Northeast Ethiopia. Trop Med Health. 2016;44:40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41. Lovelyn OA, Betrand NO, Godswill N. Family and social determinants of health-seeking behaviour of caregivers of febrile children in an urban city of South-Eastern Nigeria. Arch Med. 2016;8:1-6. [Google Scholar]
  • 42. Uggla C, Mace R. Parental investment in child health in sub-Saharan Africa: a cross-national study of health-seeking behaviour. R Soc Open Sci. 2016;3:150460. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Sisay S, Endalew G, Hadgu G. Assessment of mothers/care givers health care seeking behavior for childhood illness in rural Ensaro District, North Shoa Zone, Amhara Region, Ethiopia. Global J Life Sci Biol Res. 2015;1:20-34. [Google Scholar]
  • 44. Anantaphruti M, Waikagul J, Maipanich W, et al. School-based health education for the control of soil-transmitted helminthiases in Kanchanaburi province, Thailand. Ann Trop Med Parasitol. 2008;102:521-528. [DOI] [PubMed] [Google Scholar]
  • 45. Gyorkos TW, Maheu-Giroux M, Blouin B, Casapia M. Impact of health education on soil-transmitted helminth infections in schoolchildren of the Peruvian Amazon: a cluster-randomized controlled trial. PLoS Negl Trop Dis. 2013;7:e2397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Albright JW, Basaric-Keys J. Instruction in behavior modification can significantly alter soil-transmitted helminth (STH) re-infection following therapeutic de-worming. Southeast Asian J Trop Med Public Health. 2006;37:48-57. [PubMed] [Google Scholar]
  • 47. Asaolu S, Ofoezie I. The role of health education and sanitation in the control of helminth infections. Acta Trop. 2003;86:283-294. [DOI] [PubMed] [Google Scholar]
  • 48. Lansdown R, Ledward A, Hall A, et al. Schistosomiasis, helminth infection and health education in Tanzania: achieving behaviour change in primary schools. Health Educ Res. 2002;17:425-433. [DOI] [PubMed] [Google Scholar]
  • 49. Albonico M, Montresor A, Crompton D, Savioli L. Intervention for the control of soil-transmitted helminthiasis in the community. Adv Parasitol. 2006;61: 311-348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Bieri FA, Gray DJ, Williams GM, et al. Health-education package to prevent worm infections in Chinese schoolchildren. N Engl J Med. 2013;368:1603-1612. [DOI] [PubMed] [Google Scholar]
  • 51. Rahman A. Assessing income-wise household environmental conditions and disease profile in urban areas: study of an Indian city. Geojournal. 2006;65:211-227. [Google Scholar]

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