Scholarly article on topic 'High prevalence of Schistosoma mansoni and other intestinal parasites among elementary school children in Southwest Ethiopia: a cross-sectional study'

High prevalence of Schistosoma mansoni and other intestinal parasites among elementary school children in Southwest Ethiopia: a cross-sectional study Academic research paper on "Health sciences"

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Academic research paper on topic "High prevalence of Schistosoma mansoni and other intestinal parasites among elementary school children in Southwest Ethiopia: a cross-sectional study"

Jejaw et al. BMC Public Health (2015) 15:600 DOI 10.1186/s12889-015-1952-6

Public Health


High prevalence of Schistosoma mansoni and other intestinal parasites among elementary school children in Southwest Ethiopia: a cross-sectional study

Ayalew Jejaw1*, Endalew Zemene2, Yayehirad Alemu1 and Zemenu Mengistie1


Background: Intestinal parasitic infections (IPIs) pose significant public health challenges in school children in developing countries. The aim of this study is to determine prevalence of intestinal parasites among elementary school children in Mizan-Aman town, southwest Ethiopia.

Methods: Institution-based cross-sectional study involving 460 elementary school children in Mizan-Aman Town was conducted from May to June 2013. The school children were selected using multistage sampling technique. Data on demography and predisposing factors of IPIs were collected using pretested questionnaire. Moreover, single stool specimen was examined microscopically after wet mount and formol-ether sedimentation concentration procedures. Infection intensity of Schistosoma mansoni and soil-transmitted helminths (STHs) was estimated using Kato-Katz egg counting method.

Results: Age of the children ranged from 5 to 17 years. Overall, 76.7 % (95%CI: 72.8-80.6) of the children harbored at least one species of intestinal parasite. Eight species of intestinal parasites were detected with S. mansoni (44.8 %) and Ascaris lumbricoides (28.7 %) being predominant. Helminths and pathogenic intestinal protozoa were detected in 73.9 and 7.8 % of the children, respectively. After adjusting for other variables, age between 5 and 9 years (AOR, 2.6, 95%CI, 1.552-4.298), male gender (AOR, 2.1, 95%CI, 1.222-3.526), attending public school (AOR, 0.1, 95%CI, 0.060-0.256), using river/well water (AOR, 2.4, 95%CI, 0.912-6.191), irregular washing of hands before meal (AOR, 0.5, 95%CI, 0.254-0.865), consuming street food (AOR, 2.3, 95%CI, 1.341-3.813) and raw vegetables (AOR, 2.7, 95%CI, 1.594-4.540) were significantly associated with IPIs in the study participants.

Conclusion: Prevalence of intestinal parasites among the school children was high. Deworming of the school children and continuous follow up is required.

Keywords: S. mansoni, Intestinal parasites, School children, Ethiopia


Intestinal parasitic infections (IPIs) are the most common infections in developing countries, where sanitary facilities are scarce. Globally, the three most common soil-transmitted helminths (STHs) Ascaris lumbricoides, Trichuris trichiura and the anthropophilic hookworms (Ancylostoma duodenale and Necator americanus) are

* Correspondence:

department of BiomedicalScience, College of Health Sciences, Mizan-Tepi University, Mizan, Ethiopia

Fulllist of author information is available at the end of the article

Bio Med Central

responsible for majority of the disease burden due to neglected tropical diseases. It is estimated that 819.0, 464.6 and 438.9 million people are infected with A. lumbricoides, T. trichiura and the hookworms, respectively [1]. Schistosomes affect an estimated 240 million people worldwide, with the risk in Africa commonly associated with development of water resources [2]. While the parasites may infect people of all ages in impoverished communities, children are more likely to get infected.

Young children and individuals with heavy worm burden suffer the most from morbidity associated with the

© 2015 Jejaw et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http:// applies to the data made available in this article, unless otherwise stated.

STH and S. mansoni infections. Although mortality due to these infections is rare, the morbidity and detrimental effects on socio-economic development resulting from these infections is enormous [3-7]. Apart from the direct health impacts, malaria-helminth co-infections may also increase severity of malarial anemia resulting in gametocyte carriage, perhaps affecting transmission dynamics of malaria in endemic areas [8].

Deworming of helminth infected children is required to reduce the nutritional deficit resulting from these infections [9, 10]. The World Health Organization (WHO) recommends mass school-based deworming of schoolage children twice a year if prevalence of the STHs > 50 %, and once every year if the prevalence is > 20 % and less than 50 % [11].

Baseline surveys of IPIs produce essential evidence to take appropriate interventions, particularly for control of STHs and Schistosoma infections. Most of the epi-demiological studies of intestinal parasites carried out in Ethiopia documented often high prevalence of intestinal parasites among school children, with the STHs being most predominant [12, 13]. School-age children in developing countries, including Ethiopia, are typically at increased risk of IPIs as a result prevailing predisposing factors [14, 15]. Despite these, no published report on the magnitude of IPIs among elementary school children in Mizan-Aman Town was obtained. This research is, therefore, initiated with the objective

of determining prevalence of intestinal parasites among school children enrolled in elementary schools in the town.


Study setting

The study was conducted in Mizan-Aman Town from May to June, 2013. Mizan-Aman Town is found in Bench Maji Zone of the Southern Nations, Nationalities and Peoples' Region of Ethiopia (Fig. 1). The town is located 550 kms southwest of the capital Addis Ababa. The area is characterized by warm climate (mean annual temperature ranges between 15.1 and 27 °C), perennial rivers, and is considered ideal for agriculture and human settlement. The mean annual rainfall ranges from 400 to 2000 mm. The major economic activity of the urban inhabitants is trading while subsistence farming is the dominant means of earning a living for the surrounding rural population. In the year 2013, a total of 18 elementary schools (11 public and 7 private) were present in the town. A total of 14,393 children were enrolled in the elementary schools in the town in the year 2014.

Study design and sample size determination

School-based cross-sectional study was conducted. Sample size was determined using single population proportion formula n = Z2 p (1-p) / d2, with the following assumptions: prevalence (p) of 83.8 % from a previous

Location Map of Mizan-Aman Town

Fig. 1 Map of the study area

study [16], 95 % confidence level, 5 % margin of error, design effect of 2 and 10 % for anticipated non-response rate. Accordingly, the minimum sample size (n) was found to be 460 school children.

Multistage sampling was employed to select the study participants. First, seven of the elementary schools were randomly selected by lottery method. The sample size was allocated to the selected elementary schools proportional to the total number of student population in each of the schools. Accordingly, 145, 144, 63, 60, 31, 10 and 7 school children were sampled from Mizan Number One, Aman, Ediget Behibret, Gacheb, Mizan Misgana Academy, Aman Misgana Academy and Abune Teklehaymanot elementary schools, respectively. The school children were selected by systematic sampling technique, using list of the students as sampling frame. Children attending school in the selected elementary schools during the study period, who were voluntary to participate in the study and able to provide stool sample within the study period were included in this study.

Demographic and personal risk factors survey

Data on demographic profile of the children and factors predisposing to IPIs was gathered using pretested questionnaire. The questions included information on gender, age, shoe wearing pattern, source of drinking water, bathing in the river, habit of eating raw vegetables and street foods among others. Trained nurses who were fluent with the local languages (Amharic and Bench) interviewed the study participants.

Parasitological examination

Single stool specimen was collected from each study participant using clean plastic container labeled with unique identification number. The children were instructed on how to provide at least a thumb-sized stool specimen of their own, avoiding contamination with urine. The specimens were collected at each school and immediately transported to Clinical Laboratory of Mizan-Tepi University for processing. Direct wet smear using physiological saline and Lugol's iodine was done. Portion of the stool samples were processed by formol-ether sedimentation concentration technique, and examined microscopically following standard procedure [17]. Moreover, infection intensity of STHs and S. mansoni was determined using Kato-Katz technique. A single Kato-Katz slide was processed for each stool specimen. The specimens were processed on the same day of collection. Results of the laboratory investigation were recorded on a format prepared for this purpose.

Data analysis

Infection intensity of the STHs and S. mansoni was estimated by multiplying the total number of eggs counted by 24, which gives as the eggs per gram (epg) of stool.

Infection intensities of S. mansoni and the STHs were classified as light, moderate and heavy per the threshold set by WHO [18, 19]. The collected data were checked for completeness, entered into computer, and analyzed using SPSS version 20.0 software package. Descriptive statistics were used to summarize demographic profile of the study participants. Bivariate and multivariable logistic regression procedures were employed to identify factors associated with IPIs in the study participants. Variables appearing significantly associated with IPI by the bivariate analysis, and other biologically plausible variables were candidates for the multivariable model. The multivariable model was fitted by backward elimination technique. Statistical significance was set at p value < 0.05.

Ethical clearance

Ethical clearance was obtained from the Institute of Research and Community Support of Mizan-Tepi University. Permission was sought from Mizan-Aman Town Education and Health Offices. Informed verbal consent was obtained from the students and directors of each school. Parent/guardian consent was obtained for minors to participate in the study. Laboratory results were kept confidential. Students with positive results for intestinal parasite(s) were treated in collaboration with the health centres in the town.


Characteristics of the study participants

Table 1 shows demographic characteristics of the study participants. A total of 460 school children (50.4 % female and 49.6 % male) participated in the study. Age of the children ranged from 5 to 17 years (mean age 9.1 years). Most of the children (64.1 %) were within the age group 5-9 years.

Table 1 Demographic characteristics and intestinal parasitic infection among the school children, Mizan-Aman Town, 2013

Demographic characteristics


Positive n(%)

Negative n(%)

Gender Male Female Age group (years) 5-9 > 10 Type of school Public Private

190(83.3) 163(70.3)

242 (82.0) 111 (67.3)

336 (81.6) 17 (35.4)

38(16.7) 69(29.7)

53 (18.0)

54 (32.7)

76 (18.4) 31 (64.6)

228(49.6) 232(50.4)

295 (64.1) 165 (35.9)

412 (89.6) 48 (10.4)

Prevalence of intestinal parasites and associated risk factors

At least one species of intestinal parasite was detected in 76.7 % (95%CI: 72.8-80.6) of the children. Eight species of intestinal parasites were identified. S. mansoni was the most common intestinal parasite detected (44.8 %), followed by A. lumbricoides (28.7 %). Prevalence of each intestinal parasite is demonstrated in Fig. 2.

Out of the total children, 340 (73.9 %) were positive for at least one species of intestinal helminth, and 36 (7.8 %) were positive for protozoan parasites (Giardia lamblia and Entamoeba histolytica/dispar/moshkovskii). Risk factors associated with helminth infections include consumption of undercooked/raw vegetables (AOR 2.8, 95%CI, 1.705-4.889), consumption of street food (AOR 2.5, 95%CI, 1.523-4.368), male gender (AOR, 2.3, 95%CI, 1.392-4.043), age less than ten years (AOR 3.2, 95%CI, 1.880-5.498), being enrolled in public elementary school (AOR 0.095, 95%CI, 0.043-0.212), using river water for drinking (AOR 4.385, 95%CI, 2.504-7.679). Two hundred and sixty nine (58.5 %) of the children responded to bath and wash clothes in the river. Prevalence of S. mansoni among these children (64 %) was significantly higher than those who responded not taking bath and washing clothes in the river (data not presented).

Prevalence of intestinal parasites among the school children in each school included in the study is presented in Table 2. There was a significant difference in prevalence of intestinal parasites in the children among the schools (p <0.001). Moreover, prevalence of intestinal parasites among the school children enrolled in public elementary schools (84.1 %) was significantly higher than those enrolled in private schools (35.4 %)

(p < 0.001). Multiple IPIs were detected in 35.4 % of the infected children. S. mansoni/A. lumbricoides double infections (47 %) and S. mansoni/A. lumbricoides/T. tri-chiura triple infections (34 %) were the most commonly encountered multiple infections.

Infection intensity of S. mansoni and the STHs detected in this study is shown in Table 3. Most of the S. mansoni and T. trichiura infected children had moderate infection intensity. Heavy infection with S. mansoni, A. lumbricoides and T. trichiura was obtained 4.4, 5.3 and 3.5 % of the children infected with each of the parasites, respectively.

Independent risk factors associated with IPI among the school children is presented in Table 4. After adjusting for other variables, male gender (AOR 2.1, 95%CI, 1.222-3.526), age group within 5-9 years (AOR 2.6, 95%CI, 1.552-4.298), attending public school (AOR 0.1, 95%CI, 0.060-0.256), using well/river as source of water supply (AOR 2.4, 95%CI, 0.912-6.191), irregular washing of hands before meal (AOR 0.5, 95%CI, 0.254-0.865), habit of eating raw vegetables (AOR 2.7, 95%CI, 1.5944.540) and consumption of street foods (AOR 2.3, 95%CI, 1.341-3.813) were significantly associated with IPI among the study participants.


In this study, 76.7 % of the children were positive for at least one species of intestinal parasite. Similarly high prevalence of intestinal parasites was reported among school children in Tikur Wuha [9], Zarima [13] and Lake Tana Basin [20] in northwest Ethiopia. However, the prevalence of intestinal parasites observed in this study is higher compared to similar studies done in Yadot primary school [21], Jimma zone [22] and Gondar

Table 2 Prevalence of intestinal parasites detected among the school children in each school, Mizan-Aman Town, 2013 Name of the elementary schoolNumber of Prevalence of 95% CI

children included intestinal parasite n(%)

Gacheb 60 54 (90.0) (82.4-97.6)

Ediget Behibret 63 56 (88.9) (81.0-96.7)

Mizan Number One 145 121 (83.4) (77.3-89.5)

Aman 144 105 (72.9) (65.6-80.2)

Abune Teklehaymanota 7 3 (42.9) (6.2-79.6)

Mizan Misgana Academya 31 11 (35.5) (18.7-52.3)

Aman Misgana Academya 10 3 (30.0) (1.6-58.4)

Total 460 353 (76.7) (72.8-80.6)

Ci Confidence interval aPrivate schools

[23], in which prevalence of 26.2, 47.1 and 22.7 % were reported, respectively. Difference in environmental and socio-economic factors may account for the variation in prevalence of intestinal parasites. The high prevalence of intestinal parasites obtained in this study necessitates regular deworming of the children.

In this study, S. mansoni was the most prevalent intestinal parasite encountered. In Ethiopia, activities involving river water including fishing, taking bath and swimming in the river, and washing of clothes and utensils using river water are common denominators for infection with S. mansoni [12, 24]. In this study, it was also observed that prevalence of S. mansoni was significantly higher in children taking bath and washing clothes in the river. Snails of the genus Biomphalaria (B. sudanica and B. pfeifferi) are intermediate hosts of S. mansoni in Ethiopia [25, 26].

This study also revealed significantly higher prevalence of intestinal parasites among males and children aged 5-9 years. Male children usually play outdoors, and engage in outdoor activities compared to their female counterparts, which may predispose them to higher risks of IPI. Moreover, compared to females, male children are more likely to swim and take bath in the rivers, which might have contributed to the higher prevalence of S. mansoni observed among male children in this study. The higher prevalence of intestinal parasites in the younger children could be related to lack of awareness on transmission roots of intestinal parasites. Fentie and co-workers [20]

also reported male gender as a risk factor for S. mansoni infection.

Fruits and vegetables may be contaminated with feco-oral parasites. In this study, consumption of raw vegetables was significantly associated with IPI. Recently, Tefera et al. [27] reported parasite contamination in more than half of the fruits and vegetables collected from local markets in Jimma town. Consumption of street-food was also significantly associated with IPIs in this study, which could be due to unsafe food handling practices by the food vendors, and unhygienic environments where the foods are sold. Moreover, children who irregularly wash hands before meal, and those drinking well and river water were significantly more infected with intestinal parasites. The significant association of lack of pure water supply and unhygienic practices with IPIs was also documented by other investigators [13, 28, 29].

In this study, significantly higher prevalence of intestinal parasites was observed among children attending public schools compared to those attending private schools. The higher prevalence of intestinal parasites among the children attending public schools could be related to lower socio-economic status of their families. Association of lower-income family with higher risk of IPI in school children has been documented elsewhere [30].

Soil-transmitted helminth and schistosome infections are usually aggregated, with few proportions of individuals harboring the highest worm burden. In this study, majority of the children had moderate-to-heavy infection with the STHs and S. mansoni. Pre-school and schoolage children with moderate-to-heavy infection with STHs and S. mansoni suffer the most from health consequences of these infections [18, 31].

The major limitation of our study is that infection intensity of the STHs and S. mansoni was determined by examination of single stool specimen of each study participant. Moreover, a single Kato-Katz template was examined for each of the stool specimens. These might affect the accuracy of the egg count of the STHs and S. mansoni.


This study revealed high prevalence of intestinal parasites with S. mansoni being the most predominant. Demographic factors and hygienic practice of the school

Table 3 Infection intensity of S. mansoni and the STHs detected among the school children in Mizan-Aman Town, 2013

Parasite species Infection intensity

Light n(%) Moderate n(%) Heavy n(%) Mean egg count (epg)

S. mansoni (n = 206) 72 (35) 125 (60.7) 9 (4.4) 175 ± 107

A. lumbricoides (n = 132) 76 (57.6) 49 (37.1) 7 (5.3) 15,263 ± 1,9857

T. trichiura (n = 86) 32 (37.2) 51(59.3) 3 (3.5) 3295±4163

epg eggs per gram

Table 4 Predicators of intestinal parasitic infections among the school children (n = 460) in Mizan-Aman Town, 2013

Variables Intestinal parasite Positive n(%) Negative n(%) COR (95 % CI) AOR (95 % CI)

Age group in years 5-9 242 (82.0) 53 (18.0) 2.2 (1.430-3.451)* 2.6 (1.552-4.298)*

>10 111 (67.3) 54 (32.7) 1 1

Gender Male 190 (83.3) 38 (16.7) 2.1 (1.353-3.312)* 2.1 (1.222-3.526)*

Female 163 (70.2) 69 (29.8) 1 1

Type of school Public 336 (81.6) 76 (18.4) 0.1 (0.065-0.236)* 0.1 (0.060-0.256)*

Private 17 (35.4) 31 (64.6) 1 1

Source of water Well/river 54 (90.0) 6(10) 3.0 (1.270-7.279) * 2.4 (0.912-6.191)*

Tap 299 (74.8) 101 (25.2) 1 1

Eating raw vegetables Yes 196 (85.6) 33 (14.4) 2.8 (1.766-4.438)* 2.7 (1.594-4.540)*

No 157 (68) 74 (32) 1 1

Consumption of street foods Yes 224 (82.1) 49 (17.9) 2.1 (1.327-3.184)* 2.3 (1.341-3.813)*

No 129 (69) 58 (31) 1 1

Latrine availability at home Yes 319 (77.2) 94 (22.8) 1 1

No 34 (72.3) 13 (27.7) 0.7 (0.391-1.520) 1.3 (0.548-3.010)

Hand washing before meal Always 229 (72.5) 87 (27.5) 1 1

Sometimes 124 (86.1) 20 (13.9) 0.4 (0.249-0.723)* 0.5 (0.254-0.865)*

COR crude odds ratio, AOR adjusted odds ratio, CI confidence interval ^Statistically significant at P < 0.05

children were associated with IPIs. Deworming of the school children following WHO guideline is urgently required. Prevention of reinfection post-deworming of the school children, and monitoring of the interventions would be vital to reduce the burden of IPIs among the school children. The health extension program and school-parent forums should emphasize on school-health.

Competing interests

The authors declare that they have no competing interests. Authors' contributions

AJ conceived, designed and drafted the manuscript. YA and ZM involved in data acquisition and analysis. EZ involved in data analysis and critically reviewed the manuscript. All authors contributed to the writing of the manuscript and approved the submitted version.


We thank Mizan-Tepi University for the financial support. We are grateful to Mr. Zenawi Kiflay, who co-ordinated the data acquisition. We acknowledge the study participants and administration of the schools.

Author details

department of Biomedical Science, College of Health Sciences, Mizan-Tepi University, Mizan, Ethiopia. 2Department of Medical Laboratory Sciences and Pathology, College of Health Sciences, Jimma University, Jimma, Ethiopia.

Received: 31 October 2014 Accepted: 19 June 2015 Published online: 02 July 2015


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