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Iranian Journal of Parasitology logoLink to Iranian Journal of Parasitology
. 2016 Oct-Dec;11(4):549–558.

Intestinal Parasitic Infections and Nutritional Status among Primary School Children in Delo-mena District, South Eastern Ethiopia

Begna TULU 1,2,*, Solomon TAYE 2, Yohannes ZENEBE 1, Eden AMSALU 3
PMCID: PMC5251184  PMID: 28127367

Abstract

Background:

Although there are efforts being underway to control and prevent intestinal parasitic infections (IPIs) in Ethiopia, they are still endemic and responsible for significant morbidity. The aim of this study was to evaluate the prevalence of IPIs and their association with nutritional status among primary school children of Delo-Mena district, South Eastern Ethiopia.

Methods:

A cross-sectional study was conducted from April to May 2013. Demographic data was obtained, and IPIs was investigated in a single-stool sample by both direct stool examination and formol-ether concentration techniques. Anthropometric measurements were taken to calculate height for-age (HAZ), BMI-for-age (BAZ) and weight-for-age (WAZ) for the determination of stunting, thinness and underweight, respectively using WHO AntroPlus software. SPSS version 20 was used for statistical analysis and p value less than 0.05 was considered significant.

Results:

Among 492 children studied (51% boys, aged 6–18 years, mean 10.93 +2.4) an overall IPIs prevalence of 26.6% was found. The prevalence of S. mansoni, E. histolytica/dispar, H. nana, A. lumbricoides, G. lambilia, T. trichiura, S. stercolaris, E. vermicularis, Hookworms and Taenia spp were 9.6%, 7.7%, 5.3%, 3.7%, 2.0%, 1.6%, 1.4%, 1.2%, 0.8% and 0.2% respectively. Stunting and underweightedness were observed in 4.5% and 13.6% of children and associated with IPIs (P<0.001) and (P=0.001), respectively.

Conclusion:

IPIs and its associated malnutrition remain a public health concern in Delo-Mena district. Therefore, the overall health promotion activities coupled with snail control and de-worming to the students is crucial. Additionally, initiatives aimed at improving the nutritional status of school children are also important.

Keywords: Prevalence, Cross-sectional, Nutritional status, Intestinal parasites, Ethiopia

Background

Intestinal parasitic infections (IPIs) are amongst the most common infectious diseases worldwide. Based on WHO, approximately 2 billion people are affected by helminthic infections globally (12). About one fourth of the total population is infected with one or more nematode worms (Ascaris lumbricoides, Hookworms, Trichuris trichiura, etc.) in sub- Saharan Africa (SSA). Similarly, almost half of the school age children in SSA (181 million) were infected with one or more of these parasitic worms (3). Consequently, IPIs are responsible for high levels of morbidity and mortality, including iron-deficiency anemia, malnutrition, seizures, learning disabilities, portal hypertension, bowel obstruction, and chronic diarrhea (13).

The best global indicator of children’s well-being is growth. Irregular growth patterns in children are associated with poor and unhygienic living condition, and increased burden of communicable diseases (4). In Ethiopia, IPIs prevalence can be as high as 86.2% in Jimma (5) whereas in Babile as low as 27.2% (6). Still there is high prevalence of these infections in the country. In African schoolchildren, malnutrition associated to intestinal parasites is a common problem (7). In Ethiopia, based on the Central Statistical Agency (CSA), underweight, wasting, and stunting in children aged under-five years was 36%, 10%, and 51%, respectively (4).

Previous studies conducted in the country were largely focused on the prevalence of intestinal parasitic infections (6, 811) but not on the association with the nutritional status. Hence, the main aim of this study was to assess the prevalence of intestinal parasitic infections and its association with the nutritional status among children attending primary schools at Delo-Mena district, southeastern Ethiopia.

Methods

Study design and setting

This cross-sectional study was conducted from April 2013 to May 2013 in Yadot and Birbire primary schools in the Delo-Mena district, Bale Zone, Ethiopia. The district is situated towards South Eastern Ethiopia at about 600km from Addis Ababa, the capital city. Most of the area is known by less than 1,500 meters above sea level. The area is also known by its production of cereals, chickpeas- and haricot beans as important crops and coffee is the main cash crop (15). Yadot primary school is found in the center of Delo-Mena town where almost all the students are residence of urban setup. However, Birbire primary school is situated at the periphery of the town where majority of the students are from rural areas of Delo-Mena district.

The sample size was determined using the single population proportion formula [n=(Zα/2)2p(1−p)/d2]. The following assumptions were made: proportion was taken as 50% (P = 0.5), 95% confidence interval, margin of error 5% (d = 0.05). Study subjects were selected using simple random sampling. The schools were stratified to grades and number of study participants was allocated proportionally to each grade based on their number of sections and/or number of students. Students who were on active treatment were excluded from the study.

Sample collection and microscopic examination

Data on socio-demographic, environmental and behavioral factors, and anthropometric measurements were collected by diploma nurses who were selected and trained for the purpose of this study. To ensure reliable information, the children were interviewed in their mother tongues. For those students who were unable to respond to questions properly, their guardians were contacted through the school principal. At the time of the conversation, interviewers also inspected whether the finger nails of the students trimmed, general hygienic situation, dirty materials in their hand, and their footwear.

Children who were selected for the study were instructed on how to collect stool samples and provided by the labeled, clean plastic container, toilet tissue paper, pieces of applicator sticks. As soon as the stool samples arrived, all samples were checked for their label, quantity, time, and procedure of collection.

Laboratory procedure

Direct stool examinations were done by laboratory technologists using direct saline techniques within less than 20 minutes of stool sample collection. After completion of direct stool examination, a portion of each sample was emulsified in a 10% formalin solution and were transported to the Madawalabu University Biomedical Laboratory, where formal-ether concentration technique were performed to increase the chance of detecting parasites. Iodine staining was used to identify the cyst of E. histolytica/dispar from commensal Entamoeba coli.

Nutritional assessment

Body weight and height measurements were taken for each child to calculate anthropometric indicators. Body weight was determined to the nearest 0.1 kg on an electronic digital scale and height was measured to the nearest 0.1cm. Body Mass Index (BMI), defined as the weight in kilogram of the individual divided by the square of the height in meter, was used to determine the nutritional status of the school children into severe malnutrition (BMI < 15.9 kg/m2), moderate malnutrition (BMI = 16–16.9 kg/m2), mild malnutrition (BMI = 17–18.4 kg/m2) and normal (BMI = 18.5–25 kg/m2) as recommended by WHO. Weight, height and BMI were also used to determine z scores for weight-for-age (WAZ), height-forage (HAZ) and BMI-for-age (BAZ) using WHO reference data and United States Center for Diseases Control (USCDC) (1617).

Quality control

To ensure the quality of the result, data collectors were trained in one day on how to conduct an interview, measure weight and height and to collect stool samples. Completeness of the questionnaires was checked soon after collection. Laboratory examinations were performed by experienced medical laboratory professionals who were working in the public hospitals. Stool samples were randomly selected for quality control purpose and examined by experienced laboratory technologists who were blinded to test.

Data analysis procedures

Data entry and analysis was done using SPSS version 20 statistical package (SPSS, Inc., Chicago, IL, USA). The baseline characteristics of the study population were summarized using medians and ranges for continuous variables, simultaneously proportions and frequencies for categorical variables. Chi square test of independence was used to calculate differences in proportions for categorical variables. Student t-test analysis was used to assess differences in mean values for continuous variables. In addition, to assess poly-parasitism, a category termed “infection status” was created to denote conditions of non-infected, monoparasitism or poly-parasitism (co-infections with 2 or 3 intestinal parasites). One-way ANOVA was used to analyze differences in anthropometric mean z-scores of the study population by infection status. Separate logistic regression models were constructed to assess associations between stunting and thinness odds and infection status adjusting for age, sex and soci-economic status. Odds ratios (OR) were determined with 95% confidence intervals (CI = 95%). Statistical significance was considered for P values less than 0.05.

The Z score values for height, weight and BMI-for age relative to the WHO 2007 reference were calculated using WHO Anthro Plus software. Overweight (> + 1SD BMI-for-age Z score), obesity (> + 2SD BMI-for-age Z score), thinness/wasting (< −2SD of BMI-for-age Z score), underweight (<−2SD of weight-for-age Z score) and stunting (<−2SD of height-for-age Z score) were defined according to the WHO and USCDC references. Weight-for-age is inadequate indicator for monitoring child growth beyond pre-school years due to its inability to distinguish between relative height and body mass, therefore, BMI-for-age is recommended by the WHO to assess thinness/wasting in school-aged children and adolescents (1618).

Ethical consideration

The study was approved by the Research Ethics and Review Committee of Madwalabu University. Participation was voluntary and informed written consent was obtained from each study participants. For those children whose age was under fifteen years or was unable to understand the purpose of the study, written consent was obtained from their family through school directors. Appropriate treatment was given to those students who were positive for IPIs by local nurses.

Results

Socio-demographic characteristics

A total of 492 students from Yadot (n=339) and from Birbire (n=153) were considered in the analysis of this study with non-response rate of 5%. The mean age of the respondents was 10.93 years (satd. deviation + 2.5) and male to female ration of 1.04:1.

Demographic, household and some behavioral characteristics of the study participants according to IPIs are shown in Table 1.

Table 1:

Demographic, household and behavioral characteristics of the study sample according to IPIs

Characteristics All children n= 492 n (%) Positive for any IPIs n=131 n (%) P valueα
School Yadot 339 (68.9) 89 (26.3) 0.077
Birbire 153 (31.1) 42 (27.5)
Sex Male 251 (51.0) 86 (65.6) < 0.001
Age (yr) 6–10 236 (48.0) 67 (51.1) 0.395
11–19 256 (52.0) 64 (48.9)
Grade level 1–4 324 (65.9) 89 (67.9) 0.557
5–8 168 (34.1) 42 (32.1)
Mothers education Not literate 215 (43.7) 78 (59.5) <0.001
Literate 277 (56.3) 53 (40.5)
Fathers education Not literate 157 (31.9) 43 (32.8) 0.437
Literate 335 (68.1) 88 (67.2)
Parents occupation Employed 104 (21.1) 26 (19.8) 0.067
Merchant 163 (33.1) 45 (34.4)
Farmer 190 (38.6) 57 (43.5)
Unemployed 35 (7.1) 3 (2.3)
Household Owning telephone 462 (93.9) 123 (93.9) 0.996
Owning TV 258 (52.4) 62 (47.3) 0.171
Latrine available at home 459 (93.3) 121 (92.4) 0.621
Number of rooms ≤ 3 409 (83.1) 115 (87.8) 0.097
≥ 4 83 (16.9) 16 (12.2)
Family size ≤ 4 113 (23.0) 24 (18.3) 0.140
≥ 5 379 (77.0) 107 (81.7)
Personal hygiene Good 371 (75.4) 97 (74.0) 0.673
Poor 121 (24.6) 34 (26.1)
Eat raw or undercooked fruits or vegetables 246 (50.0) 73 (55.7) 0.126
Practice of finger nail trimming regularly 331 (67.3) 57 (57.3) 0.004
Water contact activities 341 (69.3) 102 (77.9) 0.013
Not wearing protective shoe 109 (22.2) 46 (35.1) <0.001
Previous parasitic infection 250 (50.8) 67 (51.1) 0.929
Current abdominal pain 98 (19.9) 30 (22.9) 0.318
α

value of X 2 test

Prevalence of IPIs

Based on microscopic stool sample examination, ten species of intestinal parasites were identified with an overall prevalence of 26.6%. Poly-parasitism was detected in 5.7% of the students. Double infection was observed in 4.7% of the students, triple infection in 0.8%, and quadruple infection in 0.2% (Table 2).

Table 2:

Proportion of cases with mono-parasitism and poly-parasitism of IPIs

Type of infection Number of species Most prevalent IP species in each type of infection
Species associated Cases (%)
Mono-parasitism 1 species (n=104) E. histolytica/dispar 30 (6.1)
S. mansoni 30 (6.1)
Total mono-parasitism 104 (20.9)
Poly-parasitism 2 species (n=23) A. lumbricoides and S. mansoni 5 (1.0)
Subtotal 23 (4.7)
3 species (n=4) A. lumbricoides , T. trichiura and S. mansoni 2 (0.4)
Subtotal 4 (0.8)
4 species A. lumbricoides, E. histolytica/dispar, T. 1 (0.2)
trichiura and S. mansoni
Total poly-parasitism 28 (5.7)

A total 10 different intestinal parasites were investigated in this study. The most prevalent parasites was S. mansoni 9.6%, followed by E. histolytica/dispar 7.7%, H. nana 5.3%, A. lumbricoides 3.7%, G. lambilia 2.0%, T. trichiura 1.6% S. stercolaris 1.4%, E. vermicularis 1.2%, Hook-worms 0.8% and Taenia spp 0.2%.

Children’s nutritional status

The over all malnutrition was reported among 21.0% of the children. The prevalence of stunting, thinness/wasting and underweight was found to be 4.5%, 17.1% and 13.6%, respectively. Stunting, underweight and thinness/wasting were found to be higher in boys than girls (Table 3 and 4).

Table 3:

Nutritional status versus infection status

Nutritional indicators All children N= 492 Positive for any IPIs N=131 Infection status
n (%) γ n (%) γ P value£ Not infected Mono-parasitism Poly-parasitism P value¥
n (%)γ n (%)γ n (%)γ
Mean HAZ score (n=492) −0.31 (1.03) −0.37(0.94) <0.001 −0.28(0.94) −0.36(1.28) −0.42(1.14) 0.694
Mean BAZ score (n=492) −1.14 (1.25) −1.31(1.37) 0.057 −1.07(1.21) −1.31(1.37) −1.35(1.41) 0.153
Mean WAZβ score (n=236) −0.81 (1.00) −1.06(1.12) 0.043 −0.72(0.94) −0.99(1.07) −1.25(1.28) 0.041
Stunted (< - 2 SD HAZ) 22 (4.5) 15 (11.5) <0.001 7(1.9) 10(9.7) 5(17.5) <0.001
Thinness (< - 2 SD BAZ) 84 (17.1) 25 (19.1) 0.475 58(16.1) 18(17.5) 8(27.6) 0.285
Underweight (< - 2 SD WAZ) 67 (13.6) 29 (22.1) 0.001 37(10.3) 20(19.4) 10(34.5) <0.001
Over all malnutrition 103 (21.0) 40 (30.5) 0.002 62(17.2) 28(27.2) 13(44.8) <0.001
β

WAZ calculation is not recommended for children >10 years of age.

γ

For continuous variables, values in parentheses are the standard deviation.

£

Independent t-test used for continuous variables and chi-square test used for categorical variables.

¥

One-way ANOVA used for continuous variables and chi-square test used for categorical variables.

Table 4:

Distribution of schoolchildren according to the Z scores of HAZ, WAZ and BAZ

Z score Boys Girls
Height -for-age (%) Weight-for-age (%)β BMI-for-age (%) Height -for-age (%) Weight-for-age (%)β BMI-for-age (%)
<−3 0 3 (3.0) 10 (4.0) 0 3 (2.3) 8 (3.3)
−3 to −2 17 (6.8) 13 (12.0) 41 (16.3) 4 (1.7) 2 (1.6) 25 (10.4)
−2 to −1 67 (26.7) 32 (30.0) 100 (39.8) 44 (18.3) 37 (28.7) 79 (32.8)
−1 to 0 84 (33.5) 50 (47.0) 74 (29.5) 100 (41.5) 54 (41.9) 91 (37.8)
> 0 83 (33.0) 9 (8.0) 26 (10.4) 93 (38.6) 33 (25.6) 38 (15.8)
Total 251 (100.0) 107 (100.0) 251 (100.0) 241 (100.0) 129 (100.0) 241 (100.0)
β

WAZ calculation is not recommended for children >10 yr

Associations between IPIs and nutritional status

For continues variables independent t-test and one way ANOVA was computed to see the association between mean scores of HAZ, BAZ and WAZ and IPIs and infection status of the students. Accordingly, the t-test analysis for the mean score of HAZ and WAZ of the students showed significant association with IPIs. Results of the one-way ANOVA analysis revealed that mean values for WAZ scores were significantly lower in children with polyparasitism and mono-parasitism as compared to non-infected students. Similarly, the X2 test showed that the overall malnutrition was significantly associated with IPIs and infection status (Table 3).

Based on the multivariable logistic regression analysis, stunted students were found to be almost five times (AOR=4.91, 95%CI=1.87–12.88) more likely to be infected with IPIs. Similarly, underweight students were found to be two times (AOR=1.81, 95%CI=1.02–3.22) more likely to be infected with IPIs (Table 5).

Table 5:

Associations between IPIs and nutritional status

Nutritional indicators Positive for IPIs
No. (%) Crude Odds ratio CI (>95%) P value Adjusted Odds ratio CI (>95%) P value
Stunted (< -2 SD HAZ) Yes 15 (11.5) 5.54 [2.60–16.43] < 0.001 4.91 [1.87–12.88] 0.001
No 116 (88.5) 1 1
Thinness (< - 2 SD BAZ) Yes 25 (19.1) 1.21 [0.72–2.03] 0.476 - -
No 106 (80.9) 1 -
Underweight (< - 2 SD WAZ) Yes 29 (22.1) 2.42 [1.42–4.11] 0.001 1.81 [1.02–3.22] 0.044
No 102 (77.9) 1 1
Over all malnutrition Yes 40 (30.5) 2.08 [1.31–3.29] 0.002 - -
No 91 (69.5) 1 -

Table 6 below shows the association between types of IPIs and malnutrition. S. mansoni (P=0.008), A. lumbricoides (P=0.015) and G. lambilia (P=0.006) were significantly associated with malnutrition status of the children. Similarly, those children who were infected with mono-parasitism (P=0.030) and polyparasitism (P=0.002) were more likely to be malnourished compared to children who were non-infected with intestinal parasites. However, Hookworms and other identified parasites were not significantly associated with malnutrition status (Table 6).

Table 6:

Association between type of intestinal parasite and malnutrition

Type of intestinal parasite Overall nutritional status
Not malnourished No. (%) Malnourished No. (%) Crude Odds ratio CI (>95%) P value
S. mansoni Negative 359 (80.7) 86 (19.3) 1 0.008
Positive 30 (63.8) 17 (36.5) 2.37[1.25–4.48]
E. histolytica/dispar Negative 363 (80.0) 91 (20.0) 1 0.097
Positive 26 (68.4) 12 (31.6) 1.84[0.89–3.79]
H. nana Negative 371 (79.6) 95 (2.04) 1 0.210
Positive 18 (69.2) 8 (30.8) 1.74[0.73–4.11]
A. lumbricoides Negative 379 (80.0) 95 (20.0) 1 0.017
Positive 10 (55.6) 8 (44.4) 3.19[1.23–8.31]
G. lambilia Negative 385 (79.9) 97 (20.1) 1 0.006
Positive 4 (40.0) 6 (60.0) 5.95[1.65–21.51]
T. trichiura Negative 382 (78.9) 102 (21.1) 1 0.561
Positive 7 (87.5) 1 (12.5) 0.54[0.06–4.40]
S. stercolaris Negative 383 (79.0) 102 (21.0) 1 0.666
Positive 6 (85.7) 1 (14.3) 0.63[0.07–5.25]
E. vermicluaris Negative 384 (79.0) 102 (21.0) 1 0.797
Positive 5 (83.3) 1 (16.7) 0.75[0.08–6.52]
Hookworm Negative 385 (78.9) 103 (21.1) - -
Positive 4 (100.0) 0 - -
Taenia spp Negative 388 (79.0) 103 (21.0) - -
Positive 1 (100.0) 0 - -
Overall Infection status NI* 298 (82.5) 63 (17.5) 1
MP** 75 (72.8) 28 (27.2) 1.76[1.06–2.95] 0.030
PP*** 16 (57.1) 12 (42.9) 3.55[1.60–7.87] 0.002
*

NI=not infected,

**

MP=mono-parasitism,

***

PP=poly-parasitism

Discussion

This study tried to describe the magnitude of IPIs and the nutritional status of school-children between two primary schools of Delo-Mena district, South Eastern Ethiopia. The overall prevalence of any parasitic infections was 26.6% and the mean weight-for-age, height-for-age, and BMI-for-age of the study population were lower in this study population as compared to the WHO 2007 reference values (18). Stutness and underweightedness were significantly associated with IPIs with P value < 0.05.

The prevalence of IPIs in this study was found to be consistent with other study reported in different parts of Ethiopia, Arba Mainch (27.7%) (19), Babile Twon 927.2%) (6), South and Central Tigray (28.6%) (20) and North West Ethiopia (34.2%) (21). However, the present study reported significantly lower result than reported in other parts of the country, Langano 83.8% (8), Delgi (79.8%) (9), Jimma 83%, 47.1% (11, 22) and other countries like Pakistan 54.4% (23), Nigeria 35.98%, 51.54% (24) and India 42.8% (25). On the contrary, this study reported much higher prevalence as compared to reports from Italy (13.24%, 10%) (2). These differences in prevalence could be due to the place and living standard of study subjects, and or due to a reflection of the local endemicity and geographic condition of the study area.

The highest prevalent parasite in our study area was S. mansoni 12.6%; which is consistent with study conducted in other areas of Ethiopia, South Gonder (14.6%) (12), Delgi (15.9%) (9). On the contrary, the prevalence of S. mansoni in this study was much lower than the previous studies conducted in Langano (21.2%) (10). Though we could not get published work regarding this topic, it is highly recommended to undertake further studies to identify the transmission foci that will enable to design appropriate methods of prevention and control in a systematic way. The high prevalence of S. mansoni in this study might be associated to the river Yadot, which passes through the Delo-Mena town and the behavioral factors of the students such as frequent contact, drinking and swimming in the river.

The magnitudes of other parasites identified in this study were also comparable with reports from other study areas. In localities where numerous kinds of intestinal parasites found, multiple infections were frequently encountered. In this study, double 6.2%, triple 1.2% and quadruple 0.3% infection were observed. The most frequent mixed infections were A. lumbricoides and S. mansoni. Whereas, studies from other areas showed A. lumbricoides, T. trichiura and Hookworm were the most common mixed infections (2729). This is probably due to environmental conditions and methods of transmission that was favorable for the two parasites to live together or the occurrence of high prevalence of the two parasites in the study area.

In developing countries like Ethiopia, under-nutrition is one of the major causes for children’s morbidity and mortality (2, 30). This problem is directly related to the poor economic development of the nation and accompanied by serious long-term consequences for the child (31). In this study, the over all prevalence of stunting, thinness/wasting and underweight was found to be 4.5%, 17.1% and 13.6% respectively. This result showed that the students in this study area were in a good condition as compared to the previous studies conducted in Ethiopia in Tigray, the prevalence of stunting and wasting was (26.5%) and (58.3%), respectively (32), in Gondar the prevalence of underweight, stunting and thinness/wasting was 15.1%, 25.2% and 8.9%, respectively (2) and in Angolela (11.0%), (20.8%) and (19.6%) were stunted, under-weight and wasted, respectively (1). However, the findings of this study showed that under nutrition was highly prevalent as compared to the WHO international references published in 2007 (33). This variation and higher prevalence of under nutrition can be explained by the poor socio-economic status and differences in socio-cultural experiences.

Some of the limitations of this study include the microscopy techniques used in the diagnosis of intestinal parasites may underestimate the prevalence of intestinal parasites in the study population. Other techniques like molecular assays could best estimate the prevalence of intestinal parasites among the study participants. The cross-sectional design of the study also might establish temporal relationship between IPIs and nutritional status and selection bias may also arise from convenience sampling.

Conclusion

This study showed a high prevalence of intestinal parasitic infections, as well as evidence of under-nutrition. Thus, activities to strength and expand school and community based programs that promote effective and inexpensive practices aimed at preventing the spread of parasitic diseases by promoting the use and distribution of prophylaxis and other de-worming medications while making substantial improvements in school and community-based sanitation facilities are essential. Furthermore, improving the nutritional status of schoolchildren is also pivotal.

Acknowledgements

We would like to thank Madawalabu University Research and Community Services Directorate for financial assistance, and Bale Zone Health office, Robe, Goba, and Delo-Mena hospitals for their support in providing some anti-helminthic drugs. Delo-Mena District Education office and Yadot and Birbire primary schools principals deserve our special appreciation for their cooperation. We are also grateful to the medical laboratory technologists and nurses who participated in laboratory diagnosis and treating students who were positive. Lastly, students and their families who participated in this study deserve our special thank.

Footnotes

Conflict of interest

The authors declare that there is no conflict of interest.

References

  • 1. Nguyen N, Gelaye B, Aboset N, Kumie A, Williams M, Berhane Y. Intestinal Parasitic Infection and Nutritional Status among School Children in Angolela, Ethiopia. J Prev Med Hyg. 2012; 53 (3): 157– 164. [PMC free article] [PubMed] [Google Scholar]
  • 2. Amare B, Ali J, Moges B, Bereket F, Tafess K, Woldeyohannes D, et al. Nutritional status, intestinal parasite infection and allergy among school children in Northwest Ethiopia. BMC Pediatrics. 2013; 13: 7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Harhay MO, Horton J, Olliaro PL. Epidemiology and control of human gastrointestinal parasites in children. Expert Rev Anti Infect Ther. Expert Rev Anti Infect Ther. 2010; 8 (2): 219– 234. doi: 10.1586/eri.09.119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Central Statistics Agency (CSA) of Ethiopia Ethiopia Demographic and Health Survey. 2005.
  • 5. Ali I, Mekete G, Wodajo N. Intestinal parasitism and related risk factors among students of Asendabo Elementary and Junior Secondary school, South Western Ethiopia. Ethiop J Health Dev. 1999; 3: 157– 161. [Google Scholar]
  • 6. Tadesse G. The prevalence of intestinal helminthic infections and associated risk factors among school children in Babile town, eastern Ethiopia. Ethiop J Health Dev. 2005; 19 (2): 140– 147. [Google Scholar]
  • 7. Walker A, Walker B. Moderate to mild malnutrition in African children of 10–12 years: roles of dietary and non-dietary factors. Int J Food Sci Nutr. 1997; 48: 95– 101. [DOI] [PubMed] [Google Scholar]
  • 8. Legesse M, Erko B. Prevalence of intestinal parasites among schoolchildren in a rural area close to southeast of Lake Langano, Ethiopia. Ethiop J Health Dev. 2004; 18: 116– 20. [Google Scholar]
  • 9. Ayalew A, Debebe T, Worku A. Prevalence and risk factors of intestinal parasites among Delgi school children, North Gondar, Ethiopia. J Parasitol Vect Bio. 2011; (5): 75– 81. [Google Scholar]
  • 10. Mengistu A, Gebre-Selassie S, Kassa T. Prevalence of intestinal parasitic infections among urban dwellers in southwest Ethiopia. Ethiop J Health Dev. 2007; 21 (1): 12– 7. [Google Scholar]
  • 11. Yami A, Mamo Y, Kebede S. Prevalence and predictors of intestinal helminthiasis among school children in Jimma Zone; A cross-sectional study. Ethiop J Health Sci. 2011; 21 (3): 167– 174. [PMC free article] [PubMed] [Google Scholar]
  • 12. Jemaneh L. The epidemiology of Schistosoma mansoni and soil-transmitted helminthes in elementary school children from the South Gondar Zone of the Amhara National Regional State Ethiopia. Ethiop Med J. 2000; 38 (2): 105– 18. [PubMed] [Google Scholar]
  • 13. Erko B, Medhin G. Human Helminthiasis in Wondo genet Southern Ethiopia with emphasis on geo helminthiasis. Ethiop Med J. 2003. 41 (4): 333– 4. [PubMed] [Google Scholar]
  • 14. Tulu B, Taye S, Amsalu E. Prevalence and its associated risk factors of intestinal parasitic infections among Yadot primary school children of South Eastern Ethiopia: a cross-sectional study. BMC Research Notes. 2014; 7: 848. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Central Statistical Agency (CSA) Population and Housing Census of Ethiopia: Results for Oromia Region, 2007.
  • 16. NCHS, CDC Growth charts U.S. Department of Health and Human Services, Centres for Disease Control and Prevention, National Centre for Health Statistics. http://www.cdc.gov/nchs. Accessed January 20, 2013.
  • 17. World Health Organization (WHO) AnthroPlus for personal computers Manual/Software for assessing growth of the world’s children and adolescents, 2009. http://www.who.int/growthref/tools/en/] Geneva, Switzerland: WHO. Accessed January 20, 2013. [Google Scholar]
  • 18. World Health Organization (WHO) WHO Child Growth Standards, 2007. http://www.who.int/growthref/en/. Accessed January 20, 2013.
  • 19. Haftu D, Deyessa N, Agedew E. Prevalence and determinant factors of intestinal parasites among school children in Arba Minch town, Southern Ethiopia. Amer J Health Res. 2014; 2 (5): 247– 254. [Google Scholar]
  • 20. Tadesse D, Tsehaye A. Impact of irrigation on the prevalence of intestinal parasite infections with emphasis on schistosomiasis in Hintalo -Wejerat, north Ethiopia. Ethiop J Health Dev. 2008; 18(2). [Google Scholar]
  • 21. Gelaw A, Anagaw B, Nigussie B, Silesh B, Yirga A, Alem M, et al. Prevalence of intestinal parasitic infections and risk factors among schoolchildren at the University of Gondar Community School, Northwest Ethiopia: a cross-sectional study. BMC Public Health. 2013; 13: 304>. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Mengistu A, Gebre-Selassie S, Kassa T. Prevalence of intestinal parasitic infections among urban dwellers in southwest Ethiopia. Ethiop J Health Dev. 2007; 21 (1): 12– 7. [Google Scholar]
  • 23. Ahsan-ul- W, Abdul B, ur RA, Khawaja F. Frequency of Intestinal Parasite infestation in children Quetta Hospital. Pakist J Med Res. 2005; 44: 87– 8. [Google Scholar]
  • 24. Omorodion AO, Goddey NOP, Clement IC, Ogbeneovo UD, Oijiangbe AA. Distribution of Intestinal Parasites among School-Age Children in Delta and Edo States of Nigeria. PUJ. 2012; 5 (2). [Google Scholar]
  • 25. Sehgal R, Gogulamudi VR, Jaco JV, Atluri VS. Prevalence of intestinal parasitic infections among school children and pregnant women in a low socio-economic area, Chandigarh, North India. RIF. 2010; 1 (2): 100– 103. [Google Scholar]
  • 26. Peruzzi S, Gorrini C, Piccolo G, Calderaro A, Dettori G, Chezzi C. Prevalence of intestinal parasites in the area of Parma during the year 2005. Acta Biomed. 2006; 77 (3): 147– 151. [PubMed] [Google Scholar]
  • 27. Agbolade O, Agu N, Adesanya O, Odejayi A, Adigun A, Adesanlu E, et al. Intestinal helminthes and schistosomiasis among school children in an urban center and some rural communities in south west Nigeria. Korean J Parasitol. 2007; 45: 233– 8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Chandrasekhar M, Nagesha C. Intestinal helminthic infestation in children. Indian J Pathol Microbiol. 2003; 46: 492– 494. [PubMed] [Google Scholar]
  • 29. Evi J, Yavo W, Barro-kikpc, Menan E, Koné M. Intestinal helminthosis in school back ground in six towns of south western Cotedivoire. Bull Soc Pathol Exot. 2007; 100: 176– 7. [PubMed] [Google Scholar]
  • 30. Alemu M, Nicola J, Belele T. Young lives project working paper on tackling child malnutrition in Ethiopia No 19. London: Save the children UK, 2005. Accessed July 10, 2013. [Google Scholar]
  • 31. Nyaruhucha CNM, Mamiro PS, Kerengi AJ, Shayo NB. Nutritional status of under five children in a pastoral community in Simanjiro district, Tanzania. Tanzan Health Res Bull. 2006; 8 (1): 32– 36. [DOI] [PubMed] [Google Scholar]
  • 32. Mulugeta A, Hagos F, Stoecker B, et al. Nutritional Status of Adolescent Girls from Rural Communities of Tigray, Northern Ethiopia. Ethiop J Health Dev. 2009; 23: 5– 11. [Google Scholar]
  • 33. de Onis M, Onyango AW, Borghi E, Siyam A, Nishida C, Siekmann J. Development of a WHO growth reference for school-aged children and adolescents. Bull WHO. 2007; 85 (9): 660– 7. [PubMed: 18026621]. [DOI] [PMC free article] [PubMed] [Google Scholar]

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