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Current status of soil-transmitted helminthiases among pre-school and school-aged children from Ile-Ife, Osun State, Nigeria

Published online by Cambridge University Press:  02 September 2010

O.A. Sowemimo  and
S.O. Asaolu
O.A. Sowemimo*
Affiliation:
Department of Zoology, Obefemi Awolowo University, Ile-Ife, Osun State, Nigeria
S.O. Asaolu
Affiliation:
Department of Zoology, Obefemi Awolowo University, Ile-Ife, Osun State, Nigeria
*
*E-mail: yomi_showemimo@yahoo.com
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Abstract

A cross-sectional survey was conducted to determine the prevalence and intensity of soil-transmitted helminths among pre-school and school-aged children attending nursery and primary schools in Ile-Ife. Single stool samples were collected between January and March, 2009 from 352 children randomly selected from a total of 456 children attending both private and government schools. The stool samples were processed using the modified Kato–Katz technique, and then examined for the eggs of soil-transmitted helminths (STHs). One hundred and twenty-one (34.4%) samples were positive for STH eggs. The overall prevalences of Ascaris lumbricoides, Trichuris trichiura and hookworm were 33.2%, 3.7% and 0.9%, respectively. The prevalence of STH infection in government schools (47.8%) was significantly higher than in private schools (16.1%) (P < 0.001). The most common type of mixed infection was the combination of A. lumbricoides and T. trichiura (6.8%). The prevalence and intensity of A. lumbricoides rose with age. The lowest prevalence and intensity (7.7%; 0.240 ± 0.136 eggs per gram (epg)) were recorded in the 2- to 3-year-old age group, while the highest prevalence and intensity (58.7%; 1.820 ± 0.237 epg) were recorded in children aged 10 years and above. A questionnaire survey indicated that 73% of the children attending private school had been treated with anthelminthics less than 2 months prior to the collection of stool specimens, while 43% of the children attending government school received anthelminthic treatment during the same period. The findings indicate that STH infections are endemic among schoolchildren in Ile-Ife and that the burden of parasitic infections is greater in government schools than in private schools.

Type
Research Papers
Information
Journal of Helminthology , Volume 85 , Issue 3 , September 2011 , pp. 234 - 238
Copyright
Copyright © Cambridge University Press 2010

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References

Adeleye, O.A. & Akinlabi, A.M. (2002) Intestinal parasitic infection among school children in a rural community Southwest Nigeria. Nigerian Journal of Parasitology 23, 11–18.Google Scholar
Agbolade, O.M., Agu, N.C., Adesanya, O.O., Odejayi, A.O., Adigun, A.A., Adesanlu, E.B., Ogunleye, F.G., Sodimu, A.O., Adeshina, S.A., Bisiriyu, G.O., Omotoso, O.I. & Udia, K.M. (2007) Intestinal helminthiases and schistosomiasis among school children in an urban center and some rural communities in Southwest Nigeria. Korean Journal of Parasitology 45, 233–238.CrossRefGoogle Scholar
Albonico, M., Allen, H., Chitsulo, L., Engels, D., Gabrielli, A. & Savioli, L. (2008) Controlling soil-transmitted helminthiases in pre-school-age children through preventive chemotherapy. PLoS Neglected Tropical Diseases 2, e126. doi:10.1371/journal.pald.0000126CrossRefGoogle ScholarPubMed
Allen, H., Sithey, G., Padmasiri, E.A. & Montresor, A. (2004) Epidemiology of soil-transmitted helminthes in the Western Region of Bhutan. Southeast Asian Journal of Tropical Medicine and Public Health 35, 777–779.Google ScholarPubMed
Asaolu, S.O., Holland, C.V., Jegede, J.O., Fraser, N.R. & Stoddart, R.C. (1992) The prevalence and intensity of soil-transmitted helminthiasis in rural communities in Southern Nigeria. Annals of Tropical Medicine and Parasitology 86, 279–287.CrossRefGoogle ScholarPubMed
Botero, D. & Restrepo, M. (1998) Parasitosis humanas. pp. 27–135. Medellin, Colombia, Ed. Corporacion para investigaciones.Google Scholar
Crompton, D.W.T. (1999) How much human helminthiases is there in the world? Journal of Parasitology 85, 397–403.CrossRefGoogle ScholarPubMed
Curtale, F., Pezzotti, P., Saad, Y. & Aloi, A. (1999) An analysis of individual, household and environmental risk factors for intestinal helminth infection among children in Qena Governorate, Upper Egypt. Journal of Tropical Paediatrics 45, 14–17.CrossRefGoogle ScholarPubMed
Ekpo, U.F., Odoemene, S.N., Mafiana, C.F. & Sam-Wobo, S.O. (2008) Helminthiasis and hygiene conditions of schools in Ikenne, Ogun State, Nigeria. PLoS Neglected Tropical Diseases 2, e146. doi:10.1371/journal.pntd.0000146CrossRefGoogle ScholarPubMed
Forrester, J.E. & Scott, M.E. (1990) Measurement of Ascaris lumbricoides infection intensity and dynamic of expulsion following treatment with mebendozole. Parasitology 100, 303–308.CrossRefGoogle Scholar
Hadju, V., Abadi, K. & Stephenson, L.S. (1997) Relationships between soil-transmitted helminthiases and growth in urban slum school children in Ujung Pandang, Indonesia. International Journal of Food Science and Nutrition 48, 85–93.CrossRefGoogle ScholarPubMed
Hagel, I., Lynch, N.R., Perez, M., Di Prisco, M.C., Lopez, R. & Rojas, E. (1993) Relationship between the degree of poverty and the IgE response to Ascaris infection in slum children. Transactions of the Royal Society of Tropical Medicine and Hygiene 87, 16–18.CrossRefGoogle ScholarPubMed
Holland, C.V., Asaolu, S.O., Crompton, D.W.T., Stoddert, R.C., MacDonald, R. & Torimiro, S.E.A. (1989) The epidemiology of Ascaris lumbricoides and other soil-transmitted helminthes in primary schoolchildren from Ile-Ife, Nigeria. Parasitology 99, 275–285.CrossRefGoogle Scholar
Kightlinger, L.K., Seed, J.R. & Kightlinger, M.B. (1995) Ascaris lumbricoides intensity in relation to environmental, socio-economic and behavioural determinants of exposure to infection in children from Southeast Madagascar. Journal of Parasitology 81, 480–484.Google Scholar
Kirwan, P., Asaolu, S.O., Abiona, T.C., Jackson, A.L., Smith, H.V. & Holland, C.V. (2009) Soil-transmitted helminth infections in Nigerian children aged 0–25 months. Journal of Helminthology 83, 261–266.CrossRefGoogle ScholarPubMed
Needham, C., Hoang, T.K., Nguyen, V.H., Cong, L.D., Michael, E., Drake, L., Hall, A. & Bundy, D.A.P. (1998) Epidemiology of soil-transmitted nematode infections in Ha Nam Province, Vietnam. Tropical Medicine and International Health 3, 904–912.CrossRefGoogle Scholar
Nwosu, A.B.C. (1981) The community ecology of soil-transmitted helminths infection of humans in hyperendemic area of Southern Nigeria. Annals of Tropical Medicine and Parasitology 75, 197–203.CrossRefGoogle Scholar
Saldiva, S.R., Silveria, A.S., Philippi, S.T., Torres, D.M., Mangini, A.C., Dias, R.M., da Silva, R.M., Buratini, M.N. & Massad, E. (1999) Ascaris–Trichuris association and malnutrition in Brazilian children. Paediatric Perinatal Epidemiology 13, 89–98.CrossRefGoogle ScholarPubMed
Sowemimo, O.A. (2007) Prevalence and intensity of Toxocara canis (Werner, 1782) in dogs and its potential public health significance in Ile-Ife, Nigeria. Journal of Helminthology 81, 433–438.CrossRefGoogle ScholarPubMed
Stoltzfus, J., Albonico, M. & Chwaya, H.M. (1996) Hemoquant determination of hookworm-related blood loss and its role in iron deficiency in African children. American Journal of Tropical Medicine and Hygiene 55, 399–404.CrossRefGoogle ScholarPubMed
Udonsi, J.K., Behnke, J.M. & Glibert, F.S. (1996) Analysis of the prevalence of infection and associations between human gastrointestinal nematodes among different age classes living in urban and sub-urban communities of Port Harcourt, Nigeria. Journal of Helminthology 70, 74–84.CrossRefGoogle Scholar