URINARY SCHISTOSOMIASIS AMONG KINDERGARTEN AND PRIMARY SCHOOL CHILDREN IN OKPECHI COMMUNITY, CROSS RIVER STATE, NIGERIA: A PRELIMINARY STUDY

Size: px

Start display at page:

Download "URINARY SCHISTOSOMIASIS AMONG KINDERGARTEN AND PRIMARY SCHOOL CHILDREN IN OKPECHI COMMUNITY, CROSS RIVER STATE, NIGERIA: A PRELIMINARY STUDY"

Gwenda Wilkerson
6 years ago
Views:

Journal of Science, Journal Engineering of Science, and Technology Engineering 1(2), and Technology September 1(2), 2012: September 23-27.

1 Journal of Science, Journal Engineering of Science, and Technology Engineering 1(2), and Technology September 1(2), 2012: September ISSN URINARY SCHISTOSOMIASIS AMONG KINDERGARTEN AND PRIMARY SCHOOL CHILDREN IN OKPECHI COMMUNITY, CROSS RIVER STATE, NIGERIA: A PRELIMINARY STUDY 1 IBOH, C. I., 2 OKON, O. E., 1 ETIM, S. E., 1 UKPONG, I. E., 1 OGBAN, E. I. & 1 PHILIP, J. I. 1 Department of Biological Sciences, CRUTECH, Calabar, 2 Department of Zoology and Environmental Biology, University of Calabar, Calabar. Corresponding author: clenaboh@yahoo.com Abstract Preliminary studies on schistosomiasis and its snail vectors were carried out between October 2010 May 2011 among Kindergarten and Primary School children in Okpechi, a rural community on the North western border of Cross river State, Nigeria. The inhabitants of Okpechi village are predominantly farmers, with only one stream, a well and some ponds as sources of water. Of the 258 urine specimens examined from these pupils, 52 (20.2%) were positive with schistosoma heamatobium ova. The prevalence of infection among boys 32(20.8%) and girls 20(19.2%) were comparable (x 2 test: P<0.05). Prevalence and intensity of infection increased significantly (x 2 test: P<0.001) with age. There was no significant difference (x 2 test: P<0.05) between intensity in boys (9.8 eggs/10ml urine) and girls (8.2 eggs/10ml urine). Among the children, 37.6% and 32.2% had haematuria and proteinuria respectively, and this was not gender specific (t- test: P<0.05). A total of four species of snails, Bulinus globosus B. truncatus, B. forskali, and B. natalensis, were identified with B. globosus being the most abundant. Keywords: Kindergarten, Primary, schistosomiasis, children, Okpechi, Nigeria. INTRODUCTION Schistosomiasis is a parasitic disease caused by fluke worms called schistosomes (Lwambo, 1988 and Anosike et al, 2006). Schistosoma haematobium, S. mansoni and S. japonicum are the most important and widespread parasites of man, while S. mekongi and S. intercalatum have a localized distribution (Rollingson & Vaughan, 1998). Schistosomiasis is endemic in 76 tropical and subtropical countries with more than 700 million people at risk of infection due to their occupational activities, which exposed them to water infection with the snail intermediate host (Nanvya et al, 2011; Opara et al, 2007). The intermediate hosts of Schistosomes are fresh water snails of the family planorbidae (Anosike et al, 2006; Akinboye et al, 2011). Bulinus globosus, B. africanus, B. nastus and B. truncatus have been incriminated as vectors of Schistosoma haematobium in Africa (Anosike et al, 2006). But B. forskali and B. senegalensis have also been reported as the intermediate hosts of S. haematobium by some investigators (Akinboye et al, 2011, Anosike et al, 2001; Betterton et al, 1983). An estimated 11 million Nigerians are infected with schistosomiasis (Nanvya et al, 2011). There are two types of schistosomiasis, namely, urinary schistosomasis (Bilhaziasis) which is caused by S. haematobium and intestinal schistosomiasis caused by S. mansoni and S. japonicum (Ukoli, 1990). Urinary and intestinal schitosomiasis are endemic in Nigeria, particularly in rural areas among primary and kindergarten school children (Ukoli, 1990; Ozumba et al, 1989, Ejezie et al, 1991, Adewunmi et al, 1991; Okoli and Odaibo 1999, Opara et al, 2001, Mafiana et al, 2003; Ekpo and Mafiana, 2004). Reports on schistosomiasis showed that different levels of infection have been documented in many parts of Nigeria (Cowpers, 1963; Dakul et al, 1997; and Houmsou et al, 2010). 50%, 8%, 0.67% 4.6%, 62.4%, 40.2%, 22.%, 45.4%, 58.8% and 50.0% have been reported in Jos Plateau, Laranto area, Jos, Panskin, Shendam, Qua anpan, Lantang South and Langtang South respectively (Cowpers, 1996, Akusangwe et al, 1996 Okpala et al, 2004; Goselle et al, 2010). Other infection levels reported are 5.5%, 21.1%, 19.8%, 44% in Oyo State, Ebonyi State and Cross River respectively (Akinboye et al, 2011; Anosike et al, 2006 and Opara et al, 2007). Both S. mansoni and S.

2 24 Iboh, C. I. et al: Urinary Schistosomiasis among Kindergarten and Primary School Children in Okpechi... haematobium are endemic in Nigeria with the latter being more widely distributed (Wilkins, 1997). Despite much research work on schistosomiasis, a lot more research need to be done to discover new endemic areas. This study was undertaken to determine the prevalence and intensity of schistosomiasis among primary and kindergarten school children in a rural community of Okpechi on the North-western border of Cross River State, Nigeria. MATERIALS AND METHODS The study was carried out in Okpechi, a rural community on the North-western border of Cross River State, Nigeria, between October, 2010 and May, Cross River State occupies an area lying between latitude and N and longitude and E. Okpechi is an agrarian community specialized in the cultivation of yams, cassava, plantain and maize. Pupils attending Okpechi primary school made up the core population of the study. The community head of Okpechi was informed about the Public Health importance of the study. The exercise was hosted in the chief s palace. The chief ensured that the cooperation of the headmaster, class teachers and parents were obtained for the study. SAMPLE COLLECTION Urine samples were collected from pupils recruited for the study with specimen bottles labeled with the needed information on age, sex and name of students. This was carried out between 10.00hours and hours during which maximum egg output is likely (Pugh and Gilles, 1997). Pupils whose ages ranged between 12 to 20 years were advised to discard the first stream of urine and also exert some pressure on their pelvic muscles so that the very last drop of urine was included in the samples (Akinboye et al, 2011). In respect of children below 5 years, parents were advised by the researcher to collect any voided urine into dark plastic bowls at the specified time above. SNAIL SAMPLING Snail samples were collected from the Ekakang stream in Okpechi with a metal scoop net. Sampling was carried out in the morning hours between 9.00 hours and hours and in the evening between hours and 18 hours. The natural vegetation was noted at points where snail samples were obtained. Snails collected were taken into glass jars transported to CRUTECH Biology laboratory for examination and identification. Identification of snails was done using the keys of Franden et al, (1980). INFECTIVITY OF SNAILS Single snails harvested from Ekakang stream, were placed in glass jars containing a mixture of dechlorinated stream water. These were exposed to laboratory bench lamps before examining the shedding of cercariae with hand lens. PARASITOLOGICAL EXAMINATION OF URINE Haematuria and proteinuria were detected in urine samples in the field within 2 hours of collection, using dipsticks. The reagent end of the dipstick was dipped into fresh urine for 45 seconds after which the test areas were compared with the standard coloured chart provided by the manufacturers. Haematuria was graded as positive when 3 to 20 erythorcytes were detected per microlitre (µl) of urine, moderately positive by presence of 50RBC/µl and highly positive by presence of more than 250 RBC/µl. Proteinuria was graded according to the concentration of protein per µl of urine. Therefore the presence of 30mg/ µl was regarded as trace, and 100mg/ µl as positive and 300mg/ µl as strongly positive. After the detection of haematuria and proteinuria, all urine samples were transported to the laboratory for detection of S. haematobium ova. The urine samples were subjected to ordinary centrifugation sedimentation techniques (WHO, 1991). Ten milliliters of urine was taken from the deposit of each specimen bottle and centrifuged at 3,000 rounds per minute (r.p.m.) for 5 minutes. The supernatant was decanted, and the sediment spread on a grease-free glass slide and covered with a cover slip. This was viewed under a binocular microscope using magnifications 10 and 40 to detect the presence of S. haematobium ova describe as golden yellowish and elliptical in shape, with characteristic terminal spines (Soulsby, 1982). The eggs were counted and expressed as number of egg per 10 millilitres of urine (egg/10ml). The intensity of infection was graded as low if less or equal to 50 eggs/10ml and high when more than 100 eggs/10ml of urine (WHO, 1983). RESULT A total of 258 urine samples were examined, 64 from kindergarten children below 5 years, and 194 from primary school children in Okpechi. Out of these, 52 (20.2%) were found to be positive for S. haematobium ova (Table 1). Infection occurred among all age groups of both sexes and were comparable between boys (32 or 20.8%) and girls (20 or 19.2%). This was not statistically significant (x 2 = 3.492, df = 4, p>0.05). The rate of infection increased progressively with age with the highest infection rate (40.0%) in pupils above 20 -years-old. The lowest infection rate (12.5%) was observed among the 6-10 years old

3 Journal of Science, Engineering and Technology 1(2), September pupils (Table 1). Table 2 illustrates the relationship between egg count, haematuria, and proteinuria among the pupils. The total haematuria prevalence rate was 37.6%. There was no significant difference (x 2 = 9.2, df = 4, P>0.05) in haematuria prevalence rate between boys (22.5%) and girls (17.4%). The overall proteinuria rate was 32.2%. The boys had a higher proteinuria rate (17.8%) than girls (14.3%). There was no significant difference (x 2 = 1.78, df = 4, P> 0.05) in proteinuria prevalence rate between boys (17.8%) and girls (14.3%). There was variation in the intensity of egg count between age groups. The overall mean egg count ranges from 5.7 to 12.9 eggs/10ml urine across the age groups. The overall mean intensity of egg count in the sampled population was 9.0 egg/10ml urine. There was strong correlation between the intensity of infection of S. haematobium and the existence of haematuria (r = 0.56) and proteinuria (r = 0.77) among children in Okpechi. The investigation result of snails revealed the presence of four species in the study area, namely, Bulinus globosus, B. forskali, B. truncatus and B. natalensis (Table 3). Bulinus globosus was the most abundant species found in the study area and lymnaea natalensis the least. DISCUSSION As revealed by this preliminary investigation, pupils in Okpechi kindergartens and primary school, showed moderate infection with S. haematobium, and overall prevalence of 20.2%. This conformed with the report of Anosike et al (2006) in parts of Ebonyi State, Table 1 Number (%) of ova positive urine among kindergarten and primary school children in Okpechi village. Age Boys Girls Total group Number Ova Number Ova Number Number (%) (years examined +ve(%) examined + ve(%) examined infected <5 36 8(22.2) 28 4(14.2) (18.8) (14.3) 16 2(12.5) 44 6 (13.6) (15.6) 18 3(16.7) 50 8 (16.0) (18.4) 24 5(20.8) (19.4) > (40.0) 18 6(33.3) (36.8) Total (20.8) (19.2) (20.2) Table 2: Prevalence (%) of mean intensity of egg count, haematuria and proteinuria according to age and gender. haematuria Proteinuria Mean intensity of egg count per 10ml urine Boys Girls Total Boys Girls Total Boys Girls Total No No (%) No No (%) No (%) No No (%) No No (%) No (%) infected infected Examine Infected examine infected examine examine infected examine infected examine 36 4(6.3) 28 3(4.7) 64 7(10.9) 36 9(14.1) 28 7(10.9) 64 16(25.0) (15.9) 16 11(17.2) 44 18(40.6) 28 8(18.2) 16 6(13.6) 44 14(31.8) (28.0) 18 10(20.0) 50 24(48.0) 32 7(14.0) 18 8(16.0) 50 15(30.0) (29.0) 24 14(22.6) 62 32(51.6) 38 16(25.8) 24 12(18.8) 62 28(45.2) (39.5) 18 7(18.4) 38 16(42.1) 20 6(15.9) 18 4(10.5) 38 10(26.3) (22.5) (17.4) (37.6) (17.8) (14.3) (32.2) Table 3: Infection rates of schistosome in fresh water snails collected from Ekakang stream Snails species No. of snails No. infected (%) total count Bulinus globosus (10.8) Bulinus forskali 63 0 Bulinus truncatus 18 0 Lymnaea natalensis 4 0 Total (6.3) (21.1%), Opara et al (2007) in Cross River State (19.1%), Anosike et al (2000) in parts of Ebonyi State (21.5%) and Khallaayoune and Lamrani (1992) in Morocco (21.2%). A lower prevalence rate has been reported by Akinboye et al (2011) in Oyo State (5.5%) and Arene et al (1989) in Port Harcourt (5.7%). In contrast to these moderate and low prevalence rates, Nanvya et al (2011) recorded a high prevalence of (41.3%) in Plateau State, while Biu et al (2009) reported 51-63%) in Zamfara State. The prevalence rate of 20.2% recorded in this study area is of public health concern in view of damages to the gentialia and cost of control intervention. This moderate prevalence could be due to the swimming activities of pupils in Ekakang stream. Infection in children is mainly due to their swimming activities when they accompany their mothers to the stream and during crossing of rivers and streams as they wade across (Anosike et al, 2006, Opara et al, 2007; Akinboye et al, 2011, Mafiana et al, 2003; Biu et al 2009). The rate of S. haematobium infection increased progressively with age as has been reported elsewhere (Opara et al, 2007; Akinboye et al, 2011). The age-related prevalence could be attributed to the higher propensity of children going out for swimming, bathing, and washing of clothes as they grow older. Secondly, older children spend more time in swimming than younger ones. (Akinboye et al, 2011; Nanvya et al, 2011, Opara et al, 2007; Okoli &. Odaibo, 1999). The sexrelated prevalence of infection showed no gender specificity. This was because girls were not restricted from most water activities such as fishing, farming and swimming that boys engaged in. This result is in contrast with the observation of Nanvya et al (2011) in plateau State. However, the pupils in Okpechi primary school visit Ekakang stream in groups to fetch drinking water and carry out other domestic activities. Aside this, pupils accompany their parents to farms where they work in several swampy areas where they contact infection in these infected water bodies (Udonsi, 1990; Okoli & Odaibo, 1999; Anosike et al, 2001, 2007). Furthermore, despite the close proximity of Obubra general hospital across the river, there is no community-based control programme targeted at enlightening the people on the aetiology of this disease. These factors could be responsible for the moderate prevalence of

4 26 Iboh, C. I. et al: Urinary Schistosomiasis among Kindergarten and Primary School Children in Okpechi... S.haematobium in these pupils. This study observed that more than half of the sampled pupils were not aware of the causative agent of schistosomiasis which is similar to report from Ebonyi State, Oyo State and Plateau State (Goselle et al 2010 Anosike et al 2006). Result from the snail survey revealed a low infection rate (6.3%) of Bulinus globosus, the proven intermediate host of S. haematobium (Wilkins, 1977; Anosike et al, 2001). This low prevalence is indicative of infection rate of S. haematobium among primary school pupils in Okpechi, compared to the high intensity reported from other parts of the country (Cowper, 1963; Houmsou et al, 2010). There was moderate haematuria and proteinuria prevalence among the studied population, with no significant difference in prevalence rate between boys and girls. It was observed that haematuria has existed long ago in Okpechi village and that is probably why the name Ntitagha for urine with blood is a common household word. It was therefore not surprising that all the sampled age groups had pupils with various levels of infection. Haematuria and proteinuria are recognized clinical signs of urinary schistosomiasis (Mafiana et al 2003; Anosike et al 2006; Opara et al, 2007). This apparent haematuria and proteinuria infection among the kindergarten and primary school pupils showed that urinary schistosomiasis is endemic and of Public Health concern in the study area. Although the people of Okpechi have lived with haematuria, control intervention is hampered by lack of knowledge of the aetiological agent, cost of diagnosis and prazinguantel - the drug of choice. We therefore recommend sound Public Health education programme as well as price reduction in cost of diagnosis and of prazinquantel to reduce the worm burden in the study area. ACKNOWLEDGEMENT The authors sincerely thank the village head of Okpechi Chief Ovarr Asibeng and his subordinates, as well as the headmaster of Okpechi primary school, for mobilizing their subjects and pupils to participate in this study. REFERENCES Adewunmi, C. O; Furu, P., Chretensen, N. Q. and Marquis, B. B. (1991). Endemicity, Seasonality, and focality of transmission of human schistosomiasis in 3 communities in south western Nigeria. Tropical Medicine and Parasitology 43, Akinboye, D. O., Agisebutu, J.U. Fawle, O. Agbonlade, O. M., Akinboye, O. O., Amosu, A. M., Atulomah, N. O. S., Awodele, O., Oduola, O., Owochnni, B. M., Rebecca, S. N. Falade, M. and Emem, O. (2011). Urinary schistosomasis water contact frequency and infectivity among secondary school students in Ibadan, Nigeria. Parasitology and Public Health Soceity of Nigeria. Nigeria Journal of Parasitology vol. 32 (1), Akufangwe, P. F. Dakul, D. A., Michael, P. D. Dajagat, P. D. and Arabs, W. L. (1996). Urinary schistosomiasis in rural communities of some Local Government Area in Plateau State, Nigeria: A preliminary parasitological and Malacogical survey. Journal of helminthology 70,(1) 3-4. Anosike J. C, Nwoke BE, Njoku A. J. (2001). The Validity of haematuria in the community diagnosis of urinary schistosomasis infections. Journal of Helminthology 75(3), Anosike, J. C., Njoku, A. J. Nwoke, B. E. B. Okere, A. N. Okoro, U. D. Obiajuru I. O. C. Ogbulie, J. N. Ohaeri, C. N. Ene, E. O. Njoku, C. J. (2001). Epidemiological and bacterial findings in some endemic foci in Ebonyi State Nigeria. International Journal of Environmental Helath and Human Development, 2(2) Anosike, J. C., Ogwuuike, U. T., Nwoke, B. E. B. Asor, J. E., Ikpeama C. A., Nwosu, D. C. and Ogbusu, F. I. (2006). Studies on Vesicle schistosomasis among rual Ezza farmers in the South eastern border of Ebonyi State, Nigeria. Annals of Agriculture and Environmental Medicine 13, Arene, F. O. Ukpeibo, E. T. Nwanze, E. A. (1989). Studies on schistosomiasis in the Niger Delta: Schistosoma intercalatum in the urban city of Port Harcourt, Nigeria. Public Health 103(4), Betterton, C. Fryer, S. G. Wright, C. A. (1983). (Bulinus senegulensis Mollusca: Planorbidae) In Northern Nigeria. Annals of Tropical Medicine and Parasitology 77(2), Biu, A. A. Kolo, H. B. and Agbadu, E. T. (2009). Prevalence of Schistosoma haematobium infection in school aged children of Konduga Local Government Area, North eastern Nigeria. International Journal of Biomedical and Health Sciences. Vol. 5(4), Cowpers, S. G. (1963). Schistosomiasis in Nigeria. Annals of Tropical Medicine and parasitology 72,

5 Journal of Science, Engineering and Technology 1(2), September Dakul, D. A. Noami, C. M., Njoku, M. O., Akufongwe, P. F. and Lapang, B. H. (1997). Urinary schistosomiasis among the Mwagvul tribe in Plateau State, Nigeria. Journla of Appleid Sceicne and Management, 1(1), Ejezie, G. C., Uko, I. E. and Braide E. I. (1991). Schistosomiasis in Cross River State, Nigeria, I. Prevalence and intensity of infection in Adim, Akamkpa Local Government Area. Journal of Hygiene Epimiology, Micro Biology and Immuniology 35(2) Ekpo, U. F. and Mafiana, C. F. (2004). Epidemiological studies of Urinary schistosomiasis in Ogun State, Nigeria. Identification of high risk communities. Nigerian Journal of Parasitology 25, Frandsen, F., McCullough, F. and Madson, H. (1980). A practical guide to the identification of African fresh water snails. Malcol Revised. 13, Goselle N. O., Anegbe, D. Imandeh, G. N. Dakul, D. A., Onwuliri A. C. F., Abba, O. J., Udeh, O. E. and Abelau, A. M. (2010). Schistosomiasis infection among school children in Jos, Nigeria. Science World Journal Vol. 5 (No.1). Houmsou, R, Kela, S. Suleiman, M. and Ogidi, J. (2010). Perceptions and assessment of rick factors in Schistosoma haematobium infection in Buruku and Katsina-Ala Local Government Area of Benue State Nigeria. The Internet Journal of Infectious Disease. Vol. 8(1) 1-4. Khallaayoune K. and Laamrani, H. (1992) Diurnal pattern in the transmission of Schistosoma haematobium in Attaouia, Morocco. Journal of Helminthology 66(2) Lwambo, N. J. S. (1988). Transmission of urinary schistobomiasis in Sukuma Land Tanzania. Journal of Helminthology, 62(3). 2( ). Mafiana, C. F. Ekpo, U.F. and Ojo, D. A. (2003). Urinary schistosomiasis in pre-school children in settlement around Oyan Reserviour in Ogun State Nigeria, Nigeria: implications for control. Tropical medicine and International Health 8 (1), Nanvya, T.N. Dakul, D.A and Mwansat, G.S. (2011). Schistosomiasis in Ndinjor district of Tangtana North Local Government Area of Plateau State, Nigeria. Nigerian Journal of parasitology vol 32(2) Okoli E. I. and Odaibo, A. B. (1999) Urinary Schistosomiasis among school children in Ibadan, an urban community in south western Nigeria. Tropical Medicine and International Health 11 (4), Okpala, H. O. Agwu, E. Agba, M. I. Chimezie, O. R. Nwosbu, G. O. and Ohihoin, A. A (2004). A survey of the prevalence of schistosomiasis among pupils in Apata and Laranta area in Jos, Plateau State. Online Journal of Health and Allied Science, 2004; Opara, K. N. Mbagwu, H. O. C. and Ekpo U. F. (2001) Qualitative diagnosis of urinary schistosomiasis in two endemic communities of Cross River Basin. West Africa Journal of Pharmacology and Drug Research 17, Opara, K. N. Udoidung, N. I. and Ukpong, I. G. (2007). Genitourinary schistosomiasis among pre-primary school children in a rural community within the Cross River Basin, Nigeria. Journal of Helminthology 81, Ozumba, N. A. G. Christensen, N. O; Nwosu, A. B. C and Nworogu, O. C. (1989). Endemicity, focality and seasonality of transmission of human schistosomiasis in Amagunze Village, Eastern Nigeria. Journal Helimthology 63, Pugh, R. N. H. and vanghan, R. S. (1997). Malumfashi endemic disease research project, III Urinary schistosomiasis longitudinal study. Annals of Tropical Medicine and Parasitology. 72: Rollingson D. and Vaughan, R. S. (1987). The genus Schistosoma. A taxonomic appraisal. In: The Biology of schistosomes from genus to latrines Rollingson D & Simpson, A. J. G. (ends). Academic press, New York. P Soulsby, J. L. (1982). Helminthes. Arthropods and protozoa of domesticated animals. 7 th ed. Bailliere Tindall, London. 809 pages. Udonsi, J. K. (1990). Human community ecology of urinary schistosomiasis in relation to snail vector bionomics in Igwun River Basin in Nigeria. Tropical Medicine and Parasitology 41, Ukoli, F. M. A. (1990). Introduction to Parasitology in Tropical Africa Textflow limited, Ibadan Nigeria p WHO (1993). Sedimentation method in basic laboratory methods in medical Parasitology, Geneva, pp WHO (1993) The control of schistosomiasis. Second Report of a World Health Organization Expert Committee, Technical Report Series No. 830, WHO Geneva Switzerland, p. 86. Wilkins, H. A. (1977). Schistosoma haematobium in a Gambia Community. I. The intensive and prevalence of infection. Annals of Tropical Medicine and Parasitology. 71 (1),

Asian Journal of Biomedical and Pharmaceutical Sciences. The Incidence of Urinary Schistosomiasis in Ohaukwu Local Government Area of Ebonyi

ISSN 2249 622X Asian Journal of Biomedical and Pharmaceutical Sciences The Incidence of Urinary Schistosomiasis in Ohaukwu Local Government Area of Ebonyi Anorue CO 1, Nwoke BEB 2, Ukaga CN 2 1 Department