H.A. Adie, A. Oyo-Ita, O.E. Okon, G.A. Arong, I.A. Atting, E.I. Braide, O. Nebe,

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Research Journal of Parasitology 10 (2): 58-65, 2015 ISSN 1816-4943 / DOI: 10.3923/jp.2015.58.65 2015 Academic Journals Inc. Evaluation of Intensity of Urinary Schistosomiasis in Biase and Yakurr Local Government Areas of Cross River State, Nigeria after Two Years of Integrated Control Measures 1 1 2 2 3 4 5 H.A. Adie, A. Oyo-Ita, O.E. Okon, G.A. Arong, I.A. Atting, E.I. Braide, O. Nebe, 6 7 U.E. Emanghe and A.A. Otu 1 Ministry of Health, Calabar, Nigeria 2 Department of Zoology and Environmental Biology, University of Calabar, Nigeria 3 Department of Medical Microbiology and Parasitology, University of Uyo/University of Uyo Teaching Hospital, Uyo, Nigeria 4 Federal University, Lafia, Nasarawa State, Nigeria 5 Federal Ministry of Health, Abuja, Nigeria 6 Department of Medical Microbiology/Parasitology, University of Calabar, Nigeria 7 Department of Internal Medicine, University of Calabar, Calabar, Nigeria Corresponding Author: H.A. Adie, Ministry of Health, Calabar, Nigeria ABSTRACT A parasitological mapping of urinary schistosomiasis using filtration method was conducted in Biase and Yakurr LGAs of Cross River State, Nigeria by the Neglected Tropical Diseases Control unit in collaboration with the schistosomiasis/soil transmitted helminths unit of the Federal Ministry of Health, Nigeria in November 2012. The results of the study revealed a mean urinary schistosomiasis prevalence of 49% for the six schools under study in Biase and 30% for the six schools under study in Yakurr LGA. The mean ova load was 0.9 for males and 0.8 for females in the two LGAs. Integrated control measures put in place, included chemotherapy of infected individuals with praziquantel and health education on the predisposing factors responsible for the transmission of urinary schistosomiasis. An evaluation of the interventions was carried out in November 2014, after two rounds of treatment with Praziquantel and intensive education were given. Urine samples were collected from 600 school children, 300 from each of the two LGAs. The evaluation study using the urine filtration technique revealed a mean schistosomiasis prevalence of 0% for the six schools under study in Biase and 0.02% for the six schools under study in Yakurr LGA with mean ova load reduced to 0.3 for males and 0 for females in the two LGAs. Data analysis with SPSS package revealed a 100% participation of all selected school children in 12 schools (6 in each LGA). Statistical analysis showed that there was no significant difference in the prevalence between male and female (p>0.005). A student t-test showed a significant difference between prevalence rates in 2012 and the results in 2014 (p>0.005). The spatial distribution showed that endemic schools were distributed within marshy areas where rice was cultivated in the two LGAs. These results showed that with wide scale integrated control measures, urinary schistosomiasis can be eliminated or reduced to a disease of no public health importance. Key words: Evaluation, intensity, urinary schistosomiasis, integrated control measures 58

INTRODUCTION Schistosomiasis, a parasitic disease that has plagued humanity for centuries is caused by a trematode or fluke of genus Schistosoma. The disease has some time ago been misconceived as the male equivalent of menstruation and has therefore been celebrated as the coming of age for young males in rural endemic communities (Amazigo et al., 1997). The widespread, uncontrolled, unmonitored proliferation of water impoundment and irrigation schemes, coupled with the phenomenon of global warming and prevailing ignorance of Schistosomiasis in most endemic areas has elevated the disease to a very serious health problem in sub-saharan Africa including Nigeria (Abdullahi et al., 2011; WHO., 2012; Useh, 2013). The disease is also considered as one of the most frequently occurring parasitic infections globally (Okon et al., 2007; WHO., 1985). About 200 million people in 76 countries are affected with schistosomiasis and 600 million people may be at risk of infection (WHO., 1985). In Cross River State, the agrarian population and suitability for the thriving of the snail intermediate host has contributed to the prevalence of S. haematobium (Ejezie et al., 1991). A national prevalence survey carried out in 1990/91 among school children aged 5-14 years, reported the presence of schistosomiasis in all 36 states of Nigeria including the Federal Capital Territory, Abuja, with an estimated number of 20 million people infected (Ekpo and Mafiana, 2004; NSCP., 1996). In Biase Local Government Area of Cross River State, Etim et al. (1999, 2012) reported 35.95 and 30.5% prevalence of urinary schistosomiasis, respectively while Okon et al. (2007, 2009) reported 35 and 45.3% prevalence, respectively from parasitological examination of urine samples from school children. Schistosomiasis can be treated effectively by giving a single oral dose of praziquantel which is effective against all the species of schistosomes. Chemotherapy with health education and provision of safe water sources can reduce transmission. Control of snail intermediate hosts of the disease is however of very limited value (NSCP., 1999). Efforts have been targeted on urinary schistosomiasis (the most common and easily diagnosed) for control (WHO., 1985). Drug administration alone cannot control the spread of schistosomiasis hence the integrated approach used by the Cross River State Neglected Tropical Diseases Control unit in curbing the spread of the disease. The objective of this study was to evaluate the efficacy of the strategies used in the control of urinary schistosomiasis among school children in Biase and Yakurr Local Government Areas. The results of this study will strengthen planning for large scale control measures. MATERIALS AND METHODS Study area: The study was carried out in Cross River State, Nigeria, situated within the tropics, between latitudes 5 32 and 4 27 North and longitude 7 50 and 9 28 East (Fig. 1). All year round rainfall of about 350 mm occurs along the coastal area. Rainfall in the hinterland is between 120 and 200 mm annually with maximum precipitation occurring from July to September. Ambient temperatures remain high throughout the year (22.4-33.2 C). Relative humidity is high (60-93%). The climate is tropical except for Obudu Plateau which has an altitude of 1,575.76 m above sea level and has temperate climate. The State has a 2015 projected population of 3,783,085 people (United Nations Fund for Population Activities (UNFPA)). Study procedure: This study received a country wide ethical clearance from the Ethical Board of the Federal Ministry of Health, Abuja. The Cross River State Health Research and Ethic Committees also provided further clearance for this study. Advocacy visits were made to the Yakurr and Biase LGAs during which the purpose of the study was explained to key opinion leaders. The 59

Yala Bekwarra Ogoja Obudu Obanliku Yakurr Ikom Boki Obubra Abi Etung Biase Odukpani Akamkpa Boundaries Calabar municipality Calabar south Bakassi Akpabuyo Study LGAs Study sites 20 0 20 40 km Fig. 1: Map of cross river state showing study LGAs and sites schools were identified and oral consent was obtained after meeting with parents of school children and explaining the study. All participants had the opportunity to opt out if they were not comfortable with participating. This cross-sectional descriptive and analytical study utilized a structured questionnaire for each urine-providing child and this was administered by a trained researcher to capture relevant socio-demographic data. Urine samples were then collected from a total of 600 school children from 12 schools, that is, 300 from each of the two LGAs. Collection of urine samples: A sterile procedure was used to collect urine samples for diagnosis of urinary schistosomiasis. This was to ensure that the samples were not contaminated, hence the samples were collected in sterilin bottles. Pupils were provided with capped sterile bottles. They were instructed to fill the bottle with urine to the 10 ml mark in the middle of a discharge and then cover the bottle with the cap. The period of urine collection for Schistosoma haematobium was between 10.00 and 14.00 h. 60

Examination of urine samples: On collection, the urine samples were examined for colour (macrohaematuria) and appearance following the guide indicated in the questionnaire. A reagent strip (hemastix) was inserted in the urine to test for microhaematuria and the observations recorded. The urine was examined further on the same day for S. haematobium eggs, the urine was further treated by fixation, this was done by adding 3 drops of formaldehyde and examining later for S. haematobium eggs following the procedure below. Each of the urine samples was thoroughly mixed and 10 ml of the sample put into a centrifuge tube with a conical tip. The centrifuge was spun for 5 min at 1500 rpm. The supernatant was removed with a pipette leaving about 0.5 ml of the fluid with the sediment at the bottom of the tube undisturbed. The remaining fluid and sediment were mixed using a pipette, then a drop of the mixture was transferred to a microscope slide and covered with a cover slip. The slides were thoroughly examined for S. haematobium eggs using the 10X objective. The total number of eggs in all the sediment were expressed per 10 ml of the urine. Collection of coordinates: A hand-held GPS (Garmin 12XL, Garmin Corp, USA) was used to determine the latitude and longitude of the schools. The coordinates were collected in the school compound, the location was marked after allowing the satellite error to come to a distance of 3-5 m. Data analysis: All data were double-entered using SPSS version 17.0 for Windows (SPSS Inc, Chicago, IL, USA). For analysis of infection data, descriptive statistics, including 95% confidence intervals (95% CI), Student t-test analysis was also used to compare differences among variables. ArcView GIS with Spatial Analyst GIS software were used for display of spatial data. The location of each school was linked to the parasitological data using unique schools identifier. RESULTS The study analyzed urine samples from six hundred pupils (300 males and 300 females) in 12 schools in Biase and Yakurr Local Government Areas. Of the 600 pupils examined before and after the implementation of the integrated control strategies in the two Local Government Areas, 231 (38.5%) and 1 (0.17%) prevalence were reported, respectively (Table 1). In Biase Local Government Area, out of the six schools re-examined after the implementation of integrated control strategies, no infection were found for both sexes while in Yakurr Local Government Area, only 1 (0.67%) prevalence was observed among the male pupils (Table 2 and 3). Table 1: Age range, percentage prevalence and intensity of urinary schistosomiasis in Biase and Yakurr Local Government Areas, Cross River State, Nigeria before and after the implementation of the integrated control strategies Prevalence before Prevalence after implementation of implementation of control strategies Mean Ova/10 ml of urine control strategies Mean Ova/10 ml of urine Age range No. of pupils -------------------------- before implementation of --------------------------- after implementation of (years) examined No. % control strategies No. % control strategies 5-10 148 68 45.9 50 0 0.00 0 11-15 244 109 44.7 85 1 0.41 12 16-20 208 54 25.9 62 0 0.00 0 Total 600 231 38.5 197 61 0.17 12 61

Table 2: Prevalence of urinary schistosomiasis among children in 6 selected schools in Yakurr LGA before and after the implementation of the integrated control strategies Prevalence be fore implementation of Prevalence after implementation integrated control strategies of strategies integrated control -------------------------------------------------------- ---------------------------------------------- No. of individuals examined M F M F -------------------------------------- -------------------- ------------------ ------------------ ---------------- Location of school M F No. % No. % No. % No. % Lekpanko 25 25 12 48 7 28 1 4.0 0 0 Nko 25 25 4 16 8 32 0 0.0 0 0 Ntam Ekori 25 25 11 44 6 24 0 0.0 0 0 Assiga old town 25 25 6 24 8 32 0 0.0 0 0 Idomi 25 25 14 56 7 28 0 0.0 0 0 Agoi Ekpo 25 25 5 20 2 8 0 0.0 0 Total 150 150 52 35 38 25 1 0.6 0 0 Table 3: Prevalence of urinary schistosomiasis among children in six selected schools in Biase LGA before and after the implementation of the integrated control strategies Prevalence be fore implementation of Prevalence after implementation integrated control strategies of strategies integrated control -------------------------------------------------------- ---------------------------------------------- No. of individuals examined M F M F --------------------------------------- -------------------- ------------------ ------------------ ------------------ Location of school M F No. % No. % No. % No. % Ugbem 25 25 14 56 9 36 0 0 0 0 Iwuru 25 25 19 76 14 56 0 0 0 0 Agwagwune 25 25 7 28 11 44 0 0 0 0 Abini 25 25 20 80 7 28 0 0 0 0 Adim 25 25 22 88 15 60 0 0 0 0 Akparavuni 25 25 9 36 12 48 0 0 0 0 Total 150 150 52 35 38 25 0 0 0 0 The intensity of urinary schistosomiasis calculated as mean ova load reduced drastically after the implementation of the integrated control strategies from the initial 197 mean ova/10 ml of urine to 12 mean ova/10 ml of urine in the two Local Government Areas (Table 1). The t-test analysis of the results using the SPSS statistical software indicated a significant difference in the prevalence rates before and after implementation of the integrated control strategies. There was also a significant difference in infection intensity rates amongst the pupils before and after implementation of the integrated control strategies (p<0.05). The only pupil that tested positive in Lekpanko was not treated, since he was absent from school when his class had treatment (Table 1). DISCUSSION Previous studies have established the endemicity of urinary schistosomiasis in parts of Cross River State (Ekanem et al., 1995; Ejezie et al., 1991; Useh and Ejezie, 1996; Etim et al., 1998, 1999, 2012; Okon et al., 2007, 2009) but without deliberate efforts at evaluating available interventions. However, Okon et al. (2010) evaluated the status of urinary schistosomiasis in Ogoja Local Government Area, Cross River State, Nigeria, further treated infected persons with artesunate and found 64% cure rate while Inyang-Etoh et al. (2008) recorded a cure rate of 88.6% also in their study in Nigeria using artesunate and praziquantel combination. 62

The present study further re-evaluated the status of urinary schistosomiasis in Biase and Yakurr Local Government Areas of Cross River State with the view of applying integrated control strategies to eradicate the infection. The prevalence rate of infection reported for the two Local Government Areas before the implementation of the control strategies were 231 (38.5%) out of the 600 pupils examined while intensity was 197 mean ova per 10 ml. This result is in consonance with previous reports in these areas as mentioned by earlier investigators. Two years after the implementation of the integrated control strategies in the two Local Government Areas, the prevalence rate reduced to 1 (0.17%) while the intensity similarly reduced to 12 mean ova per 10 ml. The integrated control strategies utilized included chemotherapy using praziquantel, health education and provision of safe water sources. Chemotherapy with praziquantel currently offers the most feasible means of controlling human schistosomiasis, at least in the short term (WHO., 2002). Most of the schools in Yakurr and Biase Local Government Areas implemented the UNICEF free open defecation programme, hence there were improved toilet and hand washing facilities in the schools. This encouraged the pupils towards improved sanitary practices which reduced the contamination of available freshwater which were sources of transmission of schistosomiasis. It is very likely that the dramatic reduction in prevalence and intensity of urinary schistosomiasis recorded in these communities is a result of the integrated health interventions introduced two years ago. The benefits of applying mass chemotherapy on a large scale in various endemic populations have been proven scientifically (WHO., 2006; Morris, 2010). Praziquantel is safe and easy to use and it is low cost. The concerns about promoting resistance to Praziquantel by large scale chemotherapy appear to be remote (Utzinger et al., 2009; Webster et al., 2008). Chemotherapy with Praziquantel is the mainstay for the control of the disease in the short term (Useh, 2013). However, there have been recent worries of the emergence of resistance in Senegal following a report of the low cure rates of 18-38% of S. mansoni infections (Danso-Appiah and de Vlas, 2002). In the long term, the most cost-effective and sustainable means of controlling endemic infectious disease is through the use of vaccination. From literature, there is great hope in the discovery of schistosome vaccine. This lies in the Sh28GST which has already undergone successful Phase 1 and 2 human trials without adverse side effects (Capron et al., 2002). Health education and health promotion have also proven to be veritable tools in Schistosoma control particularly when combined with mass chemotherapy programmes. The results of this study are in consonance with results of a study done in Poyang Lake area China to examine the short-term effects of health education and health promotion in the control of schistosomiasis and to monitor the long-term impact on re-infection patterns (Hu et al., 2005). In general, the approach of emphasizing health education and health promotion in combination with chemotherapy was highly successful in reducing prevalence and intensity in the two Local Government Areas of Cross River State, Nigeria. REFERENCES Abdullahi, M.K., S.E. Bassey and T.I. Oyeyi, 2011. The epidemiology of Schistosoma haematobium infections in the 44 local Government of Kano State, Nigeria. Niger. J. Parasitol., 32: 19-24. Amazigo, U.O., C.I. Anago-Amanze and J.C. Okeibunor, 1997. Urinary schistosomiasis among school children in Nigeria: Consequences of indigenous beliefs and water contact activities. J. Biosocial Sci., 29: 9-18. 63

Capron, A., M. Capron and G. Riveau, 2002. Vaccine development against schistosomiasis from concepts to clinical trials. Br. Med. Bull., 62: 139-148. Danso-Appiah, A. and S.J. de Vlas, 2002. Interpreting low praziquantel cure rates of Schistosoma mansoni infections in Senegal. Trends Parasitol., 18: 125-129. Ejezie, G.C., I.E. Uko and E.I. Braide, 1991. Schistosomiasis in Cross River State, Nigeria: 1. Prevalence and intensity of infection in Adim, Akamkpa Local Government Area. J. Hyg. Epidemiol. Microbiol. Immunol., 35: 141-147. Ekanem, E.E., G.C. Ejezie, A.A. Asindi and O.E. Antia-Obong, 1995. Urinary symptoms and blood pressure of children with Schistosoma haematobium infection in South-Eastern Nigeria. East Afr. Med. J., 72: 486-489. Ekpo, U.F. and C.F. Mafiana, 2004. Epidemiological studies of urinary schistosomiasis in Ogun State, Nigeria: Identification of high-risk communities. Nig. J. Parasitol., 25: 111-119. Etim, S.E., E.I. Braide and P.A. Akpan, 1999. Incidence of urinary schistosomiasis in Biase Area of Cross River State. Int. J. Trop. Environ., 1: 243-252. Etim, S.E., E.I. Braide, N. Umeche and P.A. Akpan, 1998. The epidemiology of urinary schistosomiasis in Biase Area, Cross River State and its implications for control. Niger. J. Parasitol., 19: 77-83. Etim, S.E., O.E. Okon, E.E. Oku, G.I. Ukpong, M.E. Ohioma and C.E. Uttah, 2012. Urinary schistosomiasis in a rice-farming community in Biase Area of Cross River State. Niger. J. Parasitol., 33: 197-201. Hu, G.H., J. Hu, K.Y. Song, D.D. Lin and J. Zhang et al., 2005. The role of health education and health promotion in the control of schistosomiasis: Experiences from a 12-year intervention study in the Poyang Lake area. Acta Trop., 96: 232-241. Inyang-Etoh, P.C., G.C. Ejezie, M.F. Useh and E.C. Inyang-Etoh, 2008. Efficacy of a combination of praziquantel and artesunate in the treatment of Urinary Schistosomiasis in Nigeria. Trans. R. Soc. Trop. Med. Hyg., 103: 38-44. Morris, K., 2010. Time to overcome the neglect of neglected tropical diseases. Lancet Infect. Dis., 10: 820-821. NSCP., 1996. Update on schistosomiasis control in Nigeria. National Schistosomiasis Control Programme, Vol. 1, No. 3, Federal Ministry of Health, Nigeria. NSCP., 1999. Update on schistosomiasis control in Nigeria. National Schistosomiasis Control Programme, Vol. 3, No. 1, Federal Ministry of Health, Nigeria. Okon, O.E., M.F. Udoutun, E.E. Oku, A.I. Nta, S.E. Etim, J.T. Abraham and P.A. Akpan, 2007. Prevalence of urinary schistosomiasis in Abini Community, Biase Local Government Area, Cross River State, Nigeria. Niger. J. Parasitol., 28: 28-31. Okon, O.E., A. Ememayom and K. Opara, 2009. Reliability of self-reported blood in urine for diagnosis of Schistosoma haematobium in a community in South-Eastern Nigeria. Internet J. Epidemiol., Vol. 7, No. 2. Okon, O.E., A. Obi and K. Opara, 2010. The efficacy of artesunate in the treatment of urinary schistosomiasis in Ogoja, Cross River State, Nigeria. Internet J. Trop. Med., Vol. 6, No. 2. Useh, M.F. and G.C. Ejezie, 1996. Prevalence and morbidity of Schistosoma haematobium infection in Adim community of Nigeria. Niger. J. Med. Lab. Sci., 5: 17-28. Useh, M.F., 2013. Parasitic diseases-schistosomiasis. Creative Commons Attribution License, Geneva, Switzerland, pp: 82-83. 64

Utzinger, J., G. Raso, S. Brooker, D. De Savigny and M. Tanner et al., 2009. Schistosomiasis and neglected tropical diseases: Towards integrated and sustainable control and a word of caution. Parasitology, 136: 1859-1874. WHO., 1985. The control of schistosomiasis. Report of the WHO Expert Committee, Technical Report Series No 728, World Health Organization, Geneva, Switzerland, pp: 86. WHO., 2002. Prevention and control of schistosomiasis and soil transmitted helminthiasis. World Technical Report Series No. 912, World Health Organization, Geneva. WHO., 2006. Preventive Chemotherapy in human Helminthiasis: Coordinated use of Antihelminthic Drugs in Control Interventions: A Manual for Health Professionals and Programme Managers. WHO Press, Geneva, Switzerland, pp: 1-74. WHO., 2012. World health organization fact sheet on schistosomiasis. World Health Organization, Geneva, Switzerland. Webster, J.P., C.M. Gower and A.J. Norton, 2008. Evolutionary concepts in predicting and evaluating the impact of mass chemotherapy schistosomiasis control programmes on parasites and their hosts. Evol. Applic., 1: 66-83. 65