Department of Microbiology, International American University, Vieux Fort, Saint Lucia. Abstract

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J Vector Borne Dis 47, December 2010, pp. 228 234 Epidemiology and control of Schistosomiasis and other intestinal parasitic infections among school children in three rural villages of south Saint Lucia Rajini Kurup & Gurdip S. Hunjan Department of Microbiology, International American University, Vieux Fort, Saint Lucia Abstract Objective: The purpose of this study was to determine the epidemiology of parasitic infections and the efficacy of treatment among school children in rural villages of south Saint Lucia. Method: A total of 554 school children participated in this study. Parasitic infections were confirmed by using Kato-Katz method. Results & conclusion: Overall, 61.6% of the school children were infected by any parasitic infection. The helminths identified were Ascaris lumbricoides (15.7%), Hookworm (11.9%), Strongyloides (9.7%), Trichuris trichiura (4.7%), Schistosoma mansoni (0.6%), Taenia solium (0.8%) and Enterobius vermicularis (2.1%), Entamoeba coli (9.7%), Iodameba butschlii (5%), Entamoeba histolytica (1.1%), Giardia lamblia (1.8%) and Endolimax nana (2.1%). The control intervention included treatment with albendazole 400 mg and praziquantel 40 mg/kg as well as awareness campaigns. Post-interventional assessment showed the total prevalence of intestinal parasitic infection reduced from 61.6 to 3.6% with a cure rate of 94.2%, following the control methods. Key words Control; cure rate; helminths; IPI; protozoan; risk factors; Saint Lucia; soil-transmitted helminths Introduction Intestinal protozoan and soil-transmitted helminths (STH) are major problems in health worldwide, especially in the tropical and sub-tropical regions 1. Intestinal parasitic infections are globally endemic and constitute greatest single worldwide cause of illness and disease 2,3. Schistosomiasis affects about 200 million people worldwide, and more than 650 million people live in endemic areas 4. The burden of disease caused by infection with schistosomiasis and soil-transmitted helminths (STH) remains enormous. About two billion people are affected worldwide, of whom 300 million suffer associated severe morbidity 5. Pan American Health Organization/World Health Organization estimates that 20 30% of those living in Latin America and the Caribbean are infected with one of several intestinal helminths and/or schistosomiasis. In the Caribbean, STH prevalence appears to be higher in certain countries, such as Guyana, Belize, and Jamaica whereas St. Lucia is the only country in the Caribbean Islands that is currently reporting schistosomiasis infection 6. In school age populations of developing countries, intestinal helminth infections rank first among the causes of communicable and noncommunicable diseases 7. Hygiene and play habits among male children especially make them vulnerable to schistosomiasis and STH infections. It is estimated that 400 million school-age children who are infected are often physically and intellectually compromised by anaemia, leading to attention deficits, learning disabilities, school absenteeism and higher

KURUP & HUNJAN: SCHISTOSOMIASIS & IPI AMONG SCHOOL CHILDREN IN ST. LUCIA 229 dropout rates 8. The development of effective parasite control is possible by regular periodic chemotherapy, using anti-helminthics to school-aged children delivered through the school system which can be the main intervention strategy 9,10. Unfortunately, there is no recent school based studies which provide information on the epidemiology of the parasitic infections in the Schistosoma endemic island of Saint Lucia. The present study, therefore, attempts to address this dearth of information and describes the prevalence, characteristics and control of schistosomiais and other intestinal parasitic infections among school children from three rural villages of south St. Lucia. Material & Methods Study site: Saint Lucia is a mountainous volcanic island in the eastern Caribbean Sea on the boundary with the Atlantic Ocean. The local climate is tropical, moderated by northeast trade winds, with a dry season from January to April and a rainy season from May to December. The population of Saint Lucia is of mostly African descent (82.5% of the population) with a significant mixed minority representing 11.9%, with Indo-Caribbean, small European origin minority. The total size of Saint Lucia is 620 km² with an estimated population of 160,000. The study was conducted in three rural villages Vigier, Bellvue and Grace located at south of Saint Lucia. At the time of survey Bellvue and Grace had one health center but no health center facility was present in Grace. Study design: The study populations were school children aged between 0 and 19 yr. All schools in the area participated in this study. Bellvue village has one secondary school and 2 day care centers, Grace has one secondary school and Vigier has one primary school. A total of 554 children attending the schools were examined. The objectives and method of the study were explained to the teachers and parents/guardians in a series of meetings and full informed consent was obtained. Stool samples of all students were screened for intestinal parasitic infection using Kato-Katz method and parasep concentration method. Treatment: At the end of the epidemiological survey, participants found infected with S. mansoni were treated with praziquantel single oral dose of 40 mg/kg. Individuals infected with other intestinal parasitic infections were treated with a single dose of albendazole (400 mg). To analyze the efficacy of treatment, stool samples from positive cases were tested after four months post-treatment. Treatment of infected children was administered by the nurses under supervision of District Medical Officer. Data collection Stool sample collection and laboratory testing: The school children were given the same day two dry, clean, leak proof containers labeled with their name, age and identification number. Parents/guardians were also instructed to deposit one fecal sample per day of the participant into each container and return immediately to the nearby collection center. The school children participating in the study and their parents/guardians were guided on how to collect the sample during the parents meeting. Presence of infection (prevalence) and assessment of eggs per gram of feces (intensity) were determined by analyzing two samples of stool using Kato-Katz technique 11. Slides were examined within 45 min of slide preparation to avoid clearing of hookworm eggs. Helminth s ova counts were made using the standard smear egg count technique, and the results were expressed as eggs per gram feces (epg). Statistical analysis: Data collected were analyzed using SPSS 9.0 version. Tests included analysis of variance, the chi-squared test, cross-tabulation and logistic regression analysis to identify risk and protective factors associated with parasitic infections. A significant level of 0.05 was adopted for all tests. Ethical considerations: The study was approved by the Ethics Committee of the Institute International

230 J VECTOR BORNE DIS 47, DECEMBER 2010 American University and the local health authorities of St. Lucia. The school teachers obtained written consent from parents or legal guardians on behalf of their children for participation in the study. The stool test positive children were also provided with anti-parasitic treatment, albendazole and/ or praziquantel under consultation of a physician free of cost. Results All selected 554 school children participated in the study with a response rate of 100%. The study started in April 2006 with a sampling period of six months. The study had participation of 49.5% girls and 50.5% boys. The total prevalence of children infected with parasitic infection was 61.6%, the prevalence of helminths infection was 45.6% and protozoan infection was 19.8%. The parasites found were: Ascaris lumbricoides (15.7%), hookworm (11.9%), Strongyloides stercoralis (9.7%), Trichuris trichiura (4.7%), Enterobius vermicularis (2.1%), Taenia solium (0.8%), Schistosoma mansoni (0.6%), Entamoeba coli (9.7%), Iodamoeba butschlii (5%), Endolimax nana (2.1%), Giardia lamblia (1.8%) and Entamoeba histolytica (1.1%). Table 1 shows the helminths and protozoan infections found within the male and female cohorts and within different age groups. Total intestinal parasites were more frequent in females (70.6%) than in males (60.1%) and females (51.9%) recorded more helminth infections than males (39.2%). Among the total infected cases, 17.3% of individuals harboured mixed infections. The most common combinations were infection with double helminths (9.3%) followed by double protozoans (5.3%). There were 282 subjects with single infection (50.9%), 56 with double infection (10.1%) and three with triple infection (0.5%). Egg intensity of helminths showed most cases with light infections. Ascaris had six cases of heavy infection and twelve cases of moderate infections. Hookworm showed six heavy and six moderate infections whereas Trichuris had only one heavy and five moderate infections. Only one moderate infection was recorded with Schistosoma mansoni. Table 2 shows analysis of demographic data and risk factor of parasitic infection that indicated an asso- Table 1. Prevalence and number of intestinal parasites in three rural villages in south St. Lucia by age groups and gender Parasite species Age group (yr) Male Female Total 0 4 5 9 10 14 15 19 Ascaris 1umbricoids 1 (3) 49 (16.7) 46 (16.5) 1 (10) 31 (10.1) 66 (21.3) 97 (15.7) Hookworm 36 (12.2) 35 (12.5) 2 (20) 37 (12.1) 36 (11.6) 73 (11.9) Strongyloides 30 (10.2) 27 (9.7) 3 (30.3) (10.5) 2 (9) (9.7) Enterobius vermicularis 8 (2.7) 5 (1.8) 6 (2) 7 (2.3) 13 (2.1) Trichuris trichiura 16 (5.4) 13 (4.7) 9 (2.9) 20 (6.5) 29 (4.7) Taenia solium 2 (0.7) 3 (1.1) 3 (1) 2 (0.6) 5 (0.8) Entamoeba coli 1 (3) 29 (9.9) 30 (10.8) 28 (9.2) 32 (10.3) 60 (9.7) Endolimax histolytica 3 (1) 4 (1.4) 3 (1) 4 (1.3) 7 (1.1) Endolimax nana 6 (2) 7 (2.5) 9 (2.9) 4 (1.3) 13 (2.1) Iodamoeba butschlii 13 (4.4) 17 (6.1) 1 (10) 20 (6.5) 11 (3.5) 31 (5) Schistosoma mansoni 2 (0.7) 2 (0.7) 2 (0.7) 2 (0.6) 4 (0.6) Giardia lamblia 3 (1) 8 (2.9) 4 (1.3) 7 (2.3) 11 (1.8) Figures in parentheses indicate percentages.

KURUP & HUNJAN: SCHISTOSOMIASIS & IPI AMONG SCHOOL CHILDREN IN ST. LUCIA 231 Table 2. Logistic regression analysis of parasite prevalence in three rural villages of south St. Lucia for factors associated with the infection Factors Chi-square df Sig Odds 95% CI ratio Upper Lower Wearing shoes Yes: No 28.8 1 0 3.18 2.08 4.85 Washing hands before meal Yes: No 68.5 1 0 6.06 3.96 90.29 Trim nails Yes: No 4.24 1 0.04 0.46 0.22 0.96 Recreation 11.51 3 0.01 Swimming in fresh water Yes: No 0.97 1 0.32 0.61 0.23 1.63 Fishing in fresh water Yes: No 0.16 1 0.68 0.84 0.36 1.96 Playing cricket bare feet Yes: No 10.9 1 0 0.48 0.31 0.74 Gender Male : Female 2.32 1 0.13 0.74 0.50 1.09 ciation between infection and risk factors. Children who do not wear shoes or those who do not wash their hand before having food showed high risk for acquiring parasitic infection. Treatment with albendazole and praziquantel resulted in a significant decrease in prevalence and intensity of infection after four months. The efficacy rate following treatment was determined from diagnosing the infected individual negative by using Kato-Katz method (94.2%, 321 of 341). Post-treatment of total infections showed no heavy or moderate levels of infections. Infection that persisted beyond treatment was Ascaris lumbricoides, Trichuris trichiura, Giardia lamblia and Strongyloides. Albendazole was effective with cure rate for Ascaris 96.9%, Trichuris 82.7%, Strongyloides 93.3% and Giardia lamblia 81.8% (Table 3). Discussion The study aimed to identify the prevalence and intensity of intestinal parasitic infections among school children and identify risk factors and role of pharmacological control of the infections in three rural villages of Saint Lucia. To date a systematic study on intestinal parasitic infection on school based control has not be done in the country and this study therefore focus on epidemiology of intestinal parasites as well as targets school based treatment in reducing the prevalence and intensity of intestinal parasites. More than half (61.6%) of the tested population had positive stool specimens, the majority only had a single parasite identified. Soil transmitted helminths were the most common intestinal parasites observed in the current study as seen in other parts of the world 12, 13. There are reports of high prevalence of three major intestinal helminths infections ascariasis, trichuriasis, and hookworm infection in the poorest areas of the Caribbean, particularly in the Dominican Republic, Haiti, and Jamaica, Barbados and Trinidad and Tobago as well as in other parts of the world 14, 15. Ascaris lumbricoides was the most common parasite in the given study. This could be because the infective stages of A. lumbricoides, the embryonated eggs have enormous capacity for withstanding the environmental extremes of urban environments 16. This study found older age group most heavily infected age group particularly with STH followed by the 5 9 yr age group. This increased prevalence could be due to the behavior of this particular age group. Children use to play in the environment and are more prone to exposure to contaminated soil, high level of soil contact activity and low personal hygiene in this age group. Similar finding is supported by a previous report from India 17. The prevalence rate of overall intestinal parasitic infection and helminthic infection in females (70.6 and 51.9%) was significantly higher than in males (60.1 and 39.2%). Other studies also revealed sex specific differences among para-

232 J VECTOR BORNE DIS 47, DECEMBER 2010 Table 3. Prevalence and intensity of parasitic infection within school children pre-treatment and four month post-treatment with albendazole and praziquantel Parasites Pre-treatment Post-treatment Cure rate Mean ERR (%) n (%) n (%) n (%) EPG Ascaris lumbricoides 97 (15.7) 3 (0.5) 94 (96.9) 5389 96 Hookworm 73 (11.9) 0 73 (100) 884 100 Strongyloides 60 (9.7) 4 (0.65) 56 (93.3) n.a. n.a. Trichuris trichiura 29 (4.7) 5 (0.8) 24 (82.8) 853 84 Enterobius vermicularis 13 (2.1) 0 13 (100) n.a. n.a Taenia solium 5 (0.8) 0 5 (100) n.a. n.a. Schistosoma mansoni 4 (0.6) 0 4 (100) 78 100 Entamoeba coli 60 (9.7) 0 60 (100) n.a. n.a. Entamoeba histolytica 7 (1.1) 0 7 (100) n.a. n.a. Endolimax nana 13 (2.1) 0 13 (100) n.a. n.a. Iodamoeba butschlii 31 (5) 0 31 (100) n.a. n.a. Giardia lamblia 11 (1.8) 2 (0.3) 9 (81.8) n.a. n.a. sitic infections 18. Male children were more infected than female children with Hookworm and Strongyloides as examined in other studies 19, 20. High rates of Hookworm after Ascaris infection in this study agrees with similar studies done in similar climatic conditions of tropics of Paraguay and Peru as well as in parts of Central America and in Surinam 14,21, 22. Strongyloidiasis was recorded as third high infection rate in this study is endemic in Latin America and Caribbean, with no estimates of their regional prevalence 23. Though the rate of Schistosoma mansoni infection was low in children with only one moderate case but if not treated could act as a potential infective pool for rest of the community. There are reports that almost 4400 cases of Schistosoma mansoni occur in Guadeloupe, and transmission still occurs in Saint Lucia and Antigua and Barbuda 24. Among Protozoan infection E. coli and I. butschlii were the most common intestinal protozoa among the study population were as Giardia was the common pathogenic protozoa. Both can be transmitted orally by drinking infected water and both are environmental contaminants of the water supply. There are reports of Giardia and E. coli being the most common protozoan in the western part of Turkey 25. Analysis of risk factors was evaluated based on the presence of infection. Infection rate was significantly higher in children who do not wear shoes, who do not wash hand before having food, who do not trim their nails and those who play cricket bare foot at ground 26. This current study showed successful effort to control intestinal parasitic infection, focusing the school age population. In several Asian and Latin American countries, there has been a dramatic decrease in prevalence rates, largely because of national control activities together with social and economic development 27. Treatment of infected children (albendazole 400 mg and praziquantel, according to body weight), health education campaigns using fliers and power point presentations as recommended by WHO 28, 29, during parent teacher meeting has showed high cure rates. Conclusion This study has identified prevalence and intensity of

KURUP & HUNJAN: SCHISTOSOMIASIS & IPI AMONG SCHOOL CHILDREN IN ST. LUCIA 233 intestinal parasitic infection among school children in rural St. Lucia. The control program by treatment and health education was a good demonstration of treating infected school children and creating awareness among them. Acknowledgement We are grateful to the school children, parents, principal, teachers and other staffs of the schools participated. Ministry of Health, Ministry of Environment Health and Ministry of Education of St. Lucia provided all the needed cooperation to conduct this project. We thank District Medical Officer of Vieux Fort for the support in the project. We also thank the nurses of Vieux Fort for their participation during distribution of medication of infected school children, St. Jude hospital for providing laboratory facility and PAHO for providing Kato-Katz kits. References 1. Savioli L, Bundy DAP, Tomkins A. Intestinal parasitic infections: a soluble public health problem. Trans R Soc Trop Med Hyg 1992; 86: 353 4. 2. Bethony J, Brooker S, Albonico M, Geiger SM, Loukas A, et al. Soil-transmitted helminth infections: ascariasis, trichuriasis, and hookworm. Lancet 2006; 367: 1521 32. 3. Curtale F, Pezzotti P, Sharbini AL, al Maadat H, Ingrosso P, et al. Knowledge, perceptions and behaviour of mothers toward intestinal helminths in Upper Egypt: implications for control. Health Policy Plan 1998; 13: 423 32. 4. Programmes and projects. Schistosomiasis: a major public health problem. Geneva: World Health Organization 2009. 5. Savioli L, Stansfield S, Bundy DA, Mitchell A, Bhatia, et al. Schistosomiasis and soil-transmitted helminth infections: forging control efforts. Trans R Soc Trop Med Hyg 2002; 96: 577 9. 6. Control of soil-transmitted helminth infections in the English- and French-speaking Caribbean: towards world health assembly resolution. Kingston, Jamaica: PAHO 2007; p. 54.19. 7. Prevention and control of schistosomiasis and soil-transmitted helminthiasis. WHO Tech Rep Ser No. 912. Geneva: World Health Organization 2002. 8. Control of schistosomiasis and soil-transmitted helminth infections. Report by the Secretariat. Executive Board 107th session. Provisional agenda item 3.3 (EB107/31). Geneva: World Health Organization 2001. 9. Awasthi S, Bundy DAP, Savioli L. Helminthic infections. British Med J 2003; 23: 431 3. 10. Hotez PJ, Bundy DAP, Beegle K, Brooker S, de Silva N, Montresor A, et al. Disease control priorities in developing countries: helminth infections. II edn. WHO, World Bank, NIH, Oxford University Press 2005. 11. Katz N, Chaves A, Pelligrino J. A simple device for quantitative stool thick-smear technique in Schistosomiasis mansoni. Revue Instituto Medicina Tropical 1972; 14: 817 20. 12. Escobedo A. A, Cañete R, Núñez FA. Prevalence, Risk Factors and Clinical Features Associated with Intestinal Parasitic Infections in Children from San Juan y Martínez, Pinar del Río, Cuba. West Indian Med J 2008; 57(4): 378. 13. Abolfath SA, Alaghehbandan R, Akhlaghi L, Shahi M, Rasregar AL. Prevalence of intestinal parasites in a population in south of Tehran, Iran. Rev Inst Med Trop S Paulo 2008; 50(3): 145 9. 14. De Silva NR, Brooker S, Hotez PJ, Montresor A, Engels D, et al. Soil-transmitted helminth infections: updating the global picture. Trends Parasitol 2003; 19: 547 51. 15. Peter J. Hotez, Maria Elena Bottazzi, Carlos Franco- Paredes, Steven K. Ault, and Mirta Roses Periago. The Neglected Tropical Diseases of Latin America and the Caribbean: A Review of Disease Burden and Distribution and a Roadmap for Control and Elimination. PLoS Negl Trop Dis 2008; 2(9): e300. 16. Hotez PJ, da Silva N, Brooker S, Bethony J. Soil-transmitted helminth infections: the nature, causes and burden of the condition. Working Paper No. 3: Disease Control Priority Project. Behesda, Manyland: Fogarty International Centre, National Institute 2003. 17. Naish S, McCarthy J, Williams GM. Prevalence, intensity and risk factors for soil-transmitted helminth infection in a South Indian fishing village. Acta Trop 2004; 91: 177 87. 18. Okay P, Ertug S, Gultekin B, Onen O, Beser E. Intestinal parasites prevalence and related factors in school children, a western city sample -Turkey. BMC Public Health, 2004; 4: 64. 19. Albonico M, Crompton DW, Savioli L. Control strategies for human intestinal nematode infections. Adv Parasitol 1999; 42: 277 341. 20. Odikamnoro OO, Ikeh IM. Prevalence of common intestinal nematode infection among primary School children

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