Intestinal parasitoses among under-fives in two communities in Ethiopia

Similar documents
Schistosomiasis mansoni and geo-helminthiasis in school children in the Dembia plains, Northwest Ethiopia

Intestinal parasitism among students in three localities in South Wello, Ethiopia

INTESTINAL PARASITISM AMONG JIREN ELEMENTARY AND JUNIOR SECONDARY SCHOOL STUDENTS IN SOUTH-WESTERN ETmOPIA

Soil-Transmitted Helminth Infections and Schistosomiasis mansoni in School Children from Chilga District, Northwest Ethiopia

Citation 熱帯医学 Tropical medicine 37(2). p73-7

Schistosomiasis mansoni and soil-transmitted helminthiasis in Bushulo village, southern Ethiopia

Prevalence of intestinal parasites among primary school children in Makurdi, Benue State- Nigeria

Research Article Cross-Sectional Study on the Prevalence of Intestinal Parasites and Associated Risk Factors in Teda Health Centre, Northwest Ethiopia

Intestinal parasitosis among Kara and Kwego semipastoralist tribes in lower Omo Valley, Southwestern Ethiopia

THE HELMINTHIC AND PROTOZOAL INFESTATIONS IN A RURAL POPULATION OF NORTHERN NIGERIA

Prevalence of intestinal parasites in three localities in Gaza Governorates Palestine

Aschalew Gelaw 1*, Belay Anagaw 1, Bethel Nigussie 2, Betrearon Silesh 3, Atnad Yirga 4, Meseret Alem 4, Mengistu Endris 1 and Baye Gelaw 1

Prevalence of Intestinal Parasites among Schoolchildren in a Coastal Rural Area of Maragondon, Cavite, Southern Luzon, Philippines

Intestinal parasitic infections and malnutrition amongst first-cycle primary schoolchildren in Adama, Ethiopia

Intestinal parasitic infections among under-five children and maternal awareness about the infections in Shesha Kekele, Wondo Genet, Southern Ethiopia

Intestinal Parasitic Infection and Associated Factors among Food Handlers in South Ethiopia: A Case of Wolaita Sodo Town

Intestinal Parasitism In Rural And Urban Areas Of North Central Nigeria: An Update

Prevalence of Intestinal Parasitic Infections in a Tertiary Care Hospital in Northern India: Five year retrospective study

PARASITE CONCENTRATOR FOR THE LABORATORY DIAGNOSIS OF INTESTINAL PARASITISM

INTESTINAL POLYPARASITISM IN A RURAL KENYAN COMMUNITY

PREVALENCE AND PREDICTORS OF INTESTINAL HELMINTHIASIS AMONG SCHOOL CHILDREN IN JIMMA ZONE; A CROSS-SECTIONAL STUDY

Epidemiology of soil-transmitted helminths, Schistosoma mansoni, and haematocrit values among schoolchildren in Ethiopia

Some epidemiological aspects of intestinal parasites in women workers before going abroad

Anaemia and Intestinal Parasitic Infections Among School Age Children in Behera Governorate, Egypt

Indian Journal of Basic and Applied Medical Research; September 2014: Vol.-3, Issue- 4, P

INTESTINAL PARASITOSES IN THE KANDY AREA, SRI LANKA

Journal of Tropical Diseases

CHAPTER VI CONCLUSION AND RECOMMENDATIONS

INTESTINAL PARASITES, ANAEMIA AND MALNUTRITION AMONG SCHOOL PUPILS (5-12) YEARS IN OHAFIA LOCAL GOVERNMENT AREA OF ABIA STATE, NIGERIA.

Prevalence of Soil Transmitted Helminth Infections in a Tertiary Institution in Western Nigeria

The Prevalence and Intensity of Soil-Tra nsmitted Helminthiasis Amng Pre~school Children in Orang Asli Resettlement Villages in Kelantan

JMSCR Vol 06 Issue 04 Page April 2018

Prevalence of Intestinal Parasitic Infection and Associated Factors among Pediatric Patients at Shenen Gibe Hospital, Ethiopia

INCIDENCE OF NEMATODE INFECTIONS AMONG THE CHILDREN BROUGHT TO ICDDR, B HOSPITAL, DHAKA, BANGLADESH

Intestinal Parasitic Infestation among the Outdoor Patients of Dhaka University Medical Centre, Bangladesh

INTESTINAL HELMINTH INFECTIONS AMONG CHILDREN OF DISTRICT SHOPIAN OF KASHMIR VALLEY, INDIA

Study of Intestinal Protozoan Parasites in Rural Inhabitants of Mazandaran Province, Northern Iran

Parasitology Questions. Choose the best correct answer in the following statements

INTESTINAL PARASITES IN SCHOOL-AGED CHILDREN IN VILLAGES BORDERING TONLE SAP LAKE, CAMBODIA

Parasitic helminthes infection and anemia among growing children in Nandurbar District, Maharashtra

The Prevalence of Intestinal Parasitic Infections in a Tertiary Care Hospital in Southern India - A Retrospective Study

1. Parasitology Protozoa 4

Prevalence of Intestinal Protozoan among Students Visiting Wollega University Students Clinic

Prevalence of intestinal parasites at tertiary teaching Hospital, BRIMS, Bidar

Prevalence of intestinal parasitic infections among highland and lowland dwellers in Gamo area, South Ethiopia

BRITISH BIOMEDICAL BULLETIN

COMPREHENSIVE STOOL ANALYSIS

A study of the incidence of intestinal helminthic diseases and their risk factors among school Children in Lumame town, Northwest, Ethiopia

Prevalence of Intestinal Helminths and Associated Risk Factors in Rural School-Children in Were-Abaye Sub District, Tigray Region, Northern Ethiopia

Catalog # OKDA00123 SUMMARY AND EXPLANATION

Intestinal parasitic infection and nutritional status among school children in Angolela, Ethiopia

Comparison of Formol-Ether, Direct Smear and Nigrosine Methylene Blue for the Diagnosis of Human Intestinal Parasites

Overview IMPORTANCE CLASSIFICATION SPECIMEN COLLECTION PROTOZOA WORMS BLOOD PARASITES ARTHROPODS DELUSIONAL PARASITOSIS QUIZZES GROSS

Brief Survey of Common Intestinal Parasites in the Tokyo Metropolitan Area. Tsukasa NOZAKI1), Kouichi NAGAKURA2)*, Hisae FUSEGAWA3)

HIV and Parasitic Infection and the Effect of Treatment among Adult Outpatients in Malawi

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

Recent Diagnostic Methods for Intestinal Parasitic Infections

Prevalence of intestinal parasites in rural Southern Indians

INTESTINAL HELMINTHIC INFECTIONS IN SCHOOLCHILDREN IN CAMBODIA

Journal of Family Medicine and Health Care

ENTERIC PARASITIC INFECTIONS AMONG SCHOOL CHILDREN AT RUPANDEHI, NEPAL

THE PREVALENCE OF MALNUTRITION AND GEO-HELMINTH INFECTIONS AMONG PRIMARY SCHOOLCHILDREN IN RURAL KELANTAN

JMSCR Vol 05 Issue 06 Page June 2017

Gut parasites in general practice

EDO UNIVERSITY IYAMHO

Intestinal Parasites of Man in Agusan Del Norte, Philippines with Emphasis on Schistosomiasis and Capillariasis

PREVALENCE AND DISTRIBUTION OF INTESTINAL AND BLOOD PARASITES AMONG IBANS IN THE NANGA ATOIIN THE SECOND DIVISION IN SARAWAK.

Intestinal parasitic infection in adult patients attending tertiary care hospitals: a retrospective study

HUMAN PARASITOLOGY. lumbricoides, Trichuris trichiura, hookworm. Human Parasitology (Code: ) Guideline

Prevalence of parasitic helminthes in stools of children aged 4-12 years in Ahaba Imenyi community of Abia state Nigeria.

Prevalence of Some Selected Soil Transmitted Helminthes Infections among Patients (Children) In Nekemte Hospital Oromia, Region, Western Ethiopia.

Community control of Ascaris lumbricoides in rural Oyo State, Nigeria: mass, targeted and selective treatment with levamisole

Journal of Biology, Agriculture and Healthcare ISSN (Paper) ISSN X (Online) Vol.3, No.19, 2013

Influence of human demographic Characteristics on Soil Transmitted Helminthiasis in Nsukka zone, Enugu State, Nigeria

Sanitary survey of residential areas using Ascaris lumbricoides ova as indicators of environmental hygiene, Jimma, Ethiopia

Detecting Parasites Loads in Urine Diversion Toilets.

PARASITE MRS. OHOUD S.ALHUMAIDAN

International Journal of Integrative sciences, Innovation and Technology

Comparative Evaluation of Three Stool Concentration Techniques in the Diagnosis of Intestinal Parasitic Infections

Detection and Prevalence Intestinal Parasites in Patients in Abeokuta, South-western, Nigeria

REVIEW OF LITEATURE. 3.1 Global situation

HEALTH POLICY AND PLANNING; 13(4): 423^432 ß Oxford University Press 1998

EVALUATION OF PROTOZOAN PARASITES CAUSING DIARRHOEA IN HIV POSITIVE PATIENTS

SOIL-TRANSMITTED HELMINTHIASIS AMONG INDIAN PRIMARY SCHOOL CHILDREN IN SELANGOR, MALAYSIA

Prevalence and speciation of hookworm in Plateau State, Nigeria

IV. AN EPIDEMIOLOGIC SURVEY IN YAMANASHI PREFECTURE, HONSHU, JAPAN INTRODUCTION

A Study on the Intestinal Parasitic Infections among Elementary School Students at a District (Silvana) In Urmia, West Azerbaijan

SOIL-TRANSMITTED HELMINTHS IN CHILDREN WITH CLINICAL SYMPTOMS OF INFECTION

PARASITIC INFECTIONS AMONG ORANG ASLI (ABORIGINE) IN THE CAMERON HIGHLANDS, MALAYSIA

Faculty and Department: Faculty of Science and Technology, Biomedical Sciences. Status: Option, BSc Biomedical Sciences, Westminster elective module

Prevalence of Intestinal Parasites in Medical Diagnostic Laboratories, Zahedan University of Medical Sciences-Iran

Introduction to Parasitic Helminths

PREVALENCE OF SOIL TRANSMITTED HELMINTHS IN SCHOOL CHILDREN IN THE FEDERAL TERRITORY OF MALAYSIA

Prevalence and Intensity of Soil-Transmitted Helminths Among School-Aged Children in Sigmo Primary School, Jimma Zone, South-Western Ethiopia

Diarrhea and Intestinal Parasites among HIV Infected Patients in Baringo, Kenya

Assessment of the prevalence of intestinal parasitosis and associated risk factors among primary school children in Chencha town, Southern Ethiopia

SOME BEHAVIOURAL RISK FACTORS FOR INTESTINAL HELMINTHIASIS IN NURSERY AND PRIMARY SCHOOL CHILDREN IN ENUGU, SOUTH EASTERN NIGERIA

PREVALENCE OF PARASITIC INFECTIONS AMONG PRIMARY SCHOOL CHILDREN IN BANGALORE

Anemia and hypoalbuminia as an adjunct to soiltransmitted helminthiasis among slum school children in

Transcription:

Intestinal parasitoses among under-fives in two communities in Ethiopia Hailu Birrie *, Fekade Balcha, Fekadu Abebe Abstract: The prevalence of intestinal parasites was studied among under-fives from two communities: Metehara Sugar Estate, central Ethiopia, and Jigga town, northwest Ethiopia. In the former, 89% of the children were infected with one or more of 11 species of parasites while in the latter 82% were infected with one or more of 12 species. In Jigga town, Ascaris lumbricoides (67%) and hookworms (53%) were the dominant parasites while in the Metehara Sugar Estate A. lumbricoides and Schistosoma mansoni were the dominant ones. Overall, the mean number of parasite species per infected child in Jigga town was 2.6 and was significantly higher than that in Metehara which was 1.5 (P<0.05). The possible factors responsible for the differences between the two communities, the possible adverse effects of the parasites on the nutritional and health status of the children and the actions that need to be taken are discussed. [Ethiop. J. Health Dev. 1998;12(1):63-67] Introduction In Ethiopia, malnutrition and mortality among children below five years of age (under-fives) are estimated to reach 61% and 159 per 1000, respectively (1). Although the causes of these may be many and varied the role played by intestinal parasites is expected to be significant. Evidence is steadily accumulating to show that intestinal infection with intestinal protozoa (2, 3) and helminths (4, 5) can impair nutrition and growth of children, particularly when the socioeconomic status is low (6). It is hence recommended to give high priority to de-worming programmes in areas where mild to moderate underweight exceeds 25% and where parasites are widespread, especially among the vulnerable under-fives (7). Previous studies of intestinal parasitoses in Ethiopia have focused mainly on school children (8-11). To our knowledge, only Seyoum Taticheff et al. (12) studied parasitoses among kindergarten children in Addis Ababa and reported that over 70% of the children harboured one of the 12 parasites encountered. This shows that the Ethiopian under-fives among whom malnutrition and mortality are both very high have not received due attention in the study of intestinal parasites, including schistosomiasis. The most probable reason for this neglect could be due to the fact that it is very difficult to obtain faecal samples from very young children. Much attention need to be focused on children less than five years old as this age group is considered to be particularly vulnerable (13). The objective of this study was to determine the prevalence and burden of intestinal parasites, especially schistosomiasis, among under fives living in different socioecological environments. Such information may help health workers consider intestinal parasites in the differential diagnosis of childhood malnutrition and morbidity. From the Institute of Pathobiology, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia * Methods Study areas: Two different ecological and socio-cultural settings were selected. Both areas are endemic for intestinal schistosomiasis. a) Jigga town - It is a semi-urban setting with a population of a little over 5000 in 1984 (14). It is

located at a distance of 375 km northeast of Addis Ababa at an altitude of 1800 meters above sea level (m.a.s.l.). The prevalence of schistosomiasis mansoni reaches 81% among school children (15). The source of transmission is a gently flowing stream very close to the town. Although there are few communal stand pipes in the town, due to the inadequacy of water supply, people use the stream water for almost all purposes (16). Sanitary facilities are also a lot less than desired (14). b) Chore Camp. Metehara Sugar Estate - Metehara is an irrigation setting with a population of over 30,000 (16). It is located at a distance of 190km southeast of Addis Ababa at an altitude of 1000 m.a.s.l. The overall prevalence of schistosomiasis mansoni reached 40% in the population in 1994 (17). The source of transmission are mainly drainage canals bypassing plantation camps. Although there are communal stand pipes providing underground water, the population continues to use canal water due to the hardness of the under ground water and also in fear of fluorosis which is highly prevalent in the area. The Turkish type of toilet system installed in 1965 by the Dutch Sugar Company has completely dilapidated and as a result open defecation is extremely ubiquitous in the vicinities of homes. Chore Camp is one of the 11 plantation camps of the Sugar Estate and it has a population of about 2000 people (local information). Stool Examination: In both places, trained field assistants went from house to house to identify households with under-fives, distribute screw-capped vials pre-filled with 6ml of 10% formalin and trained consenting mothers on how to collect the faecal matters of their under-fives and preserve them in the vials provided. All mothers were shown a piece of pebble to indicate to them how much faeces they should put in the vial for each child. In case of more than one under-five per household, instruction was given to mothers to keep the vials separately with identifying marks. On the next day field assistants went back to the households and collected the vials from mothers with age and sex information of each child. Some mothers returned vials without faeces giving a number of reasons, such as the faeces of their under- fives being too watery to handle. The specimens were transported to the laboratory in Addis where they were processed and examined by the formol-ether-concentration technique (18). Statistical analysis: Prevalence, were computed by species of parasites. Parasite load was estimated from the mean number of parasite species diagnosed per infected child. Differential statistics were analyzed using Chi-square test. Result Jigga Town: The number of under-fives examined constituted about 5% of the population. The species and prevalence of intestinal parasites are presented in Table 1 while the level of polyparasitism is given in Table 2. Twelve species of parasites (eight helminths and four protozoa) were encountered, the prevalence of Ascaris lumbricoides, Hookworm infection, Trichuris trichiura, Strongyloides stercolaris, Schistosoma mansoni and Hymenolepis nana reaching 67%, 53%, 23%, 16% and 10%, respectively (Table 1). Two percent of the children also harboured Taenia saginata. The prevalence of Entamoeba coli, E. histolytica, Giargia lambila and Iodamoeba butschelii cysts reached 19%, 12% and 6%, respectively (Table 1). Table 1: Prevalence of intestinal parasites among under-fives in two communities in Ethiopia, 1993. Infection status Percent positive Jigga (n=241) Metehara (n=106) Schistosoma mansoni 16 29 Ascaris lumbricoides 67 40 Trichuris trichiura 37 12 Hookworm sp. 53 7 Strongloides stercolaris 23 5 Hymenolepis nana 10 17 Taenia saginata 2 2 Enterobius vermicularis 0.4 0 Entamoeba histolytica 12 9 Entamoeba coli 19 14 Giardia lamblia 12 8 Iodamoeba butschelii 6 5

Parasite free 11 18 Only 11% of the children were parasite free, ie. 89% of them were infected by one or more of the 12 parasites encountered. Of the infected children, the majority harboured 2-4 parasites at the same time, the minimum and maximum being 1 parasite (17%) and 6 or more (2.5%), respectively, (Table 2). Overall, the mean number of parasite species per infected child was 2.6 (Table 1). Chore Camp, Metehara Sugar Estate: The number of under-fives examined constituted about 4%. The species and prevalence of intestinal parasites are presented in Table 1 while the level of polyparasitism is given in Table 2. Table 2: Polyparasitism among the under-fives (helminths and protozoa cysts combined) by locality, 1993. parasite load Jigga (N=241) Metehara (N=106) No. % No. % 0 Parasite 26 26 18 18 1 Parasite species 40 40 33 33 2 Parasite species 50 50 34 34 3 Parasite species 49 49 8 8 4 Parasite species 52 52 6 6 5 Parasite species 18 18 6 6 6 or more species 6 6 1 1 Mean* 2.6 2.6 1.5 - Total 241 241 106 100 Here, 11 species of intestinal parasites (seven helminths and four protozoa) were encountered among the under-fives, the prevalence reaching 40%, 29%, 17% and 5% for A. lumbricoides, S. mansoni, H. nana, T. trichiura, hookworm/sp and S. stercolaris, respectively (Table 1). E. vermicularis was not encountered while cases of T. saginata were found among 2% of the underfives here too. The prevalence of E. histolytica, G. lamblia and I. butschelii cysts was 14%, 9%, 8% and 5%, respectively (Table 1). Here, 18% the children were parasite free indicating that 82% of the children were infected with one or the other of the 11 intestinal parasites encountered. Of the infected children, the majority harboured 1-2 parasites at the same time, the maximum being five or more parasite (1%) (Table 2). Overall, here the parasite load was 1.5 parasite spices per infected child (Table 1). The difference between Jigga and Metehara in the mean number of parasite species per infected child was significant (P<0.05). Discussion Our finding of 11 and 12 species of intestinal parasites among under-fives in Metehara and Jigga town respectively is in conformity with previous reports in Ethiopia (8-10, 12) which showed that children are infected with a plethora of intestinal parasites. In Ghana also, 11 species of parasites have been reported among pre-school children (19). This indicates the abundance of intestinal parasites in the domestic and peri-domestic environments of young children in developing countries where water supply and sanitation are either inadequate or absent. Intestinal parasites especially Ascaris is highly prevalent among under-fives in both socioecological environments. However, children in Jigga town, representing a stream ecology and an intermediate elevation are more significantly infected with both helminths and protozoa than their counterparts in Metehara, representing an irrigation ecology and a relatively low elevation. The prevalence of A. lumbricoides (67%), hookworm infection (53%) and S. stercolaris (23%) in Jigga town are extremely high by all standards. For A. lumbricoides the corresponding worm burden is dangerously high when the prevalence exceeds 60% (20). Given the high prevalence of polyparasites, infection with four parasite species at the same time reaching 21.6% in Jigga town, the adverse health effects imposed on the under-fives at the crucial stage of their development should be of much concern. The high prevalence of hookworm infection especially in Jigga and schistosomiasis mansoni especially in Metehara are of even more concern since both are known to cause severe anaemia in Children (21). It is not surprising to find low prevalence of Enterobius vermicularis since the appropriate technique, the Scotch Tape method, for detection of the parasite was not used. Also, there could have been under estimation of the prevalence of protozoan parasites and Strongyloides because the

method used does not pick trophozoites and is relatively less sensitive for the latter. However, it is of interest to observe cases of Taenia saginata (2% in each community) among under-fives. The age of these children ranged from 3-4 years and were perhaps exposed to inadequately cooked food. Both ascariasis and schistosomiasis are health problems of under-fives in both Jigga town and Chore Camp (Metehara). However in Jigga town, representing a stream ecology and an intermediate elevation, children are infested with more parasite species at the same time than their counterparts in Metehara, representing an irrigation ecology and a low elevation. The differences in the prevalence of polyparasitism especially in hookworm infection, strongyloidiasis and hymenolepiasis may be related to a number of factors ranging from altitudinal factors, soil types to familial and household characteristics, the educational and economic standing of parents. Metehara is a semi-arid environment which may does not favour the transmission of hookworms and Strongyloides which have similar life cycle. Also, more children at Metehara may be wearing shoes that has protected them against hookworm infection. On the other hand perhaps because of the perennial drainage canals bypassing irrigation villages which encourages human-water contact and contamination the transmission of intestinal schistosomiasis appears to be more favoured in Metehara. The key question is how do so young children who cannot swim or play in the infective waters get the infection in both Jigga and Metehara. Are they infected at home through bathing or do the relatively older children accompany their mothers who do laundry in the infective water bodies and thereby get the chance of infection while paddling in the shallow section of the water bodies? In either cases, there is too much parasitoses among the under-fives and this calls for urgent action. Perhaps it is necessary to integrate health education of mothers and d-worming of children with MCH and EPI programmes if this nation has to do justice to the most vulnerable group which constitutes over 18.5% the population (1). Ethiopia is one of the countries where there is high prevalence of moderate to severe stunting and mortality rates among the 24-59 mothers of age (7). Considering the adverse health and nutritional effects by these parasites high priority needs to be given to the de-worming programme. References 1. Central statistical Abstracts. Addis Ababa. 1984. 2. World Health Organization. Intestinal protozoa and helminthic infections WHO Tech Rep Ser No. 666. World Health Organization. Geneva. 1981. 3. Gupta MC. Ascariasis and malnutrition in children: Studies in India and Guatemala. In: Ascariasis and its Public Health Significance (ed. D.W.T Croupton, M.C. Nesheim and Z.S. pacolowski). London and Basingstoke: Taylor & Francis Ltd. 1985. 4. Willett WC, Kilama WL and Kihamia CM. Ascaris and growth rates: a randomized trial of treatment. Am J Public Hlth 1979;69:987-91. 5. Stephenson LS, crompton DWT et al. Relationship between Ascaris infection and growth of malnourished preschool children in Kenya. Am J Clinical Nuta 1980;33:1165-72. 6. Cere BJ, Rohde JE and Soesanto T. Ascaris and malnutrition in a Balinese village: a conditional relationship. Trop Geogr Med 1981;33:367-73. 7. Tomkins A and Watson F. Malnutrition and infection: a Review. New York 1989. 8. Aklilu L, Mesfin D and Bahita M. Parasitological survey of Addis Ababa and Debre Zeit Schoolchildren, with emphasis on bilharziasis Ethiop Med J 1968;6:61-71. 9. Freij L. Observations on parasitic and bacterial infections of the intestine among paediatric out patients in Addis Ababa. Ethiop Med J 1973;11:13-24. 10. McConnel E and Armstrong JC. Intestinal parasitism in fifty communities on the central plateau of Ethiopia. Ethiop Med J 1976;14:159-168. 11. De Carneri I, Di Matteo L and Shibru T. A comparison of helminth infections in urban and rural areas of Addis Ababa. Trans Roy Soc Med Hyg 1992;86:000-000. 12. Siyoum T, Yaya A and Fisseha HM. Intestinal parasitic infections in pre-school children in

Addis Ababa. Ethiop Med J 1981;19:35-40. 13. Hall A. Intestinal parasitic worms and the growth of children. Trans Roy Soc Trop Med Hyg. 1993;87:241-242. 14. Fekadu A, Teklemariam A and Hailu B. The epidemiology of schistosomiasis mansoni in Jigga town, northwestern Ethiopia. IPB Research Report No. 2:14-28. 15. Hailu B. Progress Report No. 4. Expanded programme for Research and Training Towards the Control of Schistosomiasis in Ethiopia. Institute of Pathobiology, Addis Ababa University 1986;78pp. 16. Kloos H, Fekadu A, Teklemariam A, Hailu B and Fekade S. The impact of water supply and environmental control measures on human water contact patterns. Rivisita di parasitologia 1991;8:155-160. 17. Hailu B, Teklemariam A, Shibru T and Fekadu A. Transmission of schisotosomiasis in Ethiopia. Epidemiological aspect. Ethiop J Hlth Dev 1992;7:63-69. 18. Ritchie LS. An ether sedimentation technique for routine stool examination. Bull US Army Med Dept 1948;8:326-329. 19. Annon A, Crompton DWT, Walters DE and Arnold SE. An investigation of the prevalence of intestinal parasites in pre-school children in Ghana. Parasitology 1986;92:209-217. 20. Guyatt HL, Bundy DAP, Medley GF and Grenfell BT. The relationship between the frequency distribution of Ascaris lumbricoides and the prevalence and intensity of infection in human communities. Parasitology 1990; 101: 139-143. 21. Stephensen LS. Helminth parasites, a major factor in malnutrition. World Hlth Forum 1994;15:169-172.