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Comparisons of schistosome and geohelminth infection prevalences in school-aged children from selected areas of Africa: implications for rapid assessment and combined control

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TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE (1999) 93,125-126

Comparisons

of schistosome

and

geohelminth

infection

prevalences

in

school-aged

children from selected

areas of Africa: implications

for rapid

assessment

and combined

control

S. Brooker I*, M. Booth’! and H. Guyatt’ ‘The

Wellcome Trust Centre for the Epidemiology of Infectious Disease, University of Oxford, South Parks Road, Oxford OX1 3PS, UK; ‘Department of Public Health and Epidemi-

ology, Swiss Tropical Institute, CH 4002, Base& Switzerland

Keywords: geohelminths, schistosomes, multiple species in- fections, school-aged children, prevalence, disease control, rapid assessment, Africa

School-based control programmes against schisto- some and geohelminth infections have been identified as a highly cost-effective public health strategy (SAVIOLI

et al., 1997). The cost-effectiveness of this approach is said to be maximized by combining control of both types of infection, using 2 drugs: praziquantel and a benzimi- dazole derivative. Preliminary analyses (BUNDY et al.,

199 1) demonstrated that the geographical distributions of geohelminth and schistosome infections overlap suffi- ciently at the national level to warrant consideration of combined control of both types of infection. However, since infections of schistosomes and geohelminths are unevenly distributed within countries, such an approach will be cost-effective only when the 2 types of infection are endemic in the same communities. The benefits from combined control will be further determined by the ability to identify target communities for treatment using rapid assessment methods. A questionnaire-based meth- od exists for Schistosoma haematobium (LENGELER et al.,

1992), and there is increasing evidence that a similar approach may be possible for S. mansoni (HAILU et al.,

1995; BOOTH et al., 1998). Unfortunatelv, no comoar- able approach exists for tl-e geohelminths; and parasito- logical screening remains the only option, though it is expensive and time-consuming. If the prevalence of schistosome infection could be used to predict the prevalence of geohelminth infection this would improve the efficiency of targeted control programmes.

In an effort to investigate this issue, an exhaustive search was made of all nublished orevalence survevs undertaken among school-aged populations in East Africa (Kenva. Tanzania. Ethionia and Uganda) and West Afxica’(coasta1 countries of Carnero&, Nigeria, Ghana, C&e d’Ivoire, Liberia, and Sierra Leone). These countries were selected because there exist extensive data and they represent different ecological zones of Africa. Data were derived from computerized literature searches of MEDLINE and CAR Health databases using key- words relevant to helminth species infection, scrutiny of appropriate journals taken by the London School of Hygiene and Tropical Medicine and Oxford University, and with the help of colleagues in Africa. The search included only cross-sectional studies that had an ade- quate sample size (n > 30), with the present analysis including surveys which reported data on schistosome and geohelminth prevalence. Non-parametric Spear- man’s rank analysis was used to test the significance of

associations between the different snecies. Significance was tested at the 5% level.

The search located 42 publications with data on the prevalence of schistosomes and geohelminths in school- aged children, covering 139 sites in East Africa and 98 sites in West Africa. Relationshins between the nreva- lences of S. mansoniand S. haemahbium and each of the 3 main geohelminth infections (Ascaris lumbricoides, Tri- churis trichiura and hookworms) in East and West Africa are shown in the Figure. In many areas the prevalence of schistosome infection was extremely low, and commu- nities with high prevalence were restricted to a limited number of foci. Nonetheless, the data demonstrate clearly that the distribution of schistosome infection is largely independent of the distribution of each geohel- minth species in the study countries. A similar pattern was observed even when the analvsis was undertaken for each country separately. In accordance with previous work (BOOTH & BUNDY. 1992). the analvses also showed a highly significant association between A.

lumbricoides and T. trichiura prevalences (P < 0.0001) (data not shown), but here the relationship was demon- strated clearly for school-aged children. No significant relationship was observed between the prevalences of S. haematobium and S. mansoni infections in West Africa (data not shown).

Overall, these results suggest that schistosome and geohelminth infections are independently distributed within countries where they are both endemic. It follows that the prevalence of S. haematobium or S. mansoni infections cannot be used to predict the prevalence of geohehninth infections, and vice versa. Reported gastro- intestinal symptoms also appear not to be associated with geohelminth infections (BOOTH et al., 1998), confirming that parasitological screening, which adds obvious costs to any programme, is still necessary for estimating community prevalences of geohelminth infection. The results also reduce the prospects for a single strategy aimed at the combined control ofboth schistosomes and geohelminths on a national scale. Our observations therefore suggest that a more refined approach to com- bined control is required, whereby target communities are identified separately for intervention against schisto- somes and geohelminths and drugs are distributed according to local needs.

Acknowledgements

S.B. is in receipt ofa Wellcome Trust Prize Studentship. M.B. was supported by a Wellcome Trust Travelling Research Fellowship. H.G. is in receipt of a Wellcome Trust Research Career Development Fellowship.

References

Booth, M. & Bundy, D. A. P. (1992). Comparative prevalences of Ascati lumbricoides, Tri~huti trichiura, and hookworm infections and the prospects for control. Parasitology, 105,

151-157.

Booth, M., Mayombana, C. & Kilima, P. (1998). The popula- tion biology and epidemiology of schistosome and geohel- minth infections among schoolchildren in Tanzania.

Transactions of the Royal Society of Tropical Medicine and Hvpiene. 92.491-495.

Bun&, D A: P., Chandiwana, S. K., Homeida, M. M. A., Yoon, S. & Mott, K. E. (199 1). The epidemiological implica- tions of a multiple-infection approach to the control ofhuman helminth infections. Transactions of the Royal Society of

Tropical Medicine and Hygiene, 85,274-276.

Hailu, M., Jemaneh, L. & Kebede, D. (1995). The use of questionnaires for the identification of communities at risk for intestinal schistosomiasis in western Gojam. Ethiopian Med- icalJournal,33, 103-l 13.

Lengeler, C., Sala-Diakanda, D. M. & Tanner, M. (1992). Using questionnaires through an existing administrative system: a new approach to health interview surveys. Interna- tibnalJourna1 of Epidemiology, 20, 796-807.

Savioli, L., Renganathan, E., Montresor, A., Davis, A. & Behbehani, K. (1997). Control of schistosomiasis-a global picture. Parasitology Today, 13,444-448.

*Address for correspondence: e-mail simon.brooker@zoo.ox.ac.uk

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126 S. BROOKXR ETAL.

West Africa

‘.t-

East Africa

(a>

100

i

-._-___..

-__-.__-.-

.

.

*

8-l

.

. l .

Prevalence of Ascaris

b 0 a, 40 60 SO 100 0 20 40 60 80 100 s

Prevalence of Trichuris

100 1 q 1 0 0 20 40 60 so 100

cc>

100 - ,,. l . . . Bo : . . 60 -t . . . . l * 0 20 40 60 SO 100

Prevalence of hookworm

Figure. Comparative prevalences of Schistosoma mansoni and S. haematobium with Ascatti lumbrdcoides (a), Trichuris trichiura (b) and hookworm (c) in East and West Africa. (e) S. mansoni; (0) S. haemarobium. The reference list for the data sources is available from the authors.

Received 28 October 1998; revised 16 Februay 1999; accepted for publication 23 Februa y 1999

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