Impact of Different Sampling Schemes for Decision Making in Soil-Transmitted Helminthiasis Control Programs

Author:

Coffeng Luc E1,Malizia Veronica1,Vegvari Carolin2,Cools Piet3,Halliday Katherine E4,Levecke Bruno3,Mekonnen Zeleke5,Gichuki Paul M6,Sayasone Somphou7,Sarkar Rajiv8,Shaali Ame9,Vlaminck Johnny3,Anderson Roy M2,de Vlas Sake J1

Affiliation:

1. Department of Public Health, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands

2. London Centre for Neglected Tropical Disease Research, Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom

3. Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Belgium

4. Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, United Kingdom

5. Jimma University Institute of Health, Jimma University, Jimma, Ethiopia

6. Eastern and Southern Africa Centre of International Parasite Control, Kenya Medical Research Institute, Nairobi, Kenya

7. Lao Tropical and Public Health Institute, Ministry of Health, Vientiane, Lao People’s Democratic Republic

8. Division of Gastrointestinal Sciences, Christian Medical College, Vellore, Tamil Nadu, India

9. Laboratory Division, Public Health Laboratory-Ivo de Carneri, Chake Chake, United Republic of Tanzania

Abstract

Abstract Starting and stopping preventive chemotherapy (PC) for soil-transmitted helminthiasis is typically based on the prevalence of infection as measured by Kato-Katz (KK) fecal smears. Kato-Katz-based egg counts can vary highly over repeated stool samples and smears. Consequentially, the sensitivity of KK-based surveys depends on the number of stool samples per person and the number of smears per sample. Given finite resources, collecting multiple samples and/or smears means screening fewer individuals, thereby lowering the statistical precision of prevalence estimates. Using population-level data from various epidemiological settings, we assessed the performance of different sampling schemes executed within the confines of the same budget. We recommend the use of single-slide KK for determining prevalence of moderate-to-heavy intensity infection and policy decisions for starting and continuing PC; more sensitive sampling schemes may be required for policy decisions involving stopping PC. Our findings highlight that guidelines should include specific guidance on sampling schemes.

Funder

Bill and Melinda Gates Foundation

Dutch Research Council

NWO

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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