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Implications for selecting persistent hot spots of schistosomiasis from community- and school-based surveys in Blue Nile, North Kordofan, and Sennar States, Sudan

  • Hassan Ahmed Hassan Ahmed Ismail (Communicable and Non-Communicable Diseases Control Directorate, Federal Ministry of Health) ;
  • Seungman Cha (Department of Global Development and Entrepreneurship, Graduate School of Global Development and Entrepreneurship, Handong Global University) ;
  • Yan Jin (Department of Microbiology, Dongguk University College of Medicine) ;
  • Sung-Tae Hong (Department of Tropical Medicine and Parasitology, Seoul National University College of Medicine)
  • Received : 2023.02.16
  • Accepted : 2023.04.28
  • Published : 2023.05.31

Abstract

In several schistosomiasis-endemic countries, the prevalence has remained high in some areas owing to reinfection despite repeated mass drug administration (MDA) interventions; these areas are referred to as persistent hot spots. Identifying hotspots is critical for interrupting transmission. This study aimed to determine an effective means of identifying persistent hot spots. First, we investigated the differences between Schistosoma haematobium and Schistosoma mansoni prevalence among school-aged children (SAC) estimated by a community-based survey, for which local key informants purposively selected communities, and a randomly sampled school-based survey. A total of 6,225 individuals residing in 60 villages in 8 districts of North Kordofan, Blue Nile, or Sennar States, Sudan participated in a community-based survey in March 2018. Additionally, the data of 3,959 students attending 71 schools in the same 8 districts were extracted from a nationwide school-based survey conducted in January 2017. The community-based survey identified 3 districts wherein the prevalence of S. haematobium or S. mansoni infection among SAC was significantly higher than that determined by the randomly sampled school survey (e.g., S. haematobium in the Sennar district: 10.8% vs. 1.1%, P<0.001). At the state level, the prevalence of schistosomiasis among SAC, as determined by the community-based survey, was consistently significantly higher than that determined by the school-based survey. Purposeful selection of villages or schools based on a history of MDA, latrine coverage, open defecation, and the prevalence of bloody urine improved the ability for identifying persistent hot spots.

Keywords

Acknowledgement

This project was funded by the Korea International Cooperation Agency (KOICA, P-2015-00145). The funder had no role in the study design, data collection, and analysis, decision to publish, or preparation of the manuscript. The authors thank the project team members for their efforts and contributions to controlling neglected tropical diseases in Sudan. They extend their appreciation to community members, the Ministries of Heath of 18 states, and the Federal Ministry of Health, Sudan. Special thanks go to Dr. Nahid Abdelgadir, International Health Directorate Project Management Unit, the Federal Ministry of Health, Sudan, and also to Mr. Dae Seong Cho, the field manager of the SUKO project.

References

  1. Sang HC, Muchiri G, Ombok M, Odiere MR, Mwinzi PN. Schistosoma haematobium hotspots in south Nyanza, western Kenya: prevalence, distribution and co-endemicity with Schistosoma mansoni and soil-transmitted helminths. Parasit Vectors 2014;7:125. https://doi.org/10.1186/1756-3305-7-125 
  2. Zou L, Ruan S. Schistosomiasis transmission and control in China. Acta Trop 2015;143:51-57. https://doi.org/10.1016/j.actatropica.2014.12.004 
  3. Pennance T, Person B, Muhsin MA, Khamis AN, Muhsin J, et al. Urogenital schistosomiasis transmission on Unguja Island, Zanzibar: characterisation of persistent hot-spots. Parasit Vectors 2016;9(1):646. https://doi.org/10.1186/s13071-016-1847-0 
  4. World Health Organization. Ending the Neglect to Attain the Sustainable Development Goals a Road Map for Neglected Tropical Diseases 2021-2030. World Health Organization. Geneva, Switzerland. 2021. 
  5. FMOH. The Sudan National Neglected Tropical Diseases (NTDs) Strategic Plan 2021-2025. Khartum, Sudan. Federal Ministry of Health. 2021. 
  6. Cha S, Elhag MS, Lee YH, Cho DS, Ismail HAHA, et al. Epidemiological findings and policy implications from the nationwide schistosomiasis and intestinal helminthiasis survey in Sudan. Parasit Vectors 2019;12(1):429. https://doi.org/10.1186/s13071-019-3689-z 
  7. Cha S, Jin Y, Elhag MS, Kim Y, Ismail HAHA. Unequal geographic distribution of water and sanitation at the household and school level in Sudan. PLoS One 2021;16(10):e0258418. https://doi.org/10.1371/journal.pone.0258418 
  8. Pelletreau S, Nyaku M, Dembele M. Sarr B, Budge P, et al. The field testing of a novel integrated mapping protocol for neglected tropical disease. PLoS Negl Trop Dis 2011;5(11):e1380. https://doi.org/10.1371/journal.pntd.0001380 
  9. Finn TP, Stewart BT, Reid HL, Petty N, Sabasio A, et al. Integrated rapid mapping of neglected tropical diseases in three States of South Sudan: survey findings and treatment needs. PLoS One 2012;7(12):e52789. https://doi.org/10.1371/journal.pone.0052789 
  10. Andrade-Pacheco R, Rerolle F, Lemoine J, Hernandez L, Meite A, et al. Finding hotspots: development of an adaptive spatial sampling approach. Sci Rep 2020;10(1):10939. https://doi.org/10.1038/s41598-020-67666-3 
  11. Giardina F, Coffeng LE, Farrell SH, Vegvari C, Werkman M, et al. Sampling strategies for monitoring and evaluation of morbidity targets for soil-transmitted helminths. PLoS Negl Trop Dis 2019;13(6):e0007514. https://doi.org/10.1371/journal.pntd.0007514 
  12. World Health Organization. Preventive chemotherapy in human helminthiasis. World Health Organization. Geneva, Switzerland. 2006, pp 40-41. 
  13. Rudge JW, Stothard JR, Basanez MG, Mgeni AF, Khamis IS, et al. Micro-epidemiology of urinary schistosomiasis in Zanzibar: Local risk factors associated with distribution of infections among schoolchildren and relevance for control. Acta Trop 2008;105(1):45-54. https://doi.org/10.1016/j.actatropica.2007.09.006 
  14. Clennon JA, Mungai PL, Muchiri EM, King CH, Kitron U. Spatial and temporal variations in local transmission of Schistosoma haematobium in Msambweni, Kenya. Am J Trop Med Hyg 2006;75(6):1034-1041.  https://doi.org/10.4269/ajtmh.2006.75.1034
  15. Pennance T, Person B, Muhsin MA, Khamis AN, Muhsin J, et al. Urogenital schistosomiasis transmission on Unguja Island, Zanzibar: characterisation of persistent hot-spots. Parasit Vectors 2016;9(1):646. https://doi.org/10.1186/s13071-016-1847-0 
  16. Rollinson D, Knopp S, Levitz S, Stothard JR, Tchuem Tchuente LA, et al. Time to set the agenda for schistosomiasis elimination. Acta Trop 2013;128(2):423-440. https://doi.org/10.1016/j.actatropica.2012.04.013 
  17. KOICA. Project Design Document of the Schistosomiasis Elimination along the Nile-river in Sudan with Empowered People project. Internation Cooperation Agency. Seongnam, Korea. 2020. 
  18. Jin Y, Lee YH, Cha S, Choi IU, Ismail HAHA, et al. Transmission dynamics of schistosoma haematobium among school-aged children: a cohort study on prevalence, reinfection and incidence after mass drug administration in the White Nile State of Sudan. Int J Environ Res Public Health 2021;18(21):11537. https://doi.org/10.3390/ijerph182111537 
  19. Cha S, Hong ST, Lee JS, Jeong HG, Kwon IS, et al. Comparison of the change in the prevalence and intensity of Schistosoma haematobium infection between high and low prevalence areas of White Nile State, Sudan. Korean J Parasitol 2020;58(4):421-430. https://doi.org/10.3347/kjp.2020.58.4.421 
  20. Jin Y, Cha S, Lee J, Elhag MS, Hong ST, et al. Parasitological observation in schoolchildren with urogenital schistosomiasis following treatment with three different brands of praziquantel. J Korean Med Sci 2020;30;35(46):e394. https://doi.org/10.3346/jkms.2020.35.e394