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A Multidisciplinary Analysis of over 53,000 Fascioliasis Patients Along the 1995-2019 Countrywide Spread in Vietnam Defines a New Epidemiological Baseline for One Health Approaches

Abstract

Fascioliasis, only foodborne trematodiasis of worldwide distribution, is caused by and , liver flukes transmitted by freshwater snails. Southern and southeastern Asia is an emerging hot spot of , despite its hitherto less involvement in human infection. In Vietnam, increasing cases have been reported since 1995, whereas only sixteen throughout 1800-1994. A database was created to include epidemiological data of fascioliasis patients from the 63 Vietnam provinces throughout 1995-2019. Case profiles were based on serology, symptoms, eosinophilia, imaging techniques, stool egg finding, and post-specific-treatment recovery. Radio broadcasting about symptoms and costless diagnosis/treatment led patients to hospitals after symptom onset. Yearly case numbers were modelled and spatio-temporally analyzed. Missing data and confounders were assessed. The countrywide spread has no precedent. It started in the central coast, including 53,109 patients, mostly adults and females. Seasonality, linked to vegetable consumption, peaks in June, although the intensity of this peak differs according to relief/climatic zones. Incidence data and logistic regression curves are obtained for the first time in human fascioliasis. Fasciolid hybrids accompanying the spreading flukes, and climate change assessed by risk index correlations, are both ruled out as outbreak causes. Human-guided movements of livestock from an original area prove to be the way used by fasciolids and lymnaeid vectors to expand geographically. , a highly efficient transmitting and colonizing vector, played a decisive role in the spread. The use of irrigated crop fields, widely inhabited by , for livestock grazing facilitated the transmission and spread of the disease. General physician awareness and diagnostic capacity improvement proved the successful impact of such knowledge transfer in facilitating and increasing patient infection detection. Information, education and communication to the public by radio broadcasting demonstrated to be very helpful. is able to cause epidemic and endemic situations similar to . The magnitude of the human outbreak in Vietnam is a health wake-up call for southern and southeastern countries of Asia which present the highest human population densities with increasing food demands, uncontrolled livestock inter-country exchange, foreign import practices, and monsoon's increasing climate change impact.

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References
1.
Nguyen T, Dermauw V, Dahma H, Bui D, Le T, Phi N . Prevalence and risk factors associated with Clonorchis sinensis infections in rural communities in northern Vietnam. PLoS Negl Trop Dis. 2020; 14(8):e0008483. PMC: 7425981. DOI: 10.1371/journal.pntd.0008483. View

2.
Arjona R, Riancho J, Aguado J, Salesa R, Gonzalez-Macias J . Fascioliasis in developed countries: a review of classic and aberrant forms of the disease. Medicine (Baltimore). 1995; 74(1):13-23. DOI: 10.1097/00005792-199501000-00002. View

3.
Nguyen S, Nguyen D, Van Nguyen T, Huynh V, LE D, Fukuda Y . Prevalence of Fasciola in cattle and of its intermediate host Lymnaea snails in central Vietnam. Trop Anim Health Prod. 2012; 44(8):1847-53. DOI: 10.1007/s11250-012-0147-8. View

4.
Le T, De N, Agatsuma T, Blair D, Vercruysse J, Dorny P . Molecular confirmation that Fasciola gigantica can undertake aberrant migrations in human hosts. J Clin Microbiol. 2006; 45(2):648-50. PMC: 1829072. DOI: 10.1128/JCM.01151-06. View

5.
Bargues M, Artigas P, Angles R, Osca D, Duran P, Buchon P . Genetic uniformity, geographical spread and anthropogenic habitat modifications of lymnaeid vectors found in a One Health initiative in the highest human fascioliasis hyperendemic of the Bolivian Altiplano. Parasit Vectors. 2020; 13(1):171. PMC: 7137187. DOI: 10.1186/s13071-020-04045-x. View