Schistosomiasis is a helminthiasis caused by schistosomes, which are digenetic trematodes belonging to the phylum Platyhelminthes [1]. The human disease is chiefly associated with Schistosoma haematobium, S. japonicum, and S. mansoni, with minor contributions from S. intercalatum and S. mekongi in some accounts [1][2]. Source-backed detail on species-specific clinical distinctions is not yet available in the provided material [2][1].
Disease Profile
ParasiticSchistosomiasis
血吸虫病
Schistosomiasis is a parasitic helminth infection caused by schistosomes, a group of digenetic trematode flatworms [1]. It remains a major global cause of morbidity, with nearly 800 million people at risk and more than 250 million estimated to be affected worldwide [2][3]. The sources describe substantial mortality and morbidity burden, with estimates of 280,000-500,000 deaths each year [2].
The provided sources note that schistosomiasis encompasses both acute and chronic disease, and that the condition carries a significant burden of morbidity [2]. They also indicate that immunopathology is an important aspect of the disease, but they do not specify the clinical syndrome, symptom pattern, or organ complications in the supplied excerpts [2]. Source-backed detail on timing, severity pattern, and specific complications is not yet available. The material does, however, emphasize that control programs have reduced schistosomiasis-associated morbidity where implemented [3].
Schistosomiasis is reported as endemic across tropical and subtropical settings, with infection occurring in 78 countries in one source and 76 countries in another [1][2]. The disease is described as affecting more than 200 million people in the cited scholarly metadata and more than 250 million globally in the PubMed abstract, indicating a large and persistent surveillance burden [1][2][3]. The sources also state that almost 800 million people worldwide are at risk [2]. No outbreak-specific pattern or reservoir ecology is described in the supplied snippets beyond the identification of human-infecting species [2][1].
Source-backed detail on the route of transmission is not yet available in the provided snippets. The material identifies schistosomiasis as a parasitic infection with clinically significant human species, but it does not state the exposure mechanism or environmental stage of acquisition [2][1].
The sources specifically identify school-aged children as the predominant target group in earlier WHO preventive chemotherapy recommendations, reflecting their importance in endemic control programmes [3]. The 2022 guidance broadened eligibility to all age groups 2 years and older in endemic settings, suggesting that risk is not confined to children [3]. Beyond this, source-backed detail on other high-risk groups is not yet available in the provided material.
The supplied sources emphasize preventive chemotherapy as the principal public-health control approach. WHO guidance is described as recommending mass drug administration with praziquantel, historically directed mainly to school-aged children in endemic settings and later expanded in 2022 to include all age groups 2 years and older, with a lower prevalence threshold and increased treatment frequency [3]. School-based and community-based preventive chemotherapy programmes are reported to have been scaled up and to have reduced morbidity [3].
In surveillance terms, schistosomiasis should be read as a high-burden helminth infection with a wide endemic footprint and substantial at-risk population [2][1]. The sources support attention to preventive chemotherapy coverage, age eligibility, and treatment frequency as key programmatic indicators because these measures are explicitly tied to morbidity reduction and updated WHO guidance [3]. Source-backed detail on case definitions, notification thresholds, or laboratory confirmation is not yet available in the provided material.
- 1 Schistosomiasis. Medical Parasitology. 1995. doi: 10.1093/oso/9780199633012.003.0010. DOI: https://doi.org/10.1093/oso/9780199633012.003.0010
- 2 LoVerde PT et al. Schistosomiasis. Adv Exp Med Biol. 2024. PMID: 39008264. doi: 10.1007/978-3-031-60121-7_3. PubMed: https://pubmed.ncbi.nlm.nih.gov/39008264/
- 3 Lo NC et al. Review of 2022 WHO guidelines on the control and elimination of schistosomiasis. Lancet Infect Dis. 2022 Nov. PMID: 35594896. doi: 10.1016/S1473-3099(22)00221-3. PubMed: https://pubmed.ncbi.nlm.nih.gov/35594896/
- 4 Stingl P et al. [Schistosomiasis]. MMW Fortschr Med. 2017 Sep. PMID: 29468512. doi: 10.1007/s15006-017-0067-7. PubMed: https://pubmed.ncbi.nlm.nih.gov/29468512/
- 5 Schistosomiasis Schistosomiasis. DGPI Handbuch. 2026. doi: 10.1055/f-0005-0087-b000000868. DOI: https://doi.org/10.1055/f-0005-0087-b000000868
- 6 Schistosomiasis. Environmental Health Engineering in the Tropics. 2018. doi: 10.4324/9781315883946-17. DOI: https://doi.org/10.4324/9781315883946-17
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Figure 1 | Full historical trajectories across all reporting countries.
Figure 2 | Year-over-year monthly comparison for seasonality and structural shifts.
Dataset Archive
Supplementary Data | Multi-country disease dataset
Machine-readable multi-country disease dataset (JSON/CSV) with source metadata.
Source Register
Official sources and update cadences used to construct the downloadable dataset.
Brazil
Brazil Ministry of Health DATASUS/SINAN public DBC microdata aggregated to national monthly notification counts.
Official sourceChina
Monthly notifiable infectious disease reports published by China CDC.
Official sourceChina
Official China public health bulletin and query portal.
Official sourceChina
Biomedical literature discovery feed used as supplementary context.
Official source