Table 3. Population attributable fractions of modifiable factors associated with tungiasis. Floor of sand or clay inside the house Common resting place outside house without elevated costs. For example, cementing the floors of those houses with sandy or clay floor in the community would reduce prevalence of tungiasis by almost 75%. In addition, this measure will reduce transmission on the long run without any additional costs for the next years. Similar, confining pigs to pigpens and explaining to community members the location of breeding sites and areas of high transmission would reduce considerably the prevalence in the community. As a spin-off, the discussed measures References Attributable risk % exposed among cases PAF 0,89 82.5 73.7 0,86 76.2 65.5 Regular use of footwear 0,66 77.4 51.1 Presence of pigs on compound 0,94 40.1 37.9 doi:10.1371/journal.pntd.0000087.t003 1. Heukelbach J, de Oliveira FA, Hesse G, Feldmeier H (2001) Tungiasis: a neglected health problem of poor communities. Trop Med Int Health 6: 267–272. 2. Ehrenberg JP, Ault SK (2005) Neglected diseases of neglected populations: thinking to reshape the determinants of health in Latin America and the Caribbean. BMC Public Health 5: 119. 3. Molyneux DH, Hotez PJ, Fenwick A (2005) ‘‘Rapid-impact interventions’’: how a policy of integrated control for Africa’s neglected tropical diseases could benefit the poor. PLoS Med 2: e336. 4. Franck S, Feldmeier H, Heukelbach J (2003) Tungiasis: more than an exotic nuisance. Travel Medicine and Infectious Disease 1: 159–166. 5. Heukelbach J (2005) Tungiasis. Revista do Instituto de Medicina Tropical de São Paulo 47: 307–313. 6. Feldmeier H, Heukelbach J, Eisele M, Sousa AQ, Barbosa LM, Carvalho CB (2002) Bacterial superinfection in human tungiasis. Trop Med Int Health 7: 559–564. 7. Joseph JK, Bazile J, Mutter J, Shin S, Ruddle A, Ivers L, Lyon E, Farmer P (2006) Tungiasis in rural Haiti: a community-based response. Trans R Soc Trop Med Hyg 100: 970–974. 8. Feldmeier H, Eisele M, Saboia-Moura RC, Heukelbach J (2003) Severe tungiasis in underprivileged communities: case series from Brazil. Emerg Infect Dis 9: 949–955. 9. Obengui (1989) La tungose et le tétanos au C.H.U. de Brazzaville. Dakar Med 34: 44–48. 10. Tonge BL (1989) Tetanus from chigger flea sores. J Trop Pediatr 35: 94. 11. Hoeppli R (1963) Early references to the occurrence of Tunga penetrans in Tropical Africa. Acta Trop 20: 143–152. 12. Njeumi F, Nsangou C, Ndjend AG, Koga, Ostanello F, Pampiglione S (2002) Tunga penetrans au Cameroun. Revue Méd Vét 153: 176–180. 13. Ugbomoiko US, Ofoezie IE, Heukelbach J (2007) Tungiasis: High prevalence, parasite load and morbidity in a rural community in Lagos State, Nigeria. Int J Dermatol 46: 475–481. 14. Heukelbach J, Wilcke T, Harms G, Feldmeier H (2005) Seasonal variation of tungiasis in an endemic community. Am J Trop Med Hyg 72: 145–149. 15. González A, de Villalobos C, Ranalletta MA, Coscarón MC (2004) Aspectos adaptativos y biológicos de Tunga penetrans (Linné 1758). Epidemiología en comunidades aborígenes del norte argentino. Arch Argent Dermatol 54: 119–123. 16. Muehlen M, Feldmeier H, Wilcke T, Winter B, Heukelbach J (2006) Identifying risk factors for tungiasis and heavy infestation in a resource-poor community in Northeast Brazil. Trans R Soc Trop Med Hyg 100: 371–380. 17. Heukelbach J, Wilcke T, Eisele M, Feldmeier H (2002) Ectopic localization of tungiasis. Am J Trop Med Hyg 67: 214–216. probably reduce also the transmission of other parasitic diseases, such as neurocysticercosis, ancylostomiasis and strongyloidiasis. In conclusion, the presence of tungiasis in the community is associated to an important extent with a set of a few modifiable variables. Effective and sustainable intervention measures addressing these factors need to be implemented in the study area, and in other communities throughout West Africa, to reduce the burden of this neglected tropical disease. An integrated approach combining the control of animal reservoirs, housing and environmental factors, and health education is necessary. Intervention measures need to be designed by an interdisciplinary team together with the affected communities. Acknowledgments We thank the Baales and Ajido Erekiti communities for supporting the study and Mr. Durotimi Ashade and Mr. Ola Avhose for skillful assistance. LA received a PhD scholarship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior–CAPES (Brazil). Author Contributions Tungiasis in Nigeria Conceived and designed the experiments: JH UU IEO. Performed the experiments: UU. Analyzed the data: JH UU LA. Contributed reagents/ materials/analysis tools: JH. Wrote the paper: JH UU IEO LA. 18. Eisele M, Heukelbach J, van Marck E, Mehlhorn H, Meckes O, Franck S, Feldmeier H (2003) Investigations on the biology, epidemiology, pathology and control of Tunga penetrans in Brazil: I. Natural history of tungiasis in man. Parasitol Res 90: 87–99. 19. Heukelbach J, Mencke N, Feldmeier H (2002) Editorial: Cutaneous larva migrans and tungiasis: the challenge to control zoonotic ectoparasitoses associated with poverty. Trop Med Int Health 7: 907–910. 20. Heukelbach J, Costa AM, Wilcke T, Mencke N, Feldmeier H (2004) The animal reservoir of Tunga penetrans in severely affected communities of north-east Brazil. Med Vet Entomol 18: 329–335. 21. Carvalho RW, Almeida AB, Barbosa-Silva SC, Amorim M, Ribeiro PC, Serra- Freire NM (2003) The patterns of tungiasis in Araruama township, state of Rio de Janeiro, Brazil. Mem Inst Oswaldo Cruz 98: 31–36. 22. Rietschel W (1989) Beobachtungen zum Sandfloh (Tunga penetrans) bei Mensch und Hund in Französisch-Guayana. Tierärztliche Praxis 17: 189–193. 23. Cooper JE (1976) Tunga penetrans infestation in pigs. Veterinary Records 98: 472. 24. Cooper JE (1967) An outbreak of Tunga penetrans in a pig herd. Veterinary Records 80: 365–366. 25. Verhulst A (1976) Tunga penetrans (Sarcopsylla penetrans) as a cause of agalactia in sows in the Republic of Zaire. Veterinary Records 98: 384. 26. Pampiglione S, Trentini M, Gentili FM, Mendes JLX, Pampiglione C, Rivasi F (1998) Tunga penetrans (Insecta: Siphonaptera) in pigs in São Tomé (Equatorial Africa): Epidemiological, clinical, morphological and histopathological aspects. Revue Élev Méd vét Pays trop 51: 201–205. 27. Heukelbach J, Costa AM, Wilcke T, Mencke N, Feldmeier H (2004) The animal reservoir of Tunga penetrans in severely affected communities of north-east Brazil. Med Vet Entomol 18: 329–335. 28. Muehlen M, Heukelbach J, Wilcke T, Winter B, Mehlhorn H, Feldmeier H (2003) Investigations on the biology, epidemiology, pathology and control of Tunga penetrans in Brazil II. Prevalence, parasite load and topographic distribution of lesions in the population of a traditional fishing village. Parasitol Res 90: 449–455. 29. Wilcke T, Heukelbach J, Cesar Saboia MR, Regina SK-P, Feldmeier H (2002) High prevalence of tungiasis in a poor neighbourhood in Fortaleza, Northeast Brazil. Acta Trop 83: 255–258. 30. Chadee DD (1998) Tungiasis among five communities in south-western Trinidad, West Indies. Ann Trop Med Parasitol 92: 107–113. 31. Arene FO (1984) The prevalence of sand flea (Tunga penetrans) among primary and post-primary school pupils in Choba area of the Niger Delta. Public Health 98: 282–283. 32. Ade-Serrano MA, Ejezie GC (1981) Prevalence of tungiasis in Oto-Ijanikin village, Badagry, Lagos State, Nigeria. Ann Trop Med Parasitol 75: 471–472. PLoS Neglected Tropical Diseases | www.plosntds.org 7 2007 | Volume 1 | Issue 3 | e87
Original Article Epidemiology and clinical aspects of tungiasis (sand flea infestation) in Alagoas State, Brazil Jorg Heukelbach, 1,2 Anne Jackson, 3 Liana Ariza, 4 Cláudia Maria Lins Calheiros, 5 Valquíria de Lima Soares, 5 and Hermann Feldmeier 3 1 Department of Community Health, School of Medicine, Federal University of Ceará, Fortaleza, Brazil; 2 School of Public Health, Tropical Medicine and Rehabilitation Sciences, James Cook University, Townsville, Australia; 3 Institute for Microbiology and Hygiene, Campus Benjamin Franklin, Charité – University of Medicine, Berlin, Germany; 4 Post-Graduation Program in Medical Sciences, School of Medicine, Federal University of Ceará, Fortaleza, Brazil; 5 Department of Pathology, Universidade de Ciências da Saúde de Alagoas (UNCISAL), Maceió, Brazil. Abstract Background: Tungiasis (infestation with the sand flea Tunga penetrans) is common in resource-poor populations throughout Brazil. However, the epidemiological situation and the clinical aspects are not fully understood. Methodology: To describe the prevalence and severity of tungiasis, associated pathology, as well as the seasonal variation in rural northeast Brazil, we performed two cross-sectional surveys: one in the rainy season, another in the dry season. Individuals were examined for the presence of tungiasis, number of lesions, symptoms and signs. In the rainy season, 88.6% (1,015/1,146), and in the dry season 91.1% (990/1,087) of the respective target populations were examined. Results: The prevalence of tungiasis was 21.6% (95% confidence interval: 19.0-24.1) in the rainy season and 29.5% (26.6-32.3) in the dry season (p
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UNIVERSIDADE FEDERAL DO CEARÁ FACU
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LIANA DE MOURA ARIZA UM NOVO MÉTOD
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RESUMO Introdução: Existe pouco c
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1 - INTRODUÇÃO 1.1 - TUNGÍASE A
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Após a penetração na epiderme, a
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1.2 - MÉTODOS EPIDEMIOLOGICOS RÁP
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1.4 - HIPÓTESE A presença de pelo
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comunidades. A presença destas, si
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