Housing Risk Factors of Four Tropical Neglected Diseases: A Brief Review of the Recent Literature
Abstract
:1. Introduction
2. Methods of the Literature Review
3. Results of the Literature Review concerning Housing Risk Factors of Four Tropical Neglected Diseases
3.1. Chagas Disease
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- Walls containing bajareque (mud and sticks), but not adobe, were a risk factor (OR = 1.9, 95% CI 1.2–3.9) as well as earthen floors (OR = 3.4, 95% CI 1.9–6.0) and tile roofs (OR = 1.9, 95% CI 1.1–3.3); on the contrary, cement or tile floors were protective (OR = 0.3, 95% CI 0.2–0.7) as well as cinder block walls.
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- Houses with unplastered walls had a 20.7 times greater risk of infestation (p < 0.001) than those with uncracked plastered walls; similarly houses with unplastered concrete or brick, or thatched roofs had a 7.2 times greater risk of infestation than houses with plastered roofs (p < 0.001).
3.2. Leishmaniasis
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- Houses without water supply (AOR = 6.0, 95% CI 2.7–13.1) in a study from an endemic area in Brazil [30].
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- Poor interior housing conditions (OR = 2.0, 95% CI 1.0–3.93), among other major risk factors such as chronic diseases in a study from south-eastern Iran [31].
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- Non-plastered brick walls (OR = 41.5, 95% CI 13.8–124.8) in a study from southern Sri Lanka [32].
3.3. Lymphatic Filariasis
3.4. Dengue
4. Discussion
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- It is limited to a rather short period of time (10 years), thus excluding possible major studies going back to previous decades.
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- Only studies listed on a single platform were considered (PubMed), which may have contributed to missing meaningful studies, since various platforms may search additional databases.
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- Articles exclusively in the English language were considered, which might have excluded critical studies published in other languages, even more since the discussed diseases are mostly endemic in non-English-speaking countries.
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- Chagas disease: In the early 1990s, Starr et al. [41] reported from Costa Rica higher relative odds of Triatoma dimidiate infestation when the floor type was dirt versus other types of floor (OR = 1.7, 95% CI 0.8–3.8); or the wall type was earthen versus other types of wall (OR = 1.6, 95% CI 0.8–2.9); or the roof was made of tiles versus galvanized metal roof (OR = 2.4, 95% CI 1.1–5.4);
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- Leishmania: In the early 1990s, Weigel et al. [42] reported environmental risk factors of CL in Columbia, among which they mentioned roof thatch or palm leaves (OR = 2.0, 95% CI 1.3–3.2). More recently, Singh et al. [43] reported from India that housing conditions represent risk factors for VL independently of socioeconomic status Living in a thatched house (OR 2.60, 95% CI 1.50–4.48) or Living in a house with damp floors (OR 2.6, 95% CI 1.25–5.41);
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- Lymphatic filiaria: In the late 1970s, Maheudin et al. [44] reported from Indonesia that persons living in poorly built houses had a nine times higher microfila infection rate and a five times higher disease rate than people living in modern houses.
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- Dengue: In the late 1980s, Focks and Chadee [45], recognizing the need to control Aedes aegypti proliferation, estimated in the context of Trinidad that the provision of an adequate water supply system and an environmental sanitation effort would eliminate the ubiquitous small water containers (buckets, tires, etc.) would reduce mosquito densities by >80%.
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- The international community has long recognized the importance of improving housing conditions to prevent/control/eradicate, among others, the above-discussed diseases. Indeed, many projects have been initiated and implemented worldwide based on guidelines/recommendations/roadmaps, such as the following:
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- Keeping the vector out: housing improvements for vector control and sustainable development [46], which argues based on evidence that poor quality housing and neglected peridomestic environments are risk factors for the transmission of many diseases including, Chagas disease, leishmaniasis, filariasis and dengue, and those housing interventions such as screening windows, reducing cracks in walls, floors and roofs are essential.
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- WASH (Water, Sanitation and Hygiene) [47]: Safe drinking water, sanitation and hygiene are crucial to human health. Evidence suggests that clean drinking water (piped water) and connections to sewer systems will improve health outcomes, notably mortality related to diarrhea. Regarding NTDs, one of five key strategies identified to combat those diseases is “safe drinking-water, basic sanitation and hygiene services”, which can contribute to reducing the incidence and morbidity of water-associated vector-borne diseases such as dengue or filariasis or, through closed sewerage systems, decrease breeding and resting sites of vectors, such as sand-flies transmitting leishmaniasis [48];
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- WHO NTDs Roadmaps [49]: Regarding the four NTDs discussed here, the roadmap for neglected tropical diseases 2021–2030 [49] proposes, concerning risk factors due to housing conditions, core strategic interventions, such as sanitation improvements that can reduce vector breeding habitats, insecticide spraying, insecticide-treated nets and environmental management, reducing available habitats for mosquitoes (e.g., environmental modification, house construction), home cleanliness and housing improvements (e.g., crack-free walls, bed-nets).
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- Mud walls are more prone to cracks/holes that facilitate breeding sites for potential vectors. Mud walls can also retain moisture for prolonged periods, ensuring optimal humidity corresponding to a protective environment for vectors, thus potentially increasing the density of vectors; for example, shown with Culex [50,51].
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- Similarly, houses with damp floors or thatched houses could provide an adequate environment for the survival of potential vectors [29,43,44]. An inadequate sewage system, as well as backyard characteristics (swamp, for example), may also play a role in offering favorable breeding/surviving conditions to potential vectors [52].
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- Lime plastering (but not mud plastering) of walls significantly reduced (42%) the density of sand-flies (vector of VL) in India and one site in Nepal (but not a second one) in a study combining interventions [54];
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- Environmental clean-up campaigns such as waste management indoor and outdoor as well as emptying, scrubbing, covering water containers showed a reduction of dengue illness of 24.7% and a relative risk reduction among children of dengue infection of 29.5% in a study from Nicaragua and Mexico [55].
- 47% lower odds of malaria infection compared to traditional houses (AOR = 0.5; CI 95%: 0.42–0.67; p < 0.001);
- 45–65% lower odds of clinical malaria (case-control studies: AOR = 0.4, 95% CI 0.20–0.62, p < 0.001; cohort studies: AOR = 0.6, 95% CI 0.36–0.84, p = 0.005).
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- World Health Organization. Milestones in Health Promotion Statements from Global Conferences; WHO: Geneva, Switzerland, 2009; Available online: https://www.who.int/healthpromotion/Milestones_Health_Promotion_05022010.pdf (accessed on 28 February 2022).
- Ottawa Charter for Health Promotion: An International Conference on Health Promotion, Ottawa, ON, Canada, 17–21 November 1986. Available online: https://www.canada.ca/en/public-health/services/health-promotion/population-health/ottawa-charter-health-promotion-international-conference-on-health-promotion.html (accessed on 28 January 2022).
- WHO-Euro. Environmental Burden of Disease Associated with Inadequate Housing; World Health Organization Europe: Copenhagen, Denmark, 2011; Available online: http://www.euro.who.int/__data/assets/pdf_file/0003/142077/e95004.pdf (accessed on 28 January 2022).
- World Health Organization. WHO Housing and Health Guidelines; WHO/CED/PHE/18.10; World Health Organization: Geneva, Switzerland, 2018. [Google Scholar]
- Brauchbach, M.; Savelsberg, J. Social Inequalities and Their Influence on Housing Risk-Factors and Health; A Data Report Based on the WHO LARES Database; WHO Regional Office for Europe: Copenhagen, Denmark, 2009. [Google Scholar]
- GBD 2017 Risk Factor Collaborators. Global, regional, and national comparative risk assessment of 84 behavioral, environmental, and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet 2018, 392, 1923–1994. [Google Scholar] [CrossRef] [Green Version]
- WHO Europe. New Evidence from WHO: Inadequate Housing Causes More Than 100 000 Annual Deaths in Europe. 2011. Available online: https://www.euro.who.int/en/media-centre/sections/press-releases/2011/06/new-evidence-from-who-inadequate-housing-causes-more-than-100-000-annual-deaths-in-europe (accessed on 2 February 2022).
- Harker, L. Chance of a Lifetime. The Impact of Bad Housing on Children’s Lives. Shelter. 2006. Available online: https://england.shelter.org.uk/professional_resources/policy_and_research/policy_library/chance_of_a_lifetime_-_the_impact_of_bad_housing_on_childrens_lives (accessed on 5 February 2022).
- Hunt, P.; Stewart, R.; de Mesquita, J.B.; Oldring, L. Neglected Diseases: A Human Rights Analysis/(Special Topics in Social, Economic and Behavioural Research Report Series; no. 6)“TDR/SDR/SEB/ST/07.2”; World Health Organization: Geneva, Switzerland, 2007. [Google Scholar]
- Office of the United Nations High Commissioner for Human Rights. The Right to Adequate Housing; Fact Sheet No. 21/Rev.1; United Nations: Geneva, Switzerland, 2010. [Google Scholar]
- United Nations. Universal Declaration of Human Rights. 1948. Available online: https://www.un.org/en/about-us/universal-declaration-of-human-rights (accessed on 6 February 2022).
- OHCHR. International Covenant on Economic, Social and Cultural Rights. General Assembly resolution 2200A (XXI). 1966. Available online: https://www.ohchr.org/en/professionalinterest/pages/cescr.aspx (accessed on 7 February 2022).
- OHCHR. CESCR General Comment No. 4: The Right to Adequate Housing. Adopted at the Sixth Session of the Committee on Economic, Social and Cultural Rights, on 13 December 1991. Available online: https://www.refworld.org/docid/47a7079a1.html (accessed on 7 February 2022).
- Dyke, E.; McKay, B.; Ly, M.; Peeling, R. Evaluation of the WHO Neglected Tropical Diseases Programme Volume 1: Report Corporate Evaluation Commissioned by the WHO Evaluation Office. 2019. TDV Global Inc.. Available online: https://www.who.int/docs/default-source/documents/evaluation/evaluation-ntd-report.pdf?sfvrsn=351a36 (accessed on 10 February 2022).
- Keenan, J.D.; Hotez, P.J.; Amza, A.; Stoller, N.E.; Gaynor, B.D.; Porco, T.C.; Lietman, T.M. Elimination and eradication of neglected tropical diseases with mass drug administrations: A survey of experts. PLoS Negl. Trop. Dis. 2013, 7, e2562. [Google Scholar] [CrossRef] [PubMed]
- Lidani, K.C.F.; Andrade, F.A.; Bavia, L.; Damasceno, F.S.; Beltrame, M.H.; Messias-Reason, I.J.; Sandri, T.L. Chagas Disease: From Discovery to a Worldwide Health Problem. Front. Public Health 2019, 2, 166. [Google Scholar] [CrossRef] [PubMed]
- PAHO. Chagas Disease. 2020. Available online: https://www.paho.org/en/topics/chagas-disease (accessed on 10 February 2022).
- WHO. Leishmaniasis. 2022. Available online: https://www.who.int/news-room/fact-sheets/detail/leishmaniasis (accessed on 12 February 2022).
- PAHO. Lymphatic Filariasis. 2022. Available online: https://www.paho.org/en/topics/lymphatic-filariasis (accessed on 12 February 2022).
- WHO. Global Program to Eliminate Lymphatic Filariasis: Progress Report, 2020. Wkly. Epidemiol. Rec. Relev. Épidémiologique Hebd. 2021, 41, 497–508. [Google Scholar]
- WHO. Dengue/Severe Dengue. Key-Facts. 2022. Available online: https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue (accessed on 12 February 2022).
- Bhatt, S.; Gething, P.W.; Brady, O.J.; Messina, J.P.; Farlow, A.W.; Moyes, C.L.; Drake, J.M.; Brownstein, J.S.; Hoen, A.G.; Sankoh, O.; et al. The global distribution and burden of dengue. Nature 2013, 496, 504–507. [Google Scholar] [CrossRef]
- Bustamante, D.M.; De Urioste-Stone, S.M.; Juárez, J.G.; Pennington, P.M. Ecological, social, and biological risk factors for continued Trypanosoma cruzi transmission by Triatoma dimidiata in Guatemala. PLoS ONE 2014, 9, e104599. [Google Scholar] [CrossRef]
- Crocco, L.; Nattero, J.; López, A.; Cardozo, M.; Soria, C.; Ortiz, V.; Rodriguez, C.S. Factors associated with the presence of triatomines in rural areas of south Argentine Chaco. Rev. Soc. Bras. Med. Trop. 2019, 52, e20180357. [Google Scholar] [CrossRef] [Green Version]
- Lardeux, F.; Depickère, S.; Aliaga, C.; Chavez, T.; Zambrana, L. Experimental control of Triatoma infestans in poor rural villages of Bolivia through community participation. Trans. R. Soc. Trop. Med. Hyg. 2015, 109, 150–158. [Google Scholar] [CrossRef]
- Younis, L.G.; Kroeger, A.; Joshi, A.B.; Das, M.L.; Omer, M.; Singh, V.K.; Gurung, C.K.; Banjara, M.R. Housing structure including the surrounding environment as a risk factor for visceral leishmaniasis transmission in Nepal. PLoS Negl. Trop. Dis. 2020, 14, e0008132. [Google Scholar] [CrossRef] [Green Version]
- Uranw, S.; Hasker, E.; Roy, L.; Meheus, F.; Das, M.L.; Bhattarai, N.R.; Rijal, S.; Boelaert, M. An outbreak investigation of visceral leishmaniasis among residents of Dharan town, eastern Nepal, evidence for urban transmission of Leishmania donovani. BMC Infect. Dis. 2013, 13, 21. [Google Scholar] [CrossRef] [Green Version]
- Yared, S.; Deribe, K.; Gebreselassie, A.; Lemma, W.; Akililu, E.; Kirstein, O.D.; Balkew, M.; Warburg, A.; Gebre-Michael, T.; Hailu, A. Risk factors of visceral leishmaniasis: A case control study in north-western Ethiopia. Parasit. Vectors 2014, 7, 470. [Google Scholar] [CrossRef]
- Perry, D.; Dixon, K.; Garlapati, R.; Gendernalik, A.; Poche, D.; Poche, R. Visceral leishmaniasis prevalence and associated risk factors in the saran district of Bihar, India, from 2009 to July of 2011. Am. J. Trop. Med. Hyg. 2013, 88, 778–784. [Google Scholar] [CrossRef]
- Araujo, A.R.; Portela, N.C.; Feitosa, A.P.; Silva, O.A.; Ximenes, R.A.; Alves, L.C.; Brayner, F.A. Risk Factors Associated With American Cutaneous Leishmaniasis In An Endemic Area of Brazil. Rev. Inst. Med. Trop. Sao Paulo 2016, 58, 86. [Google Scholar] [CrossRef] [Green Version]
- Bamorovat, M.; Sharifi, I.; Aflatoonian, M.R.; Sharifi, H.; Karamoozian, A.; Sharifi, F.; Khosravi, A.; Hassanzadeh, S. Risk factors for anthroponotic cutaneous leishmaniasis in unresponsive and responsive patients in a major focus, southeast of Iran. PLoS ONE 2018, 13, e0192236. [Google Scholar] [CrossRef] [Green Version]
- Kariyawasam, K.K.; Edirisuriya, C.S.; Senerath, U.; Hensmen, D.; Siriwardana, H.V.; Karunaweera, N.D. Characterization of cutaneous leishmaniasis in Matara district, southern Sri Lanka: Evidence for case clustering. Pathog. Glob. Health 2015, 109, 336–343. [Google Scholar] [CrossRef] [Green Version]
- Mutheneni, S.R.; Upadhyayula, S.M.; Kumaraswamy, S.; Kadiri, M.R.; Nagalla, B. Influence of socioeconomic aspects on lymphatic filariasis: A case-control study in Andhra Pradesh, India. J. Vector Borne Dis. 2016, 53, 272–278. [Google Scholar]
- Srividya, A.; Subramanian, S.; Sadanandane, C.; Vasuki, V.; Jambulingam, P. Determinants of transmission hotspots and filarial infection in households after eight rounds of mass drug administration in India. Trop. Med. Int. Health TM IH 2018, 23, 1251–1258. [Google Scholar] [CrossRef]
- Upadhyayula, S.M.; Mutheneni, S.R.; Kadiri, M.R.; Kumaraswamy, S.; Nagalla, B. A cohort study of lymphatic filariasis on socio economic conditions in Andhra Pradesh, India. PLoS ONE 2012, 7, e33779. [Google Scholar] [CrossRef] [Green Version]
- Lippi, C.A.; Stewart-Ibarra, A.M.; Endy, T.P.; Abbott, M.; Cueva, C.; Heras, F.; Polhemus, M.; Beltrán-Ayala, E.; Ryan, S.J. Exploring the utility of social-ecological and entomological risk factors for dengue infection as surveillance indicators in the dengue hyper-endemic city of Machala, Ecuador. PLoS Negl. Trop. Dis. 2021, 15, e0009257. [Google Scholar] [CrossRef]
- Lippi, C.A.; Stewart-Ibarra, A.M.; Muñoz, Á.G.; Borbor-Cordova, M.J.; Mejía, R.; Rivero, K.; Castillo, K.; Cárdenas, W.B.; Ryan, S.J. The Social and Spatial Ecology of Dengue Presence and Burden during an Outbreak in Guayaquil, Ecuador, 2012. Int. J. Environ. Res. Public Health 2018, 15, 827. [Google Scholar] [CrossRef] [Green Version]
- Rahman, M.S.; Ekalaksananan, T.; Zafar, S.; Poolphol, P.; Shipin, O.; Haque, U.; Paul, R.; Rocklöv, J.; Pientong, C.; Overgaard, H.J. Ecological, Social, and Other Environmental Determinants of Dengue Vector Abundance in Urban and Rural Areas of Northeastern Thailand. Int. J. Environ. Res. Public Health 2021, 18, 5971. [Google Scholar] [CrossRef]
- Martin, J.L.; Lippi, C.A.; Stewart-Ibarra, A.M.; Ayala, E.B.; Mordecai, E.A.; Sippy, R.; Heras, F.H.; Blackburn, J.K.; Ryan, S.J. Household and climate factors influence Aedes aegypti presence in the arid city of Huaquillas, Ecuador. PLoS Negl. Trop. Dis. 2021, 15, e0009931. [Google Scholar] [CrossRef]
- Shah, H.; Pandey, B.D. Risk factors of adult Dengue Fever in urban community of Nepal. Glob. J. Infect. Dis. Clin. Res. 2021, 7, 64–69. [Google Scholar] [CrossRef]
- Starr, M.D.; Rojas, J.C.; Zeledón, R.; Hird, D.W.; Carpenter, T.E. Chagas’ disease: Risk factors for house infestation by Triatoma dimidiata, the major vector of Trypanosoma cruzi in Costa Rica. Am. J. Epidemiol. 1991, 133, 740–747. [Google Scholar] [CrossRef]
- Weigle, K.A.; Santrich, C.; Martinez, F.; Valderrama, L.; Saravia, N. Epidemiology of Cutaneous Leishmaniasis in Colombia: Environmental and Behavioral Risk Factors for Infection, Clinical Manifestations, and Pathogenicity. J. Infect. Dis. 1993, 168, 709–714. [Google Scholar] [CrossRef]
- Singh, S.P.; Hasker, E.; Picado, A.; Gidwani, K.; Malaviya, P.; Singh, R.P.; Boelaert, M.; Sundar, S. Risk factors for visceral leishmaniasis in India: Further evidence on the role of domestic animals. Trop. Med. Int. Health 2010, 15 (Suppl. S2), 29–35. [Google Scholar] [CrossRef] [Green Version]
- Maheudin, H.; Partono, F.; Idris, P.; Idris, K.N. Parasitological and clinical survey of bancroftian filariasis in Kepu District, Central Jakarta, Indonesia. Southeast Asian J. Trop. Med. Public Health 1977, 8, 173–178. [Google Scholar]
- Focks, D.A.; Chadee, D.D. Pupal survey: An epidemiologically significant surveillance method for Aedes aegypti: An example using data from Trinidad. Am. J. Trop. Med. Hyg. 1997, 56, 159–167. [Google Scholar] [CrossRef]
- WHO. Keeping the Vector Out: Housing Improvements for Vector Control and Sustainable Development; World Health Organization: Geneva, Switzerland, 2017. [Google Scholar]
- WHO. Water, Sanitation and Hygiene Strategy 2018–2025; WHO/CED/PHE/WSH/18.03; World Health Organization: Geneva, Switzerland, 2018. [Google Scholar]
- WHO. Water Sanitation Hygiene 2015–2020. A Global Strategy for Accelerating and Sustaining Progress on Neglected Tropical; WHO/FWC/WSH/15.12; World Health Organization: Geneva, Switzerland, 2015. [Google Scholar]
- WHO. Ending the Neglect to Attain the Sustainable Development Goals: A Road Map for Neglected Tropical Diseases 2021–2030; World Health Organization: Geneva, Switzerland, 2020. [Google Scholar]
- Chadee, D.D.; Williams, S.A.; Ottesen, E.A. Xenomonitoring of Culex quinquefasciatus mosquitoes as a guide for detecting the presence or absence of lymphatic filariasis: A preliminary protocol for mosquito sampling. Ann. Trop. Med. Parasitol. 2002, 96, 47–53. [Google Scholar] [CrossRef]
- Baruah, K.; Rai, R.N. The impact of housing structures on filarial infection. Jpn. J. Infect. Dis. 2000, 53, 107–110. [Google Scholar]
- Luz, J.G.G.; Carvalho, A.G.; Naves, D.B.; Dias, J.V.L.; Fontes, C.J.F. Are backyard characteristics relevant factors for the occurrence of human visceral leishmaniasis in Central-Western Brazil? Trans. R Soc. Trop. Med. Hyg. 2020, 114, 276–283. [Google Scholar] [CrossRef] [PubMed]
- Horstick, O.; Runge-Ranzinger, S. Protection of the house against Chagas disease, dengue, leishmaniasis, and lymphatic filariasis: A systematic review. Lancet Infect. Dis. 2018, 18, e147–e158. [Google Scholar] [CrossRef]
- Joshi, A.B.; Das, M.L.; Akhter, S.; Chowdhury, R.; Mondal, D.; Kumar, V.; Pradeep, D.; Kroeger, A.; Boelaert, M.; Petzold, M. Chemical and environmental vector control as a contribution to the elimination of visceral leishmaniasis on the Indian subcontinent: Cluster randomized controlled trials in Bangladesh, India and Nepal. BMC Med. 2009, 7, 54. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Andersson, N.; Nava-Aguilera, E.; Arosteguí, J.; Morales-Perez, A.; Suazo-Laguna, H.; Legorreta-Soberanis, J.; Hernandez-Alvarez, C.; Fernandez-Salas, I.; Paredes-Solís, S.; Balmaseda, A.; et al. Evidence based community mobilization for dengue prevention in Nicaragua and Mexico (Camino Verde, the Green Way): Cluster randomized controlled trial. BMJ 2015, 351, h3267. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tusting, L.S.; Ippolito, M.M.; Willey, B.A.; Kleinschmidt, I.; Dorsey, G.; Gosling, R.D.; Lindsay, S.W. The evidence for improving housing to reduce malaria: A systematic review and meta-analysis. Malar. J. 2015, 9, 209. [Google Scholar] [CrossRef] [Green Version]
- Tusting, L.S.; Bottomley, C.; Gibson, H.; Kleinschmidt, I.; Tatem, A.J.; Lindsay, S.W.; Gething, P.W. Housing Improvements and Malaria Risk in Sub-Saharan Africa: A Multi-Country Analysis of Survey Data. PLoS Med. 2017, 14, e1002234. [Google Scholar] [CrossRef] [Green Version]
- Rojas de Arias, A.; Ferro, E.A.; Ferreira, M.E.; Simancas, L.C. Chagas disease vector control through different intervention modalities in endemic localities of Paraguay. Bull. World Health Organ 1999, 77, 331–339. [Google Scholar]
- Nieto-Sanchez, C.; Bates, B.R.; Guerrero, D.; Jimenez, S.; Baus, G.; Peeters Grietens, K.; Grijalva, M.J. Home improvement and system-based health promotion for sustainable prevention of Chagas disease: A qualitative study. PLoS Negl. Trop. Dis. 2019, 13, e0007472. [Google Scholar] [CrossRef]
- Thomson, H.; Thomas, S.; Sellstrom, E.; Petticrew, M. The health impacts of housing improvement: A systematic review of intervention studies from 1887 to 2007. Am. J. Public Health 2009, 99 (Suppl. S3), S681–S692. [Google Scholar] [CrossRef]
- Vazquez-Prokopec, G.M.; Lenhart, A.; Manrique-Saide, B. Housing improvement: A novel paradigm for urban vector borne disease control? Trans. R Soc. Trop. Med. Hyg. 2016, 110, 567–569. [Google Scholar] [CrossRef] [Green Version]
Chagas Disease | Viscerla Leishmaniasis | Cutaneous Leishmaniasis | Lymphatic Filariasis | Dengue | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Bustamante et al. [23] 2014 | Croco et al. [24] 2019 | Lardeux et al. [25] 2015 | Younis et al. [26] 2020 | Uranw et al. [27] 2013 | Yared et al. [28] 2014 | Perry et al. [29] 2013 | Araujo et al. [30] 2016 | Bamorovat et al. [31] 2018 | Kariyawasam et al. [32] 2015 | Mutheneni et al. [33] 2016 | Srividya et al. [34] 2018 | Upadhyayula et al. [35] 2012 | Lippi et al. [36] 2021 | Lippi et al. [37] 2018 | Rahman et al. [38] 2021 | Martin et al. [39] 2021 | Shah et al. [40] 2021 | ||
Risk factor House | Poor housing conditions | OR 2.0 CI 1.0–3.9 | OR 24.6 CI 17.6–32.1 | IRR 2.0 CI 1.5–2.6 | |||||||||||||||
Thatched/mud/hut house | RR 7.2 p < 0.001 | OR 6.6 CI 1.8–23.7 | OR 1.9 CI = 1.2–3.1 | ||||||||||||||||
Unplastered concrete/brick/tiles walls | RR 20.7 p < 0.001 | OR 41.5 CI 13.8–124.8 | RR 2.0 RR 2.9 | ||||||||||||||||
Bajareque walls (Mud and sticks) | OR 1.9 CI 1.2–3.9 | ||||||||||||||||||
Bamboo walls | AOR 8.1 CI 2.4–27.6 | ||||||||||||||||||
Earthen floors | OR 3.4 CI 1.9–6.0 | ||||||||||||||||||
Cracks in walls | OR 3.9, CI 2.3–6.7 | AOR2.9 CI 0.9–9.2 | AOR 6.4 CI 1.6–25.6 | ||||||||||||||||
Unplastered roofs (tiles/thatched) | OR 1.9 CI 1.1–3.3 | OR = 3.7, CI 1.6–8.7 | OR 1.6, CI 0.5–5.0 | OR 1.3 CI = 0.8–2.0 | |||||||||||||||
Risk factor Water | Houses without or with interrupted water supply | AOR 6.0 CI 2.7–13.1 | OR 1.7 CI 1.10–2.5 | OR4.8 CI 1.1–24.1 | |||||||||||||||
Water storage in an open tank in the household | OR0.1 CI 0.01–0.1 | ||||||||||||||||||
Collection of dirty water around the house | OR1.9 CI 1.0–3.7 | ||||||||||||||||||
Water collected in discarded containers/tires | AOR6.3 CI 2.7–14.5 | ||||||||||||||||||
Kutcha drainage (uncemented) | OR 19.4 CI 3.0–126.4 | p = 0.032 | |||||||||||||||||
Proximity of U-drains to house | RR 5.8 | ||||||||||||||||||
Rainwater and open water source | |||||||||||||||||||
Risk Factor Yard | Shady condition of yard and house | OR 3.8 CI 1.3–11.5 | IRR 2.0 CI 1.5–2.6 | ||||||||||||||||
Untidy yard | |||||||||||||||||||
Protective Factor | Cement/tile floors | OR 0.3 CI 0.2–0.7 | |||||||||||||||||
Window screens in good conditions | OR 0.3 CI 0.1–0.8 | ||||||||||||||||||
Window vs. no window in thatched house | AOR 0.4 CI 0.1–0.8 | ||||||||||||||||||
Existence of air conditioning | p < 0.05 | ||||||||||||||||||
Sceptic tank system | OR 0.1 CI 0.01–0.1 | ||||||||||||||||||
Pucca drainage (masonry system | p = 0.001 |
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Chastonay, A.H.M.; Chastonay, O.J. Housing Risk Factors of Four Tropical Neglected Diseases: A Brief Review of the Recent Literature. Trop. Med. Infect. Dis. 2022, 7, 143. https://doi.org/10.3390/tropicalmed7070143
Chastonay AHM, Chastonay OJ. Housing Risk Factors of Four Tropical Neglected Diseases: A Brief Review of the Recent Literature. Tropical Medicine and Infectious Disease. 2022; 7(7):143. https://doi.org/10.3390/tropicalmed7070143
Chicago/Turabian StyleChastonay, Anouk H. M., and Oriane J. Chastonay. 2022. "Housing Risk Factors of Four Tropical Neglected Diseases: A Brief Review of the Recent Literature" Tropical Medicine and Infectious Disease 7, no. 7: 143. https://doi.org/10.3390/tropicalmed7070143
APA StyleChastonay, A. H. M., & Chastonay, O. J. (2022). Housing Risk Factors of Four Tropical Neglected Diseases: A Brief Review of the Recent Literature. Tropical Medicine and Infectious Disease, 7(7), 143. https://doi.org/10.3390/tropicalmed7070143