The Skin—A Common Pathway for Integrating Diagnosis and Management of NTDs
Abstract
:1. Introduction
2. Methodology
3. Integrated Approach to Skin NTDs
4. Diagnosis
5. Disease Mapping and Surveillance
6. Treatment
7. Morbidity Management
8. Conclusions and Future Directions
Author Contributions
Funding
Conflicts of Interest
References
- Karimkhani, C.; Dellavalle, R.P.; Coffeng, L.E.; Flohr, C.; Hay, R.J.; Langan, S.M.; Nsoesie, E.O.; Ferrari, A.J.; Erskine, H.E.; Silverberg, J.I.; et al. Global skin disease morbidity and mortality: An update from the Global Burden of Disease Study 2013. JAMA Dermatol. 2017, 153, 406–412. [Google Scholar] [CrossRef] [PubMed]
- Clucas, D.B.; Carville, K.S.; Connors, C.; Currie, B.J.; Carapetis, J.R.; Andrews, R.M. Disease burden and health-care clinic attendances for young children in remote Aboriginal communities of northern Australia. Bull. World Health Organ. 2008, 86, 275–281. [Google Scholar] [PubMed]
- Herricks, J.R.; Hotez, P.J.; Wanga, V.; Coffeng, L.E.; Haagsma, J.A.; Basáñez, M.G.; Buckle, G.; Budke, C.M.; Carabin, H.; Fèvre, E.M.; et al. The Global Burden of Disease Study 2013: What does it mean for the NTDs? PLoS Negl. Trop. Dis. 2017, 11, e0005424. [Google Scholar] [CrossRef] [PubMed]
- Hay, R.J.; Johns, N.E.; Williams, H.C.; Bolliger, I.W.; Dellavalle, R.P.; Margolis, D.J.; Marks, R.; Naldi, L.; Weinstock, M.A.; Wulf, S.K.; et al. The Global Burden of Skin Disease in 2010: An analysis of the prevalence and impact of skin conditions. J. Investig. Dermatol. 2014, 134, 1527–1534. [Google Scholar] [CrossRef] [PubMed]
- Rodrigues, M.L.; Albuquerque, P.C. Searching for a change: The need for increased support for public health and research on fungal diseases. PLoS Negl. Trop. Dis. 2018, 12, e0006479. [Google Scholar] [CrossRef] [PubMed]
- Houweling, T.A.J.; Karim-Kos, H.E.; Kulik, M.C.; Stolk, W.A.; Haagsma, J.A.; Lenk, E.J.; Richardus, J.H.; de Vlas, S.J.; et al. Socioeconomic inequalities in neglected tropical diseases: A systematic review. PLoS Negl. Trop. Dis. 2016, 10, e0004546. [Google Scholar] [CrossRef] [PubMed]
- Chandler, D.J.; Hansen, K.S.; Mahato, B.; Darlong, J.; John, A.; Lockwood, D.N.J. Household costs of leprosy reactions (ENL) in rural India. PLoS Negl. Trop. Dis. 2015, 9, e0003431. [Google Scholar] [CrossRef] [PubMed]
- Tiwari, A.; Suryawanshi, P.; Raikwar, A.; Arif, M.; Richardus, J.H. Household expenditure on leprosy outpatient services in the Indian Health System: A comparative study. PLoS Negl. Trop. Dis. 2018, 12, e0006181. [Google Scholar] [CrossRef] [PubMed]
- Tembei, A.M.; Kengne-Ouaffo, J.A.; Ngoh, E.A.; John, B.; Nji, T.M.; Deribe, K.; Enyong, P.; Nkuo-Akenji, T.; Davey, G.; Wanji, S. A comparative analysis of economic cost of podoconiosis and leprosy on affected households in the northwest region of Cameroon. Am. J. Trop. Med. Hyg. 2018, 98, 1075–1081. [Google Scholar] [CrossRef] [PubMed]
- Uranw, S.; Meheus, F.; Baltussen, R.; Rijal, S.; Boelaert, M. The household costs of visceral leishmaniasis care in south-eastern Nepal. PLoS Negl. Trop. Dis. 2013, 7, e2062. [Google Scholar] [CrossRef] [PubMed]
- Lenk, E.J.; Redekop, W.K.; Luyendijk, M.; Rijnsburger, A.J.; Severens, J.L. Productivity loss related to neglected tropical diseases eligible for preventive chemotherapy: A systematic literature review. PLoS Negl. Trop. Dis. 2016, 10, 1–19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Engelman, D.; Fuller, L.C.; Solomon, A.W.; McCarthy, J.S.; Hay, R.J.; Lammie, P.J.; Steer, A.C. Opportunities for integrated control of neglected tropical diseases that affect the skin. Trends Parasitol. 2016, 32, 843–854. [Google Scholar] [CrossRef] [PubMed]
- Mitjà, O.; Marks, M.; Bertran, L.; Kollie, K.; Argaw, D.; Fahal, A.H.; Fitzpatrick, C.; Fuller, L.C.; Izquierdo, B.G.; Hay, R.; et al. Integrated control and management of neglected tropical skin diseases. PLoS Negl. Trop. Dis. 2017, 11, e0005136. [Google Scholar] [CrossRef] [PubMed]
- Department of Control of Neglected Tropical Diseases. Recognizing Neglected Tropical Diseases Through Changes on the Skin: A Training Guide for Front-Line Health Workers; WHO: Geneva, Switzerland, 2018. [Google Scholar]
- Faye, O.; Hay, R.J.; Ryan, T.J.; Keita, S.; Traoré, A.K.; Mahé, A. A public health approach for leprosy detection based on a very short term-training of primary health care workers in basic dermatology. Lepr. Rev. 2007, 78, 11–16. [Google Scholar] [PubMed]
- Chandler, D. Integrated care and leprosy in India: A role for indian systems of medicine and traditional health practice in the eradication of leprosy. Curr. Sci. 2016, 111, 351–355. [Google Scholar] [CrossRef]
- Oswald, I.H. Are traditional healers the solution to the failures of primary health care in rural Nepal? Soc. Sci. Med. 1983, 17, 255–257. [Google Scholar] [CrossRef]
- Kaur, P.; Sharma, U.C.; Pandey, S.S.; Gurmohan, S. Leprosy care through traditional healers. Lepr. Rev. 1984, 55, 57–61. [Google Scholar] [CrossRef] [PubMed]
- Ezenduka, C.; Post, E.; John, S.; Suraj, A.; Namadi, A.; Onwujekwe, O. Cost-effectiveness analysis of three leprosy case detection methods in northern Nigeria. PLoS Negl. Trop. Dis. 2012, 6, e1818. [Google Scholar] [CrossRef] [PubMed]
- Darlong, J.; Govindharaj, P.; Darlong, F.; Mahato, N. A study of untreated leprosy affected children reporting with grade 2 disability at a referral centre in West Bengal, India. Lepr. Rev. 2017, 88, 298–305. [Google Scholar]
- Yotsu, R.R.; Kouadio, K.; Vagamon, B.; N’guessan, K.; Akpa, A.J.; Yao, A.; Aké, J.; Abbet, A.R.; Tchamba, A.A.; Bedimo, R.; et al. Skin disease prevalence study in schoolchildren in rural Côte d’Ivoire: Implications for integration of neglected skin diseases (Skin NTDs). PLoS Negl. Trop. Dis. 2018, 12, e0006489. [Google Scholar] [CrossRef] [PubMed]
- Barogui, Y.T.; Diez, G.; Anagonou, E.; Johnson, R.C.; Gomido, I.C.; Amoukpo, H.; Bachirou, Z.S.; Houezo, J.G.; Saizonou, R.; Sopoh, G.E.; et al. Integrated approach in the control and management of skin neglected tropical diseases in Lalo, Benin. PLoS Negl. Trop. Dis. 2018, 12, e0006584. [Google Scholar] [CrossRef] [PubMed]
- Mahé, A.; Faye, O.; N’Diaye, H.T.; Ly, F.; Konaré, H.; Kéita, S.; Traoré, A.K.; Hay, R. Definition of an algorithm for the management of common skin diseases at primary health care level in sub-Saharan Africa. Trans. R. Soc. Trop. Med. Hyg. 2005, 99, 39–47. [Google Scholar] [CrossRef] [PubMed]
- Steer, A.C.; Tikoduadua, L.V.; Manalac, E.M.; Colquhoun, S.; Carapetis, J.R.; Maclennan, C. Validation of an integrated management of childhood illness algorithm for managing common skin conditions in Fiji. Bull. World Health Organ. 2009, 87, 173–179. [Google Scholar] [CrossRef] [PubMed]
- Deribe, K.; Wanji, S.; Shafi, O.; Tukahebwa, M.E.; Umulisa, I.; Molyneux, D.H.; Davey, G. The feasibility of eliminating podoconiosis. Bull. World Health Organ. 2015, 93, 712–718. [Google Scholar] [CrossRef] [PubMed]
- Engelman, D.; Fuller, L.C.; Steer, A.C.; International Alliance for the Control of Scabies Delphi Panel. Consensus criteria for the diagnosis of scabies: A delphi study of international experts. PLoS Negl. Trop. Dis. 2018, 12, e0006549. [Google Scholar] [CrossRef] [PubMed]
- Brooker, S.J.; Smith, J.L. Mapping neglected tropical diseases: A global view. Community Eye Heal. 2013, 26, 32. [Google Scholar]
- Noma, M.; Nwoke, B.E.B.; Nutall, I.; Tambala, P.A.; Enyong, P.; Namsenmo, A.; Remme, J.; Amazigo, U.V.; Kale, O.O.; Sékétéli, A. Rapid epidemiological mapping of onchocerciasis (REMO): Its application by the African Programme for Onchocerciasis Control (APOC). Ann. Trop. Med. Parasitol. 2002, 96, S29–S39. [Google Scholar] [CrossRef] [PubMed]
- Sime, H.; Deribe, K.; Assefa, A.; Newport, M.J.; Enquselassie, F.; Gebretsadik, A.; Kebede, A.; Hailu, A.; Shafi, O.; Aseffa, A.; et al. Integrated mapping of lymphatic filariasis and podoconiosis: Lessons learnt from Ethiopia. Parasit. Vectors 2014, 7, 397. [Google Scholar] [CrossRef] [PubMed]
- Kebede, B.; Martindale, S.; Mengistu, B.; Kebede, B.; Mengiste, A.; H/Kiros, F.; Tamiru, A.; Davey, G.; Kelly-Hope, L.A.; Mackenzie, C.D. Integrated morbidity mapping of lymphatic filariasis and podoconiosis cases in 20 co-endemic districts of Ethiopia. PLoS Negl. Trop. Dis. 2018, 12, e0006491. [Google Scholar] [CrossRef] [PubMed]
- Mason, D.S.; Marks, M.; Sokana, O.; Solomon, A.W.; Mabey, D.C.; Romani, L.; Kaldor, J.; Steer, A.C.; Engelman, D. The prevalence of scabies and impetigo in the Solomon Islands: A population-based survey. PLoS Negl. Trop. Dis. 2016, 10, e0004803. [Google Scholar] [CrossRef] [PubMed]
- Marks, M.; Vahi, V.; Sokana, O.; Chi, K.H.; Puiahi, E.; Kilua, G.; Pillay, A.; Dalipanda, T.; Bottomley, C.; Solomon, A.W.; et al. Impact of community mass treatment with azithromycin for trachoma elimination on the prevalence of yaws. PLoS Negl. Trop. Dis. 2015, 9, e0003988. [Google Scholar] [CrossRef] [PubMed]
- Molyneux, D.H. ‘Neglected’ diseases but unrecognised successes—Challenges and opportunities for infectious disease control. Lancet 2004, 364, 380–383. [Google Scholar] [CrossRef]
- Hotez, P.J.; Remme, J.H.F.; Buss, P.; Alleyne, G.; Morel, C.; Breman, J.G. Combating tropical infectious diseases: Report of the Disease Control Priorities in Developing Countries Project. Clin. Infect. Dis. 2004, 38, 871–988. [Google Scholar] [CrossRef] [PubMed]
- Molyneux, D.H.; Hotez, P.J.; Fenwick, A. ‘Rapid-impact interventions’: How a policy of integrated control for Africa’s neglected tropical diseases could benefit the poor. PLoS Med. 2005, 2, e336. [Google Scholar] [CrossRef] [PubMed]
- Hotez, P.J.; Fenwick, A.; Ray, S.E.; Hay, S.I.; Molyneux, D.H. ‘Rapid impact’ 10 years after: The first ‘decade’ (2006-2016) of integrated neglected tropical disease control. PLoS Negl. Trop. Dis. 2018, 12, e0006137. [Google Scholar] [CrossRef] [PubMed]
- Omura, S.; Crump, A. Ivermectin: Panacea for resource-poor communities? Trends Parasitol. 2014, 30, 445–455. [Google Scholar] [CrossRef] [PubMed]
- Heukelbach, J.; Winter, B.; Wilcke, T.; Muehlen, M.; Albrecht, S.; de Oliveira, F.A.S.; Kerr-Pontes, L.R.; Liesenfeld, O.; Feldmeier, H. Selective mass treatment with ivermectin to control intestinal helminthiases and parasitic skin diseases in a severely affected population. Bull. World Health Organ. 2004, 82, 563–571. [Google Scholar] [PubMed]
- Ottesen, E.A.; Hooper, P.J.; Bradley, M.; Biswas, G. The Global Programme to Eliminate Lymphatic Filariasis: Health impact after 8 years. PLoS Negl. Trop. Dis. 2008, 2, e317. [Google Scholar] [CrossRef] [PubMed]
- Krotneva, S.P.; Coffeng, L.E.; Noma, M.; Zouré, H.G.M.; Bakoné, L.; Amazigo, U.V.; de Vlas, S.J.; Stolk, W.A. African Program for Onchocerciasis Control 1995–2010: Impact of annual ivermectin mass treatment on off-target infectious diseases. PLoS Negl. Trop. Dis. 2015, 9, e0004051. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Romani, L.; Whitfeld, M.J.; Koroivueta, J.; Kama, M.; Wand, H.; Tikoduadua, L.; Tuicakau, M.; Koroi, A.; Andrews, R.; Kaldor, J.M.; et al. Mass drug administration for scabies control in a population with endemic disease. N. Engl. J. Med. 2015, 373, 2305–2313. [Google Scholar] [CrossRef] [PubMed]
- Pacqué, M.; Muñoz, B.; Poetschke, G.; Foose, J.; Greene, B.M.; Taylor, H.R. Pregnancy outcome after inadvertent ivermectin treatment during community-based distribution. Lancet 1990, 336, 1486–1489. [Google Scholar] [CrossRef]
- Gyapong, J.O.; Chinbuah, M.A.; Gyapong, M. Inadvertent exposure of pregnant women to ivermectin and albendazole during mass drug administration for lymphatic filariasis. Trop. Med. Int. Health 2003, 8, 1093–1101. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ndyomugyenyi, R.; Kabatereine, N.; Olsen, A.; Magnussen, P. Efficacy of ivermectin and albendazole alone and in combination for treatment of soil-transmitted helminths in pregnancy and adverse events: A randomized open label controlled intervention trial in Masindi District, Western Uganda. Am. J. Trop. Med. Hyg. 2008, 79, 856–863. [Google Scholar] [CrossRef] [PubMed]
- Opoku, N.O.; Bakajika, D.K.; Kanza, E.M.; Howard, H.; Mambandu, G.L.; Nyathirombo, A.; Nigo, M.M.; Kasonia, K.; Masembe, S.L.; Mumbere, M.; et al. Single dose moxidectin versus ivermectin for Onchocerca volvulus infection in Ghana, Liberia, and the Democratic Republic of the Congo: A randomised, controlled, double-blind phase 3 trial. Lancet 2018. [Google Scholar] [CrossRef]
- Korth-Bradley, J.M.; Parks, V.; Patat, A.; Matschke, K.; Mayer, P.; Fleckenstein, L. Relative bioavailability of liquid and tablet formulations of the antiparasitic moxidectin. Clin. Pharmacol. Drug Dev. 2012, 1, 32–37. [Google Scholar] [CrossRef] [PubMed]
- Mounsey, K.E.; Walton, S.F.; Innes, A.; Cash-Deans, S.; McCarthy, J.S. In vitro efficacy of moxidectin versus ivermectin against Sarcoptes scabiei. Antimicrob. Agents Chemother. 2017, 61, e00381. [Google Scholar] [CrossRef] [PubMed]
- Ndyomugyenyi, R.; Byamungu, A.; Korugyendo, R. Perceptions on onchocerciasis and ivermectin treatment in rural communities in Uganda: Implications for long-term compliance. Int. Health 2009, 1, 163–168. [Google Scholar] [CrossRef] [PubMed]
- Coulibaly, Y.I.; Dicko, I.; Keita, M.; Keita, M.M.; Doumbia, M.; Daou, A.; Haidara, F.C.; Sankare, M.H.; Horton, J.; Whately-Smith, C.; et al. A cluster randomized study of the safety of integrated treatment of trachoma and lymphatic filariasis in children and adults in Sikasso, Mali. PLoS Negl. Trop. Dis. 2013, 7, e2221. [Google Scholar] [CrossRef] [PubMed]
- Mohammed, K.A.; Haji, H.J.; Gabrielli, A.F.; Mubila, L.; Biswas, G.; Chitsulo, L.; Bradley, M.H.; Engels, D.; Savioli, L.; Molyneux, D.H. Triple co-administration of ivermectin, albendazole and praziquantel in Zanzibar: A safety study. PLoS Negl. Trop. Dis. 2008, 2, e171. [Google Scholar] [CrossRef] [PubMed]
- Thomsen, E.K.; Sanuku, N.; Baea, M.; Satofan, S.; Maki, E.; Lombore, B.; Schmidt, M.S.; Siba, P.M.; Weil, G.J.; Kazura, J.W.; et al. Efficacy, safety, and pharmacokinetics of coadministered diethylcarbamazine, albendazole, and ivermectin for treatment of bancroftian filariasis. Clin. Infect. Dis. 2016, 62, 334–341. [Google Scholar] [CrossRef] [PubMed]
- Van ’t Noordende, A.T.; Kuiper, H.; Ramos, A.N.; Mieras, L.F.; Barbosa, J.C.; Pessoa, S.M.F.; Souza, E.A.; Fernandes, T.A.; Hinders, D.C.; Praciano, M.M.; et al. Towards a toolkit for cross-neglected tropical disease morbidity and disability assessment. Int. Health 2016, 8, i71–81. [Google Scholar] [CrossRef] [PubMed]
- Ryan, T.J. The International Society of Dermatology’s Task Force for Skin Care for All: Community dermatology. Int. J. Dermatol. 2011, 50, 548–551. [Google Scholar] [CrossRef] [PubMed]
- Kaur, P.; Singh, G. Community dermatology in India. Int. J. Dermatol. 1995, 34, 322. [Google Scholar] [CrossRef] [PubMed]
- Stocks, M.E.; Freeman, M.C.; Addiss, D.G. The effect of hygiene-based lymphedema management in lymphatic filariasis-endemic areas: A systematic review and meta-analysis. PLoS Negl. Trop. Dis. 2015, 9, e0004171. [Google Scholar] [CrossRef] [PubMed]
- Negussie, H.; Molla, M.; Ngari, M.; Berkley, J.A.; Kivaya, E.; Njuguna, P.; Fegan, G.; Tamiru, A.; Kelemework, A.; Lang, T.; et al. Lymphoedema management to prevent acute dermatolymphangioadenitis in podoconiosis in northern Ethiopia (GoLBeT): A pragmatic randomised controlled trial. Lancet Glob. Heal. 2018, 6, e795–803. [Google Scholar] [CrossRef]
- Deribe, K.; Kebede, B.; Tamiru, M.; Mengistu, B.; Kebede, F.; Martindale, S.; Sime, H.; Mulugeta, A.; Kebede, B.; Sileshi, M.; et al. Integrated morbidity management for lymphatic filariasis and podoconiosis, Ethiopia. Bull. World Health Organ. 2017, 95, 652–656. [Google Scholar] [CrossRef] [PubMed]
- Stocks, M.E.; Ogden, S.; Haddad, D.; Addiss, D.G.; McGuire, C.; Freeman, M.C. Effect of water, sanitation, and hygiene on the prevention of trachoma: A Systematic review and meta-analysis. PLoS Med. 2014, 11, e1001605. [Google Scholar] [CrossRef] [PubMed]
- Strunz, E.C.; Addiss, D.G.; Stocks, M.E.; Ogden, S.; Utzinger, J.; Freeman, M.C. Water, sanitation, hygiene, and soil-transmitted helminth infection: A systematic review and meta-analysis. PLoS Med. 2014, 11, e1001620. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Grimes, J.E.T.; Croll, D.; Harrison, W.E.; Utzinger, J.; Freeman, M.C.; Templeton, M.R. The relationship between water, sanitation and schistosomiasis: A systematic review and meta-analysis. PLoS Negl. Trop. Dis. 2014, 8, e3296. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Seward, N.; Neuman, M.; Colbourn, T.; Osrin, D.; Lewycka, S.; Azad, K.; Costello, A.; Das, S.; Fottrell, E.; Kuddus, A.; et al. Effects of women’s groups practising participatory learning and action on preventive and care-seeking behaviours to reduce neonatal mortality: A meta-analysis of cluster-randomised trials. PLoS Med. 2017, 14, e1002467. [Google Scholar] [CrossRef] [PubMed]
- Pryce, J.; Mableson, H.E.; Choudhary, R.; Pandey, B.D.; Aley, D.; Betts, H.; Mackenzie, C.D.; Kelly-Hope, L.A.; Cross, H. Assessing the feasibility of integration of self-care for filarial lymphoedema into existing community leprosy self-help groups in Nepal. BMC Public Health 2018, 18, 201. [Google Scholar] [CrossRef] [PubMed]
- Hofstraat, K.; van Brakel, W.H. Social Stigma Towards Neglected Tropical Diseases: A systematic review. Int. Health 2016, 8, i53–i70. [Google Scholar] [CrossRef] [PubMed]
© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
Chandler, D.J.; Fuller, L.C. The Skin—A Common Pathway for Integrating Diagnosis and Management of NTDs. Trop. Med. Infect. Dis. 2018, 3, 101. https://doi.org/10.3390/tropicalmed3030101
Chandler DJ, Fuller LC. The Skin—A Common Pathway for Integrating Diagnosis and Management of NTDs. Tropical Medicine and Infectious Disease. 2018; 3(3):101. https://doi.org/10.3390/tropicalmed3030101
Chicago/Turabian StyleChandler, David John, and Lucinda Claire Fuller. 2018. "The Skin—A Common Pathway for Integrating Diagnosis and Management of NTDs" Tropical Medicine and Infectious Disease 3, no. 3: 101. https://doi.org/10.3390/tropicalmed3030101
APA StyleChandler, D. J., & Fuller, L. C. (2018). The Skin—A Common Pathway for Integrating Diagnosis and Management of NTDs. Tropical Medicine and Infectious Disease, 3(3), 101. https://doi.org/10.3390/tropicalmed3030101