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Selective Intermittent Preventive Treatment of Vivax Malaria: Reduction of Malaria Incidence in an Open Cohort Study in Brazilian Amazon

DOI: 10.1155/2013/310246

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Abstract:

In children, the Intermittent Preventive Treatment (IPTc), currently called Seasonal Malaria Chemoprevention (SMC), was considered effective on malaria control due to the reduction of its incidence in Papua New Guinea and in some areas with seasonal malaria in Africa. However, the IPT has not been indicated because of its association with drug resistance and for hindering natural immunity development. Thus, we evaluated the alternative IPT impact on malaria incidence in three riverside communities on Madeira River, in the municipality of Porto Velho, RO. We denominate this scheme Selective Intermittent Preventive Treatment (SIPT). The SIPT consists in a weekly dose of two 150?mg chloroquine tablets for 12 weeks, for adults, and an equivalent dose for children, after complete supervised treatment for P. vivax infection. This scheme is recommend by Brazilian Health Ministry to avoid frequent relapses. The clinic parasitological and epidemiological surveillance showed a significant reduction on vivax malaria incidence. The results showed a reduction on relapses and recurrence of malaria after SIPT implementation. The SIPT can be effective on vivax malaria control in localities with high transmission risk in the Brazilian Amazon. 1. Introduction In Brazil 99% of malaria cases occur in Amazon areas. In recent years, the number of cases per year decreased from 500.000 (2006) to 300.000 (2011) [1]. The Artemisin-based Combination Therapy, used by Brazilian Health Ministry decreased the falciparum malaria incidence (i.e., number of total positive thick blood smear/falciparum thick blood smear 100) from 26.5 in 2006 to 12.4 in 2011. These results do not consider Asymptomatic Plasmodium Carriers (APC), found frequently in holoendemic areas of Africa and Papua New Guinea [2, 3], but not in Amazon areas [4, 5]. However, recent studies show the presence of APC in several areas of the Brazilian Amazon [6–11]. Several works showed that residual malaria may resist to conventional treatment [12–15]. Thus, the APC presence, associated with ineffective tools for vector control and population mobility in Amazon, can be regarded as important factors to explain the increase and maintenance of malaria [16]. Frequencies from 10% to 40% APC were found in adults living in different riverside areas of Madeira River, in Rond?nia state [8, 10, 12, 14]. In the same areas, relapses frequency of 6.5% was found after complete treatment with chloroquine (CQ) plus primaquine (PQ) for 14 days, and of 26.7% after the same treatment for 7 days [17]. Previous works were performed to verify

References

[1]  “Sistema de Informa??o de Vigilancia Epidemiológic-SIVEP-Malária,” Brasil, Federal Ministry of Health, 2012, http://www.saude.gov.br/sivep_malaria.
[2]  G. Covell, “Relationship between malarial parasitaemia and symptoms of the disease: a review of the literature.,” Bulletin of the World Health Organization, vol. 22, pp. 605–619, 1960.
[3]  J. F. Trape, C. Rogier, L. Konate et al., “The Dielmo project: a longitudinal study of natural malaria infection and the mechanisms of protective immunity in a community living in a holoendemic area of Senegal,” The American Journal of Tropical Medicine and Hygiene, vol. 51, no. 2, pp. 123–137, 1994.
[4]  C. A. Alvarado, “Malária,” in Ricardo Veronesi. Doen?as Infecciosas e Parasitárias, pp. 660–682, Guanabara Koogan, Rio de Janeiro, Brazil, 6th edition, 1976.
[5]  A. Prata, M. Urdaneta, P. B. McGreevy, and M. S. Tada, “Infrequency of asymptomatic malaria in an endemic area in Amazonas, Brazil,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 21, no. 2, pp. 51–54, 1998.
[6]  A. L. S. S. De Andrade, C. M. T. Martelli, R. M. Oliveira, J. R. Arias, F. Zicker, and L. Pang, “High prevalence of asymptomatic malaria in gold mining areas in Brazil,” Clinical Infectious Diseases, vol. 20, no. 2, p. 475, 1995.
[7]  E. P. Camargo, F. Alves, and L. H. Pereira da Silva, “Symptomless Plasmodium vivax infections in native Amazonians,” The Lancet, vol. 353, no. 9162, pp. 1415–1416, 1999.
[8]  L. M. A. Camargo, E. Noro?a, J. M. V. Salcedo et al., “The epidemiology of malaria in Rondonia (Western Amazon region, Brazil): study of a riverine population,” Acta Tropica, vol. 72, no. 1, pp. 1–11, 1999.
[9]  C. J. F. Fontes, Epidemiologia da malária e fatores associados à infec??o assintomática por Plasmodium em uma popula??o de garimpeiros da Amaz?nia Brasileira (Mato Grosso 1996) [Ph.D. thesis], Departamento de Clínica Médica, Federal University of Minas Gerais, Belo Horizonte, Brazil, 2001.
[10]  F. P. Alves, R. R. Durlacher, M. J. Menezes, H. Krieger, L. H. Pereira da Silva, and E. P. Camargo, “High prevalence of asymptomatic Plasmodium vivax and Plasmodium falciparum infections in native Amazonian populations,” The American Journal of Tropical Medicine and Hygiene, vol. 66, no. 6, pp. 641–648, 2002.
[11]  J. R. Coura, M. Suárez-Mutis, and S. Ladeia-Andrade, “A new challenge for malaria control in Brazil: asymptomatic Plasmodium infection: a review,” Memorias do Instituto Oswaldo Cruz, vol. 101, no. 3, pp. 229–237, 2006.
[12]  M. S. Tada, R. P. Marques, E. Mesquita et al., “Urban malaria in the Brazilian Western Amazon Region I. High prevalence of asymptomatic carriers in an urban riverside district is associated with a high level of clinical malaria,” Memorias do Instituto Oswaldo Cruz, vol. 102, no. 3, pp. 263–269, 2007.
[13]  T. H. Katsuragawa, L. H. S. Gil, M. S. Tada, and L. H. Pereira da Silva, “Endemias e epidemias na amaz?nia. Malária e doen?as emergentes em áreas ribeirinhas do Rio Madeira. Um caso de escola,” Estudos Avancados, vol. 22, no. 64, pp. 111–141, 2008.
[14]  T. H. Katsuragawa, R. P. A. Cunha, D. C. A. Souza, L. H. S. Gil, R. M. B. Cruz, et al., “Malária e aspectos hematológicos em moradores da área de influência dos futuros reservatórios das hidrelétricas de Santo Ant?nio e Jirau. Rond?nia, Brasil,” Cadernos de Saúde Pública, vol. 25, no. 7, pp. 1486–1492, 2009.
[15]  M. S. Tada, R. G. M. Ferreira, T. H. Katsuragawa, R. C. Dalla-Martha, J. D. N. Costa, et al., “Asymptomatic infections by Plasmodium falciparum and Plasmodium vivax in the Brazilian Amazon basin: to treat or not to treat?” Memórias do Instituto Oswaldo Cruz, vol. 107, no. 5, pp. 621–629, 2012.
[16]  T. H. Katsuragawa, L. H. S. Gil, M. S. Tada et al., “The dynamics of transmission and spatial distribution of malaria in riverside areas of Porto Velho, Rond?nia, in the Amazon Region of Brazil,” PLoS ONE, vol. 5, no. 2, Article ID e9245, 2010.
[17]  J. M. Villalobos-Salcedo, M. S. Tada, E. Kimura, M. J. Menezes, and L. H. Pereira-da-Silva, “In-vivo sensitivity of Plasmodium vivax isolates from Rond?nia (western Amazon region, Brazil) to regimens including chloroquine and primaquine,” Annals of Tropical Medicine and Parasitology, vol. 94, no. 8, pp. 749–758, 2000.
[18]  M. S. Tada, Epidemiologia da malária em áreas ribeirinhas urbanas e suburbanas do município de Porto Velho. Rond?nia (Amaz?nia Ocidental). Ensaios preliminares de inova??o em métodos de controle [Ph.D. thesis], Federal University of Rond?nia, Núcleo de Saúde, 2008.
[19]  N. Senn, P. Rarau, D. I. Stanisic, L. Robinson, C. Barnadas, et al., “Intermittent preventive treatment for malaria in papua new guinean infants exposed to Plasmodium falciparum and P. vivax: a randomized controlled trial,” PLoS Medicine, vol. 9, no. 3, Article ID e1001195, 2012.
[20]  M. Kweku, D. Liu, M. Adjuik et al., “Seasonal intermittent preventive treatment for the prevention of anaemia and malaria in Ghanaian children: a randomized, placebo controlled trial,” PLoS ONE, vol. 3, no. 12, Article ID e4000, 2008.
[21]  B. Cissé, C. Sokhna, D. Boulanger et al., “Seasonal intermittent preventive treatment with artesunate and sulfadoxine-pyrimethamine for prevention of malaria in Senegalese children: a randomised, placebo-controlled, double-blind trial,” The Lancet, vol. 367, no. 9511, pp. 659–667, 2006.
[22]  K. Bojang, F. Akor, O. Bittaye et al., “A randomised trial to compare the safety, tolerability and efficacy of three drug combinations for intermittent preventive treatment in children,” PLoS ONE, vol. 5, no. 6, Article ID e11225, 2010.
[23]  A. Dicko, I. Sagara, M. S. Sissoko et al., “Impact of intermittent preventive treatment with sulphadoxine-pyrimethamine targeting the transmission season on the incidence of clinical malaria in children in Mali,” Malaria Journal, vol. 7, article 123, 2008.
[24]  A. T. Konaté, J. B. Yaro, A. Z. Ouédraogo et al., “Intermittent preventive treatment of malaria provides substantial protection against malaria in children already protected by an insecticide-treated bednet in Burkina Faso: a randomised, double-blind, placebo-controlled trial,” PLoS Medicine, vol. 8, no. 2, Article ID e1000408, 2011.
[25]  B. Greenwood, “Review: intermittent preventive treatment: a new approach to the prevention of malaria in children in areas with seasonal malaria transmission,” Tropical Medicine and International Health, vol. 11, no. 7, pp. 983–991, 2006.
[26]  A. L. Wilson, “A systematic review and meta-analysis of the efficacy and safety of intermittent preventive treatment of malaria in children (IPTc),” PLoS ONE, vol. 6, no. 2, Article ID e16976, 2011.
[27]  A. T. Konaté, J. B. Yaro, A. Z. Ouédraogo, A. Diarra, A. Gansané, et al., “Morbidity from Malaria in children in the year after they had received intermittent preventive treatment of Malaria: a randomised trial,” PLoS ONE, vol. 6, no. 8, Article ID e23391, 2011.
[28]  A. Dicko, A. I. Diallo, I. Tembine et al., “Intermittent preventive treatment of malaria provides substantial protection against malaria in children already protected by an insecticide-treated bednet in mali: a randomised, double-blind, placebo-controlled trial,” PLoS Medicine, vol. 8, no. 2, Article ID e1000407, 2011.
[29]  C. Pitt, H. Diawara, D. J. Ouédraogo, S. Diarra, H. Kaboré, et al., “Intermittent preventive treatment of Malaria in children: a qualitative study of community perceptions and recommendations in Burkina Faso and Mali,” PLoS ONE, vol. 7, no. 3, Article ID e32900, 2012.
[30]  B. Greenwood, “Anti-malarial drugs and the prevention of malaria in the population of malaria endemic areas,” Malaria Journal, vol. 9, supplement 3, article S2, 2010.
[31]  G. Snounou, “Detection and identification of the four malaria parasite species infecting humans by PCR amplification,” Methods in Molecular Biology, vol. 50, pp. 263–291, 1996.
[32]  Brasil, Federal Ministry of Health, A??es de Controle da Malária. Manual para Profissionais de Saúde na Aten??o Básica. Série A. Normas e Manuais Técnicos, Federal Ministry of Health, Brasília, Brazil, 1st edition, 2006.
[33]  N. J. White, M. Van Vugt, and F. Ezzet, “Clinical pharmacokinetics and pharmacodynamics of artemether-lumefantrine,” Clinical Pharmacokinetics, vol. 37, no. 2, pp. 105–125, 1999.
[34]  O. P. Forattini, Culicidologia Médica, vol. 2, Faculdade de Saúde Pública, S?o Paulo University, 2002.
[35]  A. Bj?rkman, J. Brohult, and P. O. Pehrson, “Monthly antimalarial chemotherapy to children in a holoendemic area of Liberia,” Annals of Tropical Medicine and Parasitology, vol. 80, no. 2, pp. 155–167, 1986.
[36]  B. Ntab, B. Cissé, D. Boulanger et al., “Impact of intermittent preventive anti-malarial treatment on the growth and nutritional status of preschool children in rural Senegal (West Africa),” The American Journal of Tropical Medicine and Hygiene, vol. 77, no. 3, pp. 411–417, 2007.
[37]  S. Sesay, P. Milligan, E. Touray et al., “A trial of intermittent preventive treatment and home-based management of malaria in a rural area of the Gambia,” Malaria Journal, vol. 10, article 22, 2011.
[38]  E. A. Pereira, E. A. Y. Ishikawa, and C. J. F. Fontes, “Adherence to Plasmodium vivax malaria treatment in the Brazilian Amazon region,” Malaria Journal, vol. 10, article 355, 2011.
[39]  P. C. F. Graf, S. Durand, C. A. Antonio, C. Montalvan, A. G. Montoya, et al., “Failure of supervised chloroquina and primaquine regimen for the treatment of Plasmodium vivax in the Peruvian Amazon,” Malaria Research and Treatment, vol. 2012, Article ID 936067, 5 pages, 2012.
[40]  F. S. de Santana Filho, A. R. D. L. Arcanjo, Y. M. Chehuan et al., “Chloroquine-resistant Plasmodium vivax, Brazilian Amazon,” Emerging Infectious Diseases, vol. 13, no. 7, pp. 1125–1126, 2007.
[41]  B. Roshanravan, E. Kari, R. H. Gilman et al., “Endemic malaria in the Peruvian Amazon region of Iquitos,” The American journal of tropical medicine and hygiene, vol. 69, no. 1, pp. 42–52, 2003.
[42]  M. da Silva-Nunes, C. T. Code?o, R. S. Malafronte et al., “Malaria on the amazonian frontier: transmission dynamics, risk factors, spatial distribution, and prospects for control,” The American Journal of Tropical Medicine and Hygiene, vol. 79, no. 4, pp. 624–635, 2008.

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