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Association between the proportion of Plasmodium falciparum and Plasmodium vivax infections detected by passive surveillance and the magnitude of the asymptomatic reservoir in the community: a pooled analysis of paired health facility and community data.
Stresman, Gillian; Sepúlveda, Nuno; Fornace, Kimberly; Grignard, Lynn; Mwesigwa, Julia; Achan, Jane; Miller, John; Bridges, Daniel J; Eisele, Thomas P; Mosha, Jacklin; Lorenzo, Pauline Joy; Macalinao, Maria Lourdes; Espino, Fe Esperanza; Tadesse, Fitsum; Stevenson, Jennifer C; Quispe, Antonio M; Siqueira, André; Lacerda, Marcus; Yeung, Shunmay; Sovannaroth, Siv; Pothin, Emilie; Gallay, Joanna; Hamre, Karen E; Young, Alyssa; Lemoine, Jean Frantz; Chang, Michelle A; Phommasone, Koukeo; Mayxay, Mayfong; Landier, Jordi; Parker, Daniel M; Von Seidlein, Lorenz; Nosten, Francois; Delmas, Gilles; Dondorp, Arjen; Cameron, Ewan; Battle, Katherine; Bousema, Teun; Gething, Peter; D'Alessandro, Umberto; Drakeley, Chris.
Afiliação
  • Stresman G; Department of Infection Biology, London School of Hygiene & Tropical Medicine, London, UK. Electronic address: gillian.stresman@lshtm.ac.uk.
  • Sepúlveda N; Department of Infection Biology, London School of Hygiene & Tropical Medicine, London, UK; Centre of Statistics and Its Applications, University of Lisbon, Lisbon, Portugal.
  • Fornace K; Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
  • Grignard L; Department of Infection Biology, London School of Hygiene & Tropical Medicine, London, UK.
  • Mwesigwa J; Medical Research Council Unit The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia; Department of Global Health, University of Antwerp, Antwerp, Belgium.
  • Achan J; Medical Research Council Unit The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
  • Miller J; PATH Malaria Control and Elimination Partnership in Africa (MACEPA), National Malaria Elimination Centre, Ministry of Health, Chainama Grounds Lusaka, Zambia.
  • Bridges DJ; PATH Malaria Control and Elimination Partnership in Africa (MACEPA), National Malaria Elimination Centre, Ministry of Health, Chainama Grounds Lusaka, Zambia.
  • Eisele TP; Center for Applied Malaria Research and Evaluation, Department of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, USA.
  • Mosha J; National Institute for Medical Research, Mwanza Medical Research Centre, Mwanza, Tanzania.
  • Lorenzo PJ; Department of Parasitology, Research Institute for Tropical Medicine, Research Drive, Alabang, Muntinlupa, Metro Manila, Philippines.
  • Macalinao ML; Department of Parasitology, Research Institute for Tropical Medicine, Research Drive, Alabang, Muntinlupa, Metro Manila, Philippines.
  • Espino FE; Department of Parasitology, Research Institute for Tropical Medicine, Research Drive, Alabang, Muntinlupa, Metro Manila, Philippines.
  • Tadesse F; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands.
  • Stevenson JC; Macha Research Trust, Choma District, Zambia; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Quispe AM; School of Medicine, Universidad Continental, Huancayo, Peru.
  • Siqueira A; Fundação de Medicina Tropical Dr Heitor Vieira Dourado, Manaus, Brazil; Programa de Pós-graduação em Medicina Tropical, Universidade do Estado do Amazonas, Manaus, Brazil; Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
  • Lacerda M; Fundacao de Medicine Tropical Dr. Heitor Viera Dourado, Manaus, Brazil; Institutos Nacionais de Ciencia e Technologia (INCT), Instituto Elimina, Manaus, Brazil.
  • Yeung S; Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK.
  • Sovannaroth S; National Center for Parasitology, Entomology and Malaria Control, Phnom Penh, Cambodia.
  • Pothin E; Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, University of Basel, Basel, Switzerland; Clinton Health Access Initiative, Boston, MA, USA.
  • Gallay J; Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, University of Basel, Basel, Switzerland.
  • Hamre KE; Centers for Disease Control and Prevention, Center for Global Health, Division of Parasitic Diseases and Malaria, Malaria Branch, Atlanta, GA, USA; CDC Foundation, Atlanta, GA, USA.
  • Young A; Clinton Health Access Initiative, Port-au-Prince, Haiti.
  • Lemoine JF; Programme National de Contrôle de la Malaria, Ministère de la Santé Publique et de la Population (MSPP), Port-au-Prince, Haiti.
  • Chang MA; Centers for Disease Control and Prevention, Center for Global Health, Division of Parasitic Diseases and Malaria, Malaria Branch, Atlanta, GA, USA.
  • Phommasone K; Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos.
  • Mayxay M; Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Institute of Research and Education Development, Universit
  • Landier J; Aix Marseille Univ, IRD, INSERM, SESSTIM, Marseille, France.
  • Parker DM; Department of Population Health and Disease Prevention and Department of Epidemiology, University of California, Irvine, CA, USA.
  • Von Seidlein L; Oxford Tropical Medicine Research Unit, Mahidol University Bangkok, Thailand; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Nosten F; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Shoklo Malaria Research Unit, Mae Sot, Thailand.
  • Delmas G; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Shoklo Malaria Research Unit, Mae Sot, Thailand.
  • Dondorp A; Oxford Tropical Medicine Research Unit, Mahidol University Bangkok, Thailand; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Cameron E; Telethon Kids Institute, Perth Children's Hospital, Nedlands, WA, Australia; Curtin University, Bentley, WA, Australia.
  • Battle K; Institute for Disease Modelling, Seattle, WA, USA.
  • Bousema T; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands.
  • Gething P; Telethon Kids Institute, Perth Children's Hospital, Nedlands, WA, Australia; Curtin University, Bentley, WA, Australia.
  • D'Alessandro U; Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK; Medical Research Council Unit The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
  • Drakeley C; Department of Infection Biology, London School of Hygiene & Tropical Medicine, London, UK.
Lancet Infect Dis ; 20(8): 953-963, 2020 08.
Article em En | MEDLINE | ID: mdl-32277908
BACKGROUND: Passively collected malaria case data are the foundation for public health decision making. However, because of population-level immunity, infections might not always be sufficiently symptomatic to prompt individuals to seek care. Understanding the proportion of all Plasmodium spp infections expected to be detected by the health system becomes particularly paramount in elimination settings. The aim of this study was to determine the association between the proportion of infections detected and transmission intensity for Plasmodium falciparum and Plasmodium vivax in several global endemic settings. METHODS: The proportion of infections detected in routine malaria data, P(Detect), was derived from paired household cross-sectional survey and routinely collected malaria data within health facilities. P(Detect) was estimated using a Bayesian model in 431 clusters spanning the Americas, Africa, and Asia. The association between P(Detect) and malaria prevalence was assessed using log-linear regression models. Changes in P(Detect) over time were evaluated using data from 13 timepoints over 2 years from The Gambia. FINDINGS: The median estimated P(Detect) across all clusters was 12·5% (IQR 5·3-25·0) for P falciparum and 10·1% (5·0-18·3) for P vivax and decreased as the estimated log-PCR community prevalence increased (adjusted odds ratio [OR] for P falciparum 0·63, 95% CI 0·57-0·69; adjusted OR for P vivax 0·52, 0·47-0·57). Factors associated with increasing P(Detect) included smaller catchment population size, high transmission season, improved care-seeking behaviour by infected individuals, and recent increases (within the previous year) in transmission intensity. INTERPRETATION: The proportion of all infections detected within health systems increases once transmission intensity is sufficiently low. The likely explanation for P falciparum is that reduced exposure to infection leads to lower levels of protective immunity in the population, increasing the likelihood that infected individuals will become symptomatic and seek care. These factors might also be true for P vivax but a better understanding of the transmission biology is needed to attribute likely reasons for the observed trend. In low transmission and pre-elimination settings, enhancing access to care and improvements in care-seeking behaviour of infected individuals will lead to an increased proportion of infections detected in the community and might contribute to accelerating the interruption of transmission. FUNDING: Wellcome Trust.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reservatórios de Doenças / Malária Vivax / Malária Falciparum / Infecções Assintomáticas Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reservatórios de Doenças / Malária Vivax / Malária Falciparum / Infecções Assintomáticas Idioma: En Ano de publicação: 2020 Tipo de documento: Article