Affiliations 

  • 1 MRC Tropical Epidemiology Group, Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK; School of Public Health, University of the Witwatersrand, Johannesburg, South Africa. Electronic address: [email protected]
  • 2 MRC Tropical Epidemiology Group, Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK
  • 3 Global Malaria Programme, WHO, Geneva, Switzerland
  • 4 Federal Ministry of Health, Khartoum, Sudan; School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia
  • 5 KEMRI Centre for Geographic Medicine Research Coast, Kilifi, Kenya
  • 6 School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia; Khartoum Malaria Free Initiative, Khartoum, Sudan
  • 7 National Reference Unit (NRU) for Vector Control, The Biotechnology Center, University of Yaoundé I, Yaoundé, Cameroon
  • 8 Programme National de Lutte contre le Paludisme (PNLP), Ministère de la Santé, Cotonou, Benin
  • 9 National Institute of Malaria Research, Indian Council of Medical Research, Department of Health Research, New Delhi, India
  • 10 University of Khartoum, Faculty of Medicine, Department of Community Medicine, Khartoum, Sudan
  • 11 KEMRI/CDC Research and Public Health Collaboration, Kisumu, Kenya
  • 12 National Malaria Control Program, Ministry of Public Health, Yaoundé, Cameroon
  • 13 Organisation de Coordination pour la lutte contre les Endemies en Afrique Centrale (OCEAC), Yaoundé, Cameroon
  • 14 Organisation de Coordination pour la lutte contre les Endemies en Afrique Centrale (OCEAC), Yaoundé, Cameroon; Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon
  • 15 Centre de Recherche Entomologique de Cotonou, Cotonou, Benin
  • 16 University of Nairobi, School of Medicine, College of Health Sciences, Department of Medical Physiology, Nairobi, Kenya
  • 17 Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK
  • 18 Faculté des Sciences de la Santé, Université d'Abomey-Calavi, Cotonou, Benin
  • 19 Federal Ministry of Health, Khartoum, Sudan
  • 20 Maladies Infectieuses et Vecteurs, Ecologie, Génétique, Evolution et Contrôle (MIVEGEC), Institut de Recherche pour le Développement (IRD), CNRS, University of Montpellier, Montpellier, France
  • 21 KEMRI Eastern and Southern Africa Centre of International Parasite Control, Nairobi, Kenya
  • 22 KEMRI Centre for Biotechnology and Research Development, Nairobi, Kenya
  • 23 Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK
  • 24 Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK; Malaria Programme, Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK
Lancet Infect Dis, 2018 Jun;18(6):640-649.
PMID: 29650424 DOI: 10.1016/S1473-3099(18)30172-5

Abstract

BACKGROUND: Scale-up of insecticide-based interventions has averted more than 500 million malaria cases since 2000. Increasing insecticide resistance could herald a rebound in disease and mortality. We aimed to investigate whether insecticide resistance was associated with loss of effectiveness of long-lasting insecticidal nets and increased malaria disease burden.

METHODS: This WHO-coordinated, prospective, observational cohort study was done at 279 clusters (villages or groups of villages in which phenotypic resistance was measurable) in Benin, Cameroon, India, Kenya, and Sudan. Pyrethroid long-lasting insecticidal nets were the principal form of malaria vector control in all study areas; in Sudan this approach was supplemented by indoor residual spraying. Cohorts of children from randomly selected households in each cluster were recruited and followed up by community health workers to measure incidence of clinical malaria and prevalence of infection. Mosquitoes were assessed for susceptibility to pyrethroids using the standard WHO bioassay test. Country-specific results were combined using meta-analysis.

FINDINGS: Between June 2, 2012, and Nov 4, 2016, 40 000 children were enrolled and assessed for clinical incidence during 1·4 million follow-up visits. 80 000 mosquitoes were assessed for insecticide resistance. Long-lasting insecticidal net users had lower infection prevalence (adjusted odds ratio [OR] 0·63, 95% CI 0·51-0·78) and disease incidence (adjusted rate ratio [RR] 0·62, 0·41-0·94) than did non-users across a range of resistance levels. We found no evidence of an association between insecticide resistance and infection prevalence (adjusted OR 0·86, 0·70-1·06) or incidence (adjusted RR 0·89, 0·72-1·10). Users of nets, although significantly better protected than non-users, were nevertheless subject to high malaria infection risk (ranging from an average incidence in net users of 0·023, [95% CI 0·016-0·033] per person-year in India, to 0·80 [0·65-0·97] per person year in Kenya; and an average infection prevalence in net users of 0·8% [0·5-1·3] in India to an average infection prevalence of 50·8% [43·4-58·2] in Benin).

INTERPRETATION: Irrespective of resistance, populations in malaria endemic areas should continue to use long-lasting insecticidal nets to reduce their risk of infection. As nets provide only partial protection, the development of additional vector control tools should be prioritised to reduce the unacceptably high malaria burden.

FUNDING: Bill & Melinda Gates Foundation, UK Medical Research Council, and UK Department for International Development.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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