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Implications of insecticide resistance for malaria vector control with long-lasting insecticidal nets: a WHO-coordinated, prospective, international, observational cohort study

Authors :
Tessa B. Knox
Jonathan Lines
Dipak Kumar Swain
Jude D. Bigoga
Martin J. Donnelly
Alioun Adechoubou
Immo Kleinschmidt
Kamaraju Raghavendra
Aurore Ogouyemi-Hounto
Celestin Kouambeng
Mujahid Sheikhedin Abdin
Etienne Fondjo
Mariam Okê-Sopoh
Sylvie Cornelie
Martin Akogbeto
Neena Valecha
Philippa A. West
Khalid A Elmardi
Abraham Mnzava
Elfatih M. Malik
Vincent Corbel
Nabie Bayoh
Charles Mbogo
Teresa Kinyari
Mehul Kumar Chourasia
Luna Kamau
Krishanthi Subramaniam
Evan M. Mathenge
Hmooda Toto Kafy
Zinga José Nkuni
Bashir Adam Ismail
Michael B. Macdonald
Eric Ochomo
Josiane Etang
Rajendra M Bhatt
Achille Massougbodji
Herman Parfait Awono-Ambene
Jackie Cook
John S. Bradley
Source :
The Lancet Infectious Diseases. 18:640-649
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Summary 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.

Details

ISSN :
14733099
Volume :
18
Database :
OpenAIRE
Journal :
The Lancet Infectious Diseases
Accession number :
edsair.doi.dedup.....c57eab6539d6232cb661a030c3bfabb9
Full Text :
https://doi.org/10.1016/s1473-3099(18)30172-5