Implications of insecticide resistance for malaria vector control with long-lasting insecticidal nets: a WHO-coordinated, prospective, international, observational cohort study.
Kleinschmidt I, Bradley J, Knox TB, Mnzava AP, Kafy HT, Mbogo C, Ismail BA, Bigoga JD, Adechoubou A, Raghavendra K, Cook J, Malik EM, Nkuni ZJ, Macdonald M, Bayoh N, Ochomo E, Fondjo E, Awono-Ambene HP, Etang J, Akogbeto M, Bhatt RM, Chourasia MK, Swain DK, Kinyari T, Subramaniam K, Massougbodji A, Okê-Sopoh M, Ogouyemi-Hounto A, Kouambeng C, Abdin MS, West P, Elmardi K, Cornelie S, Corbel V, Valecha N, Mathenge E, Kamau L, Lines J, Donnelly MJ.
Date:
2018-06
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.
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