Affiliations 

  • 1 Vector Unit, Ministry of Health, Khartoum, Sudan
  • 2 School of Biological Sciences, Universiti Sains Malaysia, 11800 Pulau Penang, Malaysia
  • 3 Malaria Programme, World Health Organization, 1202 Geneva, Switzerland
  • 4 Department of Disease Control, London School of Hygiene and Tropical Medicine (LSHTM), London WC1E 7HT, United Kingdom
  • 5 Kilimanjaro Christian Medical University College, Moshi, Tanzania
  • 6 Malaria Research and Training Centre, Sennar, Sudan
  • 7 State Malaria Control Programme, Gedarif, Sudan
  • 8 Department of Infectious Disease Epidemiology, LSHTM, London WC1E 7HT, United Kingdom
  • 9 Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool L35QA, United Kingdom
  • 10 Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool L35QA, United Kingdom; janet.hemingway@lstmed.ac.uk martin.donnelly@lstmed.ac.uk Immo.Kleinschidmt@LSHTM.ac.uk
  • 11 Ministry of Health, Khartoum, Sudan
  • 12 Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA 70112
  • 13 Department of Infectious Disease Epidemiology, LSHTM, London WC1E 7HT, United Kingdom; janet.hemingway@lstmed.ac.uk martin.donnelly@lstmed.ac.uk Immo.Kleinschidmt@LSHTM.ac.uk
Proc Natl Acad Sci U S A, 2017 12 26;114(52):E11267-E11275.
PMID: 29229808 DOI: 10.1073/pnas.1713814114

Abstract

Insecticide-based interventions have contributed to ∼78% of the reduction in the malaria burden in sub-Saharan Africa since 2000. Insecticide resistance in malaria vectors could presage a catastrophic rebound in disease incidence and mortality. A major impediment to the implementation of insecticide resistance management strategies is that evidence of the impact of resistance on malaria disease burden is limited. A cluster randomized trial was conducted in Sudan with pyrethroid-resistant and carbamate-susceptible malaria vectors. Clusters were randomly allocated to receive either long-lasting insecticidal nets (LLINs) alone or LLINs in combination with indoor residual spraying (IRS) with a pyrethroid (deltamethrin) insecticide in the first year and a carbamate (bendiocarb) insecticide in the two subsequent years. Malaria incidence was monitored for 3 y through active case detection in cohorts of children aged 1 to <10 y. When deltamethrin was used for IRS, incidence rates in the LLIN + IRS arm and the LLIN-only arm were similar, with the IRS providing no additional protection [incidence rate ratio (IRR) = 1.0 (95% confidence interval [CI]: 0.36-3.0; P = 0.96)]. When bendiocarb was used for IRS, there was some evidence of additional protection [interaction IRR = 0.55 (95% CI: 0.40-0.76; P < 0.001)]. In conclusion, pyrethroid resistance may have had an impact on pyrethroid-based IRS. The study was not designed to assess whether resistance had an impact on LLINs. These data alone should not be used as the basis for any policy change in vector control interventions.

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

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