Evidence map›Paper›PMID 33076928›Full record

ArticleMalaria journal2020

Protective effects of Olyset® Net on Plasmodium falciparum infection after three years of distribution in western Kenya.

Noriko Tamari, Noboru Minakawa, George O Sonye, Beatrice Awuor, James O Kongere, Muneaki Hashimoto, Masatoshi Kataoka, Stephen Munga

Abstract readComparative Study
In one paragraph

Article in Malaria journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Noriko TamariInstitute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523, Japan. norikotamari@email.arizona.edu.ORCID http://orcid.org/0000-0002-1793-5983
Noboru MinakawaInstitute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523, Japan.
George O SonyeAbility To Solve By Knowledge Project, Mbita, Homa Bay, Kenya.
Beatrice AwuorAbility To Solve By Knowledge Project, Mbita, Homa Bay, Kenya.
James O KongereCentre for Research in Tropical Medicine and Community Development, Nairobi, Kenya.
Muneaki HashimotoNational Institute of Advanced Industrial Science and Technology (AIST), Health Research Institute, Kagawa, Japan.
Masatoshi KataokaNational Institute of Advanced Industrial Science and Technology (AIST), Health Research Institute, Kagawa, Japan.
Stephen MungaCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral types of insecticides, treating technologies and materials are available for long-lasting insecticide-treated nets (LLINs). The variations may result in different efficacies against mosquitoes and correspondingly infection risks for the Plasmodium falciparum malaria parasite. This cross-sectional study investigated whether infection risk varied among children who slept under different LLIN brands in rural villages of western Kenya.

methodsChildren sleeping under various types of LLINs were tested for P. falciparum infection using a diagnostic polymerase chain reaction (PCR) assay. Data were collected for other potential factors associated with infection risk: sleeping location (with bed/without bed), number of persons sharing the same net, dwelling wall material, gap of eaves (open/close), proportional hole index, socio-economic status, and density of indoor resting anophelines. Bed-net efficacy against the Anopheles gambiae susceptible strain was estimated using the WHO cone test and the tunnel test. The residual insecticide content on nets was measured.

resultsSeven LLIN brands were identified, and deltamethrin-based DawaPlus® 2.0 was the most popular (48%) followed by permethrin-based Olyset® Net (28%). The former LLIN was distributed in the area about six months before the present study was conducted, and the latter net was distributed at least three years before. Of 254 children analysed, P. falciparum PCR-positive prevalence was 58% for DawaPlus® 2.0 users and 38% for Olyset® users. The multiple regression analysis revealed that the difference was statistically significant (adjusted OR: 0.67, 95% credible interval: 0.45-0.97), whereas the confounders were not statistically important. Among randomly selected net samples, all DawaPlus® 2.0 (n = 20) and 95% of Olyset® (n = 19) passed either the cone test or the tunnel test.

conclusionsOlyset® was more effective in reducing infection risk compared with DawaPlus® 2.0. Although the data from the present study were too limited to explain the mechanism clearly, the results suggest that the characteristics of the former brand are more suitable for the conditions, such as vector species composition, of the study area.

Indexed as

AnimalsAnophelesChildChild, PreschoolCross-Sectional StudiesFemaleHumansInsecticidesInsecticide-Treated BednetsKenyaMalaria, FalciparumMaleMosquito ControlPrevalenceRural PopulationInsecticidesDawaPlus® 2.0DeltamethrinLlinsMalariaOlyset®PermethrinPlasmodiumRepellent effects

Identifiers

PMID33076928
PMCPMC7574443

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.