Evidence map›Paper›PMID 33284799›Full record

ArticlePLoS neglected tropical diseases2020

Population pharmacokinetics of ivermectin for the treatment of scabies in Indigenous Australian children.

Amanda Gwee, Stephen Duffull, Xiao Zhu, Steven Y C Tong, Noel Cranswick, Brett McWhinney, Jacobus Ungerer, Joshua Francis, Andrew C Steer

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 26% of its field
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

9 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 6 institutions in 2 countries.

Amanda GweeDepartment of General Medicine, The Royal Children's Hospital Melbourne, Parkville, Victoria, Australia.ORCID 0000-0003-4016-8986
Stephen DuffullSchool of Pharmacy, University of Otago, Dunedin, New Zealand.
Xiao ZhuInfection and Immunity theme, Murdoch Children's Research Institute, Parkville, Victoria, Australia.ORCID 0000-0003-3295-619X
Steven Y C TongVictorian Infectious Diseases Service, The Royal Melbourne Hospital, and Doherty Department University of Melbourne, at the Peter Doherty Institute for Infection and Immunity, Victoria, Australia.ORCID 0000-0002-1368-8356
Noel CranswickDepartment of General Medicine, The Royal Children's Hospital Melbourne, Parkville, Victoria, Australia.
Brett McWhinneyDepartment of Chemical Pathology, Pathology Queensland, Brisbane, Queensland, Australia.
Jacobus UngererDepartment of Chemical Pathology, Pathology Queensland, Brisbane, Queensland, Australia.
Joshua FrancisGlobal and tropical health division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
Andrew C SteerDepartment of General Medicine, The Royal Children's Hospital Melbourne, Parkville, Victoria, Australia.
Royal Children's Hospital · AUQueensland Health · AUCharles Darwin University · AUMurdoch Children's Research Institute · AUThe Royal Melbourne Hospital · AUUniversity of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ivermectin is a broad-spectrum antiparasitic agent used for the treatment and control of neglected tropical diseases. In Australia, ivermectin is primarily used for scabies and is licensed in children aged ≥5 years weighing >15 kg. However, young children, aged <5 years, are particularly vulnerable to scabies and its secondary complications. Therefore, this study aimed to determine an appropriate ivermectin dose for children aged 2 to 4 years and weighing ≤15 kg. We conducted a prospective, pharmacokinetic study of ivermectin in Indigenous Australian children aged between 5 and 15 years and weighing >15 kg. Doses of 200 μg/kg rounded to the nearest whole or half 3 mg tablet were given to children with scabies and ivermectin concentrations determined at two time points after dosing. A population pharmacokinetic model was developed using non-linear mixed effects modelling. A separate covariate database of children aged 2 to 4 years and weighing <15 kg was used to generate 1000 virtual patients and simulate the dose required to achieve equivalent drug exposure in young children as those aged ≥5 years. Overall, 26 children who had 48 ivermectin concentrations determined were included, 11 (42%) were male, the median age was 10.9 years and median body weight 37.6 kg. The final model was a two-compartment model with first-order absorption and linear elimination. For simulated children aged 2 to 4 years, a dose of 3 mg in children weighing 10-15 kg produced similar drug exposures to those >5 years. The median simulated area under the concentration-time curve was 976 μg∙h/L. Using modelling, we have identified a dosing strategy for ivermectin in children aged 2 to 4 years and weighing less than 15 kg that can be prospectively evaluated for safety and efficacy.

Indexed as

AustraliaChildChild, PreschoolFemaleHumansIvermectinMaleScabiesIvermectin

Identifiers

PMID33284799
PMCPMC7746298
OpenAlexW3112165889

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.