Evidence map›Paper›PMID 37798141›Full record

ArticleJournal of the Pediatric Infectious Diseases Society2023

Abacavir Drug Exposures in African Children Under 14 kg Using Pediatric Solid Fixed Dose Combinations According to World Health Organization Weight Bands.

Suthunya Chupradit, Dalton C Wamalwa, Elizabeth Maleche-Obimbo, Adeodata R Kekitiinwa, Juliet Mwanga-Amumpaire, Elizabeth A Bukusi, Winstone M Nyandiko, Joseph K Mbuthia, Alistair Swanson, DNDi Clinical Team and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Pediatric Infectious Diseases Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

13 authors at 8 institutions in 5 countries.

Suthunya ChupraditPhD's Degree Program in Pharmacy, Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.
Dalton C WamalwaDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
Elizabeth Maleche-ObimboDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
Adeodata R KekitiinwaBaylor College of Medicine Children's Foundation, Kampala, Uganda.
Juliet Mwanga-AmumpaireEpicentre, Mbarara, Uganda.
Elizabeth A BukusiCentre for Microbiology Research, Kenya Medical Research Institute, Kisumu, Kenya.
Winstone M NyandikoDepartment of Child Health and Paediatrics-Moi University, AMPATH and Moi Teaching and Referral Hospital, Eldoret, Kenya.
Joseph K MbuthiaGertrude's Children's Hospital, Nairobi, Kenya.
Alistair SwansonDrugs for Neglected Diseases Initiative, Geneva, Switzerland.
DNDi Clinical Team
Tim R CresseyAMS/IRD Research Collaboration, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.
Baralee PunyawudhoDepartment of Pharmaceutical Care, Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.
Victor MusiimeJoint Clinical Research Centre, Kampala, Uganda.
Chiang Mai University · THUniversity of Nairobi · KEBaylor College of Medicine Children’s Foundation · UGEpicentre Uganda · UGJoint Clinical Research Centre · UGKenya AIDS Vaccine Initiative · KEKenya Medical Research Institute · KEMoi University · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe pharmacokinetics of abacavir (ABC) in African children living with HIV (CLHIV) weighing <14 kg and receiving pediatric fixed dose combinations (FDC) according to WHO weight bands dosing are limited. An ABC population pharmacokinetic model was developed to evaluate ABC exposure across different World Health Organization (WHO) weight bands.

methodsChildren enrolled in the LIVING study in Kenya and Uganda receiving ABC/lamivudine (3TC) dispersible tablets (60/30 mg) according to WHO weight bands. A population approach was used to determine the pharmacokinetic parameters. Monte Carlo simulations were conducted using an in silico population with demographic characteristics associated with African CLHIV. ABC exposures (AUC0-24) of 6.4-50.4 mg h/L were used as targets.

resultsPlasma samples were obtained from 387 children. A 1-compartment model with allometric scaling of clearance (CL/F) and volume of distribution (V/F) according to body weight best characterized the pharmacokinetic data of ABC. The maturation of ABC CL/F was characterized using a sigmoidal Emax model dependent on postnatal age (50% of adult CL/F reached by 0.48 years of age). Exposures to ABC were within the target range for children weighing 6.0-24.9 kg, but children weighing 3-5.9 kg were predicted to be overexposed.

conclusionsLowering the ABC dosage to 30 mg twice daily or 60 mg once daily for children weighing 3-5.9 kg increased the proportion of children within the target and provided comparable exposures. Further clinical study is required to investigate clinical implications and safety of the proposed alternative ABC doses.

Indexed as

Anti-HIV AgentsHIV InfectionsAbacavirAdultChildDideoxynucleosidesHumansInfantKenyaUgandaAbacavirAnti-HIV AgentsDideoxynucleosidesAbacavirAfrican childrendose optimizationNONMEMpopulation pharmacokinetics

Identifiers

PMID37798141
PMCPMC10756690
OpenAlexW4387389076

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.