Evidence map›Paper›PMID 35189818›Full record

Trial reportBMC infectious diseases2022

Effectiveness and safety of artesunate-amodiaquine versus artemether-lumefantrine for home-based treatment of uncomplicated Plasmodium falciparum malaria among children 6-120 months in Yaoundé, Cameroon: a randomized trial.

Peter Thelma Ngwa Niba, Akindeh Mbuh Nji, Innocent Mbulli Ali, Lawrence Fonyonga Akam, Cedric Hermann Dongmo, Jean Paul Kengne Chedjou, Calvino Tah Fomboh, William Dorian Nana, Ornella Laetitia Ayem Oben, Abdel Aziz Selly-Ngaloumo and 20 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04565184 (Monitoring the Effectiveness and Safety of Artesunate-Amodiaquine and Artemether-Lumefantrine During the Treatment of Uncomplicated Plasmodium Falciparum Malaria Among Children in Yaounde, Cameroon), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.6field-weighted citation impact, top 11% 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.

NCT04565184 phase4completednot on this map

Monitoring the Effectiveness and Safety of Artesunate-Amodiaquine and Artemether-Lumefantrine During the Treatment of Uncomplicated Plasmodium Falciparum Malaria Among Children in Yaounde, Cameroon

TypeinterventionalSponsorUniversity of Yaounde 1Ran2019 to 2020Enrolled242ConditionsMalaria,FalciparumArmsArtesunate-amodiaquine combination, Artemether, Lumefantrine Drug Combination
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Evolution of Plasmodium falciparum antimalarial drug resistance markers post-adoption of artemisinin-based combination therapies in Yaounde, Cameroon.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2023
    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

30 authors at 8 institutions in 2 countries.

Peter Thelma Ngwa NibaMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Akindeh Mbuh NjiMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Innocent Mbulli AliThe Biotechnology Center, University of Yaoundé I, Yaoundé, Cameroon.
Lawrence Fonyonga AkamMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Cedric Hermann DongmoMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Jean Paul Kengne ChedjouMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Calvino Tah FombohMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
William Dorian NanaMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Ornella Laetitia Ayem ObenMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Abdel Aziz Selly-NgaloumoMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Marcel N MoyehMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Jude Achidi NguMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Ambassa Jean LudovicDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Pierre Martiniel AbohDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Marie Carine Enyegue AmbaniDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Pierrette Albertine Mbarga OmgbaDistrict Hospital, Cité Verte, Yaoundé, Cameroon.
Grâce Bissohong KotcholiDistrict Hospital, Cité Verte, Yaoundé, Cameroon.
Linus Moye AdzemyeDistrict Hospital, Cité Verte, Yaoundé, Cameroon.
Danielle Regine Abenkou NnaDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Adèle DouanlaDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Ze AngoDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Marie Sophie EwaneDistrict Medical Center, Minkoa-Meyos, Yaoundé, Cameroon.
Joel Tewara TichaMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Fritz Mbuh TatahMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Golwa DinzaMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Valentine Nchafor NdikumDepartment of Pharmacology and African Traditional Medicine, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Dorothy A FosahNational Malaria Control Program, Ministry of Public Health, Yaoundé, Cameroon.
Jude D BigogaMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon.
Michael AlifrangisCentre for Medical Parasitology, Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Wilfred F MbachamMARCAD-DELTAS Program, Laboratory for Public Health Research Biotechnologies, University of Yaoundé I, Yaoundé, Cameroon. wfmbacham@yahoo.com.
Université de Yaoundé I · CMUniversity Teaching Hospital of Yaounde · CMBamenda University of Science and Technology · CMCopenhagen University Hospital · DKMinistry of Public Health · CMUniversité de Dschang · CMUniversity of Buea · CMYaoundé General Hospital · CM

Funding

AAS/AESA/Wellcome trust UK grant # DEL-15-010EPA EP-C-15-010Wellcome Trust
6 · The paper itself

Abstract

backgroundMany studies have reported high efficacy and safety of artesunate-amodiaquine (AS-AQ) and artemether-lumefantrine (AL) when administered under direct observation in Cameroon. There is paucity of data to support their continuous use in home-based treatment of uncomplicated Plasmodium falciparum malaria in Cameroon. Hence, this study aimed to assess the effectiveness and safety of AS-AQ versus AL for home-based treatment of uncomplicated P. falciparum malaria among children 6-120 months in Yaoundé, Cameroon.

methodsA two-arm, open-label, randomized, controlled trial comparing the equivalence of AS-AQ (experimental group) and AL (control group) was carried out from May 2019 to April 2020 at two secondary hospitals in Yaoundé. Participants were randomized to receive either AS-AQ or AL. After the first dose, antimalarial drugs were given at home, rather than under direct observation by a study staff. The conventional on-treatment and post-treatment laboratory and clinical evaluations were not done until day 3 of the full antimalarial treatment course. The evaluation of effectiveness was mainly based on per protocol polymerase chain reaction adjusted adequate clinical and parasitological response (PP PCR adjusted ACPR) on day 28 post-treatment. Safety was based on assessment of adverse events (AEs) and severe adverse events (SAEs) from day 1 to day 28.

resultsA total of 242 children were randomized to receive AS-AQ (n = 114) and AL (n = 128). The PP PCR adjusted day 28 cure rates were [AS-AQ = 96.9% (95% CI, 91.2-99.4) versus AL = 95.5% (95% CI, 89.9-98.5), P = 0.797]. Expected mild to moderate adverse events were reported in both arms [AS-AQ = 83 (84.7%) versus AL = 99 (86.1%), P = 0.774]. The most common adverse events included: transient changes of hematologic indices and fever.

conclusionsThis study demonstrated that AS-AQ and AL are effective and safe for home management of malaria in Yaoundé. The evidence from this study supports the parallel use of the two drugs in routine practice. However, the findings from this study do not describe the likely duration of antimalarial effectiveness in holoendemic areas where multiple courses of treatment might be required.

trial registrationThis study is a randomized controlled trial and it was retrospectively registered on 23/09/2020 at ClinicalTrials.gov with registration number NCT04565184.

Indexed as

AntimalarialsArtemisininsMalaria, FalciparumAmodiaquineArtemetherArtemether, Lumefantrine Drug CombinationArtesunateCameroonChildDrug CombinationsEthanolaminesHumansInfantPlasmodium falciparumTreatment OutcomeAmodiaquineAntimalarialsArtemetherArtemether, Lumefantrine Drug CombinationArtemisininsArtesunateDrug CombinationsEthanolaminesArtemether-lumefantrineArtesunate-amodiaquineCameroonEffectivenessMalariaPlasmodium falciparumSafety

Identifiers

PMID35189818
PMCPMC8862275
OpenAlexW4213332912

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Registered trials

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.