Evidence map›Paper›PMID 32778875›Full record

SynthesisThe Journal of infectious diseases2022

Efficacy of Single-Dose Primaquine With Artemisinin Combination Therapy on Plasmodium falciparum Gametocytes and Transmission: An Individual Patient Meta-Analysis.

Kasia Stepniewska, Georgina S Humphreys, Bronner P Gonçalves, Elaine Craig, Roly Gosling, Philippe J Guerin, Ric N Price, Karen I Barnes, Jaishree Raman, Menno R Smit and 25 more

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in The Journal of infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 3 pooled it
6.3field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 3 syntheses or guidelines pooled it, 57 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

35 authors at 20 institutions in 14 countries.

Kasia StepniewskaWorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
Georgina S HumphreysWorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
Bronner P GonçalvesDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Elaine CraigWorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
Roly GoslingDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA.
Philippe J GuerinWorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
Ric N PriceWorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
Karen I BarnesWorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
Jaishree RamanUniversity of Cape Town/Medical Research Council Collaborating Centre for Optimising Antimalarial Therapy, University of Cape Town, Cape Town, South Africa.
Menno R SmitDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Umberto D'AlessandroMedical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Will J R StoneDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Anders BjorkmanDepartment of Microbiology Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Aaron M SamuelsDivision of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Maria I Arroyo-ArroyoGrupo Salud y Comunidad, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.
Guido J H BastiaensDepartment of Medical Microbiology, Radboud University Medical Center, Nijmegen, the Netherlands.
Joelle M BrownDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA.
Alassane DickoMalaria Research and Training Centre, Faculty of Pharmacy and Faculty of Medicine and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Badria B El-SayedTropical Medicine Research Institute, National Centre for Research, Khartoum, Sudan.
Salah-Eldin G ElzakiTropical Medicine Research Institute, National Centre for Research, Khartoum, Sudan.
Alice C EziefulaDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Simon KariukiKenya Medical Research Institute, Kisian, Kenya.
Titus K KwambaiDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Amanda E MaestreGrupo Salud y Comunidad, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.
Andreas MartenssonDepartment of Women's and Children's Health, International Maternal and Child Health, Uppsala University, Uppsala, Sweden.
Dominic MoshaBagamoyo Research and Training Centre, Ifakara Health Institute, Bagamoyo, Tanzania.
Richard O MwaisweloDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Billy E NgasalaDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Joseph OkebeDepartment of International Public Health, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Michelle E RohDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA.
Patrick SawaHuman Health Division, International Centre for Insect Physiology and Ecology, Mbita Point, Kenya.
Alfred B TionoDepartment of Biomedical Sciences, Centre National de Recherche et de Formation sur le Paludisme, Ouagadougou, Burkina Faso.
Ingrid ChenGlobal Health Group, Malaria Elimination Initiative, University of California, San Francisco, California, USA.
Chris J DrakeleyDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Teun BousemaDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0003-2666-094X
University of California, San Francisco · USUniversity of Oxford · GBLiverpool School of Tropical Medicine · GBLondon School of Hygiene & Tropical Medicine · GBRadboud University Nijmegen · NLMuhimbili University of Health and Allied Sciences · TZNational Centre for Research · SDUniversidad de Antioquia · COBrighton and Sussex Medical School · GBCenters for Disease Control and Prevention · USCentre National de Recherche et de Formation sur le Paludisme · BFIfakara Health Institute · TZInternational Centre of Insect Physiology and Ecology · KEKarolinska Institutet · SEKenya Medical Research Institute · KEMahidol University · THNational Health Laboratory Service · ZAUniversity of Bamako · MLUniversity of Cape Town · ZAUppsala University · SE

Funding

Medical Research Council MC_EX_MR/K007203/1Wellcome Trust 200909/Z/16/Z
6 · The paper itself

Abstract

backgroundSince the World Health Organization recommended single low-dose (0.25 mg/kg) primaquine (PQ) in combination with artemisinin-based combination therapies (ACTs) in areas of low transmission or artemisinin-resistant Plasmodium falciparum, several single-site studies have been conducted to assess efficacy.

methodsAn individual patient meta-analysis to assess gametocytocidal and transmission-blocking efficacy of PQ in combination with different ACTs was conducted. Random effects logistic regression was used to quantify PQ effect on (1) gametocyte carriage in the first 2 weeks post treatment; and (2) the probability of infecting at least 1 mosquito or of a mosquito becoming infected.

resultsIn 2574 participants from 14 studies, PQ reduced PCR-determined gametocyte carriage on days 7 and 14, most apparently in patients presenting with gametocytemia on day 0 (odds ratio [OR], 0.22; 95% confidence interval [CI], .17-.28 and OR, 0.12; 95% CI, .08-.16, respectively). Rate of decline in gametocyte carriage was faster when PQ was combined with artemether-lumefantrine (AL) compared to dihydroartemisinin-piperaquine (DP) (P = .010 for day 7). Addition of 0.25 mg/kg PQ was associated with near complete prevention of transmission to mosquitoes.

conclusionsTransmission blocking is achieved with 0.25 mg/kg PQ. Gametocyte persistence and infectivity are lower when PQ is combined with AL compared to DP.

Indexed as

AntimalarialsArtemisininsMalaria, FalciparumAnimalsArtemetherArtemether, Lumefantrine Drug CombinationHumansPlasmodium falciparumPrimaquineAntimalarialsArtemetherArtemether, Lumefantrine Drug CombinationArtemisininsPrimaquinegametocytemiaPlasmodium falciparumsingle low-dose primaquine

Identifiers

PMID32778875
PMCPMC8974839
OpenAlexW3048921488

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.