Evidence map›Paper›PMID 23520478›Full record

Trial reportPloS one2013

Reduced susceptibility of Plasmodium falciparum to artesunate in southern Myanmar.

Myat P Kyaw, Myat H Nyunt, Khin Chit, Moe M Aye, Kyin H Aye, Moe M Aye, Niklas Lindegardh, Joel Tarning, Mallika Imwong, Christopher G Jacob and 4 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02198573 (Molecular Assessment of Artemisinin Resistance Markers, K13 Kelch Propeller and Multi-drug Resistant Gene Polymorphism in Eastern and Western Border Areas of Myanmar), which is not on this map. Cited by 138 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 4 pooled it
28.4field-weighted citation impact, top 1% 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.

NCT02198573 completednot on this map

Molecular Assessment of Artemisinin Resistance Markers, K13 Kelch Propeller and Multi-drug Resistant Gene Polymorphism in Eastern and Western Border Areas of Myanmar

TypeobservationalSponsorMyat Htut NyuntRan2013 to 2014Enrolled91ConditionsDay-3 Positive of Parasitaemia, Prevalence of Drug Resistance Gene Mutation
3 · Its place in the literature

Who cites it

138 citing papers in PubMed, 4 syntheses or guidelines pooled it, 204 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Deletion of theAntimicrobial agents and chemotherapy · 2025
    Article
  11. Review
  12. Article
  13. Antimicrobial agents and chemotherapy · 2023
    Article
  14. Article
  15. A review of malaria molecular markers for drug resistance inFrontiers in cellular and infection microbiology · 2023
    Review
  16. Article
  17. Review
  18. Observational
  19. Article
  20. Article

78 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 5 countries.

Myat P KyawDepartment of Medical Research (Lower Myanmar), Yangon, The Republic of the Union of Myanmar.
Myat H Nyunt
Khin Chit
Moe M Aye
Kyin H Aye
Moe M Aye
Niklas Lindegardh
Joel Tarning
Mallika Imwong
Christopher G Jacob
Charlotte Rasmussen
Jamie Perin
Pascal Ringwald
Myaing M Nyunt
Johns Hopkins University · USMyanmar Oxford Clinical Research Unit · MMMahidol University · THUniversity of Maryland, Baltimore · US

Funding

Howard Hughes Medical InstituteWellcome Trust 089275
6 · The paper itself

Abstract

backgroundPlasmodium falciparum resistance to artemisinins, the first line treatment for malaria worldwide, has been reported in western Cambodia. Resistance is characterized by significantly delayed clearance of parasites following artemisinin treatment. Artemisinin resistance has not previously been reported in Myanmar, which has the highest falciparum malaria burden among Southeast Asian countries.

methodsA non-randomized, single-arm, open-label clinical trial of artesunate monotherapy (4 mg/kg daily for seven days) was conducted in adults with acute blood-smear positive P. falciparum malaria in Kawthaung, southern Myanmar. Parasite density was measured every 12 hours until two consecutive negative smears were obtained. Participants were followed weekly at the study clinic for three additional weeks. Co-primary endpoints included parasite clearance time (the time required for complete clearance of initial parasitemia), parasite clearance half-life (the time required for parasitemia to decrease by 50% based on the linear portion of the parasite clearance slope), and detectable parasitemia 72 hours after commencement of artesunate treatment. Drug pharmacokinetics were measured to rule out delayed clearance due to suboptimal drug levels.

resultsThe median (range) parasite clearance half-life and time were 4.8 (2.1-9.7) and 60 (24-96) hours, respectively. The frequency distributions of parasite clearance half-life and time were bimodal, with very slow parasite clearance characteristic of the slowest-clearing Cambodian parasites (half-life longer than 6.2 hours) in approximately 1/3 of infections. Fourteen of 52 participants (26.9%) had a measurable parasitemia 72 hours after initiating artesunate treatment. Parasite clearance was not associated with drug pharmacokinetics.

conclusionsA subset of P. falciparum infections in southern Myanmar displayed markedly delayed clearance following artemisinin treatment, suggesting either emergence of artemisinin resistance in southern Myanmar or spread to this location from its site of origin in western Cambodia. Resistance containment efforts are underway in Myanmar.

trial registrationAustralian New Zealand Clinical Trials Registry ACTRN12610000896077.

Indexed as

AntimalarialsArtemisininsAdultArtesunateCambodiaDrug ResistanceFemaleHumansMalaria, FalciparumMaleMyanmarPlasmodium falciparumAntimalarialsArtemisininsArtesunate

Identifiers

PMID23520478
PMCPMC3592920
OpenAlexW2020465799

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.