Evidence map›Paper›PMID 29676250›Full record

ReviewParasite (Paris, France)2018

Plasmodium falciparum resistance to artemisinin-based combination therapies: A sword of Damocles in the path toward malaria elimination.

Manel Ouji, Jean-Michel Augereau, Lucie Paloque, Françoise Benoit-Vical

Open access · goldAbstract readReview
In one paragraph

Review in Parasite (Paris, France), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 2 pooled it
19.5field-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.

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

91 citing papers in PubMed, 2 syntheses or guidelines pooled it, 177 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Observational
  8. Article
  9. Article
  10. A review on molecular markers ofJournal of parasitic diseases : official organ of the Indian Society for Parasitology · 2025
    Review
  11. Review
  12. Article
  13. Review
  14. Observational
  15. Article
  16. Article
  17. Supercritical COBiotechnology notes (Amsterdam, Netherlands) · 2025
    Review
  18. Evaluation of the transmission-blocking potential ofFrontiers in cellular and infection microbiology · 2025
    Article
  19. Article
  20. Article

31 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

4 authors at 2 institutions in 1 country.

Manel OujiLCC (Laboratoire de Chimie de Coordination du CNRS), BP 44099, 205 Route de Narbonne, 31077 Toulouse cedex 4, France - Université de Toulouse; UPS, INPT; LCC; F-31077 Toulouse, France.
Jean-Michel AugereauLCC (Laboratoire de Chimie de Coordination du CNRS), BP 44099, 205 Route de Narbonne, 31077 Toulouse cedex 4, France - Université de Toulouse; UPS, INPT; LCC; F-31077 Toulouse, France.
Lucie PaloqueLCC (Laboratoire de Chimie de Coordination du CNRS), BP 44099, 205 Route de Narbonne, 31077 Toulouse cedex 4, France - Université de Toulouse; UPS, INPT; LCC; F-31077 Toulouse, France.
Françoise Benoit-VicalLCC (Laboratoire de Chimie de Coordination du CNRS), BP 44099, 205 Route de Narbonne, 31077 Toulouse cedex 4, France - Université de Toulouse; UPS, INPT; LCC; F-31077 Toulouse, France.
Laboratoire de Chimie de Coordination · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of artemisinin-based combination therapies (ACTs), which combine an artemisinin derivative with a partner drug, in the treatment of uncomplicated malaria has largely been responsible for the significant reduction in malaria-related mortality in tropical and subtropical regions. ACTs have also played a significant role in the 18% decline in the incidence of malaria cases from 2010 to 2016. However, this progress is seriously threatened by the reduced clinical efficacy of artemisinins, which is characterised by delayed parasitic clearance and a high rate of recrudescence, as reported in 2008 in Western Cambodia. Resistance to artemisinins has already spread to several countries in Southeast Asia. Furthermore, resistance to partner drugs has been shown in some instances to be facilitated by pre-existing decreased susceptibility to the artemisinin component of the ACT. A major concern is not only the spread of these multidrug-resistant parasites to the rest of Asia but also their possible appearance in Sub-Saharan Africa, the continent most affected by malaria, as has been the case in the past with parasite resistance to other antimalarial treatments. It is therefore essential to understand the acquisition of resistance to artemisinins by Plasmodium falciparum to adapt malaria treatment policies and to propose new therapeutic solutions.

Indexed as

Drug Resistance, MultipleAfrica South of the SaharaAntimalarialsArtemisininsAsiaAsia, SoutheasternCambodiaClinical Trials as TopicDisease EradicationDrug Therapy, CombinationHumansMalariaMalaria, FalciparumPlasmodium falciparumAntimalarialsArtemisinins

Identifiers

PMID29676250
PMCPMC5909375
OpenAlexW2799282155

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.