Evidence map›Paper›PMID 33650319›Full record

ReviewClinical and translational science2021

Drugs used for the treatment of cerebral and disseminated infections caused by free-living amoebae.

Alexandre Taravaud, Zineb Fechtali-Moute, Philippe M Loiseau, Sébastien Pomel

Open access · goldAbstract readReview
In one paragraph

Review in Clinical and translational science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. The potential of nanocomposites (patuletin-conjugated with gallic acid-coated zinc oxide) against free-living amoebae pathogens.International microbiology : the official journal of the Spanish Society for Microbiology · 2025
    Article
  8. Encystment and Excystment Processes inPathogens (Basel, Switzerland) · 2025
    Review
  9. Article
  10. Article
  11. 18F-FDG PET/CT findings in fatalRadiology case reports · 2024
    Article
  12. Review
  13. DisseminatedFrontiers in medicine · 2024
    Article
  14. Induction of Programmed Cell Death inAntioxidants (Basel, Switzerland) · 2023
    Article
  15. Nanocarrier Drug Conjugates Exhibit Potent Anti-Diseases (Basel, Switzerland) · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. In Silico Structural Analysis of Serine CarboxypeptidaseInternational journal of molecular sciences · 2022
    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

4 authors at 2 institutions in 1 country.

Alexandre TaravaudBioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, Châtenay-Malabry, France.
Zineb Fechtali-MouteBioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, Châtenay-Malabry, France.
Philippe M LoiseauBioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, Châtenay-Malabry, France.
Sébastien PomelBioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, Châtenay-Malabry, France.
Université Paris-Saclay · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Free-living amoebae (FLAs) are protozoa developing autonomously in diverse natural or artificial environments. The FLAs Acanthamoeba spp., Balamuthia mandrillaris, and Naegleria fowleri represent a risk for human health as they can become pathogenic and cause severe cerebral infections, named granulomatous amoebic encephalitis (GAE), Balamuthia amoebic encephalitis (BAE), and primary amoebic meningoencephalitis (PAM), respectively. Additionally, Acanthamoeba sp. can also rarely disseminate to diverse organs, such as the skin, sinuses, or bones, and cause extracerebral disseminated acanthamebiasis (EDA). No consensus treatment has been established for cerebral FLA infections or EDA. The therapy of cerebral and disseminated FLA infections often empirically associates a large diversity of drugs, all exhibiting a high toxicity. Nevertheless, these pathologies lead to a high mortality, above 90% of the cases, even in the presence of a treatment. In the present work, a total of 474 clinical cases of FLA infections gathered from the literature allowed to determine the frequency of usage, as well as the efficacy of the main drugs and drug combinations used in the treatment of these pathologies. The efficacy of drug usage was determined based on the survival rate after drug administration. The most efficient drugs, drug combinations, and their mechanism of action were discussed in regard to the present recommendations for the treatment of GAE, EDA, BAE, and PAM. At the end, this review aims to provide a useful tool for physicians in their choice to optimize the treatment of FLA infections.

Indexed as

AmebiasisAmebicidesAmoebaCentral Nervous System Protozoal InfectionsDrug Therapy, CombinationHumansSurvival RateTreatment OutcomeAmebicides

Identifiers

PMID33650319
PMCPMC8212752
OpenAlexW3134004284

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.