Evidence map›Paper›PMID 30201918›Full record

ReviewToxins2018

Venomous Arachnid Diagnostic Assays, Lessons from Past Attempts.

Camila Dias-Lopes, Ana Luiza Paiva, Clara Guerra-Duarte, Franck Molina, Liza Felicori

Abstract readReview
In one paragraph

Review in Toxins, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. 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

5 authors.

Camila Dias-LopesDepartamento de Bioquímica e Imunologia, UFMG, Belo Horizonte 31270901, Brazil. camiladlopes@gmail.com.
Ana Luiza PaivaFundação Ezequiel Dias (FUNED), Belo Horizonte 30510010, Brazil. analubpaiva@gmail.com.
Clara Guerra-DuarteFundação Ezequiel Dias (FUNED), Belo Horizonte 30510010, Brazil. claragd@gmail.com.
Franck MolinaSys2Diag UMR 9005 CNRS Alcediag, 34000 Montpellier, France. franck.molina@sys2diag.cnrs.fr.
Liza FelicoriDepartamento de Bioquímica e Imunologia, UFMG, Belo Horizonte 31270901, Brazil. liza@icb.ufmg.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diagnostic tests for arachnid accidents remain unavailable for patients and clinicians. Together with snakes, these accidents are still a global medical concern, and are recognized as neglected tropical issues. Due to arachnid toxins' fast mechanism of action, quick detection and quantification of venom is required to accelerate treatment decisions, rationalize therapy, and reduce costs and patient risks. This review aims to understand the current limitations for arachnid venom identification and quantification in biological samples. We benchmarked the already existing initiatives regarding test requirements (sample or biomarkers of choice), performances (time, detection limit, sensitivity and specificity) and their validation (on animal models or on samples from envenomed humans). Our analysis outlines unmet needs for improving diagnosis and consequently treatment of arachnid accidents. Hence, based on lessons from past attempts, we propose a road map for raising best practice guidelines, leading to recommendations for future progress in the development of arachnid diagnostic assays.

Indexed as

AnimalsAntiveninsBiological AssayDiagnostic Tests, RoutineHumansSpider BitesSpider VenomsAntiveninsSpider Venomsantivenomarachnidsdiagnosisenvenomationspiders and scorpions

Identifiers

PMID30201918
PMCPMC6162545

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.