Evidence map›Paper›PMID 32107679›Full record

ArticleDigestive diseases and sciences2021

Acute Anisakiasis: Pharmacological Evaluation of Various Drugs in an Animal Model.

Magdalena Gómez-Mateos, Francisco Arrebola, María Concepción Navarro, María Carmen Romero, José María González, Adela Valero

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In one paragraph

Article in Digestive diseases and sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

6 authors at 2 institutions in 1 country.

Magdalena Gómez-MateosDepartment of Parasitology, Faculty of Pharmacy, University of Granada, Campus de Cartuja s/n, 18071, Granada, Spain. magda86@correo.ugr.es.ORCID 0000-0003-1375-1519
Francisco ArrebolaDepartment of Histology, Faculty of Medicine, University of Granada, Avenida de la Investigación 11, 18071, Granada, Spain.
María Concepción NavarroDepartment of Pharmacology, Faculty of Pharmacy, University of Granada, Campus de Cartuja s/n, 18071, Granada, Spain.
María Carmen RomeroDepartment of Parasitology, Faculty of Pharmacy, University of Granada, Campus de Cartuja s/n, 18071, Granada, Spain.
José María GonzálezPharmacy Services, University Hospital San Cecilio of Granada, Calle Dr. Olóriz, 16, 18012, Granada, Spain.
Adela ValeroDepartment of Parasitology, Faculty of Pharmacy, University of Granada, Campus de Cartuja s/n, 18071, Granada, Spain.
Universidad de Granada · ESInstituto de Investigación Biosanitaria de Granada · ES

Funding

Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía BIO-243
6 · The paper itself

Abstract

backgroundThe accidental ingestion of the third larval stage of Anisakis can cause acute clinical symptoms, which are relieved via extraction of the larvae. Although this is a highly effective technique, it can only be practiced when the larvae are found in accessible areas of the gastrointestinal tract, and therefore instead the condition has often been treated using various different drugs.

aimsThis study evaluates the effectiveness of gastric acid secretion inhibitors (omeprazole and ranitidine), gastric mucosal protectants (sucralfate) and anthelmintics (mebendazole and flubendazole) in treating anisakiasis in Wistar rats.

methodsRats were infected with Anisakis-type I larvae and administered the drugs via a gastric probe. Data were recorded regarding the number of live and dead larvae, their location both within the animal and in its feces, and the presence of gastrointestinal lesions. Additionally, gastric pH was measured and histology performed.

resultsWhile rats in all experimental groups exhibited lesions; those treated with ranitidine and mebendazole showed significantly fewer lesions (50% and 35% of rats exhibited lesions, respectively). Histological examination of the gastric lesions revealed infection-induced changes, but no significant differences were observed between the treated and untreated rats.

conclusionsMebendazole was found to be most efficacious in preventing gastrointestinal lesions, followed by ranitidine, which was the most effective antacid of those studied. Both these drugs could thus be considered as part of the conservative management of anisakiasis.

Indexed as

Disease Models, AnimalAcute DiseaseAnimalsAnisakiasisAnthelminticsAntinematodal AgentsAnti-Ulcer AgentsDrug Evaluation, PreclinicalFemaleFishesGastrointestinal TractMebendazoleOmeprazoleRanitidineRatsRats, WistarAnthelminticsAntinematodal AgentsAnti-Ulcer AgentsMebendazoleOmeprazoleRanitidineSucralfateAnisakiasisAnthelminticsDrug therapyGastric acidityStomach histological sections

Identifiers

PMID32107679
OpenAlexW3007258297

What Socratic holds

Textmetadata
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 Socratic graph.