Evidence map›Paper›PMID 28691548›Full record

ReviewCritical reviews in toxicology2017

Characterizing chronic and acute health risks of residues of veterinary drugs in food: latest methodological developments by the joint FAO/WHO expert committee on food additives.

Alan Boobis, Carl Cerniglia, Alan Chicoine, Vittorio Fattori, Markus Lipp, Rainer Reuss, Philippe Verger, Angelika Tritscher

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Critical reviews in toxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  6. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Alan Boobisa Department of Medicine, Centre for Pharmacology & Therapeutics , Imperial College London , London , UK.
Carl Cernigliab Division of Microbiology, National Center for Toxicological Research, Food and Drug Administration , Jefferson , AR , USA.
Alan Chicoinec Department of Veterinary Biomedical Sciences , University of Saskatchewan , Saskatoon , Canada.
Vittorio Fattorid Food Safety and Quality Unit, Agriculture and Consumer Protection Department , Food and Agriculture Organization of the United Nations , Rome , Italy.
Markus Lippd Food Safety and Quality Unit, Agriculture and Consumer Protection Department , Food and Agriculture Organization of the United Nations , Rome , Italy.
Rainer Reusse Food Data Analysis Section, Food Information Science and Technology Branch, Food Standards Australia New Zealand , Barton , Australia.
Philippe Vergerf Department of Food Safety and Zoonoses, World Health Organization , Geneva , Switzerland.
Angelika Tritscherf Department of Food Safety and Zoonoses, World Health Organization , Geneva , Switzerland.

Funding

World Health Organization 001
6 · The paper itself

Abstract

The risk assessment of residues of veterinary drugs in food is a field that continues to evolve. The toxicological end-points to be considered are becoming more nuanced and in light of growing concern about the development of antimicrobial resistance, detailed analysis of the antimicrobial activity of the residues of veterinary drugs in food is increasingly incorporated in the assessment. In recent years, the Joint FAO/WHO Expert Committee on Food Additives (JECFA) has refined its approaches to provide a more comprehensive and fit-for-purpose risk assessment. This publication describes in detail the consideration of acute and chronic effects, the estimation of acute and chronic dietary exposure, current approaches for including microbiological endpoints in the risk assessment, and JECFA's considerations for the potential effects of food processing on residues from veterinary drugs. JECFA now applies these approaches in the development of health-based guidance values (i.e. safe exposure levels) for residues of veterinary drugs. JECFA, thus, comprehensively addresses acute and chronic risks by using corresponding estimates for acute and chronic exposure and suitable correction for the limited bioavailability of bound residues by the Gallo-Torres model. On a case-by-case basis, JECFA also considers degradation products that occur from normal food processing of food containing veterinary drug residues. These approaches will continue to be refined to ensure the most scientifically sound basis for the establishment of health-based guidance values for veterinary drug residues.

Indexed as

AnimalsDietary ExposureDrug ResiduesFood ContaminationHumansRisk AssessmentVeterinary DrugsWorld Health OrganizationVeterinary Drugsexposure assessmentfood safetyJECFAmicrobiological effectsrisk assessmenttoxicological effectsVeterinary drug residues

Identifiers

What OpenQuestion 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 OpenQuestion graph.