Verification of documentation plausibility in equine passports–drug documentation for geldings in comparison to self-reported veterinarian drug usage for equine castrations in Germany

Author:

Schneider Shary TamaraORCID,Isbrandt Rudi,Gehlen Heidrun,Langkabel NinaORCID,Meemken Diana

Abstract

The ‘positive list for equines’ (Regulation (EC) No 1950/2006) was implemented in the European Union in 2006. The drugs listed are approved for use in slaughter equines under certain conditions, although those drugs are not approved for use in livestock and are not listed in Table 1 of the annex to Regulation (EU) No 37/2010. The usage of such drugs has to be documented in the equine passport and a withdrawal period of six months must be adhered to before the equine can be slaughtered for human consumption. Since the withdrawal period is long, correct documentation is particularly important. This study compared the results of two sub-studies. In sub-study 1, 116 veterinarians and nine equine clinics in Germany were surveyed about the methods and drugs used for castration of equine stallions. In sub-study 2, the documentational findings of 195 equine passports, belonging to 194 horses and one donkey, were analyzed. Regarding sub-study 1, the most commonly used method for castration was reported as ‘laid down’. Drug combinations entailing at least one drug from the ‘positive list’ were used by 86.7% (91/105) of veterinarians castrating horse stallions ‘laid down’ and by 64.3% (36/56) of veterinarians utilizing this method on donkey stallions. Regarding sub-study 2, drug documentation was verified in the passports of 4.6% (9/195) of all equines and in just 12.0% (3/25) of those belonging to slaughter equine geldings. Anesthetics from the ‘positive list’ were documented in 4.0% (1/25) of equine passports belonging to slaughter geldings. Because of the high discrepancy of the drug combinations used by veterinarians and the documentation actually found in equine passports, we conclude that drug administration is very seldom documented in equine passports in Germany. This could result in drug residues in equine meat and poses a potential risk for consumers.

Funder

Freie Universität Berlin

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference19 articles.

1. COMMISSION REGULATION (EC) No 504/2008 of 6 June 2008 implementing Council Directives 90/426/EEC and 90/427/EEC as regards methods for the identification of equidae. Latest consolidated version: 21/11/2014 [Internet]. [cited 2023 Jan 05]. Available from: https://eur-lex.europa.eu/eli/reg/2008/504/oj.

2. COMMISSION IMPLEMENTING REGULATION (EU) 2015/262 of 17 February 2015 laying down rules pursuant to Council Directives 90/427/EEC and 2009/156/EC as regards the methods for the identification of equidae (Equine Passport Regulation) [Internet]. [cited 2023 Jan 05]. Available from: http://data.europa.eu/eli/reg_impl/2015/262/oj.

3. COMMISSION IMPLEMENTING REGULATION (EU) 2021/963 of 10 June 2021 laying down rules for the application of Regulations (EU) 2016/429, (EU) 2016/1012 and (EU) 2019/6 of the European Parliament and of the Council with regard to the identification and registration of equine animals and establishing model identification documents for those animals [Internet]. [cited 2023 Jan 05]. Available from: http://data.europa.eu/eli/reg_impl/2021/963/oj.

4. COMMISSION REGULATION (EC) No 1950/2006 of 13 December 2006 establishing, in accordance with Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products, a list of substances essential for the treatment of equidae. Current consolidated version: 16/02/2013 [Internet]. [cited 2023 Jan 05]. Available from: http://data.europa.eu/eli/reg/2006/1950/oj.

5. COMMISSION REGULATION (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin. Current consolidated version: 23/03/2023 [Internet]. [cited 2023 Jan 05]. Available from: http://data.europa.eu/eli/reg/2010/37(1)/oj.

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