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Veterinary parasitology2010; 171(1-2); 116-122; doi: 10.1016/j.vetpar.2010.03.001

Selective anthelmintic therapy of horses in the Federal states of Bavaria (Germany) and Salzburg (Austria): an investigation into strongyle egg shedding consistency.

Abstract: For 9 consecutive months (March-November 2008), faecal samples were collected monthly from 129 horses residing within 40 km of Salzburg, Austria. Samples were analysed quantitatively using a modified McMaster egg counting technique. Whenever a faecal egg count (FEC) result exceeded 250 eggs per gram (EPG), the horse was treated with pyrantel, ivermectin or moxidectin. In 52 of 129 horses (40.3%), no strongyle eggs were ever detected over the course of 9 months. In 39 horses (30.2%), strongyle eggs were detected in at least 1 sample, but the egg count never exceeded 250 EPG. The remaining 38 (29.5%) horses were treated at least once in response to a FEC that exceeded 250 EPG. As a result of this selective anthelmintic scheme, the total number of anthelmintic treatments was reduced to 54% of the number of treatments administered to the same horses in the previous year. Both the maximum and mean FEC dropped significantly after initiation of the study. A statistically significant, negative correlation was demonstrated between the maximum and mean FEC of a horse and its age. Pasture hygiene appeared to reduce FECs, but the effect was not statistically significant. The magnitude of the initial FEC was significantly correlated with the maximum FECs in the subsequent 8 months (p<0.01). The same relationship was observed for the maximum FEC of the first 2 samples. Furthermore, horses which required several anthelmintic treatments had a higher initial FEC and a greater maximum FEC in the first 2 samples than horses which received only one or no treatment. These results suggest that selective anthelmintic treatment accomplished a reduced pasture contamination with strongyle eggs, while simultaneously decreasing the number of anthelmintic treatments. Sustained implementation of a selective treatment strategy has the potential to reduce selection pressure for anthelmintic resistance. These results reported herein will assist equine practitioners in designing and monitoring sustainable anthelmintic treatment programs.
Publication Date: 2010-03-07 PubMed ID: 20356680DOI: 10.1016/j.vetpar.2010.03.001Google Scholar: Lookup
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  • Journal Article

Summary

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This study explores the use of selective anthelmintic treatment for horses in the areas of Bavaria, Germany and Salzburg, Austria. The research found this method, which involves only treating horses when strongyle egg counts exceed a certain threshold, to result in reduced overall use of anthelmintic treatments and an associated decrease in strongyle egg pasture contamination.

Research Methodology

  • Over the course of nine months (from March to November 2008), 129 horses within 40 km of Salzburg, Austria had faecal samples collected each month.
  • These samples went through a quantitative analysis using a modified McMaster egg counting technique.
  • If a faecal egg count (FEC) result exceeded 250 eggs per gram (EPG), the horse received treatment with either pyrantel, ivermectin, or moxidectin.

Key Findings

  • Out of 129 horses, no strongyle eggs were detected in 52 horses (40.3%) over the nine-month duration.
  • In 39 horses (30.2%), strongyle eggs surfaced in at least one sample, but the egg count never exceeded 250 EPG.
  • The remaining 38 horses (29.5%) received at least one treatment in response to a FEC that crossed 250 EPG.
  • Through this selective anthelmintic scheme, the total number of anthelmintic treatments significantly reduced to 54% of that administered to the same horses in the preceding year.
  • Both the maximum and mean FEC considerably reduced post the onset of this study.
  • A significant negative correlation was demonstrated between a horse’s maximum and mean FEC and its age.
  • Despite observing a decrease in FEC with better pasture hygiene, the effect was not statistically significant.

Implications of the Study

  • The initial FEC of a horse was found to be significantly correlated with the maximum FECs in the subsequent eight months, suggesting that higher initial FEC may be predictive of higher subsequent FECs.
  • Horses which necessitated multiple anthelmintic treatments had a higher initial FEC and a greater maximum FEC in the first two samples compared to horses which required only one or no treatment.
  • This research underscores that selective anthelmintic treatment can lead to reduced pasture contamination with strongyle eggs, while also decreasing the number of utilized anthelmintic treatments.
  • Persistent implementation of a selective treatment strategy could potentially lower the selection pressure for anthelmintic resistance.
  • The study’s findings provide valuable insights to aid equine practitioners in conceptualizing and overseeing sustainable anthelmintic treatment programs.

Cite This Article

APA
Becher AM, Mahling M, Nielsen MK, Pfister K. (2010). Selective anthelmintic therapy of horses in the Federal states of Bavaria (Germany) and Salzburg (Austria): an investigation into strongyle egg shedding consistency. Vet Parasitol, 171(1-2), 116-122. https://doi.org/10.1016/j.vetpar.2010.03.001

Publication

ISSN: 1873-2550
NlmUniqueID: 7602745
Country: Netherlands
Language: English
Volume: 171
Issue: 1-2
Pages: 116-122

Researcher Affiliations

Becher, A M
  • Equine Practice Dr. Müller, Hauptstr. 9, 83395 Freilassing, Germany. annebecher@gmx.de
Mahling, M
    Nielsen, M K
      Pfister, K

        MeSH Terms

        • Animals
        • Anthelmintics / administration & dosage
        • Anthelmintics / therapeutic use
        • Austria / epidemiology
        • Feces / parasitology
        • Female
        • Gastrointestinal Diseases / drug therapy
        • Gastrointestinal Diseases / epidemiology
        • Gastrointestinal Diseases / parasitology
        • Gastrointestinal Diseases / veterinary
        • Germany / epidemiology
        • Horses
        • Male
        • Parasite Egg Count / veterinary
        • Seasons
        • Statistics, Nonparametric
        • Strongyle Infections, Equine / drug therapy
        • Strongyle Infections, Equine / epidemiology
        • Strongyle Infections, Equine / parasitology
        • Strongyloidea / growth & development

        Citations

        This article has been cited 10 times.
        1. Whitlock F, van Dijk J, Hodgkinson JE, Grewar JD, Newton JR. Reasons to be fearful? Rising proportions of positive faecal worm egg counts among UK horses (2007-2023). Equine Vet J 2025 Nov;57(6):1572-1583.
          doi: 10.1111/evj.14478pubmed: 39840839google scholar: lookup
        2. Nielsen MK, Slusarewicz P, Kuzmina TA, Denwood MJ. US-wide equine strongylid egg count data demonstrate seasonal and regional trends. Parasitology 2024 May;151(6):579-586.
          doi: 10.1017/S0031182024000489pubmed: 38629125google scholar: lookup
        3. Elghryani N, McAloon C, Mincher C, McOwan T, de Waal T. Comparison of the Automated OvaCyte Telenostic Faecal Analyser versus the McMaster and Mini-FLOTAC Techniques in the Estimation of Helminth Faecal Egg Counts in Equine. Animals (Basel) 2023 Dec 16;13(24).
          doi: 10.3390/ani13243874pubmed: 38136911google scholar: lookup
        4. Ramalho Sousa S, Anastácio S, Nóvoa M, Paz-Silva A, Madeira de Carvalho LM. Gastrointestinal Parasitism in Miranda Donkeys: Epidemiology and Selective Control of Strongyles Infection in the Northeast of Portugal. Animals (Basel) 2021 Jan 11;11(1).
          doi: 10.3390/ani11010155pubmed: 33440886google scholar: lookup
        5. Roelfstra L, Quartier M, Pfister K. Preliminary Data from Six Years of Selective Anthelmintic Treatment on Five Horse Farms in France and Switzerland. Animals (Basel) 2020 Dec 15;10(12).
          doi: 10.3390/ani10122395pubmed: 33333748google scholar: lookup
        6. Harvey AM, Meggiolaro MN, Hall E, Watts ET, Ramp D, Šlapeta J. Wild horse populations in south-east Australia have a high prevalence of Strongylus vulgaris and may act as a reservoir of infection for domestic horses. Int J Parasitol Parasites Wildl 2019 Apr;8:156-163.
          doi: 10.1016/j.ijppaw.2019.01.008pubmed: 30815358google scholar: lookup
        7. Misuno E, Clark CR, Anderson SL, Jenkins E, Wagner B, Dembek K, Petrie L. Characteristics of parasitic egg shedding over a 1-year period in foals and their dams in 2 farms in central Saskatchewan. Can Vet J 2018 Mar;59(3):284-292.
          pubmed: 29599559
        8. Kaspar A, Pfister K, Nielsen MK, Silaghi C, Fink H, Scheuerle MC. Detection of Strongylus vulgaris in equine faecal samples by real-time PCR and larval culture - method comparison and occurrence assessment. BMC Vet Res 2017 Jan 11;13(1):19.
          doi: 10.1186/s12917-016-0918-ypubmed: 28077153google scholar: lookup
        9. Schneider S, Pfister K, Becher AM, Scheuerle MC. Strongyle infections and parasitic control strategies in German horses - a risk assessment. BMC Vet Res 2014 Nov 12;10:262.
          doi: 10.1186/s12917-014-0262-zpubmed: 25387542google scholar: lookup
        10. Becher AM, Pfister K. [The efficacy of anthelmintic drugs against horse strongyles in the area of Salzburg and preliminary results of selective anthelmintic treatment]. Wien Klin Wochenschr 2010 Oct;122 Suppl 3:71-5.
          doi: 10.1007/s00508-010-1441-ypubmed: 20924696google scholar: lookup