Monitoring equine ascarid and cyathostomin parasites: Evaluating health parameters under different treatment regimens.

BACKGROUND Strongylid and ascarid parasites are omnipresent in equine stud farms, and ever-increasing levels of anthelmintic resistance are challenging the industry with finding more sustainable and yet effective parasite control programs. OBJECTIVES To evaluate egg count levels, bodyweight, and equine health under defined parasite control protocols in foals and mares at two Standardbred and two Thoroughbred stud farms. STUDY DESIGN Longitudinal randomised field trial. METHODS A total of 93 foals were enrolled and split into two treatment groups, and 99 mares were enrolled and assigned to three treatment groups. All horses underwent a health examination, and episodes of colic or diarrhoea were recorded at each faecal collection date. Bodyweights were assessed using a weight tape, and mares were body condition scored. Group A foals (FA) were dewormed at two and five months of age with a fenbendazole/ivermectin/praziquantel product, while group B foals (FB) were dewormed on a monthly basis, alternating between the above-mentioned product and an oxfendazole/pyrantel embonate product. Group A mares (MA) were dewormed twice with fenbendazole/ivermectin/praziquantel, group B mares (MB) were dewormed with the same product, when egg counts exceeded 300 strongylid eggs per gram, and group C mares (MC) were dewormed every two months, alternating between the two products. Health data were collected monthly for 6 months (foals) and bimonthly for 13 months (mares). Data were analysed with mixed linear models and interpreted at the α=0.05 significance level. RESULTS There were no significant bodyweight differences between foal groups, but MA mares were significantly lighter than the other two groups. Very few health incidents were recorded. Foals in group FA had significantly higher ascarid and strongylid egg counts, whereas no significant differences were observed between mare groups. Main limitations: Study duration limited to one season. CONCLUSIONS Anthelmintic treatment intensity was lowered from the traditional intensive regimes without measurable negative health consequences for mares and foals.

[1]  E. Morgan,et al.  A survey of the level of horse owner uptake of evidence-based anthelmintic treatment protocols for equine helminth control in the UK. , 2019, Veterinary parasitology.

[2]  M. K. Nielsen,et al.  Managing anthelmintic resistance in cyathostomin parasites: Investigating the benefits of refugia-based strategies , 2019, International journal for parasitology. Drugs and drug resistance.

[3]  M. K. Nielsen,et al.  Anthelmintic efficacy of single active and combination products against commonly occurring parasites in foals. , 2019, Veterinary parasitology.

[4]  J. Matthews,et al.  Equine de-worming: a consensus on current best practice , 2019, UK-Vet Equine.

[5]  E. Morgan,et al.  Analysis of Strongyle Egg Shedding Consistency in Horses and Factors That Affect It , 2018 .

[6]  M. K. Nielsen,et al.  Encysted cyathostomin larvae in foals - progression of stages and the effect of seasonality. , 2017, Veterinary parasitology.

[7]  E. Wilkes,et al.  Efficacy of a morantel–abamectin combination for the treatment of resistant ascarids in foals , 2017, Australian veterinary journal.

[8]  M. K. Nielsen,et al.  Dynamics of Parascaris and Strongylus spp. parasites in untreated juvenile horses. , 2016, Veterinary parasitology.

[9]  M. K. Nielsen Equine tapeworm infections: Disease, diagnosis and control , 2016 .

[10]  M. K. Nielsen,et al.  Objective evaluation of two deworming regimens in young Thoroughbreds using parasitological and performance parameters. , 2016, Veterinary parasitology.

[11]  M. K. Nielsen Evidence‐based considerations for control of Parascaris spp. infections in horses , 2016 .

[12]  M. K. Nielsen,et al.  Attitudes towards implementation of surveillance-based parasite control on Kentucky Thoroughbred farms - Current strategies, awareness and willingness-to-pay. , 2015, Equine veterinary journal.

[13]  C. Rogers,et al.  Questionnaire study on parasite control practices on Thoroughbred and Standardbred breeding farms in New Zealand. , 2015, Veterinary parasitology.

[14]  I. Scott,et al.  Anthelmintic resistance in equine helminth parasites – a growing issue for horse owners and veterinarians in New Zealand? , 2015, New Zealand veterinary journal.

[15]  M. K. Nielsen,et al.  Selective therapy in equine parasite control--application and limitations. , 2014, Veterinary parasitology.

[16]  M. K. Nielsen,et al.  Anthelmintic resistance in important parasites of horses: does it really matter? , 2014, Veterinary parasitology.

[17]  E. Gee,et al.  Sub-optimal efficacy of ivermectin against Parascaris equorum in foals on three Thoroughbred stud farms in the Manawatu region of New Zealand , 2014, New Zealand veterinary journal.

[18]  E. Lyons,et al.  Strongyloides westeri and Parascaris equorum: Observations in field studies in Thoroughbred foals on some farms in Central Kentucky, USA , 2014, Helminthologia.

[19]  C. Laugier,et al.  Prevalence of Parascaris equorum infection in foals on French stud farms and first report of ivermectin-resistant P. equorum populations in France. , 2012, Veterinary parasitology.

[20]  S. S. Collins,et al.  Analysis of multiyear studies in horses in Kentucky to ascertain whether counts of eggs and larvae per gram of feces are reliable indicators of numbers of strongyles and ascarids present. , 2010, Veterinary parasitology.

[21]  M. K. Nielsen,et al.  Selective anthelmintic therapy of horses in the Federal states of Bavaria (Germany) and Salzburg (Austria): an investigation into strongyle egg shedding consistency. , 2010, Veterinary parasitology.

[22]  N. Côté,et al.  Acute small intestinal obstruction associated with Parascaris equorum infection in young horses: 25 cases (1985–2004) , 2006, New Zealand veterinary journal.

[23]  Dorothee Bienzle,et al.  Larval cyathostominosis in horses in Ontario: an emerging disease? , 2006, The Canadian veterinary journal = La revue veterinaire canadienne.

[24]  D. French,et al.  PREVALENCE OF STRONGYLE NEMATODES IN NATURALLY INFECTED PONIES OF DIFFERENT AGES AND DURING DIFFERENT SEASONS OF THE YEAR IN LOUISIANA , 2003, The Journal of parasitology.

[25]  D. Mellor,et al.  Pathogenicity of cyathostome infection. , 1999, Veterinary parasitology.

[26]  S. Reid,et al.  Epidemiological risk factors associated with a diagnosis of clinical cyathostomiasis in the horse. , 1995, Equine veterinary journal.

[27]  C. Uhlinger Uses of fecal egg count data in equine practice , 1993 .

[28]  J. Georgi,et al.  Equine helminth infections: control by selective chemotherapy. , 1991, Equine veterinary journal.

[29]  J. Duncan,et al.  Preliminary observations on an alternative strategy for the control of horse strongyles. , 1991, Equine veterinary journal.

[30]  B. F. Yeates,et al.  Relationship between condition score, physical measurements and body fat percentage in mares. , 1983, Equine veterinary journal.

[31]  H. Clayton,et al.  Clinical signs associated with parascaris equorum infection in worm-free pony foals and yearlings , 1978 .

[32]  A. F. Russell The development of helminthiasis in thoroughbred foals. , 1948, The Journal of comparative pathology and therapeutics.