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Epidemiological study on factors influencing the occurrence of helminth eggs in horses in Germany based on sent-in diagnostic samples

https://doi.org/10.1007/s00436-022-07765-4
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/vetr.332openalex-snapshot
Anthelmintic resistance in equids
inferredcites →https://doi.org/10.1007/s00436-011-2362-zopenalex-snapshot
Prevalence of helminths in horses in the state of Brandenburg, Germany
inferredcites →https://doi.org/10.1007/s00436-011-2379-3openalex-snapshot
Further evaluation in field tests of the activity of three anthelmintics (fenbendazole, oxibendazole, and pyrantel pamoate) against the ascarid Parascaris equorum in horse foals on eight farms in Central Kentucky (2009–2010)
inferredcites →https://doi.org/10.1007/s00436-012-3150-0openalex-snapshot
Prevalence, intensity and seasonality of gastrointestinal parasites in abattoir horses in Germany
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Efficacy of selected anthelmintic drugs against cyathostomins in horses in the federal state of Brandenburg, Germany
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10-year parasitological examination results (2003 to 2012) of faecal samples from horses, ruminants, pigs, dogs, cats, rabbits and hedgehogs
inferredcites →https://doi.org/10.1016/0020-7519(79)90076-6openalex-snapshot
The migration and development of Parascaris equorum in the horse
inferredcites →https://doi.org/10.1016/0020-7519(94)00214-9openalex-snapshot
The prevalence and epidemiology of gastrointestinal parasites of horses in Victoria, Australia
inferredcites →https://doi.org/10.1016/j.cveq.2009.04.003openalex-snapshot
Parasitism and Colic
inferredcites →https://doi.org/10.1016/j.exppara.2008.10.001openalex-snapshot
Species-specific identification of equine cyathostomes resistant to fenbendazole and susceptible to oxibendazole and moxidectin by macroarray probing
inferredcites →https://doi.org/10.1016/j.ijpara.2014.03.006openalex-snapshot
Anthelmintic efficacy on UK Thoroughbred stud farms
inferredcites →https://doi.org/10.1016/j.ijpddr.2014.10.003openalex-snapshot
Anthelmintic resistance in equine nematodes
inferredcites →https://doi.org/10.1016/j.ijpddr.2020.09.004openalex-snapshot
Importation of macrocyclic lactone resistant cyathostomins on a US thoroughbred farm
inferredcites →https://doi.org/10.1016/j.ijppaw.2019.01.008openalex-snapshot
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
inferredcites →https://doi.org/10.1016/j.jevs.2012.05.072openalex-snapshot
Determining Treatment to Control Two Multidrug-Resistant Parasites on a Texas Horse Farm
inferredcites →https://doi.org/10.1016/j.tvjl.2016.11.003openalex-snapshot
Shortened egg reappearance after ivermectin or moxidectin use in horses in the UK
inferredcites →https://doi.org/10.1016/j.vetpar.2005.11.019openalex-snapshot
The detection of anthelmintic resistance in nematodes of veterinary importance
inferredcites →https://doi.org/10.1016/j.vetpar.2006.09.036openalex-snapshot
Cases of reduced cyathostomin egg-reappearance period and failure of Parascaris equorum egg count reduction following ivermectin treatment as well as survey on pyrantel efficacy on German horse farms
inferredcites →https://doi.org/10.1016/j.vetpar.2007.10.014openalex-snapshot
Parascaris equorum in foals and in their environment on a Swedish stud farm, with notes on treatment failure of ivermectin
inferredcites →https://doi.org/10.1016/j.vetpar.2009.09.043openalex-snapshot
Effects of fecal collection and storage factors on strongylid egg counts in horses
inferredcites →https://doi.org/10.1016/j.vetpar.2010.08.007openalex-snapshot
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
inferredcites →https://doi.org/10.1016/j.vetpar.2011.08.015openalex-snapshot
Evaluation of conventional PCR for detection of Strongylus vulgaris on horse farms
inferredcites →https://doi.org/10.1016/j.vetpar.2011.10.009openalex-snapshot
Anthelmintic resistance in non-strongylid parasites of horses
inferredcites →https://doi.org/10.1016/j.vetpar.2011.10.010openalex-snapshot
Anthelmintic resistance in equine parasites – detection, potential clinical relevance and implications for control
inferredcites →https://doi.org/10.1016/j.vetpar.2011.11.048openalex-snapshot
An inconvenient truth: Global worming and anthelmintic resistance
inferredcites →https://doi.org/10.1016/j.vetpar.2013.11.030openalex-snapshot
Anthelmintic resistance in equine parasites—Current evidence and knowledge gaps
inferredcites →https://doi.org/10.1016/j.vetpar.2014.01.004openalex-snapshot
Anthelmintic resistance in important parasites of horses: Does it really matter?
inferredcites →https://doi.org/10.1016/j.vetpar.2014.03.020openalex-snapshot
Selective therapy in equine parasite control—Application and limitations
inferredcites →https://doi.org/10.1016/j.vetpar.2014.08.028openalex-snapshot
The efficacy of ivermectin, pyrantel and fenbendazole against Parascaris equorum infection in foals on farms in Australia
inferredcites →https://doi.org/10.1016/j.vetpar.2016.07.024openalex-snapshot
Strongylids in domestic horses: Influence of horse age, breed and deworming programs on the strongyle parasite community
inferredcites →https://doi.org/10.1016/j.vetpar.2016.08.021openalex-snapshot
Repeatability of strongyle egg counts in naturally infected horses
inferredcites →https://doi.org/10.1016/j.vetpar.2017.02.018openalex-snapshot
Strongyle egg reappearance period after moxidectin treatment and its relationship with management factors in UK equine populations
inferredcites →https://doi.org/10.1016/j.vetpar.2018.05.006openalex-snapshot
Risk factors associated with strongylid egg count prevalence and abundance in the United States equine population
inferredcites →https://doi.org/10.1016/j.vetpar.2018.07.001openalex-snapshot
Equine parasite control and the role of national legislation – A multinational questionnaire survey
inferredcites →https://doi.org/10.1016/j.vetpar.2019.08.004openalex-snapshot
Risk factors for equine intestinal parasite infections and reduced efficacy of pyrantel embonate against Parascaris sp.
inferredcites →https://doi.org/10.1016/j.vetpar.2019.108926openalex-snapshot
A survey of the level of horse owner uptake of evidence-based anthelmintic treatment protocols for equine helminth control in the UK
inferredcites →https://doi.org/10.1016/j.vetpar.2021.109494openalex-snapshot
Diagnosing Strongylus vulgaris in pooled fecal samples
inferredcites →https://doi.org/10.1016/j.vetpar.2021.109509openalex-snapshot
What makes a good fecal egg count technique?
inferredcites →https://doi.org/10.1016/j.vetpar.2022.109676openalex-snapshot
World association for the advancement of veterinary parasitology (WAAVP): Third edition of guideline for evaluating the efficacy of equine anthelmintics
inferredcites →https://doi.org/10.1016/s0034-5288(18)32899-6openalex-snapshot
The development of immunity to Parascaris equorum infection in the foal
inferredcites →https://doi.org/10.1016/s0749-0739(17)30718-6openalex-snapshot
Ascarids: Recent Advances
inferredcites →https://doi.org/10.1017/s003118201200128xopenalex-snapshot
Variation in fecal egg counts in horses managed for conservation purposes: individual egg shedding consistency, age effects and seasonal variation
inferredcites →https://doi.org/10.1017/s0031182012001941openalex-snapshot
Helminth egg excretion with regard to age, gender and management practices on UK Thoroughbred studs
inferredcites →https://doi.org/10.1017/s0031182018001786openalex-snapshot
Anthelmintic resistance and novel control options in equine gastrointestinal nematodes
inferredcites →https://doi.org/10.1051/vetres:2002035openalex-snapshot
Anthelmintic resistance in nematodes of horses
inferredcites →https://doi.org/10.1111/eve.12536openalex-snapshot
Evidence‐based considerations for control of Parascaris spp. infections in horses
inferredcites →https://doi.org/10.1111/eve.12541openalex-snapshot
Control of helminth parasites in juvenile horses
inferredcites →https://doi.org/10.1111/j.2042-3292.2012.00454.xopenalex-snapshot
Determination of anthelmintic efficacy against equine cyathostomins and P arascaris equorum in F rance
inferredcites →https://doi.org/10.1111/j.2042-3306.2010.00065.xopenalex-snapshot
Practical aspects of equine parasite control: A review based upon a workshop discussion consensus
inferredcites →https://doi.org/10.1111/j.2042-3306.2011.00397.xopenalex-snapshot
An update on cyathostomins: Anthelmintic resistance and diagnostic tools
inferredcites →https://doi.org/10.1136/inp.i5287openalex-snapshot
Anthelmintic resistance in equine helminths and mitigating its effects
inferredcites →https://doi.org/10.1136/vr.154.2.39openalex-snapshot
Prevalence of benzimidazole resistance on horse farms in Germany
inferredcites →https://doi.org/10.1186/1751-0147-51-45openalex-snapshot
Anthelmintic efficacy on Parascaris equorum in foals on Swedish studs
inferredcites →https://doi.org/10.1186/1756-3305-2-s2-s1openalex-snapshot
Equine cyathostomins: a review of biology, clinical significance and therapy
inferredcites →https://doi.org/10.1186/1756-3305-2-s2-s2openalex-snapshot
Anthelmintic resistance in cyathostomin populations from horse yards in Italy, United Kingdom and Germany
inferredcites →https://doi.org/10.1186/1756-3305-2-s2-s3openalex-snapshot
Effects of worm control practices examined by a combined faecal egg count and questionnaire survey on horse farms in Germany, Italy and the UK
inferredcites →https://doi.org/10.1186/1756-3305-2-s2-s8openalex-snapshot
Diagnosis and control of anthelmintic-resistant Parascaris equorum
inferredcites →https://doi.org/10.1186/s12917-014-0262-zopenalex-snapshot
Strongyle infections and parasitic control strategies in German horses ― a risk assessment
inferredcites →https://doi.org/10.1186/s13028-021-00569-zopenalex-snapshot
Anthelmintic resistance of horse strongyle nematodes to ivermectin and pyrantel in Lithuania
inferredcites →https://doi.org/10.1186/s13071-019-3445-4openalex-snapshot
Systematic review of gastrointestinal nematodes of horses from Australia
inferredcites →https://doi.org/10.1186/s13071-020-04318-5openalex-snapshot
Investigations on the occurrence of tapeworm infections in German horse populations with comparison of different antibody detection methods based on saliva and serum samples
inferredcites →https://doi.org/10.1186/s13071-020-04396-5openalex-snapshot
Meta-analysis of cyathostomin species-specific prevalence and relative abundance in domestic horses from 1975–2020: emphasis on geographical region and specimen collection method
inferredcites →https://doi.org/10.1186/s13071-021-05103-8openalex-snapshot
Cyathostomin resistance to moxidectin and combinations of anthelmintics in Australian horses
inferredcites →https://doi.org/10.1186/s13071-022-05168-zopenalex-snapshot
Parasite dynamics in untreated horses through one calendar year
inferredcites →https://doi.org/10.1186/s13071-022-05266-yopenalex-snapshot
Comparison of FECPAKG2, a modified Mini-FLOTAC technique and combined sedimentation and flotation for the coproscopic examination of helminth eggs in horses
inferredcites →https://doi.org/10.2174/138920112800399310openalex-snapshot
Macrocyclic Lactones for Parasite Control in Equids
inferredcites →https://doi.org/10.21836/pem20150401openalex-snapshot
Management factors and their impact on helminthic fecal egg count in horses
inferredcites →https://doi.org/10.2460/javma.2004.225.903openalex-snapshot
Prevalence of anthelmintic resistant cyathostomes on horse farms
inferredcites →https://doi.org/10.2478/bvip-2013-0030openalex-snapshot
Effect of Storage and Preservation of Horse Faecal Samples on the Detectability and Viability of Strongylid Nematode Eggs and Larvae
inferredcites →https://doi.org/10.2478/helm-2020-0042openalex-snapshot
The effects of seasonality and group size on fecal egg counts in wild Przewalski’s horses ( Equus ferus przewalskii , Poljakov, 1881) in the Chernobyl Exclusion Zone, Ukraine during 2014 – 2018
inferredcites →https://doi.org/10.2746/042516409x471485openalex-snapshot
Endoparasite control management on horse farms – lessons from worm prevalence and questionnaire data
inferredcites →https://doi.org/10.2746/095777308x356956openalex-snapshot
A review of the use of moxidectin in horses
inferredcites →https://doi.org/10.3389/fcimb.2017.00283openalex-snapshot
Nematode Species Identification—Current Status, Challenges and Future Perspectives for Cyathostomins
inferredcites →https://doi.org/10.3390/ani11051345openalex-snapshot
The Use of Molecular Profiling to Track Equine Reinfection Rates of Cyathostomin Species Following Anthelmintic Administration
inferredcites →https://doi.org/10.3390/ani9121156openalex-snapshot
Parasites in Horses Kept in A 2.5 Year-Round Grazing System in Nordic Conditions without Supplementary Feeding
inferredcites →https://doi.org/10.3390/vetsci8030042openalex-snapshot
Reduced Efficacy of Fenbendazole and Pyrantel Pamoate Treatments against Intestinal Nematodes of Stud and Performance Horses
inferredcites →https://doi.org/10.4102/jsava.v74i2.505openalex-snapshot
Anthelmintic treatment in horses : the extra-label use of products and the danger of under-dosing

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Prevalence and Risk Factors of Gastrointestinal Helminths Infection in Brazilian Horses: A Retrospective Study of a 12-Year (2008-2019) Diagnostic Data
inferred← citeshttps://doi.org/10.1007/s00436-024-08417-5openalex-snapshot
Changes in equine strongylid communities after two decades of annual anthelmintic treatments at the farm level
inferred← citeshttps://doi.org/10.1007/s00436-024-08438-0openalex-snapshot
Prevalence, risk factors, and species diversity of strongylid nematodes in domesticated Thai horses: insights from ITS-2 rDNA metabarcoding
inferred← citeshttps://doi.org/10.1007/s44338-025-00096-5openalex-snapshot
Occurrence of gastrointestinal helminthiasis and efficacy of anthelmintics in equines in Shashemene and Asella districts, Oromia, Ethiopia
inferred← citeshttps://doi.org/10.1016/j.jevs.2026.106050openalex-snapshot
Age-related comparative study of C-reactive protein, lipid profile biomarkers, and strongyle nematode gastrointestinal parasitic burden in horses
inferred← citeshttps://doi.org/10.1016/j.parint.2025.103115openalex-snapshot
Mapping the epidemiology and intensity of Parascaris equorum infection in equids in Erbil Province, Iraq
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2023.106100openalex-snapshot
Prevalence and seasonal dynamic of gastrointestinal parasites in equids in France during two years
inferred← citeshttps://doi.org/10.1016/j.rvsc.2024.105272openalex-snapshot
Prevalence and risk factors of gastrointestinal helminths infection in Brazilian horses: A retrospective study of a 12-year (2008–2019) diagnostic data
inferred← citeshttps://doi.org/10.1016/j.vas.2026.100821openalex-snapshot
Prevalence, distribution, and associated risk factors of major equine endoparasitic infections in South Gondar Zone, Northwest Ethiopia
inferred← citeshttps://doi.org/10.1016/j.vetpar.2023.110094openalex-snapshot
Understanding temporal and spatial distribution of intestinal nematodes of horses using faecal egg counts and DNA metabarcoding
inferred← citeshttps://doi.org/10.1016/j.vprsr.2025.101328openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.vprsr.2026.101581openalex-snapshot
Study of risk factors for the infection by Parascaris spp. of young equids in Normandy (Northwestern France)
inferred← citeshttps://doi.org/10.1051/npvequi/2025031openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/evj.14036openalex-snapshot
BEVA primary care clinical guidelines: Equine parasite control
inferred← citeshttps://doi.org/10.1111/evj.14478openalex-snapshot
Reasons to be fearful? Rising proportions of positive faecal worm egg counts among UK horses (2007–2023)
inferred← citeshttps://doi.org/10.1186/s13071-025-07192-1openalex-snapshot
Characterizing mixed strongyle infections in foals and broodmares using cytochrome c oxidase subunit I deep amplicon sequencing
inferred← citeshttps://doi.org/10.2139/ssrn.5043185openalex-snapshot
The Effect of Social Rank on Gastrointestinal Helminth Prevalence, Intensity, and Species Richness in Semi-Domesticated Horses Elliott, J. A & Thomas, G.R.* Aa Department of Bioscience, Swansea University, Singleton Park, Swansea, Wales UK Sa2 8pp Corresponding Author: * G.R.Thomas@Swansea.Ac.Uk…
inferred← citeshttps://doi.org/10.2478/helm-2026-0019openalex-snapshot
Coprological assessment of gastrointestinal helminths in Arabian Thoroughbred horses housed in a stable in the Constantine region, Algeria
inferred← citeshttps://doi.org/10.3390/ani13182928openalex-snapshot
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inferred← citeshttps://doi.org/10.4142/jvs.23291openalex-snapshot
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