AAEP Internal Parasite Control Guidelines

Mission Statement

Commonly used strategies for parasite control in adult horses are based largely on knowledge
and concepts that are more than 50 years old. However, much has changed over this time and
information presented on current product labels represents historic information about anti-
parasitic efficacy but does not necessarily reflect current product performance. This
development necessitates a re-examination of recommendations for parasite control. In
response to this need, the AAEP formed a Task Force charged with producing a comprehensive
set of recommendations for helping veterinarians develop improved strategies and programs for
parasite control in horses of all ages. Guidelines will be specified separately for adult and young
horses (less than 3 years).

Recommendations developed in this document are based on the following:

1. Important changes in the parasitic fauna of horses have occurred such that Strongylus
vulgaris and other large strongyles are now rare, and cyathostomins (small strongyles)
and tapeworms are now the major parasites of concern in adult horses, while Parascaris
spp. remains the most important parasite infecting foals and weanlings.
2. Anthelmintic resistance is highly prevalent in cyathostomins and Parascaris spp., and
this must be factored into treatment decisions (Kaplan and Nielsen, 2010).
3. Adult horses vary greatly in their innate susceptibility to infection with cyathostomins and
their level of strongyle egg shedding and thus, require individualized attention to their
parasite control needs.
4. Horses less than about 3 years of age require special attention as they are more
susceptible to parasite infection, and are more at risk for developing disease. This article
will detail the separate approach taken for parasite control in this age group.

AAEP Parasite Control Guidelines

Introduction

Traditional parasite control programs involving rotational treatment with anthelmintics at regular
intervals are commonly recommended by veterinarians. However, this approach is based on
concepts and strategies developed more than 50 years ago when Strongylus vulgaris (large
strongyle bloodworm) was the most important parasitic pathogen of horses (Drudge and Lyons,
1966). The rationale for this parasite control scheme was rather simple: to kill S. vulgaris worms
before they could mature and lay eggs that would contaminate the environment. Since it took
about two months for strongyle eggs to reappear after treatment, treatment every two months
prevented S. vulgaris eggs from being shed on pastures. This approach was very successful in
controlling S. vulgaris infections, and disease from S. vulgaris is now very rare in managed
horse populations.
It is noteworthy that cyathostomins (small strongyles), were not considered important pathogens
at that time, as their pathogenic potential was over-shadowed by S. vulgaris. However, that
situation has changed and currently, cyathostomins (small strongyles), are recognized as a
primary equine parasite pathogen (Love et al., 1999). Similarly, Parascaris spp. is recognized
as a major parasitic pathogen in foals and weanlings (Nielsen, 2016a), and Anoplocephala
perfoliata has been recognized as a cause of ileal colic in the horse (Nielsen, 2016b). The
biology, life-cycles and host-parasite dynamics of the cyathostomins, A. perfoliata and
Parascaris spp. are very different from S. vulgaris, thus strategies designed for controlling S.
vulgaris will not be appropriate or very effective for controlling these parasites.

Decades of frequent anthelmintic use have selected for high levels of anthelmintic drug
resistance in cyathostomin and Parascaris spp. populations (Peregrine et al., 2014), which
emphasizes that the traditional approaches for parasite control are not sustainable and that new
strategies are needed.

Cyathostomins are truly ubiquitous, and all grazing horses are infected. But they are relatively
mild pathogens and only produce disease when infections reach extremely high levels. Thus
disease from strongyle parasites is much less of a concern in adult horses today than it was
decades ago when S. vulgaris was highly prevalent. Frequent anthelmintic treatments are
therefore not needed to keep adult horses healthy. What is needed are properly timed
treatments with effective anthelmintics administered at the appropriate time of the year, which
correspond to the epidemiological cycles of transmission and the relative parasite burdens in
individual horses. In this document we aim to provide the information necessary to implement
parasite control programs for adult horses based on the best available evidence.

TERMINOLOGY TO KNOW AND UNDERSTAND

There are definitions and terminology that are used by parasitologists when discussing equine
parasitology. Commonly used terms have been included to assist in developing a common
verbiage for both the veterinarian and horse owner.

ANTHELMINTIC RESISTANCE
“Resistance is the ability of worms in a population to survive treatments that are generally
effective against the same species and stage of infection. Anthelmintic resistance is an inherited
trait. The development of resistance first requires that resistance genes are present. The rate
of development of resistance is determined by selection pressure and the extent to which
worms surviving treatment pass their genes on to the next generation. With continued selection
and reproduction of resistant worms, the frequency of resistance genes in the local worm
population increases to the point where treatment fails. Once resistance is present, the
population of resistant parasites do not appear to revert to susceptibility, so the aims of
resistance control are to prevent the first steps in the development of resistance and then to
delay the accumulation of resistance genes.” (Sangster, 1999)
 • Anthelmintics (dewormers) select for parasites in the population that have mutations that
confer drug resistance to that drug. Repeated anthelmintic treatments allow the resistant
parasites to preferentially survive and increase in frequency over time.
• The Fecal Egg Count Reduction Test (FECRT) is the only method currently available for
detecting resistance in parasites of horses.

Current levels of anthelmintic resistance in equine parasites are summarized in table 1. The
occurrence of resistance is very variable and large differences can be found between individual
farms, and resistance cannot be concluded on any given farm without proper testing. Thus,
table 1 only presents which parasites are most likely to show resistance to which drug class.

Table 1. Current levels of resistance documented in peer-reviewed studies in major nematode parasites
to the three anthelmintic classes in managed horse herds. These are world-wide trends that have also
been reported in several US surveys.
Drug class Cyathostomins Large strongyles Parascaris spp.
Benzimidazoles Widespread None Early indications
Pyrimidines Common None Early indications
Macrocyclic lactones Early indications None Widespread
Widespread: reported on multiple continents with high farm prevalences often above 80%
Common: reported on multiple continents with varying farm prevalences
Early indications: few single farm cases of reduced efficacy (ascarids) or reports of reduced egg reappearance
periods (strongyles)

PARASITE REFUGIA
Refugia refer to the portion of a population of parasites (or stages of parasites) that eludes the
drug at the time of a treatment event. This sub-population includes stages of parasites in the
horse not affected by the treatment (e.g., encysted cyathostomins when non-larvicidal
treatments are used), all free-living parasite stages on the pasture, and all parasites in animals
that were not treated. The higher the proportion of worms in refugia, the more slowly resistance
develops. The worms in refugia are not under selection pressure for resistance, thus resistant
worms remain diluted by susceptible worms, which continue to make up the majority of the
worm population (Leathwick et al., 2008; Waghorn et al., 2008).

Examples of anthelmintic formulations that do not treat all parasitic stages within the horse
include pyrantel formulations that have no efficacy against parasite stages present outside the
gastrointestinal lumen, and ivermectin which has no documented efficacy against encysted
cyathostomin larvae.

The concept of refugia can be utilized by keeping the frequency of drug treatments at a
minimum when pasture refugia is low (e.g., during the temperature extremes of cold winters or
hot summers and during droughts). Consequently, the old practice of “dose-and-move”, is now
considered to select more strongly for resistance, as moving newly dewormed horses to a new
pasture removes the dilution effect that would have been provided by a good size pasture
refugia (Waghorn et al., 2009).
Furthermore, refugia can be utilized by leaving some horses untreated at every deworming.
Fecal egg counts can be used to select the moderate and high egg shedders for anthelmintic
treatment. One study illustrated that if highly effective drugs are used, treating all adult horses
exceeding a strongyle FEC of 200 EPG, only leads to treating about 50% of the horse
population, but still provides about 95% reduction of the overall egg shedding (Kaplan and
Nielsen, 2010).

FECAL EGG COUNT REDUCTION TEST (FECRT)

The FECRT is used to determine if strongyles and/or ascarids are resistant to a given
anthelmintic. However, a finding of reduced efficacy may or may not mean there is resistance
present. Therefore, suggested cutoffs should be viewed as a guide for interpretation, but not be
viewed as the final answer. To perform the FECRT a fecal sample is collected prior to
deworming. The anthelmintic in question is administered and a fecal sample is collected 10-14
days following treatment. Using the equation below, the number of eggs in the pre-treatment
and post-treatment fecal samples is used to calculate the percent reduction in FEC for a group
of horses. The mean reduction for all horses tested is calculated to determine the percent
reduction for the farm or stable. This value is then used to make inferences regarding possible
presence or absence of drug resistance.

EPG (pre-treatment) – EPG (14 day post-treatment) X 100 = FECRT

EPG (pre-treatment)

Specific guidelines for FECRT in horses do not currently exist, but are being developed by
parasitologists under the auspices of the World Association for the Advancement of Veterinary
Parasitology (WAAVP). Until those guidelines are published, the cutoff values listed in Table 2
should be used as a guide for interpreting the results of a FECRT.
Table 2: Suggested cutoff values (mean percent reduction in FEC) for interpreting results of strongyle
FECRT
Expected Observed Results of the FECRT
efficacy if Susceptible Suspected Resistant
no (no evidence resistant
Anthelmintic resistance of resistance)
Fenbendazole/Oxibendazole 99% >95% 90-95% <90%
Pyrantel 94-99% >90% 85-90% <85%
Ivermectin/Moxidectin 99.9% >98% 95-98% <95%*
* As of March 2019, full-fledged strongyle resistance as diagnosed with a standard FECRT to ivermectin
or moxidectin has not been reported in the peer-reviewed literature. Therefore, any FECRT result that
yields <95% reduction for these drugs should be repeated before concluding there is resistance.

It is recommended to include at least six egg count positive horses in a FECRT on each farm to
evaluate treatment efficacy. Furthermore, it is recommended to always recruit the horses with
the highest possible pre-treatment egg count for the FECRT, and to use an egg counting
technique with a limit for detection of less than 25 EPG (see Appendix A). Horses should not
have received anthelmintic treatment at least 8 weeks prior to the FECRT, and should
preferably have been residents on the given farm for at least one year for their parasites to be
representative of the general parasitic fauna on the farm. When interpreting results of a FECRT
it is important to appreciate that there are many factors that can affect the observed results of a
FECRT (see Vidyashankar et al., 2012 for details). FEC are by their very nature quite variable,
so if testing is done with few horses there is potential for high variability, which could lead to an
incorrect inference. An FECRT can be carried out with fewer than six horses, but the results
should be interpreted with caution. In case of borderline results or cases of reduced efficacy
indicated only in some, but not all horses, the test should be repeated before any firm
conclusion is made.

In addition, all horses sharing pastures share the same population of parasites, and resistance
should always be evident across that population. It is not biologically possible that resistant
worms are present in some horses but not others. However, unless efficacy is very high for all
horses tested, high variability in results among the horses is quite common. Ultimately, FECRT
results can only be interpreted for the population (herd) and not on the individual level. It
should always be borne in mind that a borderline reduced efficacy can be caused by factors
other than resistance, such as incorrect dosage, incorrect storage, and expired product used.

EGG REAPPEARANCE PERIOD (ERP)

The ERP is defined as the time interval between the last effective anthelmintic treatment and
the resumption of strongyle egg shedding. Leading equine parasitologists in the US suggest the
following definition be used: the post-treatment week when the percent reduction in FEC
decreases below a cutoff value of 80% for benzimidazoles and pyrantel, and below 90%
efficacy for ivermectin and moxidectin. This is measured by performing weekly FECRTs until
egg reappearance is seen. The ERP is irrelevant if drug resistance to a particular anthelmintic is
already present on a given property, as there is no egg disappearance. Monitoring ERP on a
farm over time has value because a shortening of the ERP is a precursor to the development of
resistance. Monitoring ERPs has the most practical implication for measuring possible
emergence of resistance to ivermectin and moxidectin. Table 3 shows the usual ERP for the
common equine anthelmintics, when they are fully effective at two weeks post treatment, as well
as recently reported ranges of shortened ERPs. Macrocyclic lactones are characterized by very
long ERPs, but recent reports have documented them shortened to just 4-5 weeks for both
ivermectin and moxidectin on managed farms (Lyons et al., 2008a; Rossano et al., 2010; Lyons
et al., 2011; Bellaw et al., 2018).This is interpreted as emerging resistance in cyathostomins to
this drug class (Sangster, 1999). Thus, for macrocyclic lactones it can be of value to run one set
of post-treatment egg counts at approximately 4-6 weeks to gage the ERP status on a given
farm.

Table 3: Cyathostomin egg reappearance periods (ERP) for equine anthelmintics

Anthelmintic Usual ERP when ERP when drug ERPs on farms
drug is effective was first with emerging
introduced resistance
Fenbendazole/Oxibendazole 4-5 weeks 6 weeksa -e

Pyrantel 4-5 weeks 5-6 weeksb -e

Ivermectin 6-8 weeks 9-13 weeksc 3-5 weeks

Moxidectin 10-12 weeks 16-22 weeksd 4-6 weeks

aMcBeath et al., 1978.
bBoersema et al., 1995; 1996.
cBorgsteede et al., 1993, Boersema et al., 1996, Demeulenaere et al., 1997.

dJacobs et al., 1995, DiPietro et al., 1997, Demeulenaere et al., 1997.

e Resistance so commonly reported that ERPs have not been measured.

STRONGYLE EGG SHEDDING/CONTAMINATION POTENTIAL

Although horses grazing together share the same parasite population, they demonstrate huge
differences in their levels of strongyle egg shedding. Within any group of mature horses (> 3 yrs.
of age), strongyle egg counts are highly concentrated in certain horses, such that 15 – 30% of
adult horses usually shed approximately 80% of the eggs (Kaplan and Nielsen, 2010). This
distribution of parasite egg shedding among hosts is common to all species and is referred to as
over-dispersion. This characteristic for a horse is very stable over time, when it is otherwise in
good health, pasture management practices are sound, and the horse has not recently moved
from one farm to another. Thus, a healthy pastured horse with a low egg shedding potential will
tend to always have a low FEC, while a healthy pastured horse with a high egg shedding
potential will tend to always have a high FEC (Nielsen et al., 2006; Becher et al., 2010).

In order to determine the egg shedding potential for an individual horse, it is necessary to collect
a fecal sample and perform a fecal egg count (FEC) after the effects of the last dewormer
administered are completely gone. If you do not wait a suitable period of time following the last
anthelmintic treatment, the results of the FEC will only reflect the efficacy of the last dewormer
used, rather than measuring the innate ability of the horse’s immune system to regulate levels of
cyathostomin egg shedding. Older studies have illustrated that parasites reduce their egg
shedding outside the grazing season, where conditions are less favorable for parasite
transmission (Poynter, 1954), but this pattern may well depend on geographical and climatic
conditions and it is not certain to which extent this is a global phenomenon.

To evaluate the egg shedding status in adult horses (> 3 yrs. of age), a fecal sample should be
collected a minimum of 4 weeks beyond the Egg Reappearance Period (ERP) for the last drug
used. Given the information in Table 3, a washout period of 8 weeks should suffice in the large
majority of cases, but it can be extended for macrocyclic lactones in cases where ERPs are not
reduced to the 4-5 week range.

There are little data available for scientifically setting the FEC thresholds used for dividing adult
horses into low, moderate and high categories for egg shedding. However, one study reported
that strongyle FEC cutoff values up to the level of 500 EPG yielded significantly different
strongyle worm counts, whereas no differences were found at higher cutoffs. These data
therefore support usage of cutoffs for treatment in the 0-500 EPG range (Nielsen et al., 2010a).
Nonetheless, currently recommended thresholds are based largely on the opinions of a majority
of equine parasitologists, and as such could change as more data are collected and analyzed.
Guidelines for classifying horses on the basis of egg contamination potential are presented in
table 4.

Table 4. Suggested guidelines for classifying horses into different levels of strongyle
egg shedding and the expected percentage of the horse population belonging to each
group (Kaplan and Nielsen, 2010).
Egg count level Percentage of adult populationa
Low contaminators: 0-200 EPG 50-75
Moderate contaminators: 200-500 EPG 5-15
High contaminators: >500 EPG 10-30
a
These values are only estimates and the actual percentage of horses in each category will
vary among farms depending on a multitude of factors

It is generally advised to classify adult horses to the three strongyle contaminative groups based
on more than just one egg count performed at one point in time. In a Danish study where FEC
were performed every six months over three years, greater than 90% of horses with FEC < 200
EPG on two consecutive fecal exams had a FEC of less than 200 EPG on the third (Nielsen et
al., 2006). Thus, it appears that egg shedding categories for most horses remain consistent, but
some horses may switch categories, particularly those with FEC near the cutoff values.

GOALS OF PARASITE CONTROL

The true goal of parasite control in horses (and other equids) is to limit parasite infections so
animals remain healthy and clinical illness does not develop. The goal is NOT to eradicate all
parasites from a particular individual. Not only is eradication impossible to achieve, the
inevitable result is accelerated development of parasite drug resistance. In addition, both small
and large strongyles cause the greatest disease during their larval stages, which are refractory
to most anthelmintic treatments. Consequently, most treatments that kill only adult strongyle
worms yield limited direct benefit to the horse. However, treatments effective against adult
stages have an indirect benefit in that they prevent further contamination of the environment
with infective stages. The resulting corollary is that to achieve good parasite control, one must
prevent contamination of the living environment of a horse or horses with high numbers of
parasite eggs and larvae. Thus, treatments should be timed to control the level of egg shedding
into the environment. This relies on the use of deworming medications that are effective for
their intended use. But treatments are only necessary when the environmental conditions are
conducive to egg and larval development and survival. If strongyle eggs and developing larvae
will be rapidly killed by the adverse environmental conditions (such as hot summers) or
temperatures are too low to allow egg hatching and larval development to the third infective
stage (such as cold winters) (Nielsen et al., 2007), then little is gained by deworming the horse if
the horse is not showing any clinical symptoms of parasitic disease.

The goal of any parasite control program can therefore be summarized as follows:

1. To minimize the risk of parasitic disease.

2. To control parasite egg shedding.
3. To maintain efficacious drugs and avoid further development of anthelmintic resistance
as much as possible.

To achieve these goals, it is important to know the magnitude of egg shedding of individual
horses. This information can only be generated by performing periodic FEC surveillance. As
noted above, the acceptable limits of strongyle EPG for a horse remain debated, and the egg
shedding status of a horse may change over time as a result of changes in the horse’s immune
status and level of parasite exposure. In addition, no exact guidelines have been published
regarding the “acceptable” number of Parascaris spp. eggs in young horses. However, even
with these limitations in our knowledge, the magnitude of the FEC is the only means available to
estimate the worm burden and egg contamination potential of a horse, and determine the
effectiveness of anthelmintics. Consequently performing FEC surveillance is necessary to
properly develop and monitor any parasite control program.

FECAL SAMPLING AND FECAL EXAMINATION

There is a large number of techniques available for generating fecal egg counts in equines, and
Appendix A provides protocols for two of the most widely used techniques. Automated
smartphone-based egg counting systems are currently under development and will be made
commercially available to veterinarians in the near future.

REASONS TO PERFORM FECAL EGG COUNTS (FEC)

• To evaluate the anthelmintic efficacy using the FECRT.
• To evaluate and monitor the strongyle egg reappearance period (ERP) of the most
recently administered dewormer.
• To determine the shedding status of the adult horse at the time of sampling.
• To determine whether parasite burdens in foals and weanlings are primarily Parascaris
spp. or strongyle.

LIMITATIONS OF FEC
 • They do not accurately reflect the total adult strongyle or Parascaris spp. burden of the
horse.
• They do not detect immature or larval stages of parasites including migrating large
strongyles and ascarids, and/or encysted cyathostomins.
• Tapeworm infections are often missed or underestimated by fecal float techniques, and
modified techniques are required.
• Pinworm eggs are usually missed since they are adhered as egg packets around the
anus rather than being shed in the feces.

RECOMMENDATIONS FOR FECAL SAMPLING AND STORAGE

• Samples should be stored in airtight and leak-proof containers or plastic bags.
• Collected manure should be as fresh as possible. Samples less than 12 hours old are
acceptable, but should be refrigerated immediately after collection (Nielsen et al., 2010b).
• Refrigeration is always recommended for storage of fecal samples, but anaerobic storage
at room temperature will also prevent eggs from hatching. Anaerobic storage can be
achieved by squeezing all the air out of the bag, or by using a vacuum-sealing device.
Note that anaerobic storage works best on wet feces; if feces are dry, it is difficult to
achieve an anaerobic state.
• Samples should preferably be tested within 7 days of collection, although there are
indications that eggs can remain intact for longer if adequately refrigerated.
• Fecal samples that are or have been frozen are not acceptable, as this will damage the
eggs and decrease the recovery rate.
• Diarrhea samples are not acceptable for FEC, but can be used for qualitative testing.
Note that if a horse has diarrhea that may be associated with parasitism, deworming may
be indicated per clinician’s recommendations without regard to results of the FEC.

FEC Training and Microscope Maintenance

• Make sure that microscope lenses are adjusted to the working distance offered by
parasitology slides used for the egg counts.
• Make good use of contrast (aperture condenser) to get a better image of morphological
features.
• To improve skills at parasite egg identification, several resources are available online and
through use of textbooks. One should consider review by a veterinary parasitologist if
questions arise.
• It is recommended that microscopes be equipped with an ocular micrometer so that eggs
and other questionable objects can be measured. Having measurements can greatly
assist in the identification. Cheap digital cameras can now be acquired with software
allowing these measurements.

INTERPRETATION OF EGG COUNT DATA

In managed horses, greater than 99% of all strongyle eggs seen in a fecal sample are from the
cyathostomins. In feral horses or in cases of severe neglect, 90-99% of the eggs seen will be
from the cyathostomins and the remaining few percent will be from several large strongyle
species, which are potentially more pathogenic. It is not possible to distinguish a large strongyle
egg from a small strongyle egg while doing a FEC. Identification of large strongyle parasites
requires culturing the feces and recovering and identifying the L3 larvae. This procedure is not
difficult to learn but does require training. Arval culture and ID procedure presently is not
offered by commercial laboratories but may be available in a few university veterinary diagnostic
laboratories. An ELISA test recently has been developed to detect the presence of Strongylus
vulgaris larvae in the bloodstream (Andersen et al., 2013). This is currently commercially
available in Europe and is offered by the Nielsen Laboratory at the University of Kentucky in the
USA.

"OTHER" GASTROINTESTINAL PARASITES

Anoplocephala perfoliata (Tapeworms)

Necropsy surveys performed in Kentucky reported prevalences for Anoplocephala perfoliata of
approximately 50% both prior to and after the introduction of widespread use of cestocidal drugs
in horses (Lyons et al., 1984; Lyons et al., 2000; Lyons et al., 2018). The prevalence in other
areas is unknown; however in much of the US tapeworms remain common. Oribatid mites
serve as the intermediate host for tapeworms, and are commonly found on grass pastures.
Though epidemiological data are limited, it appears that higher densities of oribatid mites occur
where moist environmental conditions are found and in arid areas few or low numbers of
oribatid mites are present leading to a lower incidence of tapeworm infection.

In recent years, parasite A. perfoliata has received growing attention as a potential pathogen
causing various types of colic (Proudman et al., 1998; Nielsen, 2016b). Several studies have
found an association between presence of tapeworms and colic originating from the ileocecal
region (Nielsen, 2016b). Tapeworms produce small mucosal erosions at the site of attachment
and when present in relatively high numbers, have been associated with ileocecal impactions
and spasmodic colic (Proudman et al., 1998). However, most horses infected with tapeworms
tend to have relatively few worms, and these likely produce little in the way of pathogenic
consequences.

The diagnostic sensitivity of the general McMaster technique for diagnosing equine tapeworm
infections is less than 10% (Nielsen, 2016b). Consequently, unless a horse is infected with a
large burden of tapeworms, seeing tapeworm eggs in the feces is a chance event, when a
standard egg counting method is used. A modification of a centrifugation-based egg counting
technique based on analyzing 40 grams of feces has been validated to have a diagnostic
sensitivity and specificity of 0.61 and 0.98, respectively (Proudman and Edwards, 1992). For
detecting tapeworm burdens of 20 worms and above, the sensitivity of this method was found to
be 0.90, which is very good for a parasitological diagnostic test. One study has found a
Wisconsin method set to analyze 5 grams of feces to have a diagnostic sensitivity of 0.62
(Slocombe, 2004). The number of eggs seen is not highly relevant, and fecals should just be
interpreted as being either negative or positive. To greatly increase the sensitivity of detection
for tapeworms, horses can be treated with either praziquantel or a cestocidal dose of pyrantel,
and then 24 hour later fecals are performed (Sanada et al., 2009; Slocombe, 2006). If the horse
was infected with tapeworms, there is a high probability that tapeworm eggs will be seen in the
feces post treatment.

The research group led by Proudman at University of Liverpool developed the first fully
validated and commercially available serological diagnostic test for diagnosing equine tapeworm
infection (Proudman and Trees, 1996). This assay measures A. perfoliata-specific antibodies
and titer levels that have been found to correlate with worm burdens. However, being an
antibody-based test, it more reflects exposure than actual infection, and horses can remain
seropositive for months after treatment (Abbott et al., 2008). A different serological test is also
available to test for the presence of antibodies to A. perfoliata at the University of Tennessee,
but at present the test lacks sufficient validation as a quantitative assay for use in detecting
current infections or for measuring worm burdens in individual horses. Most recently, a saliva-
based ELISA has been validated for diagnosing tapeworms and made commercially available in
the United Kingdom (Lightbody et al., 2016).

Because tapeworms are relatively common and widely distributed, have a strong seasonality of
transmission, have potential to cause disease, and are difficult to diagnose, it is likely that a
properly timed single annual tapeworm treatment would be beneficial for most horses. Even if
this treatment is not needed for the health of an individual horse, a properly timed annual
treatment given to all horses on a property should diminish transmission the following grazing
season. However, there is no evidence that frequent tapeworm treatments throughout the year
would provide any additional health benefit. Drug choices for treatment of tapeworms include
praziquantel (licensed in the US for horses only in combination with ivermectin or moxidectin),
or a cestocidal (double the nematode dose) of pyrantel pamoate. In most areas, this treatment
should be given in the late fall or early winter after tapeworm transmission ends due to cold
weather. It should also be noted that horses living in dry arid regions may have little or no
exposure to tapeworms and thus would not require any cestocidal treatments. In these areas
performing ELISA testing would be valuable, as low or negative titers would suggest that annual
treatment is unnecessary.

Parascaris spp. (Roundworms; Ascarids)

This parasite is the most important in foals causing ill-thrift and poor growth. Migrating larvae
can cause signs of airway inflammation, including cough and nasal discharge (Clayton, 1986).
Further, infection poses a risk for small intestinal impactions, which are associated with a
guarded prognosis for survival, and can be further complicated by intestinal rupture (Cribb et al.,
2006). Current evidence suggests that deworming of a heavily parasitized foal with an
efficacious anthelmintic that has a paralytic mode of action can cause acute small intestinal
impaction (Nielsen, 2016a). This association has not been found with benzimidazole type drugs,
and these may therefore represent a better treatment choice for Parascaris spp. infections. The
parasite is practically ubiquitous in breeding operations and the eggs are characterized by being
particularly resistant to environmental influences and can remain present and infectious from
year to year, if organic matter is present in the soil (Ihler, 1995).

Parascaris spp. infections may occasionally be diagnosed in immunocompetent adult horses,

but clinical disease would be an extremely rare event. No specific evidence shows that the
biology of Parascaris spp. has changed, but it appears empirically that more adult horses are
positive for Parascaris spp. on fecal exams than in previous years. However, the increased fecal
testing on farms may be rendering positive horses that previously went undiscovered.

High levels of resistance have been documented across the world to ivermectin and moxidectin
(Peregrine et al., 2014), and some early findings suggest pyrantel and benzimidazole resistance
as well (Lyons et al., 2008b; Armstrong et al., 2014). Given that benzimidazoles have a non-
paralytic mode of action, they appear to represent the best choice for Parascaris treatment on
many properties, but pyrantel salts may be considered as well. Given the levels of resistance
found to ivermectin and moxidectin on a large majority of farms, fenbendazole given at 10
mg/kg for five consecutive days may be the only remaining option for larvicidal treatment.

Oxyuris equi (Pinworms)

Clinical disease from pinworms historically was seen mostly in young horses; however, in recent
years cases in adult horses appear to be becoming increasingly more common (Reinemeyer
and Nielsen, 2014). Pinworm infections tend to be sporadic, and usually only one or a few
horses are affected out of a group. Clinical signs vary in intensity, but in severe cases, intense
tail rubbing and hindquarter and/or perineal skin excoriations are seen. Some adult horses may
have patent pinworm infections without showing any specific clinical signs. Definitive diagnosis
is made by identifying the O. equi eggs. Eggs can sometimes be found on a fecal exam, but the
scotch tape test or examination of perineal scrapings (using a tongue depressor and lube) are
more sensitive. As a consequence of rubbing, horses can spread pinworm eggs throughout the
horse’s environment; transmission can occur in stalls and from contact with grooming materials,
tail wraps, fence posts, etc. Furthermore, pinworm eggs are rather hardy, and can persist on the
perianal region and in the environment for relatively long periods of time.

Apparent resistance to ivermectin in O. equi has been described in several recent reports and
appears to be relatively common (Rock et al., 2013; Wolf et al., 2014; Sallé et al., 2016). If
resistance is suspected, the available evidence suggests benzimidazoles should be given
priority over pyrantel salts due to better historic efficacy levels (Reinemeyer and Nielsen, 2014).
It should be emphasized that rectal lavage using liquid formulations of various anthelmintic
products is very unlikely to have any effect as O. equi do not inhabit the rectum or descending
colon.
Because the pruritus secondary to pinworm infections is caused by the material secreted
by the female when depositing her eggs, washing the perineum and perianal region may help to
relieve symptoms. After scrubbing, all materials should be discarded or washed in hot water
with soap and/or disinfectants.

Bots (Gasterophilus spp.)

Bots are rarely associated with measureable disease, but they can be aesthetically unpleasing.
It is often recommended to treat with a boticide once each year during late fall or early winter as
a clean-out treatment, which will help to decrease transmission in the next season. Currently,
ivermectin and moxidectin are the only available parasiticides for horses with activity against
bots. Recent data suggests variable efficacy of moxidectin against bot larvae (Reinemeyer et
al., 2015).

METHODS OF PARASITE CONTROL

Environment-based approaches
Equine strongyle parasites begin life as an egg in a manure pile, which then must develop to
infective larvae in the feces, get out onto the pasture, and then be ingested by a horse. Thus,
infection of horses could be prevented if all feces were promptly removed from the pasture.
In a bygone era, the most elite stables employed pasture grooms, who followed grazing horses
with a scoop shovel and a broom. Their job was to remove manure as quickly as it was
dropped. In the 1980s, a similar approach was evaluated using updated technology. Studies at
Newmarket in Great Britain examined the efficacy of cleaning horse pastures with a large
commercial vacuum unit that was originally designed for golf course maintenance. Twice-
weekly vacuuming was demonstrated to control pasture infectivity more effectively than routine
deworming (Herd, 1986). However, the cost of the vacuum units was prohibitively expensive for
the average horse owner, and the process only worked well on level, relatively dry pastures.
Despite this, several commercial devices are now available for cleaning pastures, and these
have found use on many horse farms.

Environmental Control
Strongyle eggs hatch and develop into infective larvae under conditions of moderate
temperature and moisture. Cold slows the rate of development or stops it altogether, and
excessive heat kills eggs and larvae. It is possible to heat manure sufficiently to kill the
parasites, including even ascarid eggs (Gould et al., 2012). Proper composting of manure and
soiled bedding will generate relatively high internal temperatures, and strongyle larvae in
manure are virtually eradicated by exposure to temperatures over 40 ºC for a minimum of one
week (Gould et al., 2012). Composting is a practice that should already be in place at any
stable.

Non-composted horse manure should never be spread on pastures as this will increase the
level of parasite contamination. This practice has been associated with higher Parascaris spp.
prevalences in Germany (Fritzen et al., 2010).

Leaving pastures unoccupied for several months of the year may or may not reduce the risk of
infection depending on the time of the year and the climate where the farm is located. Infective
strongyle larvae (L3) can survive for only a few days to a few weeks in hot weather
(temperatures around 40˚C), but for as many as six to nine months during colder weather
(Nielsen et al., 2007). Consequently, L3 survival in the environment will vary greatly from region
to region and season to season. Thus, strategies for environmental control must be made
based on local conditions.

Strongyle infective third-stage (L3) larvae can survive in wide extremes of weather and climate,
but there are sets of conditions that are optimal and sets of conditions where development
and/or survival are poor (Table 5). Therefore, it is recommended to focus anthelmintic
treatments at times of the year that are most optimal for larval development, i.e. when
transmission of strongyles is most likely. Doing so will reduce pasture contamination with
infective stages, thereby decreasing the acquisition of new infections. In addition, a time when
transmission is likely is also the time of year when adequate refugia are present, thus selection
pressure for anthelmintic resistance is theoretically lessened. Conversely, it is recommended to
avoid or limit treatments of equine strongyles during the winter months in cold temperate
climates and during summer months in warm/hot climates (times of low refugia), in order to
reduce the development of anthelmintic resistance.
 Table 5. Effects of temperature on the survival, development and persistence of free-living
stages (eggs, L1, L2, L3) of strongyles (Nielsen et al., 2007)
Development Temperature Survival
Range
No development above this level > 40 oC Free-living stages die rapidly. Intact fecal
> 104 oF balls may retain enough humidity to
enable L3 to survive for some weeks.
Optimal temperature range for 25 -33 oC Larvae survive on the shorter term (ie a
development of eggs and larvae. 77 - 91 oF few weeks), but conditions are too warm
Reach infective L3 stage in as little for long term survival
as 4 days.
Eggs develop into L3 within 2-3 10-25 oC L3 capable of surviving for several weeks
weeks. 50-77 oF to a few months
Lower limit for egg hatching is 6-10 oC L3 survive for many weeks and months
about 6 oC. At temperatures in this 43-50 oF under these circumstances
range, development will take
several weeks to a few months.
No hatching and no development 0-6 oC Eggs and L3 can survive for several
32-43 oF months at temperatures just above the
freezing point
No development during frost < 0 oC Developing larvae (L1 and L2) are killed,
< 32 oF but unembryonated eggs and L3 can
survive and persist for long periods (i.e.
months)
Alternation between freezing and < 0 > oC Repeated freeze-thaw cycles are
thawing will usually not lead to < 32 > oF detrimental to egg and larval survival
development unless temperatures
exceed 6 oC

It is practically feasible to temporarily turn a grazing pasture into a hay field and recover the
forage. Grazing infected pastures with ruminants may also assist in control (Eysker et al.,
1986). Equine strongyle larvae are quite host-specific; they cannot infect cattle, sheep, goats or
camelids. The only exception is the stomach worm, Trichostrongylus axei, which can infect both
ruminants and equids, but this parasite has become very rare in equine establishments.

The environmental control of worms using nematophagous fungi has shown promising results.
Several researchers have used these fungi that are harmless to people, and the environment
(Larsen et al., 1999). Unfortunately, these biological control agents are not commercially
available at present.

Alternative remedies
An increasing number of so-called organic or herbal dewormers are appearing in tack shops
and online, but the efficacy of these products has never been demonstrated in formal, controlled
evaluations. These products exist primarily because they exploit differences in the labeling
requirements for drugs vs. non-drug items. Before a drug can earn label claims for activity
against parasites, this fact must be proven unequivocally to the Food and Drug Administration
by extensive efficacy and safety testing. Once a dewormer is approved by the FDA, the claims
that can be made in advertising that drug are regulated by the FDA.

In contrast, products that are not considered drugs do not require FDA approval for marketing,
so advertisers of non-FDA approved products can say just about anything they want, and their
products do not have to be effective.

Anthelmintic Formulations Available

Benzimidazoles: These drugs interfere with a worm’s energy metabolism on a cellular level.
They bind to beta tubulin and prevent its polymerization into microtubules. They are available in
paste, liquid and pelleted formulations.

Tetrahydropyrimidines: Pyrantel pamoate and pyrantel tartrate act at the neuromuscular

junction causing an irreversible rigid paralysis. Pyrantel salts only affect adult parasites that
reside in the lumen of the gastrointestinal tract. Pyrantel pamoate is available in suspension
and paste formulations, while pyrantel tartrate is formulated in alfalfa pellets and must be fed on
a continual basis, serving only as a preventive, not a purge dewormer.

Heterocyclic Compounds: Several dewormers are classified as heterocyclic compounds, but

piperazine is the only one used in horses. Piperazine works by depolarizing muscular
membranes, which renders them resistant to the action of acetylcholine. The action of
piperazine is limited to adult parasites. Piperazine is used infrequently in horses, and there is
currently no formulation marketed for equine usage in the US, but one product is listed in
Canada. It was available as a liquid or powder formulation which required nasogastric
intubation.

Macrocyclic Lactones: These act on glutamate-gated chloride channels in nematode nerve

and muscle cells, disturbing the normal transmission of nervous stimuli to muscles. The result
is flaccid paralysis. Macrocyclic lactones are the most potent killers of worms, being effective at
less than one-tenth the dosage of other classes of dewormers. They also have the unique
quality of killing external parasites, such as lice, mites, and the cutaneous larvae of Onchocerca,
Habronema, and Draschia. Macrocyclic lactones are available in paste (ivermectin) and as an
oral gel (moxidectin).

Isoquinoline-Pyrozines: Praziquantel is the sole member of the isoquinolone class used in

horses. It is also unique in that it has no activity against nematodes. Praziquantel is effective
only against tapeworms. In North America, praziquantel is currently marketed only in
combination with macrocyclic lactones, and the combination formulation is that of the parent
compound (ivermectin if paste, moxidectin if a gel). Praziquantel is available as a single drug
formulation in some European countries.

Parasite Control Programs: Points to Ponder

Information about prepatent periods for the different parasites (i.e., the period of time from
ingestion of parasite infective stages until eggs are being shed in the feces), can be important
for making decisions on when to treat. This information can be found in Appendix B.
Considerations for mature horses:
Focus on control of cyathostomins. Depending on climatic conditions, one or two yearly
treatments are sufficient to prevent occurrence of large strongyles. Consider including a
treatment effective against encysted cyathostomins at a time when the mucosal burden is at its
peak. Typically, this is more likely to occur towards the end of the grazing season, i.e., fall in
northern climates, and spring in the more tropical and subtropical climates. Include a cestocide
at least annually if they are a problem in your region.

Deworming programs for adult horses should be designed with the following principles in mind:

• Evaluate the efficacy of the dewormers used on each farm at least every three
years using the FECRT.
• A basic foundation of anthelmintic treatments should be considered to all horses.
This should consist of one or two yearly treatments to target large strongyles,
tapeworms, bots, and spirurid nematodes responsible for causing summer sores
(Habronema spp. and Draschia spp.). In most cases, one or two yearly
treatments will achieve this goal.
• All further treatments should be targeting horses with a high strongyle
contamination potential.
• Focus anthelmintic treatments during seasons of peak transmission (usually
spring and fall when pasture refugia are at their highest).

Considerations for foals, weanling, yearlings

• Targeted treatments (selective therapy) based on FEC is NOT recommended in
this age group. However, FECs are still important in this age group for other
purposes and the following considerations should be made.
• During the first year of life foals should receive a minimum of four anthelmintic
treatments. First deworming should be carried out at about 2-3 months of age,
and a benzimidazole drug is recommended to ensure efficacy against ascarids.
Second deworming is recommended just before weaning (approximately 4-6
months of age). An extra treatment can be justified before weaning if the time
period between the two treatments exceeds 3 months. At weaning, FECs are
recommended to determine whether worm burdens are primarily strongyles or
ascarids, to facilitate the right choice of drug class. Third and fourth treatments
should be considered at about 9 and 12 months of age, respectively, and
treatment should primarily be targeting strongyles. In areas, where tapeworms
are present, a tapeworm-directed treatment should be included in the 9-month
treatment, or before the end of the first calendar year.
• Perform FECRT yearly to evaluate the efficacy of anthelmintics against
strongyles and ascarids.
• Strongyloides westeri is rarely a cause of diarrhea in young foals thanks to the
advent of the benzimidazoles and macrocyclic lactones. It is widely used to
deworm mares around foaling to prevent the lactogenic transmission of this
parasite. However, there is no evidence to support this procedure.
 • Recently weaned foals should be turned out onto the “cleanest” pastures with the
lowest parasite contamination levels.
• Yearlings and two-year olds should continue to be treated as “high” shedders,
and receive about three-four yearly treatments with efficacious drugs, depending
on the duration of the grazing season.

General points to consider

• Do not under-dose horses and foals; use weight tapes or scales to determine
body weights.
• Cyathostomins, large strongyles, and tapeworms are acquired on pasture.
Ascarids and pinworms can be acquired in confinement as well as on pasture.
• Use properly performed FECs to determine shedding status and drug efficacy of
new arrivals before turnout in common pastures.
• Consider using tapeworm serology (ELISA) submitted on at least 20% of resident
herd members to determine exposure potential for tapeworms.
• Concentrate drug treatments when the local climate favors parasite transmission.
• Decrease strongyle-directed treatments when climate conditions are adverse (hot
summer / freezing winter) for larval survival and / or transmission.
• Design a parasite control program that considers the farm’s management
practices and climatic region. Consider the following:
▪ Stocking density: Many horses and / or many different owners may make
it more difficult and labor intensive to treat each horse as an individual.
Heavy stocking rates resulting in a consistently high level of parasite
exposure can challenge even the best deworming program.
▪ Time horses spend on pasture: Limited access or the absence of grass
often contributes to low FECs.
▪ Age of horses on the farm: Are there foals/ weanlings/yearlings and / or
mature adults. Treat youngsters as high shedders.
▪ Is this an “open” herd: Institute a biosecurity program for all new arrivals
that includes a FEC and larvicidal deworming prior to turn-out with
resident horses.
▪ What is the farm’s ability or willingness to “clean up” the environment
using non-chemical means such as pasture rotation, cross-grazing with
other species, manure removal and composting?

Summary for Parasite Control

Given the information provided in this document, what is a rational worm control program?
Worm control programs are best viewed as a yearly cycle starting at the time of year when
worm transmission to horses changes from negligible to probable. Furthermore, it is critical that
all treatment recommendations be viewed in the proper context. All treatment and non-
treatment recommendations are made within the context of a preventive program where FEC
surveillance is being performed. These recommendations, which are based on epidemiological
principles, may not apply to individual horses on farms. Thus, if presented with a horse showing
evidence of parasitic disease during the times of the year when treatments are not
recommended (e.g., summer in south, winter in north), then this horse should be treated – and if
the horse is showing overt symptoms of strongyle-associated disease, a larvicidal treatment for
targeting encysted cyathostomin larvae should be considered. Two recent blinded anthelmintic
efficacy studies performed in the US with two different equine populations have documented a
clear loss of larvicidal efficacy of the five-day double-dose fenbendazole regimen, whereas
moxidectin had intact larvicidal efficacy in both studies (Reinemeyer et al., 2015; Bellaw et al.,
2018). Given the widespread occurrence of benzimidazole resistance in cyathostomin parasites
across the world, moxidectin would be the treatment of choice in a large majority of locations.

It is important to keep in mind that these are just suggestions; thus, there are many variations of
these suggested programs that would still meet the same goals and follow the same principles.
Ultimately, each farm (with veterinary guidance) should develop its own program tailored to the
specific needs of the farm and each animal. There is no such thing as a “one size fits all”
program.

As outlined, all adult horses should benefit from a basic foundation of one or two treatments per
year. Low strongyle egg shedding horses with naturally strong immunity to cyathostomins will
need no other treatments because the two treatments have covered the needs of the other
parasites and these horses are generally protected naturally from disease caused by
cyathostomins by their immune state. In traditional deworming programs, repeated treatment of
low shedder horses every 2-3 months accomplishes little to improve their health, but it does
promote drug resistance. Moderate and high egg shedders will need a third and sometimes a
fourth treatment for cyathostomins.

Any additional treatments would be given on an “as needed” basis depending on whether a
specific parasitic infection or disease is diagnosed. For example, if Anoplocephala eggs are
seen when performing FEC, a second tapeworm treatment during the year might be warranted.
Likewise, if pinworms are diagnosed, any horse showing symptoms should be treated with an
effective anthelmintic. Ivermectin and moxidectin remain the foundation for control of strongyle
parasites, although signs of emerging resistance have been reported. In contrast, resistance to
these drugs is common in Parascaris spp. and Oxyuris equi.

Strongyle resistance is well documented against pyrantel, fenbendazole, and oxibendazole, and
these drugs can therefore only be used if a FECRT has documented good efficacy. In addition,
resistance in Parascaris spp. is still uncommon for these drugs, thus these are often solid
choices when targeting this parasite.

Developed by the AAEP Parasite Control Subcommittee of the AAEP Infectious Disease
Committee in 2013. Original subcommittee members included: Martin K. Nielsen, DVM, Ph.D.,
Dipl. EVPC (chair), Linda Mittel, MSPH, DVM, Amy Grice, VMD, Michael Erskine, DVM, Dipl.
ABVP, Emily Graves, VMD, Dipl. ACVIM, Wendy Vaala, VMD, Dipl. ACVIM, Richard C. Tully,
DVM, Dennis D. French, DVM, Ph.D, Dip. ABVP, Richard Bowman, DVM, Ray M. Kaplan, DVM,
Ph.D, Dipl. ACVM, Dipl. EVPC.

Reviewed and updated in 2019 by the AAEP Infectious Disease Committee with
additional review by the original subcommittee above.
Recommended reading:
• Reinemeyer, C.R, Nielsen, M.K, 2018. Handbook of Equine Parasite Control, 2nd Edition.
Wiley-Blackwell, John Wiley & Sons Inc., Hoboken, NJ, USA, 2018.
• Kaplan, R.M., Nielsen, M.K., 2010. An evidence-based approach to equine parasite
control: It ain’t the 60s anymore. Equine Vet. Educ. 22, 306-316.
• Peregrine, A.S., Molento, M.B., Kaplan, R.M., Nielsen, M.K., 2014. Anthelmintic
resistance in important parasites of horses: does it really matter? Vet. Parasitol. 201, 1-
8.
• Reinemeyer, C.R., Nielsen, M.K., 2014. Review of the Biology and Control of Oxyuris
equi. Equine Vet. Educ. 26, 584-591.
• Nielsen, M.K., 2016. Evidence-based considerations for control of Parascaris spp.
infections in horses. Equine Vet. Educ. 28, 224-231.
• Reinemeyer, C.R., Nielsen, M.K., 2017. Control of helminth parasites in juvenile horses.
Equine Vet. Educ. 29, 225-237.
• Nielsen, M.K., 2016. Equine tapeworm infections – disease, diagnosis, and control.
Equine Vet. Educ. 28, 388-395.

References:
• Abbott, J.B., Mellor, D.J., Barrett, E.J., Proudman, C.J., Love, S., 2008. Serological
changes observed in horses infected with Anoplocephala perfoliata after treatment with
praziquantel and natural reinfection. Vet. Rec. 162, 50-53.
• Armstrong, S.K., Woodgate, R.G., Gough, S., Heller, J., Sangster, N.C. Hughes, K.J.,
2014. The efficacy of ivermectin, pyrantel and fenbendazole against Parascaris equorum
infection in foals on farms in Australia. Vet. Parasitol. 205, 575-580.
• Andersen, U.V., Howe, D.K., Dangoudoubiyam, S., Toft, N., Reinemeyer, C.R., Lyons,
E.T., Olsen, S.N., Monrad, J., Nejsum, P., Nielsen, M.K., 2013. rSvSXP: A Strongylus
vulgaris antigen with potential for prepatent diagnosis. Parasite Vector 6: 84.
• Bellaw, J.L., Krebs, K., Reinemeyer, C.R., Norris, J.K., Scare, J.A., Pagano, S., Nielsen,
M.K., 2018. Anthelmintic therapy of equine cyathostomin nematodes – larvicidal efficacy,
egg reappearance period, and drug resistance. Int. J. Parasitol. 48, 97-105.
• Becher, A., Mahling, M., Nielsen, M.K., 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, 116-122.
• Boersema, J.H., Borgsteede, F.H.M., Eysker, M., Saedt, I., 1995. The reappearance of
strongyle eggs in feces of horses treated with pyrantel embonate. Vet. Quart. 17, 18 –
20.
• Boersema, J.H., Eysker, M., Maas, J., van der Aar, W.M., 1996. Comparison of the
reappearance of strongyle eggs in foals, yearlings, and adult horses after treatment with
ivermectin or pyrantel. Vet. Quart. 18, 7 – 9.
• Borgsteede, F.H.M., Boersma, J.H., Gaasenbeek, C.P.H., Vanderburg, W.P.J., 1993.
The reappearance of eggs in feces of horses after treatment with ivermectin. Vet. Quart.
15, 24 – 26.
• Clayton, H.M., 1986, Ascarids. Recent advances. Vet. Clin. North Am. Equine Pract. 2,
313-328.
• Cribb, N.C., Cote, N.M., Boure, L.P., Peregrine, A.S., 2006. Acute small intestinal
obstruction associated with Parascaris equorum infection in young horses: 25 cases
(1985–2004). New Zeal. Vet. J. 54, 338-343.
• Demeulenaere, D., Vercruysse, J., Dorny, P., Claerebout, E., 1997. Comparative studies
of ivermectin and moxidectin in the control of naturally acquired cyathostome infections
in horses. Vet. Rec.15, 383–386.
• DiPietro, J.A., Hutchens, D.E., Lock, T.F., Walker, K., Pau, A.J., Shipley, C., Rulli, D.,
1997. Clinical trial of moxidectin oral gel in horses. Vet. Parasitol. 72, 167–177.
• Drudge, J.H., Lyons, E.T., 1966. Control of internal parasites of the horse. J. Am. Vet.
Med. Assoc. 148, 378-383.
• Eysker, M., Jansen, J., Mirck , M.H., 1986. Control of strongylosis in horses by alternate
grazing of horses and sheep and some other aspects of the epidemiology of
strongylidae infections. Vet. Parasitol. 19, 103-115.
• Fritzen, B., Rohn K. Schnieder, T., von Samson-Himmelstjerna, G., 2010. Endoparasite
control management on horse farms – lessons from worm prevalence and questionnaire
data. Equine Vet. J. 42, 79-83.
• Gould, J.C., Rossano, M.G., Lawrence, L.M., Burk, S.V., Ennis, R.B., Lyons, E.T., 2012.
The effects of windrow composting on the viability of Parascaris equorum eggs. Vet.
Parasitol. 191, 73-80.
• Herd, R.P., 1986. Epidemiology and control of equine strongylosis at Newmarket.
Equine Vet. J. 18, 447-52.
• Ihler, C.F., 1995. The distribution of Parascaris equorum eggs in the soil-profile of bare
paddocks in some Norwegian studs. Vet. Res. Comm. 19, 495-501.
• Jacobs, D.E., Hutchinson, M.J., Parker, L., Gibbons, L.M. 1995. Equine cyathostome
infection - Suppression of faecal egg output with moxidectin. Vet. Rec. 137, 545.
• Kaplan, R.M., Nielsen, M.K., 2010. An evidence-based approach to equine parasite
control: It ain’t the 60s anymore. Equine Vet. Educ. 22, 306-316.
• Larsen, M., 1999. Biological control of helminths. Int. J. Parasitol. 29, 139-146.
• Leathwick, D.M., Miller, C.M., Atkinson, D.S., et al. 2008. Managing anthelmintic
resistance: Untreated adult ewes as a source of unselected parasites, and their role in
reducing parasite populations. New Zeal. Vet. J. 56, 184-195.
• Lightbody, K.L., Davis, P.J., Austin, C.J. 2016. Validation of a novel saliva-based ELISA
test for diagnosing tapeworm burden in horses. Vet. Clin. Pathol. 45, 335-346.
• Love, S., Murphy, D., Mellor, D., 1999. Pathogenicity of cyathostome infection. Vet.
Parasitol. 85, 113-121.
• Lyons, E., Drudge, J., Tolliver, S., Swerczek, T., Crowe, M., 1984. Prevalence of
Anoplocephala perfoliata and lesions of Draschia megastoma in Thoroughbreds in
Kentucky at necropsy. Am. J. Vet. Res. 45, 996-999.
• Lyons, E.T., Swerczek, T.W., Tolliver, S.C., Bair, H.D., Drudge, J.H., Ennis, L.E., 2000.
Prevalence of selected species of internal parasites in equids at necropsy in central
Kentucky (1995-1999). Vet. Parasitol. 92, 51-62.
• Lyons, E.T., Tolliver, S.C., Ionita, M., Lewellen, A., Collins, S.S., 2008a. Field studies
indicating reduced activity of ivermectin on small strongyles in horses on a farm in
Central Kentucky. Parasitol. Res. 103, 209-215.
• Lyons, E.T., Tolliver, S.C., Ionita, M., Collins, S.S., 2008b. Evaluation of parasiticidal
activity of fenbendazole, ivermectin, oxibendazole, and pyrantel pamoate in horse foals
with emphasis on ascarids (Parascaris equorum) in field studies on five farms in Central
Kentucky in 2007. Parasitol. Res. 103 , 287–291.
• Lyons, E., Tolliver, S., Collins, S., Ionita, M., Kuzmina, T., Rossano, M., 2011. Field tests
demonstrating reduced activity of ivermectin and moxidectin against small strongyles in
horses on 14 farms in Central Kentucky in 2007–2009. Parasitol. Res. 108, 355-360.
• McBeath, D.G., Best, J.M., Preston, N.K., Duncan, J.L., 1978. Studies on the faecal egg
output of horses after treatment with fenbendazole. Equine Vet. J. 10, 5–8.
• Nielsen, M.K., 2016a. Evidence-based considerations for control of Parascaris spp.
infections in horses. Equine Vet. Educ. 28, 224-231.
• Nielsen, M.K., 2016b. Equine tapeworm infections – disease, diagnosis, and control.
Equine Vet. Educ. 28, 388-395.
• Nielsen, M.K., Baptiste, K.E., Tolliver, S.C., Collins, S.S., Lyons, E.T., 2010a. 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.
Vet. Parasitol. 174, 77-84.
• Nielsen, M.K., Haaning, N., Olsen, S.N., 2006. Strongyle egg shedding consistency in
horses on farms using selective therapy in Denmark. Vet. Parasitol. 135, 333-335.
• Nielsen, M.K., Kaplan, R.M., Thamsborg, S.M., Monrad, J., Olsen, S.N., 2007. Climatic
influences on development and survival of free-living stages of equine strongyles:
Implications for worm control strategies and managing anthelmintic resistance. Vet. J.
174, 23-32.
• Nielsen, M.K., Vidyashankar, A.N., Andersen, U.V., DeLisi, K., Pilegaard, K., Kaplan,
R.M., 2010b. Effects of fecal collection and storage factors on strongylid egg counts in
horses. Vet. Parasitol. 167, 55-61.
• Peregrine, A.S., Molento, M.B., Kaplan, R.M., Nielsen, M.K., 2014. Anthelmintic
resistance in important parasites of horses: does it really matter? Vet. Parasitol. 201, 1-
8.
• Poynter, D., 1954. Seasonal fluctuations in the number of parasite eggs passed in
horses. Vet. Rec. 66, 74-78.
• Proudman, C.J., Edwards, G.B., 1992. Validation of a centrifugation/flotation technique
for the diagnosis of equine cestodiasis. Vet. Rec. 131, 71-72.
• Proudman, C.J., French, N.P., Trees, A.J., 1998. Tapeworm infection is a significant risk
factor for spasmodic colic and ileal impaction colic in the horse. Equine Vet. J. 30, 194–
199.
• Proudman, C.J., Trees, A.J., 1996. Use of excretory / secretory antigens for the
serodiagnosis of Anoplocephala perfoliata cestodosis. Vet. Parasitol.61, 239-247.
• Reinemeyer, C.R., Nielsen, M.K., 2014. Review of the Biology and Control of Oxyuris
equi. Equine Vet. Educ. 26, 584-591.
• Reinemeyer, C.R., Prado, J.C., Nielsen, M.K., 2015. Comparison of the larvicidal
efficacies of moxidectin or a five-day regimen of fenbendazole in horses harboring
cyathostomin populations resistant to the adulticidal dosage of fenbendazole. Vet.
Parasitol. 214, 100-107.
• Rock, C., Pomroy, W., Gee, E., Scott, I., 2013. Macrocyclic lactone resistant Oxyuris
equi in New Zealand. Proceedings of 24th International Conference of the WAAVP, 25–
29 August, p. 520.
• Rossano, M.G., Smith, A.R., Lyons, E.T., 2010. Shortened strongyle-type egg
reappearance periods in naturally infected horses treated with moxidectin and failure of
a larvicidal dose of fenbendazole to reduce fecal egg counts. Vet. Parasitol. 173, 349-
352.
• Sallé, G., Cortet, J., Koch, C., Gascogne, T., Reigner, F., Cabaret, J., 2016. Ivermectin
failure in the control of Oxyuris equi in a herd of ponies in France. Vet. Parasitol. 229,
73–75.
• Sanada, Y., Senba, H., Mochizuki, R., Arakaki, H., Gotoh, T., Fukumoto, S., Nagahata,
H., 2009. Evaluation of marked rise in fecal egg output after bithionol administration to
horse and its application as a diagnostic marker for equine Anoplocephala perfoliata
infection. J.Vet. Med. Sci. 71, 617-620.
• Sangster, N.C., 1999. Pharmacology of anthelmintic resistance in cyathostomes: will it
occur with the avermectin/milbemycins? Vet.Parasitol. 85, 189–201.
• Slocombe, J.O.D., 2004. A modified critical test for the efficacy of pyrantel pamoate for
Anoplocephala perfoliata in equids. Can. J. Vet. Res. 68, 112-117.
• Slocombe, J.O.D., 2006. A modified critical test and its use in two dose titration trials to
assess efficacy of praziquantel for Anoplocephala perfoliata in equids. Vet. Parasitol.
136, 127-135.
• Vidyashankar, A.N., Hanlon, B.M., Kaplan, R.M., 2012. Statistical and biological
considerations in evaluating drug efficacy in equine strongyle parasites using fecal egg
count data. Vet. Parasitol. 185, 45-56.
• Waghorn, T.S., Leathwick, D.M., Miller, C.M., Atkinson, D.S., 2008. Brave or gullible:
Testing the concept that leaving susceptible parasites in refugia will slow the
development of anthelmintic resistance. New Zeal. Vet. J. 56, 158-163.
• Waghorn, T.S., Miller, C.M., Oliver, A.M., Leathwick, D.M., 2009. Drench-and-shift is a
high-risk practice in the absence of refugia. New Zeal. Vet. J. 57, 359-363.
• Wolf, D., Hermosilla, C., Taubert, A., 2014. Oxyuris equi: lack of efficacy in treatment
with macrocyclic lactones. Vet. Parasitol. 201, 163-168.
Appendix A: Egg counting techniques

Modified McMaster Fecal Egg Count (FEC) Procedure

The method described below has a detection limit of 25 EPG, which makes it useful for
identifying high egg shedders, but less appropriate for the FECRT.

Supplies needed:

• Disposable paper cup (Dixie cup) or small container for feces

• Small strainer (household)
• Pipette, eye dropper or syringe to dispense fecal solution
• Cheese cloth or gauze sponge
• McMaster Slide
• Flotation medium

Procedure Steps:
1. Weigh out 4 g of feces in a small container or paper cup.
2. Add 26 mls of flotation medium (to bring the volume up to 30 ml) to feces. Mix well.
a. Note: If you do not have a scale, you can add feces to the 26 ml of solution and
when the volume reaches 30 mls, you have added 4 g.
3. Strain through one or two layers of cheesecloth, one layered gauze squares, or tea
strainer), mix well.
4. Mix the sample well and then immediately withdraw about 1 ml of the suspension with a
pipette or syringe and fill the first counting chamber of the McMaster slide.
a. Repeat the process to fill the second chamber.
b. Let the slide stand for two to five minutes to allow eggs to float to top.
i. If visible air bubbles are present, the chamber should be emptied and
refilled.
5. Steps three and four should be done at the same time without letting the sample sit
between steps, since eggs are in flotation fluid and will immediately begin to rise to the
top of the fluid. You want to be sure to get a representative sample of the mixed solution.
6. Once chambers are filled, step three can be started for the next sample.
7. Once filled, the chambers can set for 60 minutes before counting without causing
problems if using sodium nitrate. Longer than this and drying/crystal formation can
begin. With sodium chloride, crystal formation occurs much more quickly.
8. Count all eggs inside of grid areas (only count the eggs which have more than half of
their area inside the outer lines of the grid) at 100x total magnification (10x ocular lens
and 10x objective lens). Focus on the top layer, which contains the very small air
bubbles (small black circles). Count both chambers.
a. Count only strongyle eggs (oval-shaped, about 90 microns long). Ascarid eggs
(round, about 80-90microns long) can also be counted, but should be counted
separately from the strongyle eggs. Do not count Strongyloides (oval, about 50
microns long), tapeworm eggs (D-shaped), or Eimeria leuckarti (large brown
oocysts of the same size as strongyle eggs)--only notations are made as to the
presence of these other parasites.
9. Multiply the number of counted eggs in each category by 25 to achieve the number of
eggs per gram (EPG) per egg type
Modified Wisconsin Technique
This technique does not require specialized slides, but involves centrifugation using a swing-
bucket rotor. The detection limit is 1 EPG, which makes the technique very suitable for the
FECRT.

Supplies Needed:
• Small strainer (household)
• Pipette, eye dropper or syringe to dispense fecal solution
• Cheese cloth or gauze sponges
• Test tube - 15 mls or centrifuge tube - 15 mls
• Centrifuge – swinging head centrifuge not fixed
• Sheather’s solution (sugar solution)

Procedure Steps:
1. Weigh out 1 g fecal sample in a small beaker (50-100 ml).
2. Add 20 ml of tap water in the fecal material.
3. Stir very well with a spatula and mash the material until it is completely broken apart.
4. Pour the mixture through the funnel with one layer of cheesecloth (or tea strainer) into
another beaker (150-250 ml), stirring the material in the funnel while pouring. Press the
material remaining in the funnel with the spatula until nearly dry.
5. Add 10 ml of tap water to the beaker and rinse into a mixture the material clinging to the
sides and bottom, and then pour this mixture through the material in the funnel, stirring
the material in the funnel while pouring. Press the material in the funnel until dry again,
and then discard.
6. Stir the material in the beaker and immediately pour the contents of the beaker into two
15 ml tubes, being careful to divide it as equally as possible. There should not be any
material left in the beaker.
7. Centrifuge the tubes for 5 to 7 minutes at 300 g to pull fecal debris to the bottom of tube.
8. Pour off the supernatant, leaving the pellet at the bottom of the tubes.
9. Fill the tubes to just over the top with Sheather's solution and place a cover slip onto the
meniscus.
10. Centrifuge at 300 g for 10 minutes.
a. Note that if a swing-bucket rotor is not available then a fixed-angle rotor can be
used, but cover slips may fall off. If using a fixed-angle rotor the procedure
should be modified as follows: the tube is initially filled only ¾ fill with Sheather’s
solution and then after centrifugation the tube is filled with Sheather's solution
until a positive meniscus forms. Then a coverslip is placed on the tube and the
tube is left to sit for 10-15 minutes before removing the coverslip and placing it on
a slide for counting.
11. Let sit for about 5 minutes, and then remove the cover slip and place on a slide.
12. Examine the entire cover slip from both tubes and count the number of eggs that you
find.
13. The number of eggs counted equals the EPG as the detection limit is 1 EPG.
Appendix B: Prepatent periods of important equine parasites

Species Prepatent period References

Cyathostomins 2-3 months (Round, 1969)
Parascaris equorum 2½-3 months (Clayton and Duncan, 1977)
Anoplocephala perfoliata 1½-4 months (Bain and Kelly, 1977)
Strongylus edentatus 11-12 months (Enigk, 1970)
Strongylus vulgaris 6-7 months (Enigk, 1970)

References
• Bain, S.A., Kelly, J.D., 1977. Prevalence and pathogenicity of Anoplocephala perfoliata
in a horse population in South Auckland. N. Z. Vet. J. 25, 27-28.

• Clayton, H.M., Duncan, J.L., 1977. Experimental Parascaris equorum infection of foals.
Res. Vet. Sci. 23, 109-114.

• Enigk, K., 1970. The development of the three species of Strongylus of the horse during
the prepatent period. In: Equine Infectious Diseases. S. Karger, Basel, pp. 259-268.

• Round, M.C., 1969. The prepatent period of some horse nematodes determined by
experimental infection. J. Helminthol. 43, 185-192.

© Copyright AAEP – Revised 2019