Professional Documents
Culture Documents
Ambulatory Practice
Ron Friedman, MS, DVM
KEYWORDS
• Equine • Ambulatory • Practice • Reproduction
Equine reproduction in an ambulatory practice setting is far more common than are
in-house clinic facilities. Although ambulatory settings sometimes require adaptation
and ingenuity, most procedures for a successful breeding season are readily
adaptable to the ambulatory practice. This article will describe practice procedures
that are feasible for most ambulatory settings.
PROCEDURES: MARES
Transrectal Exam
Successful broodmare management requires serial examinations of the mare before
and shortly after ovulation. These procedures ensure that the stallion is used
efficiently and the mare is bred in a timely manner. As a general rule, the goals of
breeding management, ambulatory or otherwise, should be to:
• Utilize the stallion and mare as economically and efficiently as possible
• Achieve pregnancy in as few breedings, as close to ovulation, as possible
• Ensure that the mare’s uterus maintains a suitable, contaminant-free environ-
ment ready for the maintenance of pregnancy.
The fundamental diagnostic procedure in mare reproduction is the transrectal uterine
and ovarian palpation examination. Long a mainstay in equine reproduction, the
transrectal exam remains diagnostically useful, adding information unavailable via
other methods. Other basic reproductive procedures that require transrectal palpa-
tion as a prerequisite are:
• Uterine culture
• Uterine cytology
• Uterine biopsy
• Artificial insemination (AI)
• Uterine treatments: infusion and lavage.
Fig. 2. Using the stall door as a barrier decreases the risk to the veterinarian.
Adequate lubrication not only facilitates the transrectal exam but is a safety
consideration for the mare. Carboxymethyl-cellulose and mineral oil are the most
commonly used lubricants and help decrease rectal straining; although straining is
not necessarily a prerequisite for a rectal tear, it can contribute to this potentially
catastrophic injury. Sedation with xylazine or detomondine at recommended
dosages may help improve mare handling and safety but may not relieve rectal
straining.
In addition to the mare’s safety, excessive rectal straining can be a significant
impediment to any procedure requiring transrectal palpation. The addition of a local
anesthetic such as xylocaine HCl to the lubricant or applied to the rectal mucosa may
reduce rectal straining. Intravenous N-butylscopolaminium bromide (Buscopan;
Boehringer Ingelheim GmbH, Ingelheim, Germany) at recommended doses will
eliminate rectal straining around the arm for a short time and allow for a thorough
examination or any procedure requiring transrectal manipulation of the uterus or
ovaries. Mares being palpated for the first time commonly strain and resist palpation.
Some mares never acclimate to the procedure and will continue to strain during
subsequent exams. Even experienced mares who are normally unperturbed by
palpation will strain if the procedure exceeds a few minutes. In these instances, not
only will N-butylscopolaminium bromide decrease the risk of rectal trauma but it will
also facilitate the speed, efficiency, and accuracy of the exam findings.
The procedure for and the findings of transrectal reproductive palpation have been
described.1,2 The diagnostic goal of rectal palpation of the mare is to evaluate the size
and tone of the uterus, ovaries and follicles, and cervix. An enlarged uterus, either
from pregnancy of approximately 60 days or from a diseased state such as pyometra,
178 Friedman
progesterone at the time of twin reduction resulted in delivery of more live foals than
in untreated mares.7 The author prefers to start these treatments 24 hours before, and
continue for 3 days after, twin reduction.
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Fig. 3. Preparing the mare for intrauterine and intravaginal procedures. (A) Fold the tail on
itself, put the string through the fold, and wrap around tail twice. (B) Make a quick release
loop through the string as it passes through the fold of the tail. (C) Tighten loop: the quick
release knot can be easily opened by pulling on the loose end of the string. (D) Tie a half hitch
at the top of the tail. (E) While wrapping roll over tail, incorporating a few tags of tail hair will
secure wrap in place. (F) Fold the tail on itself and incorporate into wrap, forming a loop for
securing tail. (G) To apply plastic sleeve as a tail wrap, place sleeve over folded tail, and secure
to base of tail with adhesive tape. (H) As in A–C, wrap string around tail and through fold in
tail. (I) Tail can be secured around neck of mare, tied to halter in quick release knot, or held
by mare handler.
182 Friedman
rates of chilled shipped semen and, to a lesser extent, frozen semen, have made AI
commonplace in ambulatory practice. Equipment and supplies required are minimal:
shoulder length sleeve, sterile lube, syringe, and AI pipette. Achieving positive results
with AI can pose several challenges to the ambulatory clinician, because determina-
tion of the stage of cycle and accurate prediction of ovulation are essential for
success. Several farm visits are often required until the stage of cycle is determined.
Reproductive cycle manipulation is highly utilized and may include prostaglandin
injections or 10 days of progestins followed by prostaglandin. Hormonal manipulation
of the mare’s reproductive cycle will decrease the number of farm visits and mare
exams required, significantly increasing efficiency and economy, and will also
synchronize insemination dates with the shipping companies’ days of operation.13
The mare is examined daily or every other day during estrus until ovulation can be
reliably predicted. Ideally, when using shipped semen, semen is ordered for insemi-
nation 1 day pre-ovulation. Ovulation induction agents are commonly used to shorten
the interval between insemination and ovulation. When using frozen semen and as
ovulation nears, the mare is examined multiple times daily or examined and insemi-
nated using the timed protocol discussed later.
Because thawed frozen semen has a shorter life span compared to chilled semen,
it requires insemination much closer to ovulation than with shipped semen or live
cover, ideally within a few hours. Precise prediction of ovulation is difficult; 2 basic
breeding protocols have gained popularity for AI by frozen semen.14
The first breeding protocol for AI by frozen semen requires examination every 6 to
8 hours as the gravid follicle matures, with insemination at the time ovulation is
detected. As the life span of the ova is, at most, 12 hours, this examination protocol
ensures that sperm are introduced to the ova no more than 8 hours after ovulation and
in practice often less than 6 hours after ovulation.
The second frozen semen protocol is timed around the administration of ovulation
induction agents and uses 2 breeding doses of frozen semen. In this scenario, the
mare is examined once daily until a 35-mm follicle is detected. At that time, the mare
is administered an ovulation induction agent (human chorionic gonadotropin or
gonadotropin releasing hormone). AI is then performed at 24 hours and 40 hours after
administration of the ovulation induction agent.
Both protocols for AI with frozen semen have their drawbacks in ambulatory
practice: the first protocol requires numerous trips to the mare, and the second
protocol requires 2 breeding doses of frozen semen. An additional challenge to using
frozen semen in an ambulatory setting is that specialized AI “guns” may be
recommended by various semen producers. These “guns” hold 0.25- to 0.5-mL
straws and typically require the use of multiple straws of frozen semen, using 1 straw
at a time. Their use may also require additional assistance, which is not always
available in ambulatory practice. Additional equipment is required for thawing frozen
semen. Although recommended, an electric hot water bath is not required since an
accurate thermometer and a thermal insulated mug, a large sink, or any insulated
container can be adequate for thawing frozen semen.
Two AI techniques are commonly used in the mare: traditional AI and deep horn
artificial insemination (DHAI). Traditional AI technique deposits the semen into the
uterine body. DHAI deposits semen at the apex of the uterine horn, ipsilateral to the
gravid follicle, close to the oviductal papillae. The technique is described elsewhere.15
DHAI has been recommended for use with semen containing the lower numbers of
sperm per breeding dose that are often found with frozen semen. Some advocate the
use of endoscopy to facilitate DHAI, but utilization of this technology often requires
additional assistance not always available in an in ambulatory setting. DHAI can be
Reproduction in Ambulatory Practice 183
Embryo Transfer
Embryo transfer is not easily adaptable to ambulatory practice. Flushing embryos
from donor mares requires transport of equipment and supplies, including, but not
limited to, sterile intrauterine catheters, specialized tubing with fittings, embryo filters,
embryo locating dishes, dissection microscopes, and other equipment, as well as
several liters of heated embryo flush and holding solutions. Additional personnel are
needed for the flushing procedure and restraining the mare. Keeping the mare
adequately restrained and immobile without stocks for the duration of the procedure
will be problematic, as many mares become mildly agitated or anxious when their
uterus is distended with flush solution. Thus, clients who are interested in embryo
transfer should be referred to facilities equipped for the process.
PROCEDURES: STALLION
For the most part, stallion reproduction in ambulatory or referral settings revolves
around 2 fundamental procedures: semen collection and semen transport. Repro-
ductive procedures on stallions are inherently more complicated than those on the
mare simply because they commonly require the presence of a mare and accompa-
nying personnel. Occasionally, when working with the highly trained and experienced
stallion that has been trained for collection on a phantom mare without an estrus mare
being present, additional assistance is not necessary.
Semen Collection
Stallion semen collection in ambulatory practice, although not a difficult procedure,
does pose some hurdles not encountered when working on mares. In most cases, a
receptive mare is essential, which rarely poses a problem if the estrus mare used is
the mare to be bred. If the semen is to be shipped, having an estrus mare that
coincides with the time semen is requested can be problematic and, without
preparation, unreliable.
Semen collection can be accomplished on a mare displaying estrus or on a
“phantom mare” breeding mount if available. Either method requires additional
assistance because handlers are needed for both the mare and the stallion, as well as
a person handling the artificial vagina (AV). In contrast to reproductive procedures
carried out on mares, experienced horse handlers are critical in semen collection
because sedatives and tranquilizers for the stallion are not a viable option. Without
experienced personnel, collecting semen from stallions can be a dangerous proce-
dure, and ambulatory practitioners who do not have access to trained personnel and
proper equipment would be best served to refer to facilities that specialize in this
procedure.
Because of the very nature of the procedure, collecting a sexually stimulated
stallion in close proximity to, or on the back of a mare, who may or may not be
compliant, can rapidly lead to some unexpected and unpleasant situations extremely
quickly. Semen collection and the equipment required, as well as the methods to
produce an estrus mare, have been widely described.20
Freezing Semen
Because a laboratory full of equipment and supplies is required for cryopreservation
of stallion semen, this procedure is not readily adapted to most ambulatory practices.
In addition to the freezing apparatus itself, refrigeration, incubators, microscopes, and
assorted other supplies are needed. Handling semen and supplies in a temperature-
controlled manner is critical for success, and as such, practitioners should consider
referring this service to facilities experienced in the procedure: some of these facilities
offer mobile laboratories as part of their service.
SUMMARY
REFERENCES
1. Asbury AC. Examination of the mare. In: Colahan PT, Merritt AM, Moore JN, et al,
editors. Equine medicine and surgery, vol II. St Louis: Mosby; 1999. p 1088 –93.
2. Shindeler RK. Rectal palpation. In: McKinnon AO, Voss JL, editors. Equine reproduc-
tion. Philadelphia: Lea & Febiger; 1993. p. 204 –11.
3. McKinnon AO, Squires EL. Ultrasonic evaluation of the reproductive trac. In: Colahan
PT, Merritt AM, Moore JN, et al, editors. Equine medicine and surgery, vol II. St Louis:
Mosby; 1999. p. 1100 –14.
4. McKinnon AO. Diagnosis of pregnancy. In: McKinnon AO, Voss JL, editors. Equine
reproduction. Philadelphia: Lea & Febiger; 1993. p. 501– 8.
5. Mckinnon AO. Twin reduction techniques. In: Samper JC, Pycock JF, McKinnon AO,
editors. Current therapy in equine reproduction. Philadelphia: WB Saunders; 2007. p.
357–73.
6. Pascoe DR, Pascoe RR, Hughes JP, et al Management of twin concept by manual
embryonic reduction: comparison of two techniques and three hormone treatments.
Am J Vet Res 1987;48:1594 –9.
7. Sheerin PC, Howard CE, LeBlanc MM, et al, Effects of operator, treatment, and mare
age on the live foal rate of mares after manual twin reduction. Anim Repr Sci 2010;
Suppl:S312–3.
8. LeBlanc MM. Advances in the diagnosis and treatment of chronic infectious and
post-mating-induced endometritis in the mare. Reprod Domest Anim 2010;45
(Suppl 2):21–7.
9. Riddle WT, LeBlanc MM, Stromberg AJ. Relationships between uterine culture,
cytology and pregnancy rates in a Thoroughbred practice. Theriogenology 2007;68:
395– 402.
10. Pycock JF. Breeding management of the problem mare. In: Samper JC, editor.
Equine breeding management and artificial insemination. Philadelphia: WB Saunders;
2000. P. 195–228.
Reproduction in Ambulatory Practice 187
11. LeBlanc MM. Tutorial article. The current status of antibiotic use in equine reproduc-
tion. Equine Vet Educ 2009;21:156 – 67.
12. LeBlanc MM. Vaginal examination. In: McKinnon AO, Voss JL, editors. Equine
reproduction. Philadelphia: Lea & Febiger; 1993. p. 221– 4.
13. Bergfelt DR. Estrous synchronization. In: Samper JC, editor. Equine breeding man-
agement and artificial insemination. Philadelphia: WB Saunders; 2000. p. 165–77.
14. Loomis PR, Squires EL. Frozen semen management in equine breeding programs.
Theriogenology 2005;64:480 –91.
15. Lyle SK, Ferrer MS. Low-dose insemination—why, when and how. Theriogenology
2005;64:572–9.
16. Frazer GS, Beard WL, Abrahamsen E, et al. Systemic effects of a polyethylene
polymer-based obstetrical lubricant in the peritoneal cavity of the horse. In: Proceed-
ings of the 50th Am Assoc Equine Prac. Denver; 2004. p. 484 –7.
17. Frazer GS. Dystocia and fetotomy. In: Samper JC, Pycock JF, McKinnon AO,
editors. Current therapy in equine reproduction. Philadelphia: WB Saunders;
2007. p. 417–35.
18. Brinsko SP. How to perform uterine lavage: indications and practical techniques. In:
Proceedings 47th Am Assoc Equine Prac. San Diego; 2001. p. 407–11.
19. Blanchard TL, Macpherson ML. Postparturient abnormalities. In: Samper JC, Pycock
JF, McKinnon AO, editors. Current therapy in equine reproduction. Philadelphia: WB
Saunders; 2007. p. 465–75.
20. Hurtgen JP. Semen collection in stallions. In: Samper JC, editor. Equine breeding
management and artificial insemination. Philadelphia: WB Saunders; 2000. p. 81–90.
21. Samper JC. Artificial insemination. In: Samper JC, editor. Equine breeding manage-
ment and artificial insemination. Philadelphia: WB Saunders; 2000. p. 109 –31.
22. Brinsko SP, Rowan KR, Varner DD, et al. Effects of transport container and ambient
temperature on motion characteristics of equine spermatozoa. Theriogenology 2000;
53:1641–55.