Horsemen are strongly urged to take notice of the following medication alerts:
Endogenous substances are substances that naturally occur in the horse. It is possible, however, to elevate the the normal physiological concentration of the substance in the horse via administration. There are various reasons why this is done, but none are considered appropriate. Indeed, the primary purpose is to affect the performance of the horse. The improper administration of some endogenous substances can threaten the health and welfare of the horse. The following endogenous substances are subject to regulatory control.
A blood specimen from a horse found to contain cobalt in excess of 25 nanograms per milliliter of blood plasma or serum shall be considered a positive finding. The Stewards and Judges shall be instructed to apply this regulation in the following manner:
1) A horse which tests for cobalt between 25 nanograms per milliliter of blood plasma or serum and 50 nanograms per milliliter of blood plasma or serum shall be placed on the vets list and not be permitted to start in a race until the horse tests for cobalt below 25 nanograms per milliliter of blood plasma
or serum. All costs associated with any retesting shall be paid for by the owner of the horse.
2) A horse whose cobalt level exceeds 50 nanograms per milliliter of blood plasma or serum shall be disqualified, the trainer of the horse shall be suspended and/or fined at the discretion of the Stewards or Judges and assessed points under the multiple medication violation point system. As previously stated the horse shall be placed on the vets list and not permitted to start in a race until the horse tests for cobalt below 25 nanograms per milliliter of blood plasma or serum. All costs associated with retesting the horse shall be paid for by the owner of the horse.
Cobalt is considered a Class 3 substance under the ARCI Uniform Classification of Foreign Substances. Its Penalty Class is Class B.
GABA (gamma aminobutyric acid), a naturally occurring amino acid in the horse, has been identified as being administered, purportedly to calm a horse so that it remains calm through the paddock and into the post-parade on race day. Often, GABA is administered as a part of a substance called “Carolina Gold”. It is believed that this substance is often given at or around Lasix time. Improper administration of GABA can threaten the health and welfare of the horse. Accordingly, the administration of exogenous GABA to a horse is prohibited.
- The GABA testing threshold in the horse may not exceed 110 nanograms per milliliter in plasma/blood.
- GABA is considered a Class 3 substance under the ARCI Uniform Classification of Foreign Substances. Its Penalty Class is Class B.
The use of agents that elevate the horse’s TCO2 or base excess level above those existing naturally in the untreated horse at normal physiological concentrations is prohibited. The following levels also apply to blood-gas analysis:
The regulatory threshold for TCO2 is 37.0 millimoles per liter of plasma/serum or a base excess level of 10.0 millimoles, and;
The decision level to be used for the regulation of TCO2 is 37.0 millimoles per liter of plasma/serum plus the measurement uncertainty of the laboratory analyzing the sample, or a base excess level of 10.4 millimoles per liter of plasma/serum.
Horsemen are urged to avoid combining the non-steroidal anti-inflammatory drugs Flunixin (Banamine®), Ketoprofen (Ketofen®), Diclofenac (Surpass®), Firocoxib (Equioxx®) and Phenylbutazone (Butazolidin®). Only one NSAID can be present in a post-race test sample below established thresholds. If more than one NSAID is detected in a post-race sample above the established thresholds, it is considered stacking and is a medication violation subject to penalty.
The primary thresholds for the five NSAIDs are:
Diclofenac – 5 nanograms per milliliter in plasma;
Firocoxib – 20 nangrams per milliliter in plasma;
Flunixin – 20 nanograms per milliliter in plasma;
Ketoprofen – 2 nanograms per milliliter in plasma; and
Phenylbutazone – 2 micrograms per milliliter in plasma.
There are secondary thresholds for Flunixin, Ketoprofen and Phenylbuazone. They are:
Flunixin – 3 nanograms per milliliter in plasma;
Ketoprofen – 1 nanogram per milliliter in plasma; and
Phenylbutazone – 0.3 micrograms per milliliter in plasma.
There are three classes of NSAID stacking violations:
CLASS 1 (Penalty Class B):
2 NSAIDs above the primary threshold or 3 NSAIDs above the secondary threshold.
CLASS 2 (Penalty Class C):
1 NSAID above the primary threshold and 1 other NSAID above the secondary threshold but below the primary threshold.
CLASS 3 (fines only):
2 NSAIDs above the secondary threshold but below the primary threshold.
There are no points for a stacking violation. Points are assessed only for the underlying NSAID violation.
(Source: Mid-Atlantic advisory)
Notwithstanding the ARCI recommendation, horsemen are strongly cautioned against the use of Depo-Medrol for a horse in training. A trainer who chooses to race a horse that has been treated with Depo-Medrol despite this warning should, at his/her expense, get the horse tested prior to entry to ensure that the horse will test below the regulatory limit, which is 100 picograms per milliliter of plasma or serum.
(Source: Mid-Atlantic advisory)
Only Procaine Penicillin administrations within 30 days of a race need be reported to the state racing commission. The surveillance requirement remains in effect. The commission or the racetrack, as the case may be, will provide a security guard for the horse at the owner/trainer’s expense. Please note that the testing threshold for Procaine Penicillin is 25 nanograms per milliliter in plasma regardless of the surveillance requirement, and this testing threshold will be enforced.
- The possession or use of a drug, substance, or medication on association grounds that has not been approved by the appropriate federal agency (e.g., the United States Food and Drug Administration) for any use in (human or animal) is forbidden without prior permission of the commission or its designee.
- It is a violation of this regulation to possess, use, or distribute a compounded medication on association grounds if there is an FDA approved equivalent of that substance available for purchase. A difference in available formulations or concentrations does not alleviate the need to use FDA approved products.
- It is a violation of this regulation to possess, use, or distribute a compounded medication on association grounds made from bulk substances if an FDA-approved equivalent is available for purchase.
- Combining two or more substances with pharmacologic effect constitutes the development of a new drug. This may only be done in accordance with state and local laws and must contain FDA-approved medications, if available.
- Compounded veterinary drugs: Veterinary drugs shall be compounded in accordance with all applicable state and federal laws. Compounded medication shall be dispensed only by prescription issued by a licensed veterinarian to meet the medical needs of a specific horse and for use only in that specific horse.
- Labels on compounded veterinary drugs: All compounded medications must be labeled in accordance with section ARCI-011-020(D) Medical Labeling.
- Possession of an improperly labeled product by any person on association grounds is considered a violation of this section.
Horses can be inadvertently exposed to, or come in contact with, regulated substances that if detected in a post-race urine or blood test can result in significant penalties. The trainer responsibility rule requires that horsemen bear responsibility for the presence of unauthorized substances in a horse at the time of testing regardless of intent or the route of exposure.
The Racing Medication and Testing Consortium is offering guidance for horsemen in managing the horse’s environment to prevent contamination.
Details on preventing environmental contamination are available here.
MEDICATION LABELING (PENNSYLVANIA)
Under regulations adopted by the Pennsylvania Horse Racing Commission, effective Jan. 1, 2017, all containers of medication must be properly labeled and prescribed, and they will be subject to testing.
The PHRC Dec. 1 notified horsemen and private veterinarians of the impending rules. Any containers that aren’t labeled or those that aren’t verified after testing could result in penalties for trainers and dispensing vets, according to a memorandum.
The new regulations, which outline rules for professional conduct of vets, are outlined in the PHRC memo.
Levamisole is commercially available as a dewormer for cattle, sheep, goats and pigs. It also has
conventional off-label uses in horses as an immunostimulant and as a medication for treatment of
Equine Protozoal Myelitis (EPM).
Levamisole metabolizes in the horse to aminorex and possibly also pemoline, both of which are potent stimulants assigned a 1/A Classification in the Association of Racing Commissioners International Uniform Classification of Foreign Substances. The identification of either of these substances in a post-race sample is associated with a potential career-ending penalty.
In consideration of its conventional use in horses, the Racing Medication and Testing Consortium contemplated an administration study to develop guidance on the use of levamisole and surveyed practicing veterinarians on their use of levamisole. Survey results included indications for use; route of administration (oral or injectable); dose (500 milligrams to 2,500 milligrams); and frequency and duration of treatment (3 days to unending).
Given the prevalence of compounded levamisole products and that survey results established there is no commonly used treatment protocol, the RMTC determined an administration study would yield limited information.
Therefore, the RMTC recommends that following withdrawal of the medication, levamisole-treated
horses be subjected to testing prior to entry to verify that levamisole and its metabolites have been
eliminated from the horse. Before submitting a sample for clearance testing it is advisable to consult the regulatory authority to make sure that your sample meets the laboratory’s requirements for matrix and volume.
Glaucine, which has recently been identified in a number of post-race samples, is marketed as an anti-tussive (cough suppressant) and can have hallucinogenic effects at very high doses. No glaucine-containing products are FDA-approved in the U.S.
A Racing Medication and Testing Consortium Glaucine Task Force has reported that glaucine is not only present in some bulk shavings but is also available in injectable forms online. In shavings, it is a result of the presence of the tulip poplar tree, which contains a number of plant alkaloids—two of which are asimilobine and liriodenine. One or both of these alkaloids have been identified in all samples of shavings tested that are positive for glaucine.
Due to glaucine’s presence in bedding, a horse could ingest shavings prior to a race that could potentially result in a laboratory finding. This potential for inadvertent exposure, as well as intentional exposure, indicates that the simple use of a screening limit alone would likely not be sufficient in controlling the substance.
Therefore, the following testing recommendations have been issued for glaucine:
- 500 picograms/milliliter interim screening limit;
- Penalties: Above 500 picograms/milliliter and below 1 nanogram/milliliter—warning; above 1 nanogram/milliliter—Class B Penalty.
HORSEMEN SHOULD CONSIDER REMOVING HORSES FROM BULK SHAVINGS AT 24 HOURS PRE-RACE TO AVOID THE POSSIBILITY OF A POSITIVE TEST.
MEDICATION LABELING (NEW YORK)
The New York State Gaming Commission March 24, 2017, issued rules for the labeling of prescription medication dispensed by a veterinary pharmacy. Dispensing medication on the grounds of New York racetracks without a prescription label that meets the certain criteria may be considered professional misconduct.
The memo from New York State Equine Medical Director Dr. Scott Palmer is available here.