US20090028905A1 - Method for treatment of laminitis in animals - Google Patents
Method for treatment of laminitis in animals Download PDFInfo
- Publication number
- US20090028905A1 US20090028905A1 US11/881,607 US88160707A US2009028905A1 US 20090028905 A1 US20090028905 A1 US 20090028905A1 US 88160707 A US88160707 A US 88160707A US 2009028905 A1 US2009028905 A1 US 2009028905A1
- Authority
- US
- United States
- Prior art keywords
- botulinum toxin
- horse
- laminitis
- limb
- units
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 37
- 241001465754 Metazoa Species 0.000 title claims abstract description 28
- 238000011282 treatment Methods 0.000 title description 26
- 210000003205 muscle Anatomy 0.000 claims abstract description 29
- 108030001720 Bontoxilysin Proteins 0.000 claims abstract description 22
- 229940053031 botulinum toxin Drugs 0.000 claims abstract description 22
- 238000002347 injection Methods 0.000 claims abstract description 15
- 239000007924 injection Substances 0.000 claims abstract description 15
- 241000283073 Equus caballus Species 0.000 claims description 46
- 108010057266 Type A Botulinum Toxins Proteins 0.000 claims description 16
- 229940094657 botulinum toxin type a Drugs 0.000 claims description 10
- 206010033799 Paralysis Diseases 0.000 claims 2
- 210000000003 hoof Anatomy 0.000 description 31
- 210000002435 tendon Anatomy 0.000 description 28
- 210000000988 bone and bone Anatomy 0.000 description 12
- 210000003414 extremity Anatomy 0.000 description 12
- 210000003194 forelimb Anatomy 0.000 description 11
- 239000002775 capsule Substances 0.000 description 9
- 230000006378 damage Effects 0.000 description 9
- 210000002683 foot Anatomy 0.000 description 9
- 241000283086 Equidae Species 0.000 description 8
- 208000024891 symptom Diseases 0.000 description 8
- 229940089093 botox Drugs 0.000 description 7
- 210000002414 leg Anatomy 0.000 description 7
- 230000001154 acute effect Effects 0.000 description 6
- 210000001015 abdomen Anatomy 0.000 description 5
- 230000001684 chronic effect Effects 0.000 description 4
- 238000006073 displacement reaction Methods 0.000 description 4
- 208000014674 injury Diseases 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 230000010412 perfusion Effects 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 101710117542 Botulinum neurotoxin type A Proteins 0.000 description 3
- 206010061218 Inflammation Diseases 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 208000002193 Pain Diseases 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 230000017531 blood circulation Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000004054 inflammatory process Effects 0.000 description 3
- 210000003041 ligament Anatomy 0.000 description 3
- 230000007170 pathology Effects 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 208000011580 syndromic disease Diseases 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 230000002146 bilateral effect Effects 0.000 description 2
- 210000003010 carpal bone Anatomy 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000005021 gait Effects 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 208000030175 lameness Diseases 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 230000002040 relaxant effect Effects 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 239000003053 toxin Substances 0.000 description 2
- 231100000765 toxin Toxicity 0.000 description 2
- 208000004998 Abdominal Pain Diseases 0.000 description 1
- 241000567030 Ampulloclitocybe clavipes Species 0.000 description 1
- 241000193155 Clostridium botulinum Species 0.000 description 1
- 208000002881 Colic Diseases 0.000 description 1
- 206010011985 Decubitus ulcer Diseases 0.000 description 1
- 206010015548 Euthanasia Diseases 0.000 description 1
- 206010020710 Hyperphagia Diseases 0.000 description 1
- 238000011887 Necropsy Methods 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 206010033307 Overweight Diseases 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 208000004210 Pressure Ulcer Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 206010043101 Talipes Diseases 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 108010079650 abobotulinumtoxinA Proteins 0.000 description 1
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 1
- 229960004373 acetylcholine Drugs 0.000 description 1
- 230000009798 acute exacerbation Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000011256 aggressive treatment Methods 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 210000001142 back Anatomy 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 201000011228 clubfoot Diseases 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 210000004207 dermis Anatomy 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 229940098753 dysport Drugs 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 210000004744 fore-foot Anatomy 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 238000013160 medical therapy Methods 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229940112646 myobloc Drugs 0.000 description 1
- 210000000715 neuromuscular junction Anatomy 0.000 description 1
- 231100000189 neurotoxic Toxicity 0.000 description 1
- 230000002887 neurotoxic effect Effects 0.000 description 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 235000020830 overeating Nutrition 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 108010074523 rimabotulinumtoxinB Proteins 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- 230000008736 traumatic injury Effects 0.000 description 1
- 210000001364 upper extremity Anatomy 0.000 description 1
- 210000005166 vasculature Anatomy 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Definitions
- This invention relates to laminitis in animals. More specifically, the invention comprises a method of treating the sequela of laminitis in animals, particularly horses.
- Laminitis is a serious medical condition in horses and other hoofed animals, and despite significant advances in veterinarian medicine, remains a major reason for euthanasia of such animals.
- Laminitis is an inflammation of the lamina (the lamellar attachment between the distal phalanx (coffin bone) and the inner hoof wall.
- Laminitis is characterized by separation of the hoof wall from the distal phalanx due to the deterioration and detachment of the lamina, which holds the two together. Failure of the laminar attachments, in a majority of cases is limited to the toe region (commonly called rotation).
- Laminitis can occur secondary to many diseases of the horse, but is common following overeating, colic, fever, shock, pneumonia, injury and obesity.
- wedge shoes Elevation of the heels with wedge shoes reduces the pull of the deep digital flexor tendon on the coffin bone and therefore decreases the stress on the dorsal laminar attachment.
- the wedge shoe creates additional stresses on other regions of the foot and may cause compression of the hoof capsule during the acute phase.
- the second disadvantage to wedge shoes involves the method of attaching the wedge shoe to the hoof. If wedge shoes are nailed onto the hoof, the hoof capsule may be compressed, due to the nailing force, potentially leading to further damage. If wedge shoes are glued onto the hoof the horse may be forced to hold one foot up for an extended period of time thereby harming the opposite foot.
- wedge shoes are bandaged to the foot during the acute phase.
- the bandaged shoe slips from the hoof it could cause an abrupt strain on the deep digital flexor tendon and potential further damage to the dorsal laminar attachment.
- Another disadvantage to wedge shoes is the risk of increased damage if the angle of the wedge does not correspond to each horse's particular condition. Wedge shoes must be designed for each horse on a case by case basis based on the severity of the condition or based on the hoof's adaptation to the condition before any treatment was given. In order to properly treat the condition different horses may require the wedge shoes to be adjusted to different angles. If the angle of the wedge is improper the condition may become more severe.
- DDFT deep digital flexor tendon
- the present invention comprises a method for treatment and/or prevention of the sequela of laminitis in animals. More specifically, the present invention comprises a method for treatment of the symptoms associated with the laminitis syndrome.
- Laminitis is the condition in which the lamina becomes inflamed. This inflammation may lead to separation of the epidermal lamina from the dermal lamina associated with the distal phalanx (coffin bone) often resulting in the rotation or sinking of the distal phalanx within the hoof capsule. In the acute stage the lamina are inflamed but the distal phalanx is not yet displaced. Upon entering the chronic phase of the laminitis condition the distal phalanx may be displaced. Some horses compensate for the displacement by stabilizing the bone in its displaced position.
- the rotation of this distal phalanx may be due to a metabolic disturbance (such as carbohydrate load) or to a discrepancy between the strength of the epidermal laminae and the load they have to support.
- the forces of the deep digital flexor tendon on the palmar aspect of the digital phalanx are thought to contribute to the tearing of the laminar membrane in the toe region.
- the method of the present invention can be implemented.
- the pull of the deep digital flexor tendon on the coffin bone is thought to affect the foot in several different ways.
- the tightening may compromise the blood flow through the dorsal lamina.
- the decrease in blood flow may cause decreased laminar perfusion.
- laminar perfusion With a decrease in laminar perfusion lamina tissue is deprived of nutrients and is weakened and more subject to tearing.
- the tightening of the deep digital flexor tendon on the palmar aspect of the digital phalanx creates a force which pulls the laminar membrane away from the digital phalanx or hoof wall.
- the pull of the deep digital flexor tendon on the distal phalanx often causes the distal phalanx to become displaced as the opposing force of the laminar attachment is impaired.
- the method of treatment of the present invention may be directed at relieving the tensile forces acting on the bone, which contribute to this separation. Reducing the pull of the deep digital flexor tendon on the palmar aspect of the distal phalanx theoretically reduces the shear forces on the lamina which attaches the dorsal surface of the distal phalanx to the hoof wall. The relaxation of the deep digital flexor tendon may preserve laminar perfusion.
- the distal phalanx may prevent the distal phalanx from displacing and entering the chronic phase. If the displacement of the distal phalanx can be prevented a horse has a good chance of recovery. Where a horse has entered the chronic phase the distal phalanx is displaced downward and compresses the sole corium altering the architectural development of the hoof capsule. It is hypothesized that by relaxing the deep digital flexor tendon the distal phalanx will re-align with relation to the ground surface and the hoof capsule can begin to regenerate itself.
- the goal is to allow the hoof to reestablish normal orientation of the distal phalanx and maintain that orientation without the aid of the clinical relaxation of the deep digital flexor tendon that this treatment provides.
- Relieving the tensile forces acting on the distal phalanx is accomplished by injecting the flexor muscles of the animal with Botulinum Toxin Type A.
- the Botulinum Toxin Type A used for treatment of the animal can be administered to the animal by any suitable method.
- the Botulinum toxin type A can be injected into the muscle bellies of the flexor digitorum profundus muscle which attaches to the deep digital flexor tendon.
- the Botulinum toxin is administered in the amount of 100U to 600U over the course of 4 to 10 injections per muscle.
- the above described treatment method can also be used to treat issues/pathologies distinct from laminitis.
- treatment involves injections in the superficial and/or deep digital flexor muscle.
- pathologies include “back in the knee” (deep and superficial); club foot in foals (deep and superficial); desmitis of the distal check ligament; navicular syndrome; trauma to the involved muscle or tendon; and inflammation of the involved muscle or tendon.
- Laminitis can occur in any hoofed animal therefore the present invention should not be limited to horses.
- the present invention is directed to the prevention and/or treatment of the sequela of the laminitis condition in animals. More specifically, the present invention is directed to a method for treating the symptoms of or aiding in the recovery of a hoofed animal afflicted with the condition commonly known as laminitis.
- the method of treatment of the invention involves injecting Botulinum Toxin into the muscle bellies of the flexor digitorum profundus muscle.
- Botulinum Toxin commonly known as BOTOX, MYOBLOC, OR DYSPORT, is a neurotoxic protein produced by the bacterium Clostridium botulinum .
- the toxin blocks the release of acetylcholine at the neuromuscular junction thereby relaxing the muscle.
- the physiologic effect of BOTOX lasts ten to twelve weeks.
- Botulinum toxin type A is safe and effective for the treatment of the sequela of laminitis.
- Botulinum Toxin chemically denervates the muscle bellies effecting the tension of the deep digital flexor tendon. Due to the Botulinum Toxin the deep digital flexor tendon relaxes and reduces the force pulling on the palmar aspect of the distal phalanx.
- the disclosed treatment can be used for any laminitic animal.
- Botulinum Toxin There are seven serotypes of Botulinum Toxin (A through G). The present invention should not be limited to any one serotype of the toxin.
- the Botulinum Toxin Type A is administered to the animal by injection into the muscle belly of the flexor digitorum profundus muscle at approximately 4 to 10 different sites in the muscle.
- the total amount of Botulinum Toxin Type A intramuscularly injected ranges from about 100 units to 600 units per limb depending on the size of the horse and the involvement of the affected muscles.
- the Botulinum Toxin is administered after being reconstituted according to the manufacturer's recommendations at a desired dilution.
- a quantity of 100U of powdered BOTOX is dissolved in 2-4 cc's of preservative free, sterile saline.
- the region to be injected is prepped in a sterile fashion.
- the appropriate muscle is first identified anatomically, the muscle is then accessed utilizing an Ambu Neuroline Inoject 24 gauge, 2-3 inch coated needle electrode using EMG guidance. Botulinum Toxin is then injected through this needle into 4-6 sites in the involved deep digital flexor muscle belly.
- Treatment should begin at the onset of any symptoms of laminitis.
- treatment should begin in the contra-lateral limb as soon as an impaired weight bearing injury is evident.
- Some common symptoms include lameness, excess shifting of weight by the animal, altered heel stance, immobility, depression around the coronary band and increased frequency of animal lying down. If symptoms of laminitis do not improve the treatment should be repeated after two to six weeks. Treatment may also be repeated as needed if symptoms recur in the future.
- an animal with laminitis in one limb will eventually show symptoms of laminitis in the contralateral uninvolved limb. Therefore even if an uninvolved limb shows no symptoms of laminitis the treatment may proceed in the uninvolved limb in an effort to prevent laminitis from occurring or progressing in the uninvolved limb.
- Botulinum toxin (Botox) was reconstituted into 100 units per 2cc of normal saline. The skin overlying the flexor muscles of the fore legs was prepped with isopropyl alcohol. Using EMG guidance, 25 units of botulinum toxin was injected into 8 sites of the flexor digitorum profundus of each forelimb for a total of 400 units. The horse tolerated the procedure well with no immediate adverse effects noted. The horse was monitored over the next 12 weeks. Within 2 weeks the horse showed a marked improvement in it's ability to stand and ambulate. The horse has subsequently returned to functional use to the level of pasture comfort and occasional riding at all gaits.
- leg 1 An eight year old stallion quarter horse was experiencing severe laminitis in two legs (Obel Grade 4).
- leg 1 the deep digital flexor tendon was surgically cut utilizing accepted procedures and techniques.
- Redding shoes were applied at a 15 degree angle.
- leg 2 utilizing clean technique and EMG guidance a total of 400 units of Botulinum Toxin Type A diluted into 8 cc of normal saline was injected into 8 separate sites within the flexor digitorum profundus. Redding shoes were applied at 15 degree angles.
- the horse underwent pre and post procedure venograms with no initial difference noted between the legs. The horse tolerated both procedures well and was monitored over the subsequent 5 weeks.
- the horse experienced a recovery from an Obel grade of 4 to an Obel grade of 3 with repeat venograms showing recovery of venous flow in both digits. Comparison between the two legs revealed a more rapid return to normal venous patterns in the limb receiving surgical transection of the deep digital flexor tendon. Thirty days post treatment the venogram of the surgical and Botulinum toxin treated legs were comparable.
- botulinum toxin 200 units botulinum toxin 200 units
- botulinum toxin A botulinum toxin A
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
- Not Applicable
- Not Applicable
- Not Applicable
- 1. Field of the Invention
- This invention relates to laminitis in animals. More specifically, the invention comprises a method of treating the sequela of laminitis in animals, particularly horses.
- 2. Description of the Related Art
- Laminitis is a serious medical condition in horses and other hoofed animals, and despite significant advances in veterinarian medicine, remains a major reason for euthanasia of such animals. Laminitis is an inflammation of the lamina (the lamellar attachment between the distal phalanx (coffin bone) and the inner hoof wall. Laminitis is characterized by separation of the hoof wall from the distal phalanx due to the deterioration and detachment of the lamina, which holds the two together. Failure of the laminar attachments, in a majority of cases is limited to the toe region (commonly called rotation). It is hypothesized that without the distal phalanx properly attached to the inside of the hoof wall, the weight of the horse and the forces of locomotion by the deep digital flexor tendon cause the distal phalanx to rotate away from the hoof capsule. This process shears the vasculature and crushes the corium (dermis) of the sole, causing unrelenting pain and a characteristic lameness. Radiographic and necropsy examination of the feet of affected horses show a characteristic rotation of the dorsal border of the distal phalanx away from the dorsum of the hoof wall.
- In more rare and significantly more severe cases the failure of attachment can extend around the perimeter of the hoof. This allows the entire bony column to drop within the hoof capsule.
- Laminitis can occur secondary to many diseases of the horse, but is common following overeating, colic, fever, shock, pneumonia, injury and obesity.
- All hoofed animals, and particularly horses, are susceptible to laminitis and significant economic loss occurs due to severe pain and debilitation of these animals. Due to the insidious nature of the disease process, damage to the laminae often occurs prior to clinical evidence of abnormality.
- There is no cure for laminitis. Current medical therapies include identification and treatment of the underlying disease, systemic anti-inflammatory medications and rest. A more aggressive treatment of the sequela of laminitis involves severing the deep digital flexor tendon. Additionally, support of the sole has met with some success utilizing deep sand flooring, peat moss and foam sole pads.
- One example of treatment is the application of wedge shoes. Elevation of the heels with wedge shoes reduces the pull of the deep digital flexor tendon on the coffin bone and therefore decreases the stress on the dorsal laminar attachment. However, there are several disadvantages to the wedge shoe therapy. First, the wedge shoe creates additional stresses on other regions of the foot and may cause compression of the hoof capsule during the acute phase. The second disadvantage to wedge shoes involves the method of attaching the wedge shoe to the hoof. If wedge shoes are nailed onto the hoof, the hoof capsule may be compressed, due to the nailing force, potentially leading to further damage. If wedge shoes are glued onto the hoof the horse may be forced to hold one foot up for an extended period of time thereby harming the opposite foot. To reduce risk of further damage it is recommended that wedge shoes are bandaged to the foot during the acute phase. However, if the bandaged shoe slips from the hoof it could cause an abrupt strain on the deep digital flexor tendon and potential further damage to the dorsal laminar attachment. Another disadvantage to wedge shoes is the risk of increased damage if the angle of the wedge does not correspond to each horse's particular condition. Wedge shoes must be designed for each horse on a case by case basis based on the severity of the condition or based on the hoof's adaptation to the condition before any treatment was given. In order to properly treat the condition different horses may require the wedge shoes to be adjusted to different angles. If the angle of the wedge is improper the condition may become more severe.
- Surgical transection of the deep digital flexor tendon (DDFT) has also been used to reduce the shearing forces during the acute phase of laminitis. One study reported a 60% survival rate at 2 years after the procedure. Those animals who do recover from the severing of the deep digital flexor tendon are usually not comfortable enough to ride. Even with these issues in mind, current veterinary practices suggest that a deep digital flexor tenotomy is the fastest way to counteract the rotational forces and restore the perfusion and tissue mass to the dorsal regions of the foot.
- Accordingly, there is a need for a proactive treatment that effectively treats and/or prevents the laminitis and its sequela. This treatment would effectively treat these conditions without requiring invasive surgery and all the risks and side effects associated with such invasive surgery.
- The present invention comprises a method for treatment and/or prevention of the sequela of laminitis in animals. More specifically, the present invention comprises a method for treatment of the symptoms associated with the laminitis syndrome.
- Laminitis is the condition in which the lamina becomes inflamed. This inflammation may lead to separation of the epidermal lamina from the dermal lamina associated with the distal phalanx (coffin bone) often resulting in the rotation or sinking of the distal phalanx within the hoof capsule. In the acute stage the lamina are inflamed but the distal phalanx is not yet displaced. Upon entering the chronic phase of the laminitis condition the distal phalanx may be displaced. Some horses compensate for the displacement by stabilizing the bone in its displaced position.
- The rotation of this distal phalanx (coffin bone) may be due to a metabolic disturbance (such as carbohydrate load) or to a discrepancy between the strength of the epidermal laminae and the load they have to support. The forces of the deep digital flexor tendon on the palmar aspect of the digital phalanx are thought to contribute to the tearing of the laminar membrane in the toe region. To ease the tension of the deep digital flexor tendon, thereby reducing the pull on the distal phalanx and preventing further laminar tearing or displacement of the distal phalanx the method of the present invention can be implemented.
- The pull of the deep digital flexor tendon on the coffin bone is thought to affect the foot in several different ways. First, the tightening may compromise the blood flow through the dorsal lamina. The decrease in blood flow may cause decreased laminar perfusion. With a decrease in laminar perfusion lamina tissue is deprived of nutrients and is weakened and more subject to tearing. Second, the tightening of the deep digital flexor tendon on the palmar aspect of the digital phalanx creates a force which pulls the laminar membrane away from the digital phalanx or hoof wall. The pull of the deep digital flexor tendon on the distal phalanx often causes the distal phalanx to become displaced as the opposing force of the laminar attachment is impaired.
- Because mechanical failure of the dorsal lamina may result in separation of the distal phalanx from the hoof wall, the method of treatment of the present invention may be directed at relieving the tensile forces acting on the bone, which contribute to this separation. Reducing the pull of the deep digital flexor tendon on the palmar aspect of the distal phalanx theoretically reduces the shear forces on the lamina which attaches the dorsal surface of the distal phalanx to the hoof wall. The relaxation of the deep digital flexor tendon may preserve laminar perfusion. If the tensile forces acting on the distal phalanx are relieved, in the acute stage of the condition, it may prevent the distal phalanx from displacing and entering the chronic phase. If the displacement of the distal phalanx can be prevented a horse has a good chance of recovery. Where a horse has entered the chronic phase the distal phalanx is displaced downward and compresses the sole corium altering the architectural development of the hoof capsule. It is hypothesized that by relaxing the deep digital flexor tendon the distal phalanx will re-align with relation to the ground surface and the hoof capsule can begin to regenerate itself. The goal is to allow the hoof to reestablish normal orientation of the distal phalanx and maintain that orientation without the aid of the clinical relaxation of the deep digital flexor tendon that this treatment provides. Relieving the tensile forces acting on the distal phalanx is accomplished by injecting the flexor muscles of the animal with Botulinum Toxin Type A.
- The Botulinum Toxin Type A used for treatment of the animal can be administered to the animal by any suitable method. For example, the Botulinum toxin type A can be injected into the muscle bellies of the flexor digitorum profundus muscle which attaches to the deep digital flexor tendon. Generally, the Botulinum toxin is administered in the amount of 100U to 600U over the course of 4 to 10 injections per muscle.
- The above described treatment method can also be used to treat issues/pathologies distinct from laminitis. In some of these pathologies, treatment involves injections in the superficial and/or deep digital flexor muscle. These pathologies include “back in the knee” (deep and superficial); club foot in foals (deep and superficial); desmitis of the distal check ligament; navicular syndrome; trauma to the involved muscle or tendon; and inflammation of the involved muscle or tendon.
- Laminitis can occur in any hoofed animal therefore the present invention should not be limited to horses.
- The following description contains significant detail regarding the novel aspects of the present invention. It should not be construed, however, as limiting the scope of the invention but rather as providing examples of the preferred method for treatment of the laminitis condition. Thus, the scope of the invention should be fixed by the following claims, rather than by the examples given.
- The present invention is directed to the prevention and/or treatment of the sequela of the laminitis condition in animals. More specifically, the present invention is directed to a method for treating the symptoms of or aiding in the recovery of a hoofed animal afflicted with the condition commonly known as laminitis.
- Generally, the method of treatment of the invention involves injecting Botulinum Toxin into the muscle bellies of the flexor digitorum profundus muscle. Botulinum Toxin, commonly known as BOTOX, MYOBLOC, OR DYSPORT, is a neurotoxic protein produced by the bacterium Clostridium botulinum. The toxin blocks the release of acetylcholine at the neuromuscular junction thereby relaxing the muscle. Typically, the physiologic effect of BOTOX lasts ten to twelve weeks.
- Although much is still unknown about the laminitis condition most researchers agree that the pulling of the deep digital flexor tendon, attached to the palmar surface of the distal phalanx causes a shear force against the laminar membrane and altered blood flow to the laminar membrane. In severe cases that force may lead to the detachment or partial detachment of the lamina from the hoof wall. This detachment combined with the pull of the deep digital flexor tendon causes the distal phalanx to either rotate or sink in the hoof capsule. In severe cases the distal phalanx can protrude externally from the bottom of the hoof.
- It is hypothesized that by reducing the pull of the deep digital flexor tendon on the palmar surface of the digital phalanx lamina damage will be reduced. In acute cases the relieving of the tensile forces on the deep digital flexor tendon could prevent the distal phalanx from displacing and entering a more severe phase of the laminitis condition. In the event that the hoof of the animal has already incurred lamina damage and bone displacement the reduced pull of the deep digital flexor tendon on the distal phalanx will allow the stabilization of bones within the hoof. Where the re-alignment of bones within the hoof takes place the hoof capsule can begin to regenerate and establish the restoration of sole tissue.
- The inventor has discovered that administering Botulinum toxin type A is safe and effective for the treatment of the sequela of laminitis. Botulinum Toxin chemically denervates the muscle bellies effecting the tension of the deep digital flexor tendon. Due to the Botulinum Toxin the deep digital flexor tendon relaxes and reduces the force pulling on the palmar aspect of the distal phalanx. The disclosed treatment can be used for any laminitic animal.
- There are seven serotypes of Botulinum Toxin (A through G). The present invention should not be limited to any one serotype of the toxin. In a preferred embodiment, for each limb to be treated, the Botulinum Toxin Type A is administered to the animal by injection into the muscle belly of the flexor digitorum profundus muscle at approximately 4 to 10 different sites in the muscle. The total amount of Botulinum Toxin Type A intramuscularly injected ranges from about 100 units to 600 units per limb depending on the size of the horse and the involvement of the affected muscles. Typically the Botulinum Toxin is administered after being reconstituted according to the manufacturer's recommendations at a desired dilution. In one example a quantity of 100U of powdered BOTOX is dissolved in 2-4 cc's of preservative free, sterile saline. The region to be injected is prepped in a sterile fashion. The appropriate muscle is first identified anatomically, the muscle is then accessed utilizing an Ambu Neuroline Inoject 24 gauge, 2-3 inch coated needle electrode using EMG guidance. Botulinum Toxin is then injected through this needle into 4-6 sites in the involved deep digital flexor muscle belly.
- Treatment should begin at the onset of any symptoms of laminitis. For prevention, treatment should begin in the contra-lateral limb as soon as an impaired weight bearing injury is evident. Some common symptoms include lameness, excess shifting of weight by the animal, altered heel stance, immobility, depression around the coronary band and increased frequency of animal lying down. If symptoms of laminitis do not improve the treatment should be repeated after two to six weeks. Treatment may also be repeated as needed if symptoms recur in the future.
- Typically, an animal with laminitis in one limb will eventually show symptoms of laminitis in the contralateral uninvolved limb. Therefore even if an uninvolved limb shows no symptoms of laminitis the treatment may proceed in the uninvolved limb in an effort to prevent laminitis from occurring or progressing in the uninvolved limb.
- The reader should note that although the above description and following examples relate to the treatment of laminitis in horses, it is believed that the method for treatment will work as described with any animal.
- The present invention may be better understood with reference to the following examples.
- An 11 year old Tennessee Walking Horse with a history of laminitis was experiencing an acute exacerbation of the laminitis condition (Obel Grade 4). Botulinum toxin (Botox) was reconstituted into 100 units per 2cc of normal saline. The skin overlying the flexor muscles of the fore legs was prepped with isopropyl alcohol. Using EMG guidance, 25 units of botulinum toxin was injected into 8 sites of the flexor digitorum profundus of each forelimb for a total of 400 units. The horse tolerated the procedure well with no immediate adverse effects noted. The horse was monitored over the next 12 weeks. Within 2 weeks the horse showed a marked improvement in it's ability to stand and ambulate. The horse has subsequently returned to functional use to the level of pasture comfort and occasional riding at all gaits.
- An eight year old stallion quarter horse was experiencing severe laminitis in two legs (Obel Grade 4). In leg 1 the deep digital flexor tendon was surgically cut utilizing accepted procedures and techniques. Redding shoes were applied at a 15 degree angle. In leg 2 utilizing clean technique and EMG guidance a total of 400 units of Botulinum Toxin Type A diluted into 8 cc of normal saline was injected into 8 separate sites within the flexor digitorum profundus. Redding shoes were applied at 15 degree angles. The horse underwent pre and post procedure venograms with no initial difference noted between the legs. The horse tolerated both procedures well and was monitored over the subsequent 5 weeks. The horse experienced a recovery from an Obel grade of 4 to an Obel grade of 3 with repeat venograms showing recovery of venous flow in both digits. Comparison between the two legs revealed a more rapid return to normal venous patterns in the limb receiving surgical transection of the deep digital flexor tendon. Thirty days post treatment the venogram of the surgical and Botulinum toxin treated legs were comparable.
- A 21 year old gelding quarter horse suffered a traumatic injury to the right fore carpus. Radiograph showed disruption of the normal arrangement of the carpal bones as well as severe swelling of the palmar aspect of the carpus. He was unable to extend the carpus in the non-weight bearing limb. This horse was diagnosed with traumatic disruption of the palmar ligaments of carpal bones including the accessory ligament of the deep digital flexor tendon. In an effort to prevent the development of laminitis in the contra-lateral limb, the horse received botulinum toxin 200 units (botox) injected into the deep digital flexor muscle as described above. The horse tolerated the procedure well. A Redden “Ultimate” shoe was also placed. The horse was monitored over the next 7 months. At one week and again at one month examination found no clinical evidence of laminitis in the left fore-limb. At two months the therapeutic shoe was removed. The horse was “toe touching” with the injured (right) fore-limb. At seven months the horse shows no evidence of laminitis in the left fore-foot (clinically or radiographically). The horse is now pasture sound.
- A 23 year old female Tennessee Walking horse had chronic laminitis with rotation exceeding 20 degrees radiographically in all four feet (Obel Grade 4, recumbent). She exhibited a body condition score of 7 (significantly overweight). Examination revealed pressure sores on hips. The horse was shod with a reverse keg shoe. The dorsal aspect of hoof was shaved in the bilateral front feet to reduce the angle of deviation between dorsal aspect of coffin bone and the dorsal hoof wall. Utilizing the method described above the horse was injected with 200 u into the deep digital flexor muscle of each fore-limb. The horse tolerated the procedure well and experienced no adverse effects throughout the eight months of follow-up.
- At ten days post injection the horse had improved to an Obel grade 3. At six weeks post injection the horse had improved to an Obel grade of 2. At five months post injection the horse was an Obel grade 1. Radiographically the coffin bone is parallel to the hoof wall. She is pasture sound.
- A 12 year old Arabian gelding with a body condition score of six presented with a mis-diagnosed navicular syndrome, sequestrum of dorsal aspect of P3. He had undergone an operative procedure for this diagnosis. The horse was subsequently taken to a tertiary equine center and diagnosed with bilateral fore-limb laminitis. There the horse was treated conservatively with NSAIDs and Redden “ultimate shoes” on both forelimbs as well as stall confinement. The horse was referred to our center for ongoing care and follow-up locally.
- On examination locally the horse exhibited an Obel Grade 3, almost 4. On observing the gait the horse appeared more painful in right fore-limb. X-ray of the limbs at that point indicated increased rotation by 12 degrees since discharge from the tertiary care center.
- Due to the asymmetry the horse initially underwent injection of the right fore-limb with 200 units of botulinum toxin A (Botox) in the deep digital flexor muscle utilizing the aforementioned technique.
- 19 days after the initial injection the horse was noted to have comparably increased pain in the left (uninjected) fore-limb. The right forelimb exhibited an Obel grade of 2 turning to the right. Turning to the left the horse exhibited an Obel grade of 3. It was therefore decided to proceed with injection of the left fore-limb. The horse received 200 units of botulinum toxin A (Botox) into the deep digital flexor muscle of the left fore-limb.
- At 33 days post initial injection the horse was comfortable, exhibiting an Obel grade of 1 bilaterally.
Claims (17)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/881,607 US7473429B1 (en) | 2007-07-27 | 2007-07-27 | Method for treatment of laminitis in animals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/881,607 US7473429B1 (en) | 2007-07-27 | 2007-07-27 | Method for treatment of laminitis in animals |
Publications (2)
Publication Number | Publication Date |
---|---|
US7473429B1 US7473429B1 (en) | 2009-01-06 |
US20090028905A1 true US20090028905A1 (en) | 2009-01-29 |
Family
ID=40174931
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/881,607 Active - Reinstated 2027-08-08 US7473429B1 (en) | 2007-07-27 | 2007-07-27 | Method for treatment of laminitis in animals |
Country Status (1)
Country | Link |
---|---|
US (1) | US7473429B1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020236554A1 (en) * | 2019-05-17 | 2020-11-26 | Vetmed Therapeutics, Inc. | Methods of treating musculoskeletal deformities in quadruped animals |
WO2022115594A3 (en) * | 2020-11-25 | 2022-08-18 | Vetmed Therapeutics, Inc. | Methods of treating deep and superficiel muscle/tendon injuries, and navicular syndrome in quadruped animals. |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562907A (en) * | 1993-05-14 | 1996-10-08 | Arnon; Stephen S. | Method to prevent side-effects and insensitivity to the therapeutic uses of toxins |
US20020064536A1 (en) * | 2000-02-08 | 2002-05-30 | Allergan Sales, Inc. | Methods of treating animals with botulinum toxin pharmaceutical compositions |
US20030138460A1 (en) * | 2000-02-08 | 2003-07-24 | Allergan, Inc | Methods of treating animals with botulinum toxin pharmaceutical compositions |
US20040013687A1 (en) * | 2002-05-31 | 2004-01-22 | Thomas Jefferson University | Compositions and methods for transepithelial molecular transport |
US20050238667A1 (en) * | 2000-02-08 | 2005-10-27 | Allergan, Inc. | Botulinum toxin pharmaceutical compositions with enhanced potency with regard to a reference botulinum toxin pharmaceutical composition |
US20080003241A1 (en) * | 2006-06-29 | 2008-01-03 | Merz Pharma Gmbh & Co. Kgaa | High frequency application of botulinum toxin therapy |
-
2007
- 2007-07-27 US US11/881,607 patent/US7473429B1/en active Active - Reinstated
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562907A (en) * | 1993-05-14 | 1996-10-08 | Arnon; Stephen S. | Method to prevent side-effects and insensitivity to the therapeutic uses of toxins |
US20020064536A1 (en) * | 2000-02-08 | 2002-05-30 | Allergan Sales, Inc. | Methods of treating animals with botulinum toxin pharmaceutical compositions |
US20030138460A1 (en) * | 2000-02-08 | 2003-07-24 | Allergan, Inc | Methods of treating animals with botulinum toxin pharmaceutical compositions |
US20050238667A1 (en) * | 2000-02-08 | 2005-10-27 | Allergan, Inc. | Botulinum toxin pharmaceutical compositions with enhanced potency with regard to a reference botulinum toxin pharmaceutical composition |
US20040013687A1 (en) * | 2002-05-31 | 2004-01-22 | Thomas Jefferson University | Compositions and methods for transepithelial molecular transport |
US20080003241A1 (en) * | 2006-06-29 | 2008-01-03 | Merz Pharma Gmbh & Co. Kgaa | High frequency application of botulinum toxin therapy |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020236554A1 (en) * | 2019-05-17 | 2020-11-26 | Vetmed Therapeutics, Inc. | Methods of treating musculoskeletal deformities in quadruped animals |
WO2022115594A3 (en) * | 2020-11-25 | 2022-08-18 | Vetmed Therapeutics, Inc. | Methods of treating deep and superficiel muscle/tendon injuries, and navicular syndrome in quadruped animals. |
Also Published As
Publication number | Publication date |
---|---|
US7473429B1 (en) | 2009-01-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
van Amstel et al. | Review of pododermatitis circumscripta (ulceration of the sole) in dairy cows | |
Baxter et al. | Complications of unilateral weight bearing | |
US7473429B1 (en) | Method for treatment of laminitis in animals | |
Morrison | Long-term prognosis using deep digital flexor tenotomy and realignment shoeing for treatment of chronic laminitis | |
Taylor et al. | Clinical outcome of 14 obese, laminitic horses managed with the same rehabilitation protocol | |
Parks et al. | Treatment of acute laminitis: supportive therapy | |
AU2014210332A1 (en) | Method of treating fibrosis in skeletal muscle tissue | |
Carter et al. | A novel approach to the treatment and prevention of laminitis: botulinum toxin type A for the treatment of laminitis | |
Rucker | Clinical applications of digital venography | |
Peremans et al. | Laminitis in the pony: conservative treatment vs dorsal hoof wall resection | |
US20240016904A1 (en) | Methods of treating superficial digital flexor tendon injuries, deep and superficial muscle/tendon contracture, navicular syndrome, and suspensory ligament inflammation and injuries in quadruped animals | |
Hunt et al. | Management of clubfoot in horses: foals to adults. | |
Morrison et al. | How to use stem cells in clinical laminitis cases. | |
JP2020520971A (en) | Pharmaceutical composition for treating foot pain disease containing botulinum toxin and hyaluronic acid, and method for treating foot pain disease using the same | |
US20180326023A1 (en) | Plasminogen dosage regimen for wound healing | |
Torrent‐Crosa et al. | Clinical application of the wooden shoe to complement surgical management of laminitis and other foot‐related disease in the horse: A report of three cases | |
Orsini | Clinical Updates I—Laminitis | |
Hunt | Laminitis in the geriatric horse | |
Gopinath et al. | A study of outcome of autolougous platelet rich plasma injection in patients with chronic plantar fasciitis | |
Bras | How to use foot casts to manage horses with laminitis and distal phalanx displacement secondary to systemic disease. | |
JP2020510100A (en) | Neuromuscular toxin for use in treating abnormalities of the first metatarsophalangeal joint of the foot | |
De Gresti et al. | A singular case of traumatic total hoof capsule avulsion | |
McMullan | The Treatment of Navicular Disease | |
Safarpour et al. | Treatment of Plantar Fasciitis/Plantar Fasciopathy with Botulinum Neurotoxins | |
Mahla et al. | Clinical management of chronic laminitis-a clinical study of 12 equines |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
FPAY | Fee payment |
Year of fee payment: 4 |
|
FPAY | Fee payment |
Year of fee payment: 8 |
|
SULP | Surcharge for late payment |
Year of fee payment: 7 |
|
AS | Assignment |
Owner name: VETMED THERAPEUTICS, INC., FLORIDA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:RENFROE, J. BEN, M.D.;CARTER, DANIEL W., DVM;SIGNING DATES FROM 20161213 TO 20161222;REEL/FRAME:040901/0066 |
|
FEPP | Fee payment procedure |
Free format text: MAINTENANCE FEE REMINDER MAILED (ORIGINAL EVENT CODE: REM.); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY |
|
LAPS | Lapse for failure to pay maintenance fees |
Free format text: PATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY |
|
STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |
|
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20210106 |
|
FEPP | Fee payment procedure |
Free format text: SURCHARGE, PETITION TO ACCEPT PYMT AFTER EXP, UNINTENTIONAL. (ORIGINAL EVENT CODE: M2558); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY Free format text: PETITION RELATED TO MAINTENANCE FEES FILED (ORIGINAL EVENT CODE: PMFP); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 12TH YR, SMALL ENTITY (ORIGINAL EVENT CODE: M2553); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY Year of fee payment: 12 |
|
PRDP | Patent reinstated due to the acceptance of a late maintenance fee |
Effective date: 20210824 |
|
FEPP | Fee payment procedure |
Free format text: PETITION RELATED TO MAINTENANCE FEES GRANTED (ORIGINAL EVENT CODE: PMFG); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |