15 This chapter is divided into ophthalmic diseases in foals and adult horses. Manual restraint in foals is usually possible while in the adult horse some sedation and eyelid nerve blocks are necessary for a complete ophthalmic examination. Topical medical therapy for foals is quite easy (especially with two adults), but intensive topical therapy in the adult horse usually requires some type of subpalpebral delivery system. Microphthalmia is one of the most frequent congenital defects in foals, and is often associated with congenital cataracts (Figure 15.1). The condition is unilateral or bilateral, and the Thoroughbred appears to be predisposed. The presenting signs are reduced palpebral fissure size, prominent nictitating membrane, and a smaller than normal eye. Vision is normal or impaired, depending on the size of the eye, and other abnormalities. There is no treatment for microphthalmia. Strabismus is a deviation of the globe from its normal position. In foals, this condition occurs more commonly in the Appaloosa breed and can accompany stationary night blindness (STNB) (Figure 15.2). The globe is usually rotated upward (hypertropia), or dorsomedial or medial (estropia). If both eyes are affected, the foal may position its head as if to compensate for the strabismus. Stumbling is a common complaint. STNB should be excluded when a young animal presents with strabismus. In this condition the ocular fundus appears normal by ophthalmoscopy and the animal has clinically normal vision in daylight but night vision is profoundly impaired. This is easily noted by behavior changes when the ambient illumination is reduced. STNB has a very distinct pattern on electroretinography. Primary strabismus in foals has been treated by surgery of the involved rectus muscles (either recession or resection). Congenital entropion or the inversion of the eyelid margin is an infrequent abnormality in foals (Figure 15.3). The lower eyelid is most often affected. Microphthalmia, dehydration, prematurity/dysmaturity, and eyelid trauma are contributing disorders. Presenting signs are increased lacrimation, blepharospasm, inverted lid margin, conjunctivitis, and occasionally corneal ulceration. Temporary eversion of the lid until the underlying disease state has resolved or the foal’s growth alleviates the entropion is indicated. Temporary surgical repair should be delayed until the foal has approximated its adult size. Permanent entropion repair is rarely necessary in the horse unless the condition has resulted from cicatrix formation. Dermoids or choristomas can affect the foal’s eyelids, conjunctiva, nictitating membrane, or cornea (Figure 15.4). Most often the cornea and limbal bulbar conjunctiva are affected. The dermoid presents as a raised, pigmented, hair‐covered mass (which can be confused with a limbal‐based melanoma). Treatment is surgical removal. The development of the nasolacrimal system starts as two buds that eventually become the lacrimal puncta and canaliculi, and extend through the developing facial bones and nasal cavity to exit at the muctocutaneous junction on the floor of the external nares (easily observed). In nasolacrimal duct atresia, the distal end of the nasolacrimal duct stops prematurely and ends in a blind pouch (Figure 15.5). Clinical signs include a persistent conjunctivitis (which can respond temporarily to topical antibiotics) and epiphora, but these may not be readily apparent until the foal is several months of age. Dacryocystitis with mucoid or mucopurulent discharge develops with time. Fluorescein applied on the eye does not exit at the external nares and close examination of the external nares reveals absence of the nasal punctum. Nasolacrimal flush through the upper or lower lacrimal punctum results in the accumulation of the irrigation solution in the enlarged blind end. Dacryorhinocystography facilitates the diagnosis and localizes the endpoint of the atretic duct. Restoration of nasolacrimal duct patency is by surgery. Congenital disorders of the iris in the foal are rare, but include aniridia (in Thoroughbreds, Belgians, and Quarter Horses) and persistent pupillary membranes. In heterochromia iridis, the color of the iris is blue, blue and white, or some combination of brown, blue, and white, and affects one or both eyes (Figure 15.6). The term “wall eye” refers to a blue–white iris with a black corpora nigrum (or granula iridica), while “china eye” refers to a white iris with a black corpora nigrum. Heterochromia iridis is related to hair coat color and occurs in Appaloosa, gray, white, palomino, spotted, and chestnut horses. It can be accompanied by hypoplasia or colobomatous malformations of the iris. Congenital glaucoma is rare in foals and usually signals anomalous development of the anterior chamber angle and aqueous humor outflow pathways (Figure 15.7). Presenting signs include buphthalmia (an enlarged globe), mydriasis, variable corneal edema, lens luxation, and variable degeneration of the optic nerve head and retina. Tonometry indicates elevated intraocular pressure (IOP). Treatment is not usually attempted, but includes topical drugs to lower IOP and laser cyclophotocoagulation. Iridocyclitis in foals can be secondary to other ocular diseases (usually corneal ulcers) or associated with systemic diseases such as Salmonella sp., Rhodococcus equi, Escherichia coli, Streptococcus equi, Actinobacillus equuli, adenovirus, and equine viral arteritis as well as any other cause of septicemia, pneumonia, or any systemic inflammatory condition (Figure 15.8). The iridocyclitis is often bilateral and the foal will exhibit lacrimation, blepharospasm, and photophobia. Ophthalmic findings include eyelid swelling, corneal edema, conjunctival hyperemia, ciliary injection, aqueous flare, hypopyon and/or hyphema, and miosis. Fibrin and contact of the iris and lens can result in posterior synechiae formation and secondary cataracts. A complete general physical examination as well as a complete blood count, clinical chemistry, and thoracic radiographs should be performed. Treatment should be aimed at the underlying disease but should include symptomatic therapy for the iridocyclitis (mydriatics, and topical and/or systemic anti‐inflammatory medications). Congenital cataracts and microphthalmia are the two most frequent congenital ophthalmic anomalies in foals (Figure 15.9). Inherited cataracts occur in the Belgian, Thoroughbred, Morgan, and Rocky Mountain Horse breeds. The cataracts in the Belgian may be related to aniridia (actually hypoiridia) and are inherited as a dominant trait. Cataracts are also thought inherited in the Thoroughbred breed as a dominant trait. The Morgan Horse has inherited and bilateral nonprogressive nuclear cataracts that do not progress and interfere with vision. Congenital cataracts in the Rocky Mountain Horse are associated with multiple ocular anomalies such as megalocornea, goniosynechiae, cysts of the iris, ciliary body and peripheral retina, and retinal dysplasia. Often, a foal from a normal‐eyed mare and stallion is presented to the veterinarian because of either white opacities within the eye or vision impairment to a variable degree. Ophthalmic findings include normal or slightly smaller globes, normal pupillary light response, and mature and complete cataract formation. Ultrasonography and electroretinography are usually normal. Cataract surgery is performed most commonly in the foal for congenital cataracts (adult horses usually have uveitis cataracts) and phacoemulsification is the technique of choice. Young foals used to handling have surgery at young ages (at 1–2 months before lens‐induced uveitis occurs and the foal is more difficult to manage); success rates are over 80%. Optic nerve hypoplasia is a rare cause of congenital blindness in foals (Figure 15.10). The condition is unilateral or bilateral. Diagnosis is made with ophthalmoscopy. The optic nerve head is smaller than normal, white, and contains few retinal blood vessels. There is no treatment. Orbital cellulitis occurs occasionally in horses, and can be associated with trauma, foreign bodies, and the extension of infections from the adjacent nasal and sinus cavities as well as tooth root infections (Figure 15.11). The presenting clinical signs are acute swelling of the eyelids and supraorbital fossa, blepharospasm, exophthalmia, orbital pain, epiphora, conjunctival hyperemia, and protrusion of the nictitating membrane. Ultrasonography can assist with characterization and localization of disease as well as sample acquisition. Orbital trauma is more frequent in young horses maintained in groups. Blunt as well as penetrating trauma occurs. Orbital swelling produces a prominent or partially luxated globe, nictitans protrusion, conjunctival hyperemia and chemosis, variable corneal edema, miosis, and hyphema. An impaired blink reflex can occur, and corneal exposure with ulceration rapidly develops. Treatment consists of placement of the subpalpebral system, a complete temporary tarsorrhaphy, and topical and systemic antibiotics, mydriatics, and systemic nonsteroidal anti‐inflammatory drugs (NSAIDs). Orbital trauma can also produce fractures of the orbital bones (Figure 15.12). Clinical signs include asymmetry of the orbits, epistasis, exophthalmos, conjunctival and lid swelling, crepitus, and pain on orbital palpation. Ultrasonography and radiology are essential diagnostic modalities. Surgical treatment includes bone plates or wires for the orbital fractures with displacement, subpalpebral lavage system, and complete temporary tarsorrhaphy to protect the cornea. Orbital neoplasms are rare in horses, but include most histopathological types (Figure 15.13). The most frequent are squamous cell carcinoma (usually extending from the nictitating membrane and conjunctiva) and lymphoma (often bilateral). Clinical signs are progressive exophthalmia, strabismus, orbital and supraorbital fossa swelling, and blindness. Prognosis is usually poor. Phthisis bulbus or atrophy of the globe is a not uncommon condition in older horses (Figure 15.14). It results from severe trauma, chronic anterior uveitis, and glaucoma that eventually impair aqueous humor formation. Reduced IOP results (usually less than 5 mmHg) which can cause corneal decompensation (corneal edema), cataract formation, and retinal detachment. The condition does not respond to therapy. Eyelid lacerations are common in horses. Either the upper or lower eyelid can be affected; however, because of its size, mobility, and prominence, the upper lid is most often affected (Figure 15.15). The laceration often involves the lid margin, and must be repaired carefully to avoid a postoperative notch or defect. The cornea should be carefully examined as corneal lacerations may be also present (especially if hyphema is present). Treatment consists of two‐layer closure starting with the eyelid margin. A temporary complete tarsorrhaphy is recommended to protect the cornea during lid healing and when the blink reflex is impaired.
Equine Ophthalmology
Ophthalmic Diseases in Foals
Microphthalmia
Strabismus
Congenital Entropion
Lid and Conjunctivae Dermoids
Nasolacrimal Duct Atresia
Irial Anomalies
Congenital Glaucoma
Iridocyclitis
Congenital Cataracts
Optic Nerve Hypoplasia
Equine Ophthalmology in Adult Horses
Orbital Diseases
Orbital Inflammations
Orbital Trauma and Fractures
Orbital Neoplasia
Atrophy of the Globe or Phthisis Bulbus
Diseases of the Eyelids
Eyelid Lacerations
Eyelid Neoplasia