Ophthalmology Flashcards

1
Q

Pain scoring systems in hospitalized horses with ocular disease

A

Horses Discharged After Medical Treatment:
• Higher admission pain scores (HGS and BPS) compared to horses that later underwent enucleation.
• Pain scores decreased over time, indicating effective pain control and clinical improvement.
Horses Undergoing Enucleation:
• Showed increasing pain scores (HGS and BPS) during hospitalization.
• Temporal trends in pain scores were significantly associated with enucleation as the final outcome (P < 0.05).
Horses Undergoing Ophthalmic Surgery:
• Pain scores at admission and during hospitalization did not differ significantly from horses discharged after medical management.
• Surgical decisions often depended on lesion type and severity rather than pain progression.
Pain Score Correlations
• Moderate correlation between HGS and BPS scores (r² = 0.73), supporting their complementary use.
• Temporal increases in both scores were linked to worse clinical outcomes, such as enucleation.
Impact of NSAIDs and Analgesics
• Horses treated with NSAIDs (flunixin meglumine, firocoxib) and adjunctive analgesics (gabapentin, butorphanol) generally experienced reduced pain scores over time.
• Pain relief effectiveness varied based on the severity and type of ocular disease.

Utility of Pain Scales
• HGS and BPS are reliable tools for monitoring ocular pain in hospitalized horses:
• Facilitate real-time assessment of treatment response.
• Help predict clinical progression and the need for surgical intervention.
Management Decisions
• High pain scores at admission warrant aggressive medical management, potentially avoiding surgical interventions.
• Rising pain scores during hospitalization indicate poor prognosis for medical therapy and support decisions for enucleation.
• Admission pain scores alone were insufficient to predict clinical outcomes.
• Monitoring pain trends over time is more informative for guiding treatment plans.

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2
Q

Equine uveitis: Outcome and adverse effects after one or two intravitreal low-dose gentamicin injections

A

• 41% of eyes (13/32) achieved a positive outcome after one or two IVGIs:
• Uveitis controlled with minimal or no anti-inflammatory medication.
• A second IVGI improved outcomes for some cases:
-ERU: 24% positive outcome after one injection; improved to 67% after the second injection.
-HIK: 36% positive outcome after one injection; no response to the second injection.

Limitations in Treatment:
• Nearly half (14/32, 44%) of eyes required enucleation due to:
-Persistent inflammation.
-Complications such as glaucoma, corneal ulceration, or mineralisation.
• Success rates lower than earlier studies (88–94%), possibly due to:
-Predominantly anterior uveitis cases (91%).
-Late-stage disease in many horses.

Adverse Effects
Short-Term Complications:
• Peri-injection complications occurred in 16% (5/32) of eyes:
• Mild ocular discomfort.
• Periocular swelling and epiphora (resolved within a week).
• Rare events: generalized urticaria, ventromedial strabismus (resolved in <2 months).
Long-Term Complications:
• Retinal degeneration: Observed in 22% (7/32), often within 2–8 weeks post-IVGI.
• Cataract formation: Mature cataracts developed in 16% (5/32), mostly within 6–12 months.
• Corneal mineralisation: Detected in 38% (12/32), likely exacerbated by corticosteroid use or persistent inflammation.
• Corneal ulceration: Reported in 41% (13/32), often associated with topical corticosteroid therapy.
Effect of Leptospirosis
• Only 7/29 horses were tested for leptospirosis; one was positive (L. Grippotyphosa) but did not respond to treatment.
• Leptospiral involvement was not a prominent factor in this cohort, contrasting with studies from regions with higher leptospirosis prevalence.

Clinical Implications
• IVGI may be effective for specific uveitis cases, especially in eyes with chronic ERU:
• A second injection may improve outcomes in ERU cases.
• IVGI was less effective for anterior uveitis, possibly due to the site of inflammation being less accessible to intravitreal drugs.

Indications for IVGI
• IVGI is suitable for selected cases of chronic uveitis, particularly when:
-Medical management is insufficient.
-Uveitis involves the posterior segment.
-Early-stage disease and posterior uveitis may respond better than late-stage anterior uveitis.

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3
Q

Noninvasive diode laser–an effective and safe treatment of iris cysts in 46 eyes of 35 horses

A
  • 93% response rate, 78% good and 15% moderate
  • complications included: corneal scarring, retinal burns, corneal defects and laser induced uveitis (17% eyes)
  • polycystic, hypreplastic corpora nigra and thick walled cysts less likely to respond
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4
Q

Transcorneal aspiration formanagement of primary iris cysts in the standing horse

A

-100% improvement (61% resolution)
- no long term complications (short term uveitis and fibrin)
- adequate sedation, blocking and temprement

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5
Q

Effects of intravenous romifidine, detomidine, detomidine combined with butorphanol, and xylazine on tear production in horses

A
  • Romifidine- no effect
  • xylazine- increased
  • detomidine- decreased
  • detomidine + butorphanol- lowest annd most prolonged
  • none <15mm
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6
Q

Dorsally placed commercially available subpalpebral lavage systems have low complication rates in horses

A

• Overall Complication Rate: 29.1% (37/127 SPLs).

• Ocular Complications: 21.2% (27/127).
-Secondary corneal ulcers: 7.1%.
-SPL removal by horses: 6.3%.
-Eyelid cellulitis or abscessation: 5.5%.
•Nonocular Complications: 7.9% (10/127).
-Suture replacements: 3.1%.
-Catheter replacements: 2.4%.
-Tube tangling or stretching: 2.2%.
• Risk Factors: No Significant Associations:

• SPLs managed at home had higher (but not statistically significant) complication rates (42.3%) compared to hospital-managed SPLs (23.7%).

• Earlier reports (1997) showed higher complication rates (66%) for dorsally placed SPLs, attributed to:
-Practitioner-modified systems with irregular designs.
-Increased tissue irritation and mechanical instability.
-This study’s findings underscore the benefits of commercially available kits, which feature standardized materials and improved designs.

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7
Q

Evaluation of transpalpebral ultrasonographic measurement of optic nerve sheath diameter for indirect assessment of intracranial pressure in anesthetized and standing healthy adult horses

A

• Weak to moderate associations between ICP and ONSD were found in anesthetized horses, depending on head position:
• Lowered head position: Moderate association (R² = 63–78%).
• Elevated head position: Weak association (R² = 46–63%).
• Neutral position: No significant association.
• In standing horses, there was no significant association between ONSD and ICP (R² = 5–12%).
• Measurements were consistent across observers (intra-observer coefficient of variation ≤10%).
• ONSD increased slightly in the elevated anesthetized position compared to neutral but decreased inconsistently in other positions.

• Findings indicate that transpalpebral ONSD measurements are unlikely to be clinically useful for ICP monitoring in horses:

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8
Q

Can ocular administration of atropine cause colic?

A

• It is possible to induce mild reversible symptoms of colic through frequent administration of topical ocular atropine in normal healthy horses.
• Systemic bioavailabilty is potentially both high and rapid, even if individual horses vary naturally.
• Lower overall doses, conjunctival overflow losses, variation in pharmacokinetics and the presence of more potent risk factors probably explain why no retrospective clinical studies demonstrate an association between ocular atropine and colic in horses with ocular disease.
• Therefore, the use of ocular atropine at recommended dose rates for clinical ocular disease does not increase risk of colic.

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9
Q

Role of Leptospira spp. testing and ocular examination in horses with equine recurrent uveitis

A

• Leptospira infection significantly associated with ocular disease severity and visual prognosis:
• Aqueous humour titres correlated with:
-Vision loss at presentation (P = 0.04).
-Blindness, particularly with L. bratislava (P = 0.002).
-Serum titres linked to posterior segment disease (P = 0.01).
• Horses with positive aqueous humour PCR were younger (mean age: 9.25 years) compared to PCR-negative horses (mean age: 13.3 years, P = 0.01).
• The Goldmann-Witmer coefficient (C value) was positive (≥4) in 52.38% of eyes tested, indicating intraocular leptospiral antibody production.
• Most frequent serovars associated with positive C values:
-L. grippotyphosa (81.82% of cases).
-L. pomona (68.18% of cases).
-L. bratislava and L. hardjo were associated with worse visual outcomes, indicating their potential role in severe ERU cases.

Vision prognosis varied by serovar:
• L. bratislava: Highly correlated with blindness.
• L. grippotyphosa and L. hardjo: Associated with decreased vision at presentation.
• Serum titres were often positive for the same serovars as aqueous humour titres, supporting systemic infection prior to intraocular invasion.

Horses with leptospiral-positive ERU should be treated aggressively to prevent further visual deterioration:
• Antibiotics (e.g., doxycycline, minocycline) for systemic leptospiral infections.
• Immunosuppressive therapy (e.g., corticosteroids) to control immune-mediated damage.
• Advanced options, such as pars plana vitrectomy (PPV), may reduce recurrent uveitis in horses with intraocular leptospiral titres.
• Breeds and Risk Factors Although no significant breed predisposition was observed, previous studies suggest breeds like Appaloosas and Hanoverians may be overrepresented in ERU cases.
• Horses living in wet climates or with access to wildlife are at higher risk for leptospiral exposure, warranting regular testing in endemic regions.

• Findings align with prior studies linking L. grippotyphosa and L. pomona to ERU.
• Novel association with L. bratislava highlights the evolving understanding of serovar-specific roles in ERU pathogenesis.

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10
Q

Equine retinal detachment in the United Kingdom: 23 cases (2010-2020)

A

Causes of Retinal Detachment
•Equine Recurrent Uveitis (ERU):
-Most common cause, present in 43.5% of cases.
-Typically associated with chronic intraocular inflammation, posterior synechiae, and vitreal traction bands.
• Trauma:
-Responsible for 34.8% of cases, highlighting blunt or penetrating injuries as significant contributors.
• Other Causes:
-Post-surgical complications (13.0%).
-Congenital anomalies (4.3%).
-Primary glaucoma (4.3%).

Diagnostic Techniques
• Ultrasound: Confirmed RD in all 23/23 cases (100%). Provided a reliable diagnostic modality in cases where fundus visualization was obscured by cataracts, hyphaema, or corneal oedema.
• Ophthalmoscopy: Detected RD in only 9/23 cases (39.2%). Limited by concurrent anterior chamber and vitreal abnormalities.

Clinical Signs:
• Loss of menace response, dazzle reflex, or pupillary light reflex (PLR) in 63.7% of cases.
• Partial detachment cases retained weak PLR or menace response, consistent with residual vision.

Concurrent Ocular Pathology- Common findings included:
• Ipsilateral Cataracts: Present in 52.4% of cases.
• Posterior Synechiae: 38.1%.
• Vitreal Debris: 19.0%.
• Other abnormalities: lens subluxation, corneal oedema, or hyphaema in fewer cases.

Unilateral vs Bilateral Cases
• Unilateral RD in 91.3% of cases.
• Bilateral RD in 8.7%, primarily due to ERU or congenital defects.

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11
Q

Penetration of topically administered dexamethasone disodium phosphate and prednisolone acetate into the normal equine ocular fluids

A

Drug Penetration
• Aqueous Humour:
-Mean DEX concentration: 32.4 ng/mL (range: 15.7–58.3 ng/mL).
-Mean PRED concentration: 321.6 ng/mL (range: 119.0–605.3 ng/mL).
-PRED concentrations were approximately 10 times higher than DEX.
• Vitreous Humour:
-Neither DEX nor PRED was detectable in any samples (LOD: 2.5 ng/mL).
• Serum:
-Both corticosteroids were below the detection limit (LOD: 5 ng/mL), indicating minimal systemic absorption.
• Steady-State Achievement- Both corticosteroids reached steady-state concentrations in the aqueous humour after 24 hours of dosing every 2 hours.
• Concentrations plateaued up to 180 minutes post-administration, suggesting that frequent dosing intervals may not be necessary.

Clinical Implications
• Anterior Uveitis: Effective concentrations were achieved in the aqueous humour for both DEX and PRED, supporting their use for anterior segment inflammation.
• Posterior Uveitis: Lack of detectable levels in the vitreous humour indicates that topical administration is insufficient for posterior segment inflammation.
-Alternative administration routes (e.g., systemic, subconjunctival, or intravitreal injections) may be necessary.
• Formulation Considerations
-PRED’s lipid-soluble nature allows better penetration through the lipid-rich corneal epithelium compared to the water-soluble DEX formulation.
-However, DEX is seven times more potent than PRED, suggesting that dose differences should be considered when selecting a corticosteroid.

Clinical Recommendations
• PRED may be preferred for its higher aqueous humour concentrations, especially in severe anterior uveitis cases.
• DEX remains a valid choice due to its potency and water solubility, which may reduce ocular discomfort compared to PRED suspensions.

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12
Q

Artificial intelligence as a tool to aid in the differentiation of equine ophthalmic diseases with an emphasis on equine uveitis

A

Validation results for image classification:
Three-class model (uveitis, other diseases, healthy):
• Training accuracy: 99.82%.
• Validation accuracy: 96.66%.
• High accuracy indicates the CNN effectively identifies uveitis-related changes and differentiates healthy eyes from those with disease.

• The AI primarily focused on dorsal eye structures, particularly the transition between the pupil, iris, and sclera.
• While effective for identifying anterior segment changes (e.g., corneal opacities, miosis, fibrin deposits), the tool was limited in detecting posterior segment abnormalities (e.g., retinal detachment).
• The Equine A-Eye app allows veterinarians and horse owners to capture and analyze images in real-time.
Key features:
-Heatmap overlays highlight areas of diagnostic interest.
-Immediate feedback with probabilities for each diagnostic category.
-Limitations of the Tool: AI relied on the pupil size as a visual cue, potentially creating a bias: Diseased eyes often had dilated pupils due to prior mydriatic administration. This was mitigated by including a diverse dataset with medicated and non-medicated eyes.
- The tool does not assess posterior segment diseases unless visible through the pupil, limiting its scope for retinal or optic nerve pathologies.

Possible use in triage.

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13
Q

Comparison of four tonometers in the measurement of intraocular pressure in healthy horses

A

• Rebound Tonometers (Tonovet and Tonovet Plus):
-Provided IOP values closest to manometry in sedated horses: Tonovet: 25.7 ± 5.8 mmHg. Tonovet Plus: 24.8 ± 7.1 mmHg.
-Slight overestimation of IOP, particularly at values >25 mmHg.
• Applanation Tonometers (Tono-Pen AVIA Vet and Kowa HA-2):
-Consistently underestimated IOP compared to manometry:
• Tono-Pen AVIA Vet: 19.2 ± 4.7 mmHg.
• Kowa HA-2: 24.1 ± 1.2 mmHg.
• Kowa HA-2 had the least variability and was most consistent across measurements.

Field Study (Unsedated Horses)
• All tonometers showed higher variability in IOP measurements in unsedated horses:
• Tonovet and Tonovet Plus recorded higher IOP values (30.7 ± 5.6 and 29.6 ± 6.7 mmHg, respectively) compared to Tono-Pen AVIA Vet (27.3 ± 5.8 mmHg) and Kowa HA-2 (23.4 ± 2.2 mmHg).
• Tonovet and Tonovet Plus were easy to use and did not require topical anaesthesia, making them more practical for routine field evaluations.

Bias in Tonometer Readings
• Overestimation: Rebound tonometers (Tonovet and Tonovet Plus) overestimated IOP at higher pressures (>25 mmHg).
• Underestimation: Applanation tonometers (Tono-Pen AVIA Vet and Kowa HA-2) tended to underestimate IOP, particularly at higher values.

Clinical Implications
• Rebound Tonometers: Most suitable for routine clinical use due to ease of operation and lack of need for topical anaesthesia. Tonovet Plus provided slightly more consistent results than Tonovet.
• Applanation Tonometers: Kowa HA-2 exhibited excellent repeatability but required technical expertise and fluorescein dye, limiting its practicality in field settings.
• Tono-Pen AVIA Vet had the largest underestimation bias, reducing its reliability for IOP measurements.

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14
Q

Ultrasound biomicroscopy of the equine iridocorneal angle

A

UBM effectively imaged ICA structures in all 30 horses, demonstrating:
• Pectinate ligament trabeculae.
• Corneoscleral, uveal, and supraciliary trabecular meshworks.
• Associated structures, including the anterior chamber, iris, and cornea.
• Morphology of the ICA showed minimal variability across horses, suggesting a consistent ultrasonographic appearance in normal eyes.

UBM can assess ICA morphology in vivo, allowing for early detection of:
• Aqueous humour outflow obstructions.
• Structural changes associated with glaucoma (e.g., ciliary cleft collapse).
• Particularly valuable for evaluating horses with:
-Elevated intraocular pressure (IOP).
-Recurrent or chronic uveitis.
-Corneal oedema or other anterior segment abnormalities.
• Traditional assessment of the ICA is limited to gonioscopy, which provides a segmental and anterior-only view.
• UBM offers a high-resolution, full-depth visualization of ICA structures, including posterior segments not visible with gonioscopy.
• UBM has the potential to identify early morphological changes in glaucoma-prone horses, enabling: Early interventions to preserve vision. Better understanding of structural abnormalities that predispose to ocular hypertension.

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15
Q

Risk factors for a first episode of primary uveitis in the UK and proportion of cases that experience recurrence following this first episode

A

Risk Factors for Primary Uveitis
• Proximity to Pig Farms: Horses near pig farms had significantly increased odds of developing primary uveitis (OR: 27.8, 95% CI: 1.31–592.06; P = 0.03).
• Flooding of Turnout Fields: A history of recent flooding increased the risk of uveitis (OR: 15.44, 95% CI: 2.80–84.98; P = 0.002).
• Duration of Ownership: Longer ownership duration had a protective effect (OR: 0.79, 95% CI: 0.68–0.93; P = 0.004).

• Recurrence Rate: 18.2% (4/22 horses) experienced recurrence, defined as new episodes of uveitis ≥6 weeks after the initial episode.
• First recurrences occurred within 3 months for three horses and within 12 months for all four cases.
• Five horses (22.7%) required surgical interventions for non-resolving initial episodes: Three underwent enucleation. One had a pars plana vitrectomy. One received a cyclosporine implant.

• Flood-prone pastures and proximity to pig farms may facilitate exposure to Leptospira spp., a known cause of equine uveitis. However, this study did not confirm leptospiral infection in affected horses, and the role of Leptospira spp. in UK cases remains modest.
• Owner Influence: Longer ownership may reflect a stable environment or the absence of risk exposures, though causality is unclear.

Prognosis and Recurrence
• Approximately 59% of cases resolved without recurrence, suggesting favorable outcomes for most horses with appropriate initial treatment.
• The first 3 months post-diagnosis are critical for recurrence monitoring, warranting prolonged anti-inflammatory therapy.
• Severe Cases- Horses with persistent uveitis unresponsive to medical therapy may require surgical interventions (e.g., enucleation, cyclosporine implants) to preserve quality of life.
• Unlike continental studies, Leptospira kirschneri serovar Grippotyphosa, often implicated in Europe, is less prevalent in the UK, highlighting geographic variation in uveitis aetiology.

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16
Q

Ocular penetration of oral acetaminophen in horses

A

• Acetaminophen was detected in both serum and aqueous humour after 3 days of oral dosing at 20 mg/kg every 12 hours.
• Mean aqueous humour:serum concentration ratio: 44.9% ± 15.9%.
• This ratio is higher than reported for oral NSAIDs like flunixin meglumine (3.59%) and firocoxib (11.99%), indicating better penetration across the blood-aqueous barrier (BAB).

Mechanism of Penetration- Likely facilitated by acetaminophen’s:
• Lipid solubility.
• Low molecular weight.
• Neutral charge at physiological pH, allowing easy passage through the BAB’s tight junctions. (Contrast with NSAIDs, which circulate mainly in an ionized form, limiting their BAB penetration)

• Eicosanoids- No prostaglandins (PGE2, PGF2α) or leukotrienes were detected in aqueous humour, indicating no significant modulation of inflammatory eicosanoids in the normal eye.

Normal eyes only, 20mg/kg PO q12h for 6 days

17
Q

Noninvasive diode laser- an effective and safe treatment of iris cysts in horses

A

Short-Term Outcomes:
• 78% (36/46) of treated eyes showed significant reduction in cyst size.
• Moderate reduction occurred in 15% (7/46), minimal or no effect in 4.3% (2/46).
• Less responsive:
-Polycystic eyes: OR = 0.381, P = 0.001.
-Thick-walled cysts: OR = 0.139, P = 0.02.
-Corpora nigra involvement: OR = 0.081, P = 0.03.

Long-Term Outcomes:
• 93% of owners reported resolution or reduction in clinical signs.
• Recurrence of cysts was rare, with only two confirmed cases during a median follow-up period of 19 months (IQR: 25.5 months).

Minor complications were noted in 17% (8/46) of eyes:
• Corneal oedema (3 eyes).
• Fluorescein-positive corneal defects during post-operative medication application (3 eyes).
• Reactive uveitis (1 eye) resolving within 24 hours with standard treatment.
• Retinal burns (1 eye) attributed to laser misdirection.
• No severe complications or adverse long-term outcomes were reported.

• Diode laser treatment is a suitable, minimally invasive option for iris cysts causing:
-Vision impairment (e.g., blocking the pupillary aperture).
-Clinical signs like shying, head-shaking, or decreased performance.

Post-operative anti-inflammatory protocols (e.g., topical dexamethasone, atropine, oral meloxicam) minimized complications.
• Retreatment is rarely required but may improve outcomes for unsatisfactory cases.

18
Q

Ocular findings in a population of geriatric equids in the United Kingdom

A

• 84% of geriatric equids had at least one form of ocular pathology:
• 74% had anterior segment pathology (e.g., corneal or lens changes).
• 44% had posterior segment pathology (e.g., vitreal or fundic abnormalities).
• Despite the high prevalence, all eyes retained functional vision.

Anterior Segment:
• Cataracts were the most common (52% of animals), predominantly anterior cortical (65% of cataracts).
• Other findings included corneal lesions (10%) and iris abnormalities (e.g., focal pigmentation changes, cystic granula iridica).
Posterior Segment:
• Senile Retinopathy was the most common fundic pathology (42.9% of cases with fundic changes).
• Other abnormalities included bullet-hole chorioretinopathy and pigmentary disturbances.
Signalment Associations
• Cobs and Shetlands exhibited a higher prevalence of anterior segment pathology (100%) compared to other breeds.
•Older animals were more likely to have posterior segment pathology:
-Median age: 26 years for posterior segment pathology vs 23.5 years without it.
-Median age: 27 years for senile retinopathy vs 24 years without it.
• Horses with corneal pathology were more likely to have staff-reported visual deficits (40%) compared to those without corneal changes (4.4%). Staff-reported deficits underestimated the actual prevalence of ocular abnormalities, highlighting the need for routine examinations.

• While ocular pathology was prevalent, none of the findings caused significant vision loss or compromised quality of life, emphasizing the adaptability of equine vision to age-related changes.

19
Q

A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for ocular squamous cell carcinoma in Belgian horses

A

DDB2 Variant (c.1013C>T, p.Thr338Met)- Strongly associated with ocular SCC in Belgian horses:
• 76% of affected horses were homozygous for the risk allele (T/T).
• Relative risk for homozygous horses developing SCC: 4.0.
• No homozygous carriers were identified in the control group.
• The mutation is hypothesised to impair DDB2 protein’s ability to repair UV-induced DNA damage, leading to increased susceptibility to SCC.

• All study horses were genetically chestnut (MC1R: ee), precluding direct analysis of coat colour’s influence on SCC risk within the sample. Retrospective evidence suggests a potential link between chestnut coat colour and SCC due to increased photosensitivity.

Horses homozygous for the risk allele should:
• Avoid excessive UV exposure through stabling during peak sunlight or use of UV-protective fly masks.
• Undergo regular ophthalmic examinations to detect early signs of SCC.
• Genetic testing of breeding stock is advised to minimise transmission of the risk allele.

20
Q

Inter-user and intra-user variation of two tonometers in horses

A

Rebound Tonometer (TonoVet):
• Lower inter-user variation in unsedated horses compared to TonoPen (15.4% vs 21.7%, P = 0.01).
• Lower intra-user variation in both unsedated (9.1% vs 16.1%, P < 0.0001) and sedated horses (8.4% vs 14.7%, P < 0.0001).

Applanation Tonometer (TonoPen):
• Higher inter-user variation than TonoVet in unsedated horses but similar variation in sedated horses (16.0% vs 18.1%, P = 0.4).
• Intra-user variability was consistently higher than TonoVet in all conditions.

• Sedation reduced IOP readings for both tonometers (P < 0.0001):
• Sedation did not significantly affect intra-user or inter-user variability for TonoVet but improved inter-user consistency for TonoPen.

Ease of Use
• TonoVet: Easier to use in unsedated horses due to minimal corneal contact and faster readings.
• TonoPen: Required more contact and precise alignment, increasing variability in unsedated horses.

21
Q

Intraocular pressure following four different intravenous sedation protocols in normal horses

A

• All sedation protocols significantly decreased IOP compared to pre-sedation values (P < 0.0001).
• Maximum reduction in IOP occurred 5 minutes post-sedation (Tpost5) for all protocols:
• SED2 (detomidine + butorphanol) caused the greatest reduction (14.5 ± 2.9 mmHg) compared to the other protocols.
• SED3 (detomidine alone) resulted in the least reduction in IOP across all post-sedation time points.
• IOP gradually increased after Tpost5 but remained below baseline at 60 minutes post-sedation for all protocols.
• Timing of IOP measurements was critical as peak reduction occurred within the first 5–15 minutes.

• IOP was significantly higher when the head was allowed to hang down compared to being elevated (P < 0.0001).
• Linear correlation observed between head position (vertical distance from heart to globe) and IOP.

Repeated IOP measurements should:
• Use the same sedation protocol to ensure comparable results.
• Standardize head position during measurements to minimize variability.
• IOP readings should ideally be taken within 5–15 minutes post-sedation, as this is the period of maximum reduction.
• Post-sedation IOP trends highlight the importance of recording the time point relative to drug administration.

Results align with prior findings showing that alpha-2 adrenergic agonists (e.g., detomidine, xylazine) reduce IOP via mechanisms like:
• Ciliary body constriction.
• Decreased aqueous humour production.
• Muscle relaxation reducing orbital pressure.

22
Q

Commercial amniotic membrane extract for treatment of corneal ulcers in adult horses

A

• No significant difference in healing rate between AME-treated eyes and control eyes (P = .984).
• Healing occurred in two distinct phases:
-Rapid phase (0.88 mm²/hr for 48–54 hours): Faster initial reduction in ulcer size.
-Slow phase (0.07 mm²/hr): Gradual healing to closure.

Average healing time:
• AME-treated eyes: 162.7 ± 68.2 hours.
• Control eyes: 167.6 ± 87.4 hours.
• No significant reduction in time to complete healing with AME treatment.

• AME offers no significant advantage over standard medical therapy for uncomplicated superficial corneal ulcers in horses.
• Its application may still warrant exploration for: Infected ulcers. Malacic (melting) ulcers. Conditions with significant inflammation or delayed healing.

23
Q

Prevalence of equine ulcerative keratomycosis in Colorado and association of environmental factors

A

• Ulcerative keratomycosis was diagnosed in 16.4% (10/61) of equine ulcerative keratitis cases:
• Considerably lower than reported at other North American teaching hospitals (24–86%).
• Overall prevalence among equine ophthalmology cases was 1.1% (10/935), also lower compared to studies from Florida (2–8.62%).
• Differences likely reflect Colorado’s dry, high-altitude climate, which may inhibit fungal growth.

Fungal cases predominantly occurred in:
• Spring (50%) and Fall (40%).
• No cases reported in winter, supporting a seasonal influence linked to temperature and humidity patterns.
Environmental Factors
• Higher wind speeds were significantly associated with fungal keratitis (P = 0.047):
• Wind may increase corneal trauma from airborne debris contaminated with fungal organisms.
• Other environmental factors (temperature, humidity, elevation) showed no significant association with fungal keratitis (P > 0.05).

Outcomes for fungal ulcerative keratitis were mixed:
• Healed (40%): Three cases required keratectomy and conjunctival grafting; one resolved with medical therapy alone.
• Enucleation (30%): Often elected due to severity or poor prognosis for medical treatment success.
• Lost to follow-up (30%).
• Early aggressive treatment (e.g., antifungals, surgical intervention) was key to successful outcomes.

• Cytology was the most reliable diagnostic tool, identifying fungal hyphae in 90% of fungal cases.
• Fungal cultures were positive in only 16% of cases, highlighting the limitations of culture for identifying fungal keratitis.

Treatment:
• Cases requiring both medical and surgical management had higher healing rates.
• Prompt use of antifungals (e.g., voriconazole) is critical for controlling fungal infections and improving prognosis.

24
Q

Refinement and revalidation of the Equine Ophthalmic Pain Scale: R-EOPS

A

Inter-Observer Reliability:
• Total Score (TS): Excellent reliability (ICC ≥ 0.876).
Individual items varied:
• Moderate reliability for items like overall behaviour, tension above the eye area, and mouth strained and pronounced chin.
• Substantial to almost perfect reliability for items like blepharospasm and lacrimation.
• Challenges arose with subjectivity in scoring some facial features.

Intra-Observer Reliability:
• TS: Excellent reliability (ICC ≥ 0.915).
• Most items showed substantial to almost perfect agreement (Krippendorff’s alpha ≥ 0.61).

Validity
• For each unit increase in TS, the odds of ocular pathology increased by 2.079 times (P < 0.001).
• TS threshold of 6 achieved high sensitivity (83%) and specificity (100%) for distinguishing healthy horses from those with ophthalmic disease.
Construct Validity:
• TS values significantly differentiated between healthy and diseased horses at baseline (P < 0.001) and after one week (P = 0.005).
Responsiveness Over Time
• TS variability increased at one week post-treatment in diseased horses, suggesting partial improvement in some but not all cases.
• Responsiveness to analgesia was not validated, as pain reduction timelines varied depending on pathology.
Improvements from EOPS
• Simplified Scoring: Excluded physiological parameters that were less reliable and time-consuming.
• Reduced ambiguity in descriptors for behavioural and facial expression items.
• Enhanced Internal Consistency: R-EOPS Cronbach’s alpha: 0.847 (improved from EOPS, 0.76).
• Practical Application: Shorter application time and more straightforward scoring make R-EOPS easier to use in clinical settings.

25
Q

Systemic detectability of dexamethasone and prednisolone after eye drop application in horses

A

TID treatment with maxitrol or predforte

Dexamethasone:
• Detected in serum (0.7–43 ng/mL, mean 2.1 ng/mL) and urine (1.2–5 ng/mL, mean 0.8 ng/mL) during treatment.
• Levels were below the limit of detection (LOD) in both serum and urine 24 hours after the final dose.
Prednisolone:
• Detected in serum (1.1–32.5 ng/mL, mean 6.4 ng/mL) and urine (3.7–19 ng/mL, mean 4.6 ng/mL) during treatment.
• Below LOD in urine 24 hours after the last dose and in serum by 7 days post-treatment.

Implications for Doping Tests
• Both steroids were systemically detectable after topical administration despite low doses.
• Dexamethasone and prednisolone eye drops could produce positive doping results during and shortly after treatment, depending on detection thresholds set by regulatory bodies.
• Prednisolone had a longer systemic detectability period compared to dexamethasone.

Corticosteroids are absorbed through the conjunctiva, cornea, and nasolacrimal duct, with nasopharyngeal mucosa playing a significant role.
Systemic absorption is influenced by: Drug formulation and concentration. Individual differences in tear film turnover and blinking.

Withdrawal Guidelines:
• Dexamethasone: Stop treatment at least 24 hours before competition.
• Prednisolone: Discontinue 7 days prior to competition to ensure clearance from serum.

26
Q

Risk factors for insidious uveitis in the Knabstrupper breed

A

Prevalence:
• 20.7% of Knabstruppers in the study were diagnosed with insidious uveitis.
• The condition was predominantly bilateral (91.7% of affected horses).
Genetic Risk Factors:
• Homozygosity for the leopard complex spotting allele (LP) significantly increased the odds of developing uveitis:
• LP/LP horses: Odds ratio (OR) = 7.39 compared to N/N horses (P = 0.05).
• LP/N heterozygotes did not show significantly increased risk.
• PATN1 was not significantly associated with disease risk (P = 0.7).
Age:
• Age was a significant risk factor:
• Horses aged 11–20 years were at the highest risk.
• Odds increased for horses aged 11–15 years (OR = 7.34, P = 0.04) and 16–20 years (OR = 12.11, P = 0.01) compared to younger groups.
Leptospira spp.:
• No significant association was found between Leptospira exposure and uveitis in this cohort.

Clinical Implications
• LP genotyping is recommended for Knabstruppers to assess the risk of insidious uveitis:
• LP/LP horses, especially those aged 11–20 years, should undergo regular ocular evaluations to detect early signs of disease.
• Genetic testing for PATN1 is not currently indicated based on these findings.

27
Q

Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse

A

• The study identified a missense mutation in the GRM6 gene (c.533C>T, p.178Thr>Met) as a likely cause of congenital stationary night blindness (CSNB) in a Tennessee Walking Horse.
• GRM6 encodes a metabotropic glutamate receptor critical for night vision. This receptor plays a key role in the ON-bipolar cell signaling pathway by binding the neurotransmitter glutamate.
Proposed Mechanism:
•The mutation is hypothesized to abolish the receptor’s ability to bind glutamate effectively.
•The inability to bind glutamate disrupts signal transduction, leaving ON-bipolar cells hyperpolarized in low-light conditions, which aligns with clinical symptoms of night blindness.

Comparative Insights:
• Similar dark-adapted ERG results between the studied horse and other cases (e.g., Appaloosas with TRPM1 mutation) support the involvement of GRM6 in the same visual pathway.
• Unlike TRPM1-related CSNB cases, the affected Tennessee Walking Horse lacked associated pigmentation phenotypes.

28
Q

Subconjunctival enucleation with orbital implant placement in standing horses: 20 cases (2014-2017)

A

This study is the first to report the use of a subconjunctival approach for enucleation in standing horses, combined with orbital implant placement.
It prospectively assessed the efficacy, complications, cosmetic outcomes, and client satisfaction of the procedure.
• No intraoperative complications or surgical site infections were encountered.
• Postoperative complications were minimal, including:
-Mild postoperative colic in 4 horses.
-Incisional swelling in 1 horse.
-Occasional drainage from the surgical site in 1 horse.
• No implants were removed during the 1 to 4 years of follow-up.
• All clients were satisfied with the cosmetic outcomes of the procedure.