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Veterinary ophthalmology2025; 29(2); e70124; doi: 10.1111/vop.70124

Dexmedetomidine Prolongs the Duration of Ropivacaine Corneal Anesthesia After Subconjunctival Injection in Healthy Horses.

Abstract: Objective: To determine whether dexmedetomidine prolongs corneal anesthesia following subconjunctival ropivacaine injection in healthy equine eyes.Methods: Ten horses with normal ophthalmic exams were enrolled in a randomized, blinded, crossover experiment with a minimum 4-week washout between treatments. Baseline corneal touch thresholds (CTT, cm) were measured via esthesiometry and a subconjunctival injection was performed in the treatment eye with ropivacaine (R, 0.3 mL 0.5%) or dexmedetomidine-ropivacaine (DR, 0.1 mL 0.5 mg/mL + 0.2 mL 0.5%) and saline (control, 0.3 mL) in the contralateral eye. CTT was measured every 10 min up to 120 min, every 30 min up to 360 min, and every 60 min thereafter until return to baseline. Ambient humidity was concurrently recorded. Subconjunctival hemorrhage was scored 0, 2, and 7 days after injection. CTT values were converted to corneal pressure tolerance (CPT, g/mm2) using humidity-adjusted exponential regression. Data were compared between treatments using mixed model analysis (significance p Results: Mean ± standard deviation total anesthesia time was significantly longer with DR (196 ± 121 vs. 103 ± 47 min R, p = 0.02). Evidence of significant differences between treatments was not seen for minimum CTT, duration of minimum CTT, maximal CPT, or hemorrhage scores. However, time to minimum CTT was longer for DR (32 ± 12 vs. 16 ± 10 min R, p Conclusions: Dexmedetomidine prolongs corneal anesthesia from subconjunctival ropivacaine in horses but delays the onset. Further studies are needed to assess efficacy in diseased eyes.
Publication Date: 2025-12-01 PubMed ID: 41324135PubMed Central: PMC12963526DOI: 10.1111/vop.70124Google Scholar: Lookup
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  • Journal Article
  • Randomized Controlled Trial
  • Veterinary
  • Clinical Trial
  • Veterinary

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

In healthy horses, adding dexmedetomidine to a subconjunctival ropivacaine injection approximately doubled the duration of corneal numbness but slowed the onset to peak effect. Depth of anesthesia and local safety appeared similar to ropivacaine alone, warranting further study in diseased eyes.

What question did the study ask, and why does it matter?

  • Question: Does dexmedetomidine, an alpha-2 adrenergic agonist, prolong the duration of corneal anesthesia when added to subconjunctival ropivacaine in horses?
  • Clinical relevance: Longer, reliable corneal anesthesia can facilitate diagnostics and minor procedures while reducing reliance on repeatedly applied topical anesthetics that can be epitheliotoxic.
  • Rationale: Alpha-2 agonists can act as local anesthetic adjuvants by vasoconstriction (reducing drug washout) and direct antinociceptive effects, potentially extending block duration.

Study design at a glance

  • Population: Ten healthy horses with normal ophthalmic exams.
  • Design: Randomized, blinded, crossover with a minimum 4-week washout between treatment periods.
  • Interventions per session:
    • Treatment eye received either:
      • Ropivacaine alone (R): 0.3 mL of 0.5% ropivacaine, or
      • Dexmedetomidine + ropivacaine (DR): 0.1 mL dexmedetomidine 0.5 mg/mL plus 0.2 mL of 0.5% ropivacaine.
    • Contralateral eye received saline (0.3 mL) as control.
  • Outcome measures:
    • Corneal touch threshold (CTT, cm) via esthesiometry at high frequency initially (every 10 min to 120 min), then every 30 min to 360 min, then hourly until return to baseline.
    • Ambient humidity recorded concurrently.
    • CTT converted to corneal pressure tolerance (CPT, g/mm²) using a humidity-adjusted exponential regression to account for filament behavior.
    • Subconjunctival hemorrhage scored at days 0, 2, and 7.
  • Statistics: Mixed-model analysis comparing treatments; significance threshold not fully reported in the abstract (standard p<0.05 assumed).

Key findings

  • Total anesthesia duration:
    • DR: 196 ± 121 minutes.
    • R: 103 ± 47 minutes.
    • Between-group difference significant (p = 0.02), indicating roughly a 90-minute mean prolongation with DR.
  • Onset to peak effect:
    • Time to minimum CTT was longer with DR (32 ± 12 min) versus R (16 ± 10 min); p-value not fully provided but reported as longer for DR.
  • Depth of anesthesia and other secondary measures:
    • No significant differences between DR and R for minimum CTT achieved, duration at minimum CTT, or maximal CPT.
    • Subconjunctival hemorrhage scores did not differ between treatments at any timepoint (days 0, 2, 7).
  • Variability:
    • Greater inter-session variability noted with DR (larger SD), suggesting individual response differences.

How to interpret the results

  • Efficacy: Adding dexmedetomidine meaningfully extends the functional window of corneal anesthesia from a single subconjunctival dose of ropivacaine.
  • Onset trade-off: The adjuvant delays the time to peak corneal numbness, implying a need for longer lead time before procedures.
  • Depth unchanged: Similar minima in CTT/CPT suggest that adding dexmedetomidine does not deepen the block; it chiefly prolongs its duration.
  • Safety: Comparable hemorrhage scores imply no added local vascular complication detectable by this measure; systemic effects were not detailed in the abstract.

Mechanistic considerations

  • Vasoconstriction from alpha-2 activation likely reduces local vascular uptake of ropivacaine, slowing clearance and prolonging effect.
  • Direct alpha-2–mediated antinociception on peripheral nerve terminals may complement the sodium-channel blockade of ropivacaine.
  • Delayed onset could reflect reduced diffusion to the corneal nociceptors or altered tissue kinetics from vasoconstriction at the injection site.

Strengths

  • Randomized, blinded, crossover design limits inter-individual variability and observer bias.
  • Objective, repeated esthesiometry with a rigorous sampling schedule captures the time-course of anesthesia.
  • Humidity-adjusted conversion to CPT improves comparability by accounting for environmental effects on filament force.

Limitations

  • Small sample size (n=10) limits precision and may underpower some comparisons.
  • Population restricted to healthy eyes; effects may differ in inflamed, ulcerated, or infected corneas.
  • Some p-values and statistical thresholds are truncated in the abstract, limiting full appraisal.
  • No report of systemic dexmedetomidine levels or sedation/physiologic monitoring to rule out systemic absorption effects.
  • Single dose/concentration tested; no dose–response data for dexmedetomidine or ropivacaine volumes.

Clinical implications for equine ophthalmology

  • When planning longer procedures (e.g., extended diagnostics, debridement) or prolonged corneal analgesia, DR may provide a more sustained block.
  • Allow sufficient lead time for peak effect:
    • DR: anticipate ~30–40 minutes to peak numbness.
    • R alone: peak around ~15–20 minutes.
  • If rapid onset is essential for a brief procedure, ropivacaine alone may be preferable; if procedure length is uncertain or extended, DR offers longer coverage.
  • Local tolerance appears similar to ropivacaine alone in healthy eyes; monitor for hemorrhage or irritation as usual after subconjunctival injections.

How this fits with prior knowledge

  • Consistent with the broader regional anesthesia literature where alpha-2 agonists extend local anesthetic duration without consistently increasing block intensity.
  • Supports a strategy of using adjuvants to reduce repeat topical anesthetic dosing, potentially lowering epithelial toxicity risks.

Future directions

  • Evaluate efficacy and safety in diseased or painful corneas, where tissue permeability and inflammatory milieu differ.
  • Characterize dose–response for dexmedetomidine and explore alternative alpha-2 agonists or concentrations.
  • Assess systemic absorption, sedation, cardiovascular effects, and ocular surface health over longer follow-up.
  • Compare against other local anesthetics (e.g., bupivacaine) and techniques (periocular blocks, continuous infusions) for duration, onset, and safety.

Bottom line

  • Dexmedetomidine is a useful adjuvant to subconjunctival ropivacaine in horses, roughly doubling anesthesia duration but slowing onset; plan workflow accordingly and confirm applicability in diseased eyes with further studies.

Cite This Article

APA
Lee S, Hector RC, Hess AM, Wotman KL. (2025). Dexmedetomidine Prolongs the Duration of Ropivacaine Corneal Anesthesia After Subconjunctival Injection in Healthy Horses. Vet Ophthalmol, 29(2), e70124. https://doi.org/10.1111/vop.70124

Publication

ISSN: 1463-5224
NlmUniqueID: 100887377
Country: England
Language: English
Volume: 29
Issue: 2
Pages: e70124
PII: e70124

Researcher Affiliations

Lee, Sera
  • Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Hector, Rachel C
  • Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Hess, Ann M
  • Department of Statistics, College of Natural Sciences, Colorado State University, Fort Collins, Colorado, USA.
Wotman, Kathryn L
  • Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.

MeSH Terms

  • Animals
  • Horses
  • Ropivacaine / administration & dosage
  • Ropivacaine / pharmacology
  • Anesthetics, Local / administration & dosage
  • Anesthetics, Local / pharmacology
  • Cornea / drug effects
  • Dexmedetomidine / administration & dosage
  • Dexmedetomidine / pharmacology
  • Cross-Over Studies
  • Female
  • Male
  • Injections, Intraocular / veterinary
  • Anesthesia, Local / veterinary
  • Conjunctiva

Conflict of Interest Statement

The authors have not used AI to generate any part of the manuscript. The authors declare no conflicts of interest.

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Citations

This article has been cited 1 times.
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