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Equine veterinary journal2026; doi: 10.1002/evj.70298

Epidural 0.125% ropivacaine is safe but insufficient for induced tibiotarsal joint pain.

Abstract: Epidural injection of a low concentration of the local anaesthetic ropivacaine produces analgesia without neurological deficits or ileus in people. Objective: To determine if epidural 0.125% ropivacaine mitigates induced hindlimb lameness in horses while preserving neurological function and gastrointestinal (GI) motility. Methods: Randomised, blinded, controlled, crossover study. Methods: Eight healthy, sound horses underwent two treatments in random order, separated by at least 3 weeks: epidural saline or epidural ropivacaine. For each treatment, an epidural catheter was inserted at the first intercoccygeal space and advanced 5 cm cranially. Correct catheter placement was confirmed radiographically after injecting contrast through it. The tibiotarsal joint was injected with 75 ng of recombinant equine interleukin-1β to induce synovitis. Twelve hours later, baseline variables were recorded, including heart rate, respiratory rate, borborygmi, lameness score and neurological examination score. Thirty minutes thereafter [time = 0 h (t0)], 0.045 mL/kg of preservative-free 0.9% saline or 0.125% ropivacaine was administered through the catheter over 10 min. Data were collected at t0.5, 1, 1.5, 2.5, 3.5, 4.5, 5.5, and 6.5. Faecal piles passed the 24 h before and after t0 were counted. Continuous and categorical data were analysed using a linear mixed effects model and Fisher's exact test, respectively, with significance set at p < 0.05. Results: All horses developed moderate-to-severe lameness that did not improve after ropivacaine injection. No horses developed hindlimb neurological deficits. However, from t0.5-2.5, more horses in the ropivacaine (7/8) than saline (0/7) treatment had decreased to absent anus and tail tone (p = 0.014). There were no other significant differences between treatments. Conclusions: A single volume, concentration, and injection rate were tested. Conclusions: A single dose of 0.125% ropivacaine did not mitigate hindlimb lameness. Anus and tail tone decreased, but hindlimb neurological function and GI motility were preserved.
Publication Date: 2026-08-17 PubMed ID: 42608338DOI: 10.1002/evj.70298Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study tested whether a low concentration (0.125%) of epidural ropivacaine could reduce induced hindlimb pain in horses without causing neurological problems or affecting gastrointestinal function.
  • The researchers found that while ropivacaine was safe and did not impair neurological or GI functions, it did not relieve the induced joint pain and lameness in the horses.

Background and Purpose

  • Ropivacaine is a local anesthetic used epidurally to provide pain relief; lower concentrations are thought to reduce side effects while providing analgesia.
  • In humans, low-concentration epidural ropivacaine can produce pain relief without neurological deficits or gastrointestinal complications like ileus (loss of bowel motility).
  • The study aimed to determine if this concentration (0.125%) of epidural ropivacaine would effectively reduce pain caused by induced tibiotarsal joint inflammation in horses, without causing neurological or gastrointestinal side effects.

Study Design and Methods

  • The study was a randomized, blinded, controlled, crossover trial involving 8 healthy horses.
  • Each horse received two treatments in random order with a washout period of at least 3 weeks between treatments:
    • Epidural saline (control)
    • Epidural 0.125% ropivacaine
  • An epidural catheter was placed at the first intercoccygeal space and advanced 5 cm cranially; placement was confirmed by radiography with contrast injection.
  • Pain was induced by injecting recombinant equine interleukin-1β into the tibiotarsal joint to cause synovitis, simulating joint pain and lameness.
  • Twelve hours after induction, baseline physiological and clinical data were recorded, including:
    • Heart rate and respiratory rate
    • Borborygmi (intestinal sounds) indicating GI motility
    • Lameness score and neurological examination score
  • Thirty minutes later (designated time 0 or t0), either ropivacaine or saline was administered epidurally over 10 minutes at a dose of 0.045 mL/kg.
  • Data were collected at several time points after injection (0.5, 1, 1.5, 2.5, 3.5, 4.5, 5.5, and 6.5 hours), and fecal output was measured over 24 hours before and after treatment to assess GI motility.
  • Data analysis involved linear mixed effects models for continuous data and Fisher’s exact test for categorical data, with significance defined as p < 0.05.

Results

  • All horses developed moderate-to-severe lameness after joint inflammation induction, confirming successful pain model creation.
  • Ropivacaine treatment did not improve lameness compared to saline, indicating that 0.125% ropivacaine epidural did not mitigate the induced joint pain.
  • No horses showed hindlimb neurological deficits with either treatment, indicating neurological safety at this dose/concentration.
  • However, from 0.5 to 2.5 hours after injection:
    • 7 out of 8 horses given ropivacaine developed decreased to absent anus and tail tone (a sign of some local neurological effect), while none of the saline-treated horses did (p = 0.014).
  • Other physiological parameters such as heart rate, respiratory rate, borborygmi, and fecal output showed no significant differences between treatments, indicating preserved gastrointestinal motility.

Conclusions and Implications

  • The tested single dose, volume, and injection rate of epidural 0.125% ropivacaine was safe in horses, not causing hindlimb neurological deficits or affecting GI motility.
  • Despite safety, this concentration was ineffective at reducing joint pain and lameness induced by intra-articular interleukin-1β injection.
  • The decrease in anus and tail tone suggests some local effect on nearby nerves without broader neurological impairment.
  • These findings suggest that while low-dose epidural ropivacaine is safe, it may be insufficient alone for pain relief in equine joint conditions; higher concentrations, different dosing, or adjunct analgesics might be needed.
  • Further research may explore dosing regimens or combinations that balance efficacy and safety for epidural analgesia in horses.

Cite This Article

APA
Boesch JM, Perkins GA, Todd-Donato AB, Colbath AC. (2026). Epidural 0.125% ropivacaine is safe but insufficient for induced tibiotarsal joint pain. Equine Vet J. https://doi.org/10.1002/evj.70298

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English

Researcher Affiliations

Boesch, Jordyn M
  • Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Perkins, Gillian A
  • Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Todd-Donato, Amy B
  • Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Colbath, Aimee C
  • Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.

Grant Funding

  • Harry M. Zweig Memorial Fund for Equine Research

References

This article includes 33 references
  1. Fischer BL, Ludders JW, Asakawa M, Fortier LA, Fubini SL, Nixon AJ. A comparison of epidural buprenorphine plus detomidine with morphine plus detomidine in horses undergoing bilateral stifle arthroscopy. Vet Anaesth Analg 2009;36(1):67–76.
  2. Sysel AM, Pleasant RS, Jacobson JD, Moll HD, Warnick LD, Sponenberg DP. Systemic and local effects associated with long‐term epidural catheterization and morphine‐detomidine administration in horses. Vet Surg 1997;26(2):141–149.
  3. Douglas H, Midon M, Shroff K, Floriano D, Driessen B, Hopster K. Caudal epidural catheterization for pain management in 48 hospitalized horses: a descriptive study of demographics, complications, and outcomes. Front Vet Sci 2022;9:995299.
    doi: 10.3389/fvets.2022.995299google scholar: lookup
  4. Louro LF, Milner PI, Bardell D. Epidural administration of opioid analgesics improves quality of recovery in horses anaesthetised for treatment of hindlimb synovial sepsis. Equine Vet J 2021;53(4):682–689.
    doi: 10.1111/evj.13338google scholar: lookup
  5. Sano H, Martin‐Flores M, Santos LC, Cheetham J, Araos JD, Gleed RD. Effects of epidural morphine on gastrointestinal transit in unmedicated horses. Vet Anaesth Analg 2011;38(2):121–126.
  6. van Loon JP, van Oostrom H, Doornenbal A, Hellebrekers LJ. Lumbosacral spinal cord somatosensory evoked potentials for quantification of nociception in horses. Equine Vet J 2010;42(3):255–260.
  7. Boscan P, Van Hoogmoed LM, Pypendop BH, Farver TB, Snyder JR. Pharmacokinetics of the opioid antagonist N‐methylnaltrexone and evaluation of its effects on gastrointestinal tract function in horses treated or not treated with morphine. Am J Vet Res 2006;67(6):998–1004.
    doi: 10.2460/ajvr.67.6.998google scholar: lookup
  8. Skarda RT, Muir WW. Segmental epidural and subarachnoid analgesia in conscious horses: a comparative study. Am J Vet Res 1983;44(10):1870–1876.
  9. Taylor A, McLeod G. Basic pharmacology of local anaesthetics. BJA Educ 2020;20(2):34–41.
  10. van Loon JP, Menke ES, Doornenbal A, Back W, Hellebrekers LJ. Antinociceptive effects of low dose lumbosacral epidural ropivacaine in healthy ponies. Vet J 2012;193(1):240–245.
  11. Mehta S, Gajbhare MN, Kamble NP. Comparison of epidural analgesia using 0.2% bupivacaine and 0.2% ropivacaine for the management of postoperative pain in major orthopedic surgery. Anesth Essays Res 2018;12(2):586–591.
    doi: 10.4103/aer.aer_62_18google scholar: lookup
  12. Campbell DC, Zwack RM, Crone LA, Yip RW. Ambulatory labor epidural analgesia: bupivacaine versus ropivacaine. Anesth Analg 2000;90(6):1384–1389.
  13. Crosby E, Sandler A, Finucane B, Writer D, Reid D, McKenna J. Comparison of epidural anaesthesia with ropivacaine 0.5% and bupivacaine 0.5% for caesarean section. Can J Anaesth 1998;45(11):1066–1071.
    doi: 10.1007/bf03012393google scholar: lookup
  14. Zoumprouli A, Chatzimichali A, Papadimitriou S, Papaioannou A, Xynos E, Askitopoulou H. Gastrointestinal motility following thoracic surgery: the effect of thoracic epidural analgesia. A randomised controlled trial. BMC Anesthesiol 2017;17(1):139.
    doi: 10.1186/s12871-017-0427-ygoogle scholar: lookup
  15. Iijima T, Ishiyama T, Kashimoto S, Yamaguchi T, Andoh T, Hanawa K. A comparison of three different concentrations of ropivacaine with fentanyl for patient‐controlled epidural analgesia. Anesth Analg 2007;105(2):507–511.
  16. Percie du Sert N, Hurst V, Ahluwalia A, Alam S, Avey MT, Baker M. The ARRIVE guidelines 2.0: updated guidelines for reporting animal research.. PLoS Biol 2020;18(7):e3000410.
  17. National Research Council Committee for the Update of the Guide for the C, Use of Laboratory A. Guide for the care and use of laboratory animals.. Washington (DC): National Academies Press (US); 2011.
  18. Colbath AC, Dow SW, Hopkins LS, Phillips JN, McIlwraith CW, Goodrich LR. Induction of synovitis using interleukin‐1 beta: are there differences in the response of middle carpal joint compared to the tibiotarsal joint?. Front Vet Sci 2018;5:208.
    doi: 10.3389/fvets.2018.00208google scholar: lookup
  19. Furr M, Reed S. Examination of the nervous system.. Equine Neurology Ames, IA: John Wiley & Sons, Inc.; 2015.
    doi: 10.1002/9781118993712.ch6google scholar: lookup
  20. Colbath AC, Dow SW, Hopkins LS, Phillips JN, McIlwraith CW, Goodrich LR. Single and repeated intra‐articular injections in the tarsocrural joint with allogeneic and autologous equine bone marrow‐derived mesenchymal stem cells are safe, but did not reduce acute inflammation in an experimental interleukin‐1β model of synovitis.. Equine Vet J 2020;52(4):601–612.
    doi: 10.1111/evj.13222google scholar: lookup
  21. Espinosa P, Benoit P, Salazar I, de la Fuente J, Heiles P. Transrectal ultrasonography of equine lumbosacral nerves: pilot study in 28 healthy warmblood horses.. Vet Radiol Ultrasound 2017;58(2):228–236.
    doi: 10.1111/vru.12455google scholar: lookup
  22. De Schryver M, Oosterlinck M. An explorative anatomical study on inter‐individual variation of the tibial nerve and landmarks for perineural anesthesia in horses.. Animals (Basel) 2024;14(15):9.
    doi: 10.3390/ani14152161google scholar: lookup
  23. Goodrich LR, Nixon AJ, Fubini SL, Ducharme NG, Fortier LA, Warnick LD. Epidural morphine and detomidine decreases postoperative hindlimb lameness in horses after bilateral stifle arthroscopy.. Vet Surg 2002;31(3):232–239.
    doi: 10.1053/jvet.2002.32436google scholar: lookup
  24. Valverde A, Dyson DH, McDonell WN. Epidural morphine reduces halothane MAC in the dog.. Can J Anaesth 1989;36(6):629–632.
    doi: 10.1007/bf03005412google scholar: lookup
  25. Martins LCT, Guimaraes JB, Ferraz HT, de Oliveira FA, Gomes LS, Chafes CJC. Assessing the analgesic efficacy of lumbosacral epidural morphine in cats undergoing ovariohysterectomy: a comparative study of two doses.. Vet Sci 2024;11(8):1–11.
    doi: 10.3390/vetsci11080360google scholar: lookup
  26. Tung AS, Yaksh TL. The antinociceptive effects of epidural opiates in the cat: studies of the pharmacology and the effects of lipophilicity in spinal analgesia.. Pain 1982;12(4):343–356.
  27. Valverde A, Conlon PD, Dyson DH, Burger JP. Cisternal CSF and serum concentrations of morphine following epidural administration in the dog.. J Vet Pharmacol Ther 1992;15(1):91–95.
  28. Ossipov MH, Lozito R, Messineo E, Green J, Harris S, Lloyd P. Spinal antinociceptive synergy between clonidine and morphine, U69593, and DPDPE: isobolographic analysis.. Life Sci 1990;47(16):Pl71–Pl76.
  29. Skarda RT, Muir WW. Caudal analgesia induced by epidural or subarachnoid administration of detomidine hydrochloride solution in mares.. Am J Vet Res 1994;55(5):670–680.
  30. Choi EJ, Choi YM, Jang EJ, Kim JY, Kim TK, Kim KH. Neural ablation and regeneration in pain practice.. Korean J Pain 2016;29(1):3–11.
    doi: 10.3344/kjp.2016.29.1.3google scholar: lookup
  31. Alexander K, Dobson H. Ultrasonography of peripheral nerves in the normal adult horse. Vet Radiol Ultrasound 2003;44(4):456–464.
  32. Berti M, Casati A, Fanelli G, Albertin A, Palmisano S, Danelli G. 0.2% ropivacaine with or without fentanyl for patient‐controlled epidural analgesia after major abdominal surgery: a double‐blind study. J Clin Anesth 2000;12(4):292–297.
  33. Rédua MA, Valadão CA, Duque JC, Balestrero LT. The pre‐emptive effect of epidural ketamine on wound sensitivity in horses tested by using von Frey filaments. Vet Anaesth Analg 2002;29(4):200–206.

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