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Veterinary anaesthesia and analgesia2018; 45(6); 876-880; doi: 10.1016/j.vaa.2018.08.004

Colon constipation in horses after sustained-release buprenorphine administration.

Abstract: To investigate the pharmacological profile and side effects of buprenorphine administered as a sustained-release formulation in horses. Methods: Pilot trial. Methods: A total of four experimental horses, aged 18-27 years and weighing 508-578 kg. Methods: Buprenorphine (0.1 mg kg) was mixed as a freshly prepared sterile solution with a sustained-release drug carrier. It was administered by the subcutaneous (n = 2) or intramuscular (n = 2) route. During the experiment, the horses were closely monitored, equipped with a step counter and blood samples were collected for quantification of buprenorphine in plasma. Results: All four horses developed colon constipation requiring medical therapy, together with increased locomotor activity. One horse, requiring surgical treatment of colon constipation, was euthanized during recovery from anaesthesia for weakness and severe lower airway obstruction. The three other horses recovered fully within 5-7 days. Plasma buprenorphine concentrations were between 1 and 8 ng mL for approximately 48 hours. No local reaction was observed at the injection sites. Conclusions: Administration of the sustained-release formulation of buprenorphine at a dose of 0.1 mg kg resulted in plasma concentrations compatible with antinociceptive activity for at least 48 hours. The observed severe and undesirable effects of colon constipation and increased locomotor activity definitely preclude clinical use of sustained-release buprenorphine at this dose.
Publication Date: 2018-09-11 PubMed ID: 30297131DOI: 10.1016/j.vaa.2018.08.004Google Scholar: Lookup
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  • Journal Article

Summary

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This study explores the effects and side effects of sustained-release buprenorphine, a pain medication, in horses. The research found that while this method ensured the presence of the drug in the body for at least 48 hours, it led to serious side effects, including colon constipation and increased movement, making its clinical use undesirable.

Research Methodology

  • The study was a pilot trial involving four horses aged 18 to 27 years and weighing between 508 and 578 kilograms.
  • The researchers administered a solution of buprenorphine, mixed with a sustained-release drug carrier, to the horses either subcutaneously (under the skin) or intramuscularly (into the muscle).
  • Throughout the experiment, the horses were closely monitored, and their steps were counted. Blood samples were also collected to measure the concentration of buprenorphine in plasma.

Results

  • The study found that all four horses developed constipation that required medical intervention, and there was an increase in their locomotor activity.
  • One horse had to be euthanized during recovery due to weakness and severe obstruction in its lower airways after undergoing surgical treatment for constipation.
  • The remainder of the horses fully recovered within 5 to 7 days.
  • The presence of buprenorphine in plasma was maintained for roughly 48 hours, with concentrations ranging between 1 and 8 ng/mL.
  • No local reactions were observed at the injection sites.

Conclusions

  • While the administration of a sustained-release formulation of buprenorphine ensured a plasma concentration compatible with its pain-relieving properties for at least 48 hours, the route led to severe undesirable effects, making it unsuitable for clinical use.
  • The severe side effects observed were colon constipation and a substantial increase in movement.

Cite This Article

APA
Levionnois OL, Graubner C, Spadavecchia C. (2018). Colon constipation in horses after sustained-release buprenorphine administration. Vet Anaesth Analg, 45(6), 876-880. https://doi.org/10.1016/j.vaa.2018.08.004

Publication

ISSN: 1467-2995
NlmUniqueID: 100956422
Country: United States
Language: English
Volume: 45
Issue: 6
Pages: 876-880
PII: S1467-2987(18)30212-5

Researcher Affiliations

Levionnois, Olivier L
  • Section of Anaesthesiology and Pain Therapy, Department of Clinical Veterinary Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland. Electronic address: olivier.levionnois@vetsuisse.unibe.ch.
Graubner, Claudia
  • Swiss Institute of Equine Medicine ISME, Department of Clinical Veterinary Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Spadavecchia, Claudia
  • Section of Anaesthesiology and Pain Therapy, Department of Clinical Veterinary Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

MeSH Terms

  • Analgesics, Opioid / adverse effects
  • Animals
  • Buprenorphine / adverse effects
  • Colonic Diseases / chemically induced
  • Colonic Diseases / veterinary
  • Constipation / chemically induced
  • Constipation / veterinary
  • Delayed-Action Preparations / adverse effects
  • Horse Diseases / chemically induced
  • Horses
  • Pilot Projects

Citations

This article has been cited 3 times.
  1. Paranjape VV, Knych HK, Berghaus LJ, Giancola S, Cathcart J, Reed RA. Plasma concentrations of buprenorphine administered via matrix-type transdermal patches applied at three different anatomical locations in healthy adult horses. Front Pain Res (Lausanne) 2024;5:1390322.
    doi: 10.3389/fpain.2024.1390322pubmed: 38962712google scholar: lookup
  2. Paranjape VV, Knych HK, Berghaus LJ, Cathcart J, Giancola S, Craig H, James C, Saksena S, Reed RA. Evaluation of physical variables, thermal nociceptive threshold testing and pharmacokinetics during placement of transdermal buprenorphine matrix-type patch in healthy adult horses. Front Pain Res (Lausanne) 2024;5:1373555.
    doi: 10.3389/fpain.2024.1373555pubmed: 38529072google scholar: lookup
  3. Haralambus R, Juri M, Mokry A, Jenner F. The impact of opioid administration on the incidence of postanaesthetic colic in horses. Front Pain Res (Lausanne) 2024;5:1347548.
    doi: 10.3389/fpain.2024.1347548pubmed: 38440199google scholar: lookup