Paper Details 
Original Abstract of the Article :
Flunixin meglumine (FM), a nonselective cyclooxygenase (COX) inhibitor, is most frequently selected for the treatment of equine systemic inflammatory response syndrome (SIRS)/endotoxemia. However, FM has considerable adverse effects on gastrointestinal function. The aims of this study were to compar...See full text at original site
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引用元:
https://doi.org/10.1016/j.jevs.2022.104205

データ提供:米国国立医学図書館(NLM)

Meloxicam vs. Flunixin Meglumine: A Showdown in Equine Pain Management

This study compares the analgesic effects of meloxicam and flunixin meglumine, two common medications used to manage pain in horses. The researchers used a lipopolysaccharide (LPS)-induced inflammatory response model in thoroughbred horses to evaluate the analgesic efficacy of both drugs. The study found that both meloxicam and flunixin meglumine were effective in reducing pain and inflammation, with no significant difference in their analgesic effects.

Two Powerful Allies: Similar Efficacy, Different Profiles

This study demonstrates that both meloxicam and flunixin meglumine are effective analgesics in horses. However, meloxicam, being a COX-2 selective inhibitor, may offer a potential advantage by reducing the risk of gastrointestinal side effects compared to flunixin meglumine, a nonselective COX inhibitor.

Riding Through the Desert of Equine Pain

Imagine a horse facing the harsh desert conditions of pain and inflammation. Meloxicam and flunixin meglumine act as powerful companions, offering relief and helping the horse to navigate through this challenging terrain. Choosing the right companion depends on individual needs and considerations.

Dr.Camel's Conclusion

This study provides valuable insights into the use of meloxicam and flunixin meglumine in equine pain management. While both drugs are effective, meloxicam's COX-2 selectivity may offer a potential advantage by reducing the risk of gastrointestinal side effects.

Date :
  1. Date Completed 2023-02-14
  2. Date Revised 2023-04-05
Further Info :

Pubmed ID

36586521

DOI: Digital Object Identifier

10.1016/j.jevs.2022.104205

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English

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