Peer-reviewed veterinary case report
Pain relief after spay in cats using bupivacaine liposome injection
By Gordon-Evans, Wanda J et al.Ā·Published in Journal of feline medicine and surgeryĀ·2020Ā·College of Veterinary Medicine, United StatesĀ·View original on PubMed ā
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Original publication title: Controlled, non-inferiority trial of bupivacaine liposome injectable suspension.
- Species:
- cat
Plain-English summary
A group of cats undergoing spay surgery (ovariohysterectomy) received either a new long-lasting pain relief injection (bupivacaine liposome injectable suspension, or BLIS) or a standard pain management treatment. Both groups showed low pain scores after surgery, indicating that the new injection worked just as well as the traditional method for at least 42 hours. Only one cat from each group needed extra pain relief. This suggests that the BLIS injection can effectively manage pain after surgery, reducing the need for additional medications.
People also search for: cat spay surgery pain relief Ā· bupivacaine liposome for cats Ā· postoperative pain management in cats
Abstract
OBJECTIVES: Recently, a bupivacaine liposome injectable suspension (BLIS) became commercially available in the veterinary market that may provide local analgesia for 72 h. The purpose of this study was to compare a BLIS incisional block with a control protocol in cats after ovariohysterectomy (OHE). The hypothesis was that a BLIS block would provide equivalent pain relief. METHODS: This study was designed as a randomized, double-blind, non-inferiority trial. Students performed an OHE followed by a two-layer incisional and body wall block with either standard bupivacaine (control) or BLIS. Postoperatively, cats in the control group received robenacoxib, whereas the BLIS cats received saline. All cats were evaluated using the feline Glasgow Composite Measure Pain Scale (GCMPS) at multiple time points postoperatively. RESULTS: There were 24 control cats and 23 BLIS cats. One cat from each group required rescue medication. The mean GCMPS scores were low and the groups were equivalent at all time points ( <0.05). This study showed that BLIS was equivalent to the control group up to 42 h and pain scores remained low up to 68 h after surgery. CONCLUSIONS AND RELEVANCE: BLIS incisional block is equivalent to a control pain protocol and reduces the need for continued postoperative drug administration.
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Search related cases āOriginal publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/31833793/