Add on Bupivacaine fails to reduce pain after knee replacement surgery: JAMA

The key findings of this study were as follows:

The mean (SD) age of the 533 participants in the study was 69.0 (9.7) years; 287 patients (53.8 percent) were women, and 246 were males (46.2% ).

The baseline characteristics of the study groups were balanced.

There was no change in QoR-40 score at 72 hours or pain VAS score AUC from 6 to 72 hours between the liposomal bupivacaine and control groups.

Analyses of pain VAS and QoR-40 ratings revealed just one statistically significant difference: the liposomal bupivacaine arm had lower pain scores the evening following surgery.

There was no difference in cumulative opioid intake and functional results.

When compared to the control therapy, liposomal bupivacaine was not cost-effective.

There was no difference in adverse or severe adverse events between the control groups and liposomal bupivacaine.

In conclusion, for patients who had undergone knee replacement surgery, periarticular liposomal bupivacaine combined with bupivacaine hydrochloride did not enhance postoperative recovery or pain when compared to bupivacaine hydrochloride alone. Furthermore, the intervention was determined to be ineffective in terms of cost-effectiveness.

Reference:

Hamilton TW, Knight R, Stokes JR, et al. Efficacy of Liposomal Bupivacaine and Bupivacaine Hydrochloride vs Bupivacaine Hydrochloride Alone as a Periarticular Anesthetic for Patients Undergoing Knee Replacement: A Randomized Clinical Trial. JAMA Surg. Published online April 06, 2022. doi:10.1001/jamasurg.2022.0713