Perineural dexamethasone extends analgesia duration in upper limb surgery blocks versus bupivacaine alone
This double-blinded randomized controlled trial enrolled 90 American Society of Anesthesiologists class I or II patients undergoing upper limb orthopaedic procedures. Patients received a supraclavicular brachial plexus block with either bupivacaine plus 4 mg perineural dexamethasone (Group D) or bupivacaine plus saline (Group C). The primary outcome was analgesia duration, with secondary outcomes including Numerical Pain Rating Scale scores at 4, 8, 12, and 24 hours postoperatively and adverse events.
The primary finding was a significantly longer mean analgesia duration in the dexamethasone group: 1253.33 ± 41.00 minutes compared to 714.67 ± 32.80 minutes in the control group (p < 0.001). The dexamethasone group also showed lower pain scores at the measured time points up to 24 hours, though specific numerical scores and effect sizes were not reported.
Safety and tolerability data indicated minimal adverse events, with mild nausea being the only event reported in both groups. No serious adverse events or discontinuations were reported. Key limitations include the 24-hour follow-up period, lack of reported confidence intervals or effect sizes for pain scores, and incomplete safety reporting regarding serious adverse events. The study presents a viable adjunct for regional anesthesia, but its clinical integration requires consideration of the short-term data and limited safety profile.