Regional anesthesia

Comparing bupivacaine alone to liposomal bupivacaine plus bupivacaine in interscalene blocks for total shoulder arthroplasty: a randomized, non-inferiority trial

Reg Anesth Pain MedPublished Randomised controlled trial

Primary result · 72-h cumulative opioid consumption (oral MME)Result — go to the resultGeometric mean difference 11.9 mg 95% CI −6.9 to 30.8

Authors' conclusion

Interscalene brachial plexus blocks performed with bupivacaine alone did not demonstrate non-inferiority compared to a mixture of liposomal bupivacaine plus bupivacaine with regards to 72-hour cumulative opioid consumption following total shoulder arthroplasty.

Study context

Population
Patients undergoing primary total shoulder arthroplastycompleted the study
Participants
76 patients
Comparison
Bupi vs LB
  • Bupin = 38
  • LBn = 38reference
Primary endpoint
Cumulative postoperative opioid consumption (oral morphine equivalents); non-inferiority margin 22.5 mg
Follow-up
Up to 72 hours
Methodological detailsnon-inferiority, 1:1 randomisation, ultrasound-guided single-injection interscalene block
  • Non-inferiority
  • 1:1 randomisation
  • Ultrasound-guided single-injection interscalene block

Primary result

72-h cumulative opioid consumption (oral MME)

Geometric mean difference

11.9 mg

95% CI −6.9 to 30.8

Interscalene block with bupivacaine alone vs liposomal bupivacaine plus bupivacaine
geometric mean difference 11.9 mg (95% CI −6.9 to 30.8)

As reported in the abstract

Secondary outcomes

Pain scores, patient satisfaction with analgesia, patient-reported duration of sensory block

No meaningful differences between groups

Original publication

Comparing bupivacaine alone to liposomal bupivacaine plus bupivacaine in interscalene blocks for total shoulder arthroplasty: a randomized, non-inferiority trial. Reg Anesth Pain Med. Published 19 October 2022. doi:10.1136/rapm-2022-103997

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