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Article: Addition of liposomal bupivacaine in brachial plexus blocks: A systematic review and meta-analysis of randomized controlled trials

TitleAddition of liposomal bupivacaine in brachial plexus blocks: A systematic review and meta-analysis of randomized controlled trials
Authors
KeywordsAnesthesia, Regional
Brachial Plexus
Meta-Analysis
Nerve Block
Peripheral Nerves
Issue Date23-Jul-2025
PublisherBMJ Publishing Group
Citation
Regional Anesthesia & Pain Medicine, 2025 How to Cite?
AbstractBackground: Adding liposomal bupivacaine to brachial plexus block may improve postoperative analgesia after upper limb surgery. Objective: This study aimed to assess the postoperative analgesic efficacy of adding liposomal bupivacaine to brachial plexus block compared with non-liposomal local anesthetic. Evidence review: A systematic literature search was conducted in PubMed, Web of Science, EMBASE, ClinicalTrials.gov, and the Cochrane Library up to June 30, 2024. Randomized controlled trials (RCTs) that evaluated the postoperative pain scores in patients who received liposomal bupivacaine via brachial plexus block were identified. The primary outcome was resting pain scores (Numerical Rating Scale, 0-10) at 24 hours after nerve block injection derived from the random effects model. A mean difference (MD) of 1/10 was considered to represent a minimal clinically important difference in pain scores. The Grading of Recommendations Assessment, Development, and Evaluation (GRADE) framework was applied to examine the level of evidence. Findings: 21 RCTs (1478 participants) were included. Liposomal bupivacaine was associated with statistically significant reduction in resting pain scores at 24 hours after nerve block injection compared with non-liposomal local anesthetic (MD=-1.04, 95% CI=-1.54 to -0.53, p<0.001, 95% prediction interval=-3.05 to 0.98). This was associated with significant heterogeneity (Q=107, p<0.001, I²=81%, tau2=1.0, 95% CI=0.42 to 2.07) and a low-GRADE rating. Liposomal bupivacaine was also associated with a statistically significant reduction in resting pain scores at 48 hours and 72 hours. Opioid consumption at 0-24 hours, 25-48 hours and 49-72 hours was lower in the liposomal bupivacaine group with statistical significance (p values <0.05). Liposomal bupivacaine was associated with a lower incidence of nausea. Conclusions: There is low-level evidence that liposomal bupivacaine in brachial plexus block may reduce pain intensity after upper limb surgery, but the clinical significance may be limited.
Persistent Identifierhttp://hdl.handle.net/10722/358801
ISSN
2023 Impact Factor: 5.1
2023 SCImago Journal Rankings: 1.328

 

DC FieldValueLanguage
dc.contributor.authorShing, Chung Hin-
dc.contributor.authorWang, Fengfeng-
dc.contributor.authorLam, Pui Ming-
dc.contributor.authorTsui, Omar Wai Kiu-
dc.contributor.authorChan, Timmy Chi Wing-
dc.contributor.authorWong, Stanley Sau Ching-
dc.date.accessioned2025-08-13T07:48:08Z-
dc.date.available2025-08-13T07:48:08Z-
dc.date.issued2025-07-23-
dc.identifier.citationRegional Anesthesia & Pain Medicine, 2025-
dc.identifier.issn1098-7339-
dc.identifier.urihttp://hdl.handle.net/10722/358801-
dc.description.abstractBackground: Adding liposomal bupivacaine to brachial plexus block may improve postoperative analgesia after upper limb surgery. Objective: This study aimed to assess the postoperative analgesic efficacy of adding liposomal bupivacaine to brachial plexus block compared with non-liposomal local anesthetic. Evidence review: A systematic literature search was conducted in PubMed, Web of Science, EMBASE, ClinicalTrials.gov, and the Cochrane Library up to June 30, 2024. Randomized controlled trials (RCTs) that evaluated the postoperative pain scores in patients who received liposomal bupivacaine via brachial plexus block were identified. The primary outcome was resting pain scores (Numerical Rating Scale, 0-10) at 24 hours after nerve block injection derived from the random effects model. A mean difference (MD) of 1/10 was considered to represent a minimal clinically important difference in pain scores. The Grading of Recommendations Assessment, Development, and Evaluation (GRADE) framework was applied to examine the level of evidence. Findings: 21 RCTs (1478 participants) were included. Liposomal bupivacaine was associated with statistically significant reduction in resting pain scores at 24 hours after nerve block injection compared with non-liposomal local anesthetic (MD=-1.04, 95% CI=-1.54 to -0.53, p<0.001, 95% prediction interval=-3.05 to 0.98). This was associated with significant heterogeneity (Q=107, p<0.001, I²=81%, tau<sup>2</sup>=1.0, 95% CI=0.42 to 2.07) and a low-GRADE rating. Liposomal bupivacaine was also associated with a statistically significant reduction in resting pain scores at 48 hours and 72 hours. Opioid consumption at 0-24 hours, 25-48 hours and 49-72 hours was lower in the liposomal bupivacaine group with statistical significance (p values <0.05). Liposomal bupivacaine was associated with a lower incidence of nausea. Conclusions: There is low-level evidence that liposomal bupivacaine in brachial plexus block may reduce pain intensity after upper limb surgery, but the clinical significance may be limited.-
dc.languageeng-
dc.publisherBMJ Publishing Group-
dc.relation.ispartofRegional Anesthesia & Pain Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAnesthesia, Regional-
dc.subjectBrachial Plexus-
dc.subjectMeta-Analysis-
dc.subjectNerve Block-
dc.subjectPeripheral Nerves-
dc.titleAddition of liposomal bupivacaine in brachial plexus blocks: A systematic review and meta-analysis of randomized controlled trials-
dc.typeArticle-
dc.identifier.doi10.1136/rapm-2025-106583-
dc.identifier.scopuseid_2-s2.0-105011635895-
dc.identifier.eissn1532-8651-
dc.identifier.issnl1098-7339-

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