Evidence map›Paper›PMID 42180714›Full record

SynthesisFrontiers in medicine2026

Effectiveness and safety of liposomal bupivacaine in autologous breast reconstruction: a systematic review.

Waiel A Daghistani

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

1 author.

Waiel A DaghistaniDepartment of Anesthesia and Surgery, College of Medicine, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Autologous breast reconstruction (ABR), particularly using abdominally based free flaps such as the deep inferior epigastric perforator (DIEP) flap, is associated with significant postoperative pain. Liposomal bupivacaine, a long-acting local anesthetic, has been increasingly incorporated into multimodal analgesia protocols; however, its effectiveness in improving postoperative outcomes remains uncertain. Objective: To systematically evaluate the effectiveness and safety of liposomal bupivacaine in reducing opioid consumption and improving recovery outcomes in patients undergoing autologous breast reconstruction. Methods: A systematic review was conducted in accordance with PRISMA guidelines. A comprehensive search of PubMed, Cochrane CENTRAL, Web of Science, and Scopus was performed up to February 2025. Eligible studies included randomized controlled trials and observational cohort studies comparing liposomal bupivacaine with standard analgesic strategies in ABR. Primary outcomes were total postoperative opioid consumption and length of hospital stay. Secondary outcomes included time to ambulation, time to Foley catheter removal, time to first opioid use, and adverse events. Due to heterogeneity in study designs, interventions, and outcome reporting, a narrative synthesis was performed. Results: Ten studies (5 randomized controlled trials and 5 retrospective cohort studies) involving sample sizes ranging from 16 to 1,017 patients were included. Results for opioid consumption were heterogeneous: some studies demonstrated significant reductions with liposomal bupivacaine (e.g., 512 vs. 395 mg, Conclusion: Liposomal bupivacaine may reduce postoperative opioid consumption in selected settings; however, its overall impact on recovery outcomes in autologous breast reconstruction remains inconsistent. Its benefits appear to depend on the underlying analgesic protocol and comparator strategy. Further high-quality, standardized randomized trials are needed to better define its role within multimodal analgesia pathways.

Indexed as

autologous breast reconstructionbreastliposomal bupivacainepostoperative pain managementregional anesthesia

Identifiers

PMID42180714
PMCPMC13190593

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