Evidence map›Paper›PMID 41820856›Full record

Trial reportBMC anesthesiology2026

Analgesic efficacy of liposomal bupivacaine adductor canal block combined with periarticular infiltration after total knee arthroplasty: a prospective, double-blind, randomized controlled trial.

Zhiping Yin, Jun Chen, Tianchi Zhao, Yongyan Chen, Benfu Wang, Jianfeng Ma

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC anesthesiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Zhiping YinDepartment of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, 109 Xueyuan Road, Lucheng District, Wenzhou, Zhejiang, 325000, China.
Jun ChenDepartment of Anesthesiology, The Shanghai 7th People's Hospital, Shanghai, 200137, China.
Tianchi ZhaoDepartment of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, 109 Xueyuan Road, Lucheng District, Wenzhou, Zhejiang, 325000, China.
Yongyan ChenDepartment of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, 109 Xueyuan Road, Lucheng District, Wenzhou, Zhejiang, 325000, China.
Benfu Wang *Department of Anesthesiology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, 315010, China. 53694381@qq.com.
Jianfeng Ma *Department of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, 109 Xueyuan Road, Lucheng District, Wenzhou, Zhejiang, 325000, China. majianfeng@wmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPostoperative pain after total knee arthroplasty remains substantial despite multimodal analgesia (MMA); however, whether adding liposomal bupivacaine provides clinically meaningful benefits over conventional long-acting local anesthetics within contemporary regional anesthesia–based pathways remains unclear.

methodsIn this single-center, double-blind, randomized controlled trial, 72 patients undergoing unilateral primary TKA were randomized into three groups: levobupivacaine alone (ZB), liposomal bupivacaine alone (LB), and a combination of liposomal bupivacaine and levobupivacaine (LZB). All patients received a standardized MMA protocol including an adductor canal block (ACB) and a periarticular injection (PAI). Primary outcomes were postoperative pain intensity at rest and during activity, measured by the Visual Analogue Scale (VAS). Secondary outcomes included knee range of motion (ROM), patient-controlled intravenous analgesia (PCA) utilization, sensory disturbances within the saphenous nerve distribution, postoperative complication rates, length of hospital stay, and patient satisfaction.

resultsAmong the 62 patients who completed the study, resting pain scores showed no significant differences between groups. However, activity-related pain scores were significantly lower in the LB and LZB groups than in the ZB group between 36 and 72 h postoperatively (p < 0.05). Additionally, the time to first PCA request was significantly longer in the LB and LZB groups than in the ZB group. The LB group exhibited a higher incidence of sensory disturbances in the saphenous nerve distribution than the ZB group at 48 and 72 h postoperatively (p < 0.05). No significant differences emerged regarding ROM, opioid consumption, complication rates, length of hospital stay, or patient satisfaction.

conclusionsIn patients undergoing total knee arthroplasty, incorporating liposomal bupivacaine into an analgesic regimen involving adductor canal block and periarticular infiltration provides prolonged analgesia and superior control of activity-related pain. This may facilitate early postoperative mobilization, thereby promoting early recovery. These findings support the potential of this approach in accelerating the recovery process.

trial registrationThis study was prospectively registered in the Chinese Clinical Trial Registry (ChiCTR2400084619) on May 21, 2024.

Indexed as

Anesthetics, LocalArthroplasty, Replacement, KneeBupivacaineNerve BlockPostoperative PainAgedDouble-Blind MethodFemaleHumansInjections, Intra-ArticularLevobupivacaineLiposomesMaleMiddle AgedPain MeasurementPatient SatisfactionAnesthetics, LocalBupivacaineLevobupivacaineLiposomesAdductor canal blockLiposomal bupivacaineMultimodal analgesiaPeriarticular injectionPostoperative painTotal knee arthroplasty

Identifiers

PMID41820856
PMCPMC13097951

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.