Evidence map›Paper›PMID 41660478›Full record

ArticleJournal of thoracic disease2026

Liposomal bupivacaine for postoperative analgesia after thoracoscopic surgery: a systematic review and meta-analysis.

Hailong Jin, Bingyi Wang

Abstract read
In one paragraph

Article in Journal of thoracic disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

3 citing papers in PubMed.

  1. Review
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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

2 authors.

Hailong JinDepartment of Anesthesiology, Daxing Teaching Hospital, Capital Medical University, Beijing, China.
Bingyi WangDepartment of Anesthesiology, Peking University People's Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Thoracoscopic surgery has become the standard approach for many thoracic conditions. Despite its advantages, postoperative pain remains a significant cause of complications. Liposomal bupivacaine (LB), an extended-release local analgesic, has been introduced to enhance recovery. This meta-analysis of randomized controlled trials (RCTs) compares the efficacy of LB Methods: We systematically searched PubMed, the Cochrane Library, Embase, and Web of Science for RCTs published from the inception of each database to November 2025. The risk of bias of the included studies was evaluated with the Cochrane Risk of Bias 1 (RoB 1) tool, and the quality of evidence was graded using the GRADE system. The primary outcome was postoperative opioid consumption at 24 hours, measured in morphine milligram equivalents (MMEs). Secondary outcomes included opioid consumption at 48 hours, 72 hours, and during total hospitalization; pain scores assessed using the visual analogue scale (VAS) at 24 hours, 48 hours, 72 hours, and over the entire hospitalization period; length of hospital stay (LOS); and time to first ambulation. Data were synthesized using Review Manager (RevMan; version 5.4). Results: Nine RCTs involving 915 patients were included. Compared to the control group, LB significantly reduced opioid consumption at 24 hours [mean difference (MD) =-1.83; 95% confidence interval (CI): -2.42, -1.24; P<0.001], 48 hours (MD =-2.22; 95% CI: -2.78, -1.66; P<0.001), and 72 hours (MD =-1.73; 95% CI: -2.21, -1.25; P<0.001). Pain scores were also significantly lower in the LB group at 24 hours (MD =-0.99; 95% CI: -1.57, -0.41; P<0.001) and 48 hours (MD =-0.42; 95% CI: -0.77, -0.06; P=0.02), but the difference was not statistically significant at 72 hours (MD =-0.41; 95% CI: -0.95, 0.13; P=0.14). No significant differences were found in total opioid consumption, pain scores over the entire hospitalization period, LOS, or time to first ambulation. Conclusions: LB provides superior short-term analgesia but does not improve functional recovery outcomes compared to non-liposomal local anesthetics.

Indexed as

Liposomal bupivacaine (LB)opioidpain scorepostoperative analgesiathoracoscopic surgery

Identifiers

PMID41660478
PMCPMC12875828

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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.