Bupivacaine liposomal 133mg/10ml prolonged-release dispersion for injection vials
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Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 34 · Randomised trials: 16 · 2017–2026
Showing the 50 most relevant studies, sorted by most relevant.
N. Hussain, Jarod Speer, F. Abdallah
Anesthesiology, 2024
Alexandre Nguyen, S. Grape, M. Gobbetti, et al.
European Journal of Anaesthesiology, 2023
M. Fares, M. Daher, P. Boufadel, et al.
The American Journal of Sports Medicine, 2025
Longyi Zhang, Shun Yang, Xianchun Liu, et al.
Frontiers in Medicine, 2025
Background The quality of recovery (QoR) is a multidimensional concept used to evaluate the restoration of physical and psychological functions after surgery. It is a key measure for assessing surgical efficacy, anesthetic modalities, and the effectiveness of perioperative interventions. Liposomal bupivacaine (LB), a long-acting local anesthetic recently introduced, is characterized by its sustained-release profile and prolonged analgesic effect. However, empirical findings regarding the impact of LB on the quality of postoperative recovery remain inconclusive. Methods On 5 March 2025, we conducted a systematic search of the PubMed, Embase, Web of Science, Cochrane Library, Scopus, CNKI, and VIP databases to identify randomized controlled trials (RCTs) assessing the efficacy of LB in postoperative recovery. Eligible studies compared postoperative recovery outcomes between patients receiving LB and those in control groups who did not receive LB. The primary outcome of interest was the QoR score measured 72 h after surgery. Secondary outcomes included QoR scores at 24 and 48 h after surgery; pain scores at rest at 24, 48, and 72 h after surgery; incidence of postoperative nausea and vomiting (PONV); cumulative morphine-equivalent opioid consumption within 72 h after surgery; and patient satisfaction. Results This meta-analysis included 11 RCTs comprising a total of 1,357 patients. The findings indicate that the LB group showed a statistically significant improvement in overall QoR scores 72 h after surgery [standardized mean difference (SMD): 0.52; 95% confidence interval (CI): 0.20, 0.85; P = 0.00]. Furthermore, LB use was associated with significantly reduced pain scores at 24, 48, and 72 h after surgery. The LB group also exhibited lower cumulative morphine-equivalent opioid consumption within 72 h after surgery, a reduced incidence of PONV, and significantly higher patient satisfaction scores. Conclusion The use of LB was associated with improved QoR scores within 72 h after surgery, a reduced incidence of PONV, and decreased opioid consumption. These findings suggest that LB not only improves overall postoperative recovery but also mitigates associated adverse effects, thereby contributing to improved patient satisfaction and a more streamlined recovery trajectory. Nevertheless, further research is needed to assess its long-term efficacy and broader clinical applicability. Systematic review registration [https://www.crd.york.ac.uk/prospero/], identifier [CRD420251003585].
Abstract licence: CC BY
Machado GF, Mokhtar J, Romão VT, et al.
2026
Bo Jiao, Xiaolin Xu, Caiyi Yan, et al.
BMJ Open, 2025
- Breast
- Bupivacaine
- Anesthetics, Local
Samantha L. Harrer, Michael F. Yayac, Gregory R. Toci, et al.
Journal of surgical orthopaedic advances, 2024
Hu J, Zhang K, Ma Z, et al.
Journal of Pain Research, 2026
Qian Cao, Rong-Mu Lin, Yan Liu, et al.
Frontiers in Medicine, 2026
ZiKang Yang, ZiKang Yang, Yuang Fang, et al.
Frontiers in Pain Research, 2026
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.