Observational studyMedical science monitor : international medical journal of experimental and clinical research2026
Efficacy and Safety of Liposomal Bupivacaine in Direct Anterior Approach Total Hip Arthroplasty: A Retrospective Cohort Study.
Observational study in Medical science monitor : international medical journal of experimental and clinical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- Liposomal Bupivacaine in Perioperative Analgesia: A Comprehensive Review of Clinical Efficacy, Safety, and Economic Context.Current pain and headache reports · 2026Review
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Authors and funding
6 authors.
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No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND This retrospective observational analysis aimed to assess potential associations between liposomal bupivacaine (LB) and ropivacaine for local infiltration analgesia on early postoperative outcomes in patients undergoing direct anterior approach total hip arthroplasty (DAA-THA). MATERIAL AND METHODS A total of 129 patients with femoral neck fracture or femoral head necrosis were enrolled (inclusion criteria: no preoperative infection, normal inflammation, complete data; exclusion criteria: anesthetic allergy, severe liver/kidney dysfunction, cognitive impairment). Patients were divided into an LB group (n=61) and ropivacaine group (n=68). Primary outcomes were resting and active visual analog scale (VAS) scores on postoperative days (POD) 1-3 and 7. Secondary outcomes included sleep quality score, adverse events, and inflammatory, liver/kidney function markers. RESULTS Baseline characteristics were comparable. LB group showed significantly lower resting and active VAS scores on POD 1-3 (all P<0.05), lower sleep quality scores on POD 1-2 (both P<0.001), and lower incidence of nausea/vomiting (4.92% vs 17.65%, P=0.024). No significant differences were found in 72-hour rescue opioid use, inflammatory markers, liver and kidney function, or other adverse events (all P>0.05). CONCLUSIONS In this retrospective observational analysis of DAA-THA patients receiving standardized multimodal analgesia, LB-based local infiltration analgesia was associated with modest early pain reduction, potentially better short-term sleep quality, and lower nausea/vomiting incidence, without increasing 72-hour rescue opioid use or laboratory safety risks. These findings are associative and exploratory; they do not establish causality or clinical superiority. Prospective, large-scale studies are needed to confirm these associations and evaluate long-term functional and economic outcomes.
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