ArticleSurgical endoscopy2026
Bilateral external oblique intercostal block combined with intravenous patient-controlled analgesia for multimodal analgesia after laparoscopic cholecystectomy: a single-center randomized controlled trial.
Article in Surgical endoscopy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07332546 (External Oblique Intercostal Block for Postoperative Pain After Laparoscopic Cholecystectomy), which is not on this map. Not yet cited in PubMed.
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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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External Oblique Intercostal Block for Postoperative Pain After Laparoscopic Cholecystectomy: A Randomized Controlled Trial
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7 authors.
Funding
Abstract
backgroundPostoperative pain after laparoscopic cholecystectomy (LC) remains common and peaks within 24 h. Opioid-based analgesia improves pain but can delay recovery, prompting opioid-sparing regional techniques within ERAS pathways.
objectiveTo evaluate whether adding bilateral ultrasound-guided external oblique intercostal plane block (EOIB) to standard intravenous patient-controlled analgesia (PCA) improves early analgesia and recovery after elective LC.
methodsIn a prospective, single-centre, randomized controlled parallel trial, 56 patients were randomized (1:1) to receive bilateral EOIB (n=28) or no regional block (control, n=28). All patients received standardised anesthesia and PCA with butorphanol. The primary outcome was total butorphanol consumption within 24 h postoperatively. Secondary outcomes included pain scores, Quality of Recovery at 24 h, time to first flatus, nausea and vomiting, intraoperative haemodynamic events, and length of hospital stay.
resultsEOIB significantly reduced 24 h butorphanol consumption [median 3.7 (IQR 3.2-4.8) mg vs. 7.2 (6.2-7.6) mg, equivalent to 18.5 vs. 36.0 mg intravenous morphine]. After adjustment, opioid consumption was 46.5% lower (95% CI 38.3-53.6; P<0.001). EOIB also increased QoR-15 at 24 h (median 140 vs. 131; P<0.001) and shortened time to first flatus (median 18 vs. 20 h; P=0.031). Cough-pain VRS scores were lower with a significant group-by-time interaction (P=0.013). Intraoperative haemodynamics did not differ, and PONV was numerically lower without statistical significance.
conclusionBilateral EOIB with standard PCA provides clear opioid-sparing effects after LC without increasing safety risks. STUDY REGISTRATION: ClinicalTrials.gov, NCT07332546.
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