腹腔镜结直肠手术后竖脊平面阻滞与腹横平面阻滞在术后恢复中的比较:一项随机、双盲、对照试验。

IF 2 3区 医学 Q2 ANESTHESIOLOGY Perioperative Medicine Pub Date : 2024-12-03 DOI:10.1186/s13741-024-00475-8
Pengfei Hou, Wanxin Liu, Rongman Chen, Haiqi Mi, Shuaiying Jia, Jingyan Lin
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引用次数: 0

摘要

背景:腹腔镜结肠直肠癌切除术后患者会经历明显的术后疼痛。腹横平面阻滞(transcversus abdominis plane block, TAPB)具有有效的镇痛作用,近期研究也表明竖脊平面阻滞(erector spinae plane block, ESPB)可用于腹部手术术后镇痛。然而,两种方法在腹腔镜结直肠手术后的恢复质量方面缺乏比较。方法:60例计划行腹腔镜大肠癌根治术的患者随机分为ESPB组和TAPB组(n = 30)。两组患者均单次双侧注射0.25%罗哌卡因20 mL。主要观察指标为术后24 h的恢复质量(QoR),采用恢复质量-15 (QoR-15)量表。次要结果包括术后48小时的QoR、术后48小时静息和活动状态下的视觉模拟评分(VAS)疼痛评分、救援镇痛需求、术后阿片类药物累积消耗、患者满意度、术后恶心呕吐发生率(PONV)、首次放屁和下床时间、综合并发症指数(CCI)评分和术后住院时间。结果:术后24 h, ESPB组QoR-15评分(平均±标准差)为109.2±8.7分,显著高于TAPB组(101±10.1分)(p = 0.001)。同样,术后48 h, ESPB组QoR-15评分(118.5±8.8)高于TAPB组(113.8±8.1)(p = 0.035)。ESPB组患者术后24小时视觉模拟量表(VAS)疼痛评分较低(均p)。结论:与术前TAPB组相比,ESPB组患者恢复质量更好,镇痛效果更好,术后满意度更高。试验注册:https://www.chictr.org.cn (ChiCTR2400081157);注册日期:2024年2月24日。第一位参与者于2024年2月27日注册。
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Comparison of erector spinae plane block and transverse abdominis plane block in postoperative recovery after laparoscopic colorectal surgery: a randomized, double-blind, controlled trial.

Background: Patients experience significant postoperative pain after laparoscopic resection of colorectal cancer. Transversus abdominis plane block (TAPB) provides effective analgesia, and recent studies have also shown that erector spinae plane block (ESPB) can be used for postoperative analgesia in abdominal surgery. However, there is a lack of comparison between the two methods regarding recovery quality following laparoscopic colorectal surgery.

Methods: Sixty patients scheduled for laparoscopic radical resection of colorectal cancer were randomly assigned to receive either a ESPB with TAPB (n = 30). Both groups received a single injection of 20 mL of 0.25% ropivacaine bilaterally. The primary outcome was the quality of recovery (QoR) at 24 h postoperatively, using the quality of recovery-15 (QoR-15) scale. Secondary outcomes included the QoR at 48 h postoperatively, visual analogue scale (VAS) pain scores during the first 48 h postoperatively in both resting and active states, requirements for rescue analgesia, cumulative postoperative opioid consumption, patient satisfaction, incidence of postoperative nausea and vomiting (PONV), time to first flatus and ambulation, the Comprehensive Complication Index (CCI) score, and postoperative hospital stay.

Results: At 24 h postoperatively, the QoR-15 score (mean ± standard deviation) was significantly higher in the ESPB group (109.2 ± 8.7) compared to the TAPB group (101 ± 10.1) (p = 0.001). Similarly, at 48 h postoperatively, the QoR-15 score remained higher in the ESPB group (118.5 ± 8.8) than in the TAPB group (113.8 ± 8.1) (p = 0.035). Patients in the ESPB group reported lower visual analog scale (VAS) pain scores during the first 24 h postoperatively (all p < 0.05) compared to those in the TAPB group. The sufentanil consumption median (interquartile range) in the ESPB group at 24 h postoperatively was lower (62, 61-65 μg) compared to the TAPB group (66, 63-70 μg) (p < 0.001). Hospital stay median was 7 (6-9) days for the ESPB group and 8 (7-10) days for the TAPB group (p = 0.037).

Conclusions: Patients who received ESPB showed better recovery quality, improved analgesic effects, and higher postoperative satisfaction compared to those who underwent preoperative TAPB.

Trial registration: https://www.chictr.org.cn (ChiCTR2400081157); date of registration: February 24, 2024. The first participant was enrolled on February 27, 2024.

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