Opioid-free versus opioid-based anesthesia for day surgery laparoscopic inguinal hernia repair under ERAS protocol: a randomized non-inferiority trial.

IF 2.4 2区 医学 Q1 SURGERY
Hernia Pub Date : 2025-07-09 DOI:10.1007/s10029-025-03410-y
Chun Wang, Peng Shi, Jun Xu, Xiaohua Fan, Jinjun Bian, Lulong Bo
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引用次数: 0

Abstract

Purpose: Laparoscopic inguinal hernia repair (LIHR) is increasingly performed as a day surgery procedure under enhanced recovery after surgery (ERAS) protocol. While opioid-based anesthesia (OA) remains standard, its adverse effects may impair postoperative recovery. This randomized controlled non-inferiority trial assessed whether opioid-free anesthesia (OFA) provides non-inferior postoperative pain control to OA for day surgery LIHR under ERAS protocol and evaluated comprehensive recovery outcomes.

Methods: This single-center, prospective, randomized non-inferiority trial enrolled 90 patients scheduled for day surgery LIHR who were randomly allocated to receive either lidocaine-dexmedetomidine-based OFA (n = 45) or sufentanil-remifentanil-based OA (n = 45). The primary outcome was postoperative 24-h time-weighted average visual analog scale (TWA-VAS) pain score at rest. Secondary outcomes included extended pain assessment, quality of recovery indicators, day surgery pathway efficiency, and perioperative hemodynamic stability.

Results: The 24-h TWA-VAS scores were 1.84 ± 1.02 in the OFA group and 1.77 ± 0.88 in the OA group (mean difference: 0.07; 95% CI: -0.33-0.47), establishing non-inferiority. The OFA group experienced significantly lower rates of intraoperative hypotension (8.9% vs. 53.3%; relative risk: 0.17; P = 0.001) but longer laryngeal mask airway removal time (20 vs. 15 min; P = 0.034) and post-anesthesia care unit stay (50 vs. 45 min; P = 0.018). No significant differences were observed in Quality of Recovery-15 scores, rescue analgesia requirements, postoperative urinary retention (POUR), postoperative nausea and vomiting (PONV), or 24-h discharge success rates.

Conclusion: Under ERAS protocol, lidocaine-dexmedetomidine-based OFA provided non-inferior analgesic efficacy to OA for day surgery LIHR, while delivering superior hemodynamic stability. Despite modestly prolonged emergence times, OFA maintained comparable recovery quality and discharge success rates. These findings establish OFA as a valuable alternative anesthetic strategy for day surgery LIHR under ERAS protocol, particularly for patients at risk of opioid-related adverse effects.

Trial registration: ChiCTR2500098054, registered on February 28, 2025, retrospectively registered.

无阿片类药物与基于阿片类药物的麻醉在ERAS方案下进行日间手术腹腔镜腹股沟疝修复:一项随机非劣效性试验。
目的:腹腔镜腹股沟疝修补术(LIHR)越来越多地作为一种日间手术,在术后增强恢复(ERAS)协议下进行。虽然基于阿片类药物的麻醉(OA)仍然是标准的,但其不良反应可能会损害术后恢复。这项随机对照非劣效性试验评估了在ERAS方案下,无阿片类药物麻醉(OFA)是否为OA日间手术LIHR提供了非劣效性术后疼痛控制,并评估了综合恢复结果。方法:这项单中心、前瞻性、随机非效性试验纳入了90例计划进行日间手术LIHR的患者,他们被随机分配到以利多卡因-右美托咪定为基础的OFA组(n = 45)或以舒芬太尼-瑞芬太尼为基础的OA组(n = 45)。主要观察指标为术后24小时时间加权平均视觉模拟量表(TWA-VAS)静息疼痛评分。次要结局包括延长疼痛评估、恢复指标质量、日间手术路径效率和围手术期血流动力学稳定性。结果:OA组和OFA组24h TWA-VAS评分分别为1.84±1.02和1.77±0.88(平均差异0.07;95% CI: -0.33-0.47),建立非劣效性。OFA组术中低血压发生率显著降低(8.9% vs. 53.3%;相对风险:0.17;P = 0.001),但移除喉罩的时间较长(20 vs 15 min;P = 0.034)和麻醉后护理病房住院时间(50 vs 45 min;p = 0.018)。在恢复质量-15评分、抢救镇痛要求、术后尿潴留(POUR)、术后恶心呕吐(PONV)或24小时出院成功率方面均无显著差异。结论:在ERAS方案下,利多卡因-右美托咪定为基础的OFA为OA日间手术LIHR提供了良好的镇痛效果,同时提供了优越的血流动力学稳定性。尽管急救时间略微延长,OFA仍保持了相当的回收质量和出院成功率。这些发现证实OFA是ERAS方案下日间手术LIHR的一种有价值的替代麻醉策略,特别是对于有阿片类药物相关不良反应风险的患者。试验注册:ChiCTR2500098054,于2025年2月28日注册,回顾性注册。
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来源期刊
Hernia
Hernia SURGERY-
CiteScore
4.90
自引率
26.10%
发文量
171
审稿时长
4-8 weeks
期刊介绍: Hernia was founded in 1997 by Jean P. Chevrel with the purpose of promoting clinical studies and basic research as they apply to groin hernias and the abdominal wall . Since that time, a true revolution in the field of hernia studies has transformed the field from a ”simple” disease to one that is very specialized. While the majority of surgeries for primary inguinal and abdominal wall hernia are performed in hospitals worldwide, complex situations such as multi recurrences, complications, abdominal wall reconstructions and others are being studied and treated in specialist centers. As a result, major institutions and societies are creating specific parameters and criteria to better address the complexities of hernia surgery. Hernia is a journal written by surgeons who have made abdominal wall surgery their specific field of interest, but we will consider publishing content from any surgeon who wishes to improve the science of this field. The Journal aims to ensure that hernia surgery is safer and easier for surgeons as well as patients, and provides a forum to all surgeons in the exchange of new ideas, results, and important research that is the basis of professional activity.
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