Department of Obstetrics and Gynecology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Unit of Anesthesia, Intensive Care and Pain Management, Department of Medicine, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Gynecol Obstet Invest. 2024;89(2):103-110. doi: 10.1159/000535835. Epub 2024 Jan 24.
The aim of the study was to compare, in patients undergoing minor gynecological laparoscopic procedures, the effects of ultrasound (US)-guided transversus abdominis plane (TAP) + rectus sheath (RS) block versus no TAP/RS block in terms of post-surgical pain control using the numeric pain rating scale (NRS) and the degree of patient satisfaction, according to the main goals of Early Recovery After Surgery (ERAS) programs. The primary outcome is to value the postoperative abdominal pain using NRS in both groups. Secondary outcomes are to evaluate blood values, presence of postoperative nausea and vomiting (PONV), postoperative ileus, level of patient expected satisfaction, time of discharge, length of stay (LOS), and the amounts of additional analgesics required.
In this prospective randomized controlled trial, patients were randomly assigned to loco-regional anesthesia (LRA) group, who received TAP and RS block under US guidance, or no loco-regional anesthesia (N-LRA) group. Enrolled patients were randomized 1:1 to either receive bilateral TAP/RS block with ropivacaine or sham treatment (patches were applied on the abdominal wall of the patients under general anesthesia).
All patients aged between 18 and 75 years, with ASA (American Society of Anesthesiologists) physical status 1-2, undergoing laparoscopic minor gynecological surgery, were enrolled.
The study was conducted to the University of Campus Bio-Medico Hospital of Rome.
Half an hour before surgery, all patients received gabapentin 300 mg per os. Once the patient underwent general anesthesia, US-guided bilateral TAP/RS block was performed by the anesthesiology team, while the uterine manipulator was positioned by a gynecology resident (not involved in the study). In the operative room, all patients received the same standardized anesthetic regimen. Postoperative abdominal pain was assessed at rest, after palpation, during movement, and after a cough by evaluating the patient at 6, 12, 18, 24, 36, 48, and 72 h after surgery, using the NRS from 0 to 10 in both groups. The amount of drug used for analgesia in the first 48 h after surgery was recorded. Moreover, hemoglobin, white blood cells, and c-reactive protein levels were recorded at 24, 48, and 72 h. The presence of PONV and the postoperative ileus was recorded throughout convalescence. The expected level of patient satisfaction at discharge and finally the LOS were assessed.
The major weakness of this study is that 60 mL of 0.5% ropivacaine was administered to each patient, without considering weight differences, yet contemporary literature rarely suggests volume/dose titration in fascial blocks.
A total of 104 women, undergoing gynecological minor laparoscopic surgery, were enrolled and assigned to LRA group (53 pts) and N-LRA group (51 pts). Postoperative pain was significantly reduced in patients who received TAP/RS block. A reduction in the intake of non-steroidal anti-inflammatory drugs after surgery was registered in LRA group (p < 0.01). Moreover, a significant reduction of LOS (45.97 ± 9.87 vs. 65.08 ± 17.32 h; p < 0.01) and PONV was observed in the LRA group, as well as a better level of patient satisfaction at discharge (9.43 ± 0.94 vs. 8.26 ± 1.19; p < 0.01), compared to the N-LRA group.
US-guided TAP and RS block significantly reduces postoperative pain after minor gynecologic laparoscopic surgery and improves patients' post-operative recovery.
本研究旨在比较在接受小型妇科腹腔镜手术的患者中,超声(US)引导下腹横肌平面(TAP)+腹直肌鞘(RS)阻滞与无 TAP/RS 阻滞在术后疼痛控制方面的效果,使用数字疼痛评分量表(NRS)和患者满意度来评估,根据早期康复术后(ERAS)计划的主要目标。主要结果是使用 NRS 评估两组患者术后腹部疼痛。次要结果是评估血液值、术后恶心和呕吐(PONV)的发生、术后肠梗阻、患者预期满意度、出院时间、住院时间(LOS)和所需额外镇痛药物的数量。
在这项前瞻性随机对照试验中,患者被随机分配至局部麻醉(LRA)组,接受超声引导下的 TAP 和 RS 阻滞,或非局部麻醉(N-LRA)组。入组患者按 1:1 随机分为接受双侧 TAP/RS 阻滞的罗哌卡因或假治疗(在全身麻醉下的患者腹壁上应用贴片)。
所有年龄在 18 至 75 岁之间、ASA(美国麻醉医师协会)身体状况 1-2 级、接受腹腔镜下小型妇科手术的患者均被纳入。
该研究在罗马 Campus Bio-Medico 大学医院进行。
所有患者在手术前半小时口服 300mg 加巴喷丁。一旦患者接受全身麻醉,由麻醉科团队进行超声引导下双侧 TAP/RS 阻滞,同时由妇科住院医师(不参与研究)放置子宫操纵器。在手术室,所有患者均接受相同的标准化麻醉方案。术后评估患者在休息时、触诊后、运动时和咳嗽后 6、12、18、24、36、48 和 72 小时的腹部疼痛,使用 NRS 从 0 到 10 评估两组患者。记录术后 48 小时内使用的镇痛药物量。此外,在 24、48 和 72 小时记录血红蛋白、白细胞和 C 反应蛋白水平。记录整个恢复期的 PONV 和术后肠梗阻的发生情况。评估出院时的预期患者满意度水平和最终 LOS。
本研究的主要弱点是每例患者给予 60ml0.5%罗哌卡因,未考虑体重差异,但当代文献很少建议在筋膜阻滞中进行剂量滴定。
共有 104 名接受妇科小型腹腔镜手术的女性入组并分配至 LRA 组(53 例)和 N-LRA 组(51 例)。接受 TAP/RS 阻滞的患者术后疼痛明显减轻。LRA 组术后非甾体抗炎药的摄入量减少(p < 0.01)。此外,LRA 组的 LOS(45.97 ± 9.87 与 65.08 ± 17.32 小时;p < 0.01)和 PONV 显著减少,以及出院时患者满意度水平更高(9.43 ± 0.94 与 8.26 ± 1.19;p < 0.01),与 N-LRA 组相比。
超声引导下 TAP 和 RS 阻滞可显著减轻小型妇科腹腔镜手术后的术后疼痛,并改善患者术后康复。