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围手术期自由饮酒管理促进妇科腹腔镜手术后胃肠道功能恢复:一项随机对照试验。

Perioperative liberal drinking management promotes postoperative gastrointestinal function recovery after gynecological laparoscopic surgery: A randomized controlled trial.

机构信息

Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China; Institute of Anesthesia and Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China; Key Laboratory of Anesthesiology and Resuscitation (Huazhong University of Science and Technology), Ministry of Education, China.

Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China; Institute of Anesthesia and Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China; Key Laboratory of Anesthesiology and Resuscitation (Huazhong University of Science and Technology), Ministry of Education, China.

出版信息

J Clin Anesth. 2024 Oct;97:111539. doi: 10.1016/j.jclinane.2024.111539. Epub 2024 Jun 29.

Abstract

STUDY OBJECTIVE

This study aims to evaluate the effect of perioperative liberal drinking management, including preoperative carbohydrate loading (PCL) given 2 h before surgery and early oral feeding (EOF) at 6 h postoperatively, in enhancing postoperative gastrointestinal function and improving outcomes in gynecologic patients. The hypotheses are that the perioperative liberal drinking management accelerates the recovery of gastrointestinal function, enhances dietary tolerance throughout hospitalization, and ultimately reduces the length of hospitalization.

DESIGN

A prospective randomized controlled trial.

SETTING

Operating room and gynecological ward in Wuhan Union Hospital.

PATIENTS

We enrolled 210 patients undergoing elective gynecological laparoscopic surgery, and 157 patients were included in the final analysis.

INTERVENTIONS

Patients were randomly allocated in a 1:1:1 ratio into three groups, including the control, PCL, and PCL-EOF groups. The anesthetists and follow-up staff were blinded to group assignment.

MEASUREMENTS

The primary outcome was the postoperative Intake, Feeling nauseated, Emesis, Examination, and Duration of symptoms (I-FEED) score (range 0 to 14, higher scores worse). Secondary outcomes included the incidence of I-FEED scores >2, and other additional indicators to monitor postoperative gastrointestinal function, including time to first flatus, time to first defecation, time to feces Bristol grade 3-4, and time to tolerate diet. Additionally, we collected other ERAS recovery indicators, including the incidence of PONV, complications, postoperative pain score, satisfaction score, and the quality of postoperative functional recovery at discharge.

MAIN RESULTS

The PCL-EOF exhibited significantly enhanced gastrointestinal function recovery compared to control group and PCL group (p < 0.05), with the lower I-FEED score (PCL: 0[0,1] vs. PCL-EOF: 0[0,0] vs. control: 1[0,2]) and the reduced incidence of I-FEED >2 (PCL:8% vs. PCL-EOF: 2% vs. control:21%). Compared to the control, the intervention of PCL-EOF protected patients from the incidence of I-FEED score > 2 [HR:0.09, 95%CI (0.01-0.72), p = 0.023], and was beneficial in promoting the patient's postoperative first flatus [PCL-EOF: HR:3.33, 95%CI (2.14-5.19),p < 0.001], first defecation [PCL-EOF: HR:2.76, 95%CI (1.83-4.16), p < 0.001], Bristol feces grade 3-4 [PCL-EOF: HR:3.65, 95%CI (2.36-5.63), p < 0.001], first fluid diet[PCL-EOF: HR:2.76, 95%CI (1.83-4.16), p < 0.001], and first normal diet[PCL-EOF: HR:6.63, 95%CI (4.18-10.50), p < 0.001]. Also, the length of postoperative hospital stay (PCL-EOF: 5d vs. PCL: 6d and control: 6d, p < 0.001), the total cost (PCL-EOF: 25052 ± 3650y vs. PCL: 27914 ± 4684y and control: 26799 ± 4775y, p = 0.005), and postoperative VAS pain score values [POD0 (PCL-EOF: 2 vs. control: 4 vs. PCL: 4, p < 0.001), POD1 (PCL-EOF: 1 vs. control: 3 vs. PCL: 2, p < 0.001), POD2 (PCL-EOF: 1 vs. control:2 vs. PCL: 1, p < 0.001), POD3 (PCL-EOF: 0 vs. control: 1 vs. PCL: 1, p < 0.001)] were significantly reduced in PCL-EOF group.

CONCLUSIONS

Our primary endpoint, I-FEED score demonstrated significant reduction with perioperative liberal drinking, serving as a protective intervention against I-FEED>2. Gastrointestinal recovery metrics, such as time to first flatus and defecation, also showed substantial improvements. Furthermore, the intervention enhanced postoperative dietary tolerance and expedited early recovery.

TRIAL REGISTRATION

ChiCTR2300071047(https://www.chictr.org.cn/).

摘要

研究目的

本研究旨在评估围手术期自由液体管理,包括术前碳水化合物负荷(PCL)术前 2 小时给予和术后 6 小时早期口服喂养(EOF),对妇科患者胃肠道功能恢复和改善结局的影响。假设是围手术期自由液体管理可加速胃肠道功能恢复,提高住院期间的饮食耐受性,最终缩短住院时间。

设计

前瞻性随机对照试验。

地点

武汉协和医院手术室和妇科病房。

患者

我们纳入了 210 名择期妇科腹腔镜手术患者,最终有 157 名患者纳入最终分析。

干预措施

患者以 1:1:1 的比例随机分为三组,包括对照组、PCL 组和 PCL-EOF 组。麻醉师和随访人员对分组情况不知情。

测量

主要结局是术后摄入、恶心、呕吐、检查和症状持续时间(I-FEED)评分(范围 0 至 14,分数越高表示症状越严重)。次要结局包括 I-FEED 评分>2 的发生率,以及监测术后胃肠道功能的其他附加指标,包括首次排气时间、首次排便时间、粪便布里斯托分级 3-4 时间和耐受饮食时间。此外,我们还收集了其他 ERAS 恢复指标,包括术后恶心呕吐(PONV)发生率、并发症、术后疼痛评分、满意度评分和出院时术后功能恢复质量。

主要结果

与对照组和 PCL 组相比,PCL-EOF 组的胃肠道功能恢复明显更快(p<0.05),I-FEED 评分较低(PCL:0[0,1] vs. PCL-EOF:0[0,0] vs. 对照组:1[0,2]),I-FEED>2 的发生率也较低(PCL:8% vs. PCL-EOF:2% vs. 对照组:21%)。与对照组相比,PCL-EOF 保护患者免于发生 I-FEED 评分>2(HR:0.09,95%CI(0.01-0.72),p=0.023),并有利于促进患者术后首次排气(PCL-EOF:HR:3.33,95%CI(2.14-5.19),p<0.001)、首次排便(PCL-EOF:HR:2.76,95%CI(1.83-4.16),p<0.001)、粪便布里斯托分级 3-4(PCL-EOF:HR:3.65,95%CI(2.36-5.63),p<0.001)、耐受液体饮食(PCL-EOF:HR:2.76,95%CI(1.83-4.16),p<0.001)和耐受正常饮食(PCL-EOF:HR:6.63,95%CI(4.18-10.50),p<0.001)。此外,术后住院时间(PCL-EOF:5d 与 PCL:6d 和对照组:6d,p<0.001)、总费用(PCL-EOF:25052±3650y 与 PCL:27914±4684y 和对照组:26799±4775y,p=0.005)和术后视觉模拟评分(VAS)疼痛评分值[术后 0 天(PCL-EOF:2 与对照组:4 与 PCL:4,p<0.001)、术后 1 天(PCL-EOF:1 与对照组:3 与 PCL:2,p<0.001)、术后 2 天(PCL-EOF:1 与对照组:2 与 PCL:1,p<0.001)、术后 3 天(PCL-EOF:0 与对照组:1 与 PCL:1,p<0.001)]在 PCL-EOF 组显著降低。

结论

我们的主要终点,I-FEED 评分显著降低,提示围手术期自由液体管理是预防 I-FEED>2 的保护干预措施。胃肠道恢复指标,如首次排气和排便时间,也有明显改善。此外,该干预措施增强了术后饮食耐受性并促进了早期恢复。

试验注册

ChiCTR2300071047(https://www.chictr.org.cn/)。

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