静脉注射布洛芬和对乙酰氨基酚对腹腔镜胆囊切除术术后疼痛和曲马多消耗的疗效:前瞻性、随机、双盲临床试验

Z. Ersoy, C. Araz
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引用次数: 0

摘要

背景:包括多模式镇痛在内的许多技术已被用于控制腹腔镜胆囊切除术(LC)后的疼痛。尽管使用静脉注射布洛芬(IV)的研究数量仍然有限,但布洛芬已被证明在治疗术后疼痛方面具有潜在的作用。本研究的主要结果是评估和比较静脉注射布洛芬和对乙酰氨基酚对LC患者术后24小时阿片类药物消耗和疼痛管理的影响。研究的第二个结果是评估布洛芬和对乙酰氨基酚对阿片类药物相关不良事件(ORAE)的影响。材料与方法:本研究为前瞻性、随机、双盲临床试验。经伦理委员会批准,70名年龄在18至65岁之间,美国麻醉学会(ASA)评分为I- II的患者和计划LC的患者入组研究。患者随机分为两组。对照组(n=35)术中静脉滴注800 mg布洛芬(I组),加入100 mL生理盐水;对乙酰氨基酚组(n=35)术中滴注1000 mg布洛芬(A组)。术后所有患者均使用曲马多自控镇痛(PCA)装置。PCA装置设定为10 mg的大剂量,锁定时间为15分钟。一名盲法疼痛护士在1、2、4、6、12和24小时使用数值评定量表(NRS)评估术后镇痛。记录术后24小时恶心呕吐(PONV)发生率、曲马多总消耗量和额外镇痛药的需要。结果:70例LC患者参与了本研究。术后1、2、4、6、12、24 h静脉注射布洛芬组与对乙酰氨基酚组NRS评分差异有统计学意义(P < 0.05)。A组24小时阿片类药物消费量显著高于I组(P0.05)。布洛芬组和对乙酰氨基酚组的PONV率相似(P < 0.05)。两组间orae相似。结论:与对乙酰氨基酚相比,布洛芬作为曲马多多模式镇痛的一部分,在选择性LC手术后最初24小时内减少了曲马多的消耗。静脉布洛芬-曲马多联合用药优于对乙酰氨基酚-曲马多联合用药。两组的orae相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Intravenous Ibuprofen and Acetaminophen on Postoperative Pain and Tramadol Consumption in Laparoscopic Cholecystectomy: Prospective, Randomized, Double-blinded Clinical Trial
Background: Many techniques, including multimodal analgesia, have been used to manage postoperative pain after laparoscopic cholecystectomy (LC). Although the number of studies using intravenous ibuprofen (IV) is still limited, ibuprofen has been shown to have a potential role in managing postoperative pain. The primary outcome of this study is to evaluate and compare the impact of IV forms of ibuprofen and acetaminophen on 24-hour postoperative opioid consumption and pain management in patients undergoing LC. The second outcome of the study is to evaluate the impact of ibuprofen and acetaminophen on opioid-related adverse events (ORAE). Materials and Methods: This study was a prospective, randomized, double-blind clinical trial. Following ethical committee approval, 70 patients aged 18 to 65, American Society of Anesthesiology (ASA) score I- II, and those scheduled for LC were enrolled in the study. Patients were randomly divided into two groups. The control group (n=35) received 800 mg IV ibuprofen (group I) in 100 mL saline during surgery, while the acetaminophen group (n=35) received 1000 mg (group A). In the postoperative period, all patients received a patient-controlled analgesia (PCA) device with tramadol. The PCA device was set to a bolus dose of 10 mg and had a lockout time of 15 minutes. A blinded pain nurse assessed postoperative analgesia at 1, 2, 4, 6, 12, and 24 hours using a numerical rating scale (NRS). The incidence of postoperative nausea and vomiting (PONV), total tramadol consumption, and the need for additional analgesics during the 24-hour postoperative period were recorded. Results: Seventy patients who underwent LC participated in this study. The use of analgesic medications was statistically lower in group I than in the other group A. NRS scores between the IV ibuprofen and acetaminophen groups were statistically similar at 1, 2, 4, 6, 12, and 24 hours postoperatively (P>0.05). 24-hour opioid consumption was statistically significantly higher in group A than in group I (P0.05). PONV rates were similar in the ibuprofen and acetaminophen groups (P>0.05). ORAEs were similar between groups. Conclusion: Ibuprofen as part of tramadol-based multimodal analgesia reduced tramadol consumption compared to acetaminophen during the first 24 hours postoperatively following elective LC surgery. The IV ibuprofen-tramadol combination appeared superior to an acetaminophen-tramadol combination. ORAEs were similar in both groups.
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