Efficacy and Safety of Different Preemptive Analgesia Measures in Pain Management after Laparoscopic Cholecystectomy: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Pain and Therapy Pub Date : 2024-12-01 Epub Date: 2024-09-03 DOI:10.1007/s40122-024-00647-w
Lu Cao, Tongfei Yang, Yajing Hou, Suyun Yong, Nan Zhou
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引用次数: 0

Abstract

Introduction: The purpose of this systematic review and network meta-analysis was to evaluate the efficacy and safety of different preemptive analgesia measures given before laparoscopic cholecystectomy (LC) for postoperative pain in patients.

Methods: We conducted a comprehensive search in databases including PubMed, Web of Science, Embase, and the Cochrane Library up to March 2024, and collected relevant research data on the 26 preemptive analgesia measures defined in this article in LC surgery. Outcomes included postoperative Visual Analogue Scores (VAS) at different times (2, 6, 12, and 24 h), opioid consumption within 24 h post-operation, time to first rescue analgesia, incidence of postoperative nausea and vomiting (PONV), and incidence of postoperative headache or dizziness.

Results: Forty-nine articles involving 5987 patients were included. The network meta-analysis revealed that multimodal analgesia, nerve blocks, pregabalin, and gabapentin significantly reduced postoperative pain scores at all postoperative time points and postoperative opioid consumption compared to placebo. Tramadol, pregabalin, and gabapentin significantly extended the time to first rescue analgesia. Ibuprofen was the best intervention for reducing PONV incidence. Tramadol significantly reduced the incidence of postoperative headache or dizziness. Subgroup analysis of different doses of pregabalin and gabapentin showed that compared to placebo, pregabalin (300 mg, 150 mg) and gabapentin (600 mg, 300 mg, and 20 mg/kg) were all more effective without significant differences in efficacy between these doses. Higher doses increased the incidence of PONV and postoperative headache and dizziness, with gabapentin 300 mg having a lower adverse drug reaction (ADR) incidence.

Conclusions: Preemptive analgesia significantly reduced postoperative pain intensity, opioid consumption, extended the time to first rescue analgesia, and decreased the incidence of PONV and postoperative headache and dizziness. Multimodal analgesia, nerve blocks, pregabalin, and gabapentin all showed good efficacy. Gabapentin 300 mg given preoperatively significantly reduced postoperative pain and ADR incidence, recommended for preemptive analgesia in LC.

Trial registration: PROSPERO CRD42024522185.

Abstract Image

腹腔镜胆囊切除术后疼痛控制中不同抢先镇痛措施的有效性和安全性:随机对照试验的系统回顾和网络元分析》。
简介:本系统综述和网络荟萃分析的目的是评估腹腔镜胆囊切除术(LC)前给予不同抢先镇痛措施治疗患者术后疼痛的有效性和安全性:截至 2024 年 3 月,我们在 PubMed、Web of Science、Embase 和 Cochrane Library 等数据库中进行了全面检索,收集了本文定义的 26 种腹腔镜胆囊切除术术前镇痛措施的相关研究数据。结果包括术后不同时间(2、6、12和24小时)的视觉模拟评分(VAS)、术后24小时内的阿片类药物用量、首次镇痛抢救时间、术后恶心呕吐(PONV)发生率、术后头痛或头晕发生率:结果:共纳入49篇文章,涉及5987名患者。网络荟萃分析显示,与安慰剂相比,多模式镇痛、神经阻滞、普瑞巴林和加巴喷丁能显著降低术后所有时间点的疼痛评分和术后阿片类药物的消耗量。曲马多、普瑞巴林和加巴喷丁明显延长了首次抢救性镇痛的时间。布洛芬是降低 PONV 发生率的最佳干预措施。曲马多可明显降低术后头痛或头晕的发生率。对不同剂量的普瑞巴林和加巴喷丁进行的亚组分析表明,与安慰剂相比,普瑞巴林(300 毫克、150 毫克)和加巴喷丁(600 毫克、300 毫克和 20 毫克/千克)都更有效,但不同剂量之间的疗效无明显差异。高剂量增加了PONV以及术后头痛和头晕的发生率,而加巴喷丁300毫克的药物不良反应(ADR)发生率较低:结论:抢先镇痛可明显降低术后疼痛强度和阿片类药物的用量,延长首次抢救性镇痛的时间,并降低 PONV 以及术后头痛和头晕的发生率。多模式镇痛、神经阻滞、普瑞巴林和加巴喷丁均显示出良好的疗效。术前服用加巴喷丁 300 毫克可显著减少术后疼痛和 ADR 发生率,建议在 LC 中用于术前镇痛:试验注册:PREMCO CRD42024522185。
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来源期刊
Pain and Therapy
Pain and Therapy CLINICAL NEUROLOGY-
CiteScore
6.60
自引率
5.00%
发文量
110
审稿时长
6 weeks
期刊介绍: Pain and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of pain therapies and pain-related devices. Studies relating to diagnosis, pharmacoeconomics, public health, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, acute pain, cancer pain, chronic pain, headache and migraine, neuropathic pain, opioids, palliative care and pain ethics, peri- and post-operative pain as well as rheumatic pain and fibromyalgia. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports, trial protocols, short communications such as commentaries and editorials, and letters. The journal is read by a global audience and receives submissions from around the world. Pain and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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