彭阻滞治疗髋部发育不良患儿围手术期镇痛的疗效和安全性:一项随机、双盲、非劣效性试验的研究方案

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-01-18 DOI:10.1186/s13063-025-08725-w
Mingzhe Xu, Yi He, Zhi Li, Bin Du
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引用次数: 0

摘要

背景:手术干预是治疗儿童髋关节发育不良的关键。围手术期镇痛,通常基于高阿片类药物剂量,经常用于这些患者。在某些情况下,区域麻醉程序,如尾侧阻滞和腰丛阻滞也被使用。先前的研究表明,在成人髋关节开放性手术中,囊周神经群阻滞(PENG)具有良好的麻醉效果。彭阻滞被认为提供与尾侧阻滞相似的镇痛效果。方法:本研究是一项单中心、前瞻性、随机、双盲、非劣效性实验,纳入6个月至7岁的儿童,这些儿童计划接受发育性发育不良髋关节手术。在全身麻醉和局部阻滞(0.25%罗哌卡因,剂量为2.5 mg·kg-1,肾上腺素浓度为1:20万)后,48名患者将被随机分配到彭组或尾侧组。主要观察指标是术后24小时内FLACC(面部、腿部、活动、哭泣、安慰)得分最高。次要结局包括术中阿片类药物用量、手术24小时内镇痛剂量、开始抢救镇痛的时间、PCA泵激活次数、移除SLIPA(咽气道流线型衬垫)的时间、局部阻断手术的持续时间、不良事件发生率、血浆罗哌卡因浓度、住院时间和费用。所有数据将由盲法调查人员收集。试验的最终结果将发表在同行评议的科学杂志上。讨论:我们希望这项试验能够提供一些证据,证明PENG阻滞对于接受开放髋关节手术的儿科患者围手术期镇痛是安全有效的。试验注册:中国临床试验注册中心ChiCTR2100053128。于2021年11月12日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of perioperative analgesia in PENG block for children undergoing hip surgery with developmental dysplasia: study protocol for a randomized, double-blinded, non-inferiority trial.

Background: Surgical intervention is critical in the treatment of hip developmental dysplasia in children. Perioperative analgesia, usually based on high opioid dosages, is frequently used in these patients. In some circumstances, regional anesthetic procedures such as caudal block and lumbar plexus block have also been used. Previous research has shown that pericapsular nerve group (PENG) block provides excellent anesthetic efficacy during open hip surgery in adults. PENG block is thought to provide a similar analgesia effect comparable to caudal block.

Methods: This study is a single-center, prospective, randomized, double-blinded, non-inferiority experiment that enrolled children aged 6 months to 7 years who were scheduled for developmental dysplasia hip surgery. Following general anesthesia and regional blocks (0.25% ropivacaine at a dose of 2.5 mg·kg-1 with epinephrine at a concentration of 1:200,000), 48 individuals will be randomly assigned to either the PENG or caudal groups. The primary outcome measure is the highest FLACC (face, legs, activity, crying, consolability) score achieved within 24 h of surgery. Secondary outcomes include intraoperative opioid consumption, analgesic dosage within 24 h of surgery, time to start rescue analgesia, number of PCA pump activations, time to remove SLIPA (streamlined liner of the pharynx airway), duration of regional block procedures, incidence of adverse events, plasma ropivacaine concentrations, and hospital stays and costs. All data will be collected by blinded investigators. The trial's final results will be published in a peer-reviewed scientific journal.

Discussion: We expect this trial to provide some evidences that PENG block is safe and effective for perioperative analgesia in pediatric patients undergoing open hip surgery.

Trial registration: Chinese Clinical Trial Registry ChiCTR2100053128. Registered on November 12, 2021.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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