腹直肌鞘输注芬太尼-左布比卡因与胸腔硬膜外输注芬太尼-左布比卡因在腹部大切口腹部肿瘤手术中的围手术期比较

Doaa Abd Eltwab M Tueki, I. Ibrahim, Alaa Ali M. Elzohry
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Methods: This randomized, blinded, was registered at www.clinicaltrials.gov at no.: “NCT03460561” and was approved by local ethics committee of South Egypt Cancer Institute, Assiut University, Egypt. One hundred adult patients, (ASA grade II and III), scheduled for major elective abdominal cancer surgery with Medline incision, were randomly divided into two groups, (50 patients each); TEA group: patients in this group received TEA with standard GA and intra-operative analgesia was started before skin incision by injecting epidural bolus dose of 0.1 ml/kg of (0.125% levo-bupivacaine+fentanyl 2 μg/ml). Postoperative analgesia was provided through PCEA by injecting a bolus dose of 3 ml then continuous infusion of 0.1 ml/kg of mixture of (0.0625% levo-bupivacaine+fentanyl 2 μg/ml) for 48 hours postoperative. RSB group: patients in this group received standard GA plus ultrasound (U/S) guided rectus sheath block by a volume of 20 mL of (0.25% levo-bupivacaine+fentanyl 30 μg) in saline on either side. Before end of surgery and before closure of abdominal wall, bilateral surgically placed catheters in rectus sheath plane aiming to provide post-operative analgesia using the following; 20 mL of (0.125% levo-bupivicaine+Fentanyl 30 μg) every 12 hours in to each catheter for 48 hours. Perioperative hemodynamics (MAP and HR) were recorded. Postoperative pain was assessed over 48 hour post operatively using (VAS). Total fentanyl consumption, Peak expiratory flow rate (PEFR), postoperative and side effects of the drugs and duration of ICU and hospital stay were recorded. Results: We found a significant reduction in VAS pain scores (at rest and during cough) in both group at all postoperative period but fentanyl consumption was significantly lower in TEA group. 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引用次数: 6

摘要

背景与目的:大量的研究、系统综述和荟萃分析证明,胸椎硬膜外镇痛(TEA)是腹部大手术术后急性疼痛管理的金标准。然而,TEA有时是禁忌的,可能会导致严重的风险。直肌鞘阻滞术(Rectus Sheath Block, RSB)对于腹部中线切口的腹部手术是有效的,因为局麻药会在双侧后直肌鞘内注射,从而缓解从剑突到耻骨联合的中前壁的剧烈疼痛。该研究的目的是评估选择性腹部大癌手术中线切口患者术中和术后RSB与术中和术后TEA的对比。方法:随机、盲法,在www.clinicaltrials.gov注册,编号:。编号:NCT03460561,经埃及Assiut大学南埃及癌症研究所当地伦理委员会批准。100例ASA分级为II级和III级,计划行Medline切口腹部肿瘤大选择性手术的成年患者随机分为两组,每组50例;TEA组:该组患者在标准GA的基础上进行TEA治疗,术中于皮肤切口前开始术中镇痛,硬膜外注射剂量为0.1 ml/kg(0.125%左布比卡因+芬太尼2 μg/ml)。术后经PCEA先给药3 ml,再连续输注(0.0625%左布比卡因+芬太尼2 μg/ml)混合物0.1 ml/kg,持续48 h。RSB组:该组患者接受标准GA +超声(U/S)引导下的直肌鞘阻滞,两侧生理盐水中体积为20ml(0.25%左布比卡因+芬太尼30 μg)。手术结束前和关闭腹壁前,双侧手术置管于直肌鞘平面,目的是通过以下方式提供术后镇痛:每12小时滴入20ml(0.125%左布比卡因+芬太尼30 μg),连续48小时。记录围手术期血流动力学(MAP、HR)。术后48小时用VAS评估疼痛。记录芬太尼总用量、呼气峰流速(PEFR)、术后药物不良反应、ICU和住院时间。结果:我们发现两组患者术后所有时间的VAS疼痛评分(休息时和咳嗽时)均显著降低,但TEA组芬太尼用量显著降低。我们还发现,与RSB组相比,TEA组术中血流动力学(平均动脉压和心率)显著降低,而术后MAP和心率的统计学意义最小。两组的其他术后并发症如镇静、恶心和呕吐的发生率相当。结论:在减轻腹部肿瘤手术后疼痛强度方面,直肌鞘阻滞不逊于胸段硬膜外镇痛,并与术后48小时血流动力学稳定性相关,无手术相关不良事件或PEFR降低。
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Peri-operative Rectus Sheath Fentanyl-levobupivacaine Infusion vs. Thoracic Epidural Fentanyl Levobupvacaine Infusion in Patients Undergoing Major Abdominal Cancer Surgeries with Medline Incision
Background and Objectives: The gold standard for acute postoperative pain management in major abdominal surgeries is thoracic epidural analgesia (TEA) and this was proved by a lot of studies, systematic reviews and metaanalyses. However, TEA is sometimes contraindicated and may cause serious risks. Rectus Sheath Block (RSB) is effective for the abdominal surgeries with midline abdominal incisions as local anesthetics will be injected within the posterior rectus sheath bilaterally leading to intense pain relief for the middle anterior wall extending from the xiphoid process to the symphysis pubis. The aim of the study was to assess intra and post-operative RSB versus intra and post-operative TEA, in patients undergoing elective major abdominal cancer surgery with midline incisions. Methods: This randomized, blinded, was registered at www.clinicaltrials.gov at no.: “NCT03460561” and was approved by local ethics committee of South Egypt Cancer Institute, Assiut University, Egypt. One hundred adult patients, (ASA grade II and III), scheduled for major elective abdominal cancer surgery with Medline incision, were randomly divided into two groups, (50 patients each); TEA group: patients in this group received TEA with standard GA and intra-operative analgesia was started before skin incision by injecting epidural bolus dose of 0.1 ml/kg of (0.125% levo-bupivacaine+fentanyl 2 μg/ml). Postoperative analgesia was provided through PCEA by injecting a bolus dose of 3 ml then continuous infusion of 0.1 ml/kg of mixture of (0.0625% levo-bupivacaine+fentanyl 2 μg/ml) for 48 hours postoperative. RSB group: patients in this group received standard GA plus ultrasound (U/S) guided rectus sheath block by a volume of 20 mL of (0.25% levo-bupivacaine+fentanyl 30 μg) in saline on either side. Before end of surgery and before closure of abdominal wall, bilateral surgically placed catheters in rectus sheath plane aiming to provide post-operative analgesia using the following; 20 mL of (0.125% levo-bupivicaine+Fentanyl 30 μg) every 12 hours in to each catheter for 48 hours. Perioperative hemodynamics (MAP and HR) were recorded. Postoperative pain was assessed over 48 hour post operatively using (VAS). Total fentanyl consumption, Peak expiratory flow rate (PEFR), postoperative and side effects of the drugs and duration of ICU and hospital stay were recorded. Results: We found a significant reduction in VAS pain scores (at rest and during cough) in both group at all postoperative period but fentanyl consumption was significantly lower in TEA group. Also we found a significant reduction in intra-operative hemodynamics (mean arterial pressure and heart rate) in TEA group in comparison to RSB group while there was minimal statistically significant reduction in postoperative MAP and heart rate. The incidence of other postoperative complications such as sedation, nausea and vomiting were comparable in both groups. Conclusion: Rectus sheath block was not inferior to thoracic epidural analgesia in reduction of pain intensity after major abdominal cancer surgeries, and associated with hemodynamic stability along the 48 hours postoperative without procedure related adverse events or decreasing PEFR.
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