竖脊平面阻滞与椎旁阻滞用于乳腺癌术后镇痛的疗效比较

Arjun Singh, Nidhi Agrawal, Udismita Baruah, Surabhi Sandill
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引用次数: 0

摘要

背景:接受改良根治性乳房切除术(MRM)的患者会经历急性疼痛。术后急性疼痛控制不充分可能导致焦虑、血流动力学失衡和慢性疼痛综合征的发展。因此,镇痛是非常重要的有利结果。本研究旨在比较超声引导胸椎旁阻滞(TPVB)与超声引导胸椎竖脊平面阻滞(ESPB)联合可乐定局部麻醉对改良乳房根治术术后镇痛的效果。方法:本前瞻性随机介入性对照试验在某三级护理教学医院进行为期18个月的60例乳腺癌改良根治术患者。60例乳腺癌患者在全身麻醉下接受磁共振成像。患者被随机分为两组。E组在超声引导下行竖肌脊柱阻滞,P组在第4胸椎(T4)水平行椎旁阻滞。两组患者均给予0.5%罗哌卡因21 mL和1 μg/kg可乐定稀释于1 mL生理盐水中(使总容积达22 mL)。主要观察指标为镇痛持续时间的比较,即从阻断给药时间到患者第一次需要镇痛的时间。次要观察指标为静息时和不同时间点同侧臂外展时的平均视觉模拟评分(VAS),术后24小时内芬太尼和曲马多的总需求量;术后恶心呕吐;术后24小时患者满意度。统计学方法:定量变量比较采用独立t检验/Mann-Whitney检验(当数据集非正态分布时)。质变量比较采用卡方检验/Fisher精确检验。p值<0.05认为有统计学意义。结果:两个研究组的镇痛持续时间,即从阻滞给药到第一次抢救镇痛的时间具有可比性。E组镇痛时间平均(SD)为22.78(3.31)小时,P组为22.88(3.34)小时(P = 0.914)。两组在芬太尼需用量和总24小时曲马多需用量方面具有可比性,其他参数如术后恶心呕吐、对血流动力学的影响和患者总体满意度也具有可比性。结论:超声引导下ESPB和TPVB对改良乳房根治术患者术后镇痛效果相同。
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Comparison of Efficacy of Erector Spinae Plane Block with Paravertebral Block for Postoperative Analgesia in Patients Undergoing Breast Cancer Surgery
Background: Patients undergoing modified radical mastectomy (MRM) experience acute pain. Inadequate acute postoperative pain control may lead to anxiety, hemodynamic imbalance and development of chronic pain syndrome. Hence analgesia is extremely important for favourable outcome. This study was undertaken to compare the efficacy of ultrasound guided thoracic paravertebral block (TPVB) versus ultrasound guided thoracic erector spinae plane block (ESPB) with clonidine as an adjuvant to local anaesthetic for post-operative analgesia in modified radical mastectomy. Method: This prospective randomized interventional comparative trial, involving 60 patients were undergoing modified radical mastectomy for breast cancer surgery, was conducted in a tertiary care teaching hospital over 18 months. Sixty patients undergoing MRM for breast cancer under general anaesthesia were enrolled. The patients were randomly allocated into one of the two groups. Group E received ultrasound guided erector spinae block and Group P received Paravertebral block at the level of 4th thoracic vertebra (T4). Both the groups were given 21 mL of 0.5% ropivacaine and 1 μg/kg of clonidine diluted in 1 mL of saline (making total volume of up to 22 mL). Primary outcome measure was to compare duration of analgesia, that is from the time of block administration till the time to first rescue analgesia demanded by the patients. Secondary outcome measures were mean visual analogue scale (VAS) score at rest as well as during abduction of ipsilateral arm at various time points, total intraoperative fentanyl and tramadol requirement up to 24 hours postoperatively; postoperative nausea and vomiting; patients satisfaction at the end of 24 hours postoperatively. Statistical method used: Quantitative variables were compared using Independent t-test/Mann-Whitney Test (when the data sets were not normally distributed). Qualitative variables were compared using Chi-Square test /Fisher’s exact test.A p value of <0.05 was considered statistically significant. Results: Duration of analgesi, that is, time of first rescue analgesia from the administration of the block was comparable between the two study groups. The mean (SD) duration of analgesia in group E was 22.78 (3.31) hours and in group P was 22.88 (3.34) hours (P = 0.914). Both the groups were comparable in terms of fentanyl requirement and total 24 hours tramadol requirement Other parameters like postoperative nausea vomiting, effect on hemodynamic and overall patient satisfaction were also comparable between the two groups. Conclusions: Both ultrasound guided ESPB and TPVB are equally efficacious in providing postoperative analgesia in patients undergoing modified radical mastectomy.
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