Pv Mukundan Prasobh, Rajendran Kavya, Saxena Tripti, Vs Vinayakumar
Critical Care, Epsom and St Helier University Hospitals, London, GBR.
General Medicine, Epsom and St Helier University Hospitals, London, GBR.
Cureus. 2025 Mar 14;17(3):e80564. doi: 10.7759/cureus.80564. eCollection 2025 Mar.
Background Supraclavicular brachial plexus block (SCBPB) is a widely used regional anesthesia technique for upper limb surgeries. Intravenous dexamethasone is known to prolong postoperative analgesia, but the optimal dose remains uncertain due to potential side effects like hyperglycemia associated with high doses. This study compares the efficacy of different doses of intravenous dexamethasone in enhancing the duration of analgesia following a single-shot ultrasound-guided SCBPB. Methods This prospective, randomized study included 60 American Society of Anesthesiologists (ASA) grade I-III patients undergoing upper limb surgery. All patients received an ultrasound-guided SCBPB, followed by general anesthesia (GA) and were randomly allocated into four groups using computer-generated randomization: group 1: 0.5% levobupivacaine (20 ml) + 8 mg IV dexamethasone; group 2: 0.5% levobupivacaine (20 ml) + 4 mg IV dexamethasone; group 3: 0.5% levobupivacaine (20 ml) + 2 mg IV dexamethasone; group 4 (control): 0.5% levobupivacaine (20 ml) + IV 0.9% normal saline. Postoperative pain scores (visual analog scale, VAS), duration of analgesia, rescue analgesic requirement, incidence of nausea/vomiting, and blood glucose levels were recorded over 24 hours. Statistical analysis was performed using analysis of variance (ANOVA) and chi-square tests. Results Patients who received IV dexamethasone showed significantly prolonged analgesia compared to the control group (p < 0.001). The duration of analgesia in the 8 mg group was 13.8 ± 1.5 hours, compared to 11.2 ± 1.3 hours (4 mg), 9.4 ± 1.2 hours (2 mg), and 6.8 ± 1.1 hours in the control group. This represents a 103% increase in analgesia duration with 8 mg dexamethasone compared to the control. The incidence of postoperative nausea and vomiting (PONV) was lower in dexamethasone groups (p = 0.02). However, 8 mg dexamethasone was associated with transient hyperglycemia (p = 0.04), with blood glucose levels peaking at 185 ± 12 mg/dL compared to 145 ± 10 mg/dL in the control group. Conclusion Intravenous dexamethasone significantly prolongs analgesia following SCBPB, with 8 mg providing the longest duration (103% increase vs. control). However, 4 mg may offer a balance between efficacy and minimal side effects, particularly in avoiding postoperative hyperglycemia.
锁骨上臂丛神经阻滞(SCBPB)是上肢手术中广泛应用的区域麻醉技术。已知静脉注射地塞米松可延长术后镇痛时间,但由于高剂量可能导致如高血糖等潜在副作用,最佳剂量仍不确定。本研究比较不同剂量静脉注射地塞米松在单次超声引导下SCBPB后增强镇痛持续时间的效果。
这项前瞻性、随机研究纳入了60例接受上肢手术的美国麻醉医师协会(ASA)I - III级患者。所有患者均接受超声引导下的SCBPB,随后接受全身麻醉(GA),并使用计算机生成的随机数将其随机分为四组:第1组:0.5%左旋布比卡因(20 ml)+ 8 mg静脉注射地塞米松;第2组:0.5%左旋布比卡因(20 ml)+ 4 mg静脉注射地塞米松;第3组:0.5%左旋布比卡因(20 ml)+ 2 mg静脉注射地塞米松;第4组(对照组):0.5%左旋布比卡因(20 ml)+静脉注射0.9%生理盐水。记录术后24小时的疼痛评分(视觉模拟评分法,VAS)、镇痛持续时间、补救性镇痛需求、恶心/呕吐发生率和血糖水平。采用方差分析(ANOVA)和卡方检验进行统计分析。
与对照组相比,接受静脉注射地塞米松的患者镇痛时间显著延长(p < 0.001)。8 mg组的镇痛持续时间为13.8 ± 1.5小时,而4 mg组为11.2 ± 1.3小时,2 mg组为9.4 ± 1.2小时,对照组为6.8 ± 1.1小时。与对照组相比,8 mg地塞米松使镇痛持续时间增加了103%。地塞米松组术后恶心呕吐(PONV)的发生率较低(p = 0.02)。然而,8 mg地塞米松与短暂性高血糖有关(p = 0.04),血糖水平峰值为185 ± 12 mg/dL,而对照组为145 ± 10 mg/dL。
静脉注射地塞米松可显著延长SCBPB后的镇痛时间,8 mg剂量提供最长的镇痛持续时间(比对照组增加103%)。然而,4 mg可能在疗效和最小副作用之间提供平衡,特别是在避免术后高血糖方面。