超声引导下星状神经节阻滞治疗上肢幻肢痛--一个病例系列

Sonal Goyal, Ajit Kumar, Manasa Kantha, Ravi Shankar Sharma, Sanjay Agrawal, Girish K. Singh
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引用次数: 0

摘要

星状神经节阻滞(SGB)可有效治疗头颈部和上肢各种交感神经介导的疼痛,如复杂性区域疼痛综合征、带状疱疹后神经痛等,但很少有证据表明星状神经节阻滞可用于治疗幻肢痛(PLP)。 十名上肢幻肢痛患者接受了超声引导下的 SGB 阻滞治疗。在针尖实时可视的情况下,确保抽吸阴性后,注射 5 毫升 1%木质素卡因和 4 毫克地塞米松。记录术后疼痛评分(数字评分量表[NRS])和患者满意度评分(李克特量表),并在接下来的 60 天内对患者进行随访。 基线 NRS 评分(平均值[标准差])为 7.8 (0.748),注射后立即降至 2.8 (0.748)(P < 0.001),第 7 天降至 2.6 (0.663),第 30 天降至 2.9 [0.7],第 60 天降至 30.775。大多数患者(80%-90%)在所有随访间隔期都对治疗反应(李克特量表评分 4-5 分)比较满意或非常满意。只有两名患者出现了声音嘶哑的轻微和短暂的不良反应。 在 2 个月的随访期间,超声引导 SGB 能有效减轻截瘫后患者的疼痛,并提高患者的满意度。要提供更具体的证据,还需要更多样本量、更长时间的前瞻性随机对照试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrasound-guided Stellate Ganglion Block for Upper Extremity Phantom Limb Pain - A Case Series
Stellate ganglion block (SGB) is effectively utilized in various sympathetically mediated pain conditions of head and neck, upper limb such as complex regional pain syndrome, postherpetic neuralgias, but there has been a paucity of evidence of SGB for the management of phantom limb pain (PLP). Ten upper extremity PLP patients underwent ultrasound-guided SGB block. Under real-time needle tip visualization and after ensuring negative aspiration, 5 mL of 1% lignocaine and 4 mg of dexamethasone were injected. Postprocedure pain score (numerical rating scale [NRS]) and patient satisfaction score (Likert scale) were noted, and patients were followed-up for the next 60 days. The baseline NRS score (Mean [standard deviation]) of 7.8 (0.748) showed significant reduction (P < 0.001) to 2.8 (0.748) at immediate postinjection, to 2.6 (0.663) at day 7, at day 30 (2.9 [0.7]), and at day 60 (30.775). Most of the patients (80%–90%) were somewhat to very much satisfied with the treatment response (score 4–5 on Likert scale) at all the follow-up intervals. Only mild and transient adverse events were demonstrated in two patients who developed hoarseness of voice. Ultrasound-guided SGB effectively reduces pain and improves patient satisfaction in postamputee patients who developed PLP, over 2 months of the follow-up period. Further prospective randomized controlled trials over a larger duration with more sample size are needed to provide more concrete evidence.
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