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Efficacy of stellate ganglion blockade for the management of type 1 complex regional pain syndrome.

机译:星状神经节阻滞治疗1型复杂区域性疼痛综合征的疗效。

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INTRODUCTION: The purpose of this study was to examine the efficacy of stellate ganglion blockade (SGB) in patients with complex regional pain syndromes (CRPS I) of their hands. METHODS: After IRB approval and patient informed consent, 25 subjects, with a clinical diagnosis of CRPS I of one hand as defined by the International Association for the Study of Pain (IASP) criteria, had three SGB's performed at weekly intervals. Laser Doppler fluxmetric hand perfusion studies were performed on the normal and CRPS I hands pre- and post-SGB therapy. No patient was included in this study if they used tobacco products or any medication or substance that could affect sympathetic function. The appropriate parametric and nonparametric data analyses were performed and a p value <0.05 was used to reject the null hypothesis. RESULTS: Symptom onset of CRPS I until the initiation of SGB therapy ranged between 3 to 34 weeks. Following the SGB series, patient pain relief was as follows: group I, 10/25 (40%) had complete symptom relief; group II, 9/25 (36%) had partial relief and group III, 6/25 (24%) had no relief. The duration of symptoms until SGB therapy was: group I, 4.6 +/- 1.8 weeks, group II, 11.9 +/- 1.6 weeks and group III, 35.8 +/- 27 weeks. Compared with the normal control hand, the skin perfusion in the CRPS I affected hand was greater in group I and decreased in groups II and III. DISCUSSION: The results of our study demonstrate that an inverse relationship exists between hand perfusion and the duration of symptoms of CRPS I. On the other hand, a positive correlation exists between SGB efficacy and how soon SGB therapy is initiated. A duration of symptoms greater than 16 weeks before the initial SGB and/or a decrease in skin perfusion of 22% between the normal and affected hands adversely affects the efficacy of SGB therapy.
机译:简介:这项研究的目的是检查星状神经节阻滞(SGB)在手部复杂区域疼痛综合征(CRPS I)患者中的疗效。方法:经IRB批准并征得患者知情同意后,按照国际疼痛研究协会(IASP)标准的定义,对25例具有单手CRPS I临床诊断的受试者,每周进行3次SGB检查。在SGB治疗之前和之后,对正常手和CRPS I手进行了激光多普勒流量手灌注研究。如果他们使用过烟草产品或任何可能影响交感神经功能的药物或物质,则该研究未包括任何患者。进行了适当的参数和非参数数据分析,并使用p值<0.05来拒绝原假设。结果:开始SGB治疗之前,CRPS I的症状发作时间为3至34周。在SGB系列之后,患者的疼痛缓解如下:I组10/25(40%)完全缓解了症状;第二组9/25(36%)有部分缓解,第三组6/25(24%)没有缓解。直到进行SGB治疗的症状持续时间为:I组,4.6 +/- 1.8周,II组,11.9 +/- 1.6周,III组,35.8 +/- 27周。与正常对照组相比,CRPS I感染手的皮肤灌注在I组中更大,而在II和III组中则下降。讨论:我们的研究结果表明,手部灌注与CRPS I症状的持续时间之间存在反比关系。另一方面,SGB疗效与SGB治疗开始时间之间存在正相关。症状持续时间超过初始SGB之前的16周和/或正常手和患病手之间的皮肤灌注减少22%会对SGB治疗的疗效产生不利影响。

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