Weissenberg W
Institut für Anaesthesiologie, Klinikum Minden.
Reg Anaesth. 1987 Jul;10(3):96-103.
Blocking of sympathetic conduction aims at permanent or temporary elimination of those pain pathways conducted by the sympathetic nervous system. In order to provide an objective evaluation of sufficient blocking effect, earlier inquiries referred to parameters such as: (1) observation of clinical signs such as Horner's syndrome, Guttman's sign, anhidrosis, extended venous filling; (2) difference in skin temperature of at least 1.5 degrees C between blocked and unblocked side; (3) increase in amplitude of the pulse wave; and (4) depression of the psychogalvanic reflex (PGR) on the blocked side (Fig. 1). In clinical practice, these control parameters are effective because they are time-saving, technically simple, and highly evidential. Further parameters for evaluating sympathetic blockade are examination of hydrosis by means of color indicators such as bromocresol and ninhydrin, oscillometry, and plethysmography. The effectiveness of sympathetic blockade after stellate ganglion and sympathetic trunk blocks has been verified by various authors. In a clinical study, 16 patients were divided into four groups in order to test the effectiveness of sympathetic blockade after spinal anesthesia with 3 ml 0.75% bupivacaine (group I) and 4 ml 0.75% bupivacaine (group II) and after peridural anesthesia with 15 ml 0.75% bupivacaine (group III) and 20 ml 0.75% bupivacaine (group IV) by means of temperature difference, response of pulse wave amplitude and PGR between blocked lower and unblocked upper extremity, and sensory levels of block. The patients were classified as ASA I and II; their ages varied from 20 to 63 years.(ABSTRACT TRUNCATED AT 250 WORDS)
交感神经传导阻滞旨在永久或暂时消除由交感神经系统传导的那些疼痛通路。为了对充分的阻滞效果进行客观评估,早期的研究涉及以下参数:(1)观察临床体征,如霍纳综合征、古特曼征、无汗、静脉充盈延长;(2)阻滞侧与未阻滞侧皮肤温度相差至少1.5摄氏度;(3)脉搏波振幅增加;(4)阻滞侧精神电反射(PGR)降低(图1)。在临床实践中,这些对照参数是有效的,因为它们省时、技术简单且证据充分。评估交感神经阻滞的其他参数包括通过溴甲酚和茚三酮等颜色指示剂检查出汗情况、示波法和体积描记法。不同作者已证实星状神经节和交感干阻滞后交感神经阻滞的有效性。在一项临床研究中,16例患者被分为四组,以便通过阻滞侧下肢与未阻滞侧上肢之间的温差、脉搏波振幅反应和PGR以及感觉阻滞平面,测试0.75%布比卡因3毫升脊髓麻醉后(第一组)、0.75%布比卡因4毫升脊髓麻醉后(第二组)、0.75%布比卡因15毫升硬膜外麻醉后(第三组)和0.75%布比卡因20毫升硬膜外麻醉后(第四组)交感神经阻滞的有效性。患者被分类为ASA I和II级;年龄在20至63岁之间。(摘要截断于250字)