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[绝经后骨质疏松症慢性脊柱疼痛的治疗经验]

[Treatment experience with chronic spinal pain in involutional osteoporosis].

作者信息

Passeri M, Baroni M C, Pedrazzoni M, Vescovi P P

机构信息

Istituto di Clinica Medica Generale e Terapia Medica, Universitá degli Studi di Parma.

出版信息

Ann Ital Med Int. 1992 Jul-Sep;7(3 Suppl):137S-153S.

PMID:1297392
Abstract

The back pain syndrome which accompanies involutional osteoporosis presents a marked heterogeneity. Acute pain may be due to vertebral fractures, whereas chronic pain may eventually accompany established osteoporosis in which clinical and instrumental evidence are present. Back pain is the consequence of the mechanical (internal or external pressure) or chemical stimulation of pain receptors present in bone tissue, along the vessels, in cartilage, joints, disk, ligaments, and also in soft tissue and muscle (with secondary antalgic contracture). The compression of spinal nerves may contribute to the pain as well. An evident alteration of mood is usually present and represents an important element in the syndrome. This phenomenon interferes with the evolution of pain, in particular as regards its intensity. Besides scales for the evaluation of pain and inability, it is possible to check objective data by means of particular algometers (not easy to employ) or by electromyographic measurements of antalgic secondary contracture of spinal muscle. Gait examination (basography) of patients with painful hip prosthesis may provide objective evaluation regarding specific antalgic activity on bone of drugs. Usually the effective drugs for osteoporosis possess antalgic properties as well, with different mechanisms of action. Three drugs with evident activity are taken into consideration: calcitonin, ipriflavon, aminobutane-bisphosphonate (alendronate). Though each of them possesses some particular activity, the main mechanism of action is dependent on their effect on the local microenvironment, particularly at the level of bone tissue (calcium, cytokine and prostaglandin local concentration), on the modulation of osteoclast activity. In particular alendronate (intermittently administered intravenously) exerts the most evident antalgic activity. Subjective chronic back pain relief is accompanied by (secondary) reduction of antalgic contracture at vertebral muscle level. The activity of the substance against the painful hip prosthesis (documented by basographic gait recording) leads us to conclude that the substance really exerts a direct antalgic action at the level of bone tissue.

摘要

与更年期骨质疏松症相伴的背痛综合征具有显著的异质性。急性疼痛可能是由椎体骨折引起的,而慢性疼痛最终可能伴随已确诊的骨质疏松症出现,此时存在临床和影像学证据。背痛是骨组织、血管、软骨、关节、椎间盘、韧带以及软组织和肌肉(伴有继发性止痛性挛缩)中存在的疼痛感受器受到机械性(内部或外部压力)或化学性刺激的结果。脊神经受压也可能导致疼痛。通常会出现明显的情绪改变,这是该综合征的一个重要因素。这种现象会干扰疼痛的演变,尤其是在疼痛强度方面。除了用于评估疼痛和功能障碍的量表外,还可以通过特殊的痛觉计(使用起来不容易)或通过对脊柱肌肉继发性止痛性挛缩进行肌电图测量来检查客观数据。对疼痛性髋关节假体患者进行步态检查(足底压力测定)可以提供关于药物对骨骼特定止痛活性的客观评估。通常用于治疗骨质疏松症的有效药物也具有止痛特性,但其作用机制不同。考虑三种具有明显活性的药物:降钙素、依普黄酮、氨基丁烷双膦酸盐(阿仑膦酸盐)。尽管它们各自具有一些特殊活性,但其主要作用机制取决于它们对局部微环境的影响,特别是在骨组织水平(钙、细胞因子和前列腺素的局部浓度),以及对破骨细胞活性的调节。特别是阿仑膦酸盐(间歇性静脉给药)具有最明显的止痛活性。主观上慢性背痛缓解的同时,椎体肌肉水平的止痛性挛缩也会(继发性)减轻。该物质对疼痛性髋关节假体的活性(通过足底压力步态记录证明)使我们得出结论,该物质确实在骨组织水平发挥直接的止痛作用。

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