疼痛及其管理

Roger McFadden
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引用次数: 0

摘要

1987年5月7日,在哈罗盖特举行了“风湿病治疗的生长点”系列会议的第八届年度会议,主题是“疼痛及其管理”。90名观众由风湿病学家、负责疼痛诊所的麻醉师、行业代表和对疼痛控制感兴趣的辅助医疗专业代表组成。麻醉师对这一主题的热情与风湿病学家提交的摘要数量较少形成强烈对比。上午的会议以a Harvey博士(利兹)对疼痛的神经生理学的回顾开始。解剖在有髓鞘和无髓鞘纤维的组织学束方面被很好地定义。这种基本解剖结构可以通过神经可塑性的概念(无髓鞘C纤维激活后有关纤维连接的改变)和局部体液控制(在脊髓背角特别明显)以动态方式进行修改。神经系统在生物学上很好地适应了处理急性疼痛,但在处理慢性疼痛方面就不那么适应了。确定了干预可能针对的神经系统的不同层次。Dr J Dixon (Harrogate)回顾了各种可用于测量主观疼痛的描述性量表。新的半客观方法包括对姿态的录像记录,传统的风湿病学评估,如握力和关节压痛也反映了疼痛的因素。疼痛阈值的测量产生了一个更有限的终点,但这并不一定与受试者感知到的疼痛相同。在讨论中,大家一致认为,每日日记卡系统在规避非典型事件的特殊访问诊所方面提供了优势,并请求对适合风湿病问题的短疼痛问卷进行研究,并修改可能反映柔痛和滑膜增生的关节指数。目前尚不清楚用于风湿病学的视觉模拟量表所固有的问题是否也会在这些量表用于其他症状(如呼吸困难)时出现。三篇简短的论文提供了不同的药理学方法来控制疼痛的见解。A . Jones博士(圣巴塞洛缪医院)描述了哈默史密斯回旋加速器在人类阿片类生理研究中的工作。对一个用针刺自己的印度苦行僧的调查表明,当他不处于恍惚状态时,他对疼痛有正常的反应。高度集中状态的诱导使脑电图上的θ波活动增加(这种活动发生在睡眠期间),使他失去了正常生理反应的意识。自然产生的阿片类药物可能涉及这些药物,这些药物可能被药理学操纵。研究人员设计了一种技术,利用苯丙酚作为标记物来识别大脑中阿片结合位点浓度最高的区域。一个意想不到的发现是,这些部位的分布在睡眠期间发生了变化。H Bird博士(利兹)随后描述了两种精神药物治疗骨关节病的对照试验。由于一名药物滥用者坚持认为安非他明是唯一能完全缓解关节炎疼痛的药物,一种具有兴奋剂性质的食欲抑制剂(二乙基丙丙酮)与一种具有镇静性质的食欲抑制剂(芬氟拉明)和安慰剂在骨关节病患者中进行了比较。刺激性药物比抑制性药物更能显著缓解症状,而且这种效果与体重减轻无关。K Budd (Bradford)医生是一名麻醉师,他随后回顾了一系列新药,这些新药在麻醉师中得到了青睐,可以缓解多种疼痛。这些药物包括细胞毒性药物、抗抑郁药、儿茶酚胺拮抗剂和氨基酸,包括d -苯丙氨酸和色氨酸。最后一种药最初是作为抗抑郁药销售的。无法控制疼痛的患者有时对这些药物联合使用有反应。下午的会议以两篇关于疼痛的机械方面的论文开始。P Helliwell博士(哈罗盖特大学)使用关节成象仪测量关节僵硬度,发现只有少数关节炎患者能够区分疼痛和僵硬,这与其他作者的观点一致。用机械仪器测量的客观僵硬度并不总是与患者的主观不适感相关。客观刚度为
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Pain and its management
The eighth annual day conference in the series 'Growing points in the treatment of rheumatic diseases', which was held at Harrogate on 7 May 1987, was devoted to 'Pain and its management'. An audience of 90 was made up of rheumatologists, anaesthetists with responsibility for pain clinics, representatives from industry, and representatives of the paramedical professions that have an interest in the control of pain. The enthusiasm of anaesthetists for this topic contrasted strongly with the low number of abstracts submitted by rheumatologists. The morning session opened with a review of the neurophysiology of pain by Dr A Harvey (Leeds). Anatomy was well defined in terms of histological tracts of myelinated and unmyelinated fibres. This basic anatomy could be modified in dynamic fashion both by the concept of neuroplasticity (alteration in the connection of the fibres concerned after unmyelinated C fibre activation) and by local humoral control, which was particularly pronounced in the dorsal horn of the spinal cord. The nervous system was biologically well adapted to the handling of acute pain but less so to the handling of chronic pain. Different levels of the nervous system at which intervention might be directed were defined. Dr J Dixon (Harrogate) reviewed the various descriptive scales available for the measurement of subjective pain. Novel semiobjective methods included videotaped recording of attitude, and conventional rheumatological assessments such as grip strength and joint tenderness also reflected an element of pain. The measurement of pain threshold produced a more finite end point, but this was not necessarily the same as pain perceived by the subject. In discussion it was agreed that daily diary card systems provided advantages in circumventing the atypical event of a special visit to clinic, and a plea was made for research on short pain questionnaires that were adapted to rheumatological problems and to modified articular indices that might reflect tenderness as well as synovial proliferation. It was not clear whether the problems inherent in visual analogue scales applied to rheumatology were also experienced when these scales were used for other symptoms such as breathlessness. Three short papers offered insight into different pharmacological approaches to the control of pain. Dr A Jones (St Bartholomew's Hospital) described work performed with the Hammersmith cyclotron in the investigation of opioid physiology in man. The investigation of an Indian fakir who lanced himself with needles showed that when he was not in a trance he had a normal response to pain. The induction of a state of intense concentration produced increased theta activity on EEG (of the sort that occurs during sleep), allowing him to lose awareness of his normal physiological response. Naturally occurring opioids were implicated and these might be manipulated pharmacologically. A technique had been devised using diphenorphine as a marker to identify those areas of the brain that had the highest concentration of opioid binding sites. An unexpected finding had been the change in distribution of such sites that occurred during sleep. A controlled trial of two psychotropic agents in osteoarthrosis was then described by Dr H Bird (Leeds). Prompted by the insistence of a drug abuser that amphetamines were the only drugs that completely relieved arthritic pain, an appetite suppressant with stimulant properties (diethylpropion) had been compared with an appetite suppressant with sedative properties (fenfluramine) and placebo in patients with osteoarthrosis. The stimulant drug relieved symptoms significantly more than the depressant drug, and this effect was independent of weight loss. Dr K Budd (Bradford), an anaesthetist, then reviewed a selection of novel drugs that had found favour with anaesthetists in the relief of many sorts of pain. These included cytotoxic agents, antidepressants, catecholamine antagonists, and amino acids, including D-phenylalanine and Ltryptophan. This last drug was originally marketed as an antidepressant. Patients with uncontrollable pain sometimes responded to these drugs used in combination. The afternoon session commenced with two papers on mechanical aspects of pain. Dr P Helliwell (Harrogate) using an arthrograph to measure joint stiffness had found, in agreement with other authors, that only a minority of patients with arthritis can distinguish pain from stiffness. Objective stiffness measured by a mechanical apparatus did not always correlate with the patients' subjective perception of discomfort. Objective stiffness was
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