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局部镇痛药的药理学。

The pharmacology of topical analgesics.

出版信息

Postgrad Med. 2013 Jul;125(4 Suppl 1):7-18. doi: 10.1080/00325481.2013.1110566911.

Abstract

Pain management of patients continues to pose challenges to clinicians. Given the multiple dimensions of pain--whether acute or chronic, mild, moderate, or severe, nociceptive or neuropathic--a multimodal approach may be needed. Fortunately, clinicians have an array of nonpharmacologic and pharmacologic treatment choices; however, each modality must be chosen carefully, because some often used oral agents are associated with safety and tolerability issues that restrict their use in certain patients. In particular, orally administered nonsteroidal antiinflammatory drugs, opioids, antidepressants, and anticonvulsants are known to cause systemic adverse effects in some patients. To address this problem, a number of topical therapies in various therapeutic classes have been developed to reduce systemic exposure and minimize the risks of patients developing adverse events. For example, topical nonsteroidal anti-inflammatory drug formulations produce a site-specific effect (ie, cyclo-oxygenase inhibition) while decreasing the systemic exposure that may lead to undesired effects in patients. Similarly, derivatives of acetylsalicylic acid (ie, salicylates) are used in topical analgesic formulations that do not significantly enter the patient's systemic circulation. Salicylates, along with capsaicin, menthol, and camphor, compose the counterirritant class of topical analgesics, which produce analgesia by activating and then desensitizing epidermal nociceptors. Additionally, patches and creams that contain the local anesthetic lidocaine, alone or co-formulated with other local anesthetics, are also used to manage patients with select acute and chronic pain states. Perhaps the most common topical analgesic modality is the cautious application of cutaneous cold and heat. Such treatments may decrease pain not by reaching the target tissue through systemic distribution, but by acting more directly on the affected tissue. Despite the tolerability benefits associated with avoiding systemic circulation, topically applied analgesics are associated with application-site reactions in patients, such as dryness, erythema, burning, and discoloration. Furthermore, some adverse events that have been observed in patients may be suggestive of some degree of systemic exposure. This article reviews the mechanisms of action, pharmacokinetics, and tolerability of topical treatments for the management of patient pain.

摘要

患者的疼痛管理仍然给临床医生带来挑战。鉴于疼痛的多个维度——无论是急性还是慢性,轻度、中度还是重度,伤害感受性还是神经性——可能需要采用多模式方法。幸运的是,临床医生有一系列非药物和药物治疗选择;然而,每种方式都必须谨慎选择,因为一些常用的口服药物与安全性和耐受性问题有关,这些问题限制了它们在某些患者中的使用。特别是,口服非甾体抗炎药、阿片类药物、抗抑郁药和抗惊厥药已知会在某些患者中引起全身不良反应。为了解决这个问题,已经开发了许多不同治疗类别的局部治疗方法,以减少全身暴露并最大限度地降低患者发生不良反应的风险。例如,局部非甾体抗炎药制剂产生特定部位的作用(即环氧化酶抑制),同时减少可能导致患者出现不良影响的全身暴露。同样,乙酰水杨酸(即水杨酸酯)的衍生物用于局部镇痛制剂中,这些制剂不会显著进入患者的全身循环。水杨酸酯与辣椒素、薄荷醇和樟脑一起构成局部镇痛剂中的反刺激剂类,通过激活然后脱敏表皮伤害感受器来产生镇痛作用。此外,含有局部麻醉剂利多卡因的贴剂和乳膏,单独或与其他局部麻醉剂联合使用,也用于治疗某些急性和慢性疼痛状态的患者。也许最常见的局部镇痛方式是谨慎应用皮肤冷和热。这些治疗方法可能不会通过全身分布到达靶组织来减轻疼痛,而是通过更直接地作用于受影响的组织。尽管避免全身循环与可耐受性益处相关,但局部应用的镇痛药与患者的应用部位反应有关,如干燥、红斑、灼热和变色。此外,在患者中观察到的一些不良反应可能表明存在一定程度的全身暴露。本文综述了用于管理患者疼痛的局部治疗的作用机制、药代动力学和耐受性。

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