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局部用皮质类固醇的临床潜力。

Clinical potential of topical corticosteroids.

作者信息

Ortonne J P

机构信息

Service de Dermatologie, Centre Hospitalier, Universitaire de Nice, Hôpital Pasteur, France.

出版信息

Drugs. 1988;36 Suppl 5:38-42. doi: 10.2165/00003495-198800365-00008.

DOI:10.2165/00003495-198800365-00008
PMID:3076130
Abstract

The treatment of a variety of inflammatory skin diseases was greatly changed by the introduction, in the early 1950s, of corticosteroids for topical use. Topical corticosteroids are still the most widely used drugs in dermatology, and many preparations with quite different potencies are now available. However, attempts to eliminate the local and systemic side effects associated with topical corticosteroid therapy have not been entirely successful. Thus, dermatologists are now seeking a preparation with moderate to potent anti-inflammatory activity, which is strictly limited to the skin and has minimal or no passage into the systemic circulation, minimal or no local and/or systemic side effects and no wear-off effects. The list of dermatoses that are sensitive to treatment with topical corticosteroids is well known. However, recent reports suggest other indications, such as bullous pemphigoid, pemphigus and actinic reticuloid. The observation that potent topical corticosteroids under occlusion induce loss of dermal mast cells has opened a new therapeutic field (e.g. mastocytosis, urticaria pigmentosa) for the use of these compounds. Although topical corticosteroids have been the most extensively studied drugs in dermatology, many questions remain unanswered. We are beginning to learn about the biochemistry of glucocorticoid activity in the skin, and there is little doubt that increased knowledge in this field will help optimise the activity of these drugs. Topical corticosteroid formulations can be improved, and a better definition of proper dosage schedules is needed for each category, as defined by topical corticosteroid potency, to lower the risk-benefit ratio.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

20世纪50年代初局部使用皮质类固醇激素后,多种炎症性皮肤病的治疗发生了巨大变化。局部皮质类固醇激素仍然是皮肤科使用最广泛的药物,现在有许多效力差异很大的制剂。然而,消除与局部皮质类固醇激素治疗相关的局部和全身副作用的尝试并未完全成功。因此,皮肤科医生目前正在寻找一种具有中度至强效抗炎活性的制剂,这种制剂严格局限于皮肤,极少或不会进入体循环,极少或没有局部和/或全身副作用,也没有药效消退效应。对局部皮质类固醇激素治疗敏感的皮肤病列表是众所周知的。然而,最近的报告提出了其他适应症,如大疱性类天疱疮、天疱疮和光化性类网状细胞增多症。强效局部皮质类固醇激素在封包情况下会导致真皮肥大细胞丢失,这一观察结果为这些化合物开辟了一个新的治疗领域(如肥大细胞增多症、色素性荨麻疹)。尽管局部皮质类固醇激素是皮肤科研究最广泛的药物,但许多问题仍未得到解答。我们开始了解皮肤中糖皮质激素活性的生物化学,毫无疑问,该领域知识的增加将有助于优化这些药物的活性。局部皮质类固醇激素制剂可以改进,对于每个由局部皮质类固醇激素效力定义的类别,需要更好地确定合适的给药方案,以降低风险效益比。(摘要截短至250字)

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外用糖皮质激素。用哪种药物以及何时使用?
Drugs. 1992 Jul;44(1):65-71. doi: 10.2165/00003495-199244010-00006.
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