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新型抗组胺药:批判性观点

New antihistamines: a critical view.

作者信息

Camelo-Nunes Inês Cristina

机构信息

Departamento de Pediatria, Universidade Federal de São Paulo - Escola Paulista de Medicina (UNIFESP-EPM), São Paulo, SP, Brazil.

出版信息

J Pediatr (Rio J). 2006 Nov;82(5 Suppl):S173-80. doi: 10.2223/JPED.1552.

Abstract

OBJECTIVES

To perform a critical evaluation of the more recent H1 antihistamines and the various terms used to describe them, based on a review of evidence on their role in the treatment of allergic disorders.

SOURCES OF DATA

Original articles, reviews and consensus documents published from 1998 to 2006 and indexed in the MEDLINE and PubMed databases. Keyword: antihistamines.

SUMMARY OF THE FINDINGS

Second-generation antihistamines differ from first-generation ones because of their elevated specificity and affinity for peripheral H1 receptors and because of their lower penetration of the central nervous system (CNS), having fewer sedative effects as a result. Whilst second-generation antihistamines are in general better tolerated than their predecessors, some adverse effects, principally cardiotoxicity, have been observed with some of them. Over the last 20 years, new compounds with different pharmacokinetic properties have been synthesized. The majority of these exhibit anti-inflammatory properties that are independent of their action on the H1 receptor. More recent improvements, generally in the form of active metabolites, led to the use of the term third-generation antihistamines. This term emerged spontaneously, with no clear definition of its meaning or clinical implications, creating great confusion among healthcare professionals.

CONCLUSION

On the basis of the evidence on H1 antihistamines, none of them deserve the title "third-generation antihistamine." As the Consensus Group on New Generation Antihistamines concluded, to merit this definition, a new class of antihistamines would have to demonstrate distinct clinical advantages over existing compounds and fulfill at least three prerequisites: they should be free from cardiotoxicity, drug interactions and effects on the CNS.

摘要

目的

基于对H1抗组胺药在过敏性疾病治疗中作用的证据回顾,对近期的H1抗组胺药及其各种描述术语进行批判性评价。

数据来源

1998年至2006年发表并被MEDLINE和PubMed数据库收录索引的原创文章、综述和共识文件。关键词:抗组胺药。

研究结果总结

第二代抗组胺药与第一代不同,因其对外周H1受体具有更高的特异性和亲和力,且对中枢神经系统(CNS)的穿透性较低,因此镇静作用较少。虽然第二代抗组胺药总体上比其前代药物耐受性更好,但其中一些药物也观察到了一些不良反应,主要是心脏毒性。在过去20年中,合成了具有不同药代动力学特性的新化合物。其中大多数具有独立于其对H1受体作用的抗炎特性。最近的改进,通常以活性代谢物的形式出现,导致了“第三代抗组胺药”这一术语的使用。这个术语是自发出现的,其含义或临床意义没有明确的定义,在医疗专业人员中造成了很大的混乱。

结论

根据关于H1抗组胺药的证据,它们都不配称为“第三代抗组胺药”。正如新一代抗组胺药共识小组所总结的,要符合这一定义,一类新的抗组胺药必须证明相对于现有化合物具有明显的临床优势,并至少满足三个先决条件:它们应无心脏毒性、药物相互作用和对中枢神经系统的影响。

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