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抗癫痫药物治疗儿童癫痫的安全性和耐受性。

Safety and tolerability of antiepileptic drug treatment in children with epilepsy.

机构信息

Paediatric Neurology Unit and Laboratories, Childrens Hospital A. Meyer, University of Florence, Italy.

出版信息

Drug Saf. 2012 Jul 1;35(7):519-33. doi: 10.2165/11630700-000000000-00000.

Abstract

The aim of treating epilepsy is to control or at least decrease seizures without producing unacceptable adverse effects that impair quality of life. Antiepileptic drugs (AEDs) have been considered amongst the drugs most frequently associated with fatal suspected adverse drug reactions. Physicians must therefore be as familiar with safety and tolerability data of AEDs as they are with the expected therapeutic effects. AEDs may cause dose-related adverse effects (i.e. drowsiness, fatigue, dizziness, blurry vision and incoordination) that, in most cases, may be obviated by lowering the dosage, reducing the number of drugs or switching to a better tolerated AED. AEDs also have the potential of precipitating idiosyncratic adverse effects (i.e. serious cutaneous, haematological and hepatic events), which are more common in children and usually require withdrawal of the AED. Although occurrence of idiosyncratic adverse effects can only rarely be predicted or prevented, there are known risk factors that can help in identifying patients at high risk. Occurrence of an idiosyncratic event in a close relative, a concomitant autoimmune disease, co-treatment with specific drugs, history of a previous allergic drug reaction, starting treatment with high doses and rapid titration have all been associated with a higher risk of idiosyncratic adverse effects. New AEDs have been developed in the last two decades with the aim of improving the benefit-risk balance of AED therapy. Available evidence suggests that the newer AEDs are no more effective but may be somewhat better tolerated than older molecules. We performed a literature review with the aim of evaluating safety and tolerability of second- and third-generation AEDs in children. A PubMed search was conducted with the purpose of identifying English-language studies published between 1 January 1989 and 1 January 2011 that reported any adverse event having occurred in children with epilepsy in whom second- and third-generation AEDs were administered.

摘要

治疗癫痫的目的是控制或至少减少发作,同时避免产生不良的不良反应,从而降低生活质量。抗癫痫药物(AEDs)被认为是最常与致命疑似药物不良反应相关的药物之一。因此,医生必须熟悉 AEDs 的安全性和耐受性数据,就像他们熟悉预期的治疗效果一样。AEDs 可能会引起剂量相关的不良反应(例如嗜睡、疲劳、头晕、视力模糊和协调障碍),在大多数情况下,可以通过降低剂量、减少药物数量或改用耐受性更好的 AED 来避免。AEDs 还可能引发特发性不良反应(例如严重的皮肤、血液和肝脏事件),这些不良反应在儿童中更为常见,通常需要停用 AED。虽然特发性不良反应的发生很难预测或预防,但已知的风险因素可以帮助识别高风险患者。在近亲中发生特发性事件、同时患有自身免疫性疾病、同时使用特定药物、有以前的过敏药物反应史、开始用高剂量治疗和快速滴定都与特发性不良反应的风险增加有关。在过去的二十年中,已经开发了新的 AED,目的是改善 AED 治疗的获益-风险平衡。现有证据表明,新型 AED 并不更有效,但可能比旧分子更耐受。我们进行了文献回顾,目的是评估第二代和第三代 AED 在儿童中的安全性和耐受性。进行了 PubMed 搜索,以确定 1989 年 1 月 1 日至 2011 年 1 月 1 日期间发表的、报告了在接受第二代和第三代 AED 治疗的癫痫儿童中发生的任何不良事件的英语语言研究。

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