Asconapé Jorge J
Department of Neurology, Indiana University School of Medicine, Indianapolis, Indiana 46202-5250, USA.
Semin Neurol. 2002 Mar;22(1):27-39. doi: 10.1055/s-2002-33046.
Since 1993, eight new antiepileptic drugs (AEDs) have become available in the United States for the treatment of epilepsy: felbamate, gabapentin, lamotrigine, topiramate, tiagabine, levetiracetam, oxcarbazepine, and zonisamide. Of the older AEDs, six continue to be widely used: phenobarbital, phenytoin, primidone, ethosuximide, carbamazepine, and valproate. As a result, there is a relatively large number of alternative AEDs for the treatment of any given type of epilepsy. This has been particularly beneficial for patients with generalized epilepsies, both idiopathic and symptomatic. Given the wide availability of effective agents, the toxicity and pharmacokinetic profile of an AED have become major factors in the selection process. A number of common clinical situations may benefit from the abundance of AEDs. Chronic toxicity observed with some of the older AEDs such as osteoporosis, gingival hyperplasia, or alterations in reproductive endocrine function may be avoided with the use of the newer agents. The obese patient with epilepsy may benefit from the use of AEDs such as topiramate or zonisamide, which have a tendency to produce weight loss. In patients with a history of drug-induced skin rash, AEDs such as valproate, gabapentin, topiramate, tiagabine, and levetiracetam carry a lower risk of cross-reactivity. In patients sensitive to cognitive dysfunction, drugs with a favorable profile include gabapentin, tiagabine, lamotrigine, oxcarbazepine, and levetiracetam. A more favorable pharmacokinetic profile is observed in the majority of the newer AEDs in contraposition to the classic agents. Good absorption, linear kinetics, and low drug-drug interaction potential make these drugs easier to use. The newer AEDs are eliminated through different combinations of liver metabolism and direct renal excretion, thus providing a wider variety of choices in patients with failure of one of these organs. Some specific problems have been found with some of the newer AEDs. Hyponatremia, known to occur rarely with carbamazepine use, appears to be more common with oxcarbazepine. Felbamate has been associated with a high incidence of aplastic anemia and liver failure and should be used exceptionally. Acute angle closure glaucoma has been observed with the use of topiramate. This complication occurs early in the course of therapy and reverses rapidly with discontinuation of the drug, so physician and patient awareness of this problem is very important. In this article several common clinical situations in the management of patients with epilepsy are presented in the form of case studies. These cases illustrate some current aspects of the use of the AEDs and will give some guidelines to help the treating physician in the increasingly complex process of AED selection.
自1993年以来,美国已有八种新型抗癫痫药物(AEDs)可用于治疗癫痫:非氨酯、加巴喷丁、拉莫三嗪、托吡酯、噻加宾、左乙拉西坦、奥卡西平和唑尼沙胺。在较老的AEDs中,有六种仍被广泛使用:苯巴比妥、苯妥英、扑米酮、乙琥胺、卡马西平和丙戊酸盐。因此,对于任何给定类型的癫痫治疗,都有相对大量的替代AEDs。这对特发性和症状性全身性癫痫患者尤其有益。鉴于有效药物的广泛可得性,AED的毒性和药代动力学特征已成为选择过程中的主要因素。许多常见的临床情况可能受益于丰富的AEDs。使用较新的药物可以避免一些较老的AEDs所观察到的慢性毒性,如骨质疏松、牙龈增生或生殖内分泌功能改变。肥胖的癫痫患者可能受益于使用托吡酯或唑尼沙胺等AEDs,这些药物有导致体重减轻的倾向。在有药物性皮疹病史的患者中,丙戊酸盐、加巴喷丁、托吡酯、噻加宾和左乙拉西坦等AEDs发生交叉反应的风险较低。在对认知功能障碍敏感的患者中,具有良好特征的药物包括加巴喷丁、噻加宾、拉莫三嗪、奥卡西平和左乙拉西坦。与经典药物相比,大多数新型AEDs具有更有利的药代动力学特征。良好的吸收、线性动力学和低药物相互作用潜力使这些药物更易于使用。新型AEDs通过肝脏代谢和直接肾脏排泄的不同组合被清除,从而为其中一个器官功能衰竭的患者提供了更多样化的选择。一些新型AEDs也发现了一些特定问题。低钠血症在使用卡马西平时很少发生,但在使用奥卡西平时似乎更常见。非氨酯与再生障碍性贫血和肝衰竭的高发生率有关,应特别谨慎使用。使用托吡酯时曾观察到急性闭角型青光眼。这种并发症在治疗过程早期出现,停药后迅速逆转,因此医生和患者对这个问题的认识非常重要。在本文中,癫痫患者管理中的几种常见临床情况以病例研究的形式呈现。这些病例说明了AEDs使用的一些当前情况,并将给出一些指导方针,以帮助治疗医生在日益复杂的AED选择过程中做出决策。