Bohan KarenBeth H, Mansuri Tarannum F, Wilson Natalie M
Department of Pharmacy Practice, Nesbitt College of Pharmacy and Nursing, Wilkes University, Wilkes-Barre, Pennsylvania 18766, USA.
Pharmacotherapy. 2007 Oct;27(10):1425-39. doi: 10.1592/phco.27.10.1425.
Anticonvulsant hypersensitivity syndrome (AHS) is a delayed adverse drug reaction associated with the use of aromatic anticonvulsant drugs. It has been most commonly reported with the use of phenytoin, carbamazepine, and phenobarbital. Although its occurrence is rare, 1 in every 1000-10,000 exposures, AHS is a serious adverse event often resulting in hospitalization and even death. The clinical manifestations of AHS include a triad of symptoms consisting of dermatologic rashes, fever, and evidence of systemic organ involvement. Diagnosis is most frequently based on the recognition of this triad of symptoms and clinical judgment. The exact mechanism of AHS remains to be determined but is thought to have at least three components: deficiency or abnormality of the epoxide hydroxylase enzyme that detoxifies the metabolites of aromatic amine anticonvulsants, associated reactivation of herpes-type viruses, and ethnic predisposition with certain human leukocyte antigen subtypes. Arene oxides, the toxic intermediaries in the metabolism of anticonvulsant drugs, can accumulate and directly bind to macromolecules, causing cell death, as well as act as prohaptens that bind to T cells, initiating an immune response and systemic reactions. Management of AHS primarily includes discontinuation of the associated anticonvulsant drug. Systemic corticosteroids are usually required for full recovery. An important issue regarding AHS is the cross-sensitivity among aromatic anticonvulsant drugs, which has been reported to be 40-80%. This means that patients with a history of AHS should avoid further use of any aromatic anticonvulsant drug. In addition, a familial association with AHS exists, and family members of the patient with AHS should be educated that they may be at increased risk for developing AHS if they use aromatic anticonvulsant drugs. Anticonvulsant drugs that are generally considered safe are valproic acid and benzodiazepines. Other nonaromatic anticonvulsant drugs should also be acceptable. Pharmacists as health care providers can play an important role in the diagnosis, treatment, and prevention of AHS.
抗惊厥药超敏反应综合征(AHS)是一种与使用芳香族抗惊厥药物相关的迟发性药物不良反应。最常报道与苯妥英钠、卡马西平和苯巴比妥的使用有关。尽管其发生率很低,每1000 - 10000次用药中出现1例,但AHS是一种严重的不良事件,常导致住院甚至死亡。AHS的临床表现包括由皮肤皮疹、发热和全身器官受累证据组成的三联征症状。诊断通常基于对这三联征症状的识别和临床判断。AHS的确切机制尚待确定,但认为至少有三个组成部分:使芳香胺抗惊厥药物代谢产物解毒的环氧化物羟化酶缺乏或异常、疱疹型病毒的相关再激活以及某些人类白细胞抗原亚型的种族易感性。芳烃氧化物是抗惊厥药物代谢中的有毒中间体,可积累并直接与大分子结合,导致细胞死亡,还可作为半抗原与T细胞结合,引发免疫反应和全身反应。AHS的治疗主要包括停用相关的抗惊厥药物。通常需要全身性皮质类固醇来实现完全康复。关于AHS的一个重要问题是芳香族抗惊厥药物之间的交叉敏感性,据报道为40 - 80%。这意味着有AHS病史的患者应避免进一步使用任何芳香族抗惊厥药物。此外,AHS存在家族关联,AHS患者的家庭成员应被告知,如果他们使用芳香族抗惊厥药物,发生AHS的风险可能会增加。一般认为安全的抗惊厥药物是丙戊酸和苯二氮䓬类药物。其他非芳香族抗惊厥药物也应该是可以接受的。药剂师作为医疗保健提供者,在AHS的诊断、治疗和预防中可以发挥重要作用。