Antiepileptic drug hypersensitivity syndrome

被引:120
作者
Schlienger, RG
Shear, NH
机构
[1] Univ Toronto, Sunnybrook Hlth Sci Ctr, Div Clin Pharmacol, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Dermatol, Toronto, ON M4N 3M5, Canada
[3] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Med, Toronto, ON M4N 3M5, Canada
[4] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Pharmacol, Toronto, ON M4N 3M5, Canada
[5] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Pharm, Toronto, ON M4N 3M5, Canada
[6] Univ Toronto, Sunnybrook Hlth Sci Ctr, Glaxo Wellcome Sunnybrook Drug Safety Clin, Toronto, ON M4N 3M5, Canada
关键词
antiepileptic drugs; adverse drug reaction; hypersensitivity; syndrome;
D O I
10.1111/j.1528-1157.1998.tb01678.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The antiepileptic drug hypersensitivity syndrome (AHS) is an adverse drug reaction associated with the aromatic antiepileptic drugs (AEDs) phenytoin (PHT), carbamazepine (CBZ), phenobarbital (PB), and primidone. The syndrome is defined by the triad of fever, skin rash, and internal organ involvement. It can also be caused by other drugs, such as sulfonamides, dapsone, minocycline, terbinafine, azathioprine, and allopurinol. Diagnosis of AHS may be difficult because of the variety of clinical and laboratory abnormalities and manifestations and because the syndrome may mimic infectious, neoplastic, or collagen vascular disorders. The incidence is approximately 1 in 3,000 exposures. AHS starts with fever, rash, and lymphadenopathy, within the first 2-8 weeks after initiation of therapy. Internal manifestations include, among others, agranulocytosis, hepatitis, nephritis, and myostitis. AHS is associated with a relative excess of reactive oxidative metabolites of the AED. Insufficient detoxification may lead to cell death or contribute to the formation of antigen that triggers an immune reaction. Crossreactivity among PHT, CBZ, and PB is as high as 70-80%.
引用
收藏
页码:S3 / S7
页数:5
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