Center S A, Elston T H, Rowland P H, Rosen D K, Reitz B L, Brunt J E, Rodan I, House J, Bank S, Lynch L R, Dring L A, Levy J K
College of Veterinary Medicine, Cornell University, Ithaca, NY 14893, USA.
J Am Vet Med Assoc. 1996 Aug 1;209(3):618-25.
Acute fulminant hepatic necrosis was associated with repeated oral administration of diazepam (1.25 to 2 mg, PO, q 24 or 12 h), prescribed for behavioral modification or to facilitate urination. Five of 11 cats became lethargic, atactic, and anorectic within 96 hours of initial treatment. All cats became jaundiced during the first 11 days of illness. Serum biochemical analysis revealed profoundly high alanine transaminase and aspartate transaminase activities. Results of coagulation tests in 3 cats revealed marked abnormalities. Ten cats died or were euthanatized within 15 days of initial drug administration, and only 1 cat survived. Histologic evaluation of hepatic tissue specimens from each cat revealed florid centrilobular hepatic necrosis, profound biliary ductule proliferation and hyperplasia, and suppurative intraductal inflammation. Idiosyncratic hepatotoxicosis was suspected because of the rarity of this condition. Prior sensitization to diazepam was possible in only 1 cat, and consistent risk factors that could explain susceptibility to drug toxicosis were not identified. On the basis of the presumption that diazepam was hepatotoxic in these cats, an increase in serum transaminase activity within 5 days of treatment initiation indicates a need to suspend drug administration and to provide supportive care.
急性暴发性肝坏死与重复口服地西泮(1.25至2毫克,口服,每24或12小时一次)有关,该药用于行为矫正或促进排尿。11只猫中有5只在初始治疗的96小时内变得嗜睡、共济失调和厌食。所有猫在发病的前11天内都出现了黄疸。血清生化分析显示丙氨酸转氨酶和天冬氨酸转氨酶活性极高。3只猫的凝血试验结果显示明显异常。10只猫在首次给药后的15天内死亡或被安乐死,只有1只猫存活。对每只猫的肝组织标本进行组织学评估,发现有明显的小叶中心性肝坏死、严重的胆小管增生和化脓性导管内炎症。由于这种情况罕见,怀疑是特异质性肝中毒。只有1只猫可能先前对地西泮致敏,未发现可解释药物中毒易感性的一致危险因素。基于地西泮对这些猫具有肝毒性的推测,在开始治疗的5天内血清转氨酶活性升高表明需要暂停给药并提供支持性护理。