Yusuf Dimas, Christy Joanna, Owen David, Ho Meghan, Li David, Fishman Martin J
Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Beedie School of Business, Simon Fraser University, Vancouver, BC, Canada.
BMC Res Notes. 2018 Apr 3;11(1):228. doi: 10.1186/s13104-018-3322-9.
Nifedipine is a generic, well-known and commonly-prescribed dihydropyridine calcium channel blocker used in the treatment of hypertension and Prinzmetal's angina. A known but very rare and serious adverse effect of nifedipine is clinically-apparent hepatitis which can take months to resolve.
Here we present a case of nifedipine-induced hepatitis in a 78-year-old Caucasian female with no prior history of liver or autoimmune disease. We discuss our investigative and management approach, and present a review of prior cases. We offer an approach for patients who present with signs of acute liver injury with jaundice and high elevations in serum transaminases.
Not much is known about nifedipine-induced hepatitis due to its rare occurrence. Its prevalence is unknown. The disease appears to afflict older men and women. It can present acutely (within days) or subacutely (within 4-8 weeks after medication start) and in an idiosyncratic manner. Chronic or latent cases have also been described, some diagnosed as late as 3 years after medication start. Common symptoms include jaundice, nausea, chills, rigors, diaphoresis, fatigue, and abdominal pain. Laboratory investigations often reveal profound elevations in AST, ALT, GGT, and conjugated bilirubin. Peripheral blood smear may demonstrate eosinophilia. Histology from liver biopsy typically demonstrates infiltration of immune cells, cholestasis, and a picture of steatohepatitis. Treatment involves immediate discontinuation of the drug with supportive care. Thus far, all published instances of nifedipine-induced hepatitis were self-limiting without mortality due to fulminant liver failure. However, this disease can take months to resolve. There is no randomized evidence for other treatments such as corticosteroids.
硝苯地平是一种通用的、广为人知且常用的二氢吡啶类钙通道阻滞剂,用于治疗高血压和变异型心绞痛。硝苯地平一种已知但非常罕见且严重的不良反应是临床上明显的肝炎,这种肝炎可能需要数月才能消退。
在此,我们报告一例78岁白种女性硝苯地平诱发的肝炎病例,该女性既往无肝脏或自身免疫性疾病史。我们讨论了我们的调查和管理方法,并对既往病例进行了综述。我们为出现急性肝损伤伴黄疸和血清转氨酶大幅升高体征的患者提供了一种方法。
由于硝苯地平诱发的肝炎罕见发生,目前对此了解不多。其患病率未知。该疾病似乎在老年男性和女性中发病。它可急性发作(数天内)或亚急性发作(用药开始后4 - 8周内),且方式特异。也有慢性或潜伏病例的描述,有些病例在用药开始后3年才被诊断。常见症状包括黄疸、恶心、寒战、发冷、出汗、疲劳和腹痛。实验室检查常显示谷草转氨酶、谷丙转氨酶、γ-谷氨酰转肽酶和结合胆红素大幅升高。外周血涂片可能显示嗜酸性粒细胞增多。肝活检组织学通常显示免疫细胞浸润、胆汁淤积和脂肪性肝炎的表现。治疗包括立即停药并给予支持性护理。迄今为止,所有已发表的硝苯地平诱发肝炎病例均为自限性,未因暴发性肝衰竭导致死亡。然而,这种疾病可能需要数月才能消退。对于其他治疗方法,如使用皮质类固醇,尚无随机对照证据。