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美罗培南致胆汁消失综合征。

Meropenem-induced vanishing bile duct syndrome.

出版信息

Pharmacotherapy. 2010 Sep;30(9):953. doi: 10.1592/phco.30.9.953.

DOI:10.1592/phco.30.9.953
PMID:20812433
Abstract

Vanishing bile duct syndrome (VBDS) is a rare and potentially life-threatening disorder in which progressive destruction and disappearance of small intrahepatic bile ducts occur, with resultant cholestasis. The mechanism by which biliary epithelial cells are damaged and intrahepatic bile ducts are lost has not been fully elucidated. However, many etiologies have been reported,and several drugs have been implicated. Meropenem is a widely used, well tolerated broad-spectrum carbapenem antibiotic indicated for the treatment of intraabdominal infections, complicated skin and skin structure infections, and pediatric bacterial meningitis. We describe what we believe is the first reported case of meropenem-induced VBDS. A 60-year-old woman was diagnosed with VBDS after being treated with meropenem for a left temporal lobe brain abscess. Three weeks after starting the drug, the patient developed mixed hepatocellular and cholestatic liver injury with jaundice and pruritus.Meropenem-induced liver injury was suspected, and the drug was discontinued. Diagnostic tests ruled out other causes of cholestasis, including infectious and immunologic conditions. A liver biopsy, performed due to persistent liver injury, demonstrated an absence of bile ducts, which, in conjunction with the patient's clinical course, was consistent with the diagnosis of VBDS. Several months after the cessation of meropenem, the patient's liver function test results improved. Use of the Naranjo adverse drug reaction probability scale indicated a probable relationship (score of 6)between the patient's development of VBDS and meropenem therapy. A high index of suspicion is necessary to diagnose VBDS and other types of drug induced liver injury. Clinicians should consider VBDS as a potential diagnosis in patients receiving meropenem who have prolonged cholestasis, especially after other more probable causes have been excluded.

摘要

胆流消失综合征(VBDS)是一种罕见且潜在危及生命的疾病,其特征为小肝内胆管进行性破坏和消失,导致胆汁淤积。导致胆管上皮细胞损伤和肝内胆管丢失的机制尚未完全阐明。然而,已经报道了许多病因,并且几种药物也与之相关。美罗培南是一种广泛使用的、耐受性良好的广谱碳青霉烯类抗生素,适用于治疗腹腔内感染、复杂皮肤和皮肤结构感染以及小儿细菌性脑膜炎。我们描述了一例我们认为是首例美罗培南引起的 VBDS 病例。一位 60 岁女性因左颞叶脑脓肿接受美罗培南治疗后被诊断为 VBDS。开始使用该药物 3 周后,患者出现黄疸和瘙痒的混合性肝细胞性和胆汁淤积性肝损伤。怀疑为美罗培南引起的肝损伤,并停用该药物。诊断性检查排除了其他类型的胆汁淤积,包括感染和免疫性疾病。由于持续性肝损伤进行了肝活检,结果显示没有胆管,结合患者的临床病程,与 VBDS 的诊断一致。停用美罗培南几个月后,患者的肝功能试验结果改善。使用 Naranjo 药物不良反应概率量表表明,患者 VBDS 的发生与美罗培南治疗之间存在可能的关系(评分 6)。怀疑 VBDS 和其他类型的药物性肝损伤时,需要高度警惕。对于接受美罗培南治疗且出现长期胆汁淤积的患者,特别是在排除其他更可能的病因后,临床医生应考虑 VBDS 作为潜在的诊断。

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