阿莫西林-克拉维酸与口服抗凝剂:可能存在的危险关联。

Cristiana Cauli, Lara Fenu, Andrea Perra, Francesco Marongiu
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引用次数: 0

摘要

我们描述了一位68岁的男性患者,接受阿莫西林-克拉维酸治疗18天并口服抗凝剂。他出现胆汁淤积性肝炎,结合胆红素为11mg /dL,并伴有口服抗凝剂过量(INR 7)。阿莫西林-克拉维酸治疗41天后出现恶心、呕吐、黄疸和大瘀斑;临床表现在1周内消失,停药后48天肝脏检查恢复正常。阿莫西林-克拉维酸诱发肝炎的机制可能是免疫过敏性的;这种并发症主要发生在有代谢和/或免疫特异性的患者中。该抗生素不被细胞色素P450直接代谢,在细胞色素P450控制下同时使用药物可能会影响其药代动力学。当使用阿莫西林-克拉维酸时,应考虑到其潜在的肝毒性和可能与口服抗凝剂的相互作用。然而,这两种药物的正确适应症似乎是至关重要的。事实上,在上述患者中,阿莫西林-克拉维酸在鼻子皮肤活检后被错误地作为预防用药。对于一年前发生的单次阵发性心房颤动患者口服抗凝剂也发生了同样的情况。
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[Amoxicillin-clavulanic acid and oral anticoagulants: a possible dangerous association].

We describe a 68-year-old male patient, treated with amoxicillin-clavulanic acid for 18 days and oral anticoagulants. He developed a cholestatic hepatitis with conjugated bilirubin of 11 mg/dL and a concomitant overdose of oral anticoagulants (INR 7). Nausea, vomiting, jaundice and large ecchymoses occurred 41 days after treatment with amoxicillin-clavulanic acid; the clinical manifestations resolved within 1 week and the liver tests returned to normal 48 days after therapy withdrawal. The mechanism of the amoxicillin-clavulanate-induced hepatitis is probably immunoallergic; this complication occurs mainly in subjects with a metabolic and/or immunologic idiosyncrasy. The pharmacokinetics of this antibiotic, which is not directly metabolized by cytochrome P450, may be affected by the concomitant use of drugs under cytochrome P450 control. When using amoxicillin-clavulanic acid, one should take into account its potential hepatic toxicity and possible interaction with oral anticoagulants. However, it appears to be crucial to follow the correct indications for both drugs. In fact, in the patient described above amoxicillin-clavulanic acid was wrongly administered as prophylaxis after a cutaneous biopsy of the nose. The same occurred with the oral anticoagulants prescribed to the patient for a single episode of paroxysmal atrial fibrillation which had occurred one year previously.

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