病例报告:使用利福平治疗机械瓣膜心内膜炎的抗菌疗法陷阱--药物相互作用之王。

Pub Date : 2024-09-23 eCollection Date: 2024-10-01 DOI:10.1093/ehjcr/ytae525
Ryosuke Honda, Yusuke Akazawa, Katsuji Inoue, Takashi Higaki, Osamu Yamaguchi
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引用次数: 0

摘要

背景:利福平是肝细胞色素 P450(CYP)家族的强诱导剂,已知会与许多临床药物发生相互作用。病例摘要:一名 32 岁的女性门诊患者曾因不完全房室间隔缺损合并右心室和左心室瓣反流接受过心脏内修复术,并接受过人工瓣膜置换术。她服用的药物包括托伐普坦 15 毫克和华法林 1.25 毫克。她有轻微发烧,手指上有奥斯勒结节。血液培养瓶中培养出耐甲氧西林表皮葡萄球菌,经食道超声心动图观察到右房室机械瓣上有几个植被。她被诊断为人工瓣膜心内膜炎,并接受了包括利福平在内的抗生素治疗。一周后,她出现全身水肿,凝血酶原时间-国际标准化比值(PT-INR)明显下降。由于强烈怀疑存在药物间相互作用,医生立即停用了利福平。结果,她的充血和 PT-INR 都趋于稳定,经过 8 周的抗生素治疗后出院:讨论:利福平的引入会诱导 CYP 家族成员,如 CYP3A4 和 CYP2C9。华法林通过 CYP2C9 代谢,托伐普坦也通过 CYP3A4 代谢,因此与利福平合用时,这两种药物的血药浓度会明显降低。高血压药物与利福平之间的相互作用所带来的临床挑战可分为两大类:高血压恶化和血栓并发症。临床医生应保持警惕并了解这些潜在问题。
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A case report: pitfalls in antibacterial therapy with rifampicin for mechanical valve endocarditis-the king of drug interactions.

Background: Rifampicin is a strong inducer of the hepatic cytochrome P450 (CYP) family and is known to interact with many clinical drugs. However, to our knowledge, no case of worsening heart failure (HF) due to the interaction between rifampicin and HF drugs has been reported.

Case summary: A 32-year-old female, who had undergone intracardiac repair for an incomplete atrioventricular septal defect with dextrocardia and prosthetic valve replacements for right and left atrioventricular valve regurgitation, presented as an outpatient. Her medications included tolvaptan 15 mg and warfarin 1.25 mg. She had a slight fever and Osler nodes at her fingers. Blood culture bottles grew methicillin-resistant Staphylococcus epidermidis, and several vegetations were observed on the right atrioventricular mechanical valve with a transoesophageal echocardiogram. She was diagnosed with prosthetic valve endocarditis and treated with antibiotic agents including rifampicin. After a week, she developed systemic oedema and had a marked decrease in prothrombin time-international normalized ratio (PT-INR). Rifampicin was promptly discontinued due to a strong suspicion of a drug-drug interaction. Consequently, both her congestion and the PT-INR stabilized, and she was discharged after 8 weeks of antibiotic treatment.

Discussion: The introduction of rifampicin induces CYP family members such as CYP3A4 and CYP2C9. Warfarin is metabolized by CYP2C9 and tolvaptan is also metabolized by CYP3A4, resulting in a notable reduction of their blood levels when co-administered with rifampicin. The clinical challenges arising from interactions between HF drugs and rifampicin can be categorized into two main groups: worsening HF and thrombotic complications. Clinicians should remain vigilant and informed about these potential issues.

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