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首页> 外文期刊>BMC research notes >Probable fatal drug interaction between intravenous fenretinide, ceftriaxone, and acetaminophen: a case report from a New Approaches to Neuroblastoma (NANT) Phase I study
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Probable fatal drug interaction between intravenous fenretinide, ceftriaxone, and acetaminophen: a case report from a New Approaches to Neuroblastoma (NANT) Phase I study

机译:静脉注射芬维A胺,头孢曲松和对乙酰氨基酚之间可能发生的致命药物相互作用:来自神经母细胞瘤新方法(NANT)I期研究的病例报告

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Background Patients with relapsed/refractory stage 4 high-risk neuroblastoma were enrolled on a phase I study (NANT2004-03) of intravenous fenretinide emulsion. Pharmacokinetic samples were collected during and after the infusion, and the levels were measured using an HPLC system. A likely case of a fatal drug interaction between fenretinide, ceftriaxone, and acetaminophen is described, including the pharmacokinetics of fenretinide, laboratory data, and post-mortem autopsy in a pediatric neuroblastoma patient treated on this study. Case presentation On Day 4 of a scheduled 5-day-infusion of intravenous fenretinide, the patient developed a fever, acetaminophen was started, ceftriaxone initiated for possible bacteremia, and fenretinide level doubled from 56 to 110?μM. Over the next three days, although blood cultures remained negative, the patient’s condition deteriorated rapidly. Acute liver failure was diagnosed on Day 7, and the patient expired on Day 20 of fulminant hepatic failure with associated renal, cardiac, and hemorrhagic/coagulation toxicities. Autopsy showed extensive hemorrhagic necrosis of the liver, marked bile duct proliferation, and abundant hemosiderin, consistent with cholestasis and drug toxicity. Conclusions After extensive review of patient data, the clinical course, and the literature, we conclude that observed hepatic toxicity was likely due to a drug interaction between fenretinide and concomitant ceftriaxone and acetaminophen. None of the other 16 patients treated on this study experienced significant hepatic toxicity. Although the prevalence of cholestasis with ceftriaxone usage is relatively high, the potential drug interaction with these concomitant medications has not been previously reported. Concomitant use of fenretinide, ceftriaxone, and acetaminophen should be avoided.
机译:背景患有复发性/难治性第4期高危神经母细胞瘤的患者参加了静脉注射芬维A胺乳液的I期研究(NANT2004-03)。在输注期间和输注后收集药代动力学样品,并使用HPLC系统测量其水平。本文描述了芬维A胺,头孢曲松和对乙酰氨基酚之间致命药物相互作用的可能病例,包括芬维A胺的药代动力学,实验室数据和本研究治疗的小儿神经母细胞瘤患者的验尸尸检。病例介绍在计划的静脉输注芬维A胺的第5天第4天,患者发烧,开始使用对乙酰氨基酚,开始使用头孢曲松治疗可能的菌血症,芬维A胺水平从56倍增至110μM。在接下来的三天中,尽管血液培养仍为阴性,但患者的病情迅速恶化。在第7天诊断出急性肝衰竭,该患者在暴发性肝衰竭中死亡,并伴有相关的肾脏,心脏和出血/凝血毒性。尸检显示肝脏大量出血性坏死,明显的胆管增生和大量铁血黄素,符合胆汁淤积和药物毒性。结论在对患者数据,临床过程和文献进行全面审查之后,我们得出结论,观察到的肝毒性可能是由于芬维A胺与伴随的头孢曲松和对乙酰氨基酚之间的药物相互作用所致。在该研究中接受治疗的其他16名患者中,没有一例具有明显的肝毒性。尽管使用头孢曲松治疗胆汁淤积症的患病率较高,但以前尚未报道与这些伴随药物发生潜在的药物相互作用。应避免同时使用芬维A胺,头孢曲松和对乙酰氨基酚。

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