Ortega Andrew J, Ghafouri S Reshad, Vu Lynn, Edwards Brian, Nickel Nils
Internal Medicine, Texas Tech University Health Sciences Center El Paso Paul L. Foster School of Medicine, El Paso, USA.
Internal Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, USA.
Cureus. 2021 Oct 14;13(10):e18767. doi: 10.7759/cureus.18767. eCollection 2021 Oct.
Cefepime is a fourth-generation, cephalosporin antibiotic commonly used as a first-line empirical treatment in a wide range of bacterial infections. It is predominantly excreted renally; therefore, a reduction in kidney function allows for the accumulation of cefepime to potentially toxic levels. Here we present a case of cefepime-induced encephalopathy (CIE) in a 67 years old male patient with advanced-stage renal insufficiency and cirrhosis who was admitted to our hospital for altered mental status (AMS). The patient was initially treated for hepatic encephalopathy (HE) given an elevated ammonia level (105 µg/dL), which had significantly improved. He was also placed on intravenous (IV) cefepime for bacteremia. Four days later, the patient became drowsy and confused. A detailed workup for secondary causes of AMS was performed however no significant acute abnormalities were detected. The ammonia level remained within the normal range. There was no acute intracranial pathology reported on a head computerized tomography (CT). Furthermore, an electroencephalograph (EEG) was obtained which showed generalized periodic discharge with a tri-phasic wave pattern suggesting non-convulsive status epilepticus (NCSE). CIE was suspected at that point and cefepime administration was stopped. Following cefepime discontinuation, there was a remarkable improvement in the patient's mental status for several days after cefepime discontinuation that supported the diagnosis of CIE in our patient. Although the exact pathophysiology is unclear, CIE should be suspected in elderly patients, patients with renal dysfunction, and critical illness. Meanwhile, liver dysfunction can be an additional risk factor for CIE as it increases the permeability of the blood-brain barrier (BBB), altered neurotransmission, and neuro-inflammation.
头孢吡肟是一种第四代头孢菌素抗生素,常用于多种细菌感染的一线经验性治疗。它主要通过肾脏排泄;因此,肾功能减退会使头孢吡肟蓄积至潜在的中毒水平。在此,我们报告一例67岁男性患者发生头孢吡肟诱发的脑病(CIE),该患者患有晚期肾功能不全和肝硬化,因精神状态改变(AMS)入院。患者最初因血氨水平升高(105µg/dL)被诊断为肝性脑病(HE)并接受治疗,病情已显著改善。他还因菌血症接受静脉注射头孢吡肟治疗。四天后,患者变得嗜睡且意识模糊。对AMS的继发原因进行了详细检查,但未发现明显的急性异常。血氨水平仍在正常范围内。头部计算机断层扫描(CT)未报告急性颅内病变。此外,进行了脑电图(EEG)检查,结果显示广泛性周期性放电,呈三相波型,提示非惊厥性癫痫持续状态(NCSE)。此时怀疑为CIE并停用了头孢吡肟。停用头孢吡肟后,患者的精神状态在停药后的几天内有显著改善,这支持了我们对该患者CIE的诊断。尽管确切的病理生理学尚不清楚,但在老年患者、肾功能不全患者和危重症患者中应怀疑CIE。同时,肝功能障碍可能是CIE 的另一个危险因素,因为它会增加血脑屏障(BBB)的通透性、改变神经传递和神经炎症。