Jiang Mingzi, Yao Jing, Zhang L I, Gao Tianming, Zhang Yang, Weng Xiaoqing, Feng Ganzhu
Department of Respiratory Medicine, The First People's Hospital of Kunshan City, Affiliated to Jiangsu University, Kunshan, Jiangsu 215300, P.R. China.
Department of Respiratory Medicine, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210000, P.R. China.
Biomed Rep. 2016 Jan;4(1):40-44. doi: 10.3892/br.2015.528. Epub 2015 Oct 6.
Although known for their broad spectrum and curative efficacy on drug-resistant pathogens and as nephrotoxicity-free, impairments were observed on renal function during clinical treatment of the two most commonly used fourth-generation cephalosporins: Cefpirome and cefepime. The present study aimed to further explore the exact influences of them on renal function. , the cell viability of renal cells cultured in drug-combined medium was tested for six dilutions. , a clinical cohort study was carried out to detect the influence of cefpirome and cefepime on the serum creatinine (SCr) level of patients. Cefpirome had an inhibition rate with half maximal inhibitory concentration (IC) of 143.5 µmol/l on renal mesangial cells, which was greater compared to the IC of 7.702 µmol/l for cefepime. The clinical cohort study data revealed that cefpirome treatment could lead to a greater increase of the average SCr level compared to cefepime on days 3 and 7 during therapy, and in addition, a greater incidence of SCr >445 µmol/l, an indicator of clinical renal failure. Furthermore, patients with an average age >65 years were observed as more susceptible to an SCr rise caused by either cefpirome or cefepime, with a larger augment in the average SCr, as well as a higher incidence of SCr >445 µmol/l compared to patients aged <65 years. In conclusion, cefpirome may have more potential to cause renal impairment compared to cefepime, therefore, more caution and comprehensive analysis of patient conditions is required during the clinical choice of fourth-generation cephalosporins.
尽管第四代头孢菌素中最常用的两种药物——头孢匹罗和头孢吡肟,以其对耐药病原体的广谱抗菌活性和疗效以及无肾毒性而闻名,但在临床治疗过程中仍观察到肾功能损害。本研究旨在进一步探究它们对肾功能的确切影响。首先,检测了在药物组合培养基中培养的肾细胞在六种稀释度下的细胞活力。其次,开展了一项临床队列研究,以检测头孢匹罗和头孢吡肟对患者血清肌酐(SCr)水平的影响。头孢匹罗对肾系膜细胞的半数最大抑制浓度(IC)为143.5 μmol/l,抑制率高于头孢吡肟的7.702 μmol/l。临床队列研究数据显示,在治疗的第3天和第7天,与头孢吡肟相比,头孢匹罗治疗可导致平均SCr水平升高幅度更大,此外,SCr>445 μmol/l(临床肾衰竭指标)的发生率更高。此外,观察到平均年龄>65岁的患者比<65岁的患者更容易受到头孢匹罗或头孢吡肟引起的SCr升高影响,平均SCr升高幅度更大,SCr>445 μmol/l的发生率也更高。总之,与头孢吡肟相比,头孢匹罗可能更有导致肾功能损害的风险,因此,在临床选择第四代头孢菌素时,需要更加谨慎并全面分析患者情况。