Li Tao, Sheng Meiyan, Gu Tengzhen, Zhang Yan, Yirepanjiang Ailiyaer, Li Yu
Department of Respiratory Diseases, Qilu Hospital of Shandong University, Jinan 250012, China.
Department of Intensive Care Unit, Shandong Chest Hospital, Jinan 250013, China.
J Thorac Dis. 2018 Mar;10(3):1370-1376. doi: 10.21037/jtd.2018.02.01.
Multidrug-resistant (MDRAB) has emerged as an important pathogen of nosocomial infections. Even though cefoperazone-sulbactam is frequently used to treat MDRAB infections, this single-drug therapeutic approach often results in antibiotic resistance. Thus, combination therapy is preferred over single-drug therapy, particularly in the case of carbapenemase-producing gram negative bacteria. The aim of this study was to investigate the efficacy of cefoperazone-sulbactam combined with either tigecycline or rifampicin against clinical isolates of MDRAB.
One hundred and three MDRAB bacteria were isolated from patients in two hospitals in China. The Epsilomer test (E test) was used to determine the minimum inhibitory concentration (MIC) values for amikacin, ceftazidime, cefepime, levofloxacin, rifampicin, cefoperazone-sulbactam, meropenem, tigecycline, and gentamicin against MDRAB isolates. effects of various antibiotic combinations were measured and the fractional inhibitory concentration index (FICI) was calculated for each drug combination.
Approximately 17.5% of the isolates were resistant to tigecycline, whereas more than 84.2% isolates were resistant to other antimicrobial agents tested in this study. Cefoperazone-sulbactam revealed remarkable synergistic effects when used in combination with either tigecycline or rifampicin. However, for the isolates with MICs lower than blood peak concentration after combination therapy, the ratio was lower in highly resistant isolates compared to the least resistant bacteria.
cefoperazone-sulbactam in combination with tigecycline or rifampicin showed the highest synergistic or additive activity against MDRAB isolates. However, acquisition of highly antibiotic resistant bacteria may lessen the effectiveness of combination therapy.
多重耐药鲍曼不动杆菌(MDRAB)已成为医院感染的重要病原菌。尽管头孢哌酮 - 舒巴坦常用于治疗MDRAB感染,但这种单一药物治疗方法常导致抗生素耐药。因此,联合治疗优于单一药物治疗,特别是对于产碳青霉烯酶的革兰氏阴性菌。本研究的目的是调查头孢哌酮 - 舒巴坦联合替加环素或利福平对MDRAB临床分离株的疗效。
从中国两家医院的患者中分离出103株MDRAB细菌。采用Epsilometer试验(E试验)测定阿米卡星、头孢他啶、头孢吡肟、左氧氟沙星、利福平、头孢哌酮 - 舒巴坦、美罗培南、替加环素和庆大霉素对MDRAB分离株的最低抑菌浓度(MIC)值。测量各种抗生素组合的效果,并计算每种药物组合的抑菌浓度分数指数(FICI)。
约17.5%的分离株对替加环素耐药,而超过84.2%的分离株对本研究中测试的其他抗菌药物耐药。头孢哌酮 - 舒巴坦与替加环素或利福平联合使用时显示出显著的协同作用。然而,对于联合治疗后MIC低于血药峰浓度的分离株,高耐药分离株的比例低于低耐药细菌。
头孢哌酮 - 舒巴坦联合替加环素或利福平对MDRAB分离株显示出最高的协同或相加活性。然而,获得高度耐药菌可能会降低联合治疗的效果。