Sanders C V
Louisiana State University School of Medicine, New Orleans.
Intensive Care Med. 1994 Jul;20 Suppl 3:S21-6. doi: 10.1007/BF01745247.
Investigators assessed the efficacy and safety of piperacillin/tazobactam therapy in a study of patients with community-acquired lower respiratory tract infections and a study of patients with nosocomial, severe lower respiratory tract infections. Piperacillin 4 g/tazobactam 500 mg was given intravenously every 8 h to 193 hospitalized lower respiratory tract infection patients for a minimum of 5 days. There was a favorable response rate of 97% and eradication of the causative pathogen was documented or presumed in 93% of patients. There was a low incidence of adverse experiences and the combination was well tolerated. Seventy-one intensive care patients with severe lung disease received 4 g piperacillin/500 mg tazobactam intravenously every 6 h; afterward they were given amikacin 7.5 mg/kg every 12 h. Minimum duration of treatment was 5 days. Therapy with piperacillin/tazobactam plus amikacin was well-tolerated, produced a 74% favorable clinical response rate, and eradicated the responsible pathogen in 70% of patients.
在一项针对社区获得性下呼吸道感染患者的研究以及一项针对医院获得性严重下呼吸道感染患者的研究中,研究人员评估了哌拉西林/他唑巴坦治疗的疗效和安全性。对193名住院的下呼吸道感染患者每8小时静脉注射4克哌拉西林/500毫克他唑巴坦,至少治疗5天。有效率为97%,93%的患者记录或推测致病病原体被清除。不良事件发生率低,该联合用药耐受性良好。71名患有严重肺部疾病的重症监护患者每6小时静脉注射4克哌拉西林/500毫克他唑巴坦;之后每12小时给予阿米卡星7.5毫克/千克。最短治疗时间为5天。哌拉西林/他唑巴坦联合阿米卡星治疗耐受性良好,临床有效率为74%,70%的患者致病病原体被清除。