Kato Y, Saito A, Yajima O, Tomizawa M, Nakayma I
Jpn J Antibiot. 1976 Apr;29(4):358-65.
Basic and clinical investigation on the intravenous administration of sulbenicillin in moderate dose (510g daily) was carried out to evaluate its clinical effect in systemic infections due to gram-negative bacilli. The following results were obtained. (1) In human subjects received 5 g intravenous drip infusion, the peak blood levels were found at the end of infusion. In 6 cases with normal renal function (Ccr greater than or equal to 70ml/min.) the peak blood level was 181 mcg/ml on the average and the half-life 1.1 hours, while in 3 cases with impaired renal function (Ccr less than 70 ml/min.) the peak level 216 mcg/ml and the half-life longer than 2 hours. The height of the peak level seemed to be subjected to the duration of infusion. The renal excretion of sulbenicllin was 55.2% on the average both in cases with normal and impaired renal functions. (2) Sulbenicillin, 510g daily divided in 2 doses, was administered to 15 cases including 6 cases with acute pyelonephritis, 3 with acute cystitis, 3 with biliary tract infection, 2 with respiratory tract infection and 1 with acute prostatitis. All the cases except 3 cases with acute pyelonephritis had underlying diseases. Escherichia coli was isolated from 10 cases, Klebsiella from 2, Pseudomonas aeruginosa from 1, and unidentified gram-negative bacilli from 1. Eleven cases responded to the treatment, but 4 cases failed. In 11 cases with susceptible bacteria, 8 cases responded bacteriologically (2 cases recurred), and 3 cases failed to respond. A case with biliary tract infection due to E. coli did not respond to 5 g daily treatment, but responded to 5 g twice daily. Two cases due to organisms which were not inhibited by 200mcg/ml in vitro did not respond to the treatment. (3) A moderate decrease in red blood cell number and hemoglobin content was observed in one case. A transient increase in transaminase and alkaline phosphatase level was observed in other cases.
进行了中等剂量(每日5克)注射用磺苄西林的基础和临床研究,以评估其对革兰氏阴性杆菌所致全身感染的临床疗效。获得了以下结果。(1)在接受5克静脉滴注的人体受试者中,血药峰浓度在滴注结束时出现。6例肾功能正常(肌酐清除率大于或等于70毫升/分钟)的受试者,血药峰浓度平均为181微克/毫升,半衰期为1.1小时;而3例肾功能受损(肌酐清除率小于70毫升/分钟)的受试者,血药峰浓度为216微克/毫升,半衰期超过2小时。峰浓度的高低似乎与滴注持续时间有关。磺苄西林的肾排泄率在肾功能正常和受损的受试者中平均均为55.2%。(2)对15例患者每日给予5克磺苄西林,分2次给药,其中包括6例急性肾盂肾炎、3例急性膀胱炎、3例胆道感染、2例呼吸道感染和1例急性前列腺炎。除3例急性肾盂肾炎患者外,所有患者均有基础疾病。10例分离出大肠杆菌,2例分离出克雷伯菌,1例分离出铜绿假单胞菌,1例分离出未鉴定的革兰氏阴性杆菌。11例患者治疗有效,但4例无效。在11例感染敏感菌的患者中,8例细菌学治疗有效(2例复发),3例无效。1例大肠杆菌所致胆道感染患者每日5克治疗无效,但每日2次5克治疗有效。2例体外200微克/毫升浓度不能抑制的病原菌所致感染患者治疗无效。(3)1例患者红细胞数量和血红蛋白含量略有下降。其他患者观察到转氨酶和碱性磷酸酶水平短暂升高。