Hopefl A W
Drug Intell Clin Pharm. 1985 Mar;19(3):171-5.
Aztreonam is the first synthetic monobactam to undergo clinical studies in the U.S. Aztreonam has excellent activity against P. aeruginosa and Enterobacteriaceae, but poor activity against anaerobic and gram-positive organisms. Aztreonam has poor oral bioavailability, but can be given intramuscularly or intravenously in doses of 1-2 g q6-12h. Clinical trials of aztreonam have shown it to be effective in infections of urine, lung, skin, blood, bones and joints, and abdomen with an adverse reaction profile similar to beta-lactams. Aztreonam may be an alternate to aminoglycoside therapy, with the advantage of not being nephrotoxic.
氨曲南是美国首个进行临床研究的合成单环β-内酰胺类抗生素。氨曲南对铜绿假单胞菌和肠杆菌科细菌具有出色的活性,但对厌氧菌和革兰氏阳性菌的活性较差。氨曲南口服生物利用度低,但可通过肌肉注射或静脉注射给药,剂量为1-2克,每6-12小时一次。氨曲南的临床试验表明,它对泌尿系统、肺部、皮肤、血液、骨骼和关节以及腹部感染有效,不良反应与β-内酰胺类药物相似。氨曲南可能是氨基糖苷类治疗的替代药物,优点是没有肾毒性。