Angehrn P
Chemotherapy. 1985;31(6):440-50. doi: 10.1159/000238372.
The in vitro and in vivo activity of carumonam was tested in comparison with that of aztreonam and other beta-lactam antibiotics. With the exception of a few isolates that were overproducers of cephalosporinase, Enterobacteriaceae were highly susceptible to carumonam, 90% of the isolates being inhibited at 0.5 micrograms/ml. Aztreonam, ceftriaxone and ceftazidime were overall slightly less active than carumonam against Enterobacteriaceae. Carumonam was intermediate between ceftazidime and aztreonam as to the activity against Pseudomonas aeruginosa. Staphylococci were resistant to the monocyclic beta-lactams. In accordance with the in vitro data, carumonam was effective against experimental septicemias and infections of the thigh and the kidney that were caused by gram-negative pathogens.
将卡芦莫南的体外和体内活性与氨曲南及其他β-内酰胺类抗生素进行了比较测试。除了少数头孢菌素酶高产菌株外,肠杆菌科细菌对卡芦莫南高度敏感,90%的菌株在0.5微克/毫升时被抑制。总体而言,氨曲南、头孢曲松和头孢他啶对肠杆菌科细菌的活性略低于卡芦莫南。在对铜绿假单胞菌的活性方面,卡芦莫南介于头孢他啶和氨曲南之间。葡萄球菌对单环β-内酰胺类耐药。根据体外数据,卡芦莫南对由革兰氏阴性病原体引起的实验性败血症以及大腿和肾脏感染有效。