Phillips I, King A, Shannon K
Am J Med. 1986 Jun 30;80(6B):48-55. doi: 10.1016/0002-9343(86)90479-1.
Aminoglycoside resistance was monitored at St. Thomas' Hospital from 1975 to 1984. Gentamicin resistance had appeared in a number of species by 1975, but remained rare (less than 1 percent of isolates) in Escherichia coli throughout the study period. Gentamicin-resistant Klebsielleae had become fairly common (8 percent of isolates) by 1977, but little change has subsequently occurred in their frequency of isolation. Serratia species are not frequently isolated; gentamicin resistance in these organisms was not observed until 1979. Since then, 10 to 20 percent of isolates have been found to be resistant. Except for Providencia, most isolates of which were gentamicin-resistant, less than 5 percent of the Enterobacteriaceae isolated were found to be resistant to gentamicin during the 10-year period. Throughout the study, approximately 5 percent of the Pseudomonas aeruginosa isolates were resistant to gentamicin. Less than 5 percent of the isolates of Acinetobacter were resistant to gentamicin before 1979, at which time 40 percent were found to be resistant; subsequently, gentamicin resistance among these organisms has become somewhat less common. On the whole, tobramycin resistance has mirrored gentamicin resistance. However, before 1979, most gentamicin-resistant Klebsielleae isolates had retained susceptibility to tobramycin, as had most gentamicin-resistant isolates of Acinetobacter and P. aeruginosa. Amikacin resistance has remained very unusual in all organisms, apart from non-aeruginosa Pseudomonas species. Until 1977, nearly all the resistance among Enterobacteriaceae was attributable to AAC(3)-I, except for that caused by AAC(2') production in Providencia and the non-enzymatic resistance observed in E. coli. However, more recently, AAC(3)-II and AAD(2'') have become the most common mechanisms of resistance. The resistance of most gentamicin-resistant isolates of P. aeruginosa from 1974 to 1977 was attributable to non-enzymatic mechanisms; subsequently, such resistance was more often caused by AAC(3)-I, AAC(6'), or AAD(2''). Gentamicin resistance first appeared in Staphylococcus aureus in 1976, after which about 1 to 2 percent of the isolates from hospitalized patients were found to be resistant, mostly because of production of AAC(6') and APH(2'').
1975年至1984年期间,圣托马斯医院对氨基糖苷类抗生素耐药情况进行了监测。到1975年时,庆大霉素耐药已在一些菌种中出现,但在整个研究期间,大肠杆菌中的庆大霉素耐药情况仍很罕见(分离株中不到1%)。到1977年时,庆大霉素耐药的克雷伯菌已相当常见(分离株的8%),但此后其分离频率几乎没有变化。沙雷氏菌属不常被分离;直到1979年才观察到这些菌对庆大霉素耐药。从那时起,发现10%至20%的分离株耐药。除普罗威登斯菌属外,其大多数分离株对庆大霉素耐药,在这10年期间,分离出的肠杆菌科细菌中不到5%被发现对庆大霉素耐药。在整个研究过程中,约5%的铜绿假单胞菌分离株对庆大霉素耐药。1979年前,不动杆菌属的分离株中不到5%对庆大霉素耐药,当时发现40%耐药;随后,这些菌中的庆大霉素耐药情况变得不那么常见了。总体而言,妥布霉素耐药情况与庆大霉素耐药情况相似。然而,1979年前,大多数庆大霉素耐药的克雷伯菌分离株对妥布霉素仍敏感,不动杆菌属和铜绿假单胞菌的大多数庆大霉素耐药分离株也是如此。除非铜绿假单胞菌属的假单胞菌种外,阿米卡星耐药在所有菌种中一直非常少见。直到1977年,肠杆菌科细菌中的几乎所有耐药情况都归因于AAC(3)-I,普罗威登斯菌中由AAC(2')产生的耐药情况及大肠杆菌中观察到的非酶促耐药情况除外。然而,最近,AAC(3)-II和AAD(2'')已成为最常见的耐药机制。1974年至1977年期间,大多数铜绿假单胞菌庆大霉素耐药分离株的耐药归因于非酶促机制;随后,这种耐药更常由AAC(3)-I、AAC(6')或AAD(2'')引起。庆大霉素耐药于1976年首次出现在金黄色葡萄球菌中,此后,住院患者分离株中约1%至2%被发现耐药,主要是由于产生了AAC(6')和APH(2'')。