Farchione L A, Chudzik G M
J Clin Pharmacol. 1978 Aug-Sep;18(8-9):432-8. doi: 10.1002/j.1552-4604.1978.tb02460.x.
The ratio of the peak serum concentration after a 500-mg dose of amikacin to the pathogen minimum inhibitory concentration was determined for 95 patients under treatment for serious Gram-negative infections. There were 113 such ratios. The relationship of this inhibitory ratio to the clinical effectiveness and side effects of treatment with this new aminoglycoside was also studied. Mean peak serum concentration of drug was 25.8 microgram/ml, and mean inhibitory ratio was 13.0. Ninety-six per cent of inhibitory ratios were greater than or equal to 1.0. Therapy was rated totally effective in 85% of patients clinically evaluated and partially effective in 3%. Signs of renal or eighth cranial nerve impairment attributable to drug administration were confined to only two patients, and there were no other side effects. The reliability of amikacin therapy appears to be related to dependable serum levels and high inhibitory ratios.
测定了95例正在接受严重革兰氏阴性菌感染治疗患者在给予500毫克阿米卡星剂量后的血清峰值浓度与病原体最低抑菌浓度之比。共得到113个这样的比值。还研究了这种抑制比与使用这种新氨基糖苷类药物治疗的临床疗效和副作用之间的关系。药物的平均血清峰值浓度为25.8微克/毫升,平均抑制比为13.0。96%的抑制比大于或等于1.0。在临床评估的患者中,85%的患者治疗被评为完全有效,3%的患者部分有效。因给药导致的肾或第八颅神经损伤迹象仅局限于两名患者,且无其他副作用。阿米卡星治疗的可靠性似乎与可靠的血清水平和高抑制比有关。