Gooding P G, Berman E, Lane A Z, Agre K
J Infect Dis. 1976 Nov;134 SUPPL:S441-5. doi: 10.1093/infdis/135.supplement_2.s441.
Case records of 1,098 patients treated with amikacin at 79 research centers in 10 countries in a program of worldwide clinical trials were reviewed. Of the 697 patients eligible for use in evaluation of efficacy of the drug, 81% were cured, as evidenced by clinical remission and eradication of the infecting pathogen. The usual dosage was 7.5 mg/kg administered intramuscularly at 12-hr intervals. This dosage was modified in patients with renal impairment. Amikacin was effective in 90% of 322 patients with genitourinary infections, 85% of 97 patients with septicemia, 70% of 73 patients with infections of skin, soft tissue, or bone (excluding burns), and 69% of 68 patients with infections of the lower respiratory tract. Amikacin was effective in treatment of 88% of 85 infections due to gentamicin-resistant pathogens. The drug was generally well tolerated, and no side effects were reported in 80.6% of the 1,098 patients evaluated. Amikacin shares with other aminoglycosides the risk of ototoxicity and nephtotoxicity; previous exposure to gentamicin was a major factor in the development of such adverse effects. Other adverse reactions were relatively infrequent and in most cases were characterized as mild and transient.
对10个国家79个研究中心参与一项全球临床试验项目的1098例接受阿米卡星治疗的患者的病历进行了回顾。在697例符合药物疗效评估条件的患者中,81%获得治愈,临床缓解和感染病原体清除可证明这一点。常用剂量为7.5mg/kg,每12小时肌肉注射一次。肾功能损害患者的剂量进行了调整。阿米卡星对322例泌尿生殖系统感染患者中的90%有效,对97例败血症患者中的85%有效,对73例皮肤、软组织或骨感染(不包括烧伤)患者中的70%有效,对68例下呼吸道感染患者中的69%有效。阿米卡星对85例由庆大霉素耐药病原体引起的感染中的88%治疗有效。该药物总体耐受性良好,在接受评估的1098例患者中,80.6%未报告有副作用。阿米卡星与其他氨基糖苷类药物一样,有耳毒性和肾毒性风险;既往接触过庆大霉素是发生此类不良反应的主要因素。其他不良反应相对较少,且在大多数情况下表现为轻度和短暂性。