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简化的每日一次氨基糖苷类给药方案的验证与肾毒性及治疗监测指南

Validation and nephrotoxicity of a simplified once-daily aminoglycoside dosing schedule and guidelines for monitoring therapy.

作者信息

Prins J M, Weverling G J, de Blok K, van Ketel R J, Speelman P

机构信息

Department of Internal Medicine, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Antimicrob Agents Chemother. 1996 Nov;40(11):2494-9. doi: 10.1128/AAC.40.11.2494.

Abstract

There is no established dosing schedule for once-daily aminoglycoside dosing regimens, and accepted guidelines for monitoring therapy are lacking. We derived a simplified schedule from the Hull and Sarubbi (J. H. Hull and F. A. Sarubbi, Ann. Intern. Med. 85:183-189, 1976) nomogram, for which efficacy and safety in a once-daily dosing regimen were previously demonstrated, and prospectively followed serum aminoglycoside levels in patients. The standard treatment was gentamicin or tobramycin at 4 mg/kg of body weight given intravenously once daily. When the renal function was decreased, the daily dose was reduced, as follows: for an estimated creatinine clearance of between 50 and 80 ml/min, the daily dose was 3.25 mg/kg, for an estimated creatinine clearance of between 30 and 50 ml/min, the daily dose was 2.5 mg/kg, and for an estimated creatinine clearance of below 30 ml/min, the daily dose was 2 mg/kg. A total of 221 patients were studied (184 received gentamicin and 37 received tobramycin). First trough levels above 2 mg/liter were recorded in 11% of the patients, and they all had a baseline creatinine clearance below 50 ml/min, or a substantial decrease in clearance between enrollment and the day that the trough level was obtained. A peak level below 6 mg/liter was recorded in 6% of the patients, and half of them received the lowest daily dose. Twenty-five of the 179 evaluable patients (14%; 95% confidence interval, 9 to 19%) fulfilled the criteria for nephrotoxicity. In a multiple regression analysis, the duration of treatment and the use of other nephrotoxic antibiotics or high-dose furosemide, but not trough levels, were significant risk factors. Since the meaning of low peak levels is unclear and since most studies with multiple daily regimens confirm the lack of an association between trough levels and toxicity, we believe that monitoring of serum drug levels can be restricted to monitoring of trough levels in patients with a creatinine clearance below 50 ml/min or with a deteriorating renal function.

摘要

对于每日一次的氨基糖苷类给药方案,目前尚无既定的给药时间表,且缺乏公认的治疗监测指南。我们从赫尔和萨鲁比(J. H. 赫尔和F. A. 萨鲁比,《内科学年鉴》85:183 - 189, 1976)的列线图中推导了一个简化的时间表,此前已证明该时间表在每日一次给药方案中的有效性和安全性,并前瞻性地跟踪了患者血清氨基糖苷类水平。标准治疗方案是每日静脉注射庆大霉素或妥布霉素,剂量为4 mg/kg体重。当肾功能下降时,每日剂量会降低,具体如下:估计肌酐清除率在50至80 ml/min之间时,每日剂量为3.25 mg/kg;估计肌酐清除率在30至50 ml/min之间时,每日剂量为2.5 mg/kg;估计肌酐清除率低于30 ml/min时,每日剂量为2 mg/kg。总共研究了221名患者(184名接受庆大霉素治疗,37名接受妥布霉素治疗)。11%的患者首次谷浓度水平高于2 mg/L,他们的基线肌酐清除率均低于50 ml/min,或者在入组至获得谷浓度水平当天之间清除率大幅下降。6%的患者峰值水平低于6 mg/L,其中一半接受了最低的每日剂量。179名可评估患者中有25名(14%;95%置信区间为9%至19%)符合肾毒性标准。在多元回归分析中,治疗持续时间以及使用其他肾毒性抗生素或大剂量速尿是显著的危险因素,而谷浓度水平不是。由于低峰值水平的意义尚不清楚,且大多数每日多次给药方案的研究证实谷浓度水平与毒性之间缺乏关联,我们认为血清药物水平监测可仅限于对肌酐清除率低于50 ml/min或肾功能恶化的患者进行谷浓度监测。

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