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本文引用的文献

1
Optimizing aminoglycoside use.优化氨基糖苷类药物的使用。
Crit Care Clin. 2011 Jan;27(1):107-21. doi: 10.1016/j.ccc.2010.11.006.
2
Evaluation of the Chronic Kidney Disease Epidemiology Collaboration equation for estimating the glomerular filtration rate in multiple ethnicities.评估慢性肾脏病流行病学合作方程在多种族中估算肾小球滤过率的应用。
Kidney Int. 2011 Mar;79(5):555-62. doi: 10.1038/ki.2010.462. Epub 2010 Nov 24.
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Combating evolution with intelligent design: the neoglycoside ACHN-490.用智能设计对抗进化:新型糖基化合物 ACHN-490。
Curr Opin Microbiol. 2010 Oct;13(5):565-73. doi: 10.1016/j.mib.2010.09.004.
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Estimating the glomerular filtration rate in obese adult patients for drug dosing.估算肥胖成年患者的肾小球滤过率以进行药物剂量调整。
Adv Chronic Kidney Dis. 2010 Sep;17(5):e53-62. doi: 10.1053/j.ackd.2010.05.010.
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The future of aminoglycosides: the end or renaissance?氨基糖苷类药物的未来:终结还是复兴?
Chembiochem. 2010 May 3;11(7):880-902. doi: 10.1002/cbic.200900779.
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Detection and treatment options for Klebsiella pneumoniae carbapenemases (KPCs): an emerging cause of multidrug-resistant infection.产碳青霉烯酶肺炎克雷伯菌(KPCs)的检测与治疗选择:一种多重耐药感染的新兴病因。
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8
The use of extended-interval aminoglycoside dosing strategies for the treatment of moderate-to-severe infections encountered in critically ill surgical patients.在重症外科患者中治疗中重度感染时,使用延长间隔氨基糖苷类药物给药策略。
Surg Infect (Larchmt). 2009 Dec;10(6):563-70. doi: 10.1089/sur.2007.080.
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Extended-interval once-daily dosing of aminoglycosides in adult and pediatric patients with cystic fibrosis.成人和儿童囊性纤维化患者中氨基糖苷类药物的延长间隔一日一次给药。
Pharmacotherapy. 2010 Jan;30(1):95-108. doi: 10.1592/phco.30.1.95.
10
Continuing the use of the Cockcroft-Gault equation for drug dosing in patients with impaired renal function.继续使用Cockcroft-Gault方程对肾功能受损患者进行药物剂量计算。
Clin Pharmacol Ther. 2009 Nov;86(5):468-70. doi: 10.1038/clpt.2009.187.

简化超重和肥胖成年患者氨基糖苷类药代动力学估算。

Simplified estimation of aminoglycoside pharmacokinetics in underweight and obese adult patients.

机构信息

Albany College of Pharmacy, 106 New Scotland Ave., O'Brien Room 204, Albany, NY 12208, USA.

出版信息

Antimicrob Agents Chemother. 2011 Sep;55(9):4006-11. doi: 10.1128/AAC.00174-11. Epub 2011 Jun 13.

DOI:10.1128/AAC.00174-11
PMID:21670189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3165292/
Abstract

Aminoglycosides are an important class of agents that are used in combination antimicrobial regimens to treat bacterial pathogens. Dosing of aminoglycosides is typically based on total body weight. However, the most appropriate alternative body size descriptor for dosing aminoglycosides at the extremes of weight (underweight and obese) is not known. Also, the predictive performance of newer formulas to assess kidney function, such as the modification of diet in renal disease (MDRD) and chronic kidney disease-epidemiology (CKD-EPI) equations compared to the Cockcroft-Gault equation to predict aminoglycoside clearance, is not known. We sought to examine dosing of aminoglycosides across the extremes of weight using a variety of formulas to assess kidney function. Pharmacokinetic data were obtained from a set of prospectively collected data (1982 to 2003) of 2,073 (53.5% male) adult patients that included 497 tobramycin- and 1,576 gentamicin-treated cases. The median (minimum, maximum) age, weight, and body mass index were 66 (18, 98) years, 70.0 (29.7, 206.7) kg, and 24.4 (11.3, 73.8) kg/m(2), respectively. The percentage of underweight, normal-weight, overweight, and obese cases based on the World Health Organization classification were 8.8%, 45.5%, 26.5%, and 19.2%, respectively. The aminoglycoside volume of distribution was normalized to several alternative body size descriptors. Only lean body weight estimated by the method of S. Janmahasatian et al. (Clin. Pharmacokinet. 44:1051-1065, 2005) normalized the volume of distribution for both tobramycin and gentamicin across all weight strata, with the estimate being approximately 0.45 liter/kg. Aminoglycoside dosing can be simplified across all weight strata with the use of lean body weight. The CKD-EPI equation best predicts aminoglycoside clearance.

摘要

氨基糖苷类是一类重要的药物,常与其他抗菌药物联合用于治疗细菌病原体。氨基糖苷类药物的剂量通常基于总体重。然而,在体重极轻(消瘦)和极重(肥胖)的情况下,用于氨基糖苷类药物剂量的最合适的替代身体大小描述符尚不清楚。此外,用于评估肾功能的新公式(如肾脏病饮食改良公式(MDRD)和慢性肾脏病-流行病学合作研究公式(CKD-EPI))与 Cockcroft-Gault 公式相比,预测氨基糖苷类药物清除率的预测性能也尚不清楚。我们试图使用各种公式评估体重极端情况下的氨基糖苷类药物剂量。药代动力学数据来自一组前瞻性收集的数据(1982 年至 2003 年),共包括 2073 名(53.5%为男性)成年患者,其中包括 497 例妥布霉素和 1576 例庆大霉素治疗的病例。中位(最小,最大)年龄、体重和体重指数分别为 66(18,98)岁、70.0(29.7,206.7)kg 和 24.4(11.3,73.8)kg/m2。根据世界卫生组织分类,消瘦、正常体重、超重和肥胖的病例百分比分别为 8.8%、45.5%、26.5%和 19.2%。氨基糖苷类药物的分布容积被归一化为几种替代身体大小描述符。只有 S. Janmahasatian 等人提出的瘦体重估计方法(Clin. Pharmacokinet. 44:1051-1065, 2005)使妥布霉素和庆大霉素在所有体重分层中的分布容积归一化,估计值约为 0.45 升/千克。使用瘦体重可以简化所有体重分层中的氨基糖苷类药物剂量。CKD-EPI 方程最能预测氨基糖苷类药物清除率。