Effect of perfusate volume on amikacin concentrations after saphenous intravenous regional limb perfusion in standing, sedated horses.

Kelsey A Jurek, M. Schoonover, Megan R. Williams, P. Rudra
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Abstract

OBJECTIVE To determine the influence of perfusate volume on synovial fluid amikacin concentrations in the joints of the hind limb after standing saphenous intravenous regional limb perfusion (IVRLP). STUDY DESIGN Randomized crossover design. ANIMALS Six adult horses. METHODS Saphenous IVRLP was performed in 6 standing horses with 1 g of amikacin diluted with 0.9% NaCl to volumes of 10 ml, 60 ml, and 120 ml. Samples of synovial fluid from the tarsocrural, metatarsophalangeal, and hind limb distal interphalangeal joints were collected at 15 and 30 min after perfusate administration. Concentrations of 40 μg/ml and 160 μg/ml were considered therapeutic for susceptible and resistant pathogens, respectively. RESULTS No difference in synovial fluid amikacin concentrations was detected between volumes in any joint (P = .4). All synovial fluid amikacin concentrations were higher at 30 min compared to 15 min (P = .003). All median synovial fluid amikacin concentrations at 30 min were > 40 μg/ml using the 60 ml and 120 ml volumes. Synovial fluid amikacin concentrations >40 μg/ml were only reached in the hind limb distal interphalangeal joint when the 10 ml volume was used. All median synovial fluid amikacin concentrations observed were < 160 μg/ml. CONCLUSIONS Target concentrations for pathogens that were considered susceptible were consistently reached with perfusate volumes of 60 ml and 120 ml. However, median synovial fluid amikacin concentrations did not reach target levels for resistant pathogens. CLINICAL SIGNIFICANCE Perfusate volumes of 60 ml or 120 ml are recommended to treat infections due to susceptible pathogens in the joints of the distal hind limb. These results justify investigation of saphenous IVRLP with different perfusate volumes using higher doses of amikacin.
静置镇静马隐静脉局部肢体灌注后灌注量对阿米卡星浓度的影响。
目的探讨静置下肢局部静脉灌注(IVRLP)后,灌注量对后肢关节滑液阿米卡星浓度的影响。研究设计:随机交叉设计。六匹成年马。方法用0.9% NaCl稀释阿米卡星1 g,体积分别为10 ml、60 ml和120 ml,对6匹立马进行静脉静脉注射。灌注给药后15和30分钟采集跗跖、跖趾和后肢远端指间关节的滑液样本。40 μg/ml和160 μg/ml分别被认为对敏感和耐药病原体有治疗作用。结果各关节容积间滑膜液阿米卡星浓度无差异(P = 0.4)。所有滑膜液阿米卡星浓度在30分钟高于15分钟(P = 0.003)。在60 ml和120 ml体积下,30 min时滑液中位阿米卡星浓度均> 40 μg/ml。仅后肢远端指间关节滑膜液中阿米卡星浓度大于40 μg/ml时,用量为10 ml。所有观察到的滑液中位阿米卡星浓度均< 160 μg/ml。结论60 ml和120 ml灌注液均可达到易感病原菌的目标浓度。然而,对于耐药病原体,滑液中阿米卡星浓度未达到目标水平。临床意义后肢远端关节易感致病菌感染推荐灌注量60ml或120ml。这些结果证明了使用更高剂量的阿米卡星对不同灌注容量的隐静脉内静脉血栓的研究是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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