Capillary Filtration of Plasma is Accelerated During General Anesthesia: A Secondary Population Volume Kinetic Analysis.

IF 2.9 4区 医学
Robert G Hahn
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Abstract

How infusion fluids are distributed and eliminated is of importance to how much and how fast they should be administered. This manuscript applies population pharmacokinetic modeling to intravenous infusions of crystalloid fluid, which is a common therapy in hospital care and mandatory during surgery. The analysis was based on the hemodilution and urine output measured during and after 262 infusions of 1647 ± 461 mL (mean ± SD) of fluid over 30 min in adults. The result shows that distribution of fluid from the plasma to the interstitial fluid space occurred twice as fast during general anesthesia as compared to the conscious state. The increased rate ensures adequate nutritional flow to the cells despite decreased flow in the macrocirculation, which is a characteristic of general anesthesia. This increased capillary leakage of fluid was coupled with an even greater reduction of the urinary output and accumulation of fluid in both the fast-exchange interstitial fluid space and a remote "third fluid space," the latter of which apparently serves as an overflow reservoir. During the first hour of the experiments, 88% more fluid resided extravascularly in the presence of general anesthesia than in the awake state. General anesthesia increased the half-life from 1.8 to 16.6 h, showing marked impairment in the handling of infused crystalloid fluid.

全身麻醉时血浆毛细血管过滤加速:二次种群体积动力学分析。
输液液的分配和排出方式对输液液的剂量和速度至关重要。本文将群体药代动力学模型应用于晶体液体静脉输液,这是医院护理和手术期间的一种常见治疗方法。该分析是基于在30分钟内262次输注1647±461 mL(平均±SD)液体期间和之后测量的血液稀释和尿量。结果表明,在全身麻醉状态下,液体从血浆向组织液空间的分布速度是清醒状态下的两倍。增加的速率保证了充足的营养流到细胞,尽管减少了大循环的流量,这是全身麻醉的一个特点。这种增加的毛细血管漏液与尿量更大的减少和快速交换间质液空间和远端“第三流体空间”的液体积聚相结合,后者显然起到溢出储液器的作用。在实验的第一个小时内,全身麻醉状态下的液体比清醒状态下多88%。全身麻醉使半衰期从1.8小时增加到16.6小时,在处理输注晶体液体方面表现出明显的损害。
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来源期刊
Journal of Clinical Pharmacology
Journal of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
自引率
3.40%
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0
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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