Drobin D
Department of Anesthesiology, Södersjukhuset AB, Stockholm, Sweden.
Acta Anaesthesiol Scand. 2006 Oct;50(9):1074-80. doi: 10.1111/j.1399-6576.2006.01117.x.
Volume kinetics was developed to analyze the distribution and elimination of intravenously given fluid. However, when groups of patients are being compared, the current approach is limited by the need for several models, which yield parameters that cannot be compared. To meet the requirement to handle all patients in a group individually and without pooling, a new all-encompassing model was designed. The aim of this paper was to test whether the new model could be used to analyze all patients in a group.
The new model consists of 'rate' and 'amount' parameters instead of 'clearance' and 'dilution' parameters. With this change, a redundant parameter can be taken out, but the biexponential nature is retained. The new parameters are the volume of distribution V1 (ml), the intercompartmental rate constant kt/min and the elimination rate constant kr/min. The success rates of the new and original models in producing results within a set of pre-determined quality requirements were compared using blood dilution data from 10 volunteers challenged with intravenous lactated Ringer's solution.
The new model could be used to analyze all 10 cases within the pre-determined criteria, but the original biexponential model failed in 70% of cases. The residuals improved with the new model. The medians (interquartile ranges) were as follows: V1, 4931 ml (4239-6149 ml); kt), 0.0384/min (0.0024-0.1140/min); kr, 0.0140/min (0.0015-0.0043/min).
The new model was suited to the analysis of all cases, and is therefore a better approach to study how clinical conditions change the distribution and elimination of infused fluid.
容量动力学用于分析静脉输注液体的分布和消除情况。然而,在比较患者组时,目前的方法受到需要多个模型的限制,这些模型产生的参数无法进行比较。为满足单独处理一组中所有患者而不进行合并的要求,设计了一种新的综合模型。本文的目的是测试新模型是否可用于分析一组中的所有患者。
新模型由“速率”和“量”参数组成,而非“清除率”和“稀释”参数。通过这种改变,可以去除一个冗余参数,但保留双指数性质。新参数为分布容积V1(毫升)、隔室间速率常数kt/分钟和消除速率常数kr/分钟。使用10名接受静脉输注乳酸林格氏液挑战的志愿者的血液稀释数据,比较新模型和原始模型在一组预定质量要求内产生结果的成功率。
新模型可用于在预定标准内分析所有10例病例,但原始双指数模型在70% 的病例中失败。新模型的残差有所改善。中位数(四分位间距)如下:V1,4931毫升(4239 - 6149毫升);kt,0.0384/分钟(0.0024 - 0.1140/分钟);kr,0.0140/分钟(0.0015 - 0.0043/分钟)。
新模型适用于所有病例的分析,因此是研究临床状况如何改变输注液体的分布和消除的更好方法。