Department of Pathology and Laboratory Medicine, Saskatoon Health Region, Saskatoon, SK, Canada S7M 0Z9.
Comput Biol Med. 2013 Feb;43(2):84-90. doi: 10.1016/j.compbiomed.2012.11.008. Epub 2012 Dec 8.
Anemia is prevalent among critical care patients and is attributed to pathologic and iatrogenic processes and bleeding. The extent that diagnostic blood loss contributes to anemia among adult critical care patients is controversial and multi-factorial. The aim of this study is to describe an erythrokinetic model that integrates rates of phlebotomy, erythropoiesis and red cell senescence with patient characteristics to predict the onset of iatrogenic anemia in an objective manner. Using sex-specific parameters, the model predicts that adults with (average body weight and average blood volume), initial hemoglobin concentration at mid-reference interval, active erythropoiesis and losing 53 mL of blood per day by phlebotomy would require 40-70 days to reach 70 g/L of hemoglobin. To mimic critical care patients with low initial hemoglobin and suppressed erythropoiesis, the influence of daily blood loss and total blood volume was predicted. Simultaneous lack of erythropoiesis, initial hemoglobin concentrations at the lower limit of the reference interval (110 g/L), low body weight and increased phlebotomy accelerated onset of ~70 g/L hemoglobin transfusion threshold to 9-14 days. This computer simulation depicts the extent that adult critical care patients with anemia risk factors could benefit from conservative test ordering practices and subsequent reduced diagnostic phlebotomy.
贫血在重症监护患者中很常见,可归因于病理和医源性过程以及出血。诊断性失血在多大程度上导致成年重症监护患者贫血存在争议且具有多因素性。本研究旨在描述一个红细胞生成动力学模型,该模型将采血、红细胞生成和红细胞衰老的速率与患者特征相结合,以客观的方式预测医源性贫血的发生。使用性别特异性参数,该模型预测,每天通过采血丢失 53 毫升血液且具有(平均体重和平均血容量)、初始血红蛋白浓度处于参考区间中间值、活跃的红细胞生成的成年人,将需要 40-70 天达到血红蛋白 70 g/L。为了模拟初始血红蛋白低且红细胞生成受抑制的重症监护患者,预测了每日失血和总血容量的影响。同时缺乏红细胞生成、参考区间下限(110 g/L)的初始血红蛋白浓度、低体重和采血增加会加速达到血红蛋白 ~70 g/L 的输血阈值至 9-14 天。这种计算机模拟描述了具有贫血风险因素的成年重症监护患者在遵循保守的检验医嘱和随后减少诊断性采血方面可以受益的程度。