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使用一次性生物传感器持续监测用过的透析液尿素水平。临床评估。

Continuous monitoring of the spent dialysate urea level using a disposable biosensor. Clinical evaluation.

作者信息

Jacobs P, Sansen W, Hombrouckx R

机构信息

K. U. Leuven Department of Electronics ESAT-MICAS, Heverlee, Belgium.

出版信息

ASAIO J. 1994 Jul-Sep;40(3):M393-400. doi: 10.1097/00002480-199407000-00029.

DOI:10.1097/00002480-199407000-00029
PMID:8555545
Abstract

The first real-time, online measurements obtained using a screen-printed planar sensor to continually monitor urea in the spent dialysate are described. Evaluation of the sensor performance in the real clinical situation involves an extensive comparison of pre and post dialysis characteristics. Steady-state response and calibration curves show excellent reproducibility (typically within 5%; maximum deviation, 15%). The real-time results show that the characteristics predicted from the predialysis characterization are preserved during and after the prolonged period of continuous contact with the dialysate without needing recalibration. An operational stability of more than 10 hours of continuous use has been observed. Stability including intermittent wet-storage was found to be more than 5 days. Zero-baseline stability greater than 0.2 mmol/l (1.2 Og/dl) during the 4 hr treatment period and a resolution of 0.2 mmol/l were achieved, with a full-scale range of 15 mmol/l (90 mg/dl). A response time of less than 3 minutes allows dialysate urea levels to be monitored as a function of dialysis parameters such as varying blood flow. Parallel analysis of dialysate samples taken at 15 min intervals shows good correlation with the recorded data, although correspondence of the absolute values requires that the real-time data be rescaled. Because no degradation of the sensor performance was observed in vitro, this deviation can be explained only in terms of a dialysate based interference, probably caused by changes in pH and buffer.

摘要

本文描述了首次使用丝网印刷平面传感器对用过的透析液中的尿素进行连续监测所获得的实时在线测量结果。在实际临床情况下对传感器性能的评估涉及透析前后特征的广泛比较。稳态响应和校准曲线显示出极佳的重现性(通常在5%以内;最大偏差为15%)。实时结果表明,在与透析液长时间持续接触期间及之后,无需重新校准,预透析表征所预测的特征得以保留。已观察到连续使用超过10小时的操作稳定性。包括间歇性湿存储在内的稳定性超过5天。在4小时治疗期间实现了大于0.2 mmol/l(1.2 mg/dl)的零基线稳定性和0.2 mmol/l的分辨率,满量程范围为15 mmol/l(90 mg/dl)。小于3分钟的响应时间使得能够根据诸如不同血流量等透析参数来监测透析液尿素水平。以15分钟间隔采集的透析液样本的平行分析显示与记录数据具有良好的相关性,尽管绝对值的对应要求对实时数据进行重新缩放。由于在体外未观察到传感器性能的下降,这种偏差只能用基于透析液的干扰来解释,可能是由pH值和缓冲液的变化引起的。

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