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Cardiovascular pressure measurement in safety assessment studies: Technology requirements and potential errors

机译:安全评估研究中的心血管压力测量:技术要求和潜在错误

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In the early days of in vivo nonclinical pressure measurement, most laboratories were required to have considerable technical/engineering expertise to configure and maintain pressure transducers, amplifiers, tape recorders, chart recorders, etc. Graduate students and postdoctoral fellows typically had some training in the requirements and limitations of the technology they used and were closely engaged in the collection and evaluation of data from their own experiments. More recently, pressure sensing telemetry and data acquisition/ analysis systems are provided by vendors as turnkey systems, often resulting in a situation where users are less familiar with the technicalities of their operation. Also, investigators are now more likely to be absent and rely on technical staff for the collection of raw in vivo pressure data from their experiments than in the past. Depending on the goals of an experiment, an investigator may require the measurement of a variety of different pressure parameters, over varying periods of time. A basic understanding of the requirements and limitations that can affect the accuracy and precision of these parameters is important to ensure that the results and conclusions from an experiment are reliable. Factors to consider include the possibility of hydrostatic pressure effects from blood inside the vasculature of the animal, depending on the location of the sensor, as well as from fluid inside a fluid-filled catheter system; long-term stability (lack of drift) of a sensor over time, which can affect the interpretation of absolute pressure changes over a prolonged experiment; frequency response of the sensor and associated electronics; and the phase shift that occurs depending on location of the sensor in the vasculature or because of a fluid-filled catheter system. Each of these factors is discussed, and the particular requirements of frequency response as applied to the measurement of cardiac left ventricular pressure are emphasized. When these factors are understood, a pressure sensing and measurement system can be selected that is optimized for the experimental model being studied, thus eliminating errors or inaccurate results. (C) 2014 Published by Elsevier Inc.
机译:在体内非临床压力测量的早期,大多数实验室被要求具有相当的技术/工程专业知识,以配置和维护压力传感器,放大器,磁带记录器,图表记录器等。研究生和博士后通常都接受过一些培训。他们使用的技术的要求和局限性,并密切参与他们自己的实验数据的收集和评估。最近,卖方将压力感测遥测和数据采集/分析系统作为统包系统提供,常常导致用户不太熟悉其操作技术的情况。而且,与过去相比,现在更可能缺少研究人员,而依赖技术人员从他们的实验中收集原始体内压力数据。根据实验目的,研究人员可能需要在不同的时间段内测量各种不同的压力参数。对可能影响这些参数的准确性和精确度的要求和限制的基本理解,对于确保实验的结果和结论可靠是很重要的。需要考虑的因素包括取决于传感器位置的动物血管系统中的血液以及充满流体的导管系统中的流体产生静水压力效应的可能性;传感器随时间的长期稳定性(无漂移),可能会影响长时间实验中绝对压力变化的解释;传感器和相关电子设备的频率响应;取决于传感器在脉管系统中的位置或由于流体填充的导管系统而发生的相移。讨论了这些因素中的每一个,并强调了频率响应应用于心脏左心室压力测量的特定要求。当了解了这些因素后,便可以选择针对正在研究的实验模型进行优化的压力传感和测量系统,从而消除错误或不准确的结果。 (C)2014由Elsevier Inc.发行

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