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首页> 外文期刊>Clinical Medicine Insights: Trauma and Intensive Medicine >A Novel Electronic Device for Measuring Urine Flow Rate: A Clinical Investigation
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A Novel Electronic Device for Measuring Urine Flow Rate: A Clinical Investigation

机译:一种新型电子尿液测量装置的临床研究

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Objective:Currently, most vital signs in the intensive care unit (ICU) are electronically monitored. However, clinical practice for urine output (UO) measurement, an important vital sign, usually requires manual recording of data that is subject to human errors. In this study, we assessed the ability of a novel electronic UO monitoring device to measure real-time hourly UO versus current clinical practice.Design:Patients were connected to the RenalSense Clarity RMS Sensor Kit with a sensor integrated within a standard sterile urinary catheter drainage tube to monitor urine flow in real time. The Clarity RMS Sensor Kit was modified to incorporate a standard urinometer (Unomedical) for the nursing staff to record UO as per their standard practice. The drainage bag was placed in a container on a scientific scale (Precisa BJ) to be used as the gold standard.Interventions:Nursing records for hourly UO were collected and compared with the electronically recorded UO. Sensor measurements and nursing staff manual records of UO were compared with the scale data.Setting:The study setting was the ICU of Hadassah Hospital, Jerusalem.Patients:Data from 23 patients with a urinary catheter were observed in this study.Measurements and main results:A total of 1046?hours of UO were recorded from 23 subjects. Compared with the scale data, the measurements of hourly urine flow measured with the RenalSense system were closer, had a better correlation, and narrower limits of agreement to gravimetrically determined values than the measurements obtained by the nurses. In addition, continuous monitoring of UO provided graphical display of response to repeated diuretic administration.Conclusions:An electronic device for recording UO has been shown to provide more reliable information of UO records and patient fluid status than current practice. Future applications of this device will provide valuable information to help set protocol goals such as decisions for timely fluid and diuretic administration and response.
机译:目的:目前,重症监护病房(ICU)的大多数生命体征均通过电子方式监控。但是,尿液输出量(UO)测量的临床实践是重要的生命体征,通常需要人工记录容易受人为错误的数据。在这项研究中,我们评估了新型电子UO监测设备与当前临床实践相比每小时测量实时UO的能力设计:将患者连接到RenalSense Clarity RMS传感器套件,该传感器套件集成在标准无菌导尿管引流中管实时监测尿流。对清晰度RMS传感器套件进行了修改,以纳入标准的尿液计(标准),供护理人员按照其标准做法记录UO。将引流袋放在科学规模的容器中(Precisa BJ)作为金标准。干预措施:收集每小时UO的护理记录,并将其与电子记录的UO进行比较。将UO的传感器测量值和护理人员的手动记录与量表数据进行比较。地点:研究地点是耶路撒冷哈达萨医院的ICU。患者:本研究观察了来自23名带导尿管的患者的数据。 :从23位受试者中记录了总计1046小时的UO。与规模数据相比,与护士获得的测量值相比,使用RenalSense系统测量的每小时尿液流量测量值更接近,具有更好的相关性,并且与重量测定值的一致性较窄。此外,对UO的连续监测提供了对重复利尿剂给药反应的图形显示。结论:记录UO的电子设备已显示出比当前实践更可靠的UO记录信息和患者体液状态。该设备的未来应用将提供有价值的信息,以帮助设定协议目标,例如及时进行补液和利尿剂管理和反应的决策。

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