跳至主要内容
临床试验/NCT02185521
NCT02185521终止不适用

Hemodynamic Instability Rules Based Advisor: The Impact to Care With a New Predictive Indicator (HIRBA 2.0)

Philips Healthcare4 个研究点 分布在 1 个国家目标入组 127 人开始时间: 2016年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
127
试验地点
4
主要终点
Intensive Care Unit (ICU) Length of Stay

研究概览

简要总结

Philips has developed a new algorithm, called Hemodynamic Instability Rules Based Advisor (HIRBA 2.0) system, for the prediction of hemodynamic instability in critically ill patients, who were not previously known to be at risk. This algorithm provides with the numerical index - Hemodynamic Instability Index (HII) and its trend which are calculated from existing real time data derived from patient's current hospital stay such as heart rate and blood pressure, labs, and Admission - Discharge- Transfer (ADT) data to help healthcare providers obtain information about patient's status and make clinical decisions.

The aim of the study is to determine if the patient clinical information, displayed in the form of HII, can prompt possible patient hemodynamic status change and trigger earlier clinical care team response. We hypothesize that this real-time information on hemodynamic instability and earlier clinical decision making will lead to reduced length of stay (LOS) and ICU mortality relative to standard care practice. Study will also identify if the use of the Philips new algorithm called Hemodynamic Instability Rules Based Advisor (HIRBA 2.0) can improve outcomes for patients admitted to the intensive care units (ICUs).

During this study, upon patient admission to the ICU clinical data collection will begin. Data that will be pulled during the study includes: vital signs, medications, reason for admission to the ICU, treatments that patient may receive.

Research subjects will not be asked to do anything as far as specific activities expected to be accomplished during study participation. Subjects will be involved in the study only during their stay in ICU. HII information will be visible to clinicians, taking care of this patient only during his/ her stay in the study unit.

Study team will collect patient information and have the ability to view the HII for subjects.

Once patient leaves the ICU the study team will collect information on the remainder of patient's hospital course including date of hospital discharge. All collected data will be then fully de-identified and released to Philips for analysis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients admitted to the study unit will be invited to participate in the study.
  • Study subject has to stay in study unit for at least 12 hours.

排除标准

  • Patients who were discharged from study unit earlier then 12 hours after admission.
  • Patients who are or become dependent on extracorporeal membrane oxygenation (ECMO) support.

研究组 & 干预措施

visible HII - patient assessment

Experimental

Clinical team from study unit will observe the Hemodynamic Instability Index created by the HIRBA 2.0 system for individual subjects randomized into HII group arm.

If the HII value will cross the threshold, indicative of hemodynamic deterioration, subject from the study arm will receive intervention: clinical assessment.

干预措施: patient assessment (Other)

结局指标

主要结局

Intensive Care Unit (ICU) Length of Stay

时间窗: From time of the study subject admission to the unit until the day of discharge of that same study subject from the unit, assessed up to 12 months.

次要结局

  • Intensive Care Unit (ICU) Mortality(From date of randomization of the study subject until the date of ICU discharge, an average of 6.7 days..)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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