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临床试验/NCT01838343
NCT01838343已完成不适用

Efficacy of Ultrasound to Guide Management During a Rapid Response Event

Beth Israel Medical Center1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2013年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
200
试验地点
1
主要终点
Time in shock

研究概览

简要总结

Rapid response team systems have been implemented in numerous hospitals throughout the world with the goal of improving the identification and safety of hospitalized patients who are clinically deteriorating. Despite their theoretical benefit, rapid response systems have not been proven in the medical literature to ultimately change outcomes.

The traditional physical exam is helpful in evaluating and treating unstable medical patients during these types of events but has significant limitations of deceased sensitivity and specificity of findings. Ultrasound is a known tool for more accurately assessing patients in shock and respiratory failure in the ICU by highly trained operators but to the investigators knowledge has not been studied in the setting of rapid response events on hospital wards by critical care fellows after focused training. The investigators aim to assess the impact of ultrasound performed by critical care fellows during rapid response events.

详细描述

This is an randomized controlled trial to determine if portable critical care ultrasound use is feasible, if its findings change clinical decision making by critical care fellows and whether ultrasound can improve patient outcomes during rapid response events at Beth Israel Medical Center.

Patients for whom a rapid response has been called for cardiac or respiratory failure will be randomized to either have a bedside ultrasound performed by a critical care fellow at the time of rapid response or to undergo a bedside ultrasound only if clinically indicated and specifically requested by the RRT leader.

For all patients on whom a rapid response is called with shock or respiratory failure who are randomized to the intervention group, a designated ultrasound critical care fellow will document their ranked top 2 preliminary cause for either shock or respiratory failure on a data collection instrument (DCI). These clinical (i.e. pre-ultrasound) diagnoses will be based on history, physical exam and all ancillary testing available prior to ultrasound performance. Available ancillary testing will be documented.

An ultrasound exam will then be performed by the designated ultrasound fellow using a portable hand-carried unit (GE Vscan) and the findings documented on the same DCI. The GE Vscan will be used for all ultrasounds performed during this study. The ultrasound study will take approximately 5 -10 minutes and will not interfere with alternative evaluation or treatment modalities deemed to be necessary during the rapid response.

The critical care ultrasound fellow will then provide the RRT leader team with their 2 most likely post ultrasound diagnosis for shock and respiratory failure and then document these on the DCI. Any changes to management made as a result of the ultrasound exam, including all new ancillary tests and therapeutic interventions will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Patients for whom a rapid response is called who have:
  • Hemodynamic instability as defined by:
  • Systolic blood pressure less than 90 mmHg or less than 40 mmHg from previously established baseline
  • Heart rate greater than 130 beats per minute
  • Known elevated lactate above normal value.
  • Hypercapnic or hypoxemic respiratory failure as judged by the responding critical care fellow.

排除标准

  • Patients for whom a rapid response has been called who:
  • Are not hemodynamically unstable and not in respiratory failure.
  • Are hemodynamically unstable but who have an obvious source of bleeding to explain hemodynamic instability.

结局指标

主要结局

Time in shock

时间窗: Immediately after rapid response

Time on vasopressors following the rapid response event and for 8 weeks thereafter.

Time in respiratory failure

时间窗: From immediately after rapid response event and for 8 weeks thereafter.

Time period that the patient requires invasive or non-invasive mechanical ventilation.

次要结局

  • Mortality(During hospitaliztion or for 8 weeks thereafter.)
  • Diagnosis variation following ultrasound(Immediately after ultrasound and for 1 day thereafter.)
  • Utilization of chest x-ray(Following rapid response event and one day thereafter.)
  • Utilization of CT scan(Following rapid response event for one day thereafter.)
  • Length of stay(Following rapid response event and for 8 weeks thereafter.)
  • Management changes following ultrasound performance(Immediately following ultrasound and for one day thereafter.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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