Using Minimally Invasive Cardiac Output Data vs. Standard Care for Patients Emergently Admitted to the Intensive Care Unit Who Are Hemodynamically Unstable

Completed

• Conditions: Cardiac Output, High; Cardiac Output, Low
• Interventions: Device: minimally invasive cardiac output system consisting of arterial line sensor and cardiac output bedside monitor (device)

• Registration Number: NCT00354211
• Lead Sponsor: Edwards Lifesciences

Brief Summary

The purpose of this study is to evaluate if the continuous availability of minimally invasive cardiac output data during treatment in the intensive care unit (ICU) for hemodynamic instability, in comparison to standard of care will shorten the time needed to stabilize the patient.

The researchers hypothesize that early detection of instability improves the prognosis and treatment outcome of emergency intensive care patients with hemodynamic instability.

Detailed Description

Hemodynamic instability during the first 24-hours of Intensive Care Unit (ICU) admission is associated with increased risk of subsequent morbidity and mortality. Goal-directed hemodynamic support has been successfully used in a variety of patients to improve outcome. In contrast, a similar therapeutic approach applied later, or in patients with established multi-organ failure, has no beneficial effect and may even worsen the outcome.

It is conceivable that there is a window of opportunity during the phases of hemodynamic instability where therapeutic interventions have the greatest potential to influence the subsequent course of critical illness. Large scale uses of therapeutic protocols for early intervention have been hampered by logistic problems. The burden of installing invasive hemodynamic monitoring and protocols is labor intensive and requires a continuous presence of personnel with a thorough understanding of complex physiology. Various techniques have been introduced for monitoring cardiac output, stroke volume, or their surrogates. The disadvantage of these technologies so far have included user dependence of measurements results, need for calibration, and limitations in applicability. Edwards Lifesciences has developed a new algorithm for the determination of cardiac output using arterial pressure data. The FloTrac™ system, which includes the FloTrac™ sensor and Vigileo™ monitor, is utilized to capture the arterial pressure-based cardiac output measurement, which will be hereinafter referred to as APCO (Arterial Pressure Cardiac Output). This system uses an existing arterial catheter (placed in the femoral or radial artery) and does not require calibration by an external reference method. We hypothesize that using the FloTrac™ system to continuously monitor cardiac output, in addition to traditional vital signs, cardiovascular instability will be identified earlier and result in earlier intervention. In addition, following earlier diagnosis, more precise intervention will be available. If this can be achieved, patients will likely show better outcomes by reduced length of hospital stay, ICU time, Mechanical Ventilation time, incidence of renal compromise, and other related morbidity/mortality and need less ICUresources.

Study Timeline

• Study Start: 2006-07
• Study First Submitted: 2006-07-18
• Study First Submitted QC: 2006-07-19
• Study First Posted: 2006-07-20
• Primary Completion: 2007-09
• Study Completion: 2007-12
• Status Verified: 2013-02
• Last Update Submitted: 2013-02-08
• Last Update Posted: 2013-02-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 392

Inclusion Criteria

• Patient newly admitted to the ICU due to an emergency unplanned admission.
• Patient diagnosed with hemodynamic instability at or becomes unstable within 6 hours of ICU admission.
• Patient must require an indwelling radial or a femoral artery catheter.
• Patient is included in the study according to the specific regulations of the participating center: this may include a deferred consent, consent by designee, consent by independent physician or a combination thereof.
• Patient must be 18 years old or older.

Exclusion Criteria

• Patients with contraindications for the placement of radial, femoral, dorsalis pedis, or other arterial cannula.
• Patients with a pulmonary artery catheter.
• Patients who are hemodynamically stable.
• Patients with history or clinical findings of aortic valve regurgitation.
• Patients being treated with an intra-aortic balloon pump.
• Female patient is pregnant.
• Patient is currently participating in an investigational drug or another device study.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
1	minimally invasive cardiac output system consisting of arterial line sensor and cardiac output bedside monitor (device)	FLOTRAC™ SYSTEM

Trial Locations

Locations (3)

Kuopio University Hospital; 🇫🇮 Kuopio, Finland

Tampere Unversity Hospital; 🇫🇮 Tampere, Finland

University Hospital Bern (Inselspital); 🇨🇭 Bern, Switzerland