Value of Non Invasive Hemodynamic Monitoring in Patients Admitted to Respiratory Intensive Care Unit

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06110013
Collaborator
(none)
177
13

Study Details

Study Description

Brief Summary

This study aims to evaluate clinical application of electrical cardiometry EC in patients admitted to respiratory ICU. It will evaluate the reliability of EC in assessment of hemodynamic changes in these patients. It will estimate the effect of mechanical ventilation either invasive or non invasive hemodynamic parameters in patients admitted to ICU with respirator disorders

Condition or Disease Intervention/Treatment Phase
  • Device: Electrical cardiometry

Detailed Description

Mechanical ventilation MV is a life saving intervention in intensive care units. Access to lower airways is achieved either through tracheostomy or endotracheal intubation. More recently non invasive ventilation NIV techniques were introduced that do not require an endotracheal airway but using patient ventilator interfaces in the form of facial masks have been designed.

The haemodynamic consequences of MV are multiple and complex and may affect all the determinants of cardiac performance such as heart rate.preload.contractility .and afterload. These consequences affect both right and left ventricle and are also related to the biventricular interdependence .

Mechanically ventilated patients are considered Critically ill.and they are often hemodynamically unstable or at risk of becoming unstable owing to hypovolemia. cardiac dysfunction. or alterations of vasomotor function. leading to organ dysfunction.deterioration into multiorgan failure .and eventually death .Socardiopulmonary monitoring is crucial to ensure successful evaluation and management of these patients . With hemodynamic monitoring. The investigators aim to guide our medical management to prevent or treat organ failure and improve the outcomes of our patients. Therapeutic measures may include fluid resuscitation.vasopressors or inotropic agents .

Hemodynamic monitoring can be done by different techniques which ranges from invasive to less invasive and completely noninvasive methods to assess Cardiac output BP oxygen saturation. Some hemodynamic parameters are easy to be measured like blood pressure and heart rate but do not give a complete picture of a patient's hemodynamics .

Measuring CO and its components preload afterload and contractility will tell us if there is ongoing need for fluid resuscitation vasopressors or inotropic agents . It can be used as a diagnostic tool to determine the type of shock hypovolemic cardiogenic obstructive or distributive according to the hemodynamic profile .

Traditional invasive methods incorporate thermodilution which requires that a transvenous catheter pushed forward to the pulmonary artery PAC Swan Ganz catheter. Other invasive methods require an arterial line to measure the blood pressure signal waveform . Due to the invasiveness the associated risk invasive methods are usually employed at an advanced stage of illness .

Non invasive hemodynamic methods have less complications. Recent techniques advances led to continuous non invasive monitoring that allow for data obtaining at bedside of critically ill patients in ICU these advances help to monitor changes and allow for management before complications .

A portable Electro Cardiometer ICON Osypka Medical GmbH Berlin Germany is a Hand held Portable battery operated non invasive cardiometer for continuous measurement of different hemodynamic parameters stroke volume SV cardiac output CO contractility fluid status and oxygen status in neonate children or adults Applied to the patients through 4 ECG electrodes. It is based on the measurement of changes in thoracic impedance to an electrical current that is produced by fluctuations in thoracic blood volume with each cardiac cycle .

Newer generation Thoracic Electrical Bioimpedence methods have overcome some of the limitations that was present in old models by having faster signal processing better signal filters improved ECG triggering and respiratory filtering .

Up till now there is limited research about ICON device and it's reliability in monitoring hemodynamics specially in respiratory ICU patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
177 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Value of Non Invasive Hemodynamic Monitoring in Patients Admitted to Respiratory Intensive Care Unit
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Nov 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
A

Patients on invasive mechanical ventilation

Device: Electrical cardiometry
All included patients will be connected to Electrical cardiometry device. The electrodes will be placed over the bare skin of patients at the following sites: A. on the left neck below the ear B. directly superior to the midpoint of the left clavicle C. along the left mid-axillary line at the level of the xiphoid process D. two inches below the third electrode. High frequency signals pass through 2 acting electrodes, the other 2 measuring electrodes detect changes in bioimpedance resistance to allow continuous hemodynamic monitoring, then data will be analysed to give comprehensive picture of the hemodynamic circulatory system, allowing differential diagnosis for a patient management
Other Names:
  • ICON
  • B

    Patients on Non invasive mechanical ventilation

    Device: Electrical cardiometry
    All included patients will be connected to Electrical cardiometry device. The electrodes will be placed over the bare skin of patients at the following sites: A. on the left neck below the ear B. directly superior to the midpoint of the left clavicle C. along the left mid-axillary line at the level of the xiphoid process D. two inches below the third electrode. High frequency signals pass through 2 acting electrodes, the other 2 measuring electrodes detect changes in bioimpedance resistance to allow continuous hemodynamic monitoring, then data will be analysed to give comprehensive picture of the hemodynamic circulatory system, allowing differential diagnosis for a patient management
    Other Names:
  • ICON
  • C

    Patients Not on mechanical ventilation

    Device: Electrical cardiometry
    All included patients will be connected to Electrical cardiometry device. The electrodes will be placed over the bare skin of patients at the following sites: A. on the left neck below the ear B. directly superior to the midpoint of the left clavicle C. along the left mid-axillary line at the level of the xiphoid process D. two inches below the third electrode. High frequency signals pass through 2 acting electrodes, the other 2 measuring electrodes detect changes in bioimpedance resistance to allow continuous hemodynamic monitoring, then data will be analysed to give comprehensive picture of the hemodynamic circulatory system, allowing differential diagnosis for a patient management
    Other Names:
  • ICON
  • Outcome Measures

    Primary Outcome Measures

    1. Effectiveness of non invasive hemodynamic monitoring [Baseline]

      Effectiveness of clinical application of non invasive hemodynamic monitoring using electrical cardiometer in patients admitted to respiratory intensive care unit

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All patients admitted to respiratory intensive care unit (ICU) among both sexes Age

    18 years Old.

    Exclusion Criteria:
    1. Patients less than 18 years old .

    2. Pregnant women.

    3. Patients with injuries, burns, or wounds which precluded the proper application of the device electrodes will be also excluded from the study.

    4. those with uncontrollable fits.

    5. Patients who need electrical direct current (DC) shock.

    6. Patients who refuse to participate in the study.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Assiut University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fatma Sayed Ahmed, Resident doctor, Assiut University
    ClinicalTrials.gov Identifier:
    NCT06110013
    Other Study ID Numbers:
    • Hemodynamic monitoring
    First Posted:
    Oct 31, 2023
    Last Update Posted:
    Oct 31, 2023
    Last Verified:
    Oct 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    No

    Study Results

    No Results Posted as of Oct 31, 2023