The Impact of Noradrenaline on Ventriculo-arterial Coupling and Central Cardiovascular Energy Delivery

Sponsor
St. Olavs Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04745845
Collaborator
(none)
49
1
1
10
4.9

Study Details

Study Description

Brief Summary

The study aims to examine how noradrenaline in combination with venous return influences the energy transmission from heart to central circulation and arteries - also called arterio-ventricular coupling.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Noradrenalin
  • Procedure: Noradrenalin
  • Procedure: Noradrenalin
  • Procedure: Noradrenalin
N/A

Detailed Description

After being informed about the study 40 elective CABG patients with written informed consent will undergo assessment of their arterio-ventricular coupling postoperatively after coronary bypass graft surgery. Whilst still in deep general anesthesia on the CT ICU the study population will be assessed by echocardiographic examination (transthoracic and transesophageal), blood pressure tracing by arterial line, respiratory data and ECG in 4 different situations.

Initially the individual patient is either considered fluid responsive (SVV >13%) og non- responsive (SVV<13%) by using stroke volume variation assessed by echocardiography.

In case of fluid responsiveness a fluid bolus of 4ml/kg of crystalloid fluid is given until SVV drops below 13% and the patient can be considered as fluid NON responder.

Right afterwards the study patient is stabilized with a baseline dose of noradrenaline (NA) intravenously in a supine position (situation 1). Situation 2 will be a slight increase in NA dose stabilizing mean arterial pressure in a "baseline + 20mmHg" state. After reversing the NA dose back to base line level the patient is allowed a short period of rest to wean of drug effect (4-5 x t1/2, appr. 12min). Subsequently the patient is to be placed in a 20% semi upright position (Anti-Trendelenburg) causing an increase in fluid responsiveness (situation 3). Following a phase of equilibration the dose of NA is again titrated up to obtain a 20mmHg increase in mean arterial pressure (situation 4).

There will be logging of arterial pressure curve and VTI-tracing I LVOT simultaneously (ultrapower, uPWR) as well as calculation of energy delivery, cardiac power, oscillatory power and -fraction and both arterial and ventricular elastance in every of those 4 situations.

Study Design

Study Type:
Interventional
Actual Enrollment :
49 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
The Impact of Noradrenaline on Ventriculo-arterial Coupling and Central Cardiovascular Energy Delivery
Actual Study Start Date :
Mar 1, 2021
Actual Primary Completion Date :
Dec 31, 2021
Actual Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Noradrenalin

treatment with 2 different NA concentrations in 2 different states of fluid responsiveness

Procedure: Noradrenalin
Norepinephrine challenge (concentration 'A' ) in fluid responsive position
Other Names:
  • Anti-Trendelenburg position/Semiupright position (20degr)
  • Procedure: Noradrenalin
    Norepinephrine challenge (concentration 'A') in non-fluid responsive position
    Other Names:
  • supine position
  • Procedure: Noradrenalin
    Norepinephrine challenge (concentration 'B') in fluid responsive position
    Other Names:
  • Anti-Trendelenburg position/Semiupright position (20degr)
  • Procedure: Noradrenalin
    Norepinephrine challenge (concentration 'B') in non-fluid responsive position
    Other Names:
  • supine position
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Cardiac Power [within 30 minutes after having been stabilised on the cardiothoracic ICU after performed CABG surgery]

      Change in Cardiac Power in reaction to both different noradrenaline doses and states of fluid responsiveness. By logging invasive BP curve and tracing left ventricular outflow tract Velocity Time Integral (by echocardiography) simultaneously Total and Mean Cardiac Power (Watt) can be determined. Examining the response to different NA doses relative to fluid responsiveness the effect of NA on arterio-ventricular coupling can be examined.

    2. Change in Oscillatory Power Fraction [within 30 minutes after having been stabilised on the cardiothoracic ICU after performed CABG surgery]

      Change in Oscillatory Power Fraction (OPF) in reaction to both different noradrenaline doses and states of fluid responsiveness. By logging invasive BP curve and tracing left ventricular outflow tract Velocity Time Integral (by echocardiography) simultaneously Total Cardiac Power (TCP, Watt) and Cardiac Power Output (CPO, Watt) can be determined. By subtracting CPO from TCP, OPF (in %) can be calculated. Examining the response to different NA doses relative to fluid responsiveness the effect of NA on arterio-ventricular coupling can be examined.

    Secondary Outcome Measures

    1. Change in single beat ventricular elastance [within 30 minutes after having been stabilised on the cardiothoracic ICU after performed CABG surgery]

      Change in single beat ventricular elastance in reaction to both different noradrenaline doses and states of fluid responsiveness. Ventricular elastance (Ees) can be determined on the bedside by using a single beat measurement of left ventricular ejection fraction, stroke volume, preejection time and ejection time.

    2. Change in single beat arterial elastance [within 30 minutes after having been stabilised on the cardiothoracic ICU after performed CABG surgery]

      Change in single beat arterial elastance in reaction to both different noradrenaline doses and states of fluid responsiveness. Using an estimative formula Ea can be calculated (Ea=SBPx0.9/SV) and Ea/Ees as a marker of arterio-ventricular coupling can be evaluated.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 99 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • elective coronary artery bypass graft surgery

    • requirement for Noradrenaline/Norepinephrine

    Exclusion Criteria:
    • lack of informed consent

    • patient unsuitable for mean arterial pressure (MAP) elevation of 20mmHg

    • patient requiring different blood pressure range due to medical/surgical needs

    • poor image quality due to patient factors

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 St Olavs Hospital, Dep. for Anesthesia & Intensive care. Section of cardiothoracic Anesthesia and -intensive Care. Trondheim Norway 7006

    Sponsors and Collaborators

    • St. Olavs Hospital

    Investigators

    • Study Director: Hilde Pleym (Head of Department), md, PhD, St. Olavs Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    St. Olavs Hospital
    ClinicalTrials.gov Identifier:
    NCT04745845
    Other Study ID Numbers:
    • 2019/287
    First Posted:
    Feb 9, 2021
    Last Update Posted:
    Jan 5, 2022
    Last Verified:
    Jan 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by St. Olavs Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2022