search
Back to results

Ventricular Stimulation as Predictor of Hypovolemia After Cardiac Surgery (TESTI)

Primary Purpose

Cardiac Surgery, Hypovolemia

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Detection of hypovolemia using a ventricular stimulation without atrial pacing
Sponsored by
CMC Ambroise Paré
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Cardiac Surgery focused on measuring Preload-dependency, hypotension, cardiac surgery, delta PP, PLR, Fluid responsiveness

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Over 18 years old,
  • Programmed for cardiac surgery with the need for invasive hemodynamic monitoring (pulmonary artery catheter) according to the recommendations:

    • Euroscore with predicted mortality> 10%
    • Left ventricular ejection fraction (LVEF) <40%
    • Left ventricular ejection fraction (LVEF) <50% for mitral insufficiency
    • pulmonary artery hypertension (PAH)> 50 mmHg
    • Tricuspid insufficiency> 3.4 m / s
    • Tricuspid annular plane systolic excursion (TAPSE) <16 mm
    • Dilatation of the inferior vena cava under respiratory collapse
  • Sinus rhythm in immediate postoperative period,
  • Sedated with mechanical ventilation,
  • Having given their written participation consent in accordance with the regulations,
  • Benefiting from a social security

Exclusion Criteria:

  • Pregnant or lactating women,
  • Patient under guardianship, Under curatorship or court of justice,
  • Discomfort to communication or neuropsychic disorders,Inability to understand, to read or to write the French language,
  • Patients for whom a fluids overload seems obvious to the intensivist and for whom a crystalloids filling would be contraindicated,
  • Patients for whom respiratory changes in pulse pressure (ΔPP) measurement is not validated: patients with spontaneous ventilation, atrial fibrillation, non-sedated

Sites / Locations

  • CMC Ambroise Paré

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

VESAP

Arm Description

patient receiving stimulation test to detect hypovolemia

Outcomes

Primary Outcome Measures

Evaluate the correlation between thes stimulation test and the cardiac output
Measure the cardiac flow before and after the VESAP, and after an infusion of 500 cc of crystalloid solution.

Secondary Outcome Measures

Collection of the possible complications due to the VESAP
Number of participants with low blood presseur or with heart rhythm disorder.
Evaluate the correlation between the VESAP and the ΔP
Measure the of the blood presser before and after stimulation test and after an infusion of 500 cc of crystalloid solution
Look for pertinent VESAP threshold in correlation with the expected increase in stroke volume
Measure the of the strocke volume before and after stimulation test and after an infusion of 500 cc of crystalloid solution

Full Information

First Posted
April 17, 2019
Last Updated
November 26, 2021
Sponsor
CMC Ambroise Paré
search

1. Study Identification

Unique Protocol Identification Number
NCT03926910
Brief Title
Ventricular Stimulation as Predictor of Hypovolemia After Cardiac Surgery
Acronym
TESTI
Official Title
Test of Ventricular Stimulation as Immediate Predictor of Hypovolemia After Cardiac Surgery: Non-randomized Open Label Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
July 22, 2019 (Actual)
Primary Completion Date
October 13, 2020 (Actual)
Study Completion Date
October 14, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CMC Ambroise Paré

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to validate a ventricular pacing test as a predictor of preload dependency in post cardiac surgery patients.
Detailed Description
In the immediate postoperative period of cardiac surgery and in intensive care unit (ICU), a systemic arterial hypotension is frequently observed. This hypotension is often due to hypovolemia but also to pump dysfunction and/or vasoplegia. Early recognition of the hypotensive mechanism is necessary because it requires immediate specific treatment. The interest of a vascular filling is usually estimated by a preload dependence test (fluid responsiveness), showing an increase in the stroke volume when preload is increased according to the Starling the law of the heart. To date, a preload dependency test is usually performed by passive leg raise (PLR) or by measuring the respiratory pulse variation (ΔPP). The PLR response varies according to the legs venous volume and capacitance. The derivation of ΔPP has been validated in patients intubated, sedated, and ventilated in standard conditions, in sinus rhythm but the ΔPP directly displayed by the monitors is unreliable and the manual calculation on pressure curve is fastidious. Faced with these difficulties, the trend is to realize a blind filling with physiologic saline solution and to judge his interest on clinical and / or hemodynamic criteria. After cardiac surgery, ventricular epicardial electrodes are systematically placed allowing a temporary stimulation by an external pacemaker in case of postoperative atrio-ventricular blocks. The ventricular stimulation without atrial pacing (VESAP) leads to a loss of the atrial systole and therefore a decrease in the left ventricular preload. During the functional test of epicardial electrodes at a frequency greater than the patient's, it is possible to observe in certain circumstances a decrease of the arterial blood pressure, but of varying importance. The investigators suspect that the eventual fall in blood pressure during a ventricular pacing test, could be correlated with preload dependence. Therefore, investigator hypothesize that ventricular pacing can be used to realize a functional testing of preload dependence, easy to achieve. Indeed, if doctors admit that during a brief ventricular stimulation, heart rate and systemic vascular resistance remain unchanged, the drop in blood pressure should reflect the decrease in stroke volume. The main objective of this study is to demonstrate that the response to VESAP can predict the preload dependence of patients after a cardiac surgery. The primary endpoint will study the predictive value of the change in blood pressure during the VESAP and the change in stroke volume after an infusion of 500 cc of crystalloid solution. Secondary endpoints will 1) compare the predictive values of the VESAP and ΔPP; 2) look for pertinent VESAP threshold in correlation with the expected increase in stroke volume; and 3) collection of the possible complications due to the VESAP. 30 patients will be enrolled in this monocentric, open label, non-randomized study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Surgery, Hypovolemia
Keywords
Preload-dependency, hypotension, cardiac surgery, delta PP, PLR, Fluid responsiveness

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
VESAP
Arm Type
Experimental
Arm Description
patient receiving stimulation test to detect hypovolemia
Intervention Type
Diagnostic Test
Intervention Name(s)
Detection of hypovolemia using a ventricular stimulation without atrial pacing
Intervention Description
Upon the return in intensive care: Baseline measurements: 1) Three measurements of blood pressure during inspiration and 3 during expiration will be collected for averaging systolic blood pressure, diastolic blood pressure, mean arterial pressure and ΔPP. Data from a pulmonary artery catheter will be also collected. Realization of VESAP pacing with adjustment of the pacemaker (PM) at a heart rate 5 bpm higher than the heart rate of the patient. After 20 seconds of stimulation, recording of the blood pressure curve as done at baseline during at least 3 respiratory cycles, Then vascular filling with 500 ml of physiologic saline solution over 10 minutes and new set of measurement (same than at baseline) Second realization of VESAP pacing, and new set of measurement (same than at Baseline) Then, if the ΔPP is >10%, new vascular filling with 500 ml of physiologic saline solution over 10 min and new set of measurements as previously performed.
Primary Outcome Measure Information:
Title
Evaluate the correlation between thes stimulation test and the cardiac output
Description
Measure the cardiac flow before and after the VESAP, and after an infusion of 500 cc of crystalloid solution.
Time Frame
1 hour
Secondary Outcome Measure Information:
Title
Collection of the possible complications due to the VESAP
Description
Number of participants with low blood presseur or with heart rhythm disorder.
Time Frame
2 hours and 24 hours
Title
Evaluate the correlation between the VESAP and the ΔP
Description
Measure the of the blood presser before and after stimulation test and after an infusion of 500 cc of crystalloid solution
Time Frame
1 hour
Title
Look for pertinent VESAP threshold in correlation with the expected increase in stroke volume
Description
Measure the of the strocke volume before and after stimulation test and after an infusion of 500 cc of crystalloid solution
Time Frame
1 hour

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Over 18 years old, Programmed for cardiac surgery with the need for invasive hemodynamic monitoring (pulmonary artery catheter) according to the recommendations: Euroscore with predicted mortality> 10% Left ventricular ejection fraction (LVEF) <40% Left ventricular ejection fraction (LVEF) <50% for mitral insufficiency pulmonary artery hypertension (PAH)> 50 mmHg Tricuspid insufficiency> 3.4 m / s Tricuspid annular plane systolic excursion (TAPSE) <16 mm Dilatation of the inferior vena cava under respiratory collapse Sinus rhythm in immediate postoperative period, Sedated with mechanical ventilation, Having given their written participation consent in accordance with the regulations, Benefiting from a social security Exclusion Criteria: Pregnant or lactating women, Patient under guardianship, Under curatorship or court of justice, Discomfort to communication or neuropsychic disorders,Inability to understand, to read or to write the French language, Patients for whom a fluids overload seems obvious to the intensivist and for whom a crystalloids filling would be contraindicated, Patients for whom respiratory changes in pulse pressure (ΔPP) measurement is not validated: patients with spontaneous ventilation, atrial fibrillation, non-sedated
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe ESTAGNASIÉ, MD
Organizational Affiliation
CMC Ambroise Paré
Official's Role
Principal Investigator
Facility Information:
Facility Name
CMC Ambroise Paré
City
Neuilly-sur-Seine
State/Province
Neuilly Sur Seine Ile De France
ZIP/Postal Code
92200
Country
France

12. IPD Sharing Statement

Learn more about this trial

Ventricular Stimulation as Predictor of Hypovolemia After Cardiac Surgery

We'll reach out to this number within 24 hrs