FLOWMAPCA: Impact of Cardiopulmonary Bypass Flow on Cerebral Autoregulation

Sponsor
Clinique de la Sauvegarde (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05681741
Collaborator
(none)
40
2
8.6

Study Details

Study Description

Brief Summary

Cerebral autoregulation is defined by the capacity of the brain to maintain a constant cerebral blood flow (CBF) despite variations of arterial pressure. However, when the arterial pressure is below a critical threshold, cerebral blood decreases.

This critical threshold is called the lower limit of cerebral autoregulation (LLA).

Cardiopulmonary bypass is a unique environment wherein systemic blood flow is totally controlled by the cardiopulmonary bypass pump. It has been shown that high pump flows combined with low arterial pressures did not compromise neurologic postoperative outcomes.

Our hypothesis is that that LLA may depend on the cardiopulmonary bypass flow, ie the LLA may decrease when the cardiopulmonary bypass flow increases, explaining why low arterial pressure may be well tolerated.

Condition or Disease Intervention/Treatment Phase
  • Procedure: current versus high pump flow
N/A

Detailed Description

Cerebral tissue perfusion is partly ensured by cardiac output and arterial pressure. In cardiac surgery, and especially during bypass surgery, one of the main objectives is to maintain sufficient blood flow and an optimal mean arterial pressure (MAP) to limit the deleterious consequences of organ hypoperfusion. To have a physiological regional organ blood flow, some organs, such as the brain, need a minimum MAP threshold (the lower limit of autoregulation, LLA) to ensure a constant cerebral blood flow (CBF). This is known as the cerebral autoregulation (CA). As the brain is at high risk of ischemia and definitive functional consequences in case of cerebral hypoperfusion, maintaining MAP above the LLA of the brain limit the deleterious postoperative neurological outcome.

CA can be determined by continuously calculating the correlation between MAP and CBF. CBF is assessed by continuous monitoring of the middle cerebral artery velocity (mV). moving Pearson correlation coefficient between 30 consecutive, paired MAP and cerebral blood flow velocity values will be calculated to generate the mean velocity index (Mx). The Blood pressure in the autoregulation range is indicated by an Mx value that approaches zero (there is no correlation between flow velocity and MAP), whereas an Mx approaching 1 indicates dysregulated cerebral blood flow (flow velocity and MAP are correlated). A value of 0.4 is accepted as the threshold of CA corresponding to the LLA.

During cardiopulmonary bypass (CPB), MAP is physiologically related to bypass flow and systemic vascular resistance. The adjustment of MAP during CPB is therefore achieved by the administration of vasoconstrictors or vasodilators as well as by the variations of the pump flow.

This research assumes that a change in the pump flow rate will lead to a change in the LLA. Therefore, if the flow rate is higher, it is possible that the LLA will be lower.

In this randomized trial, two different rates of pump flow will be compared with respect to LLA testing.

Regional brain oxygen saturation, assessed by near-infrared spectroscopy will also be monitored during surgery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
parallel affectationparallel affectation
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Impact of Cardiopulmonary Bypass Flow on Cerebral Autoregulation in Cardiac Surgery, a Cross-over Study
Anticipated Study Start Date :
Jan 10, 2023
Anticipated Primary Completion Date :
Sep 29, 2023
Anticipated Study Completion Date :
Sep 29, 2023

Arms and Interventions

Arm Intervention/Treatment
Sham Comparator: current pump flow (between 2 and 2.4 l/min/m²)

the pump flow will be constant during this randomized phase

Procedure: current versus high pump flow
during each phase of randomized pump flow, arterial pressure will be increased from 40 to 90 mmHg with vasodilators and/or vasoconstrictors

Active Comparator: high pump flow (between 2.6 and 3 l/min/m²)

the pump flow will be constant during this randomized phase

Procedure: current versus high pump flow
during each phase of randomized pump flow, arterial pressure will be increased from 40 to 90 mmHg with vasodilators and/or vasoconstrictors

Outcome Measures

Primary Outcome Measures

  1. measurement of MAP LLA (mmHg) [15 to 25 min during the procedure]

    Determination of MAP LLA according to the calculation of the mean velocity index

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient, male or female, over the age of 18

  • Patient scheduled to undergo valvular heart surgery with planned CPB

  • Patient with a Euroscore below 7%

  • Patient affiliated or entitled to a social security scheme

  • Patient having received informed information about the study and having signed a free and informed consent to participate in the study

Exclusion Criteria:
  • Patient with untreated or uncontrolled severe hypertension despite treatment

  • Patient with chronic renal failure, with glomerular filtration < 30 mL/min/1.73m² or requiring a kidney transplant

  • Patient with left ventricular ejection fraction < 40%

  • Patient with a history of ischemic stroke

  • Patient having or about to benefit from renal vascular surgery

  • Patient with preoperative sepsis

  • Patient who required a norepinephrine infusion within 24 hours before surgery

  • Patient presenting with an inaccessible temporal Doppler window

  • Patient candidate for emergency surgery

  • Pregnant, parturient or breastfeeding woman

  • Patient with preoperative uni or bilateral carotid stenosis > 50%

  • Protected patient: adult under guardianship, curators or other legal protection, deprived of liberty by judicial or administrative decision

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Clinique de la Sauvegarde

Investigators

  • Principal Investigator: Olivier Desebbe, MD, Clinique de la Sauvegarde

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Johanne Beuvelot, RAMSAY SANTE, Clinique de la Sauvegarde
ClinicalTrials.gov Identifier:
NCT05681741
Other Study ID Numbers:
  • Ramsay Sante Sauvegarde Clinic
First Posted:
Jan 12, 2023
Last Update Posted:
Jan 12, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Johanne Beuvelot, RAMSAY SANTE, Clinique de la Sauvegarde

Study Results

No Results Posted as of Jan 12, 2023