Pulse CONtour and BIoimpedance for Measurements of Stroke Volume During Changes in CARdiac Preload

Anesthesia Clinical Trial

— ConBi-Car  

Official title:

Stoke Volume Measurements During Changes in Cardiac Preload: Are Pulse Contour Analysis (CLEARSIGHT) and Transthoracic Bioelectrical Impedance (NICCOMO) Equivalent?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04231656
• Other study ID #: 2019_46
• Secondary ID: 2019-A02697-50
• Status: Completed
• Phase: N/A
• Start date: February 12, 2020
• Est. completion date: May 7, 2020

Study information

• Verified date: April 2021
• Source: University Hospital, Lille
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Fluid therapy guided by stroke volume response to repeated fluid challenges is used for hemodynamic optimization during general anesthesia. Two types of devices that measure stroke volume non-invasively are primarily available for intermediate-risk surgery under general anesthesia. They are based on two different techniques, (1) pulse contour analysis, and (2) transthoracic bioimpedance. They have never been compared with each other. Therefore, it is not known (1) whether they are interchangeable for the measurement of stroke volume changes (usually assessed as the "concordance" of two techniques), and (2) whether one is better than the other. The aim is to study the concordance of these two non-invasive hemodynamic devices. it will use both of them in patients undergoing intermediate risk surgery. They will be tested during modifications of cardiac preload induced by Trendelenburg and anti-Trendelenburg positioning, as well as during intraoperative fluid challenges, vasopressor boluses and alveolar recruitment maneuvers.

Description:

The main objective is to assess the concordance of two non-invasive devices using the technology described above : the Clearsight (Edwards Lifesciences, pulse contour analysis), and the Niccomo (Medis, bioimpedance). Both will be used in each patient included in the study. They will be tested during modifications of cardiac preload induced by sequences of position changes (see below) including Trendelenburg and anti-Trendelenburg positioning, performed systematically before and after the procedure, as well as during fluid challenges, vasopressor boluses and alveolar recruitment maneuvers (performed during the procedure according to the needs of the anesthesiologist in charge of the patient). Both monitors will also be compared with an invasive monitor of stroke volume (Vigileo/Flotrac, Edwards Lifesciences), and the respiratory pulse pressure variation will also be measured during the sequences of position changes and will be used as a gold standard for fluid responsiveness.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: May 7, 2020
• Est. primary completion date: May 7, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Eligible and suitable for intermediate risk surgery, validated by anaesthesia consultation. There is no definitive definition of intermediate risk. By reference to the literature, surgeries longer than 2 hours (excluding "low risk") and less than 3% postoperative mortality (excluding high-risk surgery). It includes the majority of non-serious visceral (abdominal and gynecological) surgery, plastic or cervical-facial surgery for neoplastic removal or long-term reconstruction, or long-term spinal surgery or neurosurgery of the base of the skull.
• For which the anesthesiologist in charge has planned an invasive monitoring (radial catheter) of arterial blood pressure.

Exclusion Criteria:

• Urgent surgery
• Intracranial hypertension
• Orthostatic hypotension
• Extreme anthropometry: weight >150 kg and 30 kg, size 120 cm and >230 cm
• Related to NICCOMO monitoring:
• Rhythmic anomaly: Atrial fibrillation, tachycardia with heart rate >200 beats per minute.
• Aortic disease: Severe sclerosis
• Valve dysfunction: severe aortic regurgitation,
• Patient with aortic prosthesis or pacemaker using impedance detection.
• Occurrence of tachycardia > 200 bpm, occurrence of hypertension with mean arterial pressure >130 mm Hg
• Simultaneous use of electrical cauterization systems during surgical procedures
• Septic shock
• Related to CLEARSIGHT monitoring
• Patient with prior distal perfusion disorders
• Lower extremity obliterans arteritis stage IV

Related Conditions & MeSH terms

• Anesthesia
• Blood Pressure
• Hemodynamic, Monitoring

Intervention

Device:
• CLEARSIGHT and NICCOMO measurements in sequence A
Starting from 0° position, shift to position +20°, then tilt to -20°, and finally back to the 0° position.
• CLEARSIGHT and NICCOMO measurements in sequence B
Starting from 0° position, shift to position -20°, then tilt to +20°, and finally back to the 0° position and collect the last group of figures.

Locations

Country	Name	City	State
France	Hôpital Roger Salengro, CHU Lille	Lille

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	concordance of stroke volume changes measured with each monitor during the standardized maneuvers of sequences A and B (total: 6 observations per individual).	4-quadrant plot	during each changes of positioning (i.e., for 1-2 minutes in each condition, for a total of 10-15 minutes following initial measurements in basal conditions), during sequences A and B
Secondary	Fluid responsiveness defined by areas under the Receiver Operating Characteristic curve (sensitivity and specificity)	Comparison of areas under the Receiver Operating Characteristic curve (sensitivity and specificity). Each maneuver will be classified as "responder" or "nonresponder" according to the value of Pulse Pressure Variation (PPV) recorded before the maneuver and to the changes in PPV during the maneuver (as previously published)	during each changes of positioning (i.e., for 1-2 minutes in each condition, for a total of 10-15 minutes following initial measurements in basal conditions), during sequences A and B
Secondary	concordance of stroke volume changes measured with each monitor during the standardized maneuvers mimicking preload decrease.	4-quadrant plot	during each changes of positioning where cardiac preload is supposed to decrease (i.e., for 1-2 minutes in one out of two condition, for a total of 10-15 minutes following initial measurements in basal conditions), during sequences A and B
Secondary	concordance of stroke volume changes measured with each monitor during the standardized maneuver mimicking preload increase.	4-quadrant plot	during each changes of positioning where cardiac preload is supposed to increase (i.e., for 1-2 minutes in one out of two condition, for a total of 10-15 minutes following initial measurements in basal conditions), during sequences A and B
Secondary	concordance of stroke volume changes measured with each monitor during the surgical procedure (fluid challenges, vasopressor boluses, alveolar recruitment maneuver).	4-quadrant plot	throughout surgery (mean length expected between 3 and 5 hours). Measurements performed during sequences of 5-20 minutes that can occur several times during surgery
Secondary	interchangeability of stroke volume measurements with each monitor during sequences A and B	Bland and Altman plot for repeated measures	before and after each changes of positioning (i.e., for 1-2 minutes in each condition, for a total of 10-15 minutes following initial measurements in basal conditions), during sequences A and B
Secondary	interchangeability of stroke volume measured with each monitor during the surgical procedure (fluid challenges, vasopressor boluses, alveolar recruitment maneuver).	Bland and Altman plot for repeated measures	throughout surgery (mean length expected between 3 and 5 hours). Measurements performed before and after sequences of 5-20 minutes that can occur several times during surgery
Secondary	concordance of stroke volume changes measured with each monitor with that measured by a Vigileo/Flotrac monitor during the standardized maneuvers of sequences A and B (total: 6 observations per individual).	4-quadrant plot	during each changes of positioning (i.e., for 1-2 minutes in each condition, for a total of 10-15 minutes following initial measurements in basal conditions), during sequences A and B