Shock Clinical Trial
Official title:
Evaluation of the Cerebral Microcirculation by Non-invasive Brain Ultrasound With Enhanced Microbubbles Contrast Injection in Shock Status.
Alterations in the brain microcirculation may be involved in patients with shock. For a three-day period, we investigate the brain microcirculation using contrast-enhanced ultrasound with microbubble injection in patients with septic and non-septic shock.Ultrasound examination is performed daily to estimate global cerebral blood flow, and to evaluate the brain microcirculation, using variables of the time-intensity brain perfusion curve, after sulphur hexafluoride microbubble Sonovue injection.
Non-invasive brain ultrasound with transcranial echo-color doppler (IE 33, Philips Medical
System, the Netherlands) is performed in three steps to 1) evaluate the global cerebral blood
volume, 2) to estimate the presence or absence of cerebral autoregulation, and 3) to
qualitatively evaluate the cerebral perfusion and microcirculation by enhanced microbubbles
contrast injection (CEUS). Brain ultrasound is performed in the first 48 hours after
hemodynamic stabilization (MAP > 65mm Hg, normotherm) and respiratory parameters
stabilization (PaCO2 between 35-45mmHg and the PaO2/FiO2 > 200) after ICU admission. The
second and third examination is performed in the next 48-72 hours before sedation withdrawal
to limit the effect of change of cerebral hemodynamics.
Before performing brain ultrasound, echocardiography (IE 33, Philips medical System, the
Netherlands) is performed to evaluate left ventricular ejection fraction and cardiac output
(L/min).
First, the global cerebral blood volume (L/min) is evaluated as the sum of flow volumes of
the internal carotid (ICA) and vertebral arteries (VA) extracranial arteries of both sides.
The internal carotid artery (ICA) is examined with a 7-MHz linear array transducer with the
head of the patient slightly titled upward, in midline position. The site of measurement is
approximately 1.5cm below the carotid bulb in the in the common carotid artery (CCA) during
expansion and 1.5cm away from the bifurcation in ICA. In the presence of atheromatous
calcifications plaques, ICA doppler measurement is performed outside and before the plaques.
The B-mode bidimensional is magnified to achieve a higher resolution and details. The
internal diameter of the vessel is measured at the exact site of the pulse doppler velocity
measurement ample volume, between both endothelial layers, perpendicular of the course of the
vessel. The diameter of the vertebral artery is examined and magnified in B-mode. The
transducer is positioned along the CCA, shiftily laterally and angled until the
intertransverse segment of the VA is seen and the doppler velocity is measured at the C4-C5
transverse area along the common carotid artery exactly at the same place of diameter
measurement. The following measurements of flow velocities are taken in each artery: Peak
systolic and end-diastolic velocity, time-averaged velocity (TAV), Pulsatility Index (PI).
Flow volume (Q) of each artery is determined as Q = TAV x Area ((diameter of the artery /2)²
x PI).
Transcranial echo-color doppler is performed via temporal windows and the Pulsatility Index
(PI) and the mean flow velocities (cm/sec) are measured of MCA, at both sides are recorded.
Cerebrovascular resistance index as defined as the ration MAP/Mean Flow velocity of MCA
(mmHg/cm per second).
Second, after measuring the global cerebral blood volume, the presence or absence of cerebral
autoregulation (CA) is tested with the Transient hyperemic response (THR) by measuring the
velocity of the media cerebral artery (MCA) the following an ipsilateral common carotid
compression during 8 seconds. THR is defined as the F3/F1 ratio F1 as the MCA velocity before
compression and F3 is the second MCA velocity after compression test). THR test is valid when
onset of compression results a sudden and maximal decrease in MCA blood velocity and remains
stable during compression.
Third, after testing the THR, the brain regional microcirculation is evaluated by the
microbubbles contrast injection SONOVUE (Italy) following the European guidelines
recommendation for contrast microbubbles enhanced ultrasound. The brain parenchyma is
insonated via the temporal bone windows at the depth of 10cm with the ultrasound S5
multifrequency transducer 2-5 MHz probe. After optimizing the acoustic bone window, SONOVUE
is injected intravenously as a bolus 2.4ml followed by 10ml saline flushed. The contralateral
brain is evaluated 5 minutes after the first injection of SONOVUE to allow a complete
evacuation of contrast microbubbles.
All real-time CEUS images were stored digitally on the hard disk as DICOM (Digital Image
Communications in Medicine) images. Offline analysis used the QLAB 10 quantification software
(Philips Medical System, the Netherlands) to convert brain perfusion images into
time-intensity curves (TIC) corresponding to the five different regions of interest (ROI) of
brain parenchyma: anterior and posterior thalamus, lentiform nucleus, parieto-temporal and
posterior white matter. Four variables were extracted from these TIC curves to qualitatively
evaluate the brain microcirculation: peak intensity in dB (PI), time to peak intensity in
seconds (TTP), mean transit time in seconds (MTT), and area under the curve in dB/seconds
(AUC) .
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT05898126 -
Renin-guided Hemodynamic Management in Patients With Shock
|
N/A | |
Completed |
NCT05563701 -
Evaluation of the LVivo Image Quality Scoring (IQS)
|
||
Recruiting |
NCT05066256 -
LV Diastolic Function vs IVC Diameter Variation as Predictor of Fluid Responsiveness in Shock
|
N/A | |
Not yet recruiting |
NCT06285513 -
Cardiovascular Metabolic Remodeling in Shock
|
||
Not yet recruiting |
NCT05649891 -
Checklists Resuscitation Emergency Department
|
N/A | |
Terminated |
NCT02755155 -
Optimization of Therapeutic Human Serum Albumin Infusion in Selected Critically Ill Patients
|
Phase 4 | |
Not yet recruiting |
NCT01941472 -
Transcutaneous pO2, Transcutaneous pCO2 and Central Venous pO2 Variations to Predict Fluid Responsiveness
|
N/A | |
Completed |
NCT01680783 -
Non-Invasive Ventilation Via a Helmet Device for Patients Respiratory Failure
|
N/A | |
Terminated |
NCT01696175 -
PICU Admission Lactate and Central Venous Oxymetry Study
|
N/A | |
Recruiting |
NCT01174966 -
Assessment of Transcutaneous Oxygen Tension/Oxygen Challenge Test in Intensive Care Unit (ICU) Patients
|
N/A | |
Recruiting |
NCT01157299 -
Hemodynamic Evaluation of Preload Responsiveness in Children by Using PiCCO
|
N/A | |
Completed |
NCT00743522 -
Programming Implantable Cardioverter Defibrillators in Patients With Primary Prevention Indication
|
||
Completed |
NCT03296891 -
Point of Care Ultrasonography In The Management of Shock: A Pilot Study
|
N/A | |
Recruiting |
NCT05922982 -
Norepinephrine Weaning Guided by the Hypotension Prediction Index in Vasoplegic Shock After Cardiac Surgery
|
N/A | |
Withdrawn |
NCT04705701 -
Comparing Post Cardiac Surgery Outcomes in ESRD Patient's With Early Dialysis Versus Standard Care
|
N/A | |
Recruiting |
NCT04615065 -
Acutelines: a Large Data-/Biobank of Acute and Emergency Medicine
|
||
Completed |
NCT05330676 -
Evaluation of Microcirculatory Function and Mitochondrial Respiration After Cardiovascular Surgery
|
||
Active, not recruiting |
NCT04079829 -
Postoperative Respiratory Abnormalities
|
||
Completed |
NCT04089098 -
VOLume and Vasopressor Therapy in Patients With Hemodynamic instAbility
|
||
Completed |
NCT03190408 -
Variation in Fluids Administered in Shock
|