Electrical impedance tomography (EIT) is a recent monitoring technique that provides information on regional ventilation distribution. Following the injection of a hypertonic saline bolus, EIT can also assess regional pulmonary perfusion distribution, allowing evaluation of the ventilation/perfusion (V/Q) ratio. In adults, protocols for assessing perfusion distribution require the injection of 10 mL of a 7.5% or 10% NaCl solution or sodium bicarbonate over a few seconds. Studies have reported good hemodynamic tolerance, adequate image quality, and no significant changes in serum sodium levels. However, this volume and sodium load are not appropriate for small children. To date, no pediatric protocol exists for assessing pulmonary perfusion distribution and the ventilation/perfusion ratio using EIT. It is therefore proposed to conduct a pilot study to evaluate the feasibility of assessing pulmonary perfusion by EIT using a weight-adjusted bolus of hypertonic saline (NaCl or sodium bicarbonate).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
20
All patients will undergo EIT monitoring (Enlight 2100, Timpel, Brazil) using a belt adjusted to the thoracic circumference. Ventilation distribution will be assessed with a tidal volume of 8 mL/kg. Following a breath hold, a saline solution (sodium chloride or sodium bicarbonate) will be injected over a few seconds. Perfusion distribution, as well as impedance signal variation, will be recorded using dedicated software (Timpel, Brazil). Data acquisition will be considered valid if the impedance signal variation induced by the saline solution injection is at least equivalent to the amplitude variation observed during ventilation with a tidal volume of 8 mL/kg. 2 measurements at 4 to 6-hours intervals with volume or concentration adjustment after the first injection if needed in the group 1
Florent BAUDIN
Bron, France, France
RECRUITINGProportion of patients with pulmonary perfusion acquisition consider as valid
Data acquisition will be considered valid if the impedance signal variation induced by the saline solution injection is at least equivalent to the amplitude variation observed during ventilation with a tidal volume of 8 mL/kg.
Time frame: Hour 0 ; Between Hour 4 and Hour 6
Proportion of patients requiring an increase in volume and/or concentration of saline solution
Increase in the volume and/or concentration of the saline solution due to insufficient signal detection during the first injection (Group 1).
Time frame: Between Hour 4 and Hour 6
Proportion of respiratory acquisition failures explained by breathing movements
Data acquisition failure related to variations in the airway pressure waveform recorded by the software.
Time frame: Hour 0 ; Between Hour 4 and Hour 6
Distribution of pulmonary perfusion
Description of the distribution of regional pulmonary perfusion in children, expressed as percentages across predefined regions of interest (right versus left and anterior versus posterior).
Time frame: Hour 0 ; Between Hour 4 and Hour 6
Natremia variation after injection
Serum sodium concentration (mmol/L) measured before and after injection, with calculation of absolute (mmol/L) and relative (%) changes.
Time frame: Hour 0 ; Hour 1 ; Between Hour 5 and Hour 7
Natremia variation at day one
Serum sodium concentration (mmol/L) measured at baseline and on day 1, with calculation of absolute (mmol/L) and relative (%) changes from baseline.
Time frame: Hour 0 ; Hour 24
Heart rate variation
Heart rate (beats/min) measured before and after saline solution injection, with calculation of absolute (beats/min) and relative (%) changes
Time frame: Hour 0 ; Hour 1 ; Between Hour 5 and Hour 7
Blood pressure variation
Systolic, diastolic, and mean arterial blood pressure measured before and after saline solution injection, with calculation of absolute (mmHg) and relative (%) changes.
Time frame: Hour 0 ; Hour 1 ; Between Hour 5 and Hour 7
Significant hemodynamic events
Any change in heart rate or systolic blood pressure \> 15% from baseline
Time frame: Through study completion, an average of 24 hours
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