There is currently a consensus that non-invasive ventilation (NIV) in preterm infants is preferred over intubation. There are two ways of delivering NIV in preterm infants, nasal continuous positive airway pressure (CPAP) or nasal intermittent positive pressure ventilation (NIPPV), where ventilator inflations are delivered intermittently over a fixed end-expiratory pressure. The synchronization in conventional mode is very difficult to obtain in premature infants. In all ventilation modes PEEP (end-expiratory pressure) is fixed. Considering that preterm infants are more likely to develop atelectasis, an active and ongoing management of the PEEP is very important to prevent de-recruitment. A new respiratory support system (NeuroPAP) was developed to address these issues (synchronization problems and control the PEEP). It uses the electrical activity of the diaphragm (EDI) to control the ventilator assist continuously, both during inspiration (principle of NAVA mode) and also during expiration (based on tonic Edi level).
The mode NeuroPAP will work with the continuous Edi-level and deliver pressures according to the Edi-signal x set NeuroPAP-level, over the whole breath (inspiration and expiration). The NeuroPAP will work between two pressure levels set by the user and named higher Pressure limit (Plimit) and minimum Pressure (Pmin). A safety upper pressure limit (UPL) will also be set. A backup ventilation will be possible. A specific gastric tube equipped with an array of microelectrodes (Edi catheter, Maquet, Solna, Sweden) will be installed after inclusion, by the same oral or nasal route as the tube previously in place. Patients will then be ventilated in the 5 aforementioned conditions: * On conventional NIPPV device on clinical settings for a 30 minute period. The investigators will note the mean airway pressure being delivered with the clinical settings and the resulting peak Edi, as well as neural respiratory rate, tonic Edi, Fraction of inspired oxygen (FiO2), and Oxygen saturation by pulse oximetry (SpO2). * With NeuroPAP without modification of Pmin (=peep). The exchange of the nasal interface may be necessary, depending on the original interface. FiO2 will initially be the same as previously set in conventional NIPPV. The Pmin will initially be set at the level of PEEP used during conventional NIPPV. A titration maneuver will be conducted to identify the optimal NeuroPAP level. The infant will be ventilated for one hour. Clinical adjustments in pressures and FiO2 are permitted. Safety termination will be established. * NeuroPAP with adjusted Pmin: the Pmin in NeuroPAP will be reduced by 2 cm H2O, with the same NeuroPAP level. The patients will be ventilated for one hour. * CPAP delivery with NeuroPAP device: the device will be switched to CPAP mode, for a 15 minute period * A second 30 minutes period of the conventional NIPPV will be conducted.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
The patients will be studied during the following conditions: * On conventional NIPPV device with the clinically prescribed settings (30 min) * With NeuroPAP and no change of Pmin (=peep) (60 min) * With NeuroPAP and adjusted Pmin (decreased by 2 cmH2O) (60 min) * During CPAP delivered with NeuroPAP device (15 min) * Again with original NIPPV device and settings for 30 minutes
St. Justine's Hospital
Montreal, Quebec, Canada
Time effectively spent with NeuroPAP mode activated during the NeuroPAP period
Percentage
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Number of interruption of NeuroPAP during the NeuroPAP period
Number of interruption per patients
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in respiratory rates between standard NIV andNeuroPAP
% of change
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in cardiac rates between standard NIV andNeuroPAP
% of change
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in blood pressure between standard NIV andNeuroPAP
% of change
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in SpO2 between standard NIV andNeuroPAP
% of change
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in TcPCO2 between standard NIV andNeuroPAP
% of change
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Time spent in asynchrony between standard NIV and NeuroPAP
% of time
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in trigger delays (ms) between standard NIV andNeuroPAP
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in non assisted breaths (wasted efforts) between standard NIV andNeuroPAP
% of change
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in autotriggered breaths between standard NIV and NeuroPAP
Percentage
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in Mean Airway pressure (cmH2O) between standard NIV and NeuroPAP
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in End expiratory pressure (PEEP, cmH2O) between standard NIV and NeuroPAP
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in Mean Electrical activity of diaphragm (Edi, mcV) between standard NIV and NeuroPAP
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in Peak Electrical activity of diaphragm (Edi, mcV) between standard NIV and NeuroPAP
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
Change in Tonic Electrical activity of diaphragm (Edi, mcV) between standard NIV and NeuroPAP
Time frame: up to 30 minutes after reinstitution of the conventional NIPPV
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