Use of Gentle Synchronized Negative Pressure in Helping Babies Breathe (Neovest)

Novel Use of Negative Pressure Assist in Neonates With Respiratory Distress: a Feasibility Study Using Neovest

The NeoVest delivery device is a wearable vest/shell that surrounds the infant's abdomen. It was developed using serial body measurements of infants previously admitted to the St. Michael's Hospital NICU (REB #15-183). It gently pulls on the abdomen by applying negative pressure, thereby displacing the diaphragm. The materials used for the NeoVest are lightweight and suitable for the infants' sensitive skin.

The AIM of the present study is to demonstrate the feasibility of applying negative pressure NIV, that is synchronized and proportional to the infant's respiratory demand. The preliminary data on feasibility can be used to apply for larger grants from the CIHR, for a study of the NeoVest in smaller premature infants.

Study Overview

• Status: Recruiting
• Conditions: Respiratory Distress Syndrome; RDS of Prematurity; TTN; Respiratory Distress, Newborn
• Intervention / Treatment: Device: NeoVest

Detailed Description

Respiratory distress is a common reason why newborn infants require intensive care soon after birth. Premature infants are at risk of having immature lungs and/or weak respiratory muscles requiring the provision of respiratory support with a mechanical ventilator. Full term infants can also require respiratory support for lung disease or lung immaturity. The most commonly used form of non-invasive respiratory support is positive pressure delivered via nasal prongs or a nasal mask, also known as nasal continuous positive airway pressure (nCPAP). Nasal CPAP is thought to be effective in a variety of newborn lung disorders including respiratory distress syndrome, transient tachypnea of the newborn, etc. Although many forms of nCPAP exist, they are not typically synchronized to a baby's breathing efforts (1,2).

Furthermore, due to the infants' sensitive skin and underdeveloped nasal bridges, continued use of nasal devices can lead to skin breakdown and permanent damage to the nose (3). In order to provide optimal ventilation, these devices must be tight-fitting nasal interfaces to provide a leak-free environment (3). There is also variability in the success of nasal interfaces in providing uniform ventilation. This is because the positive pressure provided at the level of the infants' nostrils is dissipated (through the open mouth, etc.) as it travels down the infants' airways to the alveoli of their lungs (3). Additionally, prolonged use of nasal ventilation methods may impede infant bonding with their mothers via decreased skin-to-skin time, etc. Nasal CPAP is often cited as a reason why feeding (including breastfeeding) is delayed in babies requiring neonatal intensive care stay.

Negative pressure ventilation (NPV) involves the application of sub-atmospheric pressures around the abdomen to displace the diaphragm. It is a unique alternative for administering NIV to infants and would avoid complications associated with nasal interfaces. NPV has previously been used in treating infants with respiratory distress using old-fashioned, large and bulky "iron-lung" devices (4-12). One of the earliest studies using NPV for infants with respiratory failure showed that in a series of 26 patients, NPV provided a sustained increase in PaO2 (5). The infants were a mean gestational age of 32 to 33 weeks and met the criteria for respiratory failure defined by PaO2 < 40mmHg on 100% inspired oxygen and/or PCO2 > 70mmHg during bag-mask ventilation (5). Further studies on NPV, continued to show effectiveness in the ventilation of infants with lung disease with improved oxygenation (6-12).

In this study, the investigators propose a novel negative pressure interface and device that is synchronized to the infant's respiratory drive and provides intermittent application of negative pressure. The device utilizes Neurally Adjusted Ventilator Assist (NAVA) technology to achieve synchronization to the infant's underlying respiratory drive and control.

The electrical activity of the diaphragm (Edi) is measured using a specialized feeding tube catheter with miniaturized sensors at the end. There is a small balloon at the tip of the catheter that measures the gastric pressure which provides evidence that the diaphragm is being displaced. The Edi catheter has been shown in previous work to be effective in delivering both invasive and non-invasive positive pressure ventilation with the FDA-approved NAVA and a variety of interfaces (13-15). The Edi catheter is used routinely in many NICUs worldwide as a conventional nasal or oral catheter.

NAVA is a mode of ventilation that is neurally integrated with the inherent lung protective reflexes by utilizing the information obtained from the Edi catheter. During spontaneous breathing, as lung inflation progresses, stretch receptors in the lungs will eventually sense an adequate inspired volume, and "switch off" inspiration. For a patient on NAVA, where the neural inspiration also controls the assist delivery, the ventilator breath will be cycled-off when neural exhalation begins. Several studies have demonstrated that infants spontaneously choose lower peak inspiratory pressures (PIP) and tidal volume during NAVA compared to conventional ventilation (targeted by the clinician) (16-23).

"Traditional" NAVA is triggered on and off with the Edi and delivers assist proportionally to the Edi on inspiration only. The PEEP is fixed and defined by the clinician. During this "traditional NAVA" there is a fair amount of tonic Edi that is not assisted. With continuous NAVA, the Edi is used to continuously adjust the assist. The Edi controls both the inspiratory and expiratory assist. A safety and tolerance study in 20 preterm infants using neutrally adjusted PEEP (neuroPAP) was done using nasal prongs as the delivery interface (See Appendix 2).

In this study, the investigators plan to control a negative pressure delivery device (NeoVest) to deliver synchronized negative NIV for a short period of time. Preliminary data in small rats (~400g) and larger rabbits (~3-4kg) have demonstrated feasibility and efficacy in experimental conditions mimicking neonatal respiratory distress (See Appendix 3). The Neovest was able to generate multiple effective levels of ventilator support in these animals with no side effects.

The NeoVest delivery device is a wearable vest/shell that surrounds the infant's abdomen. It was developed using serial body measurements of infants previously admitted to the St. Michael's Hospital NICU (REB #15-183). It gently pulls on the abdomen by applying negative pressure, thereby displacing the diaphragm. The materials used for the NeoVest are lightweight and suitable for the infants' sensitive skin.

The AIM of the present study is to demonstrate the feasibility of applying negative pressure NIV, that is synchronized and proportional to the infant's respiratory demand. The preliminary data on feasibility can be used to apply for larger grants from the CIHR, for a study of the NeoVest in smaller premature infants.

• Study Type: Interventional
• Enrollment (Anticipated): 20
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Douglas Campbell, MD; Phone Number: 6560 416-864-6060; Email: campbelld@smh.ca

Study Locations

• Canada
  • Ontario
    • Toronto, Ontario, Canada, M5B 1W8
      • Recruiting
      • St. Michael's Hospital NICU
      • Contact: Douglas Campbell, MD; Phone Number: 416-864-5232; Email: campbelld@smh.ca

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 6 hours to 2 weeks (Child)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• 20 infants, admitted to Neonatal Intensive Care Unit (NICU) at St. Michael's Hospital
• >1.5kg birthweight
• Clinically stable, with symptoms of respiratory distress (due to transient tachypnea of the newborn, respiratory distress syndrome, etc.)
• Stable on nasal CPAP (5-8cm H2O) for a minimum of 6 hours
• Within the first two weeks of life

Exclusion Criteria:

• Infants with FiO2 requirements >0.35
• Infants with clinically significant apnoea or bradycardia (> 2 A&B in last hour, or apnea >20 sec, or bradycardia requiring significant stimulation)
• Infants with hemodynamic instability (mean BP < weeks GA), or any infant requiring fluid boluses and/or inotropic medications
• Infants with genetic conditions or dysmorphic facial features
• Infants that have been recently extubated in the last 48 hours
• Infants in whom placement of the NG tube is contra-indicated
• Infants with any clinical suspicion of upper airway distress such as symptoms of stridor
• Infants with abdominal wall defects and other visible abnormalities of the abdomen or chest
• Infants with umbilical arterial and/or venous catheters
• Infants that have allergies and/or previous skin reactions to silicone based materials

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Device Feasibility
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: NeoVest; Negative pressure ventilation using NeoVest	Device: NeoVest; Negative pressure ventilation with NeoVest; Other Names: Negative Pressure Ventilation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Feasibility of negative pressure ventilation with NeoVest	Ability to provide negative pressure ventilation with the NeoVest	22 minutes

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Diaphragm Electrical Activity	Obtained from Edi catheter	Will be obtained every 1-5 minutes, or following any change in respiratory support
Respiratory Rate	Breaths per minute	Will be obtained every 1-5 minutes, or following any change in respiratory support
Heart Rate	Beats per minute	Will be obtained every 1-5 minutes, or following any change in respiratory support
Oxygen Saturation	Percent oxygen saturation	Will be obtained every 1-5 minutes, or following any change in respiratory support
Transcutaneous Carbon Dioxide Level	Transcutaneous meassurement in mmHg	Will be obtained every 1-5 minutes, or following any change in respiratory support
Blood Pressure	Obtained with blood pressure cuff in mmHg	Will be obtained every 1-5 minutes, or following any change in respiratory support

Collaborators and Investigators

• Sponsor: Unity Health Toronto
• Investigators: Principal Investigator: Douglas Campbell, MD, Unity Health Toronto

Study record dates

Study Major Dates

• Study Start (Actual): September 2, 2019
• Primary Completion (Anticipated): June 30, 2024
• Study Completion (Anticipated): December 30, 2024

Study Registration Dates

• First Submitted: April 5, 2018
• First Submitted That Met QC Criteria: April 25, 2018
• First Posted (Actual): April 27, 2018

Study Record Updates

• Last Update Posted (Actual): May 10, 2023
• Last Update Submitted That Met QC Criteria: May 9, 2023
• Last Verified: May 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Respiration Disorders; Lung Diseases; Infant, Newborn, Diseases; Infant, Premature, Diseases; Respiratory Distress Syndrome; Respiratory Distress Syndrome, Newborn
• Other Study ID Numbers: 17-282Neovest

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No