None listed
Conditions
Brief summary
The purpose of this study is determine how the lungs start breathing air immediately after birth. We know that during the pregnancy the baby’s lungs are filled with fluid but that immediately after birth the lungs need to very quickly clear the fluid and replace it with air so normal breathing can begin (this is called ‘aeration’). Some babies struggle to do this and develop breathing problems immediately after birth. This is very common in babies born prematurely but also occurs in at least 10% of healthy term babies. It is known from studies in animals that the process of aeration is very complex and breathing problems are most likely if aeration does not occur equally throughout both lungs at birth. At present we don't know how babies lungs aerate at birth, despite this being something every baby needs to do. This is because measuring aeration is hard to do. Recently, our team have developed a special method of measuring aeration at birth, it uses a simple device called electrical impedance tomography or EIT). EIT does not interfere with the normal behaviour of a baby or their clinical care, and is free from radiation (unlike x-rays), meaning that EIT can measure aeration and breathing in a baby for long periods of time. We would like to use EIT describe, for the first time, how healthy term and preterm lungs aerate immediately after birth. This will assist us in determining how we may be able to better understand how to develop treatments for sick babies who cannot achieve aeration properly.
Interventions
As soon as practical after birth a custom-built non-adhesive elastic neonatal 32 electrode EIT belt appropriate for estimated birth weight (RIEDEL system, Swisstom AG, Switzerland; CTN-04696-11-04) will be secured with a Velcro fastener around the chest at nipple level of the newly born infant and imaging commenced. A pulse oximetry probe will also be placed on the right hand (Masimo SET pulse oximeter, Masimo Corp., Irvine, CA) to measure preductal peripheral oxygen saturation (SpO2) and heart rate. Clinical care will then proceed as per Neonatal Resuscitation Program guidelines. If respiratory support is applied pressure, flow and tidal volume will be measured using a Florian Respiratory Mechanics monitor (Acutronic, Hizel, Switzerland). The resuscitation will be video recorded. Measurements will cease when the infant is moved from the resuscitation trolley. There will be no interruption or alteration to normal clinical care. For preterm infants all measurements will be repeated daily until 72 hours of life (subject to reaffirmation of parental consent) using our previously validated protocol of 6 x two minute recordings over a 30 min period of quiet activity. This will allow us to determine the relationship between the physiological and clinical respiratory events occurring in the Delivery Room and the impact on subsequent respiratory status in NICU.
Sponsors
Eligibility
Inclusion criteria
Need for any assessment in the Delivery Room by a health care practitioner at birth, such that participation in the study will not interfere with normal mother-baby interactions. This includes infants being born preterm at any gestation less than 36 weeks, term infants with low-risk of needing resuscitation but still require attendance of a midwife or medical staff, and infants being born via immediate and delayed umbilical cord clamping.
Exclusion criteria
1. Any infant with known congenital anomalies or pulmonary hypoplasia. 2. Infants born to guardians’ unable to or refusing consent.