The RAM Cannula interface is used as routine interface for newborn infants receiving CPAP
treatment for respiratory distress. Compared to the standard systems that have been used
for more than 50 years, the interface has high resistance and has not been extensively
studied. The delivered quality of the CPAP support is likely to be negatively affected by
the interface resistance.
We hypothesise that exhalations through the device is uncommon and that the interface
resistance restricts flow from the patient. If expiratory flows are uncommon the RAM
interface provide support clinically comparable to other systems based on unidirectional
flow such as humidified high-flow cannula.
This is a cross-sectional, observational study (no intervention) in newborn infants that
are clinically stable and on respiratory support with the RAM interface connected to a
bCPAP circuit. This is the most common support in the Phu San neonatal unit. The time
needed for data collection is short and collection is expected to take approximately five
minutes (less than 15 minutes) in a quiet infant. The collection can be planned to
minimize disturbances for the infant, parents and staff. For example, the busiest times
of the day can be avoided to not intervene with daily care, ward rounds or examinations
of the infant.
Data on flow and pressure will be collected within the respiratory support circuit at the
connection to the RAM interface. The measurements are passive, and no tests or
manipulation of the infant is planned. There will be brief interruptions (<1 min) in
respiratory support when the meters are connected. Similar interruptions are very common
and occurs several times per day during normal care.
Data will be collected in case report forms (CRF) with REDCap electronic data capture
tool. All personal identifiers will be removed before data export from REDCap and further
analysis only using enrolment numbers.
Background variables describing the pregnancy, delivery and the infant will be collected.
We also will record details of the RAM-cannula interface, such as size, protective
dressing, gastric feeding tube, obvious leak at nares and mouth.
During the measurement the infant will be monitored for vital signs and any problems will
be addressed and recorded. This includes oxygen need, CPAP support and breathing
problems. The flow and pressure data for one minute of quiet breathing will be stored
locally with the enrolment number as identifier. The analysis after collection of flow
and pressure will include average flow in the CPAP circuit, the flow to the patient,
average absolute leak and delivered pressure. If a variation with breathing can be seen
this will be described. These output variables directly relate to the research questions.
What flows and pressure can be observed in the breathing circuit? [Measured average
flows, pressure and variability between patients]
Do infants exhale through the RAM interface? [Measured expiratory flows at the
interface]
What is the level of leak for the interface? [Measured absolute leak]
The RAM cannula interface has been widely introduced but is not CE-marked for CPAP
support. It has an advantage of being more comfortable and light weight with less nasal
injury in most trials. The high resistance of the RAM interface has been discussed as
problematic by several authors, but the clinical importance is not known. Comparing RAM
interface to other CPAP interfaces in clinical trials is difficult and, if RAM has a
treatment effect similar to HHFNC, very large trials of high quality would be needed.
The described study will generate new knowledge on the RAM interface by describing
patient flow through the interface and illustrate the importance of resistance and leak.
The study is not strictly a physiological study but investigate flow in an airway
interface. The most likely outcome is that exhalation is uncommon, and this would support
that the RAM interface has more similarities with HHFNC than conventional CPAP.