Background: Newborn resuscitation is commonly performed in the presence of face mask leak. Leak is highly variable, pressure dependent and often unrecognised. The effectiveness of resuscitation devices to deliver adequate inflations in the presence of leak is unknown. Bench models simulating continuous leak have disadvantages of not accurately reflecting leak occurring during clinical resuscitation. A dynamic leak model based on pressure release valves was thus developed. Aim: To assess self-inflating bag (SIB) and T-piece resuscitator (TPR) ventilation performance in the presence of dynamic (DLM) compared to continuous (CLM) leak models in a bench study. Method: Five predefined leak levels were tested for each leak model (0-87%). Resuscitation devices were connected to a test lung (compliance 0.6 mL/cmH2O) and respiratory parameters were measured using respiratory function monitors before (patient interface) and after (actual) an induced leak at 40, 60, 80 inflations/min. Results: 3,600 inflations were analysed. DLM showed a decrease in actual tidal volumes from 0%-87% leak with tidal volume differences (SIB 4.8mL, TPR 2.9mL), contrasting to minimal change for CLM (SIB -0.6mL, TPR 0.3mL). CLM demonstrated larger differences between patient interface and actual leak. The absolute difference at 60 inflations/min at 87% leak were SIB 37.5%, TPR 18.2% for CLM compared to SIB 4.6%, TPR 1.4% for DLM. Conclusion: CLM may underestimate the impact of resuscitation device performance with poor correlation between patient interface and actual delivered volume. DLM demonstrates several advantages with more accurate representation of face mask leak and will prove useful in modelling all systems delivering PPV.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementWe acknowledge funding support from a PhD Research Grant awarded by Cerebral Palsy Alliance. This research is also supported by an Australian Government Research Training Program (RTP) Scholarship.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present work are contained in the manuscript and supplementary material.
留言 (0)