Elsevier

Resuscitation

Volume 80, Issue 1, January 2009, Pages 120-125
Resuscitation

Experimental paper
The use of the Laerdal infant resuscitator results in the delivery of high oxygen fractions in the absence of a blender

https://doi.org/10.1016/j.resuscitation.2008.08.021Get rights and content

Summary

Background

High oxygen increases morbidity and mortality. Current guidelines in Neonatal Resuscitation Programme (NRP) state if self-inflating bags are used with an input FiO2 of 1.0 without an oxygen reservoir a delivered safe FiO2 of approximately 0.40 is achieved. This conflicts with manufacturer findings (Laerdal infant resuscitator® (LIR)). We assessed FiO2 delivery by the LIR, varying oxygen reservoir (OR) use, ventilation and input flowrates.

Methods

A test lung was connected to the LIR and oxygen analyzer. FiO2 delivery was measured under these four conditions: LIR plus OR and FiO2 1.0 or FiO2 0.40; LIR minus OR and FiO2 of 1.0 and 0.40. Variations of ventilation patterns in random order, assessed tidal volumes (from 20 and 40 mL), ventilation rates (from 30, 40 and 60 breaths/min), and input flowrates (from 1, 3, 5, 8, and 10 Lpm). A wash-out period of 1 min of ventilation was followed by measure of FiO2 during manual ventilation.

Results

The measured FiO2 with the LIR delivered the same source FiO2 under all experimental conditions for flowrates of 5 Lpm and greater; irrespective of the OR presence or absence. At flowrates of 1 and 3 Lpm, FiO2 was lower, with and without the reservoir, but the reservoir was visibly identified as not filled.

Conclusion

Our findings support the manufacturers performance specification that high input FiO2 results in high delivered FiO2 with/without an OR. These results dispute the 2006 NRP guidelines that state “in the absence of a reservoir (oxygen) the delivered oxygen is reduced to about 40%”.

Introduction

The delivery of high oxygen fractions to premature infants carries a potential for increased mortality during newborn resuscitation. Recently, a systematic review provides strong evidence to argue for a reduction in the FiO2 used at newborn resuscitation to below 1.0.1 The Neonatal Resuscitation Program (NRP) of the American Heart Association acknowledges this evidence and is currently amending its recommendations.2, 3, 4 However how technically to achieve this may require re-consideration. Currently, the American Heart Association Neonatal Resuscitation Programme Guidelines2 advise that with the self-inflating bag, a high fraction of oxygen (FiO2) is not achieved when the oxygen reservoir is removed. This is in direct conflict with the Laerdal infant resuscitator® (LIR) findings.5

An existing discrepancy between the LIR manufacturer recommendations and the NRP guidelines is of potential concern. The most widely used generic resuscitation device in newborns, is the self-inflating bag, as identified by 33 out of 40 neonatal intensive care centres across 19 countries.6 Although a 2006 global inventory lists over 100 trade-brands of self-inflating bags,7 the Laerdal infant resuscitator® was identified as the most widely used self-inflating bag.6 The LIR manufacturers state that a high FiO2 of 0.97–1.0 is delivered to the patient with or without the oxygen reservoir, when connected to an oxygen source. These recommendations are based on testing at tidal volumes of 20 mL and ventilation rates of 40–60 bpm, and flowrates of 3, 8, and 10 Lpm.5 In contrast, NRP currently states the FiO2 delivered is reduced to approximately 0.40 by a self-inflating bag without the oxygen reservoir; the test methods of this data are not detailed by NRP though they acknowledge that the ventilation pattern will influence the actual FiO2 delivered.2

Our objectives were first, to explore this discrepancy by determining whether the FiO2 delivered by the LIR does vary with and without a reservoir; and second to determine if a FiO2 less than 1.0 can be delivered by the LIR when connected to an O2 source. If a consistent FiO2 less than 1.0 can be delivered from the self-inflating bag, this would be reassuring for use during newborn resuscitation. Finally, we wished to determine the influence of tidal volume, ventilation rate, and gas flowrate (to the LIR) upon the FiO2 delivery with and without the reservoir. We hypothesized that there would be great variability in the FiO2 delivery without the reservoir, and that FiO2 delivery would be inconsistent depending on tidal volume, ventilation rate and gas flowrate.

Section snippets

Test conditions: use of reservoir and input gas FiO2

In vitro experimental conditions were created to assess the influence of a reservoir and the separate influence of the gas FiO2 delivered to the LIR (input gas). First we tested two conditions using a FiO2 of 1.0: the LIR with and without the oxygen reservoir bag, while attached to an oxygen gas input. We then varied the input gas FiO2 to 0.40 by attaching the LIR to an air/oxygen blender set to deliver a FiO2 of 0.40, both with and without the reservoir bag. In total this created four

Results

We display the data as plotted in Figure 2, Figure 3; and tabulated in Table 1. As well Table 2 displays relevant statistical analysis.

Discussion

We used an in vitro model to test the competing recommendations of the Laerdal manufacturers and the NRP regarding the maintenance of appropriate FiO2 during newborn manual ventilation. Our results confirm that the LIR does not provide an adequately low FiO2 when attached to an oxygen source of 1.0, at the NRP recommended flow rates of 5–10 Lpm. Provided flow rates of greater than 5 Lpm are used, the source FiO2 is maintained irregardless of the presence or absence of the reservoir. If a

Conclusion

If it is desired to deliver a FiO2 significantly lower than 1.0, then it is necessary to use a gas source that is of the desired air/oxygen mix. The absence of an oxygen reservoir assembly, does not influence the FiO2 delivered by the LIR at flowrates recommended by NRP. In addition, the removal of the oxygen reservoir may make it more difficult to discern if adequate gas flow is being achieved. Furthermore, it may not be as important as NRP suggests in achieving the gas source delivery with

Conflict of interest

None.

Acknowledgements

The authors wish to thank Dirk Bassler (McMaster University and Tubingen Children's H Germany) and Noori Akhtar-Danesh (Department Clinical Epidemiology, McMaster University) for assisting with the statistical analysis of the data.

References (9)

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A Spanish translated version of the summary of this article appears as Appendix in the final online version at doi:10.1016/j.resuscitation.2008.08.021.

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