Performance and Acceptability of Two Self-Inflating Bag-Mask Neonatal Resuscitator Designs

被引:13
作者
Coffey, Patricia S. [1 ]
Saxon, Eugene A. [1 ]
Narayanan, Indira [1 ]
DiBlasi, Robert M. [2 ,3 ]
机构
[1] PATH, Seattle, WA 98109 USA
[2] Seattle Childrens Hosp, Dept Resp Therapy, Seattle, WA USA
[3] Seattle Childrens Hosp, Ctr Dev Therapeut, Res Inst, Seattle, WA USA
关键词
ventilation; medical devices; evaluation; newborn asphyxia; adverse intrapartum events; neonatal resuscitation; MANUAL VENTILATION; PRETERM INFANTS; DELIVERY ROOM; EDUCATED HAND; TIDAL VOLUME; LUNG INJURY; SURFACTANT; MORTALITY; PRESSURE; MODEL;
D O I
10.4187/respcare.03867
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: A self-inflating bag-mask device is specified by international policy guidelines as standard prototype of care for newborn resuscitation. Our hypothesis is that a new bag-mask design would be as effective and easy to use as a standard, self-inflating resuscitation bag-mask. METHODS: We conducted a comparative evaluation of the performance and acceptability of the Laerdal 220-mL resuscitator with a size-1 mask (NeoNatalie) and a Laerdal prototype Upright resuscitator with a modified mask. Participants evaluated the devices in random order using a commercially available test lung and training mannikin with an integrated chest-rise module. The test lung was configured with healthy and sick newborn lung mechanics. Two user groups participated: (1) frequent users who had used manual resuscitators to resuscitate infants and (2) infrequent users who received competency-based training and had not previously used manual resuscitators to resuscitate infants. RESULTS: Thirty-eight individuals participated in the study during March 2013. Both resuscitators are capable of delivering the minimum required tidal volumes to newborns. The Upright device provided a significant reduction in the percentage of inadequate ventilations (< 12.5 mL) compared with the NeoNatalie. Although the test sequences with low-compliance lung settings showed no difference in the percentage of excessive ventilations (> 37.5 mL) between the Upright and NeoNatalie, the test sequences with normal-compliance lung settings showed a higher percentage of excessive ventilations with both, and the increase was greater with the Upright than with the NeoNatalie (85.92% vs 71.39%, P <.001). The subjective acceptability and disassembly/reassembly tests were supportive of the new device design. CONCLUSIONS: The performance and acceptability of the Upright device in this user population suggest that the device may be suitable for effective ventilation by infrequent users in low-resource settings. The Upright device should be tested in such a setting. (c) 2015 Daedalus Enterprises
引用
收藏
页码:1227 / 1237
页数:11
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