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ORIGINAL RESEARCH article

Front. Pediatr., 06 October 2023
Sec. Neonatology
This article is part of the Research Topic Neonatal Non-Invasive Ventilation View all 4 articles

Evaluation of NAVA-PAP in premature neonates with apnea of prematurity: minimal backup ventilation and clinically significant events

\r\nAlison Protain
&#x;Alison Protain1*Kimberly Firestone,&#x;Kimberly Firestone2,†Saima Hussain,&#x;Saima Hussain3,†Daniel Lubarsky,&#x;Daniel Lubarsky4,†Howard Stein,&#x;\r\nHoward Stein5,†
  • 1Pediatrix Medical Group Akron Ohio, Akron Children’s Hospital, Akron, OH, United States
  • 2Department of Neonatology, Akron Children’s Hospital, Akron, OH, United States
  • 3Department of Pediatrics, ProMedica Russell J. Ebeid Children’s Hospital, Toledo, OH, United States
  • 4Department of Pediatrics, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, TN, United States
  • 5Northwest Ohio Neonatal Associates, ProMedica Russell J. Ebeid Children’s Hospital, Toledo, OH, United States

Background: Neonates with apnea of prematurity (AOP) clinically deteriorate because continuous positive airway pressure (CPAP) provides inadequate support during apnea. Neurally adjusted ventilatory assist (NAVA) provides proportional ventilator support from the electrical activity of the diaphragm. When the NAVA level is 0 cmH2O/mcV (NAVA-PAP), patients receive CPAP when breathing and backup ventilation when apneic. This study evaluates NAVA-PAP and time spent in backup ventilation.

Methods: This was a prospective, two-center, observational study of preterm neonates on NAVA-PAP for AOP. Ventilator data were downloaded after 24 h. The number of clinically significant events (CSEs) was collected. A paired t-test was used to perform statistical analysis.

Results: The study was conducted on 28 patients with a gestational age of 25 ± 1.8 weeks and a study age of 28 ± 23 days. The number of CSEs was 4 ± 4.39/24 h. The patients were on NAVA-PAP for approximately 90%/min, switched to backup mode 2.5 ± 1.1 times/min, and spent 10.6 ± 7.2% in backup.

Conclusion: Preterm neonates on NAVA-PAP had few CSEs with minimal time in backup ventilation.

1. Introduction

Premature neonates remain vulnerable to the physiologic consequences of apnea of prematurity (AOP). Periods of clinical deterioration characterized by bradycardia and desaturation, referred to as clinically significant events (CSEs), are frequently encountered in the neonatal intensive care unit (NICU) (1). Caffeine citrate and continuous positive airway pressure (CPAP) are commonly used therapeutic modalities that demonstrate significant benefits (24). Unfortunately, increasing respiratory support may be required for the smallest and most fragile premature neonates. Non-invasive respiratory strategies have shown promise, with synchronization of nasal ventilation showing further improvement for respiratory stability (5), although intubation and mechanical ventilation may be needed for severe apnea (2, 3, 6).

Neurally adjusted ventilatory assist (NAVA) provides support in synchrony with the respiratory efforts of a patient based on the detected electrical activity of the diaphragm (Edi). It is delivered with the Servo-I/U/N ventilator (Getinge, Germany) using NAVA software. The NAVA level is a proportionality factor that converts the Edi signal into a pressure above the positive end-expiratory pressure (PEEP) supporting each spontaneous breath. If no Edi signal is detected for a predetermined amount of time (apnea time), the ventilator switches into pressure control ventilation until the patient breathes spontaneously again, which provides a minimum rate (7). If the NAVA level is set at 0 cmH2O/mcV, the patient receives minimal synchronized support above the baseline PEEP while breathing (CPAP) and backup ventilation when apneic (Figure 1).

FIGURE 1
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Figure 1. Screenshot for the Servo-I ventilator. The bottom line represents the Edi signal. The next lineup is volume, and the third lineup is flow. The top line is pressure. Patient interface resistance compensation in the NAVA software program provides minimal support above CPAP when breathing. Backup ventilation is provided when apneic. Auto-triggering does not occur as neural triggering is the mechanism for initiation.

Although NAVA ventilation has been in use for over a decade, only one previous study has shown a statistically significant reduction in CSEs for premature neonates ventilated on non-invasive NAVA of 0 (NAVA-PAP) vs. CPAP via the RAM cannula (1). However, the mechanism for this improvement was not studied. This study aims to evaluate NAVA-PAP acting as CPAP with backup ventilation further. The primary outcomes focus on the time in NAVA vs. backup ventilation and delineating ventilator pressures and respiratory rates (RRs).

2. Materials and methods

This was a prospective, two-center, observational study of preterm patients admitted to the NICUs of ProMedica Ebeid Children's Hospital and Akron Children's Hospital during the period between August 2019 and February 2020. The patients were placed on NAVA-PAP for AOP at the treating provider's discretion. IRB approval and informed consent were obtained. Akron Children's Hospital Institutional Review Board and ProMedica IRB reviewed and approved the studies involving human/animal participants. The patients/participants (legal guardian/next of kin) provided written informed consent to participate in this study. All research was conducted in accordance with the ethical standards of all applicable national and institutional committees and the World Medical Association's Helsinki Declaration. Ventilator data were downloaded after 24 h of using NAVA-PAP. Each data point was the breath-to-breath data averaged over 1 min. Therefore, 1,440 data points were collected for each subject. The demographics and number of CSEs were collected. CSEs were defined as bradycardia (less than 80 beats/min) or desaturation (less than 90%) lasting more than 10 s. CSEs were retrospectively collected from the electronic health record during the data collection on NAVA-PAP. A paired t-test was used to perform statistical analysis.

3. Results

A total of 28 patients on NAVA-PAP were enrolled. In total, 40,320 data points (each data point = 1 averaged minute) were collected for the 28 patients. All patients experienced AOP, were treated with caffeine, and were on the RAM cannula nasal interface. Table 1 shows the demographics of the patients. Ventilator settings were a NAVA level of 0, an apnea time of 2 s (minimum rate of 30 breaths per minute), a peak inspiratory pressure (PIP) limit of 35–40 cmH2O, a PEEP of 7.9 ± 0.8 cmH2O, backup settings of PIP 19 ± 3.6 cmH2O,, and a rate of 43 ± 5.48. Patients were in NAVA-PAP for approximately 54 s per minute, went into the backup ventilation mode 2.5 ± 1.1 times per minute, and spent approximately 6 s of each minute in the backup mode (Figure 2). This calculates to an average of 150 brief switches per hour for a collective total of 6 min/h in the backup mode. The total RR was slightly higher than the spontaneous RR. Figure 3 shows that the number of CSEs was 4 ± 4.39/24 h. The mean airway pressure (MAP) was higher than the measured PEEP, and the average PIP was higher than MAP. The RAM nasal interface had a 91.9 ± 4.5% leak, with a mean supplemental oxygen requirement of 23.2 ± 3.3%.

TABLE 1
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Table 1. Demographics.

FIGURE 2
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Figure 2. Distribution of RR, Edi, and switches to backup. Units are noted in parentheses following each variable. The box plots show the median and first and third quartiles. The whiskers are the minimum and maximum values. #p < 0.05 compared with total RR.

FIGURE 3
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Figure 3. Average (SD) of PEEP, MAP, PIP, CSE, and FiO2. Units are noted in parentheses following each variable. #p < 0.05 compared with PEEP, *p < 0.05 compared with MAP.

4. Discussion

The expanded use of non-invasive ventilation strategies to decrease the need for intubation and invasive ventilation remains a high priority (8). CPAP still remains the gold standard, although a significant percentage of preterm neonates will require increased respiratory support (6, 9, 10). Non-invasive respiratory support subsequently evolved with options such as nasal intermittent positive pressure ventilation (NIPPV) to augment lung inflation and respiratory muscle unloading (11). The flow-triggered synchronized mode of NIPPV was also found to have beneficial effects on reducing apnea and desaturations compared with CPAP and NIPPV (12).

NAVA, a novel mode of ventilation, changed the paradigm by providing synchronized ventilation in which the patient controls both timing and degree of ventilatory assistance. Several studies have demonstrated decreased PIPs, oxygen requirement, and apnea in preterm neonates receiving NAVA ventilation compared with those receiving traditional synchronized intermittent mechanical ventilation (SIMV) and pressure control ventilation (1316).

Compared with CPAP, some data suggest that NIV NAVA in neonates may reduce the need for intubation, facilitate early extubation, and decrease extubation failures (1719). NIV NAVA has also been shown to decrease the number of CSEs compared with non-synchronous, non-invasive ventilation (20).

NAVA-PAP is the only non-invasive mode that delivers CPAP while breathing and backup ventilation when the patient is apneic. Utilizing NAVA-PAP as a strategy in neonates with AOP while on CPAP was recently studied and demonstrated significant benefits in reducing CSEs (1). This approach offers the advantage of reducing CSEs while minimizing exposure to non-invasive ventilation.

When NIV NAVA is set at 0 cmH2O/mcV, the Servo-I/U delivers a PIP of 2 cmH2O above PEEP in synchrony with the spontaneous breaths of the patient (1). NAVA software has patient interface resistance compensation and accounts for this small increase in pressure observed above PEEP. Buzzella et al. (21) previously demonstrated that higher CPAP levels resulted in fewer extubation failures. Owen et al. (22) showed that NIPPV did not deliver any measurable tidal volume during periods of apnea. Therefore, it is possible that the minimally augmented pressure delivered with each breath translating into a higher overall MAP is responsible for the improvement noted in CSEs in previous studies (1) but could also be related to the stimulation of the patient's respiratory drive during backup ventilation.

Even though the average set PIP delivered 19 cmH2O with each breath, the measured average PIP was only 10.9 cmH2O. Since there was no proximal sensor in use at the nasal interface, this decrease in the overall average measured PIP was expected considering that there were so few set backup breaths delivered each minute. The average PIP was higher than MAP (10.9 vs. 9.1 cmH2O). This was because the intermittent backup breaths delivered occur only during backup ventilation and did not deliver any additional pressure with any spontaneous breaths. Both Edi peak and minimum were within previously described ranges for preterm neonates (23).

Our data demonstrate that the time preterm neonates spent in backup ventilation was quite low. Studies have shown improved patient–ventilator synchrony with NAVA ventilation, with a resultant decrease in the number of apneic events (14, 20). Although these studies attributed the decreased CSEs to being on NIV NAVA, perhaps it is the additional breaths delivered during periods of apnea that contributed to the decrease in the number of CSEs. These additional backup breaths account for the total RR higher than the spontaneous RR (64 vs. 58 breaths per minute) but remains well within the normal RR range for neonates. Using an apnea time of 2 s meant that all patients had a minimum rate of 30 breaths per minute. Because of this short apnea time, there were multiple brief switches to backup pressure control ventilation, but the percentage of time spent in the backup mode was low. This short apnea time may have prevented any extended periods of apnea and contributed to the improvement in CSEs, as supported by a previous pilot trial that demonstrated that short apnea times should be utilized for neonatal patients ventilated with NIV NAVA to promote clinical stability and decrease the occurrence of clinically important events (24).

This study is limited by several factors. This was a descriptive study, so no control group was needed. Reliance was on bedside charting to determine the number of CSEs. In addition, there was an inability to determine the exact mechanism for the CSE reduction reported by a previous study. Prospective randomized controlled studies are needed to further explore the reduction in CSEs and other potential benefits of NAVA-PAP. This study only included neonates on the RAM cannula interface, which limits the generalizability of the findings to other nasal interfaces. However, useful data were provided to support further investigation of NAVA-PAP for treatment of preterm neonates with AOP.

In conclusion, NAVA-PAP in preterm neonates acted as minimally augmented CPAP during spontaneous ventilation and provided backup ventilation when apneic. Increased MAP and total RR may explain why this mode was effective. Despite the large leak, the RAM nasal interface was effective at delivering CPAP (NAVA level of 0) with backup ventilation. This modality may offer a safe and effective option to avoid excessive non-invasive ventilation or intubation in premature neonates failing CPAP because of frequent CSEs.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human/animal participants were reviewed and approved by Akron Children’s Hospital Institutional Review Board and ProMedica IRB. The patients/participants (legal guardian/next of kin) provided written informed consent to participate in this study.

Author contributions

AP, KF, SH, DL, and HS all equally contributed to the manuscript and shared the first authorship. All authors contributed to the article and approved the submitted version.

Acknowledgments

The authors acknowledge their colleagues at Akron Children's Hospital Mahoning Valley NICU for coining the phrase NAVA-PAP. The original version of this manuscript is available on the preprint server Research Square (25).

Conflict of interest

HS and KF are on the Speakers’ Bureau for Getinge and Chiesi USA Inc.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Firestone KS, Al Horany B, Belden L, Stein HM. Nasal continuous positive airway pressure versus non-invasive NAVA in preterm neonates with apnea of prematurity: a pilot study with a novel approach. J Perinatol. (2020) 40:1211–5. doi: 10.1038/s41372-020-0661-x

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Eichenwald E, Newborn CoFa. Apnea of prematurity. Pediatrics. (2016) 137(1):1097–105. doi: 10.1542/peds.2015-3757

CrossRef Full Text | Google Scholar

3. Sammour I, Karnati S. Non-invasive respiratory support of the premature neonate: from physics to bench to practice. Front Pediatr. (2020) 8:214–8. doi: 10.3389/fped.2020.00214

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Moschino L, Zivanovic S, Hartley C, Trevisanuto D, Baraldi E, Roehr CC. Caffeine in preterm infants: where are we in 2020? ERJ Open Res. (2020) 6. doi: 10.1183/23120541.00330-2019

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Moretti C, Gizzi C, Montecchia F, Barbara C, Midulla F, Sanchez-Luna M, et al. Synchronized nasal intermittent positive pressure ventilation of the newborn: technical issues and clinical results. Neonatology. (2016) 109(4):359–65. doi: 10.1159/000444898

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Hussain WA, Marks JD. Approaches to noninvasive respiratory support in preterm infants: from CPAP to NAVA. NeoReviews. (2019) 20(4):e213–21. doi: 10.1542/neo.20-4-e213

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Sinderby C, Beck J. Neurally adjusted ventilatory assist. In: Tobin MJ, editor. Principles and practice of mechanical ventilation. 3rd ed. McGraw Hill/Medical (2012). p. 351–75

8. Sweet D, Carnielli V, Greisen G, Hallman M, O’zek E, te Pas A, et al. European consensus guidelines on the management of respiratory distress syndrome—2019 update. Neonatology. (2019) 115(4):432–50. doi: 10.1159/000499361

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Dargaville PA, Gerber A, Johansson S, De Paoli A, Kamlin OF, Orsini F, et al. Incidence and outcome of CPAP failure in preterm infants. Pediatrics. (2016) 138(1):e20153985. doi: 10.1542/peds.2015-3985

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Morley C, Davis P, Doyle L, Brion L, Hascoet J, Carlin J. Nasal CPAP or intubation at birth for very preterm infants. N Engl J Med. (2008) 358(7):700–8. doi: 10.1056/NEJMoa072788

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Kiciman NM, Andréasson B, Bernstein G, Mannino FL, Rich W, Henderson C, et al. Thoracoabdominal motion in newborns during ventilation delivered by endotracheal tube or nasal prongs. Pediatr Pulm. (1998) 25(3):175–81. doi: 10.1002/(SICI)1099-0496(199803)25:3%3C175::AID-PPUL7%3E3.0.CO;2-L

CrossRef Full Text | Google Scholar

12. Gizzi C, Montecchia F, Panetta V, Castellano C, Mariani C, Campelli M, et al. Is synchronised NIPPV more effective than NIPPV and NCPAP in treating apnoea of prematurity (AOP)? A randomised cross-over trial. Arch Dis Child Fetal Neonatal Ed. (2015) 100:F17–23. doi: 10.1136/archdischild-2013-305892

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Stein HM, Howard D. Neurally adjusted ventilatory assist (NAVA) in neonates less than 1,500 grams: a retrospective analysis. J Pediatr. (2012) 160(5):786–9. doi: 10.1016/j.jpeds.2011.10.014

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Mally P, Beck J, Sinderby C, Caprio M, Bailey S. Neural breathing pattern and patient–ventilator interaction during neurally adjusted ventilatory assist and conventional ventilation in newborns. Pediatr Crit Care Med. (2018) 19(1):48–55. doi: 10.1097/PCC.0000000000001385

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Shetty S, Hunt K, Peabody J, Ali K, Greenough A. Crossover study of assist control ventilation and neurally adjusted ventilatory assist. Eu J Pediatr. (2017) 176:509–13. doi: 10.1007/s00431-017-2866-3

CrossRef Full Text | Google Scholar

16. Protain AP, Firestone KS, McNinch N, Stein H. Evaluating peak inspiratory pressures and tidal volume in premature neonates on NAVA ventilation. Eur J Pediatr. (2021) 180(1):167–75. doi: 10.1007/s00431-020-03728-y

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Yagui AC, Meneses J, Z’olio BA, Brito GM, Justino da Silva R, Rebello CM. Nasal continuous positive airway pressure (NCPAP) or noninvasive neurally adjusted ventilatory assist (NIV-NAVA) for preterm infants with respiratory distress after birth: a randomized controlled trial. Pediatr Pulmonol. (2019) 54(11):1704–11. doi: 10.1002/ppul.24466

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Lee BK, Shin S, Jung Y, Kim E, Kim H. Comparison of NIV-NAVA and NCPAP in facilitating extubation for very preterm infants. BMC Pediatr. (2019) 19:1683–4. doi: 10.1186/s12887-019-1683-4

CrossRef Full Text | Google Scholar

19. Makker K, Cortez J, Jho K, Shah S, Nandula P, Lowrie D, et al. Comparison of extubation success using noninvasive positive pressure ventilation (NIPPV) versus noninvasive neurally adjusted ventilatory assist (NI-NAVA). J Perinatol. (2020) 40(8):1202–10. doi: 10.1038/s41372-019-0578-4

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Tabacaru CR, Moores RR, Khoury J, Rozycki HJ. NAVA—synchronized compared to nonsynchronized noninvasive ventilation for apnea, bradycardia, and desaturation events in VLBW infants. Pediatr Pulmonol. (2019) 54(11):1742–6. doi: 10.1002/ppul.24464

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Buzzella B, Claure N, D’Ugard C, Bancalari E. A randomized controlled trial of two nasal continuous positive airway pressure levels after extubation in preterm infants. J Pediatr. (2014) 164(1):46–51. doi: 10.1016/j.jpeds.2013.08.040

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Owen LS, Morley C, Davis P. Effects of synchronisation during SiPAP-generated nasal intermittent positive pressure ventilation (NIPPV) in preterm infants. Arch Dis Child Fetal Neonatal Ed. (2015) 100:F24–30. doi: 10.1136/archdischild-2013-305830

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Stein H, Hall R, Davis K, White DB. Electrical activity of the diaphragm (Edi) values and Edi catheter placement in non-ventilated preterm neonates. J Perinatol. (2013) 33(9):707–11. doi: 10.1038/jp.2013.45

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Morgan EL, Firestone KS, Schachinger SW, Stein H. Effects of changes in apnea time on the clinical status of neonates on NIV-NAVA. Resp Care. (2019) 64(9):1096–100. doi: 10.4187/respcare.06662

CrossRef Full Text | Google Scholar

25. Protain A, Firestone K, Hussain S, Lubarsky D, Stein H. The effect of NIV NAVA O on ventilation in premature neonates. October 29, 2021. Research square [Preprint]. doi: 10.21203/rs.3.rs-1004905/v1. https://www.researchsquare.com/article/rs-1004905/v1. Last accessed 29 October 2021

CrossRef Full Text | Google Scholar

Keywords: neurally adjusted ventilatory assist (NAVA), premature neonates, apnea of prematurity (AOP), continuous positive airway pressure (CPAP), NAVA-PAP

Citation: Protain A, Firestone K, Hussain S, Lubarsky D and Stein H (2023) Evaluation of NAVA-PAP in premature neonates with apnea of prematurity: minimal backup ventilation and clinically significant events. Front. Pediatr. 11:1234964. doi: 10.3389/fped.2023.1234964

Received: 5 June 2023; Accepted: 21 September 2023;
Published: 6 October 2023.

Edited by:

Jonathan Michael Davis, Tufts University, United States

Reviewed by:

Paolo Biban, Integrated University Hospital Verona, Italy
Martin Keszler, Women & Infants Hospital of Rhode Island, United States

© 2023 Protain, Firestone, Hussain, Lubarsky and Stein. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Alison Protain aprotain@akronchildrens.org

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.