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 Table of Contents  
ORIGINAL ARTICLE
Year : 2021  |  Volume : 10  |  Issue : 3  |  Page : 330-335

Pressure support ventilation in neonates – Is it safe?


1 Department of Respiratory Therapy, Manipal College of Health Professions, Manipal Academy of Higher Education, Manipal, Karnataka, India
2 Department of Respiratory Care Therapy, Batterjee Medical College, Jeddah, Saudi Arabia
3 Department of Pediatrics, Kasturba Medical College, Manipal, Karnataka, India

Date of Submission25-Jan-2021
Date of Decision15-Jul-2021
Date of Acceptance26-Jul-2021
Date of Web Publication13-Sep-2021

Correspondence Address:
Leslie Edward Lewis
Department of Pediatrics, Kasturba Medical College, Manipal, Karnataka
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijrc.ijrc_13_21

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  Abstract 


Introduction: Pressure support ventilation (PSV) is a common weaning mode in adults, but it is less familiar among the neonatal population due to lack of awareness and safety concerns associated with leaks around uncuffed endotracheal tube. There is limited evidence addressing this issue in the literature. Therefore, the study focuses on the safety of PSV among neonates. Subjects and Methods: The prospective observational study was done among 57 neonates (gestational age from 26 to 37 weeks) requiring mechanical ventilation. PSV mode was used 30 min before extubation and assessed for any changes in hemodynamic and ventilator parameters for two time points, during the initiation of PSV, and the end of 30 min of the trial. The incidence of reintubation within 72 h was also noted. Results: There were no wide variations in hemodynamic and ventilator parameters during the trial. The average heart rate, respiratory rate, and saturation of oxygen were noted to be 146 bpm, 54/min, and 95%, respectively. The average mean airway pressure was found to be 7.2 cm H2O during PSV. The reintubation rate was found to be 8.2%, with a mortality rate of 5.2%. Conclusion: The current study findings conclude that PSV in neonates can be used safely as an independent mode during weaning.

Keywords: Neonatal ventilation, pressure support, respiratory severity score, spontaneous breathing trial


How to cite this article:
Rajan A, Krishna GG, Lewis LE. Pressure support ventilation in neonates – Is it safe?. Indian J Respir Care 2021;10:330-5

How to cite this URL:
Rajan A, Krishna GG, Lewis LE. Pressure support ventilation in neonates – Is it safe?. Indian J Respir Care [serial online] 2021 [cited 2021 Oct 26];10:330-5. Available from: http://www.ijrc.in/text.asp?2021/10/3/330/325874




  Introduction Top


Mechanical Ventilation (V˙e) is a lifesaving therapy in managing critically ill neonates, but its prolonged use can cause severe complications such as bronchopulmonary dysplasia, ventilator-associated pneumonia, and barotrauma. Therefore, it is necessary to wean from the ventilator as early as possible. Although weaning strategies are well established and practiced in the adult population, the evidence-based weaning in neonates is still lacking. Several studies showed that 3-min spontaneous breathing trial (SBT) would benefit in the smooth transition from mechanical V˙e to noninvasive support in neonates.[1],[2] A 2–3-min continuous positive airway pressure (CPAP) is the commonest SBT trial used in neonates. The major drawback during CPAP trial is the unaccounted endotracheal tube resistance, which may further worsen or reduce the functional residual capacity and cause weaning failure.

Pressure support ventilation (PSV) is a commonly used weaning mode in adults and pediatrics. PSV assists spontaneously breathing with inspiratory pressure support along with baseline pressure, which helps in overcoming the endotracheal tube resistance.[3] Additionally, PSV assists the respiratory muscle, improves the efficacy of patient effort, and reduces the work of breathing (WOB).[4],[5],[6] Proper titration of pressure support level is essential since a higher or lower level of pressure can result in hyperinflation or hypoventilation.[7]

The use of PSV is limited among the neonatal population. The use of an uncuffed endotracheal tube is a unique challenge causing leak around the endotracheal tube, which can mimic as a spontaneous breath and cause serious complications such as air-leak syndromes and significant hemodynamic instability. The neonatal weaning approach should be gradual with frequent small changes made at regular interval that allows the neonates to progressively assume greater responsibility of gas exchange while reducing ventilator support.[1] Premature ventilator discontinuation can cause respiratory muscle fatigue and gas exchange failure leading to invasive ventilator support. Three-minute CPAP trial predicts extubation failure but does not provide ample transition time from invasive V˙e. Longer duration in a lower level of invasive support will help in assessing the extubation readiness as well as provide a smooth transition from invasive V˙e. Furthermore, lower level of ventilator support can help in easy transition to spontaneous breathing than from a higher level of support.[8]

Recent advancements in microprocessor technology and the introduction of dedicated flow sensors help in overcoming the trigger dyssynchrony associated with tube leak. The present-day neonatal ventilators are convenient to use with its leak compensation technique, which adjusts the delivered tidal volume (VT) for the endotracheal tube leak and automatically adapts to the trigger sensitivity.[9],[10]


  Subjects and Methods Top


The current prospective observational study was done at a multispecialty tertiary care center and teaching institute in South India after the approval from the Institutional Review Board and Institution Ethical Committee on April 2018. Neonates were screened based on the inclusion and exclusion criteria of the study. Written consent was taken from the parents/guardian of the neonates prior to recruiting the study (May 2018–March 2019). The neonates with gestational age from 26 to 37 weeks who required invasive V˙e were included in the study. Neonates with multiple congenital anomalies, air-leak syndrome, severe hemodynamic instability, and without informed consent were excluded. The predetermined sample size was not calculated in the current study. Subjects who met the study criteria were enrolled. A total of 57 neonates were eligible for the study.

The existing unit protocol used CPAP trial for an extended duration (3–5-min CPAP trial) under close monitoring to assess the extubation readiness. PSV trial is also given for neonates requiring prolonged duration of mechanical V˙e. Neonates <36 weeks of gestation also receive a dose of caffeine (20 mg/kg) 30 min prior to extubation. Postextubation, neonates are initiated on any of the noninvasive support (nasal CPAP, nasal synchronized intermittent mandatory ventilation [SIMV], and heated humidified high flow nasal cannula) accordingly. If the neonate presents with any hemodynamic instability, the mode is switched over to conventional V˙e.

The primary mode of V˙e was set based on our neonatal intensive care unit (NICU) protocol, started on either SIMV with pressure control or volume guarantee (SIMV-PC or VG) mode of V˙e, inspired oxygen concentration (FiO2) (0.25–1), pressure control (targeting the VT of 4–6 ml/kg), positive end-expiratory pressure (PEEP) (5–6 cmH2O), and respiratory rate of 45 bpm. The criteria to switch over from SIMV to PSV were FiO2 (0.25), peak inspiratory pressure (PIP/14 cmH2O), PEEP (5 cmH2O), respiratory rate (f/30 bpm), inspiratory time (Ti/0.5 s), and inspiratory flow (7 L/min). The neonates were ventilated on PSV mode for 30 min before extubation. Initial settings on PSV were FiO2 (21%–40%), targeting SpO2 (88%–99%), PS (targeting a VT of 4–6 ml/kg), PEEP (5–6 cmH2O), backup rate (20–25/min), and inspiratory time (Ti) – 50% more than spontaneous Ti. After 30 min of V˙e on PSV, the neonates were extubated onto noninvasive ventilator support with the permission from an attending physician [Figure 1].[11],[12],[13],[14],[15],[16],[17]
Figure 1: Pressure support ventilation weaning protocol

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Pressure support ventilation failure

It is defined as hemodynamic instability with more than 60% endotracheal tube leak, high variation between set and measured VT, and presence of clinical signs of distress. If neonates presented with any of these, they were switched back to the previous mode, and further care was decided based on the attending physician.

The primary outcome was to assess the changes in hemodynamic and ventilator parameters at 0 min and 30 min of PSV. The secondary outcome was to determine any incidence of air leak immediately post-PSV trial, the incidence of reintubation, the total duration of invasive V˙e, and noninvasive support.

Tools and equipment used included Philips Intellivue MP20 for monitoring vitals and Philips M11193A for pulse oximetry monitoring. Dräger Babylog® 8000 plus ventilator was used for infants between 26 and 34 weeks of gestation and SLE5000 (version 5.0) (SLE5000 infant ventilator- version5.0(SLE Limited,South Croydon,UK))or SLE6000 infant ventilator (version 2.0) software (SLE6000 infant ventilator-version2.0(SLE Limited,South Croydon,UK)) for infants of higher gestation 35–37 weeks.

The data were collected using an expert, validated pro forma. It included demographic data such as mode of birth, gestational age, gender, and birth weight. The ventilator parameters and vitals were recorded during the PSV trial. The set ventilator parameter includes (FiO2, PS, PEEP, and flow),measured parameters[(Minute ventilation) minute V˙e, PIP, mean airway pressure (Paw), VT, compliance (C), and compliance at the last 20 s of breath cycle to total lung compliance (C20/C)],calculated parameters[Respiratory severity score (RSS) = Paw × FiO2 with a cutoff value 1.26 and 2.6 [Pediatr Neonatal. 2017 December and SpO2/FiO2) and vitals[Heart rate,respiratory rate and SpO2].

Statistical analysis

Data were analyzed using IBM (IBM Corp. Released 2011. IBM SPSS Statistics for Windows, version 20.0. Armonk, NY, USA: IBM Corp). Continuous variables (duration of invasive V˙e, noninvasive V˙e, and hospital days); ventilator and hemodynamic parameters were expressed in mean and standard deviation. Categorical variables (gender and mode of delivery) expressed as n (%). Paired t-test was used to compare the ventilator parameters and hemodynamic parameters at two time points of PSV trial. P =0.05 or less was considered statistically significant.


  Results Top


A total of 187 subjects required respiratory support during the hospital stay, 57 of whom were enrolled in the study as per the inclusion criteria [Figure 2]. [Table 1] represents the demographical data of the enrolled subjects. Respiratory distress syndrome was the primary reason requiring ventilator assistance (54%). Meconium aspiration syndrome, postsurgical cases, sepsis, and asphyxia constituted 44%. Hemodynamic and ventilator parameters during PSV are represented in median and interquartile range [Table 2]. There was no significant difference observed in these parameters, comparing the two time points.
Figure 2: Neonates admitted and intubated during the study period

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Table 1: Demographic data of the enrolled subjects

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Table 2: Ventilator parameters, illness severity, and vital signs at initiation and at 30-min pressure support ventilation trial

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There was no incidence of air leak post-PSV trial. Two neonates were switched from PSV to the previous mode due to severe hypoxemia (PSV failure) and were successfully extubated following the second PSV attempt.

Five neonates needed reintubation. Two got reintubated due to severe hypoxemia (within 72 h) and the remaining three due to inadequate secretion clearance and severe bleeding associated with surgery (after 72 h). The duration of mechanical V˙e was expressed in median and interquartile range as 48 (24–72) h, and duration of noninvasive V˙e was 72 (48–120) h. The neonates were extubated to either nasal CPAP (49%), high flow nasal cannula (47%), or nasal SIMV (4%). The average NICU stay and hospital stay were 15 ± 13.05 and 19 ± 15.02 days, respectively. The total mortality rate was 5.2%.


  Discussion Top


The current study focused on assessing the safety of PSV as a stand-alone mode for weaning. During the investigation, no significant change in hemodynamic or measured ventilator parameters during the 30-min trial was observed. PSV did not result in any adverse effects. PSV resulted in a smooth transition from invasive V˙e to noninvasive V˙e.

Thirty-minute PSV was found to be safe in ventilating neonates without any hemodynamic instability or clinical deterioration in our study. Perren et al.[18] had concluded that an SBT trial for 30 min identified patients ready for extubation and the results were in accordance with the results obtained by 2-h SBT trial, with no difference in extubation failure among pediatric group. PSV was also used to assess patient–ventilator synchrony among neonates with congenital cardiac disorders where they had used pressure levels of 5 cmH2O and 10 cmH2O, respectively. Each pressure level was kept for 30 min, and they observed that PSV can augment spontaneous breathing effort with patient–ventilator synchrony.[19] Hence, 30 min of PSV trial was chosen to assess its safety in ventilating neonates.

Miqliori and Cavazza[20] compared SIMV with PSV, where they observed an increase in minute ventilation (V˙E), VT, and a reduction in respiratory rate on PSV compared to SIMV. Similarly, Gupta et al.[21] also observed an increase in V˙E when SIMV combined with PS than SIMV alone. The addition of PS resulted in improvement in V˙E. In both studies however, they did not observe these changes for PSV mode alone which was in contradiction to Nayeri et al.[11] in which they did not find any differences in VT, PIP, and incidence of pneumothorax between SIMV and PSV mode, but with PSV, the duration of mechanical V˙e was found to be less than SIMV.

In our study, as per the protocol, pressure support was set to achieve a target VT of 4–6 ml/kg, which remained in the target range throughout the study. Furthermore, V˙E also remained the same without any increase in the respiratory rate, which may indicate less WOB during the trial.

In the Miqliori and Cavazza[20] study, they did not find any difference in the HR or saturation of oxygen and did not require any titration of FiO2 in PSV group. Similarly, in our study, we did not find any significant difference in hemodynamics. Instead of PaO2/FiO2, we used noninvasive indicator SpO2/FiO2 (SF ratio) since blood gas analysis was not performed routinely.

The previous literature on PSV did not observe the C20/C index (a calculation of the compliance of the last 20% of a breath in relation to the compliance of the entire breath) and calculated parameters (RSS and S/F ratio) during the PSV trial. Fisher et al.[22] studied lung overdistension associated with mechanical V˙e in neonates, and they have used C20/C to determine lung overdistension. They had concluded that C20/C <0.8 had overdistension on the flow-volume loop, and C20/C >1 was with a normal flow-volume loop. In the current study, we measured C20/C, which is an index of lung distention, and the average C20/C observed at 0 min and 30 min was 1.36 and 1.47, respectively. No graphical correlation of values was done.

Farhadi et al.[23] used PSV as a stand-alone mode with two different pressure levels (10 cmH2O and 14 cmH2O). They observed the statistical significance of higher Paw (P < 0.025) with pressure support of 14 cmH2O, which can be related to the high-pressure level used between the groups. In this current study, the pressure support range of 10–14 cmH2O with a Paw range of 5.1–10 was observed. Subjective approach of setting PS (as per the VT target of 4–6 ml/kg) resulted in a lower Paw which might have helped in smooth transition from invasive V˙e.

In 2013, a systematic review[24] on defining extubation success stated that apt window time for monitoring for reintubation following extubation depends on the study population. Neonates with BW <1000 g, a monitoring time for more than 1 week, will be required. We had observed a total of five reintubations. Among them, two were within 72 h and three after 72 h of extubation. One of these had a birth weight <1000 g and was reintubated after 72 h due to apnea of prematurity. Others were reintubated due to deterioration of underlying lung pathology and critical illness.

Mhanna et al.[25] observed that RSS, a multiple of Paw and FiO2, could be criteria for predicting extubation readiness, with a minimum cutoff value of 1.26 and a maximum cutoff value of 2.6. They observed a higher RSS score among the extubation failures (reintubation within 48 h) among 45/147 neonates, which was contradictory to the present study. There was not much variation in Paw or FiO2 which could change the RSS value during the trial. Even though the study population and reintubation rate were comparatively less, there were no observed changes in RSS value. The RSS score among the neonates requiring re-intubation(n=5) ranged from 1.47- 2.80 and among non-intubated cases the RSS score ranged from 1.50-3.50. Neonates with higher RSS (contributed by either a high Paw or FiO2) were also extubated successfully, which could be related to the resolving of underlying primary illness.

Farhadi et al.[23] observed incidence of pneumothorax with a pressure of 14 cmH2O, which was not statistically proven. In our study, none of the neonates had pneumothorax or required high-frequency oscillatory V˙e due to PSV mode. Pressure support was set according to the target VT (4–6 ml/kg) for neonates with gestational age >26 weeks, and the Paw was also on the lower limit. The individualized approach toward setting pressure support might have resulted in less incidence of pneumothorax.

Neonates are highly sensitive and are vulnerable to injury, even with a small change in care. Lack of funding to take care of such injuries limited the conduct of a controlled study. PSV being a promising mode for weaning in neonatal V˙e, further studies with a control group should be conducted to provide more substantial evidence.


  Conclusion Top


PSV mode can be safely used as a stand-alone mode for weaning in neonates with appropriate settings and close monitoring. It is not associated with any significant changes in hemodynamic or measured ventilator parameters.

Acknowledgment

I would like to thank Mr. Ramesh Unnikrishnan for his expert advice by helping me in molding my research work and special thanks to Mrs. Tisha Ann Skariah, NICU nurses, and other NICU consultants who helped me in completing the study with their cooperation. I would also like to extend my special gratitude to the statistician for helping me with the result analysis of the study.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Slutsky AS. History of mechanical ventilation from vesalius to ventilator-induced lung injury. Am J Respir Crit Care Med 2015;191:1106-15.  Back to cited text no. 1
    
2.
Goldsmith JP, Karotkin E, Suresh G, Keszler M. Assisted Ventilation of the Neonate E-Book: Evidence-Based Approach to Newborn Respiratory Care. 6th ed. Philadelphia: Elsevier; 2016. p. 242.  Back to cited text no. 2
    
3.
Cernada M, Brugada M, Golombek S, Vento M. Ventilator-associated pneumonia in neonatal patients: An update. Neonatology 2014;105:98-107.  Back to cited text no. 3
    
4.
Stevens TP, Harrington EW, Blennow M, Soll RF. Early surfactant administration with brief ventilation vs. selective surfactant and continued mechanical ventilation for preterm infants with or at risk for respiratory distress syndrome. Cochrane Database Syst Rev 2007; Issue 8, October 17:CD003063.  Back to cited text no. 4
    
5.
Kamat SS. Practical Applications of Mechanical Ventilation. 2nd ed. New Delhi: Jaypee Brothers Medical Publishers; 2016. p. 414.  Back to cited text no. 5
    
6.
Avery GB. Avery's Neonatology: Pathophysiology and Management of the Newborn. 6th ed.United States:Lippincott Williams & Wilkins;2005.  Back to cited text no. 6
    
7.
Aschner JL, Polin RA. An Issue of Clinics in Perinatology-E-Book.1st ed. Volume 39:Issue 3;2012. p. 429.  Back to cited text no. 7
    
8.
Putensen C, Muders T, Varelmann D, Wrigge H. The impact of spontaneous breathing during mechanical ventilation. Curr Opin Crit Care 2006;12:13-8.  Back to cited text no. 8
    
9.
Rozé JC, Krüger T. Pressure Support Ventilation – A New Triggered Ventilation Mode for Neonates. Available from: https://www.draeger.com/Library/Content/rsp_pressure_support_ventilation_booklet_9097499_en.pdf. [Last accessed on 2020 Dec 17].  Back to cited text no. 9
    
10.
Esteban A, Alía I, Tobin MJ, Gil A, Gordo F, Vallverdú I, et al. Effect of spontaneous breathing trial duration on outcome of attempts to discontinue mechanical ventilation. Spanish Lung Failure Collaborative Group. Am J Respir Crit Care Med 1999;159:512-8.  Back to cited text no. 10
    
11.
Nayeri F, Goudarzi R, Nili F, Amini E. Neonatal weaning from ventilator: PSV versus SIMV mode. Tehran Univ Med J 2009;66:740-5.  Back to cited text no. 11
    
12.
Sarkar S, Donn SM. In support of pressure support. Clin Perinatol 2007;34:117-28.  Back to cited text no. 12
    
13.
Reyes ZC, Claure N, Tauscher MK, D'Ugard C, Vanbuskirk S, Bancalari E. Randomized, controlled trial comparing synchronized intermittent mandatory ventilation and synchronized intermittent mandatory ventilation plus pressure support in preterm infants. Pediatrics 2006;118:1409-17.  Back to cited text no. 13
    
14.
Ramanathan R. Synchronized intermittent mandatory ventilation and pressure support: To sync or not to sync? Pressure support or no pressure support? J Perinatol 2005;25 Suppl 2:S23-5.  Back to cited text no. 14
    
15.
Olsen SL, Thibeault DW, Truog WE. Crossover trial comparing pressure support with synchronized intermittent mandatory ventilation. J Perinatol 2002;22:461-6.  Back to cited text no. 15
    
16.
Nottingham Neonatal Services: Clinical Guideline B1. Available from: https://www.academia.edu/35358507/Nottingham_Neonatal_Service_Clinical_Guidelines_Guideline_B1_Mechanical_Ventilation_in_Neonates_B1. [Last accessed on 2020 Dec 17].  Back to cited text no. 16
    
17.
Neonatal Clinical Practice Guideline: Mechanical Ventilation of Newborn; December, 2015. Available from: https://professionals.wrha.mb.ca/old/extranet/eipt/files/EIPT-044-001.pdf. [Last accessed on 2020 Dec 17].  Back to cited text no. 17
    
18.
Perren A, Domenighetti G, Mauri S, Genini F, Vizzardi N. Protocol-directed weaning from mechanical ventilation: Clinical outcome in patients randomized for a 30-min or 120-min trial with pressure support ventilation. Intensive Care Med 2002;28:1058-63.  Back to cited text no. 18
    
19.
Tokioka H, Nagano O, Ohta Y, Hirakawa M. Pressure support ventilation augments spontaneous breathing with improved thoracoabdominal synchrony in neonates with congenital heart disease. Anesth Analg 1997;85:789-93.  Back to cited text no. 19
    
20.
Miqliori C, Cavazza A. Effect on respiratory function of pressure support ventilation versus synchronized intermittent ventilation in preterm infants. Pediatr Pulmonol 2003;35:364-7.  Back to cited text no. 20
    
21.
Gupta S, Sinha SK, Donn SM. The effect of two levels of pressure support ventilation on tidal volume delivery and minute ventilation in preterm infants. Arch Dis Child Fetal Neonatal Ed 2009;94:F80-3.  Back to cited text no. 21
    
22.
Fisher JB, Mammel MC, Coleman JM, Bing DR, Boros SJ. Identifying lung overdistention during mechanical ventilation by using volume-pressure loops. Pediatr Pulmonol 1988;5:10-4.  Back to cited text no. 22
    
23.
Farhadi R, Lotfi HR, Alipour A, Nakhshab M, Ghaffari V, Hashemi SA. Comparison of two levels of pressure support ventilation on success of extubation in preterm neonates: A randomized clinical trial. Glob J Health Sci 2015;8:240-7.  Back to cited text no. 23
    
24.
Giaccone A, Jensen E, Davis P, Schmidt B. Definitions of extubation success in very premature infants: A systematic review. Arch Dis Child Fetal Neonatal Ed 2014;99:F124-7.  Back to cited text no. 24
    
25.
Mhanna MJ, Iyer NP, Piraino S, Jain M. Respiratory severity score and extubation readiness in very low birth weight infants. Pediatr Neonatol 2017;58:523-8.  Back to cited text no. 25
    


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