|Year : 2017 | Volume
| Issue : 1 | Page : 41
A comparative study of the effect of nasal intermittent positive pressure ventilation and nasal continuous positive airway pressure on the regional brain tissue oximetry in premature newborns weighing <1500 g
Alireza Sadeghnia, Marzieh Zamani Foroshani, Zohreh Badiei
Department of Pediatrics, School of Medicine, Child Growth and Development Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
|Date of Submission||27-Jun-2016|
|Date of Acceptance||08-Feb-2017|
|Date of Web Publication||01-Jun-2017|
Department of Pediatrics, School of Medicine, Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-communicable Disease, Isfahan University of Medical Sciences, Isfahan
Source of Support: None, Conflict of Interest: None
Background: Near-infrared spectroscopy (NIRS) provides the capability of monitoring oxygenation levels in cerebral microscopic vessels, enabling the operator to observe the spontaneous changes in the levels of hemoglobin concentration in tissue and interpret the resulting fluctuations. The current study tried to investigate whether brain's autoregulatory mechanisms in premature newborns have the potential to prevent the adverse effects caused by asynchronous changes of pressure in the rib cage. Therefore, NIRS method was applied to newborns that were alternatively shifted from nasal continuous positive airway pressure (nCPAP) to nasal intermittent positive pressure ventilation (NIPPV) and vice versa. Methods: This study was done as a crossover randomized clinical trial on 30 very low-weight newborns under nCPAP, who had received surfactant as a result of respiratory distress syndrome diagnosis, from April 2015 to April 2016, in Isfahan Shahid Beheshti Educational Hospital. The newborns were 72 h old, experiencing continuous distending pressure (CDP) = 4–6 cmH2O with FiO2 = 30%–40%. The respiratory support would alternate from nCPAP to NIPPV and vice versa (with indicators of expiratory PAP (EPAP) = CDP and inspiratory PAP = EPAP + 4 cmH2O), and the cerebral regional oxygen saturation (CrSO2) was monitored using NIRS. Results: The study results indicated that newborns significantly showed higher levels of CrSO2(84.93,P= 0.005) and oxygenation (94.63,P= 0.007) under nCPAP rather than NIPPV (82.43 and 93.43, respectively). The respiratory rate was also meaningfully slower when newborns were under nCPAP (P = 0.013). Conclusions: This study revealed that applying NIPPV may have an unfavorable effect on the premature newborn's brain tissue perfusion. However, more studies are needed to ensure solid outcomes.
Keywords: Cerebral regional oxygen saturation, nasal continuous positive airway pressure, nasal intermittent positive pressure ventilation
|How to cite this article:|
Sadeghnia A, Foroshani MZ, Badiei Z. A comparative study of the effect of nasal intermittent positive pressure ventilation and nasal continuous positive airway pressure on the regional brain tissue oximetry in premature newborns weighing <1500 g. Int J Prev Med 2017;8:41
|How to cite this URL:|
Sadeghnia A, Foroshani MZ, Badiei Z. A comparative study of the effect of nasal intermittent positive pressure ventilation and nasal continuous positive airway pressure on the regional brain tissue oximetry in premature newborns weighing <1500 g. Int J Prev Med [serial online] 2017 [cited 2021 Oct 19];8:41. Available from: https://www.ijpvmjournal.net/text.asp?2017/8/1/41/207382
| Introduction|| |
Intracranial hemorrhage (ICH) in premature newborns is a serious damage with potentially irrecoverable effects on the morbidity and mortality rates as well as long-term outcomes of the development of nervous system. During the recent decades, despite the significant improvements in supportive interventional procedures for premature newborns and the resulting decrease in mortality, ICH still presents a significantly harmful risk for these newborns.
A number of mechanisms cause germinal matrix-intraventricular hemorrhage (GM-IVH), including susceptibility of GM structure to damage, coagulopathy and platelet dysfunctions, genetic factors, cytokines, and finally hemodynamic factors. Hemodynamic factors are influenced by two interventional systems of intrinsic and extrinsic indicators.
The fluctuations in cerebral blood flow (CBF), which are caused by the increase in the pressure of cerebral venous drainage during respiratory distress syndrome (RDS), positive pressure ventilation (PPV), out-of-synchrony in PPV, and pneumothorax, are major ground stones for the development of GM-IVH.
RDS is among the most exclusively challenging conditions for Neonatal Intensive Care Unit (NICUs) and hence needs special management. The most prevalent pathology affecting the newborns <32 weeks of gestational age is RDS. In this regard, a significant portion of the long-term morbidity and mortality cases is ascribed to RDS and its outcomes.,
So far, nasal continuous positive airway pressure (nCPAP) has been considered as the standard care for the management of RDS for more than four decades. nCPAP improves the oxygenation in the newborns involved in the process of RDS through recruitment of pulmonary volumes, prevention of atelectasis, stabilizing the rib cage, alternation of pulmonary compliance, and decreasing the work of breathing. nCPAP decreases the intrapulmonary shunt by enhancing the efficiency of the ventilation to perfusion ratio. Studies have revealed that even in newborns who suffer frequent central apnea, the gas pressure nCPAP imposes on the upper parts of the respiratory system that can prevent the mentioned pauses in respiration through its stimulating effect. Needless to say, nCPAP shows a promising mechanism in maintaining open airways in obstructive apnea.
Nasal intermittent PPV (NIPPV) was first developed for the primary application of apnea of prematurity control. It has been a while since NIPPV has been introduced as primary mode (when NIPPV is administered for a newborn with RDS, equal or <2 h after birth, either with or without surfactant administration) in NICUs; however, taking this approach to treat RDS has revealed a high level of diversity; as in the U. K., its difference in application ranges from 48% in England to 61% in Ireland.
Although it is always stressed that the brain's autoregulatory mechanism (though not developed) accompanied by an average systematic blood pressure (BP) above 30 mmHg is enough to maintain the cerebral blood perfusion, Evans et al. showed that other factors, such as intrathoracic pressure level, can affect the intracranial blood flow, and interventions involving respiratory support are among those which are markedly accompanied by significant changes in intrathoracic pressure.
The improvement in our capability to evaluate the changes in cerebral oxygenation levels and the interventional mechanisms affecting the CBF had led to a development of our understanding of these fluctuations and their potential harm to the developing brain tissue. Premature newborns are in danger of developmental delays in “CBF autoregulatory system,” and this, in turn, increases the risk of facing unusual perfusion flows (and hence facing unusual levels of oxygenation) during hemodynamic instabilities. So far, very few technologies have been implemented for monitoring CBF in endangered newborns. Near-infrared spectroscopy (NIRS), due to the low thickening of scalp and calvarium in newborns, especially premature newborns, has the capability to monitor oxygenation levels in microscopic vascularity in fact the system monitors the hemoglobin chromophore levels which absorb the wavelength of 700–1000 nm as the basis for its monitoring and also calculates the oxyhemoglobin saturation (StO2) through differentiating the oxygenated hemoglobin (O2 Hb) from deoxygenated hemoglobin (HHb) using the following formula:
StO2 = O2 Hb + HHb, and tHb = total Hb
As a result, the operator can relate continuous changes to the changes in tissue hemoglobin concentration (or the blood volume in the tissue, resulting from tissue perfusion and CBF) and interpret its outcome records.
Due to the concerns regarding the adverse effects related to out-of-synchrony performance in the application of NIPPV, this study tried to challenge this type of respiratory support versus nCPAP through studying the brain tissue oxygenation in newborns that are frequently altered between these two forms of respiratory support.
| Methods|| |
Study design and participants
This study is a randomized clinical trial (RCT)-crossover done on very low-weight newborns who were under nCPAP respiratory support in the NICU Department of Isfahan Shahid Beheshti Hospital from October 2015 to May 2016. The newborns who entered the study were diagnosed with RDS (with demonstrations of tachypnea, intracostal retraction, nasal flaring, and grunting  as well as chest X-ray compatible with RDS) and had received surfactant in their first 2 h from birth (Survanta was administered in case FiO2 ≥30% and continuous distending pressure (CDP) ≥5 cmH2O was needed to maintain SpO2 in the range of 89%–95% in the right hand).
These newborns were placed under nCPAP respiratory support at 72 h from birth (when they entered the study) to maintain SpO2 in the range of 89%–95% in the right hand with CDP of 4–6 cmH2O and FiO2 of 30%–40%. The exclusion criteria included perinatal asphyxia (5 min Apgar of 0–3, umbilical cord pH of <7, and umbilical cord bicarbonate of <12 mEq/L), congenital malformation, not receiving surfactant or administration of surfactant later than 2 h from birth, newborns who revealed evidence of patent ductus arteriosus in echocardiography, newborns who received inotropic drugs, newborns who revealed evidence of Grades III to IV GM-IVH in cranial sonogram, as well as newborns involved in air leak syndrome.
Due to the primary goal of the study which included the evaluation and monitoring of cerebral tissue oxygen content, a NIRS transducer (INVOS 4100 Somanetics Corp., Troy, MI, USA) was placed on the scalp of the newborns who realized the conditions of inclusion criteria, right on the frontal region, and the system was activated. The newborns were monitored for 2 h for the inclusion criteria indicators while they were under BabyFlow Injector (Draeger Medical, Lubeck, Germany) and Babylog 8000 plus ventilator (Draeger Medical, Lubeck, Germany) and were supported with nCPAP respiratory support. The newborns were not fed during that period and upon 90 min of monitoring the cerebral regional oxygen saturation (CrSO2), oxygen (O2) saturation, respiratory rate, and heart rate which was recorded every 30 min; capillary gasometry was done from the newborn's heel through heel stick, and systemic BP evaluation was done on the right hand.
Then, indicators of inspiratory PAP (IPAP) and expiratory PAP (EPAP) were defined for the ventilator (as Ti = 0.5, rate = 30 breath/min, IPAP = EPAP + 4 cmH2O), and IPPV mode was activated at the end of this initial 2 h period. While under NIPPV support, which was about 2 h, the newborns were not fed, their CrSO2, O2 saturation, respiratory rate, and heart rate were monitored every 30 min and after 90 min; gasometry and mean arterial BP tests were done on the newborn.
Considering the 95% confidence interval and the power of 80% with 0.37 error, the data on 30 newborns were analyzed with IBM SPSS statistical software version 18, (Armonk, New York, U.S) using paired samples t-test and Pearson's correlation coefficient. Demographics characteristics of newborn are shown in [Table 1].
| Results|| |
This study was done with a crossover design not to let the participants' physiology interfere with the interventions with nCPAP and NIPPV, as in most RCT trials, in which the physiological conditions are kept similar to study the effect of such mechanisms on brain tissue perfusion regardless of other not intended interfering factors.
Regarding the period effect, 2 h upon birth, the newborn, who had been treated with nCPAP or NIPPV, would be assessed, and the need to administer surfactant would be indicated. Therefore, in case, the newborn did not need to receive surfactant, and it could be concluded that the interventions directed at CDP achieved their optimal effective status during the specified period of treatment.
The studied indicators are shown in [Table 2], and the statistical analysis results on correlation and paired samples t-test are given in [Table 3] and [Table 4], respectively. The results indicated the respiratory rate was significantly higher under NIPPV (60.96 ± 4.16, P= 0.013), and the results from correlation analysis indicated a strong relationship between the method and the respiratory rate (0.722, significant = 0.000) while PCO2 levels were also higher in NIPPV group but not statistically meaningful (47.34 ± 10.20, P= 0.063). Newborns showed significantly lower O2 saturation (P = 0.007) and CrSO2 (P = 0.005) levels when under NIPPV rather than nCPAP. Mean BP and heart rates showed no significant differences between nCPAP and NIPPV groups (P = 0.736 and P= 0.579, respectively).
| Discussion|| |
Considering a number of researches done to compare the two approaches of nCPAP and NIPPV respiratory support to treat RDS, it is observed that in the majority of the studies, some of which are referred to in the following, the methodology had not addressed the cerebral function monitoring.
In a study done by Sai Sunil Kishore et al., which lasted from January 2007 to April 2008, nCPAP and NIPPV were compared for the respiratory management of RDS in premature newborns. The newborns had a gestational range of 28–32 weeks, and in case, they had experienced Downes score of equal or higher than 4 in the first 6 h from birth, and they would be randomly assigned to two interventional groups of nCPAP and NIPPV. Around 39 newborns were placed in nCPAP group, and the maximum setup was considered with CDP = 7 cmH2O and FiO2 ≤70%. A total of 37 newborns entered the NIPPV group, and the initial setup was rate = 40–50/min, Ti = 0.3–035 s, positive end-expiratory pressure (PEEP) =5 cmH2O, and peak inspiratory pressure (PIP) =15–16 cmH2O; however, regarding the gasometry data, the setup could be raised to rate = 60/min, PEEP = 6 cmH2O, and PIP = 24–26 cmH2O. In nCPAP group, at CDP = 4 cmH2O and FiO2 ≤30%, the respiratory support would be discontinued, while in the NIPPV group, the respiratory support would be discontinued at rate = 30/min, PEEP = 4 cmH2O, PIP = 14 cmH2O, and FiO2 ≤30%. The need for invasive respiratory support during 48 h and a week from the discontinuation showed a significant increase in the nCPAP group rather than the NIPPV group.
In another study done by Bhandari et al. to compare synchronized NIPPV (SNIPPV) and nCPAP at two hospitals in Yale and San Diego universities, 469 preterm newborns weighing <1250 g, who were under mechanical respiratory support due to RDS, were extubated and entered the two groups of SNIPPV and nCPAP noninvasive respiratory support if during treatment, the ventilator management system indicated PIP ≤16 cmH2O, PEEP ≤5 cmH2O, rate = 15–25, and FiO2 ≤35% to maintain pH = 7.25–7.45, PaCO2 =40–55 mmHg, and PaO2 =50–80 mmHg. Synchronization management in Infant Star ventilator (invasive or noninvasive) is done through the placement of Graseby capsule on the newborn's abdomen. In this study which lasted from 2002 to 2004, upon extubation, the newborns who entered the SNIPPV group (n = 242) were put under respiratory support with Inca (Infant nCPAP Assembly) and the same invasive ventilation rate, yet PIP was increased 2–4 cmH2O, and PEEP was set as equal or <6 cmH2O, and FiO2 was set to a level to maintain the O2 saturation in the range of 85%–95%. If FiO2 of lower than 30% was needed, the newborn was detached from the ventilator (respiratory support). Bronchopulmonary dysplasia prevalence showed a significant decrease in SNIPPV group while PVL prevalence was significantly lower in non-SNIPPV group.
In a study done by Ramanathan et al. in 2012, 110 premature newborns with &360;30-week gestational age who had RDS and were treated with surfactant within the 1st h from birth entered the two groups of nCPAP and NIPPV treatment and were studied for 7 days (from birth). About 40% of the newborns in the nCPAP group demonstrated a need for mechanical ventilation during 7 days from birth, whereas in the NIPPV group, 7% of the newborns needed mechanical ventilation in the same period.
Among the few studies done to monitor the brain tissue oximetry for newborns with RDS under nCPAP treatment, we can refer to the one done by Dani et al. in 2007. In that study, 14 newborns with RDS and gestational age of <30 weeks were treated with nCPAP. After 12 h from extubation, while nCPAP was administered with FiO2 ≤40%, CDP was set to 2 cmH2O for 30 min, followed by a 60-min nCPAP support at CDP = 4 cmH2O, then a subsequent period of 60 min with CDP of equal to 6 cmH2O and eventually a final 30-min nCPAP support at CDP = 2 cmH2O, and the CrSO2 was monitored throughout the process. The results did not show any significant difference between the CrSO2s at different levels of CDP.
In the study done by Lemmers et al., 38 newborns with gestational age of <32 weeks were monitored for CrSO2 for 72 h upon birth. Among these newborns, 18 were involved in RDS and were supported with conventional mechanical ventilation, and the respiratory management ensured PCO2 of 40–50 mmHg. The results of this study did not show any significant difference between the two groups of CrSO2 and fractional tissue oxygen extraction (FTOE); however, the recorded CrSO2 and FTOE levels showed a wide and significantly different range of variance at different times in the RDS group.
Limitations of the study and suggestions for further research
One of the biggest challenges faced by the researcher was the crossover nature of the study. As the number of patients entering the study was limited, the researcher had to perform the study as a crossover. This limited the outcomes of the study, and further studies on this subject are recommended in which a larger population could be studied in a noncrossover approach.
| Conclusions|| |
The current study revealed that the newborns showed significantly meaningful lower levels of CrSO2 while under NIPPV (compared to the time they were under nCPAP). Moreover, by activating the NIPPV mode, the newborns' O2 saturation levels also decreased significantly. The study done by Bhandari et al. revealed that PVL prevalence was significantly lower among newborns in the nCPAP group than those in the NIPPV group. It seems that the results of the current study provide grounds for the outcomes of the study done by Bhandari, as at least part of the background for PVL, more specifically brain tissue ischemia, can be attributed to lower levels of CrSO2 during NIPPV treatment. Respiratory rate has also been significantly higher in the NIPPV group. The question is whether the decrease in brain tissue oxygen content is due to the decrease in O2 saturation or the instability in brain tissue perfusion, as the increase in respiratory rate or the increase in CO2 pressure in blood flow, with their relevant mechanisms of increasing asynchrony and inducing out-of-control pressures in thorax (regarding the increase in respiratory rate), as well as increasing brain tissue perfusion (regarding the increase in PCO2), may result in fluctuations or CBF. Therefore, it seems necessary to perform a wider range of research (in terms of the magnitude of the samples and the focus on long-term outcomes) before one could consider applying two different pressure levels in an out-of-synchrony fashion in respiratory management of newborns involved in RDS.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
du Plessis AJ. Cerebral blood flow and metabolism in the developing fetus. Clin Perinatol 2009;36:531-48.
Bassan H. Intracranial hemorrhage in the preterm infant: Understanding it, preventing it. Clin Perinatol 2009;36:737-62, v.
Hamrick SE, Miller SP, Leonard C, Glidden DV, Goldstein R, Ramaswamy V, et al.
Trends in severe brain injury and neurodevelopmental outcome in premature newborn infants: The role of cystic periventricular leukomalacia. J Pediatr 2004;145:593-9.
Jeenakri R, Drayton M. Management of respiratory distress syndrome. Pediatr Child Health 2009;15:158-62.
Abdel H, Nasef N. Respiratory management of the preterm newborn in the delivery room. Res Rep Neonatol 2012;2:39-53.
Jane Pillow J. Which continuous positive airway pressure system is best for the preterm infant with respiratory distress syndrome? Clin Perinatol 2012;39:483-96.
Bhandari V. Noninvasive respiratory support in the preterm infant. Clin Perinatol 2012;39:497-511.
Evans N, Osborn D, Kluckow M. Preterm circulatory support is more complex than just blood pressure. Pediatrics 2005;115:1114-5.
Goff DA, Buckley EM, Durduran T, Wang J, Licht DJ. Noninvasive cerebral perfusion imaging in high-risk neonates. Semin Perinatol 2010;34:46-56.
Kribs A, Pillekamp F, Hünseler C, Vierzig A, Roth B. Early administration of surfactant in spontaneous breathing with nCPAP: Feasibility and outcome in extremely premature infants (postmenstrual age ≤27 weeks). Paediatr Anaesth 2007;17:364-9.
Stevens TP, Blennow M, Myers EH, Soll R. 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 2009;4:CD003063.
Dani C, Bertini G, Cecchi A, Corsini I, Pratesi S, Rubaltelli FF. Brain haemodynamic effects of nasal continuous airway pressure in preterm infants of less than 30 weeks' gestation. Acta Paediatr 2007;96:1421-5.
Mazzella M, Bellini C, Calevo MG, Campone F, Massocco D, Mezzano P, et al.
A randomised control study comparing the infant flow driver with nasal continuous positive airway pressure in preterm infants. Arch Dis Child Fetal Neonatal Ed 2001;85:F86-90.
Lemmers PM, Toet M, van Schelven LJ, van Bel F. Cerebral oxygenation and cerebral oxygen extraction in the preterm infant: The impact of respiratory distress syndrome. Exp Brain Res 2006;173:458-67.
Migliori C, Motta M, Angeli A, Chirico G. Nasal bilevel vs. continuous positive airway pressure in preterm infants. Pediatr Pulmonol 2005;40:426-30.
Sai Sunil Kishore M, Dutta S, Kumar P. Early nasal intermittent positive pressure ventilation versus continuous positive airway pressure for respiratory distress syndrome. Acta Paediatr 2009;98:1412-5.
Bhandari V, Finer NN, Ehrenkranz RA, Saha S, Das A, Walsh MC, et al.
Synchronized nasal intermittent positive-pressure ventilation and neonatal outcomes. Pediatrics 2009;124:517-26.
Ramanathan R, Sekar KC, Rasmussen M, Bhatia J, Soll RF. Nasal intermittent positive pressure ventilation after surfactant treatment for respiratory distress syndrome in preterm infants <30 weeks' gestation: A randomized, controlled trial. J Perinatol 2012;32:336-43.
[Table 1], [Table 2], [Table 3], [Table 4]