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 Table of Contents  
ORIGINAL ARTICLE
Year : 2015  |  Volume : 6  |  Issue : 1  |  Page : 33

High flow nasal cannula as a method for rapid weaning from nasal continuous positive airway pressure


1 Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Child Growth and Development Center, Isfahan, Iran
2 Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Date of Submission01-May-2014
Date of Acceptance25-Feb-2015
Date of Web Publication10-Apr-2015

Correspondence Address:
Zohreh Badiee
Al Zahra Hospital, Hezarjarib Avenue, Isfahan
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2008-7802.154922

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  Abstract 

Background: To compare two methods of weaning premature infants from nasal continuous positive airway pressure (NCPAP).
Methods: Between March and November 2012, 88 preterm infants who were stable on NCPAP of 5 cmH 2 O with FIO 2 <30% for a minimum of 6 h were randomly allocated to one of two groups. The high flow nasal cannula (HFNC) group received HFNC with flow of 2 L/min and FIO 2 = 0.3 and then stepwise reduction of FIO 2 and then flow. The non-HFNC group was maintained on NCPAP of 5 cmH 2 O and gradual reduction of oxygen until they were on FIO 2 = 0.21 for 6 h, and we had weaned them directly from NCPAP (with pressure of 5 cmH 2 O) to room air.
Results: No significant differences were found between 2 study groups with regards to gestational age, birth weight, Apgar score at 1 and 5 min after birth, patent ductus arteriosus and use of xanthines. The mean duration of oxygen therapy after randomization was significantly lower in HFNC group compared to non-HFNC group (20.6 ± 16.8 h vs. 49.6 ± 25.3 h, P < 0.001). Also, the mean length of hospital stay was significantly lower in HFNC group compared to non-HFNC group (11.3 ± 7.8 days vs. 14.8 ± 8.6 days, P = 0.04). The rate of successful weaning was not statistically different between two groups.
Conclusions: Weaning from NCPAP to HFNC could decrease the duration of oxygen therapy and length of hospitalization in preterm infants.

Keywords: Continuous positive airway pressure, high flow nasal cannula, preterm infant, weaning


How to cite this article:
Badiee Z, Eshghi A, Mohammadizadeh M. High flow nasal cannula as a method for rapid weaning from nasal continuous positive airway pressure. Int J Prev Med 2015;6:33

How to cite this URL:
Badiee Z, Eshghi A, Mohammadizadeh M. High flow nasal cannula as a method for rapid weaning from nasal continuous positive airway pressure. Int J Prev Med [serial online] 2015 [cited 2017 Jul 24];6:33. Available from: http://www.ijpvmjournal.net/text.asp?2015/6/1/33/154922


  Introduction Top


Despite technological and clinical improvement in neonatal care, pulmonary disease is the most important cause of morbidity in premature neonates whose lungs are not fully developed. In the past decades, it was common to start endotracheal intubation and mechanical ventilation in newborns with moderate to severe respiratory problems. [1]

It has been well documented that endotracheal intubation and mechanical ventilation may lead to barotrauma, volutrauma, and endotrauma. In addition, intubation and mechanical ventilation could increase the risk of infection. [2,3]

The high incidence of pulmonary complications of mechanical ventilation has led to a tendency to use alternative methods of respiratory support in preterm infants.

Nasal continuous positive airway pressure (NCPAP) is a noninvasive method that provides a constant positive pressure to the airways of spontaneously breathing infants. This constant pressure improves oxygenation by increasing functional residual capacity and recruitment of collapsed alveoli. In addition, NCPAP promotes redistribution of lung fluid and reduces upper airway resistance. [4] As a result, it is a useful and relatively safe method for treatment of respiratory problems especially in preterm infants.

Although NCPAP was primarily used for treatment of respiratory distress syndrome, it is a useful method for prevention of extubation failure and treatment of apnea of prematurity. [5, 6, 7]

Despite many documented benefits of NCPAP, it is a form of respiratory support that has its complications including traumatic injuries to the nose, pulmonary air leak syndromes and gaseous distension of the stomach. [8, 9, 10] Therefore, reducing the duration of NCPAP application could decrease the associated complications. However, premature discontinuation of NCPAP has potential hazards including increased apnea, oxygen demand and the need to restart NCPAP, and occasionally mechanical ventilation.

There is no consensus on the best method to wean from NCPAP. Many centers have used graded time off NCPAP to wean from NCPAP. It means removing NCPAP for a predefined number of hours each day (for example 4 h off and 20 h on) and step by step increasing the time off NCPAP every day pending NCPAP can be completely stopped, while the others gradually decrease the NCPAP pressure and FIO 2 during weaning. [11,12]

For several years, low flow nasal cannula (with flow rates of ≤1 L/min) has been used for delivering oxygen. [13] However, it has not provided significant respiratory support in newborn infants. Recently, some neonatologists have used a nasal cannula in premature newborns for weaning from NCPAP. High flow nasal cannula (HFNC) is defined as delivery of heated humidified and blended oxygen through the nasal cannula at flow rates of more than 1 L/min. This novel method could decrease airway water loss, airway cooling, thickened secretions and nasal irritation. [14,15]

The humidified HFNC system has been adopted as a primary support for respiratory distress syndrome, [16] for treating apnea of prematurity and to support premature neonates after extubation as an alternative to NCPAP. However, its efficacy for earlier weaning from NCPAP has not been well studied.

The objective of this study was to examine whether the use of HFNC with earlier discontinuation of NCPAP could decrease the duration of oxygen therapy and length of hospital stay in premature infants.


  Methods Top


Study design and participants

Between March and November 2012, we conducted a randomized controlled trial at the neonatal Intensive Care Unit (NICU) of Al-Zahra University Hospital, affiliated to Isfahan University of Medical Sciences, Isfahan, Iran. Inborn infants with gestational ages of 28-36 weeks who were met the following criteria were enrolled into the study: Receiving NCPAP at a pressure of 5 cmH 2 O with FIO 2 requirement of 30% to maintain an oxygen saturation of 88-95%, the lack of apnea (pauses of respiration for more than 20 s associated with bradycardia or cyanosis with more than 2 episodes in 12 h or more than 3 episodes in 24 h with at least one which needed bag and mask ventilation) [17] or signs of respiratory distress including tachypnea, moderate or severe intercostal or subcostal retraction and nasal flaring under these NCPAP setting. Exclusion criteria were major congenital malformation, grade 3 or 4 intraventricular hemorrhage, neuromuscular disorders, pulmonary hypoplasia, cleft lip and palate, chest wall deformity, cyanotic congenital heart disease.

The study protocol was approved by the Ethics Committee of Isfahan University of Medical Sciences. Parents of eligible newborns were approached for participation in the study, and informed consent was obtained from them.

Procedures and variable assessment

We have been used a uniform protocol for the management of respiratory distress syndrome in our NICU. Concisely, all newborns with spontaneous respiration that have signs of respiratory distress are placed on NCPAP with 5-6 cmH 2 O. The continuous positive airway pressure (CPAP) pressure could increase up to 8 cmH 2 O if respiratory distress is not alleviated. NCPAP failure is defined as increased work of breathing characterized by ongoing tachypnea (respiratory rate of more than 60 per min for more than 2 h), significant retraction, apnea as explained above, abnormal blood gases (2 samples with an interval of more than 2 h) with low pH of <7.2, PCO 2 of more than 65 mmHg and PaO 2 of <50 mmHg with FIO 2 of >60%).

Once the newborns remained stable for 6 h, we initiated NCPAP weaning. FIO 2 was lowered gradually down to 30%, then NCPAP pressure was reduced down to 5 cmH 2 O.

The HFNC group was given HFNC with flow of 2 L/min and FIO 2 = 0.3 after discontinuation from NCPAP. FIO 2 were adjusted to maintain oxygen saturation between 88 and 95%. HFNC flow was kept at 2 L/min until FIO 2 requirements were 0.21. After that, we had lowered HFNC flow 0.5 L/min every 1 h until a flow of 0.5 L/min achieved. At this time, the infants were separated from HFNC. In the non-HFNC group the newborns were maintained on NCPAP and FIO 2 gradually decreased to 0.21. Patients stable on this setting for 6 h were weaned directly from NCPAP (with pressure of 5 cmH 2 O) to room air. If their oxygen saturation has fallen below 88%, we have administered free flow oxygen by blender to achieve FIO 2 of 88-95. Successful weaning was defined as the absence of respiratory distress and no requirements of more than 0.21 for 72 h on room air. In the presence of any of the following conditions we applied NCPAP again in both groups: (1) The need for FIO 2 >60% to maintain oxygen saturation of more than 88%, (2) signs of respiratory distress including nasal flaring, retraction, tachypnea (respiratory rate of more than 70 for more than 1 h), (3) Apnea during first 48 h after discontinuation of NCPAP.

We recorded oxygen saturation and heart rate on Masimo Pulse Oxymeter (Masimo CO, Irvin, California, USA) during the study. We were used Bubble CPAP System (Fisher and Pykel Healthcare, Auckland, New Zealand) and short binasal cannula for NCPAP administration. HFNC system included a gas source, air/O 2 blender and a humidifier rendering air/O 2 via short nasal cannula (Fisher and Pykel RT329, Salter Labs).

We have started methylxanthines for treatment of apnea of prematurity on the basis of our NICU protocols. We have recorded newborn information including birth weight, gestational age, route of delivery, prenatal steroid use, prolonged rupture of membranes for more than 18 h before delivery, surfactant therapy. Presence of patent ductus arteriosus (PDA) and the need for methylxanthines.

Primary outcome

The main outcome was the duration of oxygen requirement.

Secondary outcomes

The secondary outcomes were duration of respiratory support, rate of successful weaning and duration of hospitalization.

Statistical analysis

Sample size calculation and data analysis

We calculated that a sample size of 41 infants in each group was needed to detect a difference of 30% for the duration of oxygen dependency with 80% power and significance of 0.05.

Randomization

Computer generated random numbers were used for randomization. Infants were randomized to one of two CPAP weaning groups from concealed envelopes opened by nonstudy personnel.

Blinding

The investigators in this trial were not blinded to study intervention.

Data were analyzed with the use of SPSS software (version 20, SPSS Inc., Chicago, IL, USA). Differences between groups were evaluated by Fischer's exact test and Chi-square for each categorical variable and by Student's t-test for each continuous variable.


  Results Top


A total of 109 preterm newborn with gestational ages of 28-36 weeks were recruited for the study. From these infants, 89 patients were enrolled in the trial and were randomized as shown in [Figure 1]. Of the 89 infants who enrolled the study, 88 newborns completed the study. We did not find any significant differences between 2 study groups with regards to gestational age, birth weight, route of delivery, Apgar score at 1 and 5 min after birth, PDA, use of xanthines, prolonged rupture of membranes and maternal pregnancy induced hypertension and prenatal steroid usage [Table 1]. There was no significant difference in the number of infants who successfully trailed off NCPAP in the first attempt between the HFNC group (3 infants) and non-HFNC group (2 infants) (P = 0.8). The infants were successfully weaned off supplemental oxygen at postconceptional ages of 36.5 ± 2.1 weeks in non-HFNC group and 33.2 ± 1.9 weeks in HFNC group [Figure 2]. The postconceptional age when the newborns came from respiratory support (NCPAP or HFNC) was not significantly different between HFNC group (P = 0.8). The mean duration of oxygen therapy was significantly lower in HFNC group compared to non-HFNC group (20.6 ± 16.8 h vs. 49.6 ± 25.3 h, P < 0.001). Also, the mean length of hospital stay was significantly lower in HFNC group compared to non-HFNC group (11.3 ± 7.8 days vs. 14.8 ± 8.6 days, P = 0.04).
Figure 1: The study fl ow

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Figure 2: Comparison of two groups based on postmenstrual age at: Continuous positive airway pressure onset, FiO2 of 30% and final trial off

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Table 1: Baseline characteristics of the study population

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Eleven infants (25%) in the non-HFNC group and 17 infants (38.6%) in the HFNC had significant apnea, (P = 0.12) and received methylxanthines.

Four neonates (9.1%) in the nonHFNC group required mechanical ventilation because of respiratory failure, but no infant in HFNC group required mechanical ventilation (P = 0.05). Outcome indicators of both groups are represented in [Table 2].
Table 2: Outcome indicators in both groups

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  Discussion Top


We were trying to find a method for faster weaning from NCPAP in premature infants. Our study has shown an average of 12 h decrease in the duration of oxygen therapy and a 3.5 days decrease in the length of hospital stay in newborns weaned prematurely from NCPAP to HFNC.

Singh et al. conducted a study on 112 premature infants who were stable on NCPAP and needed <0.3 FIO 2 . They used two methods for weaning from NCPAP. The first method included gradual lowering of CPAP pressure to a predetermined level of pressure and the second method included stepwise increasing duration of time off NCPAP. They found that the median time on NCPAP was significantly lower in the first group. The mean number of days on NCPAP in the pressure group was 1.5 days that is very close to our results. [11]

Soe et al. compared the success rate of two weaning methods of decreasing airway pressure and graded time off from NCPAP in preterm newborns and found that successful weaning was significantly higher in the pressure group. [12]

Although we did not use the graded time off method, we also found that gradual decreasing of NCPAP pressure to a predetermined level of pressure is a very useful method for weaning from NCPAP.

Todd and Associates randomized 154 preterm newborns to one of the three methods of NCPAP weaning: Rapid discontinuation of NCPAP, graded time off without using nasal cannula and graded time off using nasal cannula. They found that infants in the first method group had significantly shorter duration of weaning period and length of hospital stay. [18] Although we did not use a graded time off method, the rapid discontinuation of NCPAP in this study is very similar to non-HFNC method in our study. However, the mean duration of oxygen therapy using rapid discontinuation of NCPAP was about 24 days that is much longer than the figure of 2 days in our study of the non-HFNC group. This difference is probably due to lower gestational ages of newborns enrolled in Todd's study. Because more premature infants have lower lung compliance and a longer time is needed to reach normal lung compliance. In addition, bronchopulmonary dysplasia is more likely to develop in more premature infants.

Abdel-Hady et al. conducted a study to find the better approach for weaning preterm infants from NCPAP and found that weaning off directly from a pressure of 5 cmH 2 O and FIO 2 of = 21% to room air could significantly decrease duration of oxygen therapy in comparison to using HFNC (2 L/min) after discontinuation of NCPAP with a pressure of 5 cmH 2 O and FIO 2 of ≤30%. However, the length of hospitalization and other outcomes did not differ significantly between two groups. [19]

In contrast, our study revealed that the mean duration of oxygen therapy was significantly lower in HFNC group compared to non-HFNC group. Also, the mean length of hospital stay was significantly lower in HFNC group compared to non-HFNC group. These differences may be due to differences in methodology. The mean duration of oxygen therapy in non-HFNC group in our study was about 2 days compared to 5 days in that study. This difference could partially be due to shorter maintenance on NCPAP after initial stabilization in our study (6 h instead of 24 h). Moreover, they were kept flow rate at 2 L/min until the FIO 2 requirements were 0.21and then the HFNC flow was lowered step by step by 0.5 L/min every 6 h until a flow of 0.5 L/min was attained. We also did not lower flow rate until the FIO 2 requirements were 0.21 but, the HFNC flow was decreased gradually 0.5 L/min every 1 h until a flow of 0.5 L/min was attained. So it seems that using the most similar methods could yield more similar results.

We found that the need for intubation and mechanical ventilation was higher in newborns who enrolled in the non-HFNC group but, this difference was not significant. We speculated that this difference may be due to higher number of infants suffered from severe intraventricular hemorrhage in non-HFNC group.

Recently, Rastogi et al. conducted a study to compare rapid (sudden cessation of NCPAP when infants were stable for 48 h on NCPAP of 5 cmH 2 O and FIO 2 of = 21% to room air) and gradual (cycling off for 3 h alternating with cycling on for 3 h for 48 h) weaning from NCPAP in infants <32 weeks gestation. They did not find significant differences between groups with regards to the success rate of initial weaning, length of hospital stay and postmenstural age at time of weaning from supplemental oxygen and concluded that factors other than CPAP weaning method, such as maturity of the lungs may affect the success of NCPAP weaning in premature newborns. [20]

We also found that successful weaning was not significantly different between two groups.

To the best of our knowledge and belief, this study is the first on NCPAP weaning method that used such aggressive timetable and producing such promising results. However, our study had some limitations. First of all blinding of care providers was not possible because of the nature of the study using two different devices for respiratory support. Secondly, although we defined the success and failure of the weaning methods by clinical guidelines, it is likely that subjectivity of the care providers' decision could affect the final results.


  Conclusions Top


Weaning premature infants off NCPAP could successfully be done by HFNC or by decreasing FIO 2 to 21% after reaching NCPAP pressure of 5 cmH 2 O. HFNC can decrease the duration of oxygen therapy and length of hospital stay.


  Acknowledgements Top


The authors are grateful to all staff involved in this study for their assistance. They would also like to thank the Bureau for Research, Isfahan University of Medical Sciences, for funding the study.

 
  References Top

1.
de Winter JP, de Vries MA, Zimmermann LJ. Clinical practice: Noninvasive respiratory support in newborns. Eur J Pediatr 2010;169:777-82.  Back to cited text no. 1
    
2.
Morley CJ, Davis PG. Continuous positive airway pressure: Scientific and clinical rationale. Curr Opin Pediatr 2008;20:119-24.  Back to cited text no. 2
    
3.
Hutchison AA, Bignall S. Non-invasive positive pressure ventilation in the preterm neonate: Reducing endotrauma and the incidence of bronchopulmonary dysplasia. Arch Dis Child Fetal Neonatal Ed 2008;93:F64-8.  Back to cited text no. 3
    
4.
Polin RA, Sahni R. Newer experience with CPAP. Semin Neonatol 2002;7:379-89.  Back to cited text no. 4
    
5.
Davis PG, Henderson-Smart DJ. Nasal continuous positive airways pressure immediately after extubation for preventing morbidity in preterm infants. Cochrane Database Syst Rev 2003;2:CD000143.  Back to cited text no. 5
    
6.
Mathew OP. Apnea of prematurity: Pathogenesis and management strategies. J Perinatol 2011;31:302-10.  Back to cited text no. 6
    
7.
Morley CJ, Davis PG, Doyle LW, Brion LP, Hascoet JM, Carlin JB, et al. Nasal CPAP or intubation at birth for very preterm infants. N Engl J Med 2008;358:700-8.  Back to cited text no. 7
    
8.
Diblasi RM. Nasal continuous positive airway pressure (CPAP) for the respiratory care of the newborn infant. Respir Care 2009;54:1209-35.  Back to cited text no. 8
    
9.
Thompson MA. Early nasal continuous positive airway pressure to minimize the need for endotracheal intubation and ventilation. Neoreviews 2005;6:e184-8.  Back to cited text no. 9
    
10.
Jatana KR, Oplatek A, Stein M, Phillips G, Kang DR, Elmaraghy CA. Effects of nasal continuous positive airway pressure and cannula use in the neonatal intensive care unit setting. Arch Otolaryngol Head Neck Surg 2010;136:287-91.  Back to cited text no. 10
    
11.
Singh SD, Bowe L, Clarke P, Glover K, Pasquill A, Robinson MJ, et al. Is decreasing pressure or increasing time off the better strategy in weaning VLBW infants from nasal CPAP. Eur J Pediatr Book Abstr Eur Acad Pediatr 2006;165:48.  Back to cited text no. 11
    
12.
Soe A, Hodgkinson J, Jani B, Ducker DA. Nasal continuous positive airway pressure weaning in preterm infants. Eur J Paediatr Book Abstr Eur Acad Paediatr 2006;165:48-9.  Back to cited text no. 12
    
13.
Finer NN, Bates R, Tomat P. Low flow oxygen delivery via nasal cannula to neonates. Pediatr Pulmonol 1996;21:48-51.  Back to cited text no. 13
    
14.
Bouaram BA, Fernandes CJ. Heated, humidified high-flow nasal cannula therapy: Yet another way to deliver continuous positive airway pressure? Pediatrics 2008;122:218-9.  Back to cited text no. 14
[PUBMED]    
15.
Dani C, Pratesi S, Migliori C, Bertini G. High flow nasal cannula therapy as respiratory support in the preterm infant. Pediatr Pulmonol 2009;44:629-34.  Back to cited text no. 15
    
16.
Manley BJ, Owen LS, Doyle LW, Andersen CC, Cartwright DW, Pritchard MA, et al. High-flow nasal cannulae in very preterm infants after extubation. N Engl J Med 2013;369:1425-33.  Back to cited text no. 16
    
17.
Rastogi S, Rajasekhar H, Gupta A, Bhutada A, Rastogi D, Wung JT. Factors Affecting the Weaning from Nasal CPAP in Preterm Neonates. Int J Pediatr 2012;2012:416073.  Back to cited text no. 17
    
18.
Todd DA, Wright A, Broom M, Chauhan M, Meskell S, Cameron C, et al. Methods of weaning preterm babies <30 weeks gestation off CPAP: A multicentre randomised controlled trial. Arch Dis Child Fetal Neonatal Ed 2012;97:F236-40.  Back to cited text no. 18
    
19.
Abdel-Hady H, Shouman B, Aly H. Early weaning from CPAP to high flow nasal cannula in preterm infants is associated with prolonged oxygen requirement: A randomized controlled trial. Early Hum Dev 2011;87:205-8.  Back to cited text no. 19
    
20.
Rastogi S, Wong W, Gupta A, Bhutada A, Deepa Rastogi, Maimonides Neonatal Group. Gradual versus sudden weaning from nasal CPAP in preterm infants: A pilot randomized controlled trial. Respir Care 2013;58:511-6.  Back to cited text no. 20
    


    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1], [Table 2]


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