1.gif (1892 bytes)                      

Short Communications

Indian Pediatrics 2008; 45:-312-314

A Simple Circuit to Deliver Bubbling CPAP

 

Charanjit Kaur, Akatoli Sema, Rajbir S Beri and Jacob M Puliyel

From the Department of Pediatrics, St Stephens Hospital, Tis Hazari, Delhi 110 054, India.

Correspondence to: J M Puliyel, Department of Pediatrics, St Stephens Hospital, Tis Hazari, Delhi 110 054, India. E-mail: [email protected]

Manuscript received: June 4, 2007; Initial review completed: September 15, 2007;
Revision accepted: November 19, 2007.

Abstract

Nasal continuous positive airway pressure (CPAP), especially ‘bubbling CPAP’, is known to reduce the need for more invasive ventilation. We here describe a circuit that can deliver bubbling CPAP in resource poor settings. We describe how the oxygen concentration can be altered from 98% to 21% oxygen using this system. Addition of a humidifier in the circuit has the effect of reducing the oxygen concentration by 1 to 5%. The cost of putting together the system is approximately Rs 5000.

Key words: CPAP, Nasal, Newborn.

Introduction

In the quest to bring down the neonatal mortality rate, the challenge is to develop low cost technology that can be used in remote settings(1,2). It is known that early use of continuous positive airway pressure (CPAP) reduces the incidence of chronic lung disease(3) and it may be used as an alternative to intubation and ventilation is some cases(4-7). Recent literature suggests that ‘bubbling CPAP’ is better than conventional CPAP. The bubbling CPAP is a form of oscillatory pressure delivery in which mechanical vibrations are transmitted to the chest secondary to non-uniform flow of gas bubbles across the downstream of a water seal(8) and this system results in waveforms similar to those produced by high-frequency ventilation when recorded by a transducer attached to the infant’s airway. The chest vibrations produced contribute to gas exchange by facilitated diffusion(9). We describe a circuit which delivers bubbling CPAP, is easy to assemble and can be adapted for use in any health facility where oxygen and compressed air are available.

Methods

In its most basic form, pressurized oxygen from an oxygen cylinder is delivered to the nasopharynx of the baby. An under water ‘T tube’ that acts as a blow off valve is interposed between the oxygen source and the baby. Adjusting the height of the water column above the exit of the ‘T tube’ can regulate the pressure in the system and the amount of CPAP delivered to the baby. The constant bubbling of gas through the blow off mechanism delivers the bubbling CPAP effect. Oxygen may be delivered by nasal prongs or more cheaply by a shortened endotrachel tube or a nasopharyngeal catheter (8F) inserted into the nose to a depth equal to the distance from the side of the nose to the front of the ear so the tip of the catheter is just visible in the pharynx below the soft palate when the mouth of the infant is open(10). This system however delivers 100% oxygen and can harm premature babies.

The system can be modified by having a Y tube deliver a mixture of air and oxygen from 2 separate cylinders. Flow meters indicate the flow rate of the gases and the relative concentration of oxygen. A humidifier can also be added so the gas mixture is not dry and it does not irritate the airway. This humidifier consists of a heating element that keeps the water at 37degrees centigrade and the air that passes over it is saturated with moisture at body temperature (Fig. 1).

Fig. 1. Circuit for bubbling CPAP with blow-off valve 4 cm under water and autoclavable-glass humidifier unit.

In centers where it is available, a saturation monitor can be used to adjust the air: oxygen mix to maintain saturations of 92 to 98% in the baby, and minimize the risk of oxygen toxicity.

We have used different flow rates of oxygen and air and measured the resultant oxygen concentration using a MiniOX 111 oxygen meter. The readings were taken three times and the mean values are reported. The resultant table can help guide adjustment of flow rates to deliver the desired oxygen concentration. This is similar to the theoretical values achieved which are also shown in the table. For the theoretical calculations we assumed partial pressure of humidity saturated at 37ºC is 47 mm of Hg or approximately 5% of the total atmospheric pressure at sea level. The oxygen concentration is given by the formula:

Final O2 concentration = nn×5/100 where n is the oxygen concentration before saturation with humidity.

Results

Table I shows the oxygen mix when the total flow rate is 8 liters /minute and the ratio of air and oxygen is varied. The use of a humidifier reduces the oxygen concentration from 1% to 5% as shown in the Table.

Table I

Saturations of Oxygen Achieved with Different Flow Rates for Oxygen and Air
Flow rate of
Oxygen (L)
Flow rate of
air (L)
Theoretical O2 concentration (%)
(without humidity)
Theoretical O2 concentration (%)
(humidity  saturated at 37ºC )
Mean saturation
achieved in three tests (%)
8 0 100 95.0 98.7
7 1 90 86.5 84.5
6 2 80 76.0 72.5
5 3 70 66.5 61.3
4 4 60 57.0 53.6
3 5 50 47.5 38.8
2 6 40 38.0 23.5
1 7 30 28.5 21.2
0 8 20 19.0 21.2

Discussion

CPAP helps maintain the functional residual capacity (FRC) of infants, prevents atelectasis, augments surfactant production, reduces fatigue in ventilatory muscles, provides respiratory stimulation against apnea and allows gas exchange(11). Oxygen is ideally used only in neonates who are continuously monitored. The flow mix of oxygen and air can be adjusted to keep the saturation around 96%. However in areas where saturation monitors are not available, bubbling air for CPAP would be safe. Bubbling CPAP has been found safe to be used by nurses(2). Use of the table provided in this study will help users to determine the quantities of oxygen being delivered to the child.

A single prong CPAP, using a cut down endotracheal tube, or a large bore suction tube may be used. This has shown to be as comfortable for the baby as the more expensive nasal prongs(12). This is a cheaper alternative to nasal prongs. Mouth closure is not considered essential although it can raise pharyngeal pressure(13).

The authors have utilized this system within their neonatal unit for the last 10 years both for neonates with respiratory distress prior to ventilation (with a view to reduce the need for mechanical positive pressure ventilation) and also for weaning from the ventilator. A commercial version of the CPAP system is available in the market for Rs 155,000. All elements of the system described here can be bought for Rs 500 ($10) except the humidifier which is available for Rs 4500 ($100). Widespread use of this system has the potential for saving lives in small hospitals where there is no facility for mechanical ventilation of babies.

Contributors: RSB and JP conceived the project, CK and AS did the measurements. All authors contributed to the manuscript preparation. JP will be guarantor.

Funding: None.

Competing interests: None stated.

 


What This Study Adds?

• We describe a simple circuit to deliver bubbling CPAP in newborn infants.
 


 

References

 

1. Bhargava SK. The challenge of neonatal mortality in India. Indian Pediatr 2004; 41: 657-662.

2. Koyamaibole L, Kado J, Qovu JD, Colquhoun S, Duke T. An evaluation of bubble-CPAP in a neonatal unit in a developing country: Effective respiratory support that can be applied by nurses. Trop Pediatr 2006; 52: 249-253.

3. Avery ME, Tooley WH, Keller JB, Hurd SS, Bryan MH, Cotton RB, et al. Is chronic lung disease in low birth weight infants preventable? A survey of eight centres. Pediatrics 1987; 79: 26-30.

4. Jacobsen T, Grønvall J, Petersen S, Andersen GE. "Minitouch" treatment of very low-birth-weight infants. Acta Paediatr 1993; 82: 934-938.

5. Gittermann MK, Fusch C, Gittermann AR, Regazzoni BM, Moessinger AC. Early nasal continous positive airway pressure treatment reduces the need for intubation in very low birth weight infants. Eur J Pediatr 1997; 156: 384-388.

6. Lindner W, Vossbeck S, Hummler H, Pohlandt F. Delivery room management of extremely low birth weight infants: spontaneous breathing or intubation? Pediatrics 1999; 103: 961-967.

7. Thomson MA. Early nasal CPAP + prophylactic surfactant for neonates at risk of RDS. The IFDAS trial. Pediatr Res 2001; 50: 304A.

8. Narendran V, Donovan EF, Hoath SB, Akinbi HT, Stteichen JJ, Jobe AH. Early CPAP and outcomes in ELBW preterm infants. J Perinatol 2003; 23: 195-199.

9. Kyong-Soon Lee, Dunn MS, Fenwick M, Shennan AT. A comparison of underwater bubble CPAP with ventilator derived CPAP in premature neonates ready for extubation. Biol Neonate 1998; 73: 69-75

10. Frey B, Shann F. Oxygen administration in infants. Arch Dis Child Fetal Neonatal Ed 2003; 88: F84-F88.

11. Millar D, Kirpalani H. Benefits of non-invasive ventilation. Indian Pediatr 2004; 41: 1008-1017.

12. Ahluwalia JS, White DK, Morley CJ. Infant flow driver or single prong nasal continuous positive airway pressure: short-term physiological effects. Acta Paediatr 1998; 87: 325-327.

13. De Paoli AG, Morley C, Davis PG. Nasal CPAP for neonates: what do we know in 2003? Arch Dis Child Fetal Neonatal Ed 2003; 88: F168- F172.

Home

Past Issue

About IP

About IAP

Feedback

Links

 Author Info.

  Subscription