This study seeks to determine if standard continuous positive airway pressure, known as CPAP is as effective as a more complicated approach that generates intermittent increases in airway pressure applied to the nostrils via a breathing machine. The latter is known as NIPPV and requires costly equipment to operate. Previous studies did not ensure that the average pressure applied to the lungs was equal and thus did not make for a fair comparison. The investigators believe that when the same average pressure is applied with the two techniques, CPAP is just as effective as NIPPV and may have fewer side effects, such as blowing air into the stomach. Each baby will receive CPAP or NIPPV in a random sequence for a period of 12 hours, followed by 12 hours on the alternate technique.
This is a pilot clinical trial to evaluate the comparative effectiveness of two commonly used types of non-invasive respiratory support. Preterm infants \< 34 weeks gestational age, who are stable on either of the two modalities of support will be studied in a cross-over study design, such that each subject acts as his/her own control. The study will assess the relative efficacy of these modalities when used with equal mean airway pressure comparing measures of oxygenation, CO2 removal, apnea/bradycardia/desaturation events and work of breathing. The initial phase of the study is complete and preliminary analysis supports the hypothesis that there is no difference between the modalities when the mean airway pressure is equal. However we recognized that use of the RAM cannula, which does not transmit pressure effectively is an important study limitation. The findings are valid, but may only be applicable to this interface, which is widely used, but increasingly recognized as flawed. We are now extending the study to determine if the findings will be the same when short bi-nasal prongs are used.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
52
Continuous positive airway pressure is applied for 12 hours at a mean airway pressure that is the same as the subject was receiving prior to entry into the study
NIPPV is applied for 12 hours at a mean airway pressure that is the same as the subject was receiving prior to entry into the study
Women and Infants Hospital of Rhode Island
Providence, Rhode Island, United States
Number of Apnea/bradycardia events
Number of episodes of apnea and/or bradycardia that trigger alarm on the bedside monitor
Time frame: Duration of intervention (12 hours)
Number of of desaturation events
Number of episodes of pulse oximetry readings that trigger alarm on the bedside monitor
Time frame: Duration of intervention (12 hours)
Mean oxygen saturation by pulse oximetry and proportion of time below 88%
Mean oxygen saturation by pulse oximetry and proportion of time at saturation \<88%
Time frame: Duration of intervention (12 hours)
Mean transcutaneous PCO2 and proportion of time >55 torr
Mean transcutaneous PCO2 and proportion of time at PCO2 \> 55 torr
Time frame: Duration of intervention (12 hours)
Mean fraction of inspired oxygen
Mean fraction of inspired oxygen (FIO2)
Time frame: Duration of intervention (12 hours)
Mean respiratory rate
Mean respiratory rate
Time frame: Duration of intervention (12 hours)
Mean degrees of phase lag by RIP
Estimate of work of breathing based on phase angle as determined by respiratory inductive plethysmography
Time frame: Duration of intervention (12 hours)
Number of episodes of feeding intolerance
number of instances of interruption of feeding, abdominal radiographs
Time frame: Duration of intervention (12 hours)
Instances of treatment failure
Inability to tolerate assigned treatment by pre-defined criteria
Time frame: Duration of intervention (12 hours)
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