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Published on: January 29, 2011
Permissive hypercapnia in extremely low birthweight infants (PHELBI): a randomised controlled multicentre trial
Ulrich H Thome1, Orsolya Genzel-Boroviczeny2, Bettina Bohnhorst3
1Division of Neonatology, University Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany.
Insights
Higher partial pressure of carbon dioxide (pCO2) targets in ventilated preterm infants did not reduce bronchopulmonary dysplasia or death. This study found no significant difference in outcomes between higher and lower pCO2 groups.
Area of Science:
- Neonatal Medicine
- Pediatric Critical Care
- Respiratory Physiology
Background:
- Mechanical ventilation in extremely low birthweight infants carries risks like ventilator-induced lung injury and bronchopulmonary dysplasia.
- Tolerating higher partial pressure of carbon dioxide (pCO2) is hypothesized to mitigate these risks.
Purpose of the Study:
- To investigate if higher target ranges for pCO2 decrease the incidence of bronchopulmonary dysplasia or death in mechanically ventilated preterm infants.
- To evaluate the impact of higher pCO2 targets on mortality, intraventricular hemorrhage, and retinopathy.
Main Methods:
- A randomized multicenter trial involving 362 preterm infants (400-1000g birthweight, 23-28 weeks gestational age) requiring mechanical ventilation.
- Infants were assigned to either a high target pCO2 group (ranging from 55-75 mmHg) or a control group (40-60 mmHg) over 14 days.
- The primary outcome was death or moderate to severe bronchopulmonary dysplasia at 36 weeks postmenstrual age.
Main Results:
- The rate of bronchopulmonary dysplasia or death was 36% in the high target group versus 30% in the control group (p=0.18), showing no significant difference.
- Mortality rates were 14% (high target) and 11% (control) (p=0.32).
- Rates of severe intraventricular hemorrhage (15% vs 12%) and retinopathy (11% vs 14%) also did not differ significantly between groups.
Conclusions:
- Targeting higher pCO2 levels in ventilated preterm infants did not reduce the rate of bronchopulmonary dysplasia or death.
- No significant differences in mortality, intraventricular hemorrhage, or retinopathy were observed between the higher and control pCO2 target groups.
- These findings suggest that higher pCO2 targets do not offer additional lung protection benefits in this population.
Background:
Tolerating higher partial pressure of carbon dioxide (pCO2) in mechanically ventilated, extremely low birthweight infants might reduce ventilator-induced lung injury and bronchopulmonary dysplasia. We aimed to test the hypothesis that higher target ranges for pCO2 decrease the rate of bronchopulmonary dysplasia or death.
Methods:
In this randomised multicentre trial, we recruited infants from 16 tertiary care perinatal centres in Germany with birthweight between 400 g and 1000 g and gestational age 23-28 weeks plus 6 days, who needed endotracheal intubation and mechanical ventilation within 24 h of birth. Infants were randomly assigned to either a high target or control group. The high target group aimed at pCO2 values of 55-65 mm Hg on postnatal days 1-3, 60-70 mm Hg on days 4-6, and 65-75 mm Hg on days 7-14, and the control target at pCO2 40-50 mmHg on days 1-3, 45-55 mm Hg on days 4-6, and 50-60 mm Hg on days 7-14. The primary outcome was death or moderate to severe bronchopulmonary dysplasia, defined as need for mechanical pressure support or supplemental oxygen at 36 weeks postmenstrual age. Cranial ultrasonograms were assessed centrally by a masked paediatric radiologist. This trial is registered with the ISRCTN registry, number ISRCTN56143743.
Results:
Between March 1, 2008, and July 31, 2012, we recruited 362 patients of whom three dropped out, leaving 179 patients in the high target and 180 in the control group. The trial was stopped after an interim analysis (n=359). The rate of bronchopulmonary dysplasia or death in the high target group (65/179 [36%]) did not differ significantly from the control group (54/180 [30%]; p=0·18). Mortality was 25 (14%) in the high target group and 19 (11%; p=0·32) in the control group, grade 3-4 intraventricular haemorrhage was 26 (15%) and 21 (12%; p=0·30), and the rate of severe retinopathy recorded was 20 (11%) and 26 (14%; p=0·36).
Interpretation:
Targeting a higher pCO2 did not decrease the rate of bronchopulmonary dysplasia or death in ventilated preterm infants. The rates of mortality, intraventricular haemorrhage, and retinopathy did not differ between groups. These results suggest that higher pCO2 targets than in the slightly hypercapnic control group do not confer increased benefits such as lung protection.
Funding:
Deutsche Forschungsgemeinschaft.
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