Peer-Reviewed Journal Details
Mandatory Fields
Hawkes, GA;Kenosi, M;Finn, D;O'Toole, JM;O'Halloran, KD;Boylan, GB;Ryan, AC;Dempsey, EM
2015
January
Archives of Disease In Childhood-Fetal and Neonatal Edition
Delivery room end tidal CO2 monitoring in preterm infants < 32weeks
Validated
Optional Fields
NEONATAL INTENSIVE-CARE ARTERIAL CARBON-DIOXIDE PERIVENTRICULAR LEUKOMALACIA MASK VENTILATION HYPOCAPNIA RESUSCITATION AIRWAY UNIT
101
62
65
Objectives To determine the feasibility of end tidal (EtCO2) monitoring of preterm infants in the delivery room, to determine EtCO2 levels during delivery room stabilisation, and to examine the incidence of normocapnia (5-8kPa) on admission to the neonatal intensive care unit in the EtCO2 monitored group compared with a historical cohort without EtCO2 monitoring. Patients and methods Preterm infants (<32weeks) were eligible for inclusion in this observational study. The evolution of EtCO2 values immediately after delivery was assessed and linear least-squares methods were used to fit a line to EtCO2 recordings. The partial pressure of CO2 in blood (PCO2) from the infants who received EtCO2 monitoring was compared with a historical cohort without EtCO2 monitoring. Results EtCO2 monitoring was feasible in the delivery room. EtCO2 values were successfully obtained in 39 (88.7%) of the 44 infants included in the study. EtCO2 gradually increased over the first 4min. Intubated infants had higher EtCO2 values compared with infants who were not intubated, with median (IQR) values of 4.7 (3.3-8.4) kPa versus 3.2 (2.6-4.2) kPa (p=0.05). No difference was found between the proportions of PCO2 values within the range of normocapnia among infants who received EtCO2 monitoring compared with those who did not (56.8% vs 47.9%, p=0.396). Conclusions Delivery room EtCO2 monitoring is feasible and safe. EtCO2 values obtained after birth reflect the establishment of functional residual capacity and effective ventilation. The potential short-term and long-term consequences of EtCO2 monitoring should be established in randomised controlled trials.
LONDON
1359-2998
10.1136/archdischild-2015-308315
Grant Details