{Reference Type}: Journal Article
{Title}: Achieved oxygen saturations and risk for bronchopulmonary dysplasia with pulmonary hypertension in preterm infants.
{Author}: Gentle SJ;Singh A;Travers CP;Nakhmani A;Carlo WA;Ambalavanan N;
{Journal}: Arch Dis Child
{Volume}: 0
{Issue}: 0
{Year}: 2024 Jun 27
{Factor}: 4.92
{DOI}: 10.1136/archdischild-2024-327014
{Abstract}: <B>OBJECTIVE: </B>Characterisation of oxygen saturation (SpO2)-related predictors that correspond with both bronchopulmonary dysplasia-associated pulmonary hypertension (BPD-PH) development and survival status in infants with BPD-PH may improve patient outcomes. This investigation assessed whether (1) infants with BPD-PH compared with infants with BPD alone, and (2) BPD-PH non-survivors compared with BPD-PH survivors would (a) achieve lower SpO2 distributions, (b) have a higher fraction of inspired oxygen (FiO2) exposure and (c) have a higher oxygen saturation index (OSI).<BR><B>METHODS: </B>Case-control study between infants with BPD-PH (cases) and BPD alone (controls) and by survival status within cases.<BR><B>METHODS: </B>Single-centre study in the USA.<BR><B>METHODS: </B>Infants born at <29 weeks' gestation and on respiratory support at 36 weeks' postmenstrual age.<BR><B>METHODS: </B>FiO2 exposure, SpO2 distributions and OSI were analysed over the week preceding BPD-PH diagnosis.<BR><B>METHODS: </B>BPD-PH, BPD alone and survival status in infants with BPD-PH.<BR><B>RESULTS: </B>40 infants with BPD-PH were compared with 40 infants with BPD alone. Infants who developed BPD-PH achieved lower SpO2 compared with infants with BPD (p<0.001), were exposed to a higher FiO2 (0.50 vs 0.34; p=0.02) and had a higher OSI (4.3 vs 2.6; p=0.03). Compared with survivors, infants with BPD-PH who died achieved a lower SpO2 (p<0.001) and were exposed to a higher FiO2 (0.70 vs 0.42; p=0.049).<BR><B>CONCLUSIONS: </B>SpO2-related predictors differed between infants with BPD-PH and BPD alone and among infants with BPD-PH by survival status. The OSI may provide a non-invasive predictor for BPD-PH in preterm infants.