Objective: To analyse early risk factors for mortality in preterm infants treated with inhaled nitric oxide (iNO) in China.
Design: A retrospective observational case-control study.
Setting: 8 tertiary hospitals in 5 regions of China.
Patients: 726 preterm infants treated with iNO for hypoxic respiratory failure or persistent pulmonary hypertension of newborns.
Interventions: None.
Measurements: The primary outcome was survival status at discharge.
Main Results: (1) The mortality rate was 27.1% (197/726), and which significantly reduced with increasing gestational age (GA) and birth weight. (2) Compared with the survival group, the death group had significantly greater use of assisted reproductive technology, higher multiple pregnancy rates and lower caesarean section rates. Infants in the death group had a significantly higher incidence of small for GA (SGA), Apgar score ≤3 at 1 min after birth, pneumorrhagia, sepsis and shock. In the death group, the utilisation rate of a pulmonary surfactant (PS) was significantly lower, whereas the oxygenation index (OI) before iNO treatment was significantly higher. The maximum dose of iNO in the death group was significantly higher than that in the survival group. (3) The Cox proportional hazard model showed that SGA (HR 1.800, 95% CI (1.113 to 2.911)), sepsis (HR 1.488, 95% CI (1.093 to 2.027)), shock (HR 1.473, 95% CI (1.033 to 2.100)), OI before iNO treatment (HR 1.016, 95% CI (1.006 to 1.026)) and the maximum dose of iNO treatment (HR 1.070, 95% CI (1.035 to 1.105)) were risk factors for death in preterm infants treated with iNO. Furthermore, GA (HR 0.876, 95% CI (0.831 to 0.924)), PS (HR 0.433, 95% CI (0.296 to 0.633)) and a higher initial dose of iNO (HR 0.926, 95% CI (0.891 to 0.962)) were identified as protective factors. (4) Stratified analysis and sensitivity analysis determined the stability of the core results in preterm infants with GA between 28 and 36 weeks.
Conclusion: Premature infants treated with iNO had a high mortality rate. SGA, sepsis, shock and higher OI before iNO treatment increased the mortality risk in infants with GA between 28 and 36 weeks. A higher GA the use of PS, and a higher initial iNO dose could improve the survival outcome of these babies.
Trial Registration Number: The study was registered in the Chinese Clinical Trials Registry (http://www.chictr.org.cn; registration number: ChiCTR2200066935).
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http://dx.doi.org/10.1136/bmjpo-2024-003204 | DOI Listing |
J Matern Fetal Neonatal Med
December 2025
Fetal Medicine and Gynecology Department, Medical University of Lodz, Lodz, Poland.
Objective: We aimed to compare the perinatal outcomes in women with cervical dilatation with fetal membranes visible before 26 weeks of gestation managed with an adjunctive pessary after emergency cervical cerclage or emergency cerclage alone.
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J Dev Orig Health Dis
March 2025
Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, USA.
The current study examines the application of the Pediatric-Buccal-Epigenetic (PedBE) clock, designed for buccal epithelial cells, to endothelia. We evaluate the association of PedBE epigenetic age and age acceleration estimated from human umbilical vein endothelial cells (HUVECs) with length of gestation and birthweight in a racially and ethnically diverse sample (analytic sample = 333). PedBE age was positively associated with gestational age at birth ( = 0.
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March 2025
Department of Obstetrics and Gynecology, General Hospital of Northern Theater Command, No.83, Wenhua Road, Shenhe District, Shenyang, 110016, China.
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BMC Pediatr
March 2025
Partners in Health, P. O Box 56, Neno, Malawi.
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View Article and Find Full Text PDFEur J Pediatr
March 2025
Medway NHS Foundation Trust, Kent, UK.
Unlabelled: In this brief report, we present the findings of a survey which explores the learning curve that was achieved during the 'Serial Lung Ultrasound in predicting the need for surfactant and Respiratory course in Preterm infants' (SLURP) study. The aim of this survey was to evaluate the training lung ultrasound operators received in order to scan patients who were recruited into the SLURP study. The aim of the SLURP study was to validate the optimal lung ultrasound (LU) 'cut off' score using standard and extended LU zones that predict surfactant need in babies born ≤ 34 weeks on non-invasive respiratory support when clinicians had various levels of experience in LU.
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