scholarly journals N-Terminal Pro-B Type Natriuretic Peptide as a Marker of Bronchopulmonary Dysplasia or Death in Very Preterm Neonates: A Cohort Study

PLoS ONE ◽  
2015 ◽  
Vol 10 (10) ◽  
pp. e0140079 ◽  
Author(s):  
Anna Sellmer ◽  
Vibeke Elisabeth Hjortdal ◽  
Jesper Vandborg Bjerre ◽  
Michael Rahbek Schmidt ◽  
Patrick J. McNamara ◽  
...  
2020 ◽  
Vol 56 (10) ◽  
pp. 1607-1612 ◽  
Author(s):  
Jasmine Antoine ◽  
Garry D T Inglis ◽  
Mandy Way ◽  
Peter O'Rourke ◽  
Mark W Davies

2013 ◽  
Vol 49 (11) ◽  
pp. 1106-1111 ◽  
Author(s):  
Vaneet Kumar Kalra ◽  
Sanjeev Aggarwal ◽  
Prem Arora ◽  
Girija Natarajan

2021 ◽  
Vol 5 (1) ◽  
pp. e001149
Author(s):  
Nem Yun Boo ◽  
Seok Chiong Chee ◽  
Siew Hong Neoh ◽  
Eric Boon-Kuang Ang ◽  
Ee Lee Ang ◽  
...  

ObjectivesTo determine a 10-year trend of survival, morbidities and care practices, and predictors of in-hospital mortality in very preterm neonates (VPTN, gestation 22 to <32 weeks) in the Malaysian National Neonatal Registry.DesignRetrospective cohort study.Setting43 Malaysian neonatal intensive care units.Patients29 010 VPTN (without major malformations) admitted between 1 January 2009 and 31 December 2018.Main outcome measuresCare practices, survival, admission hypothermia (AH, <36.5°C), late-onset sepsis (LOS), pneumothorax, necrotising enterocolitis grade 2 or 3 (NEC), severe intraventricular haemorrhage (sIVH, grade 3 or 4) and bronchopulmonary dysplasia (BPD).ResultsDuring this 10-year period, there was increased use of antenatal steroid (ANS), lower segment caesarean section (LSCS) and early continuous positive airway pressure (eCPAP); but decreased use of surfactant therapy. Survival had increased from 72% to -83.9%. The following morbidities had decreased: LOS (from 27.9% to 7.1%), pneumothorax (from 6.0% to 2.7%), NEC (from 8.1% to 4.7%) and sIVH (from 12.2% to 7.5%). However, moderately severe AH (32.0°C–35.9°C) and BPD had increased. Multiple logistic regression analyses showed that lower birth weight, no ANS, no LSCS, admission to neonatal intensive care unit with <100 VPTN admissions/year, no surfactant therapy, no eCPAP, moderate and severe AH, LOS, pneumothorax, NEC and sIVH were significant predictors of mortality.ConclusionSurvival and major morbidities had improved modestly. Failure to use ANS, LSCS, eCPAP and surfactant therapy, and failure to prevent AH and LOS increased risk of mortality.


2020 ◽  
Vol 149 ◽  
pp. 105142
Author(s):  
Anna Sellmer ◽  
Vibeke E. Hjortdal ◽  
Jesper V. Bjerre ◽  
Michael R. Schmidt ◽  
Bodil H. Bech ◽  
...  

Author(s):  
Clémence Guiraut ◽  
Nadine El Raichani ◽  
Guillaume Morin ◽  
Ibrahim Mohamed ◽  
Jean-Claude Lavoie

Most very premature newborns (&lt; 32 weeks of gestation) receive parenteral nutrition (PN) that is inherently contaminated with peroxides. Oxidative stress induced by PN is associated with bronchopulmonary dysplasia, a main pathological complication in these babies who have weak antioxidant capacity to detoxify peroxides because of their glutathione deficiency. In animals, glutathione supplementation of PN prevented oxidative stress and alveolar loss (the main characteristic of bronchopulmonary dysplasia). Of its two forms - disulfide (GSSG) and free thiol (GSH) - GSSG was used because of its better stability in PN. However, a 30% loss of GSSG in PN is observed. The potentially high therapeutic benefits of GSSG supplementation on the health of very premature babies makes the study of its stability highly important. Thus, GSSG was incubated in combination with the following components of PN: dextrose, multivitamins, Primene, Travasol, as well as with cysteine, cystine and peroxides for 24h. Total glutathione in these solutions was measured 0-24h after the addition of GSSG. The combination of cysteine and multivitamins caused the maximum loss of glutathione. Removing the cysteine prevented the degradation of glutathione. GSSG reacts with cysteine to form cysteine-glutathione disulfide, another suitable glutathione substrate for preterm neonates.


Sign in / Sign up

Export Citation Format

Share Document