A24 Clinical outcomes of very-low-birth-weight infants who receive non-invasive ventilator support

2012 ◽  
Vol 88 ◽  
pp. S108-S109
Author(s):  
E. Okulu ◽  
S. Arsan ◽  
I.M. Akin ◽  
S. Alan ◽  
A. Kilic ◽  
...  
Perinatology ◽  
2016 ◽  
Vol 27 (4) ◽  
pp. 244
Author(s):  
Mina Jeon ◽  
Juhyun Jin ◽  
Jeong Eun Shin ◽  
Soon Min Lee ◽  
Ho Seon Eun ◽  
...  

2015 ◽  
Vol 7 (6) ◽  
pp. 328-337 ◽  
Author(s):  
Fauzia Shakeel ◽  
Anthony Napolitano ◽  
Melanie Newkirk ◽  
Jo Ellen Harris ◽  
Sharon R. Ghazarian

2014 ◽  
Vol 90 (12) ◽  
pp. 791-795 ◽  
Author(s):  
Anna W. Anderson ◽  
P. Brian Smith ◽  
Kristin M. Corey ◽  
Kevin D. Hill ◽  
Kanecia O. Zimmerman ◽  
...  

2020 ◽  
Vol 25 (5) ◽  
pp. 437-444
Author(s):  
Shubham Bakshi ◽  
Taylor Koerner ◽  
Alexander Knee ◽  
Rachana Singh ◽  
Ruben Vaidya

OBJECTIVE Administration of fluid bolus in very low birth weight (VLBW) infants is a common practice in the NICU, but one without clear evidence demonstrating benefits in clinical outcomes. On the contrary, recent observational studies have suggested a potential detrimental effect of empiric fluid bolus in preterm infants, especially in the absence of clear indications. The aim of this study was to assess the impact of fluid bolus on various clinical outcomes in VLBW infants. METHODS Retrospective cohort study of VLBW infants born at ≤34 weeks' gestation and/or ≤1500-g birth weight at a single level III NICU from January 1, 2008, to December 31, 2013, and who received at least one fluid bolus within the first 48 hours of life. Outcomes studied were in-hospital mortality, need for home oxygen, incidence of chronic lung disease (CLD), prevalence of patent ductus arteriosus (PDA), and intraventricular hemorrhage (IVH). RESULTS Of 516 infants, 112 (21.7%) received a fluid bolus within the first 48 hours of life for various indications. Propensity models suggested no statistical difference for CLD or mortality, but exposed infants had an increased incidence of home on oxygen (p = 0.018), PDA prevalence (p = 0.008), and IVH prevalence (p = 0.038). CONCLUSIONS Fluid bolus in the first 48 hours of life may be associated with increased incidence of need for home oxygen and higher prevalence of PDA and IVH in VLBW infants. Future studies are needed to address these important adverse outcomes.


2020 ◽  
Vol 19 (3) ◽  
pp. 18-25
Author(s):  
D. R. Sharafutdinova ◽  
E. N. Balashova ◽  
O. V. Ionov ◽  
A. R. Kirtbaya ◽  
J. M. Golubtsova ◽  
...  

Near-infrared spectroscopy (NIRS), or cerebral oximetry, is a non-invasive method for assessing the oxidative status (saturation of hemoglobin with oxygen) mainly in the blood of cerebral venous vessels, which is increasingly used in clinical practice, in particular in neonatology. This method allows us to evaluate not only tissue perfusion, but also to determine the differences between the indicators of cerebral and peripheral oxygenation. Few studies have described improvements in tissue oxygenation indicators determined by NIRS after red blood cells transfusion in premature newborns. In our study we registered the oximetry indicators before and after red blood cells transfusion in extremely and very low birth weight infants (n = 55). This clinical study was approved by the Biomedical Research Ethics Committee (Protocol No. 19 dated 17 November 2016) and the Scientific Council of the Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology of Ministry of Healthcare of the Russian Federation (Protocol No. 19 dated 29 November 2016). Our study demonstrated a statistically significant increase in CrSO2 , SrSO2 , RrSO2 and SCOR and a decrease in C-FTOE, S-FTOE after a blood transfusion. The study also showed that a decrease in NIRS values (SCOR ≤ 0.76, C-FTOE ≥ 0.29, CrSO2 ≤ 64%, SrSO2 ≤ 54%, and RrSO2 ≤ 56%) can serve as an additional non-invasive measure of anemia and its progression; it helps detect a decrease in cerebral oxygenation at an early, preclinical stage of disease, and can also be used as an additional indicator of the need for red blood cell transfusions. 


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