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血红蛋白和低蛋白血症的降低:发展中国家晚发性败血症新生儿并发症的可能预测因子
Authors Cai N, Liao W, Chen Z, Tao M, Chen S
Received 5 April 2022
Accepted for publication 28 July 2022
Published 13 August 2022 Volume 2022:15 Pages 6583—6589
DOI https://doi.org/10.2147/IJGM.S369550
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Scott Fraser
Objective: The main purpose of our study was to determine the predictors of complications in neonates with late-onset sepsis (LOS).
Materials and methods: This was a retrospective cohort study conducted in a neonatal intensive care unit between June 2016 and February 2020. Neonates with LOS were enrolled in this study. According to whether complications were merged after LOS, neonates were divided into a complicated group and a noncomplicated group. The demographic data, perinatal conditions, blood cell count analysis, blood cultures, hypoproteinemia within 1 week after the onset of sepsis and treatment measures were compared between the groups.
Results: A total of 87 neonates with LOS were enrolled in this study. Significant differences were observed between the complicated and noncomplicated groups with regard to hemoglobin (Hb), a decrease in Hb, hypoproteinemia and red blood cell transfusions (P < 0.05). Further comparison found that neonates with LOS who had moderate or severe anemia at the time of sepsis onset were more likely to have complications than those with mild or no anemia. The results of binomial stepwise logistic regression suggested that a decrease in Hb (OR=0.045, P=0.025 < 0.05) and hypoproteinemia (OR=0.266, P=0.007 < 0.05) were independent predictors of complications in neonates with LOS. A receiver operating characteristic analysis showed that the area under the curve was 0.807 for a decrease in Hb.
Conclusion: A decrease in Hb and hypoproteinemia were independent predictors of complications and may help to predict the occurrence of complications in neonates with LOS in the early stage.
Keywords: sepsis, complications, hemoglobin, anemia, decrease in Hb, hypoalbuminemia