• Annals of medicine · Dec 2023

    Clinical value of procalcitonin-to-albumin ratio for identifying sepsis in neonates with pneumonia.

    • Tiewei Li, Xiaojuan Li, Zhiwei Zhu, Xinrui Liu, Geng Dong, Zhe Xu, Min Zhang, Ying Zhou, Jianwei Yang, Junmei Yang, Panpan Fang, and Xiaoliang Qiao.
    • Zhengzhou Key Laboratory of Children's Infection and Immunity, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, P.R. China.
    • Ann. Med. 2023 Dec 1; 55 (1): 920925920-925.

    BackgroundIt is possible that neonates with pneumonia also have unrecognized sepsis. Identifying sepsis in neonates with pneumonia may cause some trouble for clinicians. This study aimed to evaluate the clinical value of the procalcitonin-to-albumin ratio (PAR) in identifying sepsis in neonates with pneumonia.MethodsWe retrospectively included 912 neonates with pneumonia from January 2016 to July 2021. Clinical and laboratory data were collected from electronic medical records. Among neonates with pneumonia, 561 neonates were diagnosed with sepsis, according to the International Pediatric Sepsis Consensus. Neonates were divided into a sepsis group and a pneumonia group. A multivariate logistic regression analysis was used to evaluate whether PAR was a potential independent indicator for identifying sepsis in neonates with pneumonia. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the diagnostic value of PAR in sepsis.ResultsNeonates with sepsis have a higher PAR (p < 0.001). Correlation analysis showed that PAR was positively correlated with the level of C-reactive protein (r = 0.446, p < 0.001). Multiple logistic regression analysis showed that PAR was an independent predictor of the presence of sepsis in neonates with pneumonia. ROC curve analysis revealed that PAR had good power in identifying sepsis in neonates with pneumonia (area under curve (AUC) = 0.72, 95% confidence interval (CI), 0.68-0.75, p < 0.001).ConclusionPAR can be used as a new biomarker to identify sepsis in neonates with pneumonia.

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