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Individual and combined bioscore model of presepsin, procalcitonin, and high sensitive C - reactive protein as biomarkers for early diagnosis of paediatric sepsis

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dc.contributor.author Sakyi, Samuel Asamoah
dc.contributor.author Enimil, Anthony
dc.contributor.author Kwabena Adu, David
dc.contributor.author Ephraim, Richard Dadzie
dc.contributor.author Danquah, Kwabena Owusu
dc.contributor.author Fondjo, Linda
dc.contributor.author Baidoe-Ansah, David
dc.contributor.author Adoba, Prince
dc.contributor.author Toboh, Emmanuel
dc.contributor.author Afranie, Bright Oppong
dc.date.accessioned 2023-10-24T11:22:29Z
dc.date.available 2023-10-24T11:22:29Z
dc.date.issued 2020
dc.identifier.uri http://hdl.handle.net/123456789/9948
dc.description.abstract Background: Paediatric sepsis remains a major public health problem with significant morbidity and mortality especially in developing countries. Clinical symptoms associated with sepsis are unreliable and laboratory pa- rameters unspecific, making an early diagnosis of paediatric sepsis difficult. The lack of definitive biomarker(s) for early diagnosis of sepsis further leads to the misuse of antibiotics. Diagnosis based on a single biomarker does not provide adequate accuracy. Subsequently, combining multiple biomarkers into a single score will help clinicians make a better diagnostic judgment. Aims: This study for the first time evaluated the individual and combined diagnostic accuracy of procalcitonin (PCT), presepsin (sCD14-ST) and high sensitive C-reactive protein (hs-CRP) using a Bioscore model. Materials and methods: In a case control study conducted at the Paediatric Emergency Unit (PEU) and the Mother and Baby Unit (MBU) of Komfo Anokye Teaching Hospital (KATH), sixty (60) paediatric subjects aged zero to six (0–6) years, were diagnosed with sepsis using case-definition by the national neonatal bloodstream infection surveillance and Pediatric Sepsis Consensus Congress. Thirty (30) other paediatric subjects, aged and sex matched without sepsis or inflammatory conditions were used as controls. One-time blood sample was taken at the time of admission for blood culture and measurement of PCT, hs-CRP, and presepsin by ELISA. The Statistical Package for Social Sciences (SPSS release 20.0, Copyright ©SPSS Inc.) was used for analysis. Results: Out of the sixty septic paediatric subjects, 14 patients (23.3%) had positive blood cultures (LCS) and 46 (76%) had negative for blood cultures (CS). Klebsiella spp. recorded the highest median levels of PCT, and hs-CRP while Pseudo. Aeruginasa recorded the highest of sCD14-ST levels. Significant elevations in PCT, sCD14-ST and hs- CRP levels were observed among septic cases in comparison to controls (p < 0.0001). Individually, PCT showed better accuracy (AUC ¼ 78.7%) followed by hs-CRP (AUC ¼ 78.4%) and sCD14-ST (AUC ¼ 74.8%). Combination of PCT þ hs-CRP had the highest accuracy (AUC ¼ 80.1%) followed by hs-CRP þ sCD14-ST (AUC ¼ 77.2%), PCT þ sCD14-ST þ hs-CRP (AUC ¼ 77.0%) and PCT þ sCD14-ST (AUC ¼ 75.9%). Conclusion: hs-CRP, PCT, and sCD14-ST are independent predictors of paediatric sepsis due to their high prog- nostic values. Moreover, Bioscore combination of these biomarkers was significantly associated with increased odds for sepsis. The incorporation of these biomarkers into routine diagnostic tests will aid in prompt diagnosis of paediatric sepsis. en_US
dc.language.iso en en_US
dc.publisher Heliyon en_US
dc.title Individual and combined bioscore model of presepsin, procalcitonin, and high sensitive C - reactive protein as biomarkers for early diagnosis of paediatric sepsis en_US
dc.type Article en_US


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