Literature DB >> 16982493

Values of C-reactive protein, procalcitonin, and Staphylococcus-specific PCR in neonatal late-onset sepsis.

Imad R Makhoul1, Afeefi Yacoub, Tatiana Smolkin, Polo Sujov, Imad Kassis, Hannah Sprecher.   

Abstract

AIM: To evaluate the predictive value of relevant clinical and laboratory parameters (complete blood count (CBC), C-reactive protein (CRP), procalcitonin (PCT) and Staphylococcus-specific polymerase chain reaction (PCR)) in neonates with suspected late-onset sepsis (LOS).
METHODS: NICU neonates were prospectively followed for septic events. One hundred and eleven neonates developed 148 suspected septic events beyond 3 d of age. We recorded the clinical signs and laboratory abnormalities at onset of sepsis, serum CRP and PCT, Staphylococcus-specific PCR, microbiological data, and empiric antimicrobial therapy.
RESULTS: Variables significantly associated with subsequently confirmed LOS included hypotension (relative risk (RR) = 5.6, 95% CI 3.29-9.53), mechanical ventilation (RR = 2.46, 95% CI 1.24-4.86), immature/total neutrophil ratio (I/T) > 0.2 (RR = 5.13, 95% CI 2.54-10.31), CRP > 1.0 mg/dl (RR = 2.85, 95% CI 1.32-6.15), and small-for-gestational-age (SGA) status (RR = 2.13, 95% CI 1.03-4.38). PCT was not significantly associated with LOS. For detection of staphylococcal bacteremia, Staphylococcus-specific PCR showed: sensitivity 57.1%, specificity 94.7%, positive predictive value 53.3%, and negative predictive value 95.4%.
CONCLUSION: Hypotension, mechanical ventilation, I/T > 0.2, CRP > 1.0 mg/dl, and SGA status at onset of sepsis are significant predictors of proven neonatal LOS. Staphylococcus-specific PCR might be of value in ruling out staphylococcal sepsis.

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Year:  2006        PMID: 16982493     DOI: 10.1080/08035250600554250

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  10 in total

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Review 2.  Molecular microbiological methods in the diagnosis of neonatal sepsis.

Authors:  Mohan Venkatesh; Angela Flores; Ruth Ann Luna; James Versalovic
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Review 3.  Molecular assays for the diagnosis of sepsis in neonates.

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4.  Laboratory aid to the diagnosis and therapy of infection in the neonate.

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5.  Dependence of the severity of the systemic inflammatory response on resistance to hypoxia in male Wistar rats.

Authors:  Dzhuliia Sh Dzhalilova; Anna M Kosyreva; Mikhail E Diatroptov; Elena A Ponomarenko; Ivan S Tsvetkov; Natalia A Zolotova; Vladimir A Mkhitarov; Dmitry N Khochanskiy; Olga V Makarova
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6.  Prognostic nutrition index is associated with the all-cause mortality in sepsis patients: A retrospective cohort study.

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7.  Serum amyloid A, procalcitonin, tumor necrosis factor-alpha, and interleukin-1beta levels in neonatal late-onset sepsis.

Authors:  Birsen Ucar; Bilal Yildiz; M Arif Aksit; Coskun Yarar; Omer Colak; Yildiz Akbay; Ertugrul Colak
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8.  Performance of a Novel Molecular Method in the Diagnosis of Late-Onset Sepsis in Very Low Birth Weight Infants.

Authors:  Jonathan Davis; Sharon Christie; Derek Fairley; Peter Coyle; Richard Tubman; Michael D Shields
Journal:  PLoS One       Date:  2015-08-25       Impact factor: 3.240

9.  C-reactive protein for late-onset sepsis diagnosis in very low birth weight infants.

Authors:  Marc Beltempo; Isabelle Viel-Thériault; Roseline Thibeault; Anne-Sophie Julien; Bruno Piedboeuf
Journal:  BMC Pediatr       Date:  2018-01-30       Impact factor: 2.125

10.  Morphological Characteristics of the Thymus and Spleen and the Subpopulation Composition of Lymphocytes in Peripheral Blood during Systemic Inflammatory Response in Male Rats with Different Resistance to Hypoxia.

Authors:  Dzhuliia Sh Dzhalilova; Anna M Kosyreva; Mikhail E Diatroptov; Natalia A Zolotova; Ivan S Tsvetkov; Vladimir A Mkhitarov; Olga V Makarova; Dmitry N Khochanskiy
Journal:  Int J Inflam       Date:  2019-04-01
  10 in total

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