Serum Neutrophil Gelatinase-Associated Lipocalin: A Diagnostic Marker in Pediatric Sepsis.

Pediatr Crit Care Med

All authors: Department of Pediatrics, Faculty of Medicine, Menoufia University Hospital, Menoufia Governorate, Egypt.

Published: June 2017

AI Article Synopsis

  • Sepsis is a critical condition caused by the body’s extreme response to infection, and current detection methods for it are insufficient.
  • Researchers aimed to explore the potential of serum neutrophil gelatinase-associated lipocalin (NGAL) as a diagnostic and prognostic marker for sepsis in critically ill children, measuring its levels at admission and correlating it with clinical progress.
  • The study, conducted at Menoufia University Hospital, involved 120 critically ill children and revealed that NGAL levels are significantly higher in patients with sepsis compared to healthy controls, indicating its potential role in early sepsis diagnosis and assessing patient outcomes.

Article Abstract

Objectives: Sepsis is a life-threatening condition that arises when the response of the body to infection injures its own tissues and organs. The early prediction of sepsis by current clinical and laboratory methods remains inadequate. Serum neutrophil gelatinase-associated lipocalin level is increased in sepsis irrespective of renal dysfunction. Therefore, we aimed to correlate the serum neutrophil gelatinase-associated lipocalin value determined at admission with clinical progression and severity of disease in critically ill children and to declare its role as a potential diagnostic and prognostic marker for sepsis in critically ill children in the emergency department.

Design: A prospective cohort study.

Setting: The study carried out at the PICU of Menoufia University Hospital.

Patients: We serially enrolled 120 critically ill children admitted to the PICU at 2 fixed days per week in addition to 40 healthy children served as controls.

Interventions: Clinical examination was performed including calculation of the Pediatric Risk of Mortality and Pediatric Index of Mortality 2. Serum neutrophil gelatinase-associated lipocalin measurement was performed for patients at admission and for the controls. Patients were followed up for 30 days. The discriminatory power of neutrophil gelatinase- associated lipocalin was determined using the receiver-operating characteristic and other predictive likelihood values.

Measurements And Main Results: Serum neutrophil gelatinase-associated lipocalin level was significantly higher among the total patient cohort and those with sepsis than among the controls (p < 0.001), also in patients with systemic inflammatory response syndrome without sepsis and patients without systemic inflammatory response syndrome (p = 0.04 and <0.001). Furthermore, plasma level of neutrophil gelatinase-associated lipocalin was significantly elevated in nonsurvivors compared with survivors (p < 0. 001). Receiver-operating characteristic curve analysis exhibited an area under the curve of 0.84 for neutrophil gelatinase-associated lipocalin for diagnosis of sepsis, whereas C-reactive protein had an area under the curve of 0.79. Regarding the prognosis, neutrophil gelatinase-associated lipocalin had an area under the curve of 0.74 for prediction of mortality, whereas the area under the curve for Pediatric Risk of Mortality, Pediatric Index of Mortality 2, and C-reactive protein were 0.59, 0.58, and 0.62, respectively.

Conclusion: Overall, the data support the view that measurement at admission, serum neutrophil gelatinase-associated lipocalin results in substantial added value for early diagnosis and prognostication of sepsis in critically sick children.

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Source
http://dx.doi.org/10.1097/PCC.0000000000001186DOI Listing

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