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Plasma secretory phospholipase A2 as an early marker for late‐onset sepsis in preterm infants—a pilot study
Journal article   Peer reviewed

Plasma secretory phospholipase A2 as an early marker for late‐onset sepsis in preterm infants—a pilot study

J. Hibbert, N.J. Armstrong, C. Granland, S. Ng, K. Simmer, P. Richmond, D. Burgner, T. Strunk and A. Currie
Acta Paediatrica, Vol.110(11), pp.3011-3013
2021

Abstract

Preterm infants are particularly susceptible to bacterial late-onset sepsis (LOS). Diagnosis by blood culture and inflammatory markers have sub-optimal sensitivity and specificity and prolonged reporting times. There is an urgent need for more rapid, accurate adjunctive diagnostics in LOS to improve management and minimise antibiotic exposure. We measured the diagnostic performance of secretory phospholipase A2 type IIA (sPLA2-IIA) in very preterm infants (<30 weeks gestational age) with suspected LOS. Plasma sPLA2-IIA levels were elevated in infants with LOS (n = 28) compared to those without LOS (n = 21; median 30,970 vs. 2534 pg/ml, p < 0.0001). The mean area under the curve was 0.884 (95% CI: 0.771, 0.977) with a sensitivity of 0.907 (95% CI: 0.667, 1.00) and specificity of 0.804 (95% CI: 0.600, 1.00). The positive and negative predictive values were 0.833 (95% CI: 0.664, 0.927) and 0.842 (95% CI: 0.624, 0.945), respectively. This pilot study suggests that sPLA2-IIA may have clinical utility for the early diagnosis of LOS in very preterm infants, potentially informing clinical management and antibiotic stewardship.

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Collaboration types
Industry collaboration
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.23 Antibiotics & Antimicrobials
1.23.1757 Group B Streptococcus
Web Of Science research areas
Pediatrics
ESI research areas
Clinical Medicine
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