Prognostic value of combined platelet and fibrinogen levels on mortality in pediatric patients with sepsis
- Journal
- Annals of medicine (Q1)
- Published
- 17 August 2026
- Study design
- Prospective / inception cohort
- Evidence level
- Level 2, Moderate (CEBM 2b)
- Authors
- Wei Zhao, Lijian Chen, Yang Liu, Guanxue Li, Mengyao Li, Zhijiang Chen, et al.
- PMID
- 42608955
- DOI
- 10.1080/07853890.2026.2715785
Why clinicians should know about it
- Picked for Critical Care and Intensive Care Medicine (paper of the day, 19 August 2026): Platelet + fibrinogen prognostic value in pediatric sepsis
Abstract
BACKGROUND: Sepsis causes high mortality in pediatric intensive care units (PICUs), often involving coagulation dysfunction. While platelets and fibrinogen are crucial, their combined prognostic value in pediatric sepsis remains unclear. We investigated their additive utility on in-PICU mortality. METHODS: This retrospective cohort study included 282 pediatric sepsis patients admitted to the Zhujiang Hospital PICU (June 2022-December 2024). Multivariable Cox regression evaluated biomarkers continuously and categorically based on admission levels: platelets (cutoff: 150×109/L) and fibrinogen (cutoff: 2 g/L). Patients formed four combined groups: high/high (HPHF), high/low, low/high, and low/low (LPLF) platelets/fibrinogen. RESULTS: Decreased platelet and fibrinogen levels independently increased mortality risk (HR: 1.89, 95% CI: 1.16-3.06; and HR: 1.55, 95% CI: 1.08-2.24 per standard deviation). Categorically, low platelets (<150×109/L) and low fibrinogen (<2 g/L) independently predicted mortality (HR: 2.67, 95% CI: 1.29-5.51; HR: 1.98, 95% CI: 1.01-3.89). The LPLF group had significantly higher mortality than HPHF (HR: 4.05, 95% CI: 1.62-10.11). No significant interaction was observed. These associations were primarily significant in children ≥2 years. CONCLUSIONS: Low platelet and fibrinogen levels at PICU admission independently predict mortality in pediatric sepsis. Their concurrent assessment provides additive prognostic value for early risk stratification, especially in children ≥2 years. Prospective multicenter validation is warranted.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.