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Procalcitonin kinetics in critically ill children: impact of continuous kidney replacement therapy modality and dose
Arife Ufacık Yöndem1, Servet Yüce2, Emrullah Aygüler3
1Department of Pediatrics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Insights
In critically ill children on continuous kidney replacement therapy (CKRT), procalcitonin (PCT) levels do not significantly change due to CKRT itself. PCT reliably reflects infection or inflammation during early pediatric CKRT.
Area of Science:
- Pediatric Critical Care Medicine
- Nephrology
- Infectious Diseases
Background:
- Acute kidney injury (AKI) is prevalent in critically ill children, often requiring continuous kidney replacement therapy (CKRT).
- Procalcitonin (PCT) is a key infection biomarker, but its behavior during pediatric CKRT is not well understood.
- Limited and inconsistent adult data exist on PCT clearance by extracorporeal circuits.
Purpose of the Study:
- To investigate the short-term kinetics of procalcitonin (PCT) in critically ill children undergoing continuous kidney replacement therapy (CKRT).
- To determine if CKRT parameters influence PCT levels in pediatric patients.
- To assess the reliability of PCT for infection monitoring in this population.
Main Methods:
- Prospective observational study of 40 critically ill children receiving CKRT.
- Serum PCT levels measured at CKRT initiation, 12 hours, and 24 hours.
- Analysis of PCT kinetics in relation to CKRT modality, effluent dose, and membrane type.
Main Results:
- Median PCT levels showed no statistically significant changes from CKRT initiation to 24 hours (p=0.68).
- PCT trajectories were independent of CKRT modality, effluent dose, or membrane type.
- No correlation was observed between effluent dose and PCT changes.
Conclusions:
- Short-term PCT dynamics in pediatric CKRT are primarily influenced by underlying sepsis or inflammation, not CKRT parameters.
- PCT reliably supports infection monitoring and antibiotic stewardship during the initial phase of pediatric CKRT.
- Further research is needed to explore long-term PCT behavior and prognostic value in this context.
Background:
Acute kidney injury (AKI) is common in critically ill children, frequently necessitating continuous kidney replacement therapy (CKRT). Procalcitonin (PCT) is widely used as an infection biomarker, yet its interpretation during CKRT remains unclear. Adult data regarding extracorporeal clearance of PCT are inconsistent, while pediatric evidence is limited.
Methods:
In this prospective observational study (May 2021-October 2023), 40 critically ill children receiving CKRT in a tertiary PICU were enrolled. Serum PCT was measured at CKRT initiation (T0), 12 h (T12), and 24 h (T24). CKRT modalities (CVVH, CVVHD, CVVHDF), effluent doses, and membrane types (PS, PAES, AN69-ST) were recorded. PCT kinetics were analyzed using non-parametric tests, with correlation assessed by Spearman's rank.
Results:
Median baseline PCT was 3.6 ng/mL (IQR 0.5-27.2), rising to 7.4 (0.6-29.5) at T12 and stabilizing at 7.7 (0.6-30.5) at T24. Differences across time points were not statistically significant (p = 0.68). PCT trajectories were unaffected by CKRT modality, effluent dose, or membrane type, and no correlation was found between effluent dose and PCT changes. Stratification by high versus low effluent dosing revealed no significant differences. CKRT-related complications occurred in 17.5%, mainly filter clotting, without influencing PCT. PICU mortality was 35%, reflecting illness severity rather than CKRT.
Conclusions:
In pediatric CKRT, short-term PCT dynamics are driven by the underlying septic or inflammatory process rather than CKRT parameters. PCT typically peaks within 12 h of CKRT initiation and then stabilizes, supporting its reliability for infection monitoring and antibiotic stewardship during early CKRT. Larger studies are warranted to define long-term PCT behavior and prognostic utility.
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