Evidence map›Paper›PMID 41670654›Full record

Observational studyPediatric nephrology (Berlin, Germany)2026

Procalcitonin kinetics in critically ill children: impact of continuous kidney replacement therapy modality and dose.

Arife Ufacık Yöndem, Servet Yüce, Emrullah Aygüler, Ali Genco Gencay, Demet Demirkol

Abstract readObservational Study
In one paragraph

Observational study in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Arife Ufacık YöndemDepartment of Pediatrics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-7116-4841
Servet YüceDepartment of Public Health, Istanbul Provincial Health Directorate, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-5264-3038
Emrullah AygülerDepartment of Pediatric Intensive Care, Istanbul Faculty of Medicine, Istanbul University, Millet Cad. Fındıkzade, Topkapı, Istanbul, 34093, Turkey.ORCID http://orcid.org/0000-0002-5017-2260
Ali Genco GencayDepartment of Pediatric Intensive Care, Istanbul Faculty of Medicine, Istanbul University, Millet Cad. Fındıkzade, Topkapı, Istanbul, 34093, Turkey.ORCID http://orcid.org/0000-0001-5236-3557
Demet DemirkolDepartment of Pediatric Intensive Care, Istanbul Faculty of Medicine, Istanbul University, Millet Cad. Fındıkzade, Topkapı, Istanbul, 34093, Turkey. ddemirkol@istanbul.edu.tr.ORCID http://orcid.org/0000-0001-9578-9267

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute 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.

methodsIn 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.

resultsMedian 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.

conclusionsIn 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.

Indexed as

Acute Kidney InjuryContinuous Renal Replacement TherapyProcalcitoninBiomarkersChildChild, PreschoolCritical IllnessFemaleHumansInfantIntensive Care Units, PediatricMaleProspective StudiesBiomarkersProcalcitoninAcute kidney injuryContinuous kidney replacement therapyCritically ill childrenPediatric intensive careProcalcitoninSepsis

Identifiers

PMID41670654
PMCPMC13197258

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.