Observational studyEuropean journal of pediatrics2026
Comparison of standard care versus a biomarker algorithm to guide antibiotic stewardship in pediatric intensive care unit: a prospective observational cohort study with historical control (the BASIP study).
Observational study in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Nano-Enabled Microfluidic Platforms for Functional Immunomonitoring in Pediatric Sepsis.International journal of nanomedicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The purpose of this study is to evaluate the effectiveness and safety of an integrated antimicrobial stewardship approach in critically ill children with suspected infection admitted to a pediatric intensive care unit (PICU). The approach combined procalcitonin (PCT)-guided decision-making with serial clinical and microbiological assessment to reduce antibiotic duration. Secondary aims included evaluating additional biomarkers, such as pancreatic stone protein (PSP) and C-reactive protein (CRP) in the context of antibiotic de-escalation. This prospective observational cohort study with historical control was conducted in a tertiary PICU. PCT and pediatric Sequential Organ Failure Assessment (p-SOFA) scores were assessed at baseline, 48-72 h, and 5-7 days. Microbiological samples were obtained before initiation of empirical antibiotic therapy and repeated when clinically indicated. Antibiotic decisions were made through multidisciplinary reassessment and were based on predefined PCT thresholds integrated with microbiological findings and clinical status. PSP and CRP were measured. Fifty-three children were prospectively enrolled. Median days of therapy (DOT) were lower compared with the historical cohort (10 days [IQR 5-16] vs. 16 days [IQR 7-29]). No increase in short-term adverse outcomes was observed. Restart of intravenous antibiotics or PICU readmission within 7 days occurred in 7.1% of cases. PCT levels differed significantly between confirmed and nonconfirmed bacterial infections (p = 0.001) and were associated with decisions regarding antibiotic de-escalation or discontinuation. CRP and PSP did not demonstrate statistically significant discriminatory capacity.
conclusionImplementation of a structured PCT-guided reassessment algorithm within an antimicrobial stewardship framework was feasible and associated with reduced antibiotic exposure without apparent safety concerns. WHAT IS KNOWN: • Antimicrobial stewardship programs (AMS) are essential to reduce unnecessary antibiotic use and prevent antimicrobial resistance, especially in pediatric intensive care settings. • Although procalcitonin (PCT) has been validated in adult studies to guide antibiotic discontinuation, its integration into pediatric clinical decision-making remains poorly explored. WHAT IS NEW: • This study evaluates a real-world implementation of a PCT-based reassessment algorithm in a tertiary PICU in critically ill children. • An integrated, biomarker-guided algorithm using procalcitonin, alongside clinical and microbiological evaluation was associated with reduced antibiotic exposure without short-term safety signals.
Indexed as
Identifiers
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Registered trials
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.