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The PRORATA trial evaluated a procalcitonin-guided strategy for starting and stopping antibiotics in critically ill adults with suspected bacterial infection. The goal was to reduce unnecessary antimicrobial exposure without increasing mortality or recurrent infection. The trial showed that biomarker-guided treatment could reduce antibiotic exposure while maintaining comparable clinical outcomes. Procalcitonin was used within a predefined algorithm rather than interpreted in isolation. This is important for modern antimicrobial stewardship because prolonged antibiotic courses can drive toxicity and selection of multidrug-resistant organisms. At the same time, biomarkers are imperfect and should not be allowed to override obvious clinical evidence of ongoing infection or inadequate source control. CritiCARE 2026 explicitly discusses antibiotic stewardship, procalcitonin and antibiotic dosing in AKI, making this study highly relevant. For HCPs, the practical use of procalcitonin is as a structured aid to reassess whether continued antibiotics remain necessary. The strongest approach combines the trajectory of the patient, microbiology, source-control status, organ function and biomarker trends. The trial therefore supports a stewardship mindset: every antibiotic course should have a reassessment plan, an indication for continuation and a stopping decision.

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The PRORATA trial evaluated a procalcitonin-guided strategy for starting and stopping antibiotics in critically ill adults with suspected bacterial infection. The goal was to reduce unnecessary antimicrobial exposure without increasing mortality or recurrent infection. The trial showed that biomarker-guided treatment could reduce antibiotic exposure while maintaining comparable clinical outcomes. Procalcitonin was used within a predefined algorithm rather than interpreted in isolation. This is important for modern antimicrobial stewardship because prolonged antibiotic courses can drive toxicity and selection of multidrug-resistant organisms. At the same time, biomarkers are imperfect and should not be allowed to override obvious clinical evidence of ongoing infection or inadequate source control. CritiCARE 2026 explicitly discusses antibiotic stewardship, procalcitonin and antibiotic dosing in AKI, making this study highly relevant. For HCPs, the practical use of procalcitonin is as a structured aid to reassess whether continued antibiotics remain necessary. The strongest approach combines the trajectory of the patient, microbiology, source-control status, organ function and biomarker trends. The trial therefore supports a stewardship mindset: every antibiotic course should have a reassessment plan, an indication for continuation and a stopping decision.
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