Luisa Agnello , Fabio Del Ben , Andrea Cortegiani , Giuseppe Biundo , Aurora Giglia , Caterina Maria Gambino , Marcello Ciaccio
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引用次数: 0
Abstract
Aim
This study explores the value of midregional proadrenomedullin (mr-proADM), C-reactive protein (CRP), procalcitonin (PCT), and presepsin (PSP) in predicting mortality, considering both their absolute values at different time points and their dynamic kinetics.
Methods
We conducted a retrospective observational study including all consecutive adult ICU admissions. Biomarkers were measured at admission (T0), day 3 (T3), and day 5 (T5). We assessed absolute values, relative variations, and categorized changes (≥50 % increase or decrease).
Results
A total of 99 patients were included. mr-proADM at T3 had the highest predictive value for ICU mortality (AUC = 0.77), followed by PSP at T3 (AUC = 0.70). Cox regression identified mr-proADM at T3 as an independent predictor of mortality (HR: 1.16, p < 0.001), with a ≥ 50 % increase in mr-proADM from T0 to T3 significantly associated with mortality risk (HR: 4.15, p < 0.001). In patients with low baseline mr-proADM levels, a ≥ 50 % increase at T3 was significantly associated with mortality (HR: 4.43, p = 0.04), while in those with high baseline levels, the absolute value at T3 was more predictive.
Conclusion
Our findings suggest that mr-proADM at T3 is the most informative biomarker for predicting ICU mortality, with its absolute value and dynamic increase providing valuable prognostic insights. Importantly, stratified analysis highlights that different risk stratification approaches may be necessary based on baseline mr-proADM levels.
期刊介绍:
The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells.
The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.