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Point-of-care pancreatic stone protein measurement in critically ill COVID-19 patients.
Melegari, Gabriele; Giuliani, Enrico; Di Pietro, Giulia; Alberti, Francesco; Campitiello, Mattia; Bertellini, Elisabetta; Barbieri, Alberto.
Afiliação
  • Melegari G; Department of Anaesthesia and Intensive Care, Azienda Ospedaliero Universitaria Di Modena, Modena, Italy. melegari.gabriele@gmail.com.
  • Giuliani E; Neuron Guard Ltd, Cambridge, UK.
  • Di Pietro G; School of Anaesthesia and Intensive Care, University of Modena and Reggio Emilia, Modena, Italy.
  • Alberti F; School of Anaesthesia and Intensive Care, University of Modena and Reggio Emilia, Modena, Italy.
  • Campitiello M; School of Anaesthesia and Intensive Care, University of Modena and Reggio Emilia, Modena, Italy.
  • Bertellini E; Department of Anaesthesia and Intensive Care, Azienda Ospedaliero Universitaria Di Modena, Modena, Italy.
  • Barbieri A; School of Anaesthesia and Intensive Care, University of Modena and Reggio Emilia, Modena, Italy.
BMC Anesthesiol ; 23(1): 226, 2023 06 30.
Article em En | MEDLINE | ID: mdl-37391718
ABSTRACT

INTRODUCTION:

Pancreatic stone protein (PSP) is a novel biomarker that is reported to be increased in pneumonia and acute conditions. The primary aim of this study was to prospectively study plasma levels of PSP in a COVID-19 intensive care unit (ICU) population to determine how well PSP performed as a marker of mortality in comparison to other plasma biomarkers, such as C reactive protein (CRP) and procalcitonin (PCT).

METHODS:

We collected clinical data and blood samples from COVID-19 ICU patients at the time of admission (T0), 72 h later (T1), five days later (T2), and finally, seven days later. The PSP plasma level was measured with a point-of-care system; PCT and CRP levels were measured simultaneously with laboratory tests. The inclusion criteria were being a critical COVID-19 ICU patient requiring ventilatory mechanical assistance.

RESULTS:

We enrolled 21 patients and evaluated 80 blood samples; we found an increase in PSP plasma levels according to mixed model analysis over time (p < 0.001), with higher levels found in the nonsurvivor population (p < 0.001). Plasma PSP levels achieved a statistically significant result in terms of the AUROC, with a value higher than 0.7 at T0, T1, T2, and T3. The overall AUROC of PSP was 0.8271 (CI (0.73-0.93), p < 0.001). These results were not observed for CRP and PCT.

CONCLUSION:

These first results suggest the potential advantages of monitoring PSP plasma levels through point-of-care technology, which could be useful in the absence of a specific COVID-19 biomarker. Additional data are needed to confirm these results.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: COVID-19 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: BMC Anesthesiol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: COVID-19 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: BMC Anesthesiol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália