ŽUREK, Jiří, Michal KÝR, Martin VAVŘINA a Michal FEDORA. Pancreatic stone protein – A possible biomarker of multiorgan failure and mortality in children sepsis. Cytokine. Academic Press, 2014, roč. 66, č. 2, s. 106-111. ISSN 1043-4666. Dostupné z: https://dx.doi.org/10.1016/j.cyto.2014.01.009.
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Základní údaje
Originální název Pancreatic stone protein – A possible biomarker of multiorgan failure and mortality in children sepsis
Autoři ŽUREK, Jiří (203 Česká republika, garant, domácí), Michal KÝR (203 Česká republika, domácí), Martin VAVŘINA (203 Česká republika, domácí) a Michal FEDORA (203 Česká republika, domácí).
Vydání Cytokine, Academic Press, 2014, 1043-4666.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30209 Paediatrics
Stát vydavatele Velká Británie a Severní Irsko
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.664
Kód RIV RIV/00216224:14110/14:00075154
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/j.cyto.2014.01.009
UT WoS 000333729200003
Klíčová slova anglicky Children; Mortality; Pancreatic stone protein; Regenerating protein 1 alpha; Sepsis
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Mgr. Věra Pospíšilíková, učo 9005. Změněno: 9. 7. 2014 12:17.
Anotace
Pancreatic stone protein is associated with infection. Pancreatic stone protein did not differ between SIRS and sepsis. Pancreatic stone protein levels were higher in patients who died. Pancreatic stone protein (PSP)/regenerating protein 1-alpha (reg) is associated with inflammation, infection, and other disease-related stimuli. The prognostic value of PSP/. reg among critically ill pediatric patients is unknown. The aim of this pilot study was to evaluate PSP/. reg in children with systemic inflammatory response syndrome or sepsis.Prospective observational study, a five day evaluation period in children 0-19. years old with systemic inflammatory response syndrome or septic state. Blood tests to determine levels of PSP/. reg were obtained as long as the patient met the criteria for systemic inflammatory response syndrome or sepsis.PSP/. reg levels did not differ between patients with systemic inflammatory response syndrome and septic condition until organ dysfunction signs were present. PSP/. reg levels were significantly higher in patients with a PELOD score of 12 or higher or in those with MODS. Patients who died tended to have higher PSP/. reg levels.
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