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Protein C zymogen in adults with severe sepsis or septic shock
Crivellari, M; Silvetti, S; Gerli, C; Landoni, G; Franco, A; Bove, T; Pappalardo, F; Zangrillo, A.
Afiliación
  • Crivellari, M; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Silvetti, S; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Gerli, C; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Landoni, G; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Franco, A; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Bove, T; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Pappalardo, F; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
  • Zangrillo, A; San Raffaele Scientific Institute. Department of Anesthesia and Intensive Care. Milano. Italy
Med. intensiva (Madr., Ed. impr.) ; 38(5): 278-282, jun.-jul. 2014. ilus, tab
Article en En | IBECS | ID: ibc-126393
Biblioteca responsable: ES1.1
Ubicación: BNCS
RESUMEN

INTRODUCTION:

Activated protein C is associated with a risk of bleeding and its effects on survival in septic shock patients are questionable. Protein C zymogen has no risk of bleeding and improves the outcome of patients with septic shock. We hereby describe the largest published case series of adult patients receiving protein C zymogen. Design, setting and

participants:

A prospective study on 23 adult patients with severe sepsisor septic shock, two or more organ failures and at high risk for bleeding, treated with protein C zymogen (50 IU/kg bolus followed by continuous infusion of 3 IU/kg/h for 72 h).

RESULTS:

The Z-test evidenced a significant reduction between the expected mortality (53%)and the observed mortality 30% (Z value = 1.99, p = 0.046) in our sample population. Protein Clevels increased from 34 ± 18% to 66 ± 22% at 6 h after PC bolus (p < 0.001), and kept on increasing during 72 h of administration (p < 0.001 to baseline). Sequential Organ Failure Assessment(SOFA), score of organ dysfunction, decreased from baseline to 7 days after administration of protein C from 14 ± 2 to 7 ± 4 (p < 0.001). No adverse event drug related was noted.

CONCLUSION:

Protein C zymogen administration is safe and its use in septic patients should be investigated through a randomized controlled trial
Asunto(s)

Texto completo: 1 Colección: 06-national / ES Base de datos: IBECS Asunto principal: Choque Séptico / Proteína C / Sepsis Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Med. intensiva (Madr., Ed. impr.) Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 06-national / ES Base de datos: IBECS Asunto principal: Choque Séptico / Proteína C / Sepsis Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Med. intensiva (Madr., Ed. impr.) Año: 2014 Tipo del documento: Article
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