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Deleterious effects of plasma-derived cellular debris in a porcine model of hemorrhagic shock.
Buckley, Colin T; Lee, Yannleei L; Michele Schuler, A; Langley, Raymond J; Kutcher, Matthew E; Barrington, Robert; Audia, Jonathon P; Simmons, Jon D.
Afiliação
  • Buckley CT; Department of Surgery, University of South Alabama, Mobile, AL, United States.
  • Lee YL; Department of Surgery, University of South Alabama, Mobile, AL, United States.
  • Michele Schuler A; Department of Comparative Medicine, University of South Alabama, United States; Department of Microbiology and Immunology, University of South Alabama, United States.
  • Langley RJ; Department of Cellular & Molecular Pharmacology, University of South Alabama, United States.
  • Kutcher ME; Department of Surgery, University of Mississippi, United States.
  • Barrington R; Department of Microbiology and Immunology, University of South Alabama, United States.
  • Audia JP; Department of Microbiology and Immunology, University of South Alabama, United States.
  • Simmons JD; Department of Surgery, University of South Alabama, Mobile, AL, United States; Department of Cellular & Molecular Pharmacology, University of South Alabama, United States. Electronic address: jdsimmons@health.southalabama.edu.
Injury ; 55(5): 111300, 2024 May.
Article em En | MEDLINE | ID: mdl-38160196
ABSTRACT

BACKGROUND:

Recent studies identify large quantities of inflammatory cellular debris within Fresh Frozen Plasma (FFP). As FFP is a mainstay of hemorrhagic shock resuscitation, we used a porcine model of hemorrhagic shock and ischemia/reperfusion to investigate the inflammatory potential of plasma-derived cellular debris administered during resuscitation.

METHODS:

The porcine model of hemorrhagic shock included laparotomy with 35 % hemorrhage (Hem), 45 min of ischemia from supraceliac aortic occlusion with subsequent clamp release (IR), followed by protocolized resuscitation for 6 h. Cellular debris (Debris) was added to the resuscitation phase in three groups. The four groups consisted of Hem + IR (n = 4), Hem + IR + Debris (n = 3), Hem + Debris (n = 3), and IR + Debris (n = 3). A battery of laboratory, physiologic, cytokine, and outcome data were compared between groups.

RESULTS:

As expected, the Hem + IR group showed severe time dependent decrements in organ function and physiologic parameters. All animals that included both IR and Debris (Hem + IR + Debris or IR + Debris) died prior to the six-hour end point, while all animals in the Hem + IR and Hem + Debris survived. Cytokines measured at 30-60 min after initiation of resuscitation revealed significant differences in IL-18 and IL-1ß between all groups.

CONCLUSIONS:

Ischemia and reperfusion appear to prime the immune system to the deleterious effects of plasma-derived cellular debris. In the presence of ischemia and reperfusion, this model showed the equivalency of 100 % lethality when resuscitation included quantities of cellular debris at levels routinely administered to trauma patients during transfusion of FFP. A deeper understanding of the immunobiology of FFP-derived cellular debris is critical to optimize resuscitation for hemorrhagic shock.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Hemorrágico Limite: Animals / Humans Idioma: En Revista: Injury Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Hemorrágico Limite: Animals / Humans Idioma: En Revista: Injury Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos