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Serial Measurements of Protein Biomarkers in Sepsis-Induced Acute Respiratory Distress Syndrome.
Yang, Philip; Iffrig, Elizabeth; Harris, Frank; Holder, Andre L; Martin, Greg S; Esper, Annette M.
Afiliación
  • Yang P; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University and Grady Memorial Hospital, Atlanta, GA.
  • Iffrig E; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University and Grady Memorial Hospital, Atlanta, GA.
  • Harris F; Department of Pediatrics, Emory University, Atlanta, GA.
  • Holder AL; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University and Grady Memorial Hospital, Atlanta, GA.
  • Martin GS; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University and Grady Memorial Hospital, Atlanta, GA.
  • Esper AM; Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University and Grady Memorial Hospital, Atlanta, GA.
Crit Care Explor ; 4(10): e0780, 2022 Oct.
Article en En | MEDLINE | ID: mdl-36284549
ABSTRACT
The role of early, serial measurements of protein biomarkers in sepsis-induced acute respiratory distress syndrome (ARDS) is not clear.

OBJECTIVES:

To determine the differences in soluble receptor for advanced glycation end-products (sRAGEs), angiopoietin-2, and surfactant protein-D (SP-D) levels and their changes over time between sepsis patients with and without ARDS. DESIGN SETTING AND

PARTICIPANTS:

Prospective observational cohort study of adult patients admitted to the medical ICU at Grady Memorial Hospital within 72 hours of sepsis diagnosis. MAIN OUTCOMES AND

MEASURES:

Plasma sRAGE, angiopoietin-2, and SP-D levels were measured for 3 consecutive days after enrollment. The primary outcome was ARDS development, and the secondary outcome of 28-day mortality. The biomarker levels and their changes over time were compared between ARDS and non-ARDS patients and between nonsurvivors and survivors.

RESULTS:

We enrolled 111 patients, and 21 patients (18.9%) developed ARDS. The three biomarker levels were not significantly different between ARDS and non-ARDS patients on all 3 days of measurement. Nonsurvivors had higher levels of all three biomarkers than did survivors on multiple days. The changes of the biomarker levels over time were not different between the outcome groups. Logistic regression analyses showed association between day 1 SP-D level and mortality (odds ratio, 1.52; 95% CI, 1.03-2.24; p = 0.03), and generalized estimating equation analyses showed association between angiopoietin-2 levels and mortality (estimate 0.0002; se 0.0001; p = 0.04). CONCLUSIONS AND RELEVANCE Among critically ill patients with sepsis, sRAGE, angiopoietin-2, and SP-D levels were not significantly different between ARDS and non-ARDS patients but were higher in nonsurvivors compared with survivors. The trend toward higher levels of sRAGE and SP-D, but not of angiopoietin-2, in ARDS patients may indicate the importance of epithelial injury in sepsis-induced ARDS. Changes of the biomarker levels over time were not different between the outcome groups.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Crit Care Explor Año: 2022 Tipo del documento: Article País de afiliación: Gabón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Crit Care Explor Año: 2022 Tipo del documento: Article País de afiliación: Gabón