Evaluation of serum NT-pCNP as a diagnostic and prognostic biomarker for sepsis in dogs

Background: There is a need for diagnostic biomarkers that can rapidly differentiate dogs with sepsis from dogs with non-infectious forms of systemic inflammatory response syndrome (NSIRS). Objectives: To compare serum NT-pCNP concentrations among dogs with various forms of sepsis, NSIRS, and health...

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Bibliographic Details
Published inJournal of veterinary internal medicine Vol. 25; no. 3; pp. 453 - 459
Main Authors DeClue, A.E, Osterbur, K, Bigio, A, Sharp, C.R
Format Journal Article
LanguageEnglish
Published Malden, USA J.B. Lippincott 01.05.2011
Blackwell Publishing Inc
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Summary:Background: There is a need for diagnostic biomarkers that can rapidly differentiate dogs with sepsis from dogs with non-infectious forms of systemic inflammatory response syndrome (NSIRS). Objectives: To compare serum NT-pCNP concentrations among dogs with various forms of sepsis, NSIRS, and healthy controls and to evaluate the use of serum NT-pCNP for the diagnosis of various forms of sepsis in dogs. Animals: One hundred and twelve dogs including 63 critically ill dogs (sepsis n = 29; NSIRS n = 34) and 49 healthy control dogs. Methods: Prospective clinical investigation. Serum samples were collected for NT-pCNP measurement from dogs with sepsis or NSIRS within 24 hours of intensive care unit admission or at the time of presentation for healthy dogs. Dogs with sepsis were subclassified based on the anatomic region of infection. Serum NT-pCNP concentrations were compared among sepsis, NSIRS and healthy groups as well as among sepsis subgroups. The area under the curve (AUC), sensitivity, and specificity for identifying dogs with sepsis were determined. Results: Using a cut-off value of 10.1 pmol/L, AUC, sensitivity, and specificity of NT-pCNP for differentiating dogs with sepsis from dogs with NSIRS or healthy control dogs were 0.71 (95% CI, 0.58–0.85), 65.5% (45.7–82.1%), and 89.2% (80.4–94.9%), respectively. Serum NT-pCNP had poor sensitivity for peritoneal sources of sepsis; AUC [0.92 (0.81–1.0)], sensitivity [94% (71–100%)], and specificity [89% (80–95%)] improved when these dogs were excluded. Serum NT-pCNP concentration was not associated with survival in the sepsis group. Conclusions and Clinical Importance: Serum NT-pCNP is a promising diagnostic biomarker for sepsis but is a poor indicator of septic peritonitis.
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ArticleID:JVIM713
This work was done at the College of Veterinary Medicine, Veterinary Medical Teaching Hospital, University of Missouri, Columbia, MO. A portion of these data were presented in abstract form at the 15th Annual International Veterinary Emergency and Critical Care Symposium, Chicago, IL and the 28th Annual American College of Veterinary Internal Medicine Forum, Anaheim, CA.
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ISSN:0891-6640
1939-1676
1939-1676
DOI:10.1111/j.1939-1676.2011.0713.x