Author: Viitanen, S.J.; Lappalainen, A.K.; Christensen, M.B.; Sankari, S.; Rajamäki, M.M.
Title: The Utility of Acute-Phase Proteins in the Assessment of Treatment Response in Dogs With Bacterial Pneumonia Document date: 2016_12_29
ID: tchf7pb2_11
Snippet: Hematology, serum biochemistry, arterial blood gas analysis, blood cultures, and fecal analysis along with cytological and microbiological analysis of respiratory samples were performed as previously described. 18 Coagulation parameters prothrombin time (PT) and activated partial thromboplastin time (aPTT) were evaluated with commercial test kits for dogs, a,b . Serum samples obtained for APP analysis either were immediately analyzed or stored at.....
Document: Hematology, serum biochemistry, arterial blood gas analysis, blood cultures, and fecal analysis along with cytological and microbiological analysis of respiratory samples were performed as previously described. 18 Coagulation parameters prothrombin time (PT) and activated partial thromboplastin time (aPTT) were evaluated with commercial test kits for dogs, a,b . Serum samples obtained for APP analysis either were immediately analyzed or stored at À80°C until analyzed. [38] [39] [40] CRP was analyzed by magnetic permeability-based immunoassay c validated for dogs. 41 Creactive protein values below the detection limit for the CRP assay (<10 mg/L) were set at 5 mg/L. Results above the upper detection limit for the assay (>210 mg/L) were set at 211 mg/L. A CRP ratio (CRP concentrations at 24, 48, and 72 hour divided by the initial concentration), describing the decrease in CRP during early recovery, was calculated after initiation of treatment in dogs with samples available for the time point in question. Samples for SAA analysis were sent on dry ice to an external laboratory d and measured by an automated e latex agglutination test f validated for dogs. 42 Haptoglobin was measured by a commercial colorimetric method g validated for dogs. 43
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