ABSTRACT
The application of the erythrocyte sedimentation rate (ESR) in feline medicine is currently unavailable, while in canine medicine it has been rediscovered due to the introduction of an automated ESR device. Our aims were to (1) define the reference interval (RI) of the ESR in healthy cats, (2) evaluate the ESR values between healthy and ill cats, (3) evaluate relationships between the ESR and some inflammatory markers, and (4) assess ESR changes in different durations of illness (acute, chronic, or acute-on-chronic). A prospective multicentric cohort study on 200 client-owned cats: 57 healthy cats and 143 ill cats for the other aims. Healthy cats were blood donors, or young cats underwent desexing procedures. Ill cats with full clinical medical records, hematobiochemical profiles, and diagnostic procedures to reach a final diagnosis were included. The ESR was performed with MINI-PET using the same K3-EDTA tubes used for CBC, with no additional sample required. The total leukocyte count (WBC), neutrophil-to-lymphocyte ratio (NLR), fibrinogen, serum amyloid A, and albumin/globulin ratio (A/G) were concurrently measured. Based on the clinical presentation and the final diagnosis, cats were classified as having the following: acute, chronic, and acute-on-chronic conditions. The RI of the ESR ranged between 1 and 23 mm/h. Ill cats showed a significantly higher ESR (median 29 mm/h; range 12-46 mm/h) than healthy cats (median 10 mm/h; range 1-12 mm/h; p < 0.0001). The ESR was positively correlated only with fibrinogen (p < 0.001; r = 0.43). Cats with acute-on-chronic diseases had the highest ESR (median 47 mm/h; range 35-56 mm/h) compared with acute (median 16 mm/h; range 14-42 mm/h; p=0.003) and chronic cats (median 14 mm/h; range 10-31 mm/h; p < 0.0001). Although further studies are needed, the ESR could be a useful ancillary inflammatory marker in cats, specifically in cats with acute diseases, with or without an underlying chronic condition.
ABSTRACT
We aimed to test the influence of storage temperature and time for canine and feline ESR. Forty dogs and 12 cats were included and randomly allocated in "room temperature" and "refrigerated" groups. Both groups had the T0 ESR measures few minutes after complete blood count. Afterwards, room temperature group had ESR measured at 2, 4, 6 and 8h after T0, whereas the "refrigerated" group had the blood sample stored at 4-6°C for 24 and then T24h ESR was measured. In each ESR measurement, [1] blood samples were put on a tube rocker waiting for ESR analysis; [2] before inserting the blood tube in the MINI-PET ESR instrument, samples were gently mixed again by complete inversion 10 times; (3) each mixed blood tube was inserted in the one of the four MINI-PET tubes position; (4) on the machine display, patient's species has to be chosen and the 14 minutes countdown started; (5) after the 14 minutes optical reading, the ESR result (mm/h) is displayed on the machine. ESR of canine samples at room temperature were significantly stable until T6, while feline samples remained stable at T8. After 24h at refrigerated temperature, both canine and feline samples were stable. ⢠MINI-PET is an ESR automatic continuous-loading instrument that can analyze up to four EDTA blood samples simultaneously using an optical system that measures the erythrocytes sedimentation level ⢠We aimed to test influence of storage temperature and time for canine and feline ESR ⢠At room temperature, dogs' samples were stable within 6 hours from collection, and cats' samples were stable until 8h. At refrigerated temperature, there was no difference in T0-T24 ESR in both canine and feline samples.