کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2456409 | 1110540 | 2008 | 5 صفحه PDF | دانلود رایگان |

Samples from 75 clinically ill dogs were utilised in the study. APTT and PT tests were performed immediately on fresh citrated plasma samples (Fresh). The remaining plasma was stored at −20 °C for less than 4 months (n = 36 samples) or between 4 and 7 months (n = 39 samples). In batches of five, frozen samples were thawed rapidly and APTT and PT tests were performed on the thawed samples immediately (0RT) and after storage at room temperature (23 °C, range: 22–25 °C) for 24 h (24RT) and 48 h (48RT). The median APTT value from the (0RT) samples was significantly longer than that obtained from fresh samples (15 s vs. 13.2 s) but the PT value was not statistically different (7.8 s vs. 7.6 s). The median APTT (15 s) and PT (7.5 s) results from the (24RT) samples were not statistically different to those from the (0RT) samples (APTT: 15 s, PT: 7.6 s) but both tests were significantly longer (APTT: 16.5 s, PT: 9.2 s) from the (48RT) samples. We concluded that long term batching and freezing of clinical samples at −20 °C is acceptable for measurement of PT but not of APTT. We demonstrated that APTT and PT results do not change following storage of samples at room temperature for 24 h but storage for 48 h may lead to statistically and clinically significant changes (values at least 25% higher than the high value of the laboratory’s reference interval) in both clotting times.
Journal: Research in Veterinary Science - Volume 85, Issue 1, August 2008, Pages 166–170