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- Melissa Austin, MD⇑
- Chris Ferrell, MT(ASCP)
- Morayma Reyes, MD, PhD
- Address for Correspondence: Melissa Austin, MD, Resident in Anatomic and Clinical Pathology, Departments of Pathology and Laboratory Medicine, University of Washington Medical Center, Seattle, WA, (206) 598-6400, mcaustin{at}uw.edu
Abstract
The Clinical and Laboratory Standards Institute guidelines require special processing of whole blood specimens with hematocrits greater than 55% due to the possibility of spurious prolongation of routine coagulation studies (PT, aPTT). As samples with hematocrits above 60% are rare at our institution, our study seeks to determine the effect of relative citrate excess on routine coagulation studies in samples with hematocrits of 60% to determine whether special processing is necessary. A calculated volume of 3.2% citrate was added to 1 mL aliquots of 40 whole blood samples in citrated tubes from adult patients to simulate a hematocrit of 60%. A dilutional control was created by adding an equivalent volume of saline to a separate 1 mL aliquot. Routine coagulation studies (PT, aPTT) were run on both samples on the STA Compact Analyzer in accordance with manufacturer instructions. While a paired Student's t-test demonstrated a clinically significant change in both PT and aPTT with the addition of citrate (p = 0.0002 for PT and p = 0.0234 for aPTT), clinical management would not have been altered by any observed change. More interestingly, we observed a shortening of 27/40 PTs and 23/40 aPTTs rather than the expected prolongation. Based on our data, no adjustment of citrate volume appears to be necessary in samples with hematocrits less than or equal to 60%.
ABBREVIATIONS: CLSI - Clinical and Laboratory Standards Institute, PT - prothrombin time, aPTT - activated partial thromboplastin time, CBC - Complete Blood Count
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