Monitoring oral anticoagulant treatment from plasma stored for up to 48 hours and frozen plasma.
Author(s): Grau E, Tenias JM, Olaso MA, Ferrando I, Juan MT, Pastor E, Perez A, Real E
Publication: Haematologica, 1999, Vol. 84, Page 633-6
PubMed ID: 10406906 PubMed Review Paper? No
Purpose of Paper
Conclusion of Paper
Studies
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Study Purpose
The purpose of this study was to determine the effects of storage temperature and duration and thromboplastin reagent and analyzer on PT, INR, and factor II, VII, IX, and X activity in plasma from patients on acenocoumarol therapy. Blood was collected into tubes containing 3.2% citrate, and plasma was analyzed immediately, refrigerated for 24 or 48 h before analysis, or frozen at -40 degrees C for less than 1 month before analysis.
Summary of Findings:
Only slight reductions in factor II, VII, IX, and X activity were noted when plasma was refrigerated for 24 h or frozen, but significant reductions in factor VII and IX activity were observed after 48 h or refrigeration compared to fresh plasma. Regardless of instrumentation or reagent, there were no significant differences in INRs between fresh plasma and plasma that had been refrigerated for 24 h or frozen. Correlations between INRs (calculated using PT) in fresh plasma and those of plasma that had been refrigerated for 24 or 48 h, or frozen for less than 1 month varied based on the instrumentation and thromboplastin reagent used. When Thromboplastin IS was used with the Sysmex CA-6000, correlations were very strong (0.94-0.98) between INRs of fresh plasma and refrigerated or frozen plasma. When Simplastin was used with the Thrombolyzer Chrom, correlations were very strong between INRs of fresh plasma and plasma refrigerated for 24 h (0.95) or frozen plasma (0.92), but only a modest correlation was observed between the INR or fresh plasma and plasma that had been refrigerated for 48 h (0.50). A similar phenomenon was observed when Thromborel was used with the ACL 6000, with correlations of 0.91, 0.55, and 0.98 between INRs or fresh plasma and those of plasma that had been refrigerated for 24 h, 48 h, or frozen, respectively. When Thromboplastin D+G was used with the ACL 6000, strong correlations were observed between INRs of fresh plasma and plasma that had been refrigerated for 24 h or 48 h (0.85 and 0.81, respectively), while a very strong correlation was observed between the INRs of fresh and frozen plasma (0.97).
Biospecimens
Preservative Types
- Frozen
- None (Fresh)
- Other Preservative
Diagnoses:
- Other diagnoses
Platform:
Analyte Technology Platform Morphology Hematology/ auto analyzer Protein Hematology/ auto analyzer Pre-analytical Factors:
Classification Pre-analytical Factor Value(s) Preaquisition Diagnosis/ patient condition Atrial fibrillation
Valvular prosthesis
Cardiomyopathy
Venous thromboembolism
Biospecimen Preservation Type of fixation/preservation Frozen
None (fresh)
Refrigeration
Storage Storage temperature 2-8 degrees C
-40 degrees C
Storage Storage duration 0 h
24 h
48 h
<1 month
Hematology/ auto analyzer Specific Reaction solution Thromboplastin IS
Simplastin
Thromborel
Thromboplastin D+G
Hematology/ auto analyzer Specific Technology platform Sysmex CA-6000
Thrombolyzer Chrom
ACL 6000