Background and aim: Blood transfusion plays a critical
role in modern medicine, ensuring the availability of safe and viable blood
products for patients in need. In a special medical condition like
coagulopathies, a fresh whole blood or stored FFP are often required. However,
questions arise regarding the availability of required blood constituents and
their integrity. This underscores the need to evaluate the viability of blood
products before transfusion, with a focus on comparing the viability of factor VIII and fibrinogen
in both whole blood and FFP. Methodology:
Using an
experimental study design, 32 male and female subjects with blood groups
A, B, AB, and O in equal proportion were recruited. Following a baseline
assessment for the blood under study, blood pints were collected using standard
method of phlebotomy. Some pints were fractionated into whole blood and FFP, stored at 4±20C and -600C
respectively. Manual Prothrombin time (PT),
activated partial thromboplastin time (aPTT) and enzymatic assays for
fibrinogen (FIB) and factor VIII (FVIII) were employed, and result obtained
statistically analyzed using ANOVA and significance level set at P < 0.05. Results:
At 4±2°C in WB aPTT increased to 17.02s and 41.25s on day 14 and to
24.31s and 46.63 on day 21. FIB was table in WB at day 14 (p=659) but dropped
to 11 3.63mg/dl day 35 (p=0.00), and was stable in FFP up to day 180
(p=1.00). FVIII at 2-60C
declined to 0.778% on day 14 and to 0.477% by day 35 in WB but stable at -600C
day 180 (p=0.58). Conclusion: Lower temperatures, especially freezing at
-60°C, helped maintain the stability of coagulation factors. Prolonged storage of whole blood led to significant
alterations in FVIII and FIB. Fresh
frozen plasma (FFP) should therefore be
considered as the preferred option for haemostatic transfusion therapy due to
its stability in maintaining intrinsic and extrinsic coagulation factors.