ID 10. Beginning of
clotting (method of Lee-White) (min)
ID 11. End of clotting
(method of Lee-White) (min)
In the body, when an injury and/or bleeding occurs, the clotting
process called hemostasis begins. This process involves in part a series of
sequential chemical reactions called the coagulation cascade, in which
coagulation or "clotting" factors are activated one after another and
result in the formation of a clot. There must be a sufficient quantity of each
coagulation factor, and each must function properly, in order for normal
clotting to occur. Too little can lead to excessive bleeding; too much may lead
to excessive clotting.
Lee-White clotting time (LWCT) is considered normal when sample
clotted in up to 9 minutes. Besides, the interval between the beginning and the
end of clotting is important, and it should exceed 30 seconds.
The interaction between plasma kallikreins and tissue kallikreins
(of the pancreas, salivary glands, kidneys and intestinal wall) determines the
time of beginning and end of blood coagulation. An equally important role in
the formation of this time interval belongs to platelets and haematocrit.
The plasma kinin system also called the kinin–kallikrein system,
consists of blood proteins that play an important role in inflammation, blood
pressure control, coagulation and pain. Kinins are polypeptides derived from
naturally occurring plasma protein substrates (kininogen). It is known that
kinins are inflammatory mediators that cause dilation of blood vessels and
increased vascular permeability. Five principal pharmacological actions have
been attributed to plasma kinins: stimulation of some smooth muscle, increase
in vascular permeability, vasodilation, leucotaxis and induction of pain.
The current model of coagulation in vivo emphasizes tissue factor
as an initiator of coagulation activation, underlines the main role of thrombin
in amplification of coagulation, and the interaction of coagulation factors
with blood cells and endothelial cells (Hoffman & Monroe, 2007).
Abnormalities. Disorders or diseases caused or related.
The reasons for abnormal results include hemophilia, liver
disease, vitamin K deficiency, or a coagulation factor deficiency (e.g., factor
VII deficiency). It’s also useful in monitoring those who take medications that
affect clotting, such as warfarin (Coumadin).
In people with abnormalities of coagulation time, the test for
prothrombin time (PT) and a partial thromboplastin time (PTT) is recommended
for differentiation.
PT
RESULT |
PTT RESULT |
EXAMPLE
OF CONDITIONS THAT MAY BE PRESENT |
Prolonged |
Normal |
Liver disease, vitamin K
insufficiency, decreased or defective factor VII, chronic low-grade disseminated intravascular coagulation (DIC), anticoagulation drug
(warfarin) therapy |
Normal |
Prolonged |
Decreased or defective
factor VIII, IX, XI, or XII, von Willebrand disease (severe type), presence
of lupus anticoagulant, autoantibody against a specific factor (e.g.,
factor VIII) |
Prolonged |
Prolonged |
Decreased or defective
factor I, II, V or X, severe liver disease, acute DIC, warfarin
overdose |
Normal |
Normal or slightly
prolonged |
May indicate normal hemostasis; however, PT and PTT can
be normal in conditions such as mild deficiencies in coagulation factor(s),
mild form of von Willebrand disease, and presence of weak lupus
anticoagulant. Further testing may be required to diagnose these conditions. |
Some antibiotics can increase the time of coagulation.
Barbiturates, oral contraceptives and hormone-replacement therapy (HRT), and
vitamin K (either in a multivitamin or liquid nutrition supplement) may
decrease clotting time.
Drinking alcohol can also affect the results. Certain foods, such
as beef and pork liver, green tea, broccoli, chickpeas, kale, turnip greens,
and soybean products, contain large amounts of vitamin K and can alter the
results. It is important that a healthcare provider knows about all of the
drugs, supplements, and foods that you have consumed recently so that the
results are interpreted and used correctly.
1.
Jose Diego de Brito Sousa et al. Accuracy of the
Lee–White Clotting Time Performed in the Hospital Routine to Detect
Coagulopathy in Bothrops atrox Envenomation. Am J Trop Med Hyg. 2018 May;
98(5): 1547–1551, doi: 10.4269/ajtmh.17-0992
2.
Duchene (2011). "Kallikrein-kinin kystem in
inflammatory diseases". Kinins. De Gruyter. pp. 261–272. ISBN
978-3-11-025235-4.
3.
MELMON, K., CLINE, M. Interaction of Plasma Kinins and
Granulocytes. Nature 213, 90–92 (1967).
https://doi.org/10.1038/213090a0
Published on 9 May 2024