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BLEEDING AND
CLOTTING
DISORDERS
LEARNING OUTCOMES
 ENUMERATE BLEEDING DISORDERS
 ENUMERATE THROMBOEMBOLIC
CONDITIONS
IN THE HUMAN BEING
 ENUMERATE BLOOD COAGULATION TESTS
Decreased Prothrombin, Factor
VII,
Factor IX, and Factor X Caused by
Vitamin K Deficiency
 Diseases of the liver such as hepatitis,
cirrhosis, and acute yellow atrophy can
sometimes depress the clotting system so
greatly that the patient develops a severe
tendency to bleed.
Conditions That Cause Excessive
Bleeding in Human Beings
 Bleeding caused by
(1) Vitamin K deficiency
(2) Hemophilia
(3) Thrombocytopenia (platelet deficiency).
 Another cause of depressed formation of
clotting factors by the liver is vitamin K
deficiency.
 Vitamin K is necessary for liver formation
of five of the important clotting factors:
prothrombin, Factor VII, Factor IX, Factor
X, and protein C.
APPLIED
 Thus, liver disease often causes decreased production
of prothrombin and some other clotting factors both
because of poor vitamin K absorption and because of
the diseased liver cells.
 Because of this, vitamin K is injected into all surgical
patients with liver disease or with obstructed bile
ducts before performing the surgical procedure.
 Ordinarily, if vitamin K is given to a deficient patient
4 to 8 hours before the operation and the liver
parenchymal cells are at least one-half normal in
function, sufficient clotting factors will be produced to
prevent excessive bleeding during the operation.
Hemophilia
 Hemophilia is a bleeding disease that
occurs almost exclusively in males.
 In 85 per cent of cases, it is caused by an
abnormality or deficiency of Factor VIII;
this type of hemophilia is called
hemophilia A or classic hemophilia.
 Factor VIII has two active components, a
large component with a molecular weight in
the millions and a smaller component with a
molecular weight of about 230,000.
 The smaller component is most important in
the intrinsic pathway for clotting, and it is
deficiency of this part of Factor VIII that
causes classic hemophilia.
 Another bleeding disease with somewhat
different characteristics, called von
Willebrand’s disease, results from loss of
the large component
 When a person with classic hemophilia
experiences severe prolonged bleeding,
almost the only therapy that is truly
effective is injection of purified Factor
VIII.
 The cost of Factor VIII is high
 Its availability is limited because it can be
gathered only from human blood and only
in extremely small quantities
Thrombocytopenia
 PURPURA
 They measure 0.3–1 cm (3–10 mm),
whereas petechiae measure less than 3
mm, and ecchymoses greater than 1 cm.
ITP
Thromboembolic Conditions
in the Human Being
 An abnormal clot that develops in a blood
vessel is called a thrombus.
 Once a clot has developed, continued flow
of blood past the clot is likely to break it
away from its attachment and cause the
clot to flow with the blood; such freely
flowing clots are known as emboli.
Cause of Thromboembolic
Conditions
(1) Any roughened endothelial surface of a
vessel—as may be caused by
arteriosclerosis, infection, or trauma—is
likely to initiate the clotting process.
(2)Blood often clots when it flows very
slowly through blood vessels, where
small quantities of thrombin and other
procoagulants are always being formed
Use of t-PA in Treating
Intravascular Clots.
 Genetically engineered t-PA (tissue
plasminogen activator) is available.
 When delivered directly to a thrombosed
area through a catheter, it is effective in
activating plasminogen to plasmin, which
in turn can dissolve some intravascular
clots.
Femoral Venous Thrombosis and
Massive Pulmonary Embolism
Because clotting almost always occurs
when
 Blood flow is blocked for many hours in
any vessel of the body
 The immobility of patients confined to bed
 The practice of propping the knees with
pillows often causes intravascular clotting
because of blood stasis in one or more of
the leg veins for hours at a time.
Disseminated Intravascular
Coagulation
 Occasionally the clotting mechanism
becomes activated in widespread areas of
the circulation, giving rise to the condition
called disseminated intravascular
coagulation.
 This often results from the presence of
large amounts of traumatized or dying
tissue in the body that releases great
quantities of tissue factor into the blood.
 This occurs especially in patients with
widespread septicemia, in which either
circulating bacteria or bacterial toxins—
especially endotoxins— activate the clotting
mechanisms.
 Plugging of small peripheral vessels greatly
diminishes delivery of oxygen and other
nutrients to the tissues—a situation that
leads to or exacerbates circulatory shock. It
is partly for this reason that septicemic shock
is lethal in 85 per cent or more of patients
Blood Coagulation
Tests
Bleeding Time
 When a sharp-pointed knife is used to
pierce the tip of the finger or lobe of the
ear, bleeding ordinarily lasts for 1 to 6
minutes.
 The time depends largely on the depth of
the wound and the degree of hyperemia
in the finger or ear lobe at the time of the
test.
 Lack of any one of several of the clotting
factors can prolong the bleeding time, but
it is especially prolonged by lack of
platelets.
Clotting Time
 Unfortunately, the clotting time varies
widely, depending on the method used for
measuring it, so it is no longer used in
many clinics. Instead, measurements of
the clotting factors themselves are made,
using sophisticated chemical procedures.
Prothrombin Time
 Blood removed from the patient is immediately
oxalated so that none of the prothrombin can
change into thrombin.Then, a large excess of
calcium ion and tissue factor is quickly mixed
with the oxalated blood.
 The excess calcium nullifies the effect of the
oxalate, and the tissue factor activates the
prothrombin-to thrombin reaction by means of
the extrinsic clotting pathway. The time required
for coagulation to take place is known as the
prothrombin time.
 The shortness of the time is determined mainly
by prothrombin concentration. The normal
prothrombin time is about 12 seconds.

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BLEEDING AND CLOTTING DISORDERS: CAUSES AND TESTS

  • 2. LEARNING OUTCOMES  ENUMERATE BLEEDING DISORDERS  ENUMERATE THROMBOEMBOLIC CONDITIONS IN THE HUMAN BEING  ENUMERATE BLOOD COAGULATION TESTS
  • 3. Decreased Prothrombin, Factor VII, Factor IX, and Factor X Caused by Vitamin K Deficiency  Diseases of the liver such as hepatitis, cirrhosis, and acute yellow atrophy can sometimes depress the clotting system so greatly that the patient develops a severe tendency to bleed.
  • 4. Conditions That Cause Excessive Bleeding in Human Beings  Bleeding caused by (1) Vitamin K deficiency (2) Hemophilia (3) Thrombocytopenia (platelet deficiency).
  • 5.  Another cause of depressed formation of clotting factors by the liver is vitamin K deficiency.  Vitamin K is necessary for liver formation of five of the important clotting factors: prothrombin, Factor VII, Factor IX, Factor X, and protein C.
  • 6. APPLIED  Thus, liver disease often causes decreased production of prothrombin and some other clotting factors both because of poor vitamin K absorption and because of the diseased liver cells.  Because of this, vitamin K is injected into all surgical patients with liver disease or with obstructed bile ducts before performing the surgical procedure.  Ordinarily, if vitamin K is given to a deficient patient 4 to 8 hours before the operation and the liver parenchymal cells are at least one-half normal in function, sufficient clotting factors will be produced to prevent excessive bleeding during the operation.
  • 7. Hemophilia  Hemophilia is a bleeding disease that occurs almost exclusively in males.  In 85 per cent of cases, it is caused by an abnormality or deficiency of Factor VIII; this type of hemophilia is called hemophilia A or classic hemophilia.
  • 8.  Factor VIII has two active components, a large component with a molecular weight in the millions and a smaller component with a molecular weight of about 230,000.  The smaller component is most important in the intrinsic pathway for clotting, and it is deficiency of this part of Factor VIII that causes classic hemophilia.  Another bleeding disease with somewhat different characteristics, called von Willebrand’s disease, results from loss of the large component
  • 9.  When a person with classic hemophilia experiences severe prolonged bleeding, almost the only therapy that is truly effective is injection of purified Factor VIII.  The cost of Factor VIII is high  Its availability is limited because it can be gathered only from human blood and only in extremely small quantities
  • 10. Thrombocytopenia  PURPURA  They measure 0.3–1 cm (3–10 mm), whereas petechiae measure less than 3 mm, and ecchymoses greater than 1 cm.
  • 11. ITP
  • 12. Thromboembolic Conditions in the Human Being  An abnormal clot that develops in a blood vessel is called a thrombus.  Once a clot has developed, continued flow of blood past the clot is likely to break it away from its attachment and cause the clot to flow with the blood; such freely flowing clots are known as emboli.
  • 13. Cause of Thromboembolic Conditions (1) Any roughened endothelial surface of a vessel—as may be caused by arteriosclerosis, infection, or trauma—is likely to initiate the clotting process. (2)Blood often clots when it flows very slowly through blood vessels, where small quantities of thrombin and other procoagulants are always being formed
  • 14. Use of t-PA in Treating Intravascular Clots.  Genetically engineered t-PA (tissue plasminogen activator) is available.  When delivered directly to a thrombosed area through a catheter, it is effective in activating plasminogen to plasmin, which in turn can dissolve some intravascular clots.
  • 15. Femoral Venous Thrombosis and Massive Pulmonary Embolism Because clotting almost always occurs when  Blood flow is blocked for many hours in any vessel of the body  The immobility of patients confined to bed  The practice of propping the knees with pillows often causes intravascular clotting because of blood stasis in one or more of the leg veins for hours at a time.
  • 16. Disseminated Intravascular Coagulation  Occasionally the clotting mechanism becomes activated in widespread areas of the circulation, giving rise to the condition called disseminated intravascular coagulation.  This often results from the presence of large amounts of traumatized or dying tissue in the body that releases great quantities of tissue factor into the blood.
  • 17.  This occurs especially in patients with widespread septicemia, in which either circulating bacteria or bacterial toxins— especially endotoxins— activate the clotting mechanisms.  Plugging of small peripheral vessels greatly diminishes delivery of oxygen and other nutrients to the tissues—a situation that leads to or exacerbates circulatory shock. It is partly for this reason that septicemic shock is lethal in 85 per cent or more of patients
  • 19. Bleeding Time  When a sharp-pointed knife is used to pierce the tip of the finger or lobe of the ear, bleeding ordinarily lasts for 1 to 6 minutes.  The time depends largely on the depth of the wound and the degree of hyperemia in the finger or ear lobe at the time of the test.  Lack of any one of several of the clotting factors can prolong the bleeding time, but it is especially prolonged by lack of platelets.
  • 20. Clotting Time  Unfortunately, the clotting time varies widely, depending on the method used for measuring it, so it is no longer used in many clinics. Instead, measurements of the clotting factors themselves are made, using sophisticated chemical procedures.
  • 21. Prothrombin Time  Blood removed from the patient is immediately oxalated so that none of the prothrombin can change into thrombin.Then, a large excess of calcium ion and tissue factor is quickly mixed with the oxalated blood.  The excess calcium nullifies the effect of the oxalate, and the tissue factor activates the prothrombin-to thrombin reaction by means of the extrinsic clotting pathway. The time required for coagulation to take place is known as the prothrombin time.  The shortness of the time is determined mainly by prothrombin concentration. The normal prothrombin time is about 12 seconds.