complications of Hemophilia
1) JOINT DAMAGE
v Joint damage
or also called as Hemophilia Arthopathy is most common complication of bleeding in hemophilia. Individuals with
hemophilia can bleed into the joint space after an injury, at times or
sometimes without any clear cause. Not only that, this joint damage may occur
after repeated bleeding into the same joint or after serious bleeding at the
joint. The blood filling pressure at the joint cavity which causes a symbolic
pain that leads to chronic swelling and deformity.
The joint damage occurs in the cartilage of
around the bones and also the synovium. When there is blood flowing in the joint,
the synovium will absorbs it and the blood containing iron actually causes the
lining of synovium to grow thicker. The bleeding will affect the cartilage
around the bone area which has the smooth surface on the ends of the bones and
allows both bones connecting each other to move without any friction. The rubbing
of bones becomes more painful as the cartilage erodes and becomes pitted. Joints
that bleed are usually referred to as “target joints” and as the join damage
continues, the movement may become more restricted in that joint. The common symptoms
when joint bleeds are swelling, pain, loss of motion, stiffness and tingling
inside the joint.
2)
INHIBITORS
v Complications of bleeding in hemophilia
may also arise from the inhibitors in the body. Inhibitors are antibodies that
the immune system develops because of the infused clotting factors act as
foreign substance that need to be destroyed. Besides that, an estimated of 20
to 30% of individuals are affected by inhibitors as result with severe
hemophilia A. This is much likely to occur with mild or moderate hemophilia A
approximately of 5 to 8%. About 2 to 3 % of individuals with hemophilia B
develop inhibitors and hemophilia B is less common than hemophilia A. The risk
factors to type and severity of hemophilia are family history of an inhibitor,
age of exposure to factor product and gene mutation.
3)
INFECTIONS
v Infections
are one of the complications of bleeding in hemophilia. Approximately 90% of
individuals with severe hemophilia usually were infected with HIV (Human Immunodeficiency
Virus), Hepatitis and blood-borne infections.
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