Hemophilia in children

1. Paediatric Hemophilia
I. M. Sechenov First
Moscow State Medical
University
Presented by: Alizada Elshad
Group 83/ 5th Year

2. What is hemophilia?
Hemophilia is an inherited bleeding disorder. Children
with hemophilia can’t stop bleeding because they
don’t have enough clotting factor in their blood.
Clotting factors are needed for blood to clot. Blood
clots to prevent excessive bleeding.
There are many blood clotting factors involved in the
forming of clots to stop bleeding. Two common factors
that affect blood clotting are factor VIII and factor IX.

3. The 3 main forms of hemophilia include:
• Hemophilia A. This is caused by a lack of the blood clotting factor
VIII. About 9 out of 10 people with hemophilia have type A disease. This
is also referred to as classic hemophilia or factor VIII deficiency.
• Hemophilia B. This is caused by a deficiency of factor IX. This is
also called Christmas disease or factor IX deficiency.
• Hemophilia C. Some doctors use this term to refer to a lack of
clotting factor XI.

4. What causes hemophilia in
children?
Hemophilia types A and B are inherited diseases. They are passed
on from parents to children through a gene on the X chromosome.
Females have two X chromosomes, while males have one X and
one Y chromosome.
• A female carrier has the hemophilia gene on one of her X
chromosomes. When a hemophilia carrier female is pregnant, there is
a 50/50 chance that the hemophilia gene will be passed on to the
baby.
• If the gene is passed on to a son, he will have the disease.
• If the gene is passed on to a daughter, she will be a carrier.

5. •
• If the father has hemophilia but the mother does not carry the hemophilia gene,
then none of the sons will have hemophilia disease, but all of the daughters will be
carriers.
In about one-third of the children with hemophilia, there is no family history of the
disorder. In these cases, it’s believed that the disorder could be related to a new
gene flaw.
Carriers of the hemophilia gene often have normal levels of clotting factors but may:
• Bruise easily
• Bleed more with surgeries and dental work
• Have frequent nosebleeds
• Have heavy menstrual bleeding
Hemophilia C usually doesn’t cause problems, but people may have increased
bleeding after surgery.

6. y 25% - 1/3 – спонтанные мутации

7. What are the symptoms of
hemophilia?
The most common symptom of this disorder is heavy, uncontrollable
bleeding.
The severity of haemophilia depends on the amount of clotting factors in the
blood. Those affected with haemophilia that have levels greater than
5% (100% being average for unaffected children) most often have bleeding
only with major surgeries or tooth extractions. These children may not even
be diagnosed until bleeding complications from a surgery occur.
Severe haemophilia is when the factor VIII or IX is less than 1%. Bleeding
can occur in these children, even with the minimal activities of daily life.
Bleeding may also occur from no known injury. Bleeding most often occurs
in the joints and in the head.

8. Patient's symptoms may also include:
• Bruising. Bruises can occur from even small accidents. This can result in a large build up of blood
under the skin causing swelling (hematoma). For this reason, most children are diagnosed around 12 to
18 months of age. This is when the child is more active.
• Bleeds easily. A tendency to bleed from the nose, mouth, and gums with minor injury. Bleeding
while brushing teeth or having dental work often suggests hemophilia.
• Bleeding into a joint. Hemarthrosis (bleeding into a joint) can cause pain, immobility, and deformity
if not treated. This is the most common site of complications due to hemophilia bleeding. These joint
bleeds can lead to chronic, painful, arthritis, deformity, and crippling with repeated occurrences.
• Bleeding into the muscles. Bleeding into the muscles can cause swelling, pain, and redness.
Swelling from excessive blood in these areas can increase pressure on tissues and nerves in the area.
This can cause permanent damage and deformity.
• Bleeding in the brain from injury or spontaneously. Bleeding from injury, or spontaneously in the
brain, is the most common cause of death in children with hemophilia and the most serious bleeding
complication. Bleeding in or around the brain can occur from even a small bump on the head or a fall.
Small bleeds in the brain can result in blindness, intellectual disability, a variety of neurological deficits. It
can lead to death if not spotted and treated right away.
• Other sources of bleeding. Blood found in the urine or stool may also signal hemophilia.

9. How is hemophilia in children
diagnosed?
The diagnosis of haemophilia is based on patient`s family history,
patient`s medical history, and a physical exam. Blood tests include:
• Complete blood count (CBC). A complete blood count checks the
red and white blood cells, blood clotting cells (platelets), and sometimes,
young red blood cells (reticulocytes). It includes haemoglobin and
hematocrit and more details about the red blood cells.
• Clotting factors. To check the levels of each clotting factor.
• Bleeding times. To test the speed that blood clots.
• Genetic or DNA testing. To check for abnormal genes.

10. How is hemophilia
treated?
Patient's healthcare provider will refer you to a hematologist, an expert in blood
disorders. Patient’s health care provider will figure out the best treatment based on:
• How old patient(child) is
• His or her overall health and medical history
• How sick he or she is
• How well patient(child) can handle specific medications, procedures, or therapies
• How long the condition is expected to last
Treatment depends on the type and severity of the hemophilia. Treatment for
hemophilia is aimed at preventing bleeding complications (mainly head and joint
bleeds).

11. Treatment may include:
• Bleeding in the joint may need surgery or
immobilization. Patient may need rehab of the affected
joint. This may include physical therapy and exercise to
strengthen the muscles around the area.
• Blood transfusions may be needed if major blood
loss has occurred. This is when patient gets donated
blood.
• Self-infused factor VIII or IX can allow a child with
hemophilia to lead a near normal lifestyle.

12. Factor VIII concentrates:
• Hemofil M(Baxter)
• Immunate(Baxter)
• Koate-DVI(Bayer)
Factor IX concentrates:
• Immunine(Baxter)
• Aimafix(Kedrion)

13. What are the complications of
hemophilia?
Complications of hemophilia include:
• Bleeding in the joints or muscles
• Inflammation of the joint lining
• Long-term joint problems
• Very serious tumor-like enlargements, of the muscle and bone
• Development of antibodies against clotting factors
• Infections from transfusions (HIV and hepatitis B and C are no
longer transmitted in donated blood)

14. Hemarthroses

15. Hematoma
Spontaneous
nosebleed

16. How is hemophilia
managed?
With careful management, many children with hemophilia can live relatively healthy lives with a normal
lifespan.
Managing patient's hemophilia may include:
• Taking part in activities and exercise, but avoiding those that may cause injury. These include soccer,
rugby, wrestling, motocross, and skiing.
• Receiving special care before surgery including dental work. Patient's doctor may advise factor
replacement infusions. These increase the child's clotting levels before the procedures. Patient may also get
the specific factor replacement infusions during and after the procedure. These maintain the clotting factor
levels and to improve healing and prevention of bleeding after the procedure.
• Preventing dental and gum problems with proper dental hygiene.
• Getting immunizations under the skin instead of in the muscle to prevent bleeding in the muscle.
• Avoiding aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs).
• Wearing medical identification (ID) in the case of an emergency.

17. When should parents call their
child's healthcare provider?
When parents should call will vary based on how severe patient's
condition is and what treatment he or she is getting. Since hemophilia is
a long-term condition, they should talk with patient's healthcare provider
about when they should call or get medical treatment for their child.
Parents should call child's healthcare provider if their child:
• Is injured
• Has pain
• Has bleeding that you cannot control
• Is scheduled for surgery or another procedure

18. Key points about hemophilia in
children
• Hemophilia is an inherited bleeding disorder.
It causes an affected child to have low levels of
blood clotting factors.
• The most common symptom of hemophilia is
increased, uncontrollable bleeding.
• Giving factor VIII or IX can allow a child with
hemophilia to lead a near normal lifestyle.

19. “Thank you
for your attention”
14.2.2017