Bleeding and coagulation disorder Flashcards

(31 cards)

1
Q

Hemostatic Disorders
-Classified into two main categories:
1.
2.

A

I. Bleeding Diseases.
II. Intravascular Thrombosis.

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2
Q

illustrate the def & causes of Bleeding Diseases

A
  • def :
    These are a group of diseases
    chc. by an in tendency to bleeding spontaneously or after trauma.

-causes: due to
1. Vessel wall defects.
2. Platelet disorders (Count or Function).
lead to superficial bleeding
3. Blood clotting disorders
lead to deep bleeding

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3
Q

illustrate the def & causes of Bleeding due to defect in the blood vessel (Purpura)

A
  • def :It is a bleeding tendency due to weak fragile vessel wall causing poor constriction of the injured vessel
  • causes :
    1. Hereditary.
    2. Acquired:
  • nutrient deficiency as Scurvy (Vitamin C deficiency).
  • Drugs (e.g. steroid).
  • Aging (senile purpura).
  • Infections (streptococcal).
  • Malignancies.
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4
Q

illustrate the causes of Bleeding due to platelet disorder (Purpura)

A
  1. Decreased platelet count (Thrombocytopenia)
    (Thrombocytopenic Purpura)
  2. Weak platelet function (Thrombasthenia orThrombocytopathia) (Thrombocytopathic purpura)
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5
Q

def of Bleeding due to platelet disorder caused by Decreased platelet count

A

It is a bleeding tendency due to deficient in platelet plug formation, clot retraction and poor constriction of injured vessel

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6
Q

-the normal platelet count range is ……
- Bleeding occurs when platelets count………….
-Internal bleeding occurs when platelets count………….
- Lethal (Fatal) platelets count…………..

A

150,000-410,000/mm3
< 50,000/µL.
< 20,000/ µl
< 10,000/ µl

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7
Q
  • People with thrombocytopenia have a tendency to bleed from………….
  • The skin of such people displays many small and purplish blotches called……., large………or larger…………
  • Bleeding time is …………. with……… clotting time
A
  • small blood vessel
    (venules and capillaries).
  • petechiae /ecchymosis/ecchymotic patches
  • prolonged / normal
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8
Q

illustrate Causes of Decreased platelet count

A

1.Primary:
Autoimmune disease (Idiopathic thrombocytopenic purpura) (ITP)
2.Secondary:
-Hypersplenism.
-Sever destruction of bone marrow.

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9
Q

………..It gives the same clinical picture as thrombocytopenia.

A

Weak platelet function

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10
Q

list Causes of Weak platelet function

A

1.Prolonged use of aspirin (inhibit platelet aggregation).
2. Renal failure (Toxins or dialysis machine).
3. Deficiency of Von Willebrand factor (inhibit platelet adhesion)

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11
Q

what’s the Treatment of bleeding disorders due to vessel wall or
platelet defects?

A
  1. Vitamin C administration.
  2. Platelet transfusions.
  3. Fresh whole blood transfusion that contain large number of platelets.
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12
Q

-In Bleeding due to abnormal coagulation, bleeding tendency due to…
-It is result from………..
-These people usually have a tendency to bleed from ……………..
-……………… is prolonged, while bleeding time is…………

A
  • deficient in clot formation
  • lack of any of the clotting factors
  • large blood vessel.
  • Clotting time / normal
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13
Q

list causes of Bleeding due to abnormal
coagulation

A
  1. Acquired:
    Liver diseases
    Vitamin K deficiency
  2. Congenital:
  3. Due to deficiency of one of the clotting factors
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14
Q

why the liver disease cause bleeding ?

A

because almost all clotting factors are formed by the liver.

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15
Q
  • in liver disease both PT & aPTT are ……………..
  • in early liver disease ……is prolonged & …….. is normal.
A
  • prolonged
  • PT / aPTT
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16
Q

Vitamin K deficiency lead to insufficiency of the clotting factors …………….

A

II, VII, IX and X

17
Q

illustrate causes of vitamin K deficiency.

A
  1. Liver disease:
    failure of liver to secrete bile.
  2. Failure of absorption:
    - bile duct obstruction
    - chronic diarrhea
    - gastrointestinal disease
  3. Deficient intestinal bacteria:
    - prolonged use of antibiotic
    - newly borne infant
  4. Anticoagulant drugs :(coumarin) prevent utilization of vit K by liver.
18
Q

def of Hemophilia

A
  • congenital deficiency of factor VIII or IX or XI
  • It is an inherited sex-linked anomaly, transmitted by females, who are carriers (show no symptoms), to males who manifest signs of the disease
19
Q

def of Parahemophilia

A

congenital deficiency of factor V

20
Q

def of Afibrinogenemia

A

deficiency of fibrinogen

21
Q

def of Hypoprothrombinemia

A

decreased prothrombin synthesis
by the liver, usually in vitamin K deficiency.

22
Q

illustrate the symptoms and pathological findings in hemophilia

A

*Symptoms (begin early in life):
- Bleeding either from natural orifices (spontaneously) or after injury or incisions.
- Recurrent hemarthrosis i.e., bleeding in joints, following minor trauma leading to crippling deformity due to fibrous
adhesions.
- Marked increase in clotting time

23
Q

in hemophilia :
- prolonged ……….
- normal …….

24
Q

illustrate Treatment of hemophilia

A

Supplying the patient with the deficient clotting factor (Cryoprecipitate)

25
list types of hemophilia
1.Hemophilia A (Classical hemophilia): - due to deficiency of factor VIII. - Represents 85% of hemophilic patients 2.Hemophilia B: - factor IX deficiency (Christmas disease). 3.Hemophilia C: - factor XI deficiency 4.Parahemophilia: factor V deficiency
26
Compare between Hemophilia and Purpura: from -Hereditary -Sex -Causes - Clotting Time (aPTT) -Bleeding Time
1. Hemophilia -Hereditary: Congenital -Sex: Males -Causes Lack of clotting factors - Clotting Time (aPTT): Prolonged -Bleeding Time: Normal 2. Purpura -Hereditary: Not congenital -Sex: Males & Females -Causes: Platelet defect (count & function) - Clotting Time (aPTT): Normal -Bleeding Time: Prolonged ** NOTE : PT is normal in both ** PT evaluate extrinsic pathway **aPTT evaluate intrinsic pathway
27
def Intravascular Thrombosis
Abnormal formation of clot inside the blood vessel (thrombus)
28
illustrate the causes of Intravascular Thrombosis
1.Sluggish blood flow: activation of clotting factors & enhance platelet aggregation. 2.Damaged or roughened endothelial surface of blood vessel as in atherosclerosis. 3. As a complication of septicemia (septic shock) or extensive tissue damage (crush injury). 4.Imbalance between clotting-anticlotting systems 5. Factor V Leiden
29
what's Factor V Leiden?
1- An inherited disorder with abnormal form of factor V. 2- Caused by mutation in the gene coding for clotting factor V. 3- Factor V Leiden is resistant to the action of activated protein C. 4- It leads to increased risk of developing blood clots in legs (DVT) or lungs (PE). 5-It is a life-threatening condition
30
illustrate Effects (Complications) of intravascular thrombosis
1. A thrombus may enlarge → complete occlusion of the blood vessel → prevent blood flow and oxygen from getting to tissues and organs leading to organ failure. e.g. DVT 2. A thrombus may detach or break loose → forming an embolus → stuck in a narrower blood vessel in distant sites (Thromboembolism). e.g., pulmonary embolism: obstruction of the pulmonary artery or its branches by thrombi from the leg veins.
31
Treatment of intravascular thrombosis or abnormal increase in blood coagulation is ..............
Administration of anticoagulant drugs either oral or parenteral.