Chapter 3: Patients With Blood Disorder Alterations And Anticoagulation Treatment Flashcards
Hemostasis is?
The mechanism of defence of the organism to prevent or stop a haemorrhage, maintain the integrity of the vascular system, and restore circulation when interrupted.
4 stages of hemostasis?
- Vasoconstriction
- Platelet aggregation
- Activation of coagulation cascade
- Clot formation
Vasoconstriction is caused by?
Thromboxane A2 from activated platelets and injured epithelial cells. Vasoconstriction is brief.
Platelets adhere to the collagen fibers in the vessel wall by becoming adhesive and filamentous due to the stimulus of?
Von Willebrand Factor
For large wounds, which type of hemostasis is needed?
Secondary
For minor wounds, which type of hemostasis is needed?
Primary
3 pathways of the coagulation cascade?
- Intrinsic
- Extrinsic
- Common
Primary coagulation is?
Platelet formation
Secondary hemostasis is?
Coagulation cascade, fibrin mesh
The coagulation factors usually are? And how do they work?
Serine proteases (enzymes)
Coagulation factors circulate as inactive enzyme precursors, which, upon activation, take part in the series of reactions that make up the coagulation cascade
Factors in the intrinsic pathway:
12,11,9,8
Negatively charged molecules, HMWK, prekallikrein
Factors in the extrinsic pathway:
3,7
Thrombin burst, prothrombin, fibrinogen,
Factors in the common pathway:
10
Thrombin, fibrin, platelet plug.
After all: fibrinolysis
Blood vessel alterations: hereditary
- rendu-osler diseases (telangiectasia: spontaneous bleeding)
- ehlers-danlos syndrome
- fabry disease
- marfans syndrome
Blood vessel alterations: acquired
- decreased collagen due to scurvy (vit c deficiency)
- secondary to corticosteroids
- vasculitis
- purpura
Platelet alterations: thrombocytopenias can be due to?
- Decreased production (anemia, leukemia, chemotherapy, radiotherapy, congenital).
- Due to the increased peripheral destruction (idiopathic thrombocytopenic purpura, infection, hemorrhage).
In thrombocytopenia, the platelet count is?
Less than 100,000
If the platelet count is less than 50,000:
Variable risk
If platelet count is less than 20,000:
Transfusion appropriate
If platelet count is less than 10,000:
Spontaneous hemorrhage
Thrombocytopathies are:
Alteration of the function of platelets when the time of hemorrhage is prolonged and number of platelets is normal
Congenital Thrombocytopathies:
Bernard lousier syndrome
Acquired Thrombocytopathies:
Drugs, kidney failure, chronic liver disease
So with Thrombocytopathies: we can see
Gingival bleeding
Coagulopathies: hereditary and coagulopathies
- Von Willebrand disease: factor 8
- haemophilia A: factor 8
- haemophilia B: factor 9
- deficit of other factors (2, 5, 7)
Coagulopathies:
- vit k deficiency
- chronic liver diseases
Prolonged immediate bleeding —>
Primary hemostasis
Prolonged late bleeding—>
Secondary hemostasis
Number of platelets:
When is there a risk for hemorrhage?
150,000-450,000
Less than 50,000: risk for hemorrhages
Time of hemorrhage, superior normal limit
7 minutes
H2: 3 values:
thromboplastin, prothrombin, thrombin
TTP: meaning and value
Thromboplastin time
Coagulation inside the BV
25-35 seconds
Altered by heparin
TP: meaning and value
Prothrombin time
Coagulation outside the BV
10-15 seconds