harsha-bleeding disorders Flashcards
(46 cards)
What are 5 components of haemostasis
- blood vessels and endothelial cells
- platelets
- coagulation factors
- coagulation inhibitors
- clot dissolution or fibrinolysis
Describe primary haemostasis
- damaged vessel narrows to contract lumen
- platelets activated
- adhere and clump to form a platelet plug to seal defect
- clumped activated platelets secrete chemicals to recruit more platelets to aggregate and become activated
- trigger coagulation pathway
Describe secondary haemostasis
- sequential activation of a cascade of otherwise inert pro-enzymes in the plasma-results in a stronger, stable fibrin clot (made from thrombin)
Describe regulation of coagulation and fibrinolysis
- Coagulation needs to be confined to the site of injury to prevent venous and arterial thrombosis
- The balance is obtained by naturally occuring coagulation inhibitors
- when clotting occurs to seal an injury, the fibrinolytic system is activated simultaneously which allows timely clot breakdown and re-canalization to maintain continuity of circulation
What are the 6 steps of blood circulation and haemostasis
- injury and haemorrhage
- vascular contraction
- platelet adhesion, aggregation, activation
- coagulation
- fibrinolysis
- recanalization/restoration of bloodflow
What are 4 types of bleeding disorders
- vascular defects
- platelet disorders
- coagulation disorders
- increased fibrinolysis
what are some causes of vascular defects
- age
- long-term steroid use
- hereditary haemorrhagic telengiectasia
- scurvy
what are some classes of platelet disorders
- inherited thrombocytopenia
- myeloproliferative disorders
- bone marrow failure (infection, immunologically mediated)
- Drug induced
- Platelet function disorders
What are some coagulation disorders
- von-willebrand disease
- haemophilia A
- haemophilia B
- Vitamin K deficiency
- Liver disease
What is the condition associated with increased fibrinolysis
Disseminated intravascular coagulation (DIC) (often fatal)
What are some therapeautic anticoagulants that cause bleeding disorder
- antiplatelet drugs
- coumarin anticoagulants
- NOACs
- Heparin
Describe the two types of platelet disorder
Thrombocytopenia (reduced numbers)
- decreased production
- decreased survival
- increased consumption
Defective function
- Glanzmann’s thrombasthenia
- Aspirin
- NSAIDs
- Anti-platelet drugs
what is the normal platelet count and at what platelet count may the patient experience spontaneous bleeding
- 150000-400000/ml
- less than 20000/ml
Describe spontaneous bleeding due to low platelet count (skin)
superficial bleeding in skin and mucoase
- petichiae
- purpura
- ecchymosis
What is epistaxis
nose bleeding
What is haemoptysis
coughing up blood
what is haematemisis
vomiting blood
what is haematuria
blood in urine
Orally, what may platelet defects present as
- Bleeding gums
- Prolonged bleeding after injury/extractions
What are coagulation disorders characterised by
- prolonged bleeding
- severe and often life threatening
- can bleed into deep tissue
- occurs as a result of deficiency of coagulation factors which can be acquired or congenital
What are congenital coagulation disorders
- Haemophilia A- factor 8 deficient
- Haemophilia B- factor 9 deficient
- von-willebrand disease
What are acquired coagulation disorders
- acquired antibodies to f-VIII
- vit K deficiency
- liver disease
How are coagulation disorders managed preventatively
carefully managed preventative dental care to avoid/minimise need for dental procedures
Describe haemophilia
sex linked recessive transmission, affects males but females can also be carriers. Range of severity from mild to severe