Blood- Inherited disorders Flashcards
(33 cards)
What are inherited bleeding disorders?
A defect of
- Coagulation factors
- Platelet (number and function)
- both.
Which affects the coagulation of blood.
What is haemophilia A?
Deficiency in factor 8
How do we treat haemophilia A?
Severe- recombinant factor 8.
Mild-
DDAVP- Releases factor 8 that is stuck on the endothelial cells.
Tranexamic acid- slows down clot breakdown (fibrinolysis)
What is haemophilia B?
Deficiency in factor 9
How do we treat haemophilia B?
Recombinant factor 9
DDAVP doesn’t work (no factor 9 trapped in cells)
What are inhibitors?
Antibodies produced in response to synthetic coagulation factors (8 and 9)
What is Von willebrand’s disease?
A combination of reduced platelet aggregation and deficiency of factor 8.
How do we treat von willebrand’s
DDAVPS - as factor 8 deficient
Tranexamic acid- to stop fibrinolysis.
What should be considered for haemophiliac patients undergoing extractions and oral surgery?
- Atraumatic treatment - caries removal using hand instruments.
- antibiotics if infected
- observe haemostasis (stopping bleeding)
severe patient- overnight
mild- 2-3 hours
Which local anaesthetic procedures are safe for haemophiliac patients?
- Buccal infiltration
- Intraligamentary injections
- Intra-papillary injections
Which LA procedures are more dangerous for haemophiliac patients?
- inferior alveolar nerve block
- Lingual infiltration
- Posterior superior nerve block
Why is an inferior alveolar nerve block more dangerous for Haemophiliac patients?
Because you are puncturing tissue with a needle
Bleeding won’t be obvious and it won’t stop normally.
A severe haemophiliac patient comes into your practice. They are dentate. How are they treated?
Refer to hospital
A severe haemophiliac patient comes into your practice. They are edentulous. How are they treated?
Can be treated in GDP
A mild haemophiliac patient comes into your practice. They require restorative treatment (e.g. pros). How do you treat them?
In GDP
A mild haemophiliac patient comes into your practice. They require Extraction and local anaesthetic. How do you treat them?
Refer to hospital.
What is thrombophilia?
Increased risk of blot clots developing.
What causes thrombophilia?
Increased clot production
Underproduction of fibrinolytic factors.
Compare thrombocytopenia and Thrombocytothemia?
Thrombocytopenia- decreased platelets
Thrombocytothemia- increased platelets.
What are qualitative disorders?
normal number of platelets but abonormal platelet function.
This can be acquired by cirrhosis/ drugs/ high alcohol intake.
What is drug induced coagulopathy?
This is when we use drugs to reduce a patient’s coagulation?
e.g. oral anticoagulation
Injected anticoagulants (e.g.Heparins)
Anti-platelet medication.
Give examples of patients that would have anti-coagulation as part of their treatment:
thrombophillia
atrial fibrillation
Deep vein thrombosis
Heart valve disease.
mechanical heart valves
What type of oral anti-coagulant is warfarin?
coumarin
Some drugs are potentiating to warfarin.
What does this mean?
Give examples?
How do we deal with these drugs?
Potentiating increases the effect of warfarin.
- E.g. alcohol in patients with liver disease.
- NSAIDs
- Antibiotics
Reduce the concentration of warfarin