Dental management of coagluopathies Flashcards
acquired medical conditions affecting coagluapaties
chronic kidney disease
liver diseaseHF
myeloproliferative disorders
chemotherapy
congenital med conditions affecting coaglauation
haemophilia
von willebrans
erlers danlos
haemophilia A
A factor VIII deficiency
B factor 9
haemophilia B
factor IX deficeicy
haemophilia is
X linked recessive
females become carriers
males will be symptomatic
signs and symptoms of haemophilia
nose bleeds easy brusing spontaneous gingival bleeding GI bleeds difficultiy clotting after cuts hemarthosis crainal bleeds
treatment for haempphilia
antifirbinolytic agents (transexamic acid)
DDAVP
direct factor replacement
transexamic acid
anti fibrinolytic agent that inhibits breakdown of fibrin clots
blocks binding of plasminogen and plasmin to fibrin i.e. no fibrinolysis
desmopressin DDAVP
synthetic replacement for vasopressin (hormone reducing urine production)
stimulates release of VWF and FV/VIII
what does VW do
promotes plate aggregation (primary haemostats)
carrier protien for factor VIII (Secondary haemostasis)
treatment of VW disease
DDVAP
direct factor replacemtn
types of VW disease
1 D
2 D
3 - recessive
blood test platelet counts
less than 20 spontaneous bleeding
>80 haemostatic
what do NSAIDS do blood wise
impari platlet function
what do SSRI anti depressants do blood wise
affect plateletaggregation