Hemostasis 2 Flashcards
types of hemophilia
hemophilia a: factor 8
hemophilia b: factor 9
clinically indistinguishable
t/f in males, just having 1 x chromosome will make the patient express the trait
true
if the father has hemophilia and the mother is not a carrier
all sons are normal
all daughters are obligatory carriers
if the father does not have hemophilia and the mother is a carrier
all sons have a 50% chance of being affected
all daughters have a 50% change of being carriers
symptoms of hemophilia
hemarthrosis
sites of bleeding: knees, iliopsoas, gluteal area, soft tissue, intracranial bleed
mild bleeding severity for hemophilia
5-<40% of normal clotting factor level
episodes: spontaneous bleeding with major trauma or surgery, rare spontaneous bleeding
moderate bleeding severity for hemophilia
1-5% of normal CFL
occasional spontaneous bleeding, prolonged bleeding with minor trauma or injury
severe bleeding severity for hemophilia
<1% of normal CFL
spontaneous bleeding without hemostatic challenge
treatment for hemophilia
factor replacement
antifibrinolytic therapy (txa)
rehabilitation
types of factor replacement for hemophilia
factor 8 (for a) factor 9 (for b) cryoprecipitates (a) and cryosupernates (b)
cryoprecipitEIGHTS
cryosuBernates
principle of rehabilitation for hemophilia
patients develop target joints –> always swollen –> joints will be destroyed
characteristics of dic
- uncontrolled generation of thrombin due to tissue factor being activated
- widespread intravascular fibrin formation due to excess blood protease activity
pathophysio of dic
- high fibrin + thrombin -> ischemic damage -> multiple organ failure
- rbc damage and hemolysis due to fibrin clots
- excess fibrin -> secondary fibrinolysis -> fdp production d-dimer
most sensitive test/marker for dic
fdp d-dimer
common causes of dic
sepsis (cocci) immunologic disorders trauma and tissue injury drugs vascular disorders envenomation (snake/insects) OB complications liver disease cancer (APL) misc