Bleeding Disorders and Anti-Coagulation Flashcards
What are intentional bleeding disorders?
result of tx or prevention of a disease, ie just had a stroke, preventing another
How are bleeding disorders acquired?
result of disease, side-effect of tx
3 categories of why ppl bleed:
inherited, acquired, intentional disorders
Phases of clotting;
vascular, platelet, coagulation (fibrinolytic)
Phases of clotting we are concerned w:
platelet, coagulation,
Bleeding can be instantaneous in these phases;
vascular and platelet phases
When does bleeding occur int he coagulation phase?
min to hrs later
coagulation phase is aka:
fibrinolytic phase
Pts can have issues in this phase of clotting after they leave the office:
coagulation phase (fibrinolytic)
When does the vascular phase begin?
immediately after injury
What happens during vascular phase?
vessels constrict and retract, fluid pressure from blood collapses adjacent vessels
What meds can affect the vascular phase?
none
When does the platelet phase begin?
secs after injury
What makes platelets sticky?
exposure of endothelial tissues, platelet plug seals site
How long does the coagulation phase take?
10-20m
Via which pwy(s) does blood in surrounding tissue coagulate?
both extrinsic and common pwys
Via which pwy(s) does blood in vessels coagulate?
both intrinsic and common
Intrinsic pwy:
(APPT) kininogen/ kallikrein, FXIIa, FXIa, FVIII (?), FXa, Thrombin, Fibrin
Extrinsic Pwy:
(PT) FVIIa, FX, FXa, Thrombin, Fibrin
Common Pwy:
X, Prothrombin, thrombin, fibrinogen, Fibrin
Partial Thromboplastin Time measures which pwy>?
Intrinsic
Prothrombin Time measures which pwy?
extrinsic pwy
How to measure from fibrinogen to fibrin?
thrombin time
All pwys end w formation of:
fibrin
Factors assoc w common pwy:
X, V, II, Fibrinogen, Fibrin
What activates the intrinsic pwy?
surface activation
What activates the extrinsic pwy?
tissue thromboplastin
Problems w vascular phase;
usually non-specific, confined to skin, mucosa and gingiva, petechiae, ecchymosis, purpura, aging, Cushing’;s syndrome, collagen disorders, Vit C deficiency
How can Cushing’s syndrome lead to non-specific minor bleeding problems?
high dose exogenous steroids
Collagen disorder related to CV defects and excessive growth:
Marfan
Lits 2 collagen disorders:
Marfan, Ehler-Danlos
Congenital platelet disorders, rare or common?
rare
Types of acquired thrombocytopenia:
Idiopathic, Immune
Types of immune thrombocytopenia:
lupus, HIV
What is thrombocytopenia?
low platelet count
ITP sf:
Idiopathic thrombocytopenia
Type of thrombocytopenia that can be cyclic:
idiopathic
Normal platelet count:
150,000-400,000/microL
Platelet count necessary for major surgery:
80,000
Platelet count necessary for minor surgery:
50,000+
At risk for spontaneous bleeding if platelet count is below:
20,000
TF? A pt will most likely not clot if their platelet count is ½ of low/normal.
F. probably will
How can a surgical proc be performed on a pt w low platelet count?
Call hematologist, use exogenous blood products
Thrombocytopenia can result from;
aplastic anemia, leukemia, bone marrow suppression (chemo), kidney disease
Is a platelet count needed for a pt who had chemo mos ago?
yes
TF? With platelet dysfunctino, the platelet count is normal.
T
Causes of platelet dysfunctino:
dialysis, meds
meds that can cause platelet dysfunction:
ASA, NSAIDS, platelet aggregate inhibitors
Why can dialysis lead to platelet dysfunction?
it damages platelets
Drugs that effect platelet aggregation:
aspirin, non-steroidals, plavix
How to test for platelets?
platelet count, platelet function tests
4 Platelet function tests:
closure time assay, viscoelastometry, Platelet aggregometry, flow cytometry (bleeding time)
Superficial wound healing is mainly about:
platelets
Platelet function test that is no longer done:
bleeding time
Coagulation phase disorders:
hemophilia A and B
Hemophilia A:
Factor VIII deficiency (intrinsic pwy)
hemophilia B:
Factor IX deficiency (intrinsic pwy)
hemophilia B is aka:
Christmas disease
Other factor deficiencies;
IX, X, XI, XII
TF? There are no factor deficiencies affecting the extrinsic pwy.
T. check (only 8-12)
Meds are most likely to effect which phase of clotting?
coagulation phase
hereditary disorder that effect platelet adhesion and FVIII:
Von Willebrand’s, hereditary blood clotting disorder
How many types of Von Willebrand’s are there?
4
Is Von Willebrand’s usually serious?
no
Tx for Von Willebrand’s;
nasal meds
Most severe type of Von Willebrand’s:
Type 3, low FVIII
Acquired coagulation phase bleeding disorders:
Liver disease, meds, DIC
Factors involved w Vit K dependent, acquired bleeding disorder;
II, VII, IX, X
Where are Vit K dependant factors produced?
liver
Prevalence of alcoholism:
5%
Medical/ intentional anticoagulation:
recent MI, CVA (stroke), Thromophlebitis, Atrial fibrillation, pulmonary emboli, Deep vein thrombosis, Thrombogenic implanted devices