coagulation Flashcards
Time to begin forming a clot
R time
time until clot has achieved fixed strength
K time
speed of fibrin accumulation
alpha angle
Highest verticle amplitude on the Teg. measured clot stength
MA
height of vert amp at 60 min after MA
A60
binds to antithrombin, accelerating anticoagubility
Heparin
Normal 25-35 s
aPTT
heparin: 1.5-2.5x normal
normal 90-120s
ACT
> 400s cardiac surgery
ACT is affected by 4 things
1 Hemodilution
2 Hypothermia
3 Thrombocytopenia
4 Deficiency of F1, F7, F12
Fibrinogen levels is affected by
hemorrhage
hemodilution
SE Heparin
HIT
allergy
hypotension
decrease AT concntration
contraindications of heparin
neurosurgery
HIT
regional anesthesia
reverses heparin
protamine (+)
1u per 100u heparin
SLOWLY to prevent anaphylaxis and pulmonary vasoconstriction
half life of heparin
1 hour
Warfarin Inhibits Factors
2,7, 9,10 (Vit K antagonist!)
Also, protien c & s
time for warfarin to achieve therapy
36-72 hours
antidotes for warfarin
kaycentra (prothrombin complex concentrate)
Vitamin K and FFP 1-2u
Recombinant Factor 7a
risk of vit K deficiency
diet
antibiotic kills GI flora, reducing synth
malabsorption
hepatic disease
neonates (give after delivery “phytonadione”)
anesthesia and vitamin k administration
-requires a functional liver
-takes 4-9 hours to work
-antidote for warfarin
warfarin MOA
ibhibits vit K epoxide reductase complex 1 enzymes
this enzyme produces K dep factors 2, 7, 9 10, Pc&S
pt/INR on warfarin
2-3x normal
p2y12 antagonists
Plavix
antiplatelet
Lovenox MOA
abciximab
g2b3a antagonist
antiplatelet
cox 2 inhibitors
rofecoxib
celecoxib
antiplatelet
non specific cox inibitors
ASA
NSAIDS
antiplatelet
thrombin inhibitors
bivalirudin
argatroban
Pradaxa
BAP- born a pussy
anticoagulants
plasminogen activators
tPA
Streptokinase
stimulates edogenous F8 release and vWF release
DDVAP
What carries F 8 in the plasma
vWF
labs that increased with vWF disease
ptt
bleeding time
replacing factor 8 before surgery
FFP
cryro
factor 8 concentrate
DDAVP
Recombin F 7
TXA and Aminocapric acid
hemophilia A
F8 deficiency
prolonged PTT
Hemophilia B deficiency
F 9
prolonged PTT
hemophilia a and B lab
prolonged PTT
normal INR/PT
nromal bleeding time
disorganized clotthing and fibrinolysis causing hemorrhage AND thrombosis
DIC
S/S DIC FAPD
fibrinogen and antithrombin decreased
eccymodid
petechia
mucosal bleeding
bleeding at IV sites
increased d dimer and fibrin Pt and ptt
decrease fibringogen platelets and antothombin
DIC common in STOM
sepsis #1
obstetric complications
malignancy
trauma
DIC treatment
replace blood with FFP, plts, cryro
IV heparin or LMWH
IV fluids
“feed the beast”
HIT
clot formation throughout the body
immune response against heparin
HIT type 2
IgG attack F 4 –> platelet aggregation