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56 Cards in this Set
- Front
- Back
RLS in:
glycolysis |
PFK 1
|
|
RLS in:
gluconeogenesis |
F16BP
|
|
RLS in:
TCA |
isocitrate DH
|
|
RLS in:
glycogen synthesis |
glycogen synthase
|
|
RLS in:
glycogenolysis |
glycogen phosphorylase
|
|
Diabetic drug:
lactic acidosis |
metformin
|
|
Diabetic drug:
SE of hypoglycemia |
sulfonureas
|
|
Diabetic drug:
MOA closes K channels |
sulfonureas
|
|
Diabetic drug:
inhibits a-glucosidase |
acarbose
miglitol |
|
Diabetic drug:
agonist at PPAR-y |
TZD
|
|
what anticoagulant factors are dependent on vitamin K
|
S
C |
|
what coagulant factors are dependent on vitamin K
|
10
9 7 2 |
|
effects of bradykinen
|
vasodilate
inc vascular permeability inc pain |
|
labs used to monitor:
warfarin |
PT
INR |
|
labs used to monitor:
heparin |
PTT
|
|
labs used to monitor:
enoxaparin |
factor 10a activity
|
|
Rx for HIT
|
lapirudin
bivalirudin |
|
what mineral is needed for coagulation
|
Ca
|
|
what can cause a decrease in Ca coagulation
|
citrate
|
|
in liver failure, which factor is lost first
|
7
|
|
MOA of acute hemolytic transfusion reaction
|
recurrent meningiococcal infection due to hyperstabalized C3
deficiency on properdin -would normally cleave C3 |
|
symptoms of clotting factor defect
|
bleeding
hemarthrosis |
|
symptoms of platelet defect
|
patechiae
|
|
what stimulates the release of factor 8 and vWF form endothelial cells
|
desmopressin
|
|
main symptom of hemophilia
|
hemarthrosis
|
|
lab changes in hemophilia
|
inc PTT
|
|
lab changes in vitamin K def
|
inc PT and PTT
|
|
prothrombin gene mutation
|
G20210A
|
|
what does AT3 normally activate
|
7
9 10 11 12 |
|
heparin given to AT3 def px
|
reduced inc in PTT
|
|
MOA of acute hemolytic transfusion reaction
|
recurrent meningiococcal infection due to hyperstabalized C3
deficiency on properdin -would normally cleave C3 |
|
symptoms of clotting factor defect
|
bleeding
hemarthrosis |
|
symptoms of platelet defect
|
patechiae
|
|
what stimulates the release of factor 8 and vWF form endothelial cells
|
desmopressin
|
|
main symptom of hemophilia
|
hemarthrosis
|
|
lab changes in hemophilia
|
inc PTT
|
|
lab changes in vitamin K def
|
inc PT and PTT
|
|
prothrombin gene mutation
|
G20210A
|
|
what does AT3 normally activate
|
7
9 10 11 12 |
|
heparin given to AT3 def px
|
reduced inc in PTT
|
|
liver makes all clotting factors except
|
vWF
|
|
D-dimers rise from the break down of
|
fibrin
|
|
FDP rise from the break down of
|
fibrin or fibrinogen
|
|
MOA of enoxaparin
|
inhibit factor 10a
|
|
MOA of heparin
|
increase activation of AT
|
|
MOA of HIT
|
heparin binds to platelet factor 4 causing antibody production
|
|
why are px with HIT hypercoagulable
|
platelets are dropped but remaining ones are hyperactive
|
|
MOA of argatroban
|
directly inhibits thrombin
|
|
when is lepirudin used
|
px who take heparin and develops HIT
|
|
MOA of warfarin
|
inhibits epoxide reductase
-normally recycles vit K no more y-carboxylation of factors |
|
what labs change with thrombolytics
|
inc PT and PTT
|
|
what is used in atrial fib
|
warfarin
|
|
what is used in STEMI
|
thrombolytics
|
|
MOA of thrombolytics
|
increase conversion of plasminogen to plasmin
|
|
name some thrombolytics
|
streptokinase
urokinase alteplase (tPA) APSAC (anistreplase) |
|
how does aminocaproic acid work
|
inhibits fibrinolysis
|