Pathophys II- Hemostasis Flashcards

1
Q

Which test measures Extrinsic pathway?

A

PT

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2
Q

Which test measures Intrinsic pathway?

A

aPTT

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3
Q

aPTT means

A

activated Partial Thromboplastin Time

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4
Q

Bleeding time measures=

A

PLT ability of adhesion to vessel walls

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5
Q

Normal BT value

A

3-8 min

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6
Q

BT↑ when PLT__

A

Decrease

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7
Q

If BT↑ and PLT are normal=

A

Problem with PLT function

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8
Q

What is needed for aPTT?

A

Phospholipid
Surface
Calcium

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9
Q

Normal aPTT time=

A

30-40 sec

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10
Q

When checking for aPTT, are there any PLT?

A

No

Only plasma

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11
Q

How de we detect Inhibitors?

A

We mix patient plasma with normal plasma 1:1

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12
Q

If PT and aPTT prolonged

A

Inhibitor of common pathway or strong lupus inhibitor

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13
Q

Initiation of extrinsic pathway

A

TF
Lipid
Calcium

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14
Q

Normal PT time

A

10-14 sec

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15
Q

Normal INR

A

1

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16
Q

Prolonged PT may mean-

A
Deficiency of:
I
II
V
VII
X
Oral anticoagulant
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17
Q

TT determines

A

Rate of thrombin induced fibrinogen cleavage

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18
Q

Normal value TT

A

<20 sec

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19
Q

Prolonged TT means

A

Many things-

<100 mg/dL Fibrinogen

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20
Q

Normal value Fibrinogen

A

200-400 mg/dL

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21
Q

Decreased FIbrinogen seen in

A

Liver disease

DIC

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22
Q

Which clotting factors need vitamin K?

A
II
VII
IX
X
Protein S
Protein C
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23
Q

Warfarin mechanism

A

Blocks enzyme that activates vit.K

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24
Q

D-dimer may be elevated in

A
DIC
Venous thromboembolism
Infection
Cancer
Pregnancy
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25
Heparin mecahnism
Binds Antithrombin III and activates it
26
Laboratory alteration in DIC
PLT↓ FIbrinogen↓ D-dimer in serum and urine
27
When do Purpura happens?
When small blood vessels burst
28
High MPV may mean
We produce too many PLT
29
Patient with thrombocyopenia and known history of SLE=
Idiopathic Thrombocytopenic purpura
30
What shoould we check in order to determine Idiopathic Thrombocytopenic purpura
Auto ab
31
Immune complex deposition is type __ HSN
III
32
Patient with thrombocyopenia and known history of SLE. | How can we explain the renal failure?
Lupus nephritis- Immune complex deposition
33
What can explain the anemia in this patient with SLE?
Renal failure means low EPO
34
WHy low PLT in the patient with SLE
Spleen recognize the Ab coated PLT and destroys them
35
BUN=
Blood Urea Nitrogen
36
Recurrent epileptic seizures Fever Purpura Low PLT
Thrombotic Thrombocytopenic purpura
37
Thrombotic Thrombocytopenic purpura mecahnism
- Antibodies inhibiting ADAMTS13 | - ADAMTS13 disfunction
38
ADAMTS13 job
Breaks down multimers of vWF
39
What happens when multimers of vWF are not broken down?
More prone to coagulation | Coagulation happens ,ore frequently in the microcirculation
40
Why LDH is high in Thrombotic Thrombocytopenic purpura
RBC passing microscopic clots are subject to shear stress→Membrane damage→Rupture of RBC
41
Why anemia and schistocyte in Thrombotic Thrombocytopenic purpura?
RBC passing microscopic clots are subject to shear stress→Membrane damage→Rupture of RBC
42
Why renal failure in Thrombotic Thrombocytopenic purpura?
Microthrombi in renal vessels
43
Why Haptaglobin is low in Thrombotic Thrombocytopenic purpura?
Intravascular hemolysis
44
What od we expect to see on blood smear in case of Thrombotic Thrombocytopenic purpura?
Schistocytes
45
Normal ESR values
0-20 mm/h
46
Is CK 160 U/l normal?
Yes
47
Which cardiac marker should be elevated in MI?
CK-MB
48
CK-MB means
Creatine Kinase Myocardial Band
49
Right swollen thigh Dilated superficial veins Dyspnea Chest pain
DVT with PE
50
How to confirm DVT with PE
Ultrasound Chest CT angiogram ECG
51
What pattern on ECG can we see in PE
S1Q3T3
52
Patient with: PLT↓↓↓ BT↑ Normal coagulation parameters
Severe Thrombocytopenia
53
What can cause Severe Thrombocytopenia?
Acute Leukemia Autoimmune Thrombocytopenia Drug induced
54
TT normal value | Thrombin Time
<20 sec
55
Why we see aPTT↑ in vWF disease?
Bcs it is bound to fVIII usually and without it fVIII has shorter life time and it effects the Intrinsic pathway
56
How can we make sure it is vWF disease except genetics?
Ristocetin aggregation test
57
Describe Ristocetin
Ristocetin enhance vWF ans PLT GPbI addhesion
58
GPbI deficieny is called
BSS | Bernard Soulier Syndrome
59
Normal ESR
<20 mm/h
60
TT value
<20 sec
61
Pain in the leg+elevaated D-Dimer can be due to
DVT
62
What can trigger formation of Anti-phospholipid Ab?
HLA-DR7 mutation
63
HLA-DR7 makes what protein
MHC-II on B cells
64
Young women eith SLE and aPTT↑
Antiphospholipid syndrome
65
We can diagnose TTP while checking for
ADAMTS-13