Lecture 3- Coagulation Flashcards

(31 cards)

1
Q

Primary hemostasis is … … formation

A

platelet plug

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2
Q

Seconday hemostasis is … … formation

A

fibrin clot

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3
Q

Response sequence of platelets

A

adhesion
activation
aggregation

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4
Q

Platelet adhesion involves membrane receptor …. and the adhesive protein…. and the appropriate surface ….

A

Glycoprotein Ib

von Willebrand Factor (vWF)

Subendothelial matrix (collagen)

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5
Q

In platelet activation, they secrete …. that brings fibrinogen and … which provide ionized calcium and ADP

A

alpha-granules

dense bodies

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6
Q

Platelet leads to activation of …. receptor and … reorganization and the platelet …. changes

A

GP IIb/IIIa

phospholipid

shape (rounded discs to flat planes- increased surface area)

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7
Q

3 molecules that counter primary hemostasis (platelets)

A

NO
Prostacyclin (PGI2)
ADPase

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8
Q

3 molecules that counter secondary hemostasis (coag pathways)

A

Serine protease inhibitors (antithrombin)

Protein C pathway (controls Va and VIIIa)

Fibrinolytic system (removes excess clot)

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9
Q

Activated … plus …. serve to inactivate factors Va and VIIIa

A

Protein C (APC)

Protein S

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10
Q

Protein C or Protein S deficiencies result in …

A

hypercoagulable states

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11
Q

Factor V Leiden mutation promotes…. because of resistance to enzymatic inactivation by the Protein C/S complex

A

coagulation

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12
Q

In the presence of heparin, ATIII will bind and inactivate….

A

thrombin (IIa)

and other serine proteases:
IXa, Xa, XIa, XIIa

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13
Q

Regulation of coag:

Antithrombin inhibits….

Protein C inhibits….

Plasmin removes…

A

serine proteases

cofactors (Va, VIIIa)

excess clot

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14
Q

In the presence of fibrin, … can bind to plasminogen and convert it to plasmin to break down previously cross-linked fibrin monomers into FDP

A

tPA (tissue plasminogen activator)

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15
Q

Prothrombin time (PT) screens for activity of proteins in the … pathway ( factors 5,7,2,10 and fibrinogen)

A

extrinsic

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16
Q

In a PT test, … and … are added to patients plasma with…

A

phospholipid
tissue factor
calcium

17
Q

PT time is time it takes to form a clot which should be …

A

11-13 seconds

18
Q

PT forms the basis of …

which should have a value of … if normal

A

INR (International Normalized Ratio) patient/control

0.8-1.2

19
Q

INR is used to monitor patients on…

20
Q

Partial thromboplastin time (PTT) screens for activity within the … pathway (5, 2, 9, 10, 11, 12 and fibrinogen)

21
Q

PTT often used to monitor patients on…

22
Q

In a PTT test, addition of … to patient serum together with calcium

A

negatively charged activator of Factor XII (kaolin)

23
Q

In a PTT test, clot is formed after … seconds

24
Q

The 3 classifications of vWD are

A

type 1: quantitative deficiency (partial)

type 2: qualitative deficiency

type 3: quantitative deficiency (total)

25
Hemophilia is a ... ... disorder and is a deficiency of ... symptoms are recurrent soft tissue bleeding and symptoms that start in early childhood
X-linked recessive factor VIII
26
lab abnormalities in hemophilia A
prolonged PTT | decreased factor VIII
27
... is a disorder characterized by immune-mediated destruction of platelets. What are the common targets?
Immune Thrombocytopenic Purpura (ITP) GPIb/IX and IIb/IIIa
28
bone marrow and blood findings in ITP
megakaryocytes normal to increased no microangiopathic changes on blood smear review
29
ITP therapy (4)
corticosteroids IV Ig Immunosuppression splenectomy
30
... acute disorder is characterized by intravascular platelet activation with formation of platelet-rich microthrombi throughout the circulation.
Thrombotic Thrombocytopenic Purpura (TTP)
31
TTP is due to deficiency of... which is a ... that normally degrades very high MW vWF
ADAMTS 13 | metalloproteinase