Secondary Hemostasis Flashcards

1
Q

preferred name and synonyms of factor I

A

fibrinogen

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2
Q

preferred name and synonyms of factor II

A

prothrombin

prethrombin

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3
Q

preferred name and synonyms of factor III

A

tissue factor
tissue thromboplastin
*thrombokinase

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4
Q

preferred name and synonyms of factor IV

A

calcium

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5
Q

preferred name and synonyms of factor V

A

proaccelerin
labile factor
accelerator globulin
*thrombogen

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6
Q

preferred name and synonyms of factor VII

A
proconvertin
stable factor
autoprothrombin 1
*cothromboplastin
*serum prothrombin conversion accelerator
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7
Q

preferred name and synonyms of factor VIII

A
antihemophilic factor
antihemophilic globulin
antihemophilic factor A
platelet cofactor 1
*thromboplastinigen
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8
Q

preferred name and synonyms of factor IX

A
antihemophilic factor B
autoprothrombin 2
platelet cofactor 2
Christmas factor
plasma thromboplastin component (PTC)
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9
Q

preferred name and synonyms of factor X

A

Stuart factor
Prower factor
Stuart-Prower factor
autoprothrombin 3

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10
Q

preferred name and synonyms of factor XI

A

antihemophilic factor C

plasma thromboplastin antecedent (PTA)

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11
Q

preferred name and synonyms of factor XII

A

Hageman factor
glass factor
contact factor

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12
Q

preferred name and synonyms of factor XIII

A
Laki-Lorand factor
fibrin stabilizing factor
*fibrinase
*fibrinoligase
*plasma transglutaminase
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13
Q

preferred name and synonyms of prekalikrein

A

Fletcher factor

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14
Q

preferred name and synonyms of HMWK

A

Fitzgerald factor
contact activation factor
Williams factor
Flaujeuc factor

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15
Q

a transglutaminase

A

factor XIII

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16
Q

factors that are labile in room temperature

A

factor V and VIII

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17
Q

factors that are cold labile

A

factor VII and XI

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18
Q

intrinsic pathway factors

A

factors XII, XI, HMWK and prekalikrein

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19
Q

extrinsic pathway factors

A

factor VII

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20
Q

common pathway factors

A

factors I, II, V, X

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21
Q

factors that are affected by oral anticoagulants such as coumarin, coumadin and warfarin

A

“Vitamin K dependent/Prothrombin group”
factors II, VII, IX, X
protein S and protein C

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22
Q

coagulation factors that are consumed first in coagulation

A

“Fibrinogen group”

factors I, V, VIII, XIII

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23
Q

coagulation factors that are considered as acute phase reactants

A

“Fibrinogen group”

factors I, V, VIII, XIII

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24
Q

the active enzyme of fibrinolysis that dissolves FIBRIN, FIBRINOGEN, FACTOR V, FACTOR VIII and also activates complement

25
these are the plasminogen activators
factor XIIa, kallikrien, HMWK, plasma proactivator
26
substances that act BOTH as INHIBITORS of COAGULATION and FIBRINOLYSIS
a-2-macroglobulin: thrombin, kallikrien, plasmin a-1-antitrypsin: thrombin, Xa, XIa, plasmin C1 inhibitor: kallikrein, XIIa, plasmin
27
inhibitors of coagulation that degrades factor V and VIII
protein S and protein C
28
inhibitors of thrombin
``` antithrombin III (major inhibitor) heparin cofactor II ```
29
inhibits factor VIIa tissue factor complex
extrinsic pathway inhibitor or lipoprotein associated coagulation inhibitor (LACI)
30
major inhibitor of plasmin
a-2-antiplasmin
31
FDPs that are early degradation products; have anticoagulant activity
X and Y
32
FDPs that are late degradation products
D and E
33
FDPs that inhibit fibrin polymerization
Y and D
34
FDP that is a powerful inhibitor of thrombin
E
35
pathologic fibrinolysis characterized by the degradation of fibrinogen
primary fibrinolysis
36
pathologic fibrinolysis characterized by the degradation of fibrin
secondary fibrinolysis
37
test to differentiate primary fibrinolysis ans secondary fibrinolysis
protamine sulfate test primary: negative secondary: positive
38
when does primary fibrinolysis happen?
excessive amount of plasminogen actovators
39
when does secondary fibrinolysis happen?
DIC, snake bites, neoplasm and snake bites
40
laboratory findings of qualitative and quantitative deficiencies of FIBRINOGEN
APTT, PT, TT: PROLONGED
41
treatment for afibrinogenemia
cryoprecipitate, FFP
42
laboratory findings in dysfibrinogenemia
NORMAL bleeding time, and unusually normal levels of fibrinogen that are however non/dysfunctional
43
laboratory findings in factor XIII deficiency
APTT, PT, TT: NORMAL
44
test that is never affected by heparin
reptilase time
45
other name for factor XI deficiency
Rosenthal syndrome
46
other name for factor V deficiency
parahemophilia, Owren's disease
47
acquired disorders of factor XIII can be caused by:
isoniazid
48
acquired disorders of factor X can be caused by:
amyloidosis
49
the lupus-like inhibitor may be acquired thru:
SLE | phenazothiazine
50
synergistic activity of these two substances would enhance the ability to bind and inactivate thrombin; also used to TREAT THROMBOSIS
heparin and antithrombin III
51
substance that neutralizes heparin
protamine sulfate
52
hereditary pattern of all coagulation factors except factor I and factor VIII
autosomal recessive
53
hereditary pattern of factor I and factor VIII
autosomal dominant
54
abnormality in bleeding time is caused by:
disease of primary hemostasis | von Willebrand disease
55
abnormality in PT is caused by:
abnormality in extrinsic and common pathway
56
abnormality in APTT is caused by:
abnormality in intrinsic and common pathway
57
abnormality in stypven time is caused by:
factors I, II, V, X deficiency
58
abnormality in thrombin time is caused by:
factor I deficiency
59
abnormality in Duckert's test is caused by:
factor XIII deficiency