M4 QUALITATIVE PLATELET DISORDERS (ACQUIRED) Flashcards

(34 cards)

1
Q

structural and functional modifications of
arachidonic acid pathway enzymes

A

ASPIRIN-LIKE DEFECTS

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2
Q

inhibition of cyclooxygenase

A

ASPIRIN-LIKE DEFECTS

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3
Q

absence or abnormalities of the components of the
thromboxane pathway

A

ASPIRIN-LIKE DEFECTS

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4
Q

Ibuprofen

A

Inhibits platelet function

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5
Q

Thromboxane -

A

Activate neighboring platelets

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6
Q

Bleeding caused by platelet dysfunction

A

UREMIA

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7
Q

UREMIA:
Circulating ____ or ___ Interference

A

guanidinosuccinic acid (GSA) or
hydroxy phenolic acid

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8
Q

GSA (Guanidinosuccinic Acid) is a ____

A

NO (Nitric Oxide)
donor which is a platelet inhibitor

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9
Q

COX INHIBITOR

A

ACETYLSALICYLIC ACID (ASPIRIN)

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10
Q

ACETYLSALICYLIC ACID (ASPIRIN)
Interferences:

A
  1. Platelet membrane receptor sites
  2. Prostaglandin synthesis
  3. Phosphodiesterase activity
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11
Q

competitive inhibitors of cyclooxygenase

A

IBUPROFEN AND RELATED COMPOUNDS

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12
Q

COX-1 (Irreversible)

A

Aspirin

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13
Q

COX-1 (reversible)

A

Naproxen
Sulfinpyrazone
Ibuprofen

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14
Q

ADP P2Y12 (Irreversible)

A

Clopidogrel
Prasurgel

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15
Q

ADP P2Y12 (reversible)

A

Ticagrelor
Cangrelor

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16
Q

Thrombin PAR-1

17
Q

Sticky Platelet Syndrome

A

HYPERAGGREGABLE PLATELETS

18
Q

autosomal dominant, thrombophilic disorder that is
associated with venous and arterial thromboembolic
events.

A

STICKY PLATELET SYNDROME

19
Q

Overactivation of the agonist

A

STICKY PLATELET SYNDROME

20
Q

aggregation in response to
in vitro stirring only

A

spontaneous aggregation

21
Q

Stormorken

22
Q

Sticky Platelet

A

Platelet Clot

23
Q

Autosomal
dominant

A

vWF disease
Quebec platelet
Sticky Platelet
Syndrome

24
Q

Autosomal
recessive

A

-Bernard-Soulier
syndrome
-Glanzmann
thrombasthenia
-Gray platelet
syndrome
-Thrombocytopenia absent radius (TAR)
syndrome
-Hermansky-Pudlak
syndrome

25
X-linked
Wiskott-Aldrich syndrome Scott syndrome
26
no aggregation with natural agonists - Because there is qualitative or quantitative defect of GP αIIbβ3
Glanzmann thrombasthenia (Abnormal Clot retraction)
27
decreased Thrombin generation - Because phosphatidylserine cannot translocate to the outer layer
scott
28
lack of adhesion to VWF and abnormal response to thrombin - Deficiency or mutation on GP: IX, Ibβ, and Ibα
Bernard-Soulier syndrome
29
spontaneous binding of VWF to GP Ibα - Result of binding: they are removed from the circulation
Platelet-type VWD (Type 2B)
30
Gray Platelet Syndrome Quebec Platelet Disorder α-Dense granule-storage pool deficiency Wiskott-Aldrich Syndrome
α-Granules
31
G-proteins Phospholipases
Signaling pathways
32
Hermansky-Pudlak syndrome Chediak-Higashi syndrome Dense granule-storage pool deficiency Wiskott-Aldrich Syndrome
Dense granules
33
Cyclooxygenase TXA2 synthase Lipoxygenase (Drug induced)
Enzymes in dense tubular system
34
Giant Platelet syndromes ● Large platelets Wiskott-Aldrich syndrome ● Micro Platelets or micro thrombocytes formation
Cytoskeleton