Cell Biology & Hematology Flashcards

1
Q

What types of molecules are ABO blood type antigens?

A

Glycolipids

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2
Q

What kind of molecules are HLA-type antigens?

A

Glycoproteins

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3
Q

What phase of the cell cycle is the most varible?

A

G1 – determines cell cycle length

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4
Q

What are the products of glycolysis?

A

2 ATP and 2 pyruvate
(Pyruvate enters citric acid cycle and electron transport chain to generate ATP)

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5
Q

Do RBC’s contain nuclear materials?

A

No

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6
Q

What are the three responses to vascular injury?

A

Vasoconstriction, platelet adhesion, thrombin generation

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7
Q

What factor is common amongst the intrinsic and extrinsic pathway?

A

Factor X

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8
Q

What are the intrisic and extrinsic pathways?

A

Intrinsic:
XI –> VIII–> X + V which leads to conversion of prothrombin (II) to thrombin which converts fibrinogen to fibrin

Extrinsic Pathway: Factor VII + X leads to the same conclusion

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9
Q

What is the mechanism of action of heparin?

A

Binds AT III to inactivate thrombin so you don’t get conversion of fibrinogen to fibrin

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10
Q

What are the mechanisms of action of Protein C and S?

A

C: degrades fibrin
S: protein C cofactor (lead to anticoagulation

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11
Q

What is K-centra?

A

PCC or prothrombin complex concentrate (factor II)

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12
Q

Which factor is the only one not synthesized by the liver?

A

Factor VIII (comes from endothelium along with vWF)

Highest concentration is seen in cryoprecipitate. These can be released in response to DDAVP or estrogens

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13
Q

How would you treat the following based on a TEG?
Elevated R time
Elevated K time
Low angle
Low MA
High LY30

A

R: FFP
K: Cryo
Low angle: Cryp
Low MA: Platelets
High LY30: TXA

*Think F - C - C- P

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14
Q

What is the most common congenital bleeding disorder?

A

vWF
I and II are AD
III is AR
I is most common tx w/ DDAVP
II: Cryo
III; Cryo

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15
Q

What is hemophilia A?

A

VIII deficiency (prolonged PTT)
Sex-linked recessive

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16
Q

What is hemophilia B?

A

Factor IX deficiency
AKA Christmas disease
Prolonged PTT

17
Q

What is Glanzmann’s thrombocytopenia?

A

Gp IIb/iiiA receptor deficiency

18
Q

What is Bernard Soulier?

A

GpIb receptor deficiency

19
Q

What is the mechanism of action of argatroban?

A

Direct thrombin inhibitor, used in cases of HIT
With HIT see formation of white clot

20
Q

What is the most common congenital hypercoag disorder?

A

Factor V Leiden, causes resistance to activated protein C

21
Q

What is the most common factor causing acquired hypercoagulability?

A

Tobacco

22
Q

What are indications for IVC filter? (4)

A
  1. C/i to anticoag
  2. PE while on anticoag
  3. Free floating IVC thrombus
  4. Recent pulmonary embolectomy
23
Q

What is the reversal agent for Pradaxa (Dabigatran), Eliquis and Xarelto?

A

Pradaxa (prax bind) Aka idarucizumab
Eliquis and Xarelto: Andexxa (andexanet alfa)

**PCC can also give partial reversal