Exam #1: Coagulation Studies Flashcards

1
Q

What involves splenomegaly → thrombocytopenia?

A

Splenic Sequestration

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2
Q

In what way do the following conditions affect RBCs: ITP, DIC, HIT, TMA (TTP and HUS)?

A

Increased Destruction of RBCs

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3
Q

What condition involves simultaneous clotting and bleeding?

A

Disseminated Intravascular Coagulation (DIC)

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4
Q

What condition involves significantly low platelet count – consider meds, excessive bleeding/bruising?

A

Immune Thrombocytopenia (ITP)

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5
Q

What condition involves acquired thrombocytopenia while on heparin therapy?

A

Heparin-Induced Thrombocytopenia (HIT)

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6
Q

Why MUST platelets be monitored with Heparin use?

A

Can cause thrombocytopenia

- If thrombocytopenia presents, heparin must be stopped immediately and never restarted

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7
Q

Which platelet disorder involves thrombosis in capillaries and arterioles due to endothelial injury?

A

Thrombotic Microangiopathies (TMA)

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8
Q

Which condition is associated with ADAMTS-13?

A

Thrombotic Thrombocytopenic Purpura (TTP)

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9
Q

Which platelet disorder is a medical emergency; more common in black females?

A

Thrombotic Thrombocytopenic Purpura (TTP)

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10
Q

Which condition involves the pentad of microangiopathic hemolytic anemia, thrombocytopenia, AKI, neuro deficits, fever?

A

Thrombotic Thrombocytopenic Purpura (TTP)

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11
Q

Which condition is associated with Shiga toxin-producing E. coli O157:H7?

A

Hemolytic-Uremic Syndrome (HUS)

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12
Q

Which condition is mostly seen in children and MUST present with bloody stools?

A

Hemolytic-Uremic Syndrome (HUS)

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13
Q

Which condition involves the triad of microangiopathic hemolytic anemia, thrombocytopenia, AKI?

A

Hemolytic-Uremic Syndrome (HUS)

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14
Q

Which condition shows fragmented RBCs (schistocytes/helmet cells)?

A
Thrombotic Microangiopathies (TMA)
- Includes microangiopathic hemolytic anemia
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15
Q

In what way do the following conditions affect RBCs: congenital vs. acquired bone marrow failure, chemotherapy/radiation, bone marrow infiltration (CA vs. infection), nutritional (vitamin B12/folate/iron deficiency, alcohol)?

A

Impaired Production of RBCs

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16
Q

What lab test involves the intrinsic and common pathways?

A

PTT or aPTT

- You play “table tennis” (aka TT) “INside” (aka intrinsic)

17
Q

What lab test is used to monitor UFH?

A

PTT or aPTT

18
Q

What lab test involves the extrinsic and common pathways?

A

PT

- You play “tennis” (aka T) “outside” (aka external)

19
Q

What two lab tests are used to monitor Warfarin?

A
  • INR
  • PT

NOTE: for PT, it uses external pathway and you go to “war” (aka Warfarin) with “other/external” countries (external)

20
Q

Which three anticoagulants are often preferred for outpatient treatment (do not require IV)?

A
  • Warfarin
  • Xarelto (Direct Xa inhibitor)
  • Eliquis (Direct Xa inhibitor)
21
Q

Direct Thrombin Inhibitors (Pradaxa) AND Direct Xa Inhibitors (Xarelto, Eliquis, Lixiana/Savaysa) are both examples of what?

A

Direct Oral Anticoagulants (DOACs)

22
Q

For patients with a DVT or PE WITHOUT CA, what anticoagulation treatment is recommended?

A

Direct Oral Anticoagulants (DOACs) so…

  • Direct Thrombin Inhibitors (Pradaxa)
  • Direct Xa Inhibitors (Xarelto, Eliquis, Lixiana/Savaysa)
23
Q

For patients with a DVT or PE WITH CA, what anticoagulation treatment is recommended?

A

LMWH

24
Q

What is the initial dosing of Warfarin? What should subsequent dose adjustments be based off of?

A

Initial dose of 5mg/day

- Adjust based on INR values

25
Q

What is the target INR value for Warfarin usually?

A

2.0-3.0

26
Q

What is the reversal agent used to treat Warfarin “overdose” aka supratherapeutic INR?

A

Vitamin K

27
Q

What is the reversal agent for UFH, LMWH?

A

Protamine

28
Q

What is the reversal agent for Xarelto, Eliquis?

A

Andexane

29
Q

Is acquired or congenital platelet dysfunction more common?

A

Acquired (i.e. drugs/chemo)

30
Q

What lab test is used to monitor UFH AND LMWH?

A

Anti-Factor Xa (anti-Xa)

31
Q

What lab test are these components of: antithrombin, Factor V-Leiden, Protein C, Protein S, prothrombin gene mutation, lupus anticoagulant (anti-phospholipid antibodies), MTHFR gene

A

Hypercoagulable Panel

32
Q

If starting a patient on UFH, which three labs should be ordered for baseline? Which two can be ordered for monitoring?

A

Baseline:

  • aPTT
  • PT/INR
  • CBC

Monitoring:

  • aPTT
  • Factor Xa
33
Q

If starting a patient on LMWH, which four labs should be ordered for baseline? Are monitoring tests required?

A

Baseline:

  • aPTT
  • PT/INR
  • CBC
  • Creatinine

Monitoring: NOPE

34
Q

If starting a patient on a DOAC, which three labs should be ordered for baseline? Are monitoring tests required?

A

Baseline:

  • PT/INR
  • CBC
  • Creatinine

Monitoring: NOPE

35
Q

If starting a patient on Warfarin, which five labs should be ordered for baseline? Which lab should be ordered for monitoring?

A

Baseline:

  • aPTT
  • PT/INR
  • CBC
  • Creatinine
  • LFTs

Monitoring:
- PT/INR

36
Q

For how long should parenteral anticoagulation treatment (UFH/LMWH) overlap with Warfarin?

A

At least 5 days

- And until INR is therapeutic for 24 hours or 2 days

37
Q

What is the best option for decreasing INR if life-threatening situation?

A

PCC with Vitamin K (IV)