Myeloid Proliferative Disorder Chemos Flashcards

1
Q

Polycythemia Vera definition

A

Erthyrocytosis that occurs in combination with leukocytosis, thrombocytosis and/or splenomegaly
- also presents with sticky platelets in histology slides

presents with high hemoglobin/hematocrit and red cell count

General Symptoms

  • vertigo
  • visual issues
  • systolic hypertension
  • erythema and burning/pain inextremeities
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2
Q

Treatment of polycythemia Vera

A

Most important aspect to treat is thrombocytosis via erthrocytosis

  • women = get hemoglobin below 120 g/L (42%)
  • men = get hemoglobin below 140 g/L (45%)

Treated via phlebotomy and Hydroxyurea if phlebotomy isnt treating it properly.

If hyperuricemia is present, use allopurinol to prevent excess elevation of Uric acid

Anticoagulants are indicated for thrombosis treatment also

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3
Q

TxA2 and ADP molecules

A

2 substances responsible for stimulating platelet aggregation

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4
Q

Salicylate MOA

A

Non-selective NSAID used to irreversibly inhibit Cox-1 and reversibly inhibit Cox-2 in platelets and inhibits production of TxA2

“D”

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5
Q

Heparin (HMW)

Enoxaparin (LMW) MOAs

A

Heparin is better effects but is not predictable and can causes dangerous side effects

Enoxaparin is less effective but predictable responses and less serious side effects

Both function to enhance protease Anti-thrombin 3.
- Anti-thrombin 3 functions to inactivate thrombin and Factor X

“C”

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6
Q

Rivaroxaban and Apixaban (Factor Xa inhibitors)

A

Functions to inhibit factor Xa in the coagulation cascade

“C”

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7
Q

Warfarin MOA

A

Inhibits liver vitamin K reductase which inhibits regeneration of Vitamin K
- factors 2,8,9 and 10 are all knocked out

“X” and “D” for patients with mechanical heart valves

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8
Q

Xanthine oxidase inhibitors (allopurinol) MOA

A

Inhibts xanthine oxidase which is the enzyme used to convert hypoxanthine -> xanthine and utricle acid
- reduces urate crystal formation

“B”

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9
Q

Tyrosine kinase inhibitors (ruxolitnib) MOA

A

Selectively inhibits Janus Associated Kinases (JAK 1/2)

“C”

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10
Q

Pegylated interferon (a) MOA

A

Enhance host immune system by increasing activation of T-lymphocytes, NK-cells and macrophages

“C”

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11
Q

Hydroxyurea MOA

A

Inhibits ribonucelotide reductase and inhibits DNA synthesis

“D”

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12
Q

Primary Myelofibrosis (PMF)

A

Mutations inJAK2 which increases cell growth and proliferation

Characterized by marrow fibrosis and hematopoiesis and splenomegaly

Diagnosis of exclusion once PV and thrombocytosis is excluded

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13
Q

Treatment of PMF

A

Glucocorticoids and low-dose thalidomide

  • also consider chemo/interferon treatment for splenomegaly*
  • if high uric acid levels exist = use allopurinol*
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