Myeloid Proliferative Disorder Chemos Flashcards
Polycythemia Vera definition
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
Treatment of polycythemia Vera
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
TxA2 and ADP molecules
2 substances responsible for stimulating platelet aggregation
Salicylate MOA
Non-selective NSAID used to irreversibly inhibit Cox-1 and reversibly inhibit Cox-2 in platelets and inhibits production of TxA2
“D”
Heparin (HMW)
Enoxaparin (LMW) MOAs
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”
Rivaroxaban and Apixaban (Factor Xa inhibitors)
Functions to inhibit factor Xa in the coagulation cascade
“C”
Warfarin MOA
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
Xanthine oxidase inhibitors (allopurinol) MOA
Inhibts xanthine oxidase which is the enzyme used to convert hypoxanthine -> xanthine and utricle acid
- reduces urate crystal formation
“B”
Tyrosine kinase inhibitors (ruxolitnib) MOA
Selectively inhibits Janus Associated Kinases (JAK 1/2)
“C”
Pegylated interferon (a) MOA
Enhance host immune system by increasing activation of T-lymphocytes, NK-cells and macrophages
“C”
Hydroxyurea MOA
Inhibits ribonucelotide reductase and inhibits DNA synthesis
“D”
Primary Myelofibrosis (PMF)
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
Treatment of PMF
Glucocorticoids and low-dose thalidomide
- also consider chemo/interferon treatment for splenomegaly*
- if high uric acid levels exist = use allopurinol*