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Tests to establish the cause of secondary polycythemia
What tests are useful in establishing the cause of secondary polycythemia?
2020-11-10
What tests are useful in establishing the cause of secondary polycythemia?
What antithrombotic treatment should be used in a patient with thrombosis and myeloproliferative neoplasms (MPNs)? Should antiplatelet treatment be continued?
What is your approach in a patient with a low burden of JAK2 mutation without other diagnostic criteria for myeloproliferative neoplasms (MPNs)? Does this approach change if the patient has a history of thrombosis?
What is the recommended management of prefibrotic primary myelofibrosis (pre-PMF)?
Do you use any questionnaires to assess bleeding symptoms?
Do you continue phlebotomy in patients with polycythemia vera (PV) who receive cytoreductive treatment?
Should each patient homozygous for mutation of the C282Y gene be diagnosed with hemochromatosis and treated with phlebotomy?
What is the best blood test to check if a patient has iron deficiency?
Does a negative genetic test (C282Y and H63D) result exclude hemochromatosis in a patient with transferrin saturation >45% and ferritin level >1000?
