Polycythemia medical therapy: Difference between revisions
Jump to navigation
Jump to search
Line 2: | Line 2: | ||
{{Polycythemia}} | {{Polycythemia}} | ||
{{CMG}} {{AE}}{{Debduti}} | {{CMG}} {{AE}}{{Debduti}} | ||
==Overview== | ==Overview== |
Revision as of 19:48, 6 December 2020
Polycythemia Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Polycythemia medical therapy On the Web |
American Roentgen Ray Society Images of Polycythemia medical therapy |
Risk calculators and risk factors for Polycythemia medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Debduti Mukhopadhyay, M.B.B.S[2]
Overview
- Phlebotomy is used to decrease blood thickness.
- Medicines that may be used include:[1]
- Hydroxyurea: it used to reduce red blood cells counts and other blood cells if high. It also used to prevent thrombosis in patients >60 years of age with chronic PV.
- Interferon: reduce blood cell counts.PegIFN can be used to reduce established splenomegaly but not usually to normal size.
- Anagrelide: used to treat thrombocytosis.
- Ruxolitinib (JAK1/2 inhibitor): proved to be effective in PPMF and chronic-phase PV; provided durable symptom relief, blood count control, and reduction in splenomegaly; and was superior to hydroxyurea.
- Aspirin: used to prevent thrombosis.
- Ultraviolet-B light therapy: reduce the itchiness.
References
- ↑ Spivak JL (2019). "How I treat polycythemia vera". Blood. 134 (4): 341–352. doi:10.1182/blood.2018834044. PMID 31151982.