Copyright
©The Author(s) 2015.
World J Crit Care Med. Aug 4, 2015; 4(3): 230-239
Published online Aug 4, 2015. doi: 10.5492/wjccm.v4.i3.230
Published online Aug 4, 2015. doi: 10.5492/wjccm.v4.i3.230
Figure 2 Retrospective study on the probability of cardiovascular thrombotic event-free survival (days up to 3600 d = 10 years) according to the JAK2V617F mutational state in 323 polycythemia vera and 639 essential thrombocythemia patients (Vannucchi et al[20]).
Only major thrombotic events were retrospectively recorded and the erythromelalgic peripheral, ocular and cerebral ischemic events were excluded from evaluation. The overall incidence of major thrombotic events in JAK2V617F mutated PV patients during 10 years follow-up is about 25% in the Italian study[20]. A similar incidence of thrombotic events was found in our literature analysis of 1241 ET patients not on aspirin from 14 retrospective studies[22]. Source Vannucchi et al[20] Blood 2007. ET: Essential thrombocythemia; PV: Polycythemia vera.
- Citation: Michiels JJ. Myeloproliferative and thrombotic burden and treatment outcome of thrombocythemia and polycythemia patients. World J Crit Care Med 2015; 4(3): 230-239
- URL: https://www.wjgnet.com/2220-3141/full/v4/i3/230.htm
- DOI: https://dx.doi.org/10.5492/wjccm.v4.i3.230