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. 2023 Oct 19;58(4):173–180. doi: 10.5045/br.2023.2023125

Table 1.

Patient characteristics (N=94).

Age, yr, median (range) 62 (18–90)
Male 45 (47.9)
Time of diagnosis
2002–2015 27 (28.7)
2016–2021 67 (71.3)
Palpable splenomegaly 0 (0.0)
Volumetric splenomegaly 47 (50.0)
Laboratory findings
WBC, ×109/L 11.0±4.2
Neutrophil/lymphocyte 3.9±2.4
Monocyte, ×109/L 0.6±0.5
Hemoglobin, g/dL 13.6±2.2
Platelet, ×109/L 948.2±387.7
LDH, ×ULN 1.2±0.4
Driver gene mutation
JAK2V617F 64 (72.8)
CALR 9 (9.6)
MPL 3 (3.2)
JAK2V617F VAF, % 24.8±12.8
IPSET
Low 30 (31.9)
Intermediate 27 (28.7)
High 37 (39.4)
Comorbidity
Hypertension 32 (34.0)
Diabetes mellitus 12 (13.8)
Chronic kidney disease 11 (11.7)
Dyslipidemia 19 (20.2)
Smoking 21 (22.3)
Treatments
Cytoreductive treatment 65 (67.4)
Aspirin 86 (91.5)
Initial thrombotic events
Time of occurrence
Before or at diagnosis 21 (22.3)
After diagnosis 1 (1.1)
Overall 22 (23.4)
Vessels involved
Arterial 21 (22.3)
Venous 1 (1.1)
Follow-up, yr, median (range) 2.9 (0.12–0.2)

Values are presented as number (%) or mean±standard deviation.

Abbreviations: CALR, calreticulin; IPSET, International Prognostic Score in Essential Thrombocythemia; LDH, lactate dehydrogenase; ULN, upper limit of normal; VAF, variant allele frequency.