Skip to main content
. Author manuscript; available in PMC: 2019 Oct 1.
Published in final edited form as: Exp Hematol. 2018 Jul 19;66:42–49. doi: 10.1016/j.exphem.2018.07.004

Table 1.

Patient demographics

Age (years) Range 15 –70
Mean ± SD 34.3 ± 11.8

Sex, n (%) Female 86 (65.6)
Male 45 (34.4)
Sickle Cell Type, n (%)a SS type SCD-SS 102 (77.9)
SCD-Sβ° 7 (5.3)
Others SCD-SC 15 (11.5)
SCD-Sβ+ 7 (5.3)
CPI (0–100) Range 14.8–86.5
Mean ± SD 40.6 ± 13.4
Utilization Range 0–38
Mean ± SD 4.5 ± 5.3
Utilization Groups, n (%) Zero (0) 19 (14.5)
Low (1–3) 56 (42.7)
High (4–38) 56 (42.7)
a

Sickle cell types: SCD–SS (SCD–homozygous hemoglobin S, sickle cell anemia) and SCD–Sβ° (SCD–sickle β° thalassemia); others include SCD–SC (SCD–sickle hemoglobin C) and SCD–Sβ+ (SCD–sickle β+ thalassemia).