Figure 9.
Preexisting SCIs. (A) Preexisting SCIs associated with subsequent neurological events in children with HbSS or HbSβ0 thalassemia. Time to first neurological event-stroke, seizure, TIA for children with normal or conditional TCD measurements (time averaged mean maximum velocity of <200 cm/s, nonimaging, or <185 cm/s imaging technique) and with (n = 68) and without SCIs on MRI (n = 353). (B) Associated with recurrent SCIs in adults with sickle cell anemia. A total of 54 adults with HbSS or HbSβ0 thalassemia had a minimum time of 6 months between at least 2 MRIs of the brain; in this group of adults, 43% (n = 23) had SCI at baseline and 57% (n = 31) had no SCI at baseline; individuals with overt stroke were excluded based on history and examination by a neurologist. Reprinted from Jordan et al159 (A) and Jordan et al26 (B) with permission.

Preexisting SCIs. (A) Preexisting SCIs associated with subsequent neurological events in children with HbSS or HbSβ0 thalassemia. Time to first neurological event-stroke, seizure, TIA for children with normal or conditional TCD measurements (time averaged mean maximum velocity of <200 cm/s, nonimaging, or <185 cm/s imaging technique) and with (n = 68) and without SCIs on MRI (n = 353). (B) Associated with recurrent SCIs in adults with sickle cell anemia. A total of 54 adults with HbSS or HbSβ0 thalassemia had a minimum time of 6 months between at least 2 MRIs of the brain; in this group of adults, 43% (n = 23) had SCI at baseline and 57% (n = 31) had no SCI at baseline; individuals with overt stroke were excluded based on history and examination by a neurologist. Reprinted from Jordan et al159  (A) and Jordan et al26  (B) with permission.

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