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. Author manuscript; available in PMC: 2024 Feb 1.
Published in final edited form as: Br J Haematol. 2022 Oct 20;200(3):358–366. doi: 10.1111/bjh.18507

Table 2.

Comparison of neurocognitive performance between preschool children with sickle cell disease and healthy matched controls

SCD Patients Controls
Measure Score Mean (SD) Mean (SD) Absolute Mean Difference (95% CI) Cohen’s D t p
SB-5a Working Memory 91.71 (13.65) 96.74 (13.36) 5.03 (1.49, 8.57) 0.32 −2.8 0.0056
BBCS-3:R a School Readiness 89.0 (16.70) 95.47 (16.42) 6.47 (2.08, 10.87) 0.39 −2.9 0.0041
BRIEF-P b Working Memory 55.95 (12.95) 51.37 (12.03) 4.58 (1.28, 7.89) 0.37 2.73 0.0068
BRIEF-P b Global Executive function 51.9 (13.66) 47.43 (11.54) 4.47 (1.18, 7.76) 0.35 2.68 0.0079

SCD, sickle cell disease; SD, standard deviation; SB-5, Stanford-Binet Intelligence Scales – Fifth Edition; BBCS-3:R, Bracken Basic Concept Scale – 3rd Edition: Receptive; BRIEF-P, Behavior Rating Inventory of Executive Function – Preschool.

Performance measures included the Stanford-Binet Intelligence Scales – Fifth Edition and the Bracken Basic Concepts Scale – Third Edition: Receptive. Parent ratings of executive functioning collected using the Behavior Rating Inventory of Executive Function – Preschool Version.

a

Displayed values are Standard Scores with a mean of 100 and standard deviation of 15. Higher scores are indicative of better performance

b

Displayed values are T Scores with a mean of 50 and standard deviation of 10. Higher scores are indicative of greater symptoms (i.e., more problems)