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Table 3 Comparison of patients characteristics according to the alpha thalassemia trait

From: High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte

 

Alpha thalassemia trait (n = 80)

No alpha thalassemia trait (n = 52)

P

Mean (±SD) or n (%)

Hb (g/d L)

8,2 (±0,1)

7,7 (±0,2)

0,007

Hématocrit (%)

25,6 (±0,4)

23,8 (±0,5)

0,004

MCV (fL)

73,3 (±1)

81,8 (±1,5)

< 0,001

Reticulocytes (G/L)

239,6 (±10)

288,2 (±13,8)

0,004

TCD

  

0,017

Normal

72 (90)

37 (71,2)

 

Limit

3 (3,7)

8 (15,4)

 

Pathological

5 (6,3)

7 (13,4)

 

Splenomegaly ratio

0,54 (±0,03)

0,43 (±0,05)

0,057

Cerebral vasculopathy

  

0,004

Yes

78 (91,8)

43 (72,9)

 

Pathological TCD/MRI

7 (8,2)

13 (22)

 

Stroke

0

3 (5,1)

 

RBC Transfusion

  

0,028

No

28 (29,4)

10 (15,6)

 

Occasionnally

60 (63,2)

42 (65,6)

 

Exchange transfusion

7 (7,4)

12 (18,8)