Table 4.

Risk factors associated with alloimmunization in patients with SCD

Clinical variablesLogistic regression analysis Multivariate logistic regression analysis using transfusion loadMultivariate logistic regression analysis using transfusion frequency
Adjusted OR (95% CI)P valueAdjusted OR (95% CI)P valueAdjusted OR (95% CI)P value
All patients       
Age at first transfusion (y) 0.96 (0.90, 1.03) .31 — — — — 
Sex, male vs female 0.90 (0.48, 1.69) .75 — — — — 
Hb genotype, SS/Sβ0 thalassemia vs Others  12.14 (1.64, 89.86) .015 11.22 (1.51, 83.38) .018 5.84 (0.76, 45.67) .089 
Transfusion load (units)  1.02 (1.01, 1.04) .007 1.02 (1.003, 1.04) .020 — — 
Transfusion frequency,
Chronic vs Episodic 
17.64 (8.19, 38.00) < .001 — — 14.19 (6.54, 30.80) < .0001 
Patients who received episodic transfusion       
HU yes/no 6.52 (0.85, 49.77) .071 — — — — 
HU therapy duration 1.13 (0.997, 1.28) .056 — — — — 
HU MTD (mg/kg per d) 1.06 (0.96, 1.16) .242 — — — — 
Clinical variablesLogistic regression analysis Multivariate logistic regression analysis using transfusion loadMultivariate logistic regression analysis using transfusion frequency
Adjusted OR (95% CI)P valueAdjusted OR (95% CI)P valueAdjusted OR (95% CI)P value
All patients       
Age at first transfusion (y) 0.96 (0.90, 1.03) .31 — — — — 
Sex, male vs female 0.90 (0.48, 1.69) .75 — — — — 
Hb genotype, SS/Sβ0 thalassemia vs Others  12.14 (1.64, 89.86) .015 11.22 (1.51, 83.38) .018 5.84 (0.76, 45.67) .089 
Transfusion load (units)  1.02 (1.01, 1.04) .007 1.02 (1.003, 1.04) .020 — — 
Transfusion frequency,
Chronic vs Episodic 
17.64 (8.19, 38.00) < .001 — — 14.19 (6.54, 30.80) < .0001 
Patients who received episodic transfusion       
HU yes/no 6.52 (0.85, 49.77) .071 — — — — 
HU therapy duration 1.13 (0.997, 1.28) .056 — — — — 
HU MTD (mg/kg per d) 1.06 (0.96, 1.16) .242 — — — — 

Indicated in bold, P < 0.05 is considered significant.

Adjusted for time on study, which is from patients receiving the first RBC transfusion at our center to the first newly identified antibody for patients who were alloimmunized, and to 31 December 2017 or one day before patients turning 19 years old (whichever came first) for patients who were not alloimmunized.

Others include all non-HbSS/Sβ0–thalassemia genotypes.

OR was based on a 5-unit increase.

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