Table 4:
All Sickle Cell Disease | HbSS/HbSβ° Thalassemia | HbSC/HbSβ+ Thalassemia | ||||
---|---|---|---|---|---|---|
Variable | Odds Ratio (95% CI) | p | Odds Ratio (95% CI) | p | Odds Ratio (95% CI) | p |
Age | 0.86 (0.82 – 0.90) | < 0.0001 | 0.81 (0.75 – 0.87) | <0.0001 | 0.93 (0.87 – 0.99) | 0.03 |
Male Sex | 0.16 (0.07 – 0.41) | 0.0001 | 0.13 (0.04 – 0.50) | 0.003 | 0.08 (0.02 – 0.46) | 0.004 |
Hemoglobin | 0.76 (0.61 – 0.94) | 0.01 | ||||
Weight | 0.96 (0.93 – 0.99) | 0.004 | 0.94 (0.89 – 0.99) | 0.01 | ||
Hydroxyurea Therapy | 2.99 (1.18 – 7.56) | 0.02 | ||||
Use of ACE-I/ARBs | 0.08 (0.01 – 0.75) | 0.03 | 0.07 (0.01 – 0.82) | 0.03 | ||
Lactate Dehydrogenase | 0.998 (0.997 – 1.000) | 0.03 |
ACE-I = angiotensin-converting enzyme inhibitor; ARB = angiotensin receptor blocker
For continuous variables Odds Ratios (OR) are for a one unit change.
Results from multivariable logistic regression with backward elimination for variable selection. Variables initially assessed for inclusion in the model: white blood cell count, hemoglobin, reticulocyte count, lactate dehydrogenase, total bilirubin, hydroxyurea therapy, weight, systolic blood pressure, diastolic blood pressure, acute chest syndrome, and ACE inhibitor/ARB therapy. The model was adjusted for age and sex.