Abstract Objective To investigate the risk factors for steroid-induced osteonecrosis of the femoral head (SONFH) after glucocorticoid (GC) therapy in children with immune kidney diseases. Methods This retrospective study included patients (1–18years) diagnosed with immune kidney disease treated with GCs from January 2012 to July 2022 in our hospital. Data, such as sex, age and body weight at the first GC treatment, and the GC dose, were collected. Patients were divided into SONFH and non-SONFH groups based on the occurrence of SONFH. According to the International Classification of Diseases (ICD-10), the disease diagnosis was searched on the clinical data webpage of our hospital. The descriptive statistics and binary logistic regression analyses were performed. A nomogram was constructed to predict the risk of SONFH in children with immune kidney disease after GC treatment. The predictive ability of the nomogram was evaluated using the concordance index and calibration plots. Results The SONFH and non-SONFH groups included 18 and 90 patients, respectively. Age at the first GC treatment, the six-month cumulative (oral [po.] plus intravenous [iv.]) GC dose, the total cumulative prednisone (po.) dose, total cumulative methylprednisolone (iv.) dose for pulse therapy, and total cumulative GC (po. plus iv.) dose significantly differed between the two groups. Age at the initial GC treatment, the total cumulative prednisone (po.) dose, and the total cumulative methylprednisolone (iv.) dose for pulse therapy were independent risk factors for SONFH in the multivariate analysis. Conclusions This study identified specific risk factors for developing SONFH during GC treatment. Thus, children with immune-related kidney disease undergoing GC treatment should be closely monitored based on these risk factors, which aims to avoid the irreversible damage to the femoral head.
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