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Clinical Study

Individualized scheme of immunoadsorption for the recurrence of idiopathic focal segmental glomerulosclerosis in the graft: a single center experience

, , , , , & show all
Pages 777-783 | Received 19 Oct 2014, Accepted 12 Jan 2015, Published online: 26 Feb 2015

Figures & data

Table 1. Characteristics of the kidney transplant recipients with idiopathic FSGS as primary disease.

Table 2. Course of FSGS recurrence in the graft following treatment with IA.

Figure 1. Time course of mean 24-h proteinuria (g/day) in patients with FSGS recurrence in the graft following treatment with IA.

Figure 1. Time course of mean 24-h proteinuria (g/day) in patients with FSGS recurrence in the graft following treatment with IA.

Figure 2. Serum creatinine (mg/dl) alterations from the time of FSGS recurrence to the end of follow-up.

Figure 2. Serum creatinine (mg/dl) alterations from the time of FSGS recurrence to the end of follow-up.

Table 3. Rate of FSGS recurrence in the graft among kidney transplant recipients, who received or not IA pre-operatively.

Figure 3. Time course of 24-h proteinuria (g/day), serum albumin and renal function for one of the four patients who received rituximab in addition to IA. He progressed to ESRD.

Figure 3. Time course of 24-h proteinuria (g/day), serum albumin and renal function for one of the four patients who received rituximab in addition to IA. He progressed to ESRD.

Figure 4. Time course of 24-h proteinuria (g/day), serum albumin (g/dl) and serum creatinine (mg/dl) for one of the four patients who received rituximab in addition to IA. Renal function remained stable while proteinuria went into remission.

Figure 4. Time course of 24-h proteinuria (g/day), serum albumin (g/dl) and serum creatinine (mg/dl) for one of the four patients who received rituximab in addition to IA. Renal function remained stable while proteinuria went into remission.

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