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. 2021 May 6;6(8):2134–2143. doi: 10.1016/j.ekir.2021.04.029

Table 2.

Characteristics of patients and treatment at the start of apheresis

Total population
Remission
No remission
P value
n = 21 n = 7 n = 14
Clinical and biological characteristics
Age (y) [IQR] 34 [24–50] 51 [31–65] 30 [22–40] 0.05
Min-Max (years) 16–76 16–76 16–49
Hemoglobin level (g/dl) [IQR]; n = 18/21, 6/7, 12/14 10.9 [9.2–12.3] 9.6 [9.1–11.7] 11.3 [10.1–12.8] 0.17
Platelet count (109/l) [IQR]; n = 17/21, 6/7, 11/14 299 [249–365] 294 [235–333] 319 [228–377] 0.59
Absolute neutrophil count (109/l) [IQR]; n = 16/21, 6/7, 10/14 6.1 [4.4–7.7] 4.6 [2.2–6.7] 6.4 [5.4–8.5] 0.14
Renal parameters
Systolic blood pressure (mm Hg) [IQR]; n = 18/21, 5/7, 13/14 137 [120–146] 130 [109–141] 140 [120–146] 0.27
Diastolic blood pressure (mm Hg) [IQR]; n = 18/21, 5/7, 13/14 80 [70–90] 78 [55–83] 80 [70–92] 0.32
Serum albumin concentration (g/l) [IQR] 17.0 [11.4–22.9] 20.0 [11.2–28.0] 16.6 [11.4–20.9] 0.5
Proteinuria (g/d) [IQR] 5.3 [4.0–10.5] 3.9 [3.0–5.1] 7.3 [4.9–11.0] 0.03
Absolute change in proteinuria (g/d) [IQR] −2.9 [−5.4; 2.0] −5.5 [−14.0; −2.9] 0.5 [−4.5; 3.6] 0.03
Absolute monthly change in proteinuria (g/d/mo) [IQR] 0.0 [−0.6–0.1] −0.6 [−2.9; −0.3] 0.0 [−0.2; 0.2] 0.008
Serum creatinine concentration (μmol/l) [IQR]; n = 18/21, 4/7, 14/14 142.5 [110.0–198.5] 153.5 [112.2–207.5] 142.5 [103.2–185.5] 0.87
eGFR (ml/min per 1.73 m2) [IQR]a 48.0 [25.0–66.5] 28.0 [0–52.0] 48.5 [39.8–75.0] 0.05
CKD stage
 - I (%) 2 (9.5) 0 2 (14.3) 0.79
 - II (%) 3 (14.3) 0 3 (21.4) 0.51
 - III (%) 10 (47.6) 3 (42.9) 7 (50.0) 1
 - IV (%) 2 (9.5) 1 (14.3) 1 (7.1) 1
 - V (%) 4 (19.1) 3 (42.9) 1 (7.1) 0.17
Time from diagnosis to apheresis (mo) [IQR] 10 [5–25] 8 [1–11] 19 [7–26] 0.17
Absolute change in eGFR (ml/min per 1.73 m2) [IQR] −29.0 [−54.3; −6.9] −28.0 [−83.0; −7.0] −29.0 [−51.2; −4.7] 0.68
Absolute monthly change in eGFR (ml/min per 1.73 m2/mo) [IQR] −2.9 [−6.2; −0.3] −6.8 [−12.6; −3.1] −1.5 [−3.4; −0.2] 0.04
Dialysis before apheresis /at the last follow-up
 - no/no (%) 13 (61.9) 4 (57.1) 9 (64.3) } 0.01
 - yes/no (%) 3 (14.3) 3 (42.9) 0
 - no/yes (%) 5 (23.8) 0 5 (35.7)
Specific treatments for INS before apheresis
Number of immunosuppressive drugs with corticosteroids
 - 1 immunosuppressive drug (%) 10 (47.6) 7 (100.0) 3 (20.0) 0.003
 - ≥ 2 immunosuppressive drugs (%) 11 (52.4) 0 11 (78.6) 0.003
Number of treatments without corticosteroids [IQR] 2 [1–3] 1 2 [1–3] 0.002
Min - Max 1; 6 1 1; 6
Duration of corticosteroid use before apheresis - median [IQR] (month) 7.0 [5.0–24.0] 5.0 [1.0–7.0] 15.0 [6.0–25.2] 0.05
Immunosuppressive therapy used before apheresis
 - Calcineurin inhibitor (%) 13 (61.9) 4 (57.1) 9 (64.3) 1
 Cyclosporine (%) 13 (61.9) 4 (57.1) 9 (64.3)
 Tacrolimus (%) 8 (38.1) 0 8 (57.1)
 - Cyclophosphamide (%) 4 (19.1) 2 (28.6) 2 (14.3) 0.84
 - Rituximab (%) 8 (38.1) 1 (14.3) 7 (50.0) 0.27
 - Mycophenolate mofetil (%) 7 (33.3) 0 7 (50.0) 0.07
 - Intravenous immunoglobulin (%) 1 (4.8) 0 1 (7.1) 1
Mode of apheresis
Type of apheresis
 - Plasma exchange (%) 11 (52.4) 6 (85.7) 5 (35.7) 0.09
 - Immunoadsorption (%) 6 (28.6) 0 6 (42.9) 0.12
 - Double-filtration plasmapheresis (%) 2 (9.5) 1 (14.3) 1 (7.1) 1
 - Plasma exchange followed by immunoadsorption (%) 1 (4.8) 0 1 (7.1) 1
 - Low-density lipoprotein apheresis (%) 1 (4.8) 0 1 (7.1) 1
Number of apheresis sessions [IQR] 12 [4–39] 11 [4–74] 12 [7–32] 0.97
 - ≤ 3 (%) 3 (14.3) 1 (14.3) 2 (14.3)
 - [4–15](%) 10 (47.6) 3 (42.9) 7 (50)
 - ≥ 15 (%) 8 (38.1) 3 (42.9) 5 (35.7)
Duration of apheresis (days) [IQR] 47 [17–172] 56 [13–1954] 40 [21–114] 0.56
Min-Max 6; 2296 7; 2296 6; 338
Specific treatments for INS after apheresis
Dose of corticosteroids at the start of apheresis (mg/d) [IQR] 15 [1–60] 30 [7–65] 10 [0–60] 0.36
Immunosuppressive therapy used after and during apheresis
 - Calcineurin inhibitor (%) 12 (57.1) 5 (71.5) 7 (50.0) 0.64
 Cyclosporine (%) 7 (33.3) 5 (71.5) 2 (14.3)
 Tacrolimus (%) 7 (33.3) 0 7 (50.0)
 - Cyclophosphamide (%) 2 (9.5) 2 (28.6) 0 0.19
 - Rituximab (%) 3 (14.3) 2 (28.6) 1 (7.1) 0.51
 - Mycophenolate mofetil (%) 4 (19.1) 0 4 (28.6) 0.36
 - Intravenous immunoglobulin (%) 2 (9.5) 0 2 (14.3) 0.79
 - Azathioprine (%) 2 (9.5) 1 (14.3) 1 (7.1) 1
 - Ofatumumab (%) 1 (4.8) 0 1 (7.1) 1

Qualitative data are expressed as n (%), quantitative data as medians [interquartile range; IQR], as appropriate.

Glomerular filtration rate (GFR) was estimated (eGFR) by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation.

CDK stage was defined according to National Kidney Foundation practice guidelines for CKD.

a

eGFR = 0 ml/min per 1.73 m2 for the 3 patients on dialysis.