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. 2017 Mar 1;22(4):293–300. doi: 10.1111/nep.12891

Table 1.

Patient demographic and clinical characteristics (per protocol set)

PA21 group n = 100 Sevelamer group n = 92 P‐value
Age (years), mean ± SD 61.0 ± 11.7 60.8 ± 12.0 NS
Sex, n (%) 0.048
Male 72 (72.0) 53 (57.6)
Female 28 (28.0) 39 (42.4)
Prior use of phosphate binders, n (%)
Calcium carbonate 71 (71.0) 73 (79.3)
Sevelamer hydrochloride 33 (33.0) 30 (32.6)
Lanthanum carbonate 47 (47.0) 43 (46.7)
Bixalomer 8 (8.0) 8 (8.7)
Prior use of iron preparation, n (%) 5 (5.0) 4 (4.4)
Prior use of erythropoiesis stimulating agent, n (%) 88 (88.0) 86 (93.5)
Primary disease, n
Diabetic nephropathy 32 20
Chronic glomerulonephritis 43 42
Nephrosclerosis 13 9
Polycystic kidney disease 3 5
Others 4 4
Unknown 8 12
Mode of dialysis, n (%)
Haemodialysis 87 (87.0) 82 (89.1)
Haemodiafiltration 13 (13.0) 10 (10.9)
Dialysis vintage (months), mean ± SD 104.9 ± 79.7 102.4 ± 90.6
Serum phosphorus (mmol/L), mean ± SD 2.51 ± 0.45 2.45 ± 0.39 NS
Corrected serum calcium (mmol/L), mean ± SD 2.24 ± 0.15 2.22 ± 0.14 NS
Intact parathyroid hormone (ng/L), median (interquartile range) 235 (176–339) 282 (174–386) 0.082††

Two‐sample t‐test;

Fisher's exact test;

††

Two‐sample Wilcoxon test; NS, not significant