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Table 1 Clinical characteristics

From: Diagnostic accuracy and clinical usefulness of erythrocyte creatine content to predict the improvement of anaemia in patients receiving maintenance haemodialysis

 

Study Patients

aGroup 1

bGroup 2

P Value

(n = 92)

(n = 32)

(n = 60)

Age (years)

71.9 ± 14.0

73.7 ± 12.9

71.0 ± 14.5

0.37

Gender (male/female)

62/30

20/12

42/18

0.49

Diabetes Mellitus (resent/absent)

42/50

16 / 16

26 / 34

0.54

Haemodialysis time (hours/week)

15.9 ± 4.2

15.3 ± 3.3

16.2 ± 4.6

0.36

Intradialytic ultrafiltration rate (ml/hour/kg)

8.8 ± 2.9

9.1 ± 3.0

8.6 ± 2.9

0.40

Kt/v

1.72 ± 0.48

1.7 ± 0.5

1.8 ± 0.5

0.38

Erythrocyte creatine content (μmol/gHb)

1.89 ± 0.73

2.47 ± 0.74

1.57 ± 0.49

0.0001

ESA dose (units/week)

6,396.7 ± 3,746.3

7429.7 ± 3623.0

5845.8 ± 3723.2

0.04

Low dose (< 9,000)

53

13

40

0.016

High dose (≥ 9,000)

39

19

20

 

Haemoglobin at baseline (g/dL)

10.4 ± 1.2

10.0 ± 1.3

10.6 ± 1.0

0.004

Haemoglobin at 3 months (g/dL)

10.6 ± 1.3

11.1 ± 1.4

10.3 ± 1.2

0.007

Reticulocyte (%)

14.1 ± 6.2

14.3 ± 7.3

14.0 ± 5.6

0.81

Haptoglobin (g/dL)

93.6 ± 52.2

101.1 ± 52.5

89.7 ± 52.0

0.32

Transferrin saturation (%)

27.8 ± 16.2

23.5 ± 12.3

28.5 ± 17.4

0.16

Ferritin (ng/mL)

121.3 ± 106.5

100.6 ± 89.4

145.6 ± 245.3

0.32

Iron deficiency (present/ absent)

38/54

16/16(50.0%)

22/38(36.7%)

0.27

Intact parathyroid hormone (pg/mL)

152.3 ± 102.0

170.3 ± 139.5

143.7 ± 77.9

0.30

C-reactive protein (mg/dL)

0.33 ± 0.37

0.38 ± 0.46

0.30 ± 0.31

0.33

Serum calcium (mg/dL)

9.5 ± 0.5

9.4 ± 0.5

9.5 ± 0.5

0.25

Serum phosphorus (mg/dL)

4.9 ± 1.4

4.7 ± 1.4

5.0 ± 1.3

0.32

Albumin (g/dL)

3.6 ± 0.4

3.5 ± 0.4

3.7 ± 0.4

0.05

  1. Data are represented as mean ± SD. ESA erythropoiesis stimulating agent, Kt/v urea clearance
  2. aGroup 1 ≥ 0.8 g/dL change in haemoglobin from baseline to 3 months
  3. bGroup 2 < 0.8 g/dL change in haemoglobin from baseline to 3 months