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. 2008 Aug;142(3):379–393. doi: 10.1111/j.1365-2141.2008.07181.x

Table II.

The percentage of patients who achieved the target haemoglobin concentration (110 g/l) and the mean haemoglobin concentration once target was achieved.

ESA-naïve
Prior ESA-treated
n = 144 n = 62
Patients eligible for target Hb analysis, n* 129 57
KM (95% CL) percentage who reached target Hb 82% (70, 94) 55% (40, 70)
KM (95% CL) median time to achieve the target Hb, weeks 7 (5, 9) 24 (9, NE)
Patients eligible for mean Hb analysis after target achieved, n 105 31
Mean (SD) Hb concentration of maintenance, g/l 116 (8) 117 (8)
Median (Min, Max) Hb concentration of maintenance, g/l 117 (99, 133) 118 (101, 136)
Mean Hb category after achieving target, n (%)
Less than 110 g/l 25 (24) 8 (26)
110–130 g/l 75 (71) 22 (71)
Greater than 130 g/l 5 (5) 1 (3)

ESA, erythropoiesis-stimulating agent; Hb, haemoglobin; KM, Kaplan–Meier; CL, confidence limits; Min, minimum; Max, maximum; NE, not estimable.

*Patients who had haemoglobin data either at baseline or after baseline were considered eligible except for those patients with baseline haemoglobin ≥110 g/l. Patients who had no haemoglobin data after baseline were counted as not having achieved the target level.

†Patients had to reach the target haemoglobin level (110 g/l) in the absence of a red blood cell transfusion within the preceding 28 d.

‡Patients who had baseline haemoglobin ≥110 g/l or who achieved the target haemoglobin concentration of 110 g/l were included.