Clinical Study

The NIMO Scandinavian Study: A Prospective Observational Study of Iron Isomaltoside Treatment in Patients with Iron Deficiency

Table 2

Change in iron and blood cell parameters after the first iron isomaltoside treatment.

PretreatmentPosttreatmentConcentration change valueaTime of evaluationb

Mean (SD)
Hb, g/dL
()c
10.5 (1.5)12.5 (1.4)2.0 (1.4)<0.00017.1 (6.0)
TSAT, %
()d
9.6 (6.5)21.0 (9.8)11.4 (10.0)<0.00017.6 (5.0)
Ferritin, μg/L25.0 (68.0)146.3 (173.1)121.3 (162.6)<0.00017.4 (6.5)
Median (IQR)e
()d
10.0 (6.0–20)95.0 (49–181)71.0 (35–157)

a values for concentration changes obtained by analysis of covariance test with diagnosis and dose as factors and pretreatment laboratory parameter concentration as covariate. bTime (weeks) between the last administration of first iron isomaltoside treatment and blood test follow-up. cAnaemic patients (Hb < 13 g/dL for men and Hb < 12 g/dL for women at baseline) with available pre- and posttreatment Hb measures in the total population. dPatients with available pre- and posttreatment laboratory measures in the total population. eMedian is presented for data not normally distributed. Hb: haemoglobin; IQR: interquartile range; SD: standard deviation; TSAT: transferrin saturation.