Table 4

Change in fatigue and serum iron status 12 weeks after treatment initiation with intravenous iron or intravenous placebo

Iron groupPlacebo groupP
Total study population (n = 90)    
    Change of fatigue (BFI), median −1.3 (−2.4, −0.5) −0.9 (−2.2, 0.0) ns 
    Fatigue improved (SPI), n (%) 27/43 (63%) 16/47 (34%) .006 
    Change of ferritin concentration, ng/mL 81 (49, 100) −1 (−7, 4) < .001 
    Change of transferrin saturation, % 7 (0, 17) 1 (5, 6) .006 
Population with baseline ferritin ≤ 15 ng/mL (n = 34)    
    Change of fatigue (BFI), median −2.3 (−3.2, 0.9) −0.7 (−1.3, 0.1) .03 
    Fatigue improved (SPI), n (%) 14/17 (82%) 6/17 (35%) .005 
Iron groupPlacebo groupP
Total study population (n = 90)    
    Change of fatigue (BFI), median −1.3 (−2.4, −0.5) −0.9 (−2.2, 0.0) ns 
    Fatigue improved (SPI), n (%) 27/43 (63%) 16/47 (34%) .006 
    Change of ferritin concentration, ng/mL 81 (49, 100) −1 (−7, 4) < .001 
    Change of transferrin saturation, % 7 (0, 17) 1 (5, 6) .006 
Population with baseline ferritin ≤ 15 ng/mL (n = 34)    
    Change of fatigue (BFI), median −2.3 (−3.2, 0.9) −0.7 (−1.3, 0.1) .03 
    Fatigue improved (SPI), n (%) 14/17 (82%) 6/17 (35%) .005 

Results are presented as median values (quartiles Q1, Q3) or number of patients (%). P values were calculated with the Mann Whitney U test or the χ2 test.

ns indicates not significant and no trend (P > .10).

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