Skip to main content

Table 4 Effect of daily home fortification with 3 mg iron as NaFeEDTA and 12.5 mg iron as encapsulated ferrous fumarate on categorical outcomes at 30 days after start of intervention, per protocol analysis

From: Daily home fortification with iron as ferrous fumarate versus NaFeEDTA: a randomised, placebo-controlled, non-inferiority trial in Kenyan children

Outcome/intervention group

Prevalence

(n/n)

Effect (95% CI) relative to placebo

Anaemia

 Placebo

53.3%

(56/105)

Reference

 Iron, 3 mg as NaFeEDTA

43.7%

(45/103)

–9.6% (–22.7% to 3.9%)

 Iron, 12.5 mg as ferrous fumarate

51.4%

(55/107)

–1.9% (–15.1% to 11.3%)

Iron deficiencya

 Placebo

44.6%

(25/56)

Reference

 Iron, 3 mg as NaFeEDTA

24.5%

(12/49)

–20.2% (–36.4% to –18.5%)

 Iron, 12.5 mg as ferrous fumarate

30.5%

(18/59)

–14.1% (–30.7% to 3.5%)

Plasmodium infection, by dipstick testb

 Placebo

16.2%

(17/105)

Reference

 Iron, 3 mg as NaFeEDTA

18.4%

(19/103)

2.3% (–8.1% to 12.6%)

 Iron, 12.5 mg as ferrous fumarate

22.6%

(24/106)

6.4% (–4.3% to 17.0%)

P. falciparum infection, by microscopy

 Placebo

18.5%

(19/103)

Reference

 Iron, 3 mg as NaFeEDTA

15.5%

(15/97)

–3.0% (–13.4% to 7.6%)

 Iron, 12.5 mg as ferrous fumarate

15.2%

(15/99)

–3.3% (–13.6% to 7.2%)

  1. aAnalysis restricted to children without inflammation (see text)
  2. bPresence of HRP, pLDH specific to P. falciparum or pLDH due to human Plasmodium species other than P. falciparum