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Table 1 Subject characteristics at time of enrolment

From: Effect of iron content on the tolerability of prenatal multivitamins in pregnancy

Prenatal multivitamin groups, differing in iron content

 

60 mg iron group n = 75

35 mg iron group n = 92

Total N = 167

Study inclusion:

   

a) Had not started multivitamin in current pregnancy

27 (36%)

28 (30%)

55 (33%)

b) Had discontinued multivitamin in current pregnancy

48 (64%)

64 (70%)

112 (67%)

Reasons for (a) or (b):

   

Nausea and/or vomiting (NVP)

62 (83%)

68 (74%)

130 (78%)

Tablet sizeψ, swallowing difficulties, other tablet properties (i.e. taste, smell)

33 (44%)

20 (22%)

53 (32%)

Constipationβ

4 (5%)

14 (15%)

18 (11%)

Abdominal pain, GI irritability, diarrhea, heartburn, reflux

10 (13%)

13 (14%)

23 (14%)

GI medical condition (i.e. IBS, Crohn's disease)

2 (3%)

2 (2%)

4 (2%)

Doctor's advice, not supplement taker, or lacked information

5 (7%)

6 (7%)

11 (7%)

Maternal age (years)

Mean ± standard deviation

30 ± 5

31 ± 5

31 ± 5

Gravidity:

   

First pregnancy

23 (31%)

20 (22%)

43 (26%)

Second or higher pregnancy

52 (69%)

72 (78%)

124 (74%)

Multivitamin intake in a previous pregnancy*

45/52 (87%)

59/72 (82%)

104/124 (84%)

Discontinued multivitamin in a previous pregnancy*

26/45 (58%)

28/59 (47%)

54/104 (52%)

  1. *Data missing for 1 subject.
  2. ψ For the subjects who reported issues with tablet size as the reason for non-adherence with previous multivitamins, 22/33 (66%) in the '60 mg' group and 13/20 (65%) in the '35 mg' group still commenced supplementation with the assigned multivitamins.
  3. β For the subjects who reported constipation as the reason for non-adherence with previous multivitamins, 2/4 (50%) in the '60 mg' group and 12/14 (86%) in the '35 mg' group still commenced supplementation with the assigned multivitamins.