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A pilot iron substitution programme in female blood donors with iron deficiency without anaemia.

Vox sanguinis
April 1, 2011
C Pittori et al. (8 authors)
Controlled Clinical TrialJournal ArticleResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine whether targeted iron substitution could prevent anemia and enhance donor return rates in premenopausal female blood donors with iron deficiency.

Results Summary

The study found that iron supplementation significantly increased serum ferritin levels (from 7.12 to 25.2 ng/ml) and resolved symptoms like fatigue, hair loss, and nail breakage. No cases of anemia occurred, and 60% of participants completed the program and donated blood again.

Population

Premenopausal female blood donors aged ≤50 with adequate hemoglobin levels but serum ferritin ≤10 ng/ml.

Effective Dosage

Not specified

Duration

16 weeks

Interactions

None mentioned

Extracted Claims (9)
InterventionDirectionEndpointPopulationDosageImpactClaim #
iron supplementation
increase
serum ferritin
non-anaemic premenopausal female blood donors with iron deficiency
from a mean value of 7.12 to 25.2 ng/ml
increase
#1
iron supplementation
decrease
prostration
non-anaemic premenopausal female blood donors with iron deficiency
-
resolution
#2
iron supplementation
decrease
fatigue
non-anaemic premenopausal female blood donors with iron deficiency
-
resolution
#3
iron supplementation
decrease
sleep disturbances
non-anaemic premenopausal female blood donors with iron deficiency
-
resolution
#4
iron supplementation
decrease
tension in the neck
non-anaemic premenopausal female blood donors with iron deficiency
-
resolution
#5
iron supplementation
decrease
hair loss
non-anaemic premenopausal female blood donors with iron deficiency
-
resolution
#6
iron supplementation
decrease
nail breakage
non-anaemic premenopausal female blood donors with iron deficiency
-
resolution
#7
iron supplementation
decrease
anaemia
premenopausal female blood donors with iron deficiency
No case of anaemia occurred
prevents the development
#8
iron supplementation
increase
donation return
premenopausal female blood donors with iron deficiency
Sixty per cent of the women completed the programme and donated blood again
enhances
#9
Abstract

BACKGROUND AND OBJECTIVES: Blood donation can contribute to iron deficiency. The possibly resulting anaemia importantly affects donor return rate. The determination of serum ferritin levels revealed iron deficiency in many non-anaemic premenopausal female blood donors at our Institution. We started an iron substitution programme targeting this donor group to prevent anaemia and enhance donor retain. MATERIALS AND METHODS: Women aged≤50 with haemoglobin levels adequate for donation and serum ferritin≤10 ng/ml were offered iron supplementation. Substitution lasted 16 weeks and the donation interval was extended. History collection including iron deficiency-related symptoms, whole blood count and serum ferritin determination was performed at baseline and after 2 and 6 months. Data were recorded prospectively and compared with those of 108 female controls with iron deficiency not receiving iron substitution (retrospective data). RESULTS: Of the 116 participating subjects, 60% completed the programme. Significant results were serum ferritin increase (from a mean value of 7.12 to 25.2 ng/ml), resolution of prostration, fatigue, sleep disturbances, tension in the neck, hair loss and nail breakage. No case of anaemia occurred. Sixty per cent of the women completed the programme and donated blood again. CONCLUSIONS: Targeted iron substitution prevents the development of anaemia and enhances donation return in premenopausal female blood donors with iron deficiency.

Medical Subject Headings (MeSH)
AdultBlood DonorsFemaleFerritinsHemoglobinsHumansIronIron DeficienciesIron, DietaryMiddle AgedPilot ProjectsPremenopauseTreatment OutcomeYoung Adult
Study Links
Quality Scores
Safety90
Efficacy85/10
Quality75/10
Citation Metrics
Total Citations37
Citations/Year2.6
Relative Citation Ratio1.45
NIH Percentile63.8%
Research Impact Scores
APT Score0.75
Weight Score1.34
Normalized Score0.85
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