Evidence map›Paper›PMID 38021373›Full record

ArticleEClinicalMedicine2023

Alternate day versus consecutive day oral iron supplementation in iron-depleted women: a randomized double-blind placebo-controlled study.

Hanna K von Siebenthal, Sara Gessler, Florence Vallelian, Joachim Steinwendner, Urs-Martin Kuenzi, Diego Moretti, Michael B Zimmermann, Nicole U Stoffel

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
9.3field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05105438 nacompletednot on this map

Comparing Oral Iron Supplementation Using Alternate-day Dosing to the Standard of Care Consecutive-day Dosing in Iron-depleted Women With or Without Mild Anemia

TypeinterventionalSponsorSwiss Federal Institute of TechnologyRan2021 to 2022Enrolled150ConditionsIron-deficiency, Iron Deficiency AnemiaArmsConsecutive Day Dosing, Alternate Day Dosing
NCT06555315 narecruitingnot on this mapstarted 2024, after this paper: background citation

Pilot Non-inferiority Study Investigating Daily Versus Every Other Day Dosing of Oral Iron in Premature Infants.

TypeinterventionalSponsorCHRISTUS HealthRan2024 to 2026Enrolled100ConditionsVery Low Birth Weight Infant, Premature Infants, Anemia of Prematurity, Iron Deficiency, Anaemia in ChildrenArms6 mg/kg of oral iron as ferrous sulfate administered every other day., 6 mg/kg of oral iron as ferrous sulfate administered every day.
NCT07483645 active not recruitingnot on this mapstarted 2025, after this paper: background citation

Effectiveness and Acceptability of a Liposomal Iron Supplement With Vitamin C and Fiber (LISEFEX®): Observational, Descriptive, Prospective, Longitudinal, Multicenter Study in Mexican Subjects Diagnosed With Mild to Moderate Iron Deficiency Anemia.

TypeobservationalSponsorCarnot LaboratoriesRan2025 to 2026Enrolled74ConditionsIron Deficiency Anemia
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. FIGO good practice recommendations on anemia in pregnancy, to reduce the incidence and impact of postpartum hemorrhage (PPH).International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2025
    Guideline
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  9. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2025
    Review
  10. Article
  11. Diagnosis and management of iron deficiency in females.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2025
    Review
  12. Daily Versus Alternate Day Oral Iron Replacement for Women with Iron Deficiency Anaemia: A Randomized Controlled Trial.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Hanna K von SiebenthalLaboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Switzerland.
Sara GesslerLaboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Switzerland.
Florence VallelianDivision of Internal Medicine, University Hospital and University of Zurich, Zurich, Switzerland.
Joachim SteinwendnerLaboratory of Web Science, Swiss Distance University of Applied Sciences, Zürich, Switzerland.
Urs-Martin KuenziLaboratory of Web Science, Swiss Distance University of Applied Sciences, Zürich, Switzerland.
Diego MorettiNutrition Research, Department of Health, Swiss Distance University of Applied Sciences, Zürich, Switzerland.
Michael B ZimmermannLaboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Switzerland.
Nicole U StoffelLaboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Switzerland.
Swiss Distance University of Applied Sciences · CHETH Zurich · CHJohn Radcliffe Hospital · GBUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Guidelines to treat iron deficiency recommend daily provision of oral iron, but this may decrease fractional iron absorption and increase side effects. Our objective was to compare consecutive-day versus alternate-day iron supplementation. Methods: In a double-masked, randomized, placebo-controlled trial, young Swiss women (n = 150; serum ferritin ≤30 μg/L) were assigned to: daily 100 mg iron for 90 d, followed by daily placebo for another 90 d (consecutive-day group) or the same daily dose of iron and placebo on alternate days for 180 d (alternate-day group). The study period was 24/11/2021-10/8/2022. Co-primary outcomes, at equal total iron doses, were serum ferritin and gastrointestinal side effects; secondary outcomes were iron deficiency and serum hepcidin. Compliance and side effects were recorded daily using a mobile application. Data were analysed using mixed models and longitudinal prevalence ratios (LPR). The trial was registered at ClinicalTrials.gov (NCT05105438). Findings: 75 women were assigned to each group and included in the intention-to-treat analysis. Capsule adherence and side effect reporting was >97% in both groups. At equal total iron doses, comparing consecutive-day and alternate-day groups, median serum ferritin was 43.8 μg/L (31.7-58.2) versus 44.8 μg/L (33.8-53.6) (P = 0.98), the LPR for gastrointestinal side effects on days of iron intake was 1.56 (95% CI: 1.38, 1.77; P < 0.0001), and median serum hepcidin was 3.0 nM (IQR 2.0-5.0) versus 1.9 nM (1.4-2.9) (P < 0.0001). Iron deficiency prevalence after 3 months was 5.5% versus 4.3% (P = 0.74) and after 6 months was 11.4% and 3.0% (P = 0.049). Interpretation: At equal total iron doses, compared to consecutive day dosing of iron, alternate day dosing did not result in higher serum ferritin but reduced iron deficiency at 6 months and triggered fewer gastrointestinal side effects. Funding: Swiss National Science Foundation, Bern, Switzerland.

Indexed as

Alternate dayDailyDeficiencyGastrointestinal side effectsHepcidinIronSupplementation

Identifiers

PMID38021373
PMCPMC10659995
OpenAlexW4388304580

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.