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Record W4405053703 · doi:10.1182/blood-2024-202159

Daily Versus Non-Daily Oral Iron Supplementation for the Treatment of Iron Deficiency Anemia: A Systematic Review and Meta-Analysis of Randomized Trials

2024· review· en· W4405053703 on OpenAlexaff
Prince Taylor, Archit Jain, Ali Hadi, Alla Iansavitchene, Alejandro Lazo‐Langner

Bibliographic record

VenueBlood · 2024
Typereview
Languageen
FieldMedicine
TopicIron Metabolism and Disorders
Canadian institutionsLondon Health Sciences CentreWestern University
Fundersnot available
KeywordsMedicineAnemiaIron deficiencyMeta-analysisIron-deficiency anemiaRandomized controlled trialInternal medicineGastroenterology

Abstract

fetched live from OpenAlex

Introduction Iron deficiency anemia (IDA) is a leading cause of disability worldwide affecting approximately 1.2 billion people. The primary treatment for IDA is oral iron supplementation, which is often accompanied by adverse side effects such as nausea and epigastric pain which may be dose-dependent and can lead to poor compliance. Given that the efficacy and safety of different iron supplementation regimens for managing IDA is not clear, we conducted a systematic review and meta-analysis to compare the effectiveness and tolerability of daily versus non-daily oral iron supplementation. Methods Following PRISMA guidelines, MEDLINE, EMBASE, and CENTRAL were systematically searched (via Ovid) from inception to September 2022, supplemented by targeted searching of Google Scholar and the reference lists of relevant studies, to identify randomized controlled trials comparing daily (seven days a week) versus non-daily iron supplementation for the management of IDA. The primary outcome was the mean difference in hemoglobin (Hb) levels (in g/L) before and after iron supplementation. Secondary outcomes included percentual correction of baseline Hb, and tolerability and side-effect profile. The quality of the studies was evaluated using the Jadad score and the Revised Cochrane Risk of Bias Tool for Randomized Trials. The primary meta-analysis for the mean difference between baseline and end-of-treatment Hb was done using the generic inverse variance method under a random effects model. To account for potential differences in Hb laboratory methods or reference ranges among different populations, we conducted a meta-analysis for the standardized mean differences calculated using the Hedges g statistic under a random effects model. Heterogeneity was assessed using Cochran's Q and Higgin's I2 statistics and sensitivity analyses was also conducted for different dosing regimens for the non-daily group. This review is registered with the International Prospective Register of Systematic Review (CRD42024403539). Results Study Characteristics Of the 6659 identified citations, 106 underwent full-text evaluation, and we included 19 studies involving 2783 patients. The trials were conducted in various countries, including India, Bangladesh, Jordan, Pakistan, Turkey, Brazil, China, Indonesia, Kenya, and Malawi. The study populations included children and adolescents (n=11), pregnant females (n=6), premenopausal females (n=1), and patients greater than 15 years of age (n=1). Regarding non-daily regimes used, 8/19 studies assessed once weekly iron, 2/19 assessed alternate days, 6/19 assessed twice weekly, and 3/19 evaluated both once weekly and twice weekly. Study quality was, in general, low. Primary Outcome The pooled mean difference in Hb correction over the treatment period was 3.64 g/L higher in the daily group, with sensitivity analyses showing consistent results. The primary meta-analysis did not suggest evidence of publication bias. The meta-analysis of standardized mean differences corroborated the primary findings. All comparisons showed high heterogeneity based on Cochran's Q and Higgin's I2 statistics. The averages of the percent of correction of the baseline Hb 20.9% and 16.1% in the daily and non-daily groups, respectively. Assessment of Side Effects Side effects were reported in 11 out of 19 trials and were predominantly gastrointestinal including abdominal pain, nausea, stool consistency change, and/or darker stools, in order of prevalence. Of the 11 studies, 10 reported higher percentages of side effects in the daily group compared to non-daily. One of 11 studies assessed medication compliance revealing a 2.6-fold increase in non-compliance with iron supplementation in the daily group. Conclusion Both daily and non-daily oral iron supplementation effectively increase Hb concentrations in patients with IDA. Although daily supplementation results in a slightly higher Hb increase, it is only 3.64 g/L representing approximately a 5% higher correction of the baseline Hb, and it is associated with higher incidence of side effects and reduced tolerability. Consequently, non-daily iron may offer clinically comparable outcomes to daily regimens, along with additional advantages such as improved compliance, fewer side effects and lower treatment cost, and that non-daily supplementation should be considered as a preferred alternative for managing IDA effectively.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.019
metaresearch head score (Gemma)0.038
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.027
Threshold uncertainty score0.101

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0190.038
Meta-epidemiology (narrow)0.0030.002
Meta-epidemiology (broad)0.0270.041
Bibliometrics0.0080.007
Science and technology studies0.0010.001
Scholarly communication0.0040.002
Open science0.0020.002
Research integrity0.0030.002
Insufficient payload (model declined to judge)0.0050.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.135
GPT teacher head0.416
Teacher spread0.280 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designMeta-analysis
Domainnot available
GenreReview

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2024
Admission routes1
Has abstractyes

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