Evidence map›Paper›PMID 38236513›Full record

ArticleCritical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine2023

Iron and erythropoietin to heal and recover after intensive care (ITHRIVE): A pilot randomised clinical trial.

Edward Litton, Craig French, Alan Herschtal, Simon Stanworth, Susan Pellicano, Anne Marie Palermo, Samantha Bates, Sarah Van Der Laan, Ege Eroglu, David Griffith and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 36% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

11 authors at 7 institutions in 2 countries.

Edward LittonIntensive Care Unit, Fiona Stanley Hospital, Perth 6150, WA, Australia.
Craig FrenchIntensive Care Unit, Western Health, Melbourne, 3021, VIC, Australia.
Alan HerschtalSchool of Public Health and Preventative Medicine, Monash University, 4/553 St Kilda Road, Melbourne, VIC, Australia.
Simon StanworthHaematology & Transfusion Medicine, John Radcliffe Hospital, Oxford UK.
Susan PellicanoIntensive Care Unit, Fiona Stanley Hospital, Perth 6150, WA, Australia.
Anne Marie PalermoIntensive Care Unit, Fiona Stanley Hospital, Perth 6150, WA, Australia.
Samantha BatesIntensive Care Unit, Western Health, Melbourne, 3021, VIC, Australia.
Sarah Van Der LaanIntensive Care Unit, Fiona Stanley Hospital, Perth 6150, WA, Australia.
Ege ErogluIntensive Care Unit, Fiona Stanley Hospital, Perth 6150, WA, Australia.
David GriffithCritical Care and Anaesthesia, Usher Institute, Edinburgh Medical School, Molecular, Genetic, and Population Health Sciences, The University of Edinburgh, UK.
Akshay ShahNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Fiona Stanley Hospital · AUWestern Health · AUJohn Radcliffe Hospital · GBMonash University · AUThe University of Western Australia · AUUniversity of Edinburgh · GBUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine the feasibility of a pivotal randomised clinical trial of intravenous (IV) iron and erythropoietin in adult survivors of critical illness with anaemia requiring treatment in the intensive care unit. Design: An investigator-initiated, parallel group, placebo-controlled, randomised feasibility trial. Setting: A tertiary intensive care unit (ICU) in Perth, Western Australia. Participants: Adults with anaemia (haemoglobin <100 g/L), requiring ICU-level care for more than 48 h, and likely to be ready for ICU discharge within 24 h. Interventions: A single dose of IV ferric carboxymaltose and Epoetin alfa (active group) or an equal volume of 0.9% saline (placebo group). Main outcome measures: Study feasibility was considered met if the pilot achieved a recruitment rate of ≥2 participants per site per month, ≥90% of participants received their allocated study treatment, and≥ 90% of participants were followed up for the proposed pivotal trial primary outcome - days alive and at home to day 90 (DAH Results: The 40-participant planned sample size included twenty in each group and was enrolled between 1/9/2021 and 2/3/2022. Participants spent a median of 3.4 days (interquartile range 2.8-5.1) in the ICU prior to enrolment and had a mean baseline haemoglobin of 83.7 g/L (standard deviation 6.7). The recruitment rate was 6.7 participants per month [95% confidence interval (CI) 4.8-9.0], DAH Conclusion: The iron and erythropoietin to heal and recover after intensive care (ITHRIVE) pilot demonstrated feasibility based on predefined participant recruitment, study drug administration, and follow-up thresholds.

Indexed as

AnaemiaCritical careIntensive care unit

Identifiers

PMID38236513
PMCPMC10790015
OpenAlexW4389719606

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.