Evidence map›Paper›PMID 34875022›Full record

Trial reportCardiovascular research2023

High-dose intravenous iron reduces myocardial infarction in patients on haemodialysis.

Mark C Petrie, Pardeep S Jhund, Eugene Connolly, Patrick B Mark, Michael R MacDonald, Michele Robertson, Stefan D Anker, Sunil Bhandari, Kenneth Farrington, Philip A Kalra and 6 more

Full text readRandomized Controlled Trial
In one paragraph

Trial report in Cardiovascular research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Observational
  3. Article
  4. Suppression of lncRNABioengineered · 2022
    Article
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

16 authors.

Mark C PetrieBHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.ORCID 0000-0002-6333-9496
Pardeep S JhundBHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.ORCID 0000-0003-4306-5317
Eugene ConnollyBHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.ORCID 0000-0001-5625-2344
Patrick B MarkBHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.ORCID 0000-0003-3387-2123
Michael R MacDonaldChangi General Hospital, Singapore, Singapore.ORCID 0000-0003-3501-3592
Michele RobertsonRobertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.ORCID 0000-0002-8425-2592
Stefan D AnkerCharite, Universitatsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-3331-7314
Sunil BhandariHull and East Yorkshire Hospitals NHS Trust and Hull York, Medical School, Hull, UK.ORCID 0000-0002-2748-3095
Kenneth FarringtonLister Hospital, Stevenage, UK.ORCID 0000-0001-8862-6056
Philip A KalraSalford Royal NHS Foundation Trust, Salford, UK.ORCID 0000-0001-7652-1572
David C WheelerUniversity College London, London, UK.ORCID 0000-0003-0745-3478
Charles R V TomsonFreeman Hospital, Newcastle upon Tyne, UK.ORCID 0000-0002-0224-8726
Ian FordRobertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.
John J V McMurrayBHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.ORCID 0000-0002-6317-3975
Iain C MacdougallDepartment of Renal Medicine, King's College Hospital, London, UK.
PIVOTAL Investigators and Committees

Funding

British Heart Foundation RE/18/6/34217
6 · The paper itself

Abstract

aimsTo investigate the effect of high-dose iron vs. low-dose intravenous (IV) iron on myocardial infarction (MI) in patients on maintenance haemodialysis. METHODS AND

resultsThis was a pre-specified analysis of secondary endpoints of the Proactive IV Iron Therapy in Hemodialysis Patients trial (PIVOTAL) randomized, controlled clinical trial. Adults who had started haemodialysis within the previous year, who had a ferritin concentration <400 μg per litre and a transferrin saturation <30% were randomized to high-dose or low-dose IV iron. The main outcome measure for this analysis was fatal or non-fatal MI. Over a median of 2.1 years of follow-up, 8.4% experienced a MI. Rates of type 1 MIs (3.2/100 patient-years) were 2.5 times higher than type 2 MIs (1.3/100 patient-years). Non-ST-elevation MIs (3.3/100 patient-years) were 6 times more common than ST-elevation MIs (0.5/100 patient-years). Mortality was high after non-fatal MI (1- and 2-year mortality of 40% and 60%, respectively). In time-to-first event analyses, proactive high-dose IV iron reduced the composite endpoint of non-fatal and fatal MI [hazard ratio (HR) 0.69, 95% confidence interval (CI) 0.52-0.93, P = 0.01] and non-fatal MI (HR 0.69, 95% CI 0.51-0.93; P = 0.01) when compared with reactive low-dose IV iron. There was less effect of high-dose IV iron on recurrent MI events than on the time-to-first event analysis.

conclusionIn total, 8.4% of patients on maintenance haemodialysis had an MI over 2 years. High-dose compared to low-dose IV iron reduced MI in patients receiving haemodialysis. EUDRACT REGISTRATION NUMBER: 2013-002267-25.

Indexed as

IronMyocardial InfarctionAdministration, IntravenousAdultHumansRenal DialysisTreatment OutcomeIronHaemodialysisIronMyocardial infarctionPIVOTAL

Identifiers

PMID34875022
PMCPMC10022850

What OpenQuestion holds

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Registered trials

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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.