Evidence map›Paper›PMID 39699820›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

An Ovine Model of Chronic Heart Failure Induced by Repeated Coronary Microembolizations.

Mridula Pachen, Rohit Ramchandra

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

2 authors.

Mridula PachenManaaki Manawa - The Centre for Heart Research and the Department of Physiology, University of Auckland, Auckland, New Zealand.
Rohit RamchandraManaaki Manawa - The Centre for Heart Research and the Department of Physiology, University of Auckland, Auckland, New Zealand. r.ramchandra@auckland.ac.nz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of large animals in research provides a unique bridge between preclinical findings and clinical relevance, offering a valuable perspective for advancing our understanding of the complexities of heart failure. Multiple models of heart failure have been established with advantages and limitations of each model. Many insights have been gained from these models for understanding both pathophysiological mechanisms and therapeutic interventions for heart failure. We have developed a chronic model of heart failure with reduced ejection fraction in sheep using the coronary microembolization technique. These animals gradually develop heart failure over a period of 3 months. In this chapter, we document how this model can be established. The left main coronary artery is cannulated under fluoroscopic guidance, and polystyrene latex microspheres are injected into the artery. Up to three sequential selective microembolizations are undertaken over a period of 3 weeks. Changes in ECG are monitored, and echocardiography is used to check on the progression of left ventricular dysfunction. All animals were followed for 3 months after the first embolization, and heart tissue was examined to check for changes in cardiac myocyte size. All animals developed stable signs of HF. We propose that multiple sequential intracoronary microembolizations can induce stable myocardial dysfunction with hemodynamic signs of chronic heart failure.

Indexed as

Coronary VesselsDisease Models, AnimalHeart FailureAnimalsChronic DiseaseEchocardiographyElectrocardiographyEmbolismMicrospheresSheepCoronary arteryCoronary microembolizationHeart failureHeart failure with reduced ejection fractionLarge animal model

Identifiers

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.