Evidence map›Paper›PMID 27053637›Full record

ArticleCirculation. Arrhythmia and electrophysiology2016

Transcatheter Myocardial Needle Chemoablation During Real-Time Magnetic Resonance Imaging: A New Approach to Ablation Therapy for Rhythm Disorders.

Toby Rogers, Srijoy Mahapatra, Steven Kim, Michael A Eckhaus, William H Schenke, Jonathan R Mazal, Adrienne Campbell-Washburn, Merdim Sonmez, Anthony Z Faranesh, Kanishka Ratnayaka and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation. Arrhythmia and electrophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Cardiac MRI at Low Field Strengths.Journal of magnetic resonance imaging : JMRI · 2024
    Review
  2. Article
  3. Interventional cardiovascular magnetic resonance: state-of-the-art.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2023
    Review
  4. Review
  5. Review
  6. Review
  7. Native contrast visualization and tissue characterization of myocardial radiofrequency ablation and acetic acid chemoablation lesions at 0.55 T.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2021
    Article
  8. Review
  9. Magnetic resonance imaging guidance for the optimization of ventricular tachycardia ablation.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2018
    Review
  10. Article
  11. Real-time MRI guidance of cardiac interventions.Journal of magnetic resonance imaging : JMRI · 2017
    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 1 institution in 1 country.

Toby RogersFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Srijoy MahapatraFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Steven KimFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Michael A EckhausFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
William H SchenkeFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Jonathan R MazalFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Adrienne Campbell-WashburnFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Merdim SonmezFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Anthony Z FaraneshFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Kanishka RatnayakaFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.).
Robert J LedermanFrom the Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute (T.R., W.H.S., J.R.M., A.C.-W., M.S., A.Z.F., K.R., R.J.L.) and Division of Veterinary Resources (M.A.E.), National Institutes of Health, Bethesda, MD; Global Medical Affairs (S.M.) and Therapy Development (S.K.), St Jude Medical, St Paul, MN; and Department of Cardiology, Children's National Medical Center, Washington, DC (K.R.). lederman@nih.gov.
Children's National · US

Funding

NHLBI Animal Program DivisionZIGHL006020 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI CLARK, TANNIA · 2009 to 2025
$47.3M
Novel catheter treatment of valve diseaseZIAHL006040 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEDERMAN, ROBERT J · 2010 to 2025
$23.6M
Real-time MRI guided cardiovascular interventionZIAHL005062 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEDERMAN, ROBERT J · 2009 to 2025
$21.6M
MRI catheter design and fabricationZIAHL006041 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEDERMAN, ROBERT J · 2014 to 2025
$12.2M
Real-time cardiovascular MRI and co-registration technical developmentZIAHL006039 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEDERMAN, ROBERT J · 2010 to 2024
$10.3M
Therapies enabled-cardiovascular interventional MRIZ01HL005062 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEDERMAN, ROBERT J · 2003 to 2008
$6.0M
Intramural NIH HHS Z01 HL005062Intramural NIH HHS ZIA HL005062
6 · The paper itself

Abstract

backgroundRadiofrequency ablation for ventricular arrhythmias is limited by inability to visualize tissue destruction, by reversible conduction block resulting from edema surrounding lesions, and by insufficient lesion depth. We hypothesized that transcatheter needle injection of caustic agents doped with gadolinium contrast under real-time magnetic resonance imaging (MRI) could achieve deep, targeted, and irreversible myocardial ablation, which would be immediately visible. METHODS AND

resultsUnder real-time MRI guidance, ethanol or acetic acid was injected into the myocardium of 8 swine using MRI-conspicuous needle catheters. Chemoablation lesions had identical geometry by in vivo and ex vivo MRI and histopathology, both immediately and after 12 (7-17) days. Ethanol caused stellate lesions with patchy areas of normal myocardium, whereas acetic acid caused homogeneous circumscribed lesions of irreversible necrosis. Ischemic cardiomyopathy was created in 10 additional swine by subselective transcoronary ethanol administration into noncontiguous territories. After 12 (8-15) days, real-time MRI-guided chemoablation-with 2 to 5 injections to create a linear lesion-successfully eliminated the isthmus and local abnormal voltage activities.

conclusionsReal-time MRI-guided chemoablation with acetic acid enabled the intended arrhythmic substrate, whether deep or superficial, to be visualized immediately and ablated irreversibly. In an animal model of ischemic cardiomyopathy, obliteration of a conductive isthmus both anatomically and functionally and abolition of local abnormal voltage activities in areas of heterogeneous scar were feasible. This represents the first report of MRI-guided myocardial chemoablation, an approach that could improve the efficacy of arrhythmic substrate ablation in the thick ventricular myocardium.

Indexed as

NeedlesAnimalsCatheter AblationDisease Models, AnimalElectrophysiologic Techniques, CardiacEquipment DesignEthanolHeart RateInjections, IntralesionalMagnetic Resonance Imaging, CineMyocardiumSwineTachycardia, VentricularTime FactorsEthanolcardiac electrophysiologycatheter ablationelectrophysiologymagnetic resonance imagingmagnetic resonance imaging, interventionaltachycardia, ventricular

Identifiers

PMID27053637
PMCPMC4950950
OpenAlexW2327796090

What OpenQuestion holds

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LicenceTDM
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.