Evidence map›Paper›PMID 22884560›Full record

Trial reportThe American journal of cardiology2012

Effect of ranolazine on left ventricular dyssynchrony in patients with coronary artery disease.

Rajesh Venkataraman, Ji Chen, Ernest V Garcia, Luiz Belardinelli, Fadi G Hage, Jaekyeong Heo, Ami E Iskandrian

Abstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in The American journal of cardiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Phosphorylation of cardiac sodium channel at Ser571 anticipates manifestations of the aging myopathy.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  3. American journal of physiology. Heart and circulatory physiology · 2022
    Article
  4. Left ventricular regional asynchrony: Earliest marker for ischemic cardiomyopathy?Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2021
    Article
  5. Dyssynchrony as a marker of adverse prognosis among patients with coronary artery disease and heart failure.Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2020
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Ranolazine: Multifaceted Role beyond Coronary Artery Disease, a Recent Perspective.Heart views : the official journal of the Gulf Heart Association
    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

7 authors at 3 institutions in 1 country.

Rajesh VenkataramanDivision of Cardiovascular Disease, University of Alabama at Birmingham, AL, USA. rajeshv@uab.edu
Ji Chen
Ernest V Garcia
Luiz Belardinelli
Fadi G Hage
Jaekyeong Heo
Ami E Iskandrian
University of Alabama at Birmingham · USEmory University · USGilead Sciences (United States) · US

Funding

Measuring Left Ventricular Dyssynchrony from ECG-gated Myocardial Perfusion SPECTR01HL094438 · NHLBI · EMORY UNIVERSITY · PI CHEN, JI · 2009 to 2012
$1.5M
NHLBI NIH HHS R01 HL094438
6 · The paper itself

Abstract

We previously reported that ranolazine improves exercise myocardial perfusion. Ranolazine ameliorates myocardial ischemia by augmenting myocardial blood flow; likely by a reduction in the extravascular compression of small vessels. We hypothesized that ranolazine could improve left ventricular (LV) dyssynchrony as assessed by phase analysis of gated single photon emission computed tomographic myocardial perfusion imaging. Patients (n = 32) with known or suspected coronary artery disease and reversible perfusion defects on a clinically indicated stress myocardial perfusion imaging were restudied 4 weeks after ranolazine (500 to 1,000 mg orally twice daily) was added to their conventional treatment in an open-label trial (data previously reported). The LV systolic and diastolic dyssynchrony indexes were obtained using automated phase analysis before and after ranolazine. No significant changes were found in the heart rate or blood pressure (at rest or during stress) after treatment. The perfusion pattern improved in 13 of 18 patients who had undergone exercise testing, but in only 3 of 14 patients who had undergone vasodilator stress testing. No significant changes were seen in the LV ejection fraction or volume after treatment. The systolic and diastolic LV dyssynchrony improved after ranolazine therapy; there was a significant decrease in the systolic phase SD (21 ± 17 vs 18 ± 13, p = 0.04), systolic bandwidth (69 ± 60 vs 53 ± 38, p = 0.03), diastolic SD (29 ± 18 vs 24 ± 15, p = 0.047) and diastolic bandwidth (91 ± 61 vs 72 ± 45, p = 0.02). In conclusion, the present study is the first to show improvements in diastolic and systolic LV synchrony with ranolazine as measured by automated phase analysis of gated single photon emission computed tomographic myocardial perfusion imaging.

Indexed as

AcetanilidesAgedCoronary Artery DiseaseEnzyme InhibitorsExercise TestFemaleFollow-Up StudiesGated Blood-Pool ImagingHumansMalePiperazinesRanolazineTomography, Emission-Computed, Single-PhotonTreatment OutcomeVentricular Dysfunction, LeftAcetanilidesEnzyme InhibitorsPiperazinesRanolazine

Identifiers

PMID22884560
PMCPMC3483406
OpenAlexW2037472155

What OpenQuestion holds

Textmetadata
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.