Evidence map›Paper›PMID 15547020›Full record

Trial reportHeart (British Cardiac Society)2004

Impact of nicorandil in angina: subgroup analyses.

IONA Study Group

Abstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in Heart (British Cardiac Society), 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Vasodilator Therapy: Nitrates and Nicorandil.Cardiovascular drugs and therapy · 2016
    Review
  6. Nicorandil-induced penile ulceration: a case report.Journal of medical case reports · 2016
    Article
  7. Article
  8. Review
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

IONA Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsIONA (impact of nicorandil in angina) is a randomised, double blind, placebo controlled trial of nicorandil, with a target dose of 20 mg twice daily. The consistency of benefits seen in subgroups is reported.

methodsThe primary composite end point of the study was coronary heart disease death, non-fatal myocardial infarction, or unplanned hospitalisation for cardiac chest pain. Subgroups were defined using baseline characteristics including, age, sex, histories of smoking, diabetes, hypertension, myocardial infarction, revascularisation, anginal status, anti-anginal treatment, other cardiovascular drugs, and an overall assessment of risk.

resultsA total of 5126 patients were randomised to receive nicorandil or identical placebo in addition to standard anti-anginal treatment. Overall, nicorandil reduced the incidence of the primary end point from 15.5% to 13.1% (hazard ratio (HR) 0.83, 95% confidence interval (CI) 0.72 to 0.97; p = 0.014). There was no evidence of significant heterogeneity of benefit across all subgroups studied. The absolute risk reduction was greatest and the numbers needed to treat to prevent one event was lowest in subjects at greatest risk.

conclusionsThe IONA study demonstrates a significant improvement in outcome by nicorandil treatment across a broad range of patients with stable angina.

Indexed as

Angina PectorisConfidence IntervalsCoronary DiseaseDouble-Blind MethodFemaleHospitalizationHumansMaleMiddle AgedMyocardial InfarctionNicorandilProportional Hazards ModelsRisk FactorsTreatment OutcomeVasodilator AgentsNicorandilVasodilator Agents

Identifiers

PMID15547020
PMCPMC1768587

What OpenQuestion holds

Textmetadata
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.