Evidence map›Paper›PMID 33582446›Full record

ArticleAtherosclerosis2021

The incremental value of angiographic features for predicting recurrent cardiovascular events: Insights from the Duke Databank for Cardiovascular Disease.

Michael G Nanna, Eric D Peterson, Karen Chiswell, Robert A Overton, Adam J Nelson, David F Kong, Ann Marie Navar

Open access · greenAbstract read
In one paragraph

Article in Atherosclerosis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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 2 institutions in 1 country.

Michael G NannaDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA; Duke University Medical Center, Department of Medicine, Durham, NC, USA. Electronic address: michael.nanna@duke.edu.
Eric D PetersonUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.
Karen ChiswellDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Robert A OvertonDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Adam J NelsonDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
David F KongDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA; Duke University Medical Center, Department of Medicine, Durham, NC, USA.
Ann Marie NavarUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.
Duke University · USThe University of Texas Southwestern Medical Center · US

Funding

Postdoctoral Training in Cardiovascular Clinical ResearchT32HL069749 · NHLBI · DUKE UNIVERSITY · PI MARK, DANIEL B · 2003 to 2023
$6.7M
Preventing Cardiovascular Disease through Improved Risk Prediction and CommunicationK01HL133416 · NHLBI · DUKE UNIVERSITY · PI NAVAR, ANN MARIE · 2016 to 2020
$707k
NHLBI NIH HHS K01 HL133416NHLBI NIH HHS T32 HL069749
6 · The paper itself

Abstract

BACKGROUND AND

aimsIdentifying patient subgroups with cardiovascular disease (CVD) at highest risk for recurrent events remains challenging. Angiographic features may provide incremental value in risk prediction beyond clinical characteristics.

methodsWe included all cardiac catheterization patients from the Duke Databank for Cardiovascular Disease with significant coronary artery disease (CAD; 07/01/2007-12/31/2012) and an outpatient follow-up visit with a primary care physician or cardiologist in the same health system within 3 months post-catheterization. Follow-up occurred for 3 years for the primary major adverse cardiovascular event endpoint (time to all-cause death, myocardial infarction [MI], or stroke). A multivariable model to predict recurrent events was developed based on clinical variables only, then adding angiographic variables from the catheterization. Next, we compared discrimination of clinical vs. clinical plus angiographic risk prediction models.

resultsAmong 3366 patients with angiographically-defined CAD, 633 (19.2%) experienced cardiovascular events (death, MI, or stroke) within 3 years. A multivariable model including 18 baseline clinical factors and initial revascularization had modest ability to predict future atherosclerotic cardiovascular disease events (c-statistic = 0.716). Among angiographic predictors, number of diseased vessels, left main stenosis, left anterior descending stenosis, and the Duke CAD Index had the highest value for secondary risk prediction; however, the clinical plus angiographic model only slightly improved discrimination (c-statistic = 0.724; delta 0.008). The net benefit for angiographic features was also small, with a relative integrated discrimination improvement of 0.05 (95% confidence interval: 0.03-0.08).

conclusionsThe inclusion of coronary angiographic features added little incremental value in secondary risk prediction beyond clinical characteristics.

Indexed as

Cardiovascular DiseasesCoronary Artery DiseaseMyocardial InfarctionCoronary AngiographyHumansPredictive Value of TestsPrognosisRisk AssessmentRisk FactorsAcute coronary syndromeAtherosclerosisCoronary artery diseaseRecurrent eventsRisk predictionSecondary prevention

Identifiers

PMID33582446
PMCPMC8221430
OpenAlexW3127541300

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.