Evidence map›Paper›PMID 30649251›Full record

ArticleEuropean heart journal. Quality of care & clinical outcomes2019

Cardiovascular event rates in a high atherosclerotic cardiovascular disease risk population: estimates from Swedish population-based register data.

Maria Lindh, Jonas Banefelt, Kathleen M Fox, Sara Hallberg, Ming-Hui Tai, Mats Eriksson, Guillermo Villa, Maria K Svensson, Yi Qian

Open access · bronzeAbstract read
In one paragraph

Article in European heart journal. Quality of care & clinical outcomes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  6. Lipid-lowering prescription patterns after a non-fatal acute coronary syndrome: A retrospective cohort study.International journal of cardiology. Cardiovascular risk and prevention · 2025
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  14. Novel Insights into the Molecular Mechanisms of Atherosclerosis.International journal of molecular sciences · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 3 countries.

Maria LindhQuantify Research, Hantverkargatan 8, Stockholm, Sweden.
Jonas BanefeltQuantify Research, Hantverkargatan 8, Stockholm, Sweden.
Kathleen M FoxStrategic Healthcare Solutions LLC, 133 Cottonwood Creek Lane, Aiken, SC, USA.
Sara HallbergQuantify Research, Hantverkargatan 8, Stockholm, Sweden.
Ming-Hui TaiDepartment of Global Health Economics, One Amgen center dr. Thousand Oaks, CA, USA.
Mats ErikssonDepartment of Medicine, Karolinska Institutet, Karolinska Universitetssjukhuset Huddinge, Stockholm, Sweden.
Guillermo VillaDepartment of Global Health Economics, AMGEN Europe GmbH, Suurstoffi 22, Rotkreuz, Switzerland.
Maria K SvenssonDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Yi QianDepartment of Global Health Economics, One Amgen center dr. Thousand Oaks, CA, USA.
Quantify Research (Sweden) · SEAmgen (United States) · USAmgen (Switzerland) · CHCotton (United States) · USKarolinska University Hospital · SEUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThis study aimed to estimate the rate of cardiovascular (CV) events in the real world in patients at high risk of recurrent CV events similar to the FOURIER trial population. METHODS AND

resultsA retrospective population-based cohort study was conducted using Swedish national registers from 1 July 2001 to 31 December 2015. Patients in the atherosclerotic cardiovascular disease (ASCVD) prevalent cohort met the FOURIER-like inclusion criteria, including treatment with high/moderate-intensity statins, on 1 July 2006. Additionally, two cohorts defined by diagnosis of incident ischaemic stroke (IS) and incident myocardial infarction (MI), meeting the FOURIER-like inclusion criteria were followed from date of diagnosis. Event rates were calculated for the hard major adverse cardiovascular events (MACE) composite: MI, IS, and CV death; and the ASCVD composite: MI, IS, unstable angina, coronary revascularization, and CV death. Approximately half of patients experienced a CV event (ASCVD composite) during follow-up. The MACE composite rates/100 person-years were 6.3, 11.9, and 12.3 in the ASCVD prevalent (n = 54 992), MI incident (n = 45 895), and IS incident (n = 36 134) cohorts, respectively. The ASCVD composite rates/100 person-years were 7.0, 21.7, and 12.9 in the ASCVD prevalent, MI incident, and IS incident cohorts, respectively. The multiple-event MACE composite rates/100 person-years were 8.5 (ASCVD prevalent cohort), 15.4 (MI incident cohort), and 14.4 (IS incident cohort).

conclusionIn this real-world setting, CV event rates were high in all studied cohorts. In particular, the MACE composite rates were two to three times higher than in the FOURIER clinical trial, indicating a substantial disease burden despite treatment with moderate or high-intensity statins.

Indexed as

AgedAged, 80 and overAtherosclerosisCardiovascular DiseasesCohort StudiesFemaleHumansMaleRecurrenceRegistriesRetrospective StudiesRisk AssessmentSwedenASCVDCardiovascular event ratesCardiovascular outcomesSecondary prevention

Identifiers

PMID30649251
PMCPMC6613595
OpenAlexW2910356506

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.