Evidence map›Paper›PMID 30318600›Full record

ArticleClinical cardiology2019

Protecting the gains: What changes are needed to prevent a reversal of the downward cardiovascular disease mortality trend?

Jesse D Ortendahl, Allison L Diamant, Peter P Toth, Dasha Cherepanov, Amanda L Harmon, Michael S Broder

Abstract readMulticenter Study
In one paragraph

Article in Clinical cardiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Identification of In Vivo Internalizing Cardiac-Specific RNA Aptamers.bioRxiv : the preprint server for biology · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Jesse D OrtendahlPartnership for Health Analytic Research, LLC, Beverly Hills, California.
Allison L DiamantDivision of General Internal Medicine and Health Services Research, David Geffen School of Medicine, UCLA, Los Angeles, California.
Peter P TothPreventative Cardiology, CGH Medical Center, Sterling, Illinois.
Dasha CherepanovPartnership for Health Analytic Research, LLC, Beverly Hills, California.
Amanda L HarmonPartnership for Health Analytic Research, LLC, Beverly Hills, California.ORCID https://orcid.org/0000-0002-3779-9528
Michael S BroderPartnership for Health Analytic Research, LLC, Beverly Hills, California.

Funding

Amgen
6 · The paper itself

Abstract

aimsCardiovascular disease (CVD) mortality has decreased over 60% over the past 50 years in the United States; however, emerging data indicate CVD incidence may be rising because of shifting demographics, increasing risk factor prevalence, and competing needs for limited resources. We projected CVD mortality from 2015 to 2040 given varying informed assumptions regarding changes in risk factor prevalence, uptake of current therapeutic options, and future innovations.

methodsA microsimulation model was used to project US CVD mortality trends. National Health and Nutrition Examination Survey data were used to estimate population-level trends in CVD risk factors. Risk factors were used to generate Framingham Risk Scores for cohorts of 1 000 000 individuals from the general population to determine each individuals' CVD risk. Annual cardiovascular incidence, prevalence, and mortality were projected for scenarios differing by uptake of current therapies, anticipated pharmaceutical innovations with variable efficacy, risk factor prevalence, and changes in health disparities.

resultsWhen incorporating a demographic shift, continued changes in risk factors, current treatment utilization, and no major innovations, we predicted the CVD mortality rate would increase 41% by 2040. If innovations providing incremental benefits equal to those associated with the introduction of statins are identified and widely utilized, CVD mortality could remain constant through 2040. With more efficacious innovations, CVD mortality could be further reduced.

conclusionsGiven demographic and risk prevalence changes, increasing access and adherence to current preventative therapeutics could slow the expected mortality increase, but new therapies may be needed to maintain the downward trend in CVD deaths.

Indexed as

Computer SimulationAgedCardiovascular DiseasesCause of DeathDisease ProgressionFemaleHumansMaleMiddle AgedMorbidityNutrition SurveysRetrospective StudiesRisk AssessmentRisk FactorsSurvival RateUnited Statescardiovascular diseasedisease burdenmicrosimulation modelmortalityprojections

Identifiers

PMID30318600
PMCPMC6436516

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.