Evidence map›Paper›PMID 29561843›Full record

ArticlePloS one2018

Treatment gaps and potential cardiovascular risk reduction from expanded statin use in the US and England.

Peter Ueda, Thomas Wai-Chun Lung, Yuan Lu, Joshua A Salomon, Kazem Rahimi, Philip Clarke, Goodarz Danaei

Open access · goldFull text read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  5. Review
  6. ASPC president's page: Getting back to basics one patient at a time.American journal of preventive cardiology · 2022
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  10. Observational
  11. Observational
  12. Statin-Associated Muscle Disease: Advances in Diagnosis and Management.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
  13. Article
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 7 institutions in 5 countries.

Peter UedaDepartment of Global Health and Population, Harvard School of Public Health, Boston, Massachusetts, United States of America.ORCID 0000-0002-3275-8743
Thomas Wai-Chun LungThe George Institute for Global Health, Camperdown, Australia.
Yuan LuYale/ Yale-New Haven Hospital, Center for Outcomes Research and Evaluation (CORE), New Haven, Connecticut, United States of America.
Joshua A SalomonDepartment of Global Health and Population, Harvard School of Public Health, Boston, Massachusetts, United States of America.
Kazem RahimiThe George Institute for Global Health, Oxford Martin School, University of Oxford, Oxford, United Kingdom.
Philip ClarkeCentre for Health Policy, School of Population and Global Health, The University of Melbourne, Carlton, Victoria, Australia.
Goodarz DanaeiDepartment of Global Health and Population, Harvard School of Public Health, Boston, Massachusetts, United States of America.
Harvard Global Health Institute · USHarvard University · USKarolinska Institutet · SEThe George Institute for Global Health · AUThe George Institute for Global Health · GBThe University of Melbourne · AUYale New Haven Hospital · US

Funding

Reducing disparities in diabetes through expanded insurance coverage.R01DK090435 · NIDDK · HARVARD SCHOOL OF PUBLIC HEALTH · PI DANAEI, GOODARZ · 2011 to 2014
$1.8M
NIDDK NIH HHS R01 DK090435NIH HHS 1R01-DK090435
6 · The paper itself

Abstract

backgroundThe updated national guidelines for cardiovascular risk assessment and lipid modification in the UK and US expand the indications for statin therapy in primary prevention to adults with moderate risk of cardiovascular disease (CVD) but many adults at high CVD risk remain untreated in both countries. We set out to identify treatment gaps in English and American adults at moderate and high risk of cardiovascular disease (CVD), and to estimate the number of CVD events that would be prevented from expanding statin therapy to those who are currently untreated.

methodsWe used nationally representative samples of 10,375 English adults and 7,687 US adults aged 40-75 years and free of existing CVD from the Health Survey for England 2009-2013, and the National Health and Nutrition Examination Survey 2007-2012 in the US. We used the risk algorithms and the risk thresholds for statin therapy recommended by each country's national guideline to categorize the survey participants into moderate-risk (≥10% to <20% 10-year risk of CVD in England and ≥7.5% to <20% risk in the US) or high-risk (≥20%risk) and simulated the number of events that would be prevented from expansion of statin therapy to those currently untreated.

resultsClose to half of adults at high CVD risk in England (46.0%) and the US (49.7%) were not receiving statins. Expanding statin use to 1.45 million high-risk adults in England would save 101,000 (95% CI = 81,000-120,000) CVD events in the next 10 years compared with 128,000 (103,000-154,000) CVD events that would be prevented from expanding treatment to 3.64 million untreated moderate-risk adults. In the US, expanding statin use to 5.27 million untreated high-risk adults would save 384,000 (305,000-461,000) CVD events over 10 years compared with 616,000 (493,000-738,000) CVD events that would be prevented from treating 20.29 million untreated moderate-risk adults.

conclusionsIn both England and the US, expanding statin therapy to untreated moderate-risk adults would prevent a comparable number of events as expanding statin use to a much smaller number of currently untreated high-risk adults. A large potential for CVD prevention remains from improving coverage of statin therapy among high-risk adults.

Indexed as

AdultAgedAlgorithmsCardiovascular DiseasesComputer SimulationEnglandFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedModels, BiologicalPractice Guidelines as TopicRisk AssessmentRisk Reduction BehaviorUnited StatesHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID29561843
PMCPMC5862405
OpenAlexW2792791362

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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.