Evidence map›Paper›PMID 28391887›Full record

Observational studyJournal of clinical lipidology

Investigating the prevalence, predictors, and prognosis of suboptimal statin use early after a non-ST elevation acute coronary syndrome.

Richard M Turner, Peng Yin, Anita Hanson, Richard FitzGerald, Andrew P Morris, Rod H Stables, Andrea L Jorgensen, Munir Pirmohamed

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Journal of clinical lipidology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. A microRNA Signature for the Diagnosis of Statins Intolerance.International journal of molecular sciences · 2022
    Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Review
  11. Article
  12. Article
  13. Observational
  14. 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

8 authors at 1 institution in 1 country.

Richard M TurnerDepartment of Molecular & Clinical Pharmacology, University of Liverpool, Liverpool, Merseyside, UK. Electronic address: richard.turner@liverpool.ac.uk.
Peng YinDepartment of Biostatistics, University of Liverpool, Liverpool, Merseyside, UK.
Anita HansonDepartment of Molecular & Clinical Pharmacology, University of Liverpool, Liverpool, Merseyside, UK.
Richard FitzGeraldDepartment of Molecular & Clinical Pharmacology, University of Liverpool, Liverpool, Merseyside, UK.
Andrew P MorrisDepartment of Biostatistics, University of Liverpool, Liverpool, Merseyside, UK.
Rod H StablesLiverpool Heart and Chest Hospital, Liverpool, Merseyside, UK.
Andrea L JorgensenDepartment of Biostatistics, University of Liverpool, Liverpool, Merseyside, UK.
Munir PirmohamedDepartment of Molecular & Clinical Pharmacology, University of Liverpool, Liverpool, Merseyside, UK.
University of Liverpool · GB

Funding

Department of HealthWellcome TrustWellcome Trust WT098017
6 · The paper itself

Abstract

backgroundHigh-potency statin therapy is recommended in the secondary prevention of cardiovascular disease but discontinuation, dose reduction, statin switching, and/or nonadherence occur in practice.

objectivesTo determine the prevalence and predictors of deviation from high-potency statin use early after a non-ST elevation acute coronary syndrome (NSTE-ACS) and its association with subsequent major adverse cardiovascular events (MACE) and all-cause mortality (ACM).

methodsA total of 1005 patients from a UK-based prospective NSTE-ACS cohort study discharged on high-potency statin therapy (atorvastatin 80 mg, rosuvastatin 20 mg, or 40 mg daily) were included. At 1 month, patients were divided into constant high-potency statin users, and suboptimal users incorporating statin discontinuation, dose reduction, switching statin to a lower equivalent potency, and/or statin nonadherence. Follow-up was a median of 16 months.

resultsThere were 156 suboptimal (∼15.5%) and 849 constant statin users. Factors associated in multivariable analysis with suboptimal statin occurrence included female sex (odds ratio 1.75, 95% confidence interval [CI] 1.14-2.68) and muscular symptoms (odds ratio 4.28, 95% CI 1.30-14.08). Suboptimal statin use was associated with increased adjusted risks of time to MACE (hazard ratio 2.10, 95% CI 1.25-3.53, P = .005) and ACM (hazard ratio 2.46, 95% CI 1.38-4.39, P = .003). Subgroup analysis confirmed that the increased MACE/ACM risks were principally attributable to statin discontinuation or nonadherence.

conclusionsConversion to suboptimal statin use is common early after NSTE-ACS and is partly related to muscular symptoms. Statin discontinuation or non-adherence carries an adverse prognosis. Interventions that preserve and enhance statin utilization could improve post NSTE-ACS outcomes.

Indexed as

ElectrocardiographyAcute Coronary SyndromeAgedDose-Response Relationship, DrugFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMedication AdherencePrevalencePrognosisTime FactorsHydroxymethylglutaryl-CoA Reductase InhibitorsCardiovascularDiscontinuationMortalityMuscular symptomsNonadherenceStatin

Identifiers

PMID28391887
PMCPMC5399750
OpenAlexW2562023861

What OpenQuestion holds

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LicenceCC BY
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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.