Evidence map›Paper›PMID 23973701›Full record

Trial reportJournal of the American College of Cardiology2013

Beyond medication prescription as performance measures: optimal secondary prevention medication dosing after acute myocardial infarction.

Suzanne V Arnold, John A Spertus, Frederick A Masoudi, Stacie L Daugherty, Thomas M Maddox, Yan Li, John A Dodson, Paul S Chan

Erratum issued Registry-linked trialOpen access · greenAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American College of Cardiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02468349 (IMproving reModeling in Acute myoCardial Infarction Using Live and Asynchronous TElemedicine.), which is not on this map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
7.3field-weighted citation impact, top 2% 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.

NCT02468349 naunknown statusnot on this mapstarted 2015, after this paper: background citation

IMproving reModeling in Acute myoCardial Infarction Using Live and Asynchronous TElemedicine.

TypeinterventionalSponsorNational University Heart Centre, SingaporeRan2015 to 2020Enrolled300ConditionsLeft Ventricular Remodeling, Medication Adherence, Acute Coronary SyndromeArmsTelemedicine
3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. THE IMPACT OF CARDIOVASCULAR DRUGS ON GLYCEMIC CONTROL: A REVIEW.Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists · 2017
    Pooled it
  3. Medication Discontinuation in the IMPROVE-IT Trial.Circulation. Cardiovascular quality and outcomes · 2019
    Trial
  4. Trial
  5. Trial
  6. Effect of Beta-Blocker Dose on Survival After Acute Myocardial Infarction.Journal of the American College of Cardiology · 2015
    Trial
  7. Observational
  8. Article
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  14. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Suzanne V ArnoldSaint Luke's Mid America Heart Institute, Kansas City, Missouri; University of Missouri-Kansas City, Kansas City, Missouri. Electronic address: suz.v.arnold@gmail.com.
John A Spertus
Frederick A Masoudi
Stacie L Daugherty
Thomas M Maddox
Yan Li
John A Dodson
Paul S Chan
Saint Luke's Hospital · USUniversity of Colorado Anschutz Medical Campus · USBrigham and Women's Hospital · USSaint Luke's Health System · USVA Eastern Colorado Health Care System · US

Funding

SCCOR in Cardiac Dysfunction and DiseaseP50HL077113 · NHLBI · WASHINGTON UNIVERSITY · PI KELLY, DANIEL PATRICK · 2005 to 2009
$13.4M
HEARTLAND INSTITUTE FOR CLINICAL AND TRANSLATIONAL RESEARCHUL1RR033179 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BAROHN, RICHARD J. · 2011 to 2011
$3.2M
TRAINING PROGRAM IN EPIDEMIOLOGIC RESEARCH ON AGINGT32AG000158 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI GAZIANO, J. MICHAEL · 1988 to 2015
$2.1M
Gender Disparities in Invasive CVD Procedure Use: the Role of Provider BiasK08HL103776 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI DAUGHERTY, STACIE LUTHER · 2010 to 2014
$657k
The Appropriateness Criteria for Coronary Revascularization: Feasibility of MeasuK23HL102224 · NHLBI · SAINT LUKE'S HOSPITAL · PI CHAN, PAUL SHEUNG-YAN · 2010 to 2014
$610k
NCRR NIH HHS 1UL1RR033179NCRR NIH HHS UL1 RR033179NHLBI NIH HHS K08 HL103776NHLBI NIH HHS K08HL103776NHLBI NIH HHS K23 HL102224NHLBI NIH HHS K23HL102224NHLBI NIH HHS #P50HL077113NHLBI NIH HHS P50 HL077113NIA NIH HHS T32 AG000158
6 · The paper itself

Abstract

objectivesThe aim of this study was to examine the prescribing patterns of medications quantified by the performance measures for acute myocardial infarction (AMI).

backgroundCurrent performance measures for AMI are designed to improve quality by quantifying the use of evidence-based treatments. However, these measures only assess medication prescription. Whether patients receive optimal dosing of secondary prevention medications at the time of and after discharge after AMI is unknown.

methodsWe assessed treatment doses of beta-blockers, statins, and angiotensin-converting enzyme inhibitors (ACEI)/angiotensin II receptor blockers (ARBs) at discharge and 12 months after AMI among 6,748 patients from 31 hospitals enrolled in 2 U.S. registries (2003 to 2008). Prescribed doses were categorized as none, low (<50% target [defined from seminal clinical trials]), moderate (50% to 74% target), or goal (≥ 75% target). Patients with contraindications were excluded from analyses for that medication.

resultsMost eligible patients (>87%) were prescribed some dose of each medication at discharge, although only 1 in 3 patients were prescribed these medications at goal doses. Of patients not discharged on goal doses, up-titration during follow-up occurred infrequently (approximately 25% of patients for each medication). At 12 months, goal doses of beta-blockers, statins, and ACEI/ARBs were achieved in only 12%, 26%, and 32% of eligible patients, respectively. After multivariable adjustment, prescription of goal dose at discharge was strongly associated with being at goal dose at follow-up: beta-blockers, adjusted odds ratio (OR): 6.08 (95% confidence interval [CI]: 3.70 to 10.01); statins, adjusted OR: 8.22 (95% CI: 6.20 to 10.90); ACEI/ARBs, adjusted OR: 5.80 (95% CI: 2.56 to 13.16); p < 0.001 for each.

conclusionsAlthough nearly all patients after an AMI are discharged on appropriate secondary prevention medications, dose increases occur infrequently, and most patients are prescribed doses below those with proven efficacy in clinical trials. Integration of dose intensity into performance measures might help improve the use of optimal medical therapy after AMI.

Indexed as

Adrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansHydroxymethylglutaryl-CoA Reductase InhibitorsIncidenceMaleMiddle AgedMyocardial InfarctionProspective StudiesRegistriesSecondary PreventionTreatment OutcomeAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersHydroxymethylglutaryl-CoA Reductase InhibitorsACEIacute myocardial infarctionAMIangiotensin-converting enzyme inhibitorangiotensin II receptor blockerARBCIconfidence intervalLDL-Cleft ventricularlow-density lipoprotein cholesterolLVmyocardial infarctionodds ratioORperformance measuresSBPsecondary preventionsystolic blood pressure

Identifiers

PMID23973701
PMCPMC3819453
OpenAlexW2135918142

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Registered trials

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.