Evidence map›Paper›PMID 24271648›Full record

ArticleEuropean journal of clinical pharmacology2014

Use of the recommended drug combination for secondary prevention after a first occurrence of acute coronary syndrome in France.

J Bezin, A Pariente, R Lassalle, C Dureau-Pournin, A Abouelfath, P Robinson, N Moore, C Droz-Perroteau, A Fourrier-Reglat

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Article in European journal of clinical pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  4. Incidence of clinical atrial fibrillation and related complications using a screening algorithm at a nationwide level.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
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  7. Outcomes in patients with acute myocardial infarction and new atrial fibrillation: a nationwide analysis.Clinical research in cardiology : official journal of the German Cardiac Society · 2021
    Article
  8. Intervening on fear after acute cardiac events: Rationale and design of the INFORM randomized clinical trial.Health psychology : official journal of the Division of Health Psychology, American Psychological Association · 2020
    Article
  9. Article
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  11. Article
  12. Article
  13. Usage patterns of paracetamol in France.British journal of clinical pharmacology · 2016
    Article
  14. Article
  15. Article
  16. 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

9 authors at 4 institutions in 1 country.

J BezinUniversity of Bordeaux, Bordeaux, 33076, France, julien.bezin@pharmaco.u-bordeaux2.fr.
A Pariente
R Lassalle
C Dureau-Pournin
A Abouelfath
P Robinson
N Moore
C Droz-Perroteau
A Fourrier-Reglat
Université de Bordeaux · FRBordeaux Population Health · FRCentre Hospitalier Universitaire de Bordeaux · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe recommended pharmacotherapy for secondary prevention of acute coronary syndrome (ACS) is long-term treatment with a combination of four therapeutic classes: beta-blockers, antiplatelet agents (including aspirin), statins or other lipid-lowering agents, and angiotensin-converting enzyme inhibitors or angiotensin receptor blockers. The aim of this study was to describe use and persistence of the recommended drug combination after the first occurrence of ACS in France.

methodsThis was a database cohort study of patients with first registration for ACS between 2004 and 2007 in a representative sample of the French healthcare insurance database (Echantillon Généraliste de Bénéficiaires, EGB). The drugs of interest were those recommended. Persistence was assessed for patients dispensed three or all four drug classes within 2 months following ACS. Discontinuation was defined by a gap of more than 6 weeks between two dispensations. The follow-up period was 24 months after ACS occurrence.

resultsOf 2,057 patients with incident ACS, 872 (42.4 %) had at least one dispensation of each of the four recommended drug classes, and 684 (33.3 %) had three of the four classes. Persistence to treatment at 24 months was 57.4 % (95 % CI [54.0-60.6]) for patients with four classes, and 55.5 % (95 % CI [51.6-59.1]) with three classes. Discontinuation of initial combination was higher in patients aged  ≥ 65 years at ACS occurrence, those with associated ongoing chronic disease, and in those who did not suffer myocardial infarction.

conclusionsPost-ACS secondary prevention in France is not optimal, especially in patients who did not have myocardial infarction.

Indexed as

Acute Coronary SyndromeAdrenergic beta-AntagonistsAgedAngiotensin-Converting Enzyme InhibitorsCohort StudiesDrug Therapy, CombinationFemaleFranceGuideline AdherenceHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsMaleMiddle AgedPlatelet Aggregation InhibitorsSecondary PreventionAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsPlatelet Aggregation Inhibitors

Identifiers

PMID24271648
OpenAlexW2131632783

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.