S'abonner

Early impact of guideline publication on angiotensin-receptor neprilysin inhibitor use among patients hospitalized for heart failure - 11/06/18

Doi : 10.1016/j.ahj.2018.01.009 
Nancy Luo, MD a, b, , Nicholas G. Ballew, PhD c, Emily C. O'Brien, PhD b, c, Melissa A. Greiner, MS c, Pamela N. Peterson, MD, MSPH d, e, Bradley G. Hammill, DrPH c, N. Chantelle Hardy, MPH c, Warren K. Laskey, MD, MPH f, Paul A. Heidenreich, MD, MS g, Chun-Lan Chang, PhD h, Adrian F. Hernandez, MD, MHS a, b, Lesley H. Curtis, PhD b, c, Robert J. Mentz, MD a, b, Gregg C. Fonarow, MD i
a Department of Medicine, Duke University School of Medicine, Durham, NC, United States 
b Duke Clinical Research Institute, Durham, NC, United States 
c Department of Population Health Sciences, Duke University School of Medicine, Durham, NC, United States 
d Denver Health Medical Center, Denver, CO, United States 
e University of Colorado, Anschutz Medical Center, Aurora, CO, United States 
f Division of Cardiology, University of New Mexico School of Medicine, Albuquerque, NM, United States 
g Department of Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, United States 
h Novartis Pharmaceuticals Corporation, East Hanover, NJ, United States 
i Ahmanson-UCLA Cardiomyopathy Center, University of California, Los Angeles, CA, United States 

Reprint requests: Nancy Luo, MD, Duke Clinical Research Institute, Room 0311 Terrace Level, 2400 Pratt St, Durham, NC 27705, United States.Duke Clinical Research InstituteRoom 0311 Terrace Level, 2400 Pratt StDurhamNC27705United States

Abstract

Background

On May 20, 2016, US professional organizations in cardiology published joint treatment guidelines recommending the use of angiotensin-receptor neprilysin inhibitor (ARNI) for eligible patients with heart failure with reduced ejection fraction (HFrEF). Using data from the Get With The Guidelines–Heart Failure registry, we evaluated the early impact of this update on temporal trends in ARNI prescription.

Methods

We analyzed patients with HFrEF who were eligible for ARNI prescription (EF ≤40%, no contraindications) and hospitalized from February 20, 2016, through August 19, 2016—allowing for 13weeks before and after guideline publication. We quantified trends in ARNI use associated with guidelines publication with an interrupted time-series design using logistic regression and accounting for correlations within hospitals using general estimating equation methods.

Results

Of 7,200 eligible patient hospitalizations, 51.9% were discharged in the period directly preceding publication of the guidelines, and 48.1% were discharged after. Odds ratios of ARNI prescription at discharge were significantly higher in the postguideline period compared with the preguideline period in adjusted models (adjusted odds ratio 1.29, 95% CI 1.06-1.57, P=.01). However, there was no significant interaction between observed and expected ARNI use after guideline publication (Pinteraction=.14). Results were consistent using a 6-month before and after time frame.

Conclusions

The model suggested a small increase in ARNI use in HF patients being discharged from the hospital immediately after guideline release. However, the publication of national guidelines recommending ARNI use seemed to have little influence on the adoption of this evidence-based medication in the first 3 to 6months.

Le texte complet de cet article est disponible en PDF.

Plan


 Sources of funding: This work was sponsored by Novartis Pharmaceuticals Corporation, East Hanover, NJ. Additionally, the Get With The Guidelines–Heart Failure (GWTG-HF) program is provided by the American Heart Association. GWTG-HF is sponsored, in part, by Amgen Cardiovascular and has been funded in the past through support from Medtronic, GlaxoSmithKline, Ortho-McNeil, and the American Heart Association Pharmaceutical Roundtable.
 Disclosures: E. C. O. receives research support from Janssen, Pfizer, GSK, Novartis, Sanofi, and Bristol Myers Squibb.
 L. H. C. receives research support from NIH, PCORI, Novartis, GlaxoSmithKline, Gilead, Boston Scientific, and St Jude.
C. L. C. is an employee of Novartis Pharmaceuticals Corporation and owns stock in Novartis AG.
A. F. H. receives research support from AstraZeneca, Bristol-Myers Squibb, GlaxoSmithKline, Luitpold Pharmaceuticals, Merck, and Novartis and honoraria from Bayer, Boston Scientific and Novartis.
G. C. F. receives research funding from NIH and consulting funding from Amgen, Janssen, Medtronic, Novartis, and St Jude Medical.
All other authors have no relevant disclosures.


© 2018  Elsevier Inc. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 200

P. 134-140 - juin 2018 Retour au numéro
Article précédent Article précédent
  • A Hospital Level Analysis of 30-Day Readmission Performance for Heart Failure Patients and Long-Term Survival: Findings from Get With The Guidelines-Heart Failure
  • Sawan Jalnapurkar, Xin Zhao, Paul A. Heidenreich, Deepak L. Bhatt, Eric E. Smith, Adam D. DeVore, Adrian F. Hernandez, Roland Matsouaka, Clyde W. Yancy, Gregg C. Fonarow
| Article suivant Article suivant
  • Caffeine and incidence of dyspnea in patients treated with ticagrelor
  • Daniel Lindholm, Stefan James, Jonas Andersson, Oscar Ö Braun, Susanne Heller, Peter Henriksson, Jörg Lauermann, Patrik Öhagen, Christoph Varenhorst

Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.

Déjà abonné à cette revue ?

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2025 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.