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

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.
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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. |
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Disclosures: E. C. O. receives research support from Janssen, Pfizer, GSK, Novartis, Sanofi, and Bristol Myers Squibb. |
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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. |
Vol 200
P. 134-140 - juin 2018 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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