Medicines optimization prior to discharge in patients admitted to hospital with heart failure

Author:

Cuthbert Joseph J.12ORCID,Brown Oliver I.12,Pellicori Pierpaolo3,Dobbs Karen1,Bulemfu Jeanne1,Kazmi Syed1,Sokoreli Ioanna4,Pauws Steffan C.45,Riistama Jarno M.6,Cleland John G.F.3,Clark Andrew L.2

Affiliation:

1. Clinical Sciences Centre Hull York Medical School, University of Hull Kingston upon Hull East Riding of Yorkshire UK

2. Department of Cardiology Hull University Teaching Hospital Trust, Castle Hill Hospital Kingston upon Hull East Riding of Yorkshire UK

3. British Heart Foundation Centre of Research Excellence, School of Cardiovascular and Metabolic Health University of Glasgow 126 University Place, Glasgow Glasgow G12 8TA Lanarkshire UK

4. Remote Patient Management and Chronic Care Philips Research Eindhoven Eindhoven The Netherlands

5. Department of Communication and Cognition Tilburg University Tilburg The Netherlands

6. Philips Image Guided Therapy Devices Best The Netherlands

Abstract

AbstractAimsApproximately half of patients with heart failure and a reduced ejection fraction (HeFREF) are discharged from hospital on triple therapy [angiotensin‐converting enzyme inhibitors (ACE‐Is) or angiotensin receptor blockers (ARBs), beta‐blockers (BBs), and mineralocorticoid receptor antagonists (MRAs)]. We investigated what proportion of patients are on optimal doses prior to discharge and how many might be eligible for initiation of sacubitril–valsartan or sodium‐glucose co‐transporter‐2 inhibitors (SGLT2Is).Methods and resultsBetween 2012 and 2017, 1277 patients admitted with suspected heart failure were enrolled at a single hospital serving a local community around Kingston upon Hull, UK. Eligibility for sacubitril–valsartan or SGLT2I was based on entry criteria for the PIONEER‐HF, DAPA‐HF, and EMPEROR‐Reduced trials. Four hundred fifty‐five patients had HeFREF with complete data on renal function, heart rate, and systolic blood pressure (SBP) prior to discharge. Eighty‐three per cent of patients were taking an ACE‐I or ARB, 85% a BB, and 63% an MRA at discharge. More than 60% of patients were eligible for sacubitril–valsartan and >70% for SGLT2I. Among those not already receiving a prescription, 37%, 28%, and 49% were eligible to start ACE‐I or ARB, BB, and MRA, respectively. Low SBP (≤105 mmHg) was the most frequent explanation for failure to initiate or up‐titrate therapy.ConclusionsMost patients admitted for heart failure are eligible for initiation of life‐prolonging medications prior to discharge. A hospital admission may be a common missed opportunity to improve treatment for patients with HeFREF.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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