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Medical therapy doses at hospital discharge in patients with existing and de novo heart failure

AIMS: Uptitrating angiotensin‐converting enzyme inhibitors or angiotensin receptor blockers (ACE‐I/ARBs), beta‐blockers, and mineralocorticoid receptor antagonists (MRAs) to optimal doses in heart failure with reduced ejection fraction (HFrEF) is associated with improved outcomes and recommended in...

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Autores principales: Diamant, Michael J., Virani, Sean A., MacKenzie, Winston J., Ignaszewski, Andrew, Toma, Mustafa, Hawkins, Nathaniel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676447/
https://www.ncbi.nlm.nih.gov/pubmed/31218850
http://dx.doi.org/10.1002/ehf2.12454
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author Diamant, Michael J.
Virani, Sean A.
MacKenzie, Winston J.
Ignaszewski, Andrew
Toma, Mustafa
Hawkins, Nathaniel M.
author_facet Diamant, Michael J.
Virani, Sean A.
MacKenzie, Winston J.
Ignaszewski, Andrew
Toma, Mustafa
Hawkins, Nathaniel M.
author_sort Diamant, Michael J.
collection PubMed
description AIMS: Uptitrating angiotensin‐converting enzyme inhibitors or angiotensin receptor blockers (ACE‐I/ARBs), beta‐blockers, and mineralocorticoid receptor antagonists (MRAs) to optimal doses in heart failure with reduced ejection fraction (HFrEF) is associated with improved outcomes and recommended in guidelines. Studies of ambulatory patients found that a minority are prescribed optimal doses. However, dose at hospital discharge has rarely been reported. This information may guide quality improvement initiatives during and following discharge. METHODS AND RESULTS: We assessed 370 consecutive patients with HFrEF hospitalized at two centres in Vancouver, Canada. Of those without contraindications, 86.4%, 93.4%, and 44.7% were prescribed an ACE‐I/ARB/sacubitril–valsartan, beta‐blocker, or MRA, respectively. The proportion of eligible patients prescribed target dose was respectively 28.6%, 31.7%, and 4.1%. Forty‐two of 248 eligible patients (16.9%) were prescribed ≥50% of target dose, and only three patients received target dosing of all three medication classes. In multivariate regression models, cardiologist involvement in care was independently associated with increased dose and prescription of ≥50% of target dose for all medications, whereas a history of HF was only predictive for beta‐blockers. CONCLUSIONS: In a single‐region experience of hospitalized HFrEF patients, a high proportion of eligible patients were discharged on ACE‐I/ARB or beta‐blocker. Less than half were prescribed MRAs, and few were prescribed ≥50% or target dosing of all medications. Further exploration into barriers to medication uptitration, and improvement in processes of care, is needed.
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spelling pubmed-66764472019-08-06 Medical therapy doses at hospital discharge in patients with existing and de novo heart failure Diamant, Michael J. Virani, Sean A. MacKenzie, Winston J. Ignaszewski, Andrew Toma, Mustafa Hawkins, Nathaniel M. ESC Heart Fail Original Research Articles AIMS: Uptitrating angiotensin‐converting enzyme inhibitors or angiotensin receptor blockers (ACE‐I/ARBs), beta‐blockers, and mineralocorticoid receptor antagonists (MRAs) to optimal doses in heart failure with reduced ejection fraction (HFrEF) is associated with improved outcomes and recommended in guidelines. Studies of ambulatory patients found that a minority are prescribed optimal doses. However, dose at hospital discharge has rarely been reported. This information may guide quality improvement initiatives during and following discharge. METHODS AND RESULTS: We assessed 370 consecutive patients with HFrEF hospitalized at two centres in Vancouver, Canada. Of those without contraindications, 86.4%, 93.4%, and 44.7% were prescribed an ACE‐I/ARB/sacubitril–valsartan, beta‐blocker, or MRA, respectively. The proportion of eligible patients prescribed target dose was respectively 28.6%, 31.7%, and 4.1%. Forty‐two of 248 eligible patients (16.9%) were prescribed ≥50% of target dose, and only three patients received target dosing of all three medication classes. In multivariate regression models, cardiologist involvement in care was independently associated with increased dose and prescription of ≥50% of target dose for all medications, whereas a history of HF was only predictive for beta‐blockers. CONCLUSIONS: In a single‐region experience of hospitalized HFrEF patients, a high proportion of eligible patients were discharged on ACE‐I/ARB or beta‐blocker. Less than half were prescribed MRAs, and few were prescribed ≥50% or target dosing of all medications. Further exploration into barriers to medication uptitration, and improvement in processes of care, is needed. John Wiley and Sons Inc. 2019-06-20 /pmc/articles/PMC6676447/ /pubmed/31218850 http://dx.doi.org/10.1002/ehf2.12454 Text en © 2019 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Diamant, Michael J.
Virani, Sean A.
MacKenzie, Winston J.
Ignaszewski, Andrew
Toma, Mustafa
Hawkins, Nathaniel M.
Medical therapy doses at hospital discharge in patients with existing and de novo heart failure
title Medical therapy doses at hospital discharge in patients with existing and de novo heart failure
title_full Medical therapy doses at hospital discharge in patients with existing and de novo heart failure
title_fullStr Medical therapy doses at hospital discharge in patients with existing and de novo heart failure
title_full_unstemmed Medical therapy doses at hospital discharge in patients with existing and de novo heart failure
title_short Medical therapy doses at hospital discharge in patients with existing and de novo heart failure
title_sort medical therapy doses at hospital discharge in patients with existing and de novo heart failure
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676447/
https://www.ncbi.nlm.nih.gov/pubmed/31218850
http://dx.doi.org/10.1002/ehf2.12454
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