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Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction

Glasgow city has the highest cardiovascular disease (CVD) mortality rate in the UK. Patients with left ventricular systolic dysfunction after acute myocardial infarction represent a ‘high-risk’ cohort for adverse CVD outcomes. The optimisation of secondary prevention medication in this group is ofte...

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Autores principales: Forsyth, Paul, Moir, Lynsey, Speirits, Iain, McGlynn, Steve, Ryan, Margaret, Watson, Anne, Reid, Fiona, Rush, Christopher, Murphy, Clare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730630/
https://www.ncbi.nlm.nih.gov/pubmed/31544164
http://dx.doi.org/10.1136/bmjoq-2019-000676
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author Forsyth, Paul
Moir, Lynsey
Speirits, Iain
McGlynn, Steve
Ryan, Margaret
Watson, Anne
Reid, Fiona
Rush, Christopher
Murphy, Clare
author_facet Forsyth, Paul
Moir, Lynsey
Speirits, Iain
McGlynn, Steve
Ryan, Margaret
Watson, Anne
Reid, Fiona
Rush, Christopher
Murphy, Clare
author_sort Forsyth, Paul
collection PubMed
description Glasgow city has the highest cardiovascular disease (CVD) mortality rate in the UK. Patients with left ventricular systolic dysfunction after acute myocardial infarction represent a ‘high-risk’ cohort for adverse CVD outcomes. The optimisation of secondary prevention medication in this group is often suboptimal. Our aim was to improve the use and target dosing of ACE inhibitors (ACEI), angiotensin II receptor blockers (ARBs) and beta-blockers in such patients, through pharmacist-led clinics and cardiology multidisciplinary team collaboration. Retrospective audits characterised baseline care. Prospective pharmacist-led clinics were piloted and rolled out across seven hospitals and primary care localities over four Plan–Do–Study–Act cycles. ‘Hub’ and ‘spoke’ clinics utilised independent prescribing pharmacists with different levels of cardiology experience. Pharmacists were trained through a bespoke training programme—‘Teach and Treat’. Consultant cardiologists provided senior support and governance. Patients attending prospective pharmacist-led clinics were more likely to be prescribed an ACEI (or ARB) and beta-blocker (n=856/885 (97%) vs n=233/255 (91%), p<0.001 and n=813/885 (92%) vs n=224/255 (88%), p=0.048, respectively) and be on target dose of ACEI (or ARB) and beta-blocker (n=585/885 (66%) vs n=64/255 (25%), p<0.001 and n=218/885 (25%) vs n=17/255 (7%), p<0.001, respectively) compared with baseline. The mean dose of ACEI (or ARB) and beta-blocker was also higher (79% vs 48% of target dose, p<0.001% and 48% vs 33% of target dose, p<0.001, respectively) compared with baseline. Use of secondary prevention medication was significantly improved by pharmacist and cardiology collaboration. These improvements were sustained across a 4-year period, supported by a novel approach called ‘Teach and Treat’ which linked training to defined clinical service delivery. Further work is needed to assess the impact of the programme on long-term CVD outcomes.
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spelling pubmed-67306302019-09-20 Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction Forsyth, Paul Moir, Lynsey Speirits, Iain McGlynn, Steve Ryan, Margaret Watson, Anne Reid, Fiona Rush, Christopher Murphy, Clare BMJ Open Qual Quality Improvement Report Glasgow city has the highest cardiovascular disease (CVD) mortality rate in the UK. Patients with left ventricular systolic dysfunction after acute myocardial infarction represent a ‘high-risk’ cohort for adverse CVD outcomes. The optimisation of secondary prevention medication in this group is often suboptimal. Our aim was to improve the use and target dosing of ACE inhibitors (ACEI), angiotensin II receptor blockers (ARBs) and beta-blockers in such patients, through pharmacist-led clinics and cardiology multidisciplinary team collaboration. Retrospective audits characterised baseline care. Prospective pharmacist-led clinics were piloted and rolled out across seven hospitals and primary care localities over four Plan–Do–Study–Act cycles. ‘Hub’ and ‘spoke’ clinics utilised independent prescribing pharmacists with different levels of cardiology experience. Pharmacists were trained through a bespoke training programme—‘Teach and Treat’. Consultant cardiologists provided senior support and governance. Patients attending prospective pharmacist-led clinics were more likely to be prescribed an ACEI (or ARB) and beta-blocker (n=856/885 (97%) vs n=233/255 (91%), p<0.001 and n=813/885 (92%) vs n=224/255 (88%), p=0.048, respectively) and be on target dose of ACEI (or ARB) and beta-blocker (n=585/885 (66%) vs n=64/255 (25%), p<0.001 and n=218/885 (25%) vs n=17/255 (7%), p<0.001, respectively) compared with baseline. The mean dose of ACEI (or ARB) and beta-blocker was also higher (79% vs 48% of target dose, p<0.001% and 48% vs 33% of target dose, p<0.001, respectively) compared with baseline. Use of secondary prevention medication was significantly improved by pharmacist and cardiology collaboration. These improvements were sustained across a 4-year period, supported by a novel approach called ‘Teach and Treat’ which linked training to defined clinical service delivery. Further work is needed to assess the impact of the programme on long-term CVD outcomes. BMJ Publishing Group 2019-08-28 /pmc/articles/PMC6730630/ /pubmed/31544164 http://dx.doi.org/10.1136/bmjoq-2019-000676 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Quality Improvement Report
Forsyth, Paul
Moir, Lynsey
Speirits, Iain
McGlynn, Steve
Ryan, Margaret
Watson, Anne
Reid, Fiona
Rush, Christopher
Murphy, Clare
Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
title Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
title_full Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
title_fullStr Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
title_full_unstemmed Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
title_short Improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
title_sort improving medication optimisation in left ventricular systolic dysfunction after acute myocardial infarction
topic Quality Improvement Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730630/
https://www.ncbi.nlm.nih.gov/pubmed/31544164
http://dx.doi.org/10.1136/bmjoq-2019-000676
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