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Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors
BACKGROUND: Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9is) are an important but underutilised option to help optimise lipid management. We developed a new service to improve patient access to these medicines in line with National Institute for Health and Care Excellence recommend...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991064/ https://www.ncbi.nlm.nih.gov/pubmed/35393352 http://dx.doi.org/10.1136/openhrt-2021-001931 |
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author | Khatib, Rani Khan, Mutiba Barrowcliff, Abigail Ikongo, Eunice Burton, Claire Mansfield, Michael Hall, Alistair |
author_facet | Khatib, Rani Khan, Mutiba Barrowcliff, Abigail Ikongo, Eunice Burton, Claire Mansfield, Michael Hall, Alistair |
author_sort | Khatib, Rani |
collection | PubMed |
description | BACKGROUND: Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9is) are an important but underutilised option to help optimise lipid management. We developed a new service to improve patient access to these medicines in line with National Institute for Health and Care Excellence recommendations. This paper describes the model and provides lipid-lowering results and feedback from the first 100 referred patients. METHODS: The service is based on a centralised multidisciplinary clinic that is the sole prescriber of PCSK9i therapy in the area. Referred patients are assessed for eligibility and given tailored, person-centred support, education and monitoring to promote treatment adherence and lipids optimisation. The clinic also supports referred patients that do not meet PCSK9i eligibility criteria. RESULTS: Among the first 100 patients referred (n=62 male; mean age: 62.9±10.5 years), 48 were initiated on PCSK9i therapy. Mean total cholesterol decreased from 7.7±1.6 mmol/L at baseline to 4.5±1.4 mmol/L at 3 months (41% reduction), while mean low-density lipoprotein-cholesterol (LDL-C) fell from 5.0±1.6 mmol/L to 2.1±1.3 mmol/L (58% reduction; p<0.0001) and median LDL-C decreased from 4.8 mmol/L to 1.6 mmol/L (67% reduction) over the same period. These decreases were maintained at 12 months (45%, 65% and 67% reductions, respectively; p<0.0001 for the decrease in mean LDL-C from baseline). Patient feedback on the clinic was positive and overall satisfaction was high. CONCLUSIONS: This innovative, person-centred, multidisciplinary service successfully initiated PCSK9i therapy for eligible patients and drove long-term monitoring, adherence and cholesterol lowering. It also provided medicines optimisation and adherence assistance to PCSK9i-ineligible patients. The model could be used in other areas to support better uptake and optimisation of PCSK9i therapy. |
format | Online Article Text |
id | pubmed-8991064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-89910642022-04-27 Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors Khatib, Rani Khan, Mutiba Barrowcliff, Abigail Ikongo, Eunice Burton, Claire Mansfield, Michael Hall, Alistair Open Heart Cardiac Risk Factors and Prevention BACKGROUND: Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9is) are an important but underutilised option to help optimise lipid management. We developed a new service to improve patient access to these medicines in line with National Institute for Health and Care Excellence recommendations. This paper describes the model and provides lipid-lowering results and feedback from the first 100 referred patients. METHODS: The service is based on a centralised multidisciplinary clinic that is the sole prescriber of PCSK9i therapy in the area. Referred patients are assessed for eligibility and given tailored, person-centred support, education and monitoring to promote treatment adherence and lipids optimisation. The clinic also supports referred patients that do not meet PCSK9i eligibility criteria. RESULTS: Among the first 100 patients referred (n=62 male; mean age: 62.9±10.5 years), 48 were initiated on PCSK9i therapy. Mean total cholesterol decreased from 7.7±1.6 mmol/L at baseline to 4.5±1.4 mmol/L at 3 months (41% reduction), while mean low-density lipoprotein-cholesterol (LDL-C) fell from 5.0±1.6 mmol/L to 2.1±1.3 mmol/L (58% reduction; p<0.0001) and median LDL-C decreased from 4.8 mmol/L to 1.6 mmol/L (67% reduction) over the same period. These decreases were maintained at 12 months (45%, 65% and 67% reductions, respectively; p<0.0001 for the decrease in mean LDL-C from baseline). Patient feedback on the clinic was positive and overall satisfaction was high. CONCLUSIONS: This innovative, person-centred, multidisciplinary service successfully initiated PCSK9i therapy for eligible patients and drove long-term monitoring, adherence and cholesterol lowering. It also provided medicines optimisation and adherence assistance to PCSK9i-ineligible patients. The model could be used in other areas to support better uptake and optimisation of PCSK9i therapy. BMJ Publishing Group 2022-04-06 /pmc/articles/PMC8991064/ /pubmed/35393352 http://dx.doi.org/10.1136/openhrt-2021-001931 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/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/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Cardiac Risk Factors and Prevention Khatib, Rani Khan, Mutiba Barrowcliff, Abigail Ikongo, Eunice Burton, Claire Mansfield, Michael Hall, Alistair Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors |
title | Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors |
title_full | Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors |
title_fullStr | Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors |
title_full_unstemmed | Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors |
title_short | Innovative, centralised, multidisciplinary medicines optimisation clinic for PCSK9 inhibitors |
title_sort | innovative, centralised, multidisciplinary medicines optimisation clinic for pcsk9 inhibitors |
topic | Cardiac Risk Factors and Prevention |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991064/ https://www.ncbi.nlm.nih.gov/pubmed/35393352 http://dx.doi.org/10.1136/openhrt-2021-001931 |
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