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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...

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Autores principales: Khatib, Rani, Khan, Mutiba, Barrowcliff, Abigail, Ikongo, Eunice, Burton, Claire, Mansfield, Michael, Hall, Alistair
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
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.
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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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