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The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?

OBJECTIVE: To evaluate targeting of statin prescribing for primary prevention to those with high cardiovascular disease (CVD) risk. DESIGN: Two cohort studies including the general population and initiators of statins aged 35–74 years. SETTING: UK primary care records in the Clinical Practice Resear...

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Autores principales: van Staa, Tjeerd-Pieter, Smeeth, Liam, Ng, Edmond S-W, Goldacre, Ben, Gulliford, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812879/
https://www.ncbi.nlm.nih.gov/pubmed/23735939
http://dx.doi.org/10.1136/heartjnl-2013-303698
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author van Staa, Tjeerd-Pieter
Smeeth, Liam
Ng, Edmond S-W
Goldacre, Ben
Gulliford, Martin
author_facet van Staa, Tjeerd-Pieter
Smeeth, Liam
Ng, Edmond S-W
Goldacre, Ben
Gulliford, Martin
author_sort van Staa, Tjeerd-Pieter
collection PubMed
description OBJECTIVE: To evaluate targeting of statin prescribing for primary prevention to those with high cardiovascular disease (CVD) risk. DESIGN: Two cohort studies including the general population and initiators of statins aged 35–74 years. SETTING: UK primary care records in the Clinical Practice Research Datalink. PATIENTS: 3.8 million general population patients and 300 914 statin users. INTERVENTION: Statin prescribing. MAIN OUTCOME MEASURES: Statin prescribing by CVD risk; observed 5-year CVD risks; variability between practices. RESULTS: Statin prescribing increased substantially over time to patients with high 10-year CVD risk (≥20%): 7.0% of these received a statin prior to 2007, and 30.4% in 2007 onwards. Prescribing to patients with low risk (<15%) also increased (from 1.9% to 5.0%). Only about half the patients initiating statin treatment were high risk according to CVD risk score. The 5-year CVD risks, as observed during statin treatment, reduced over calendar time (from 17.0% to 7.1%). There was a large variation between general practices in the percentage of high-risk patients prescribed a statin in 2007 onwards, ranging from 8.2% to 61.5%. For low-risk patients, these varied from 2.1% to 29.1%. CONCLUSIONS: There appeared to be substantive overuse in low CVD risk and underuse in high CVD risk (600 000 and 850 000 patients, respectively, in the UK since 2007). There is wide variation between practices in statin prescribing to patients at high CVD risk. There is a clear need for randomised trials for the best strategy to target statin treatment and manage CVD risk for primary prevention.
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spelling pubmed-38128792013-10-31 The efficiency of cardiovascular risk assessment: do the right patients get statin treatment? van Staa, Tjeerd-Pieter Smeeth, Liam Ng, Edmond S-W Goldacre, Ben Gulliford, Martin Heart Epidemiology OBJECTIVE: To evaluate targeting of statin prescribing for primary prevention to those with high cardiovascular disease (CVD) risk. DESIGN: Two cohort studies including the general population and initiators of statins aged 35–74 years. SETTING: UK primary care records in the Clinical Practice Research Datalink. PATIENTS: 3.8 million general population patients and 300 914 statin users. INTERVENTION: Statin prescribing. MAIN OUTCOME MEASURES: Statin prescribing by CVD risk; observed 5-year CVD risks; variability between practices. RESULTS: Statin prescribing increased substantially over time to patients with high 10-year CVD risk (≥20%): 7.0% of these received a statin prior to 2007, and 30.4% in 2007 onwards. Prescribing to patients with low risk (<15%) also increased (from 1.9% to 5.0%). Only about half the patients initiating statin treatment were high risk according to CVD risk score. The 5-year CVD risks, as observed during statin treatment, reduced over calendar time (from 17.0% to 7.1%). There was a large variation between general practices in the percentage of high-risk patients prescribed a statin in 2007 onwards, ranging from 8.2% to 61.5%. For low-risk patients, these varied from 2.1% to 29.1%. CONCLUSIONS: There appeared to be substantive overuse in low CVD risk and underuse in high CVD risk (600 000 and 850 000 patients, respectively, in the UK since 2007). There is wide variation between practices in statin prescribing to patients at high CVD risk. There is a clear need for randomised trials for the best strategy to target statin treatment and manage CVD risk for primary prevention. BMJ Publishing Group 2013-11-01 2013-06-04 /pmc/articles/PMC3812879/ /pubmed/23735939 http://dx.doi.org/10.1136/heartjnl-2013-303698 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Epidemiology
van Staa, Tjeerd-Pieter
Smeeth, Liam
Ng, Edmond S-W
Goldacre, Ben
Gulliford, Martin
The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
title The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
title_full The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
title_fullStr The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
title_full_unstemmed The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
title_short The efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
title_sort efficiency of cardiovascular risk assessment: do the right patients get statin treatment?
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812879/
https://www.ncbi.nlm.nih.gov/pubmed/23735939
http://dx.doi.org/10.1136/heartjnl-2013-303698
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