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Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study

OBJECTIVES: To explore population patterns of sex-based incidence and prevalence of peripheral arterial disease (PAD), guideline-directed best medical therapy prescriptions and its relationship with all-cause mortality at 1 year. DESIGN: A retrospective cohort study. SETTING: Anonymised electronic p...

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Autores principales: Benson, Ruth A, Okoth, Kelvin, Keerthy, Deepiksana, Gokhale, Krishna, Adderley, Nicola J, Nirantharakumar, Krishnarajah, Lasserson, Daniel S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915354/
https://www.ncbi.nlm.nih.gov/pubmed/35273054
http://dx.doi.org/10.1136/bmjopen-2021-055952
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author Benson, Ruth A
Okoth, Kelvin
Keerthy, Deepiksana
Gokhale, Krishna
Adderley, Nicola J
Nirantharakumar, Krishnarajah
Lasserson, Daniel S
author_facet Benson, Ruth A
Okoth, Kelvin
Keerthy, Deepiksana
Gokhale, Krishna
Adderley, Nicola J
Nirantharakumar, Krishnarajah
Lasserson, Daniel S
author_sort Benson, Ruth A
collection PubMed
description OBJECTIVES: To explore population patterns of sex-based incidence and prevalence of peripheral arterial disease (PAD), guideline-directed best medical therapy prescriptions and its relationship with all-cause mortality at 1 year. DESIGN: A retrospective cohort study. SETTING: Anonymised electronic primary care from 787 practices in the UK, or approximately 6.2% of the UK population. PARTICIPANTS: All registered patients over 40 with a documented diagnosis of peripheral arterial disease. OUTCOME MEASURE: Population incidence and prevalence of PAD by sex. Patterns of guideline-directed therapy, and correlation with all-cause mortality at 1 year (defined as death due to any outcome) in patients with and without an existing diagnosis of cardiovascular disease. Covariates included Charlson comorbidity, sex, age, body mass index, Townsend score of deprivation, smoking status, diabetes, hypertension, statin and antiplatelet prescription. RESULTS: Sequential cross-sectional studies from 2010 to 2017 found annual PAD prevalence (12.7–14.3 vs 25.6 per 1000 in men) and incidence were lower in women (11.6–12.4 vs 22.7–26.8 per 10 000 person years in men). Cox proportional hazards models created for PAD patients with and without cardiovascular disease over one full year analysed 25 121 men and 13 480 women, finding that following adjustment for age, women were still less likely to be on a statin (OR 0.69; 95% CI 0.66 to 0.72; p<0.001) or antiplatelet (OR: 0.87; 95% CI 0.83 to 0.90; p<0.001). Once fully adjusted for guideline recommended medical therapy, all-cause mortality was similar between women and men (adjusted HR (aHR) 0.95, 95% CI 0.87 to 1.03, p=0.198 for all patients, aHR 1.01, 95% CI 0.88 to 1.16, p=0.860 for those with cardiovascular disease). CONCLUSIONS: Women with a new diagnosis of PAD were not prescribed guideline-directed therapy at the same rate as men. However once adjusted for factors including age, all-cause mortality in men and women was similar.
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spelling pubmed-89153542022-03-25 Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study Benson, Ruth A Okoth, Kelvin Keerthy, Deepiksana Gokhale, Krishna Adderley, Nicola J Nirantharakumar, Krishnarajah Lasserson, Daniel S BMJ Open Cardiovascular Medicine OBJECTIVES: To explore population patterns of sex-based incidence and prevalence of peripheral arterial disease (PAD), guideline-directed best medical therapy prescriptions and its relationship with all-cause mortality at 1 year. DESIGN: A retrospective cohort study. SETTING: Anonymised electronic primary care from 787 practices in the UK, or approximately 6.2% of the UK population. PARTICIPANTS: All registered patients over 40 with a documented diagnosis of peripheral arterial disease. OUTCOME MEASURE: Population incidence and prevalence of PAD by sex. Patterns of guideline-directed therapy, and correlation with all-cause mortality at 1 year (defined as death due to any outcome) in patients with and without an existing diagnosis of cardiovascular disease. Covariates included Charlson comorbidity, sex, age, body mass index, Townsend score of deprivation, smoking status, diabetes, hypertension, statin and antiplatelet prescription. RESULTS: Sequential cross-sectional studies from 2010 to 2017 found annual PAD prevalence (12.7–14.3 vs 25.6 per 1000 in men) and incidence were lower in women (11.6–12.4 vs 22.7–26.8 per 10 000 person years in men). Cox proportional hazards models created for PAD patients with and without cardiovascular disease over one full year analysed 25 121 men and 13 480 women, finding that following adjustment for age, women were still less likely to be on a statin (OR 0.69; 95% CI 0.66 to 0.72; p<0.001) or antiplatelet (OR: 0.87; 95% CI 0.83 to 0.90; p<0.001). Once fully adjusted for guideline recommended medical therapy, all-cause mortality was similar between women and men (adjusted HR (aHR) 0.95, 95% CI 0.87 to 1.03, p=0.198 for all patients, aHR 1.01, 95% CI 0.88 to 1.16, p=0.860 for those with cardiovascular disease). CONCLUSIONS: Women with a new diagnosis of PAD were not prescribed guideline-directed therapy at the same rate as men. However once adjusted for factors including age, all-cause mortality in men and women was similar. BMJ Publishing Group 2022-03-09 /pmc/articles/PMC8915354/ /pubmed/35273054 http://dx.doi.org/10.1136/bmjopen-2021-055952 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 Cardiovascular Medicine
Benson, Ruth A
Okoth, Kelvin
Keerthy, Deepiksana
Gokhale, Krishna
Adderley, Nicola J
Nirantharakumar, Krishnarajah
Lasserson, Daniel S
Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
title Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
title_full Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
title_fullStr Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
title_full_unstemmed Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
title_short Analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
title_sort analysis of the relationship between sex and prescriptions for guideline-recommended therapy in peripheral arterial disease, in relation to 1-year all-cause mortality: a primary care cohort study
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915354/
https://www.ncbi.nlm.nih.gov/pubmed/35273054
http://dx.doi.org/10.1136/bmjopen-2021-055952
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