All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study

Objectives To evaluate the benefit and risk of low-dose acetylsalicylic acid (aspirin) in patients from remote Aboriginal communities in the Northern Territory, Australia.Design Retrospective cohort study using primary care and hospital data routinely used for healthcare. Aspirin users and non-users...

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Main Authors: Louise Maple-Brown, Yuejen Zhao, Steven Guthridge, Henrik Falhammar, Kanakamani Jeyaraman, Paul Burgess, Christine Connors
Format: Article
Language:English
Published: BMJ Publishing Group 2020-01-01
Series:BMJ Open
Online Access:https://bmjopen.bmj.com/content/10/1/e030034.full
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author Louise Maple-Brown
Yuejen Zhao
Steven Guthridge
Henrik Falhammar
Kanakamani Jeyaraman
Paul Burgess
Christine Connors
author_facet Louise Maple-Brown
Yuejen Zhao
Steven Guthridge
Henrik Falhammar
Kanakamani Jeyaraman
Paul Burgess
Christine Connors
author_sort Louise Maple-Brown
collection DOAJ
description Objectives To evaluate the benefit and risk of low-dose acetylsalicylic acid (aspirin) in patients from remote Aboriginal communities in the Northern Territory, Australia.Design Retrospective cohort study using primary care and hospital data routinely used for healthcare. Aspirin users and non-users were compared before and after controlling confounders by matching. Marginal structural models (MSM) were applied to ascertain the benefit and risk.Setting The benefit and harm of aspirin were investigated in patients aged ≥18 years from 54 remote Aboriginal communities.Participants None had a previous cardiovascular event or major bleeds. Patients on anticoagulants or other antiplatelets were excluded.Intervention Aspirin at a dose of 75–162 mg/day.Outcome measures Endpoints were all-cause, cardiovascular mortality and incidences of cardiovascular events and major bleeds.Results 8167 predominantly Aboriginal adults were included and followed between July 2009 and June 2017 (aspirin users n=1865, non-users n=6302, mean follow-up 4 years with hospitalisations 6.4 per person). Univariate analysis found material differences in demographics, prevalence of chronic diseases and outcome measures between aspirin users and non-users before matching. After matching, aspirin was significantly associated with reduced all-cause mortality (HR=0.45: 95% CI 0.34 to 0.60; p<0.001), but not bleeding (HR=1.13: 95% CI 0.39 to 3.26; p=0.820). After using MSMs to eliminate the effects of confounders, loss of follow-up and time dependency of treatment, aspirin was associated with reduced all-cause mortality (HR=0.60: 95% CI 0.47 to 0.76; p<0.001), independent of age (HR=1.06; p<0.001), presence of diabetes (HR=1.42; p<0.001), hypertension (HR=1.61; p<0.001) and alcohol abuse (HR=1.81; p<0.001). No association between aspirin and major bleeding was found (HR=1.14: 95% CI 0.48 to 2.73; p=0.765). Sensitivity analysis suggested these findings were unlikely to have been the result of unmeasured confounding.Conclusion Aspirin was associated with reduced all-cause mortality. Bleeding risk was less compared with survival benefits. Aspirin should be considered for primary prevention in Aboriginal people with high cardiovascular risk.
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spelling doaj-art-1757c2f21d514e578dbc4d72dbd56d9d2024-12-06T00:20:10ZengBMJ Publishing GroupBMJ Open2044-60552020-01-0110110.1136/bmjopen-2019-030034All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational studyLouise Maple-Brown0Yuejen Zhao1Steven Guthridge2Henrik Falhammar3Kanakamani Jeyaraman4Paul Burgess5Christine Connors6Endocrine Department, Royal Darwin Hospital, Casuarina, Northern Territory, Australia3 Population and Digital Health, NT Health, Darwin, Northern Territory, AustraliaMenzies School of Health Research, Casuarina, Northern Territory, Australia9 Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden2 Department of Endocrinology, Royal Darwin Hospital, Darwin, Northern Territory, Australia3UCL Institute of Cognitive Neuroscience, London, UKNorthern Territory Department of Health, Darwin, Northern Territory, AustraliaObjectives To evaluate the benefit and risk of low-dose acetylsalicylic acid (aspirin) in patients from remote Aboriginal communities in the Northern Territory, Australia.Design Retrospective cohort study using primary care and hospital data routinely used for healthcare. Aspirin users and non-users were compared before and after controlling confounders by matching. Marginal structural models (MSM) were applied to ascertain the benefit and risk.Setting The benefit and harm of aspirin were investigated in patients aged ≥18 years from 54 remote Aboriginal communities.Participants None had a previous cardiovascular event or major bleeds. Patients on anticoagulants or other antiplatelets were excluded.Intervention Aspirin at a dose of 75–162 mg/day.Outcome measures Endpoints were all-cause, cardiovascular mortality and incidences of cardiovascular events and major bleeds.Results 8167 predominantly Aboriginal adults were included and followed between July 2009 and June 2017 (aspirin users n=1865, non-users n=6302, mean follow-up 4 years with hospitalisations 6.4 per person). Univariate analysis found material differences in demographics, prevalence of chronic diseases and outcome measures between aspirin users and non-users before matching. After matching, aspirin was significantly associated with reduced all-cause mortality (HR=0.45: 95% CI 0.34 to 0.60; p<0.001), but not bleeding (HR=1.13: 95% CI 0.39 to 3.26; p=0.820). After using MSMs to eliminate the effects of confounders, loss of follow-up and time dependency of treatment, aspirin was associated with reduced all-cause mortality (HR=0.60: 95% CI 0.47 to 0.76; p<0.001), independent of age (HR=1.06; p<0.001), presence of diabetes (HR=1.42; p<0.001), hypertension (HR=1.61; p<0.001) and alcohol abuse (HR=1.81; p<0.001). No association between aspirin and major bleeding was found (HR=1.14: 95% CI 0.48 to 2.73; p=0.765). Sensitivity analysis suggested these findings were unlikely to have been the result of unmeasured confounding.Conclusion Aspirin was associated with reduced all-cause mortality. Bleeding risk was less compared with survival benefits. Aspirin should be considered for primary prevention in Aboriginal people with high cardiovascular risk.https://bmjopen.bmj.com/content/10/1/e030034.full
spellingShingle Louise Maple-Brown
Yuejen Zhao
Steven Guthridge
Henrik Falhammar
Kanakamani Jeyaraman
Paul Burgess
Christine Connors
All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
BMJ Open
title All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
title_full All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
title_fullStr All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
title_full_unstemmed All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
title_short All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
title_sort all cause mortality following low dose aspirin treatment for patients with high cardiovascular risk in remote australian aboriginal communities an observational study
url https://bmjopen.bmj.com/content/10/1/e030034.full
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