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Title: All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study.
Authors: Zhao, Yuejen
Jeyaraman, Kanakamani
Burgess, Paul
Connors, Christine
Guthridge, Steven
Maple-Brown, Louise
Falhammar, Henrik
Citation: BMJ open 2020-01-02; 10(1): e030034
Abstract: To evaluate the benefit and risk of low-dose acetylsalicylic acid (aspirin) in patients from remote Aboriginal communities in the Northern Territory, Australia. 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. The benefit and harm of aspirin were investigated in patients aged ≥18 years from 54 remote Aboriginal communities. None had a previous cardiovascular event or major bleeds. Patients on anticoagulants or other antiplatelets were excluded. Aspirin at a dose of 75-162 mg/day. Endpoints were all-cause, cardiovascular mortality and incidences of cardiovascular events and major bleeds. 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. 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.
Click to open PubMed article: https://www.ezpdhcs.nt.gov.au/login?url=https://www.ncbi.nlm.nih.gov/pubmed/31900264
Click to open Pubmed Article: https://www.ezpdhcs.nt.gov.au/login?url=https://www.ncbi.nlm.nih.gov/pubmed/31900264
Journal title: BMJ open
Publication Date: 2020-01-02
Type: Journal Article
URI: https://hdl.handle.net/10137/7987
DOI: 10.1136/bmjopen-2019-030034
metadata.dc.identifier.orcid: http://orcid.org/0000-0002-5622-6987
Appears in Collections:(a) NT Health Research Collection

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