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An 80-year-old lady with a history of recently diagnosed squamous cell lung cancer presented to our institution with an inferior ST-elevation myocardial infarction and was transferred emergently to the cardiac catherisation suite. Examination done in the holding bay revealed right sided neurological deficits and CT head and aortogram was organised. CT head showed an acute ischaemic stroke with a hyperdense left middle cerebral artery sign and no carotid stenosis. The CT chest showed bilateral segmental pulmonary embolus. Decision was made to proceed to coronary angiogram which showed thrombotic occlusion distal right coronary artery. An aspiration thrombectomy performed revealed a large amount of clots. The artery was smooth walled and there was no evidence of a plaque rupture angiographically. TIMI 3 flow was re-established at the end of the procedure without need for any stent placement. Patient was then transferred to interventional radiology where she had successful LMCA clot retrieval and an inferior vena cava filter inserted. Clexane was then started. Patient progressed well and had full neurological recovery 72 hours post presentation

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Background Indigenous populations globally have a higher burden of cardiovascular disease and increased mortality after acute coronary events, partly due to inequitable access to specialised care like cardiac catheterisation. Gender differences in revascularisation rates have been well described in non-Indigenous patients. Whether this applies to Indigenous patients when cardiac catheterisation facilities are readily available is unclear. Purpose We compared the rates of percutaneous coronary intervention (PCI), cardiac surgery, 30-day and long-term all-cause mortality in Indigenous (Aboriginal and Torres Strait Islanders) patients in Far North Queensland (FNQ) – a region with a large Indigenous population and 24/7 cardiac catheterisation facilities. Method All patients who presented to the tertiary referral center for FNQ, for their first inpatient angiogram between November 2012 and October 2019 were identified. The primary study outcomes were rates of PCI or cardiac surgery and all-cause mortality measured at 30 days and long term. Secondary study outcomes were significant left ventricular dysfunction (ejection fraction <50%) and valvular disease (moderate to severe) in patients who had an echocardiogram. Other differences in baseline characteristics, including age, gender, body mass index, postcode and indication for angiography were accounted for using logistic and cox regression analysis. Results 1042 patients (mean age 53.7±11.6 years, 45.5% female, median follow-up 1092 days) self-identified as Indigenous. Indigenous women were older 54.8±11.4 vs 52.8±11.7 years, p=0.005 and had different angiography indications. For Indigenous women and men respectively, rates of ST elevation myocardial infarction (STEMI) were 14.6% vs 22.9%, non-STEMI 44.3% vs 46.8%, angina 32.7% vs 21.0%, cardiac arrest 2.7% vs 3.3% and other 5.7% vs 6.0%, p<0.001. Indigenous women had significantly lower rates of PCI or cardiac surgery, 40.5% vs 60.7%, p<0.001, but similar 30-day mortality, 1.5% vs 2.3% p=0.34 and long-term all-cause mortality rates 11.2% vs 10.9%, p=0.89, in unadjusted data. 685 patients (mean age 53.8±11.5 years, 45.5% female) were included in the echocardiogram subgroup. Indigenous women had significantly more valvular disease, 23.3% vs 16.3%, p=0.022 but similar rates of left ventricular dysfunction, 30.2% vs 35.8%, p=0.12. Following adjustment for other baseline characteristics female gender independently predicted lower rates of PCI or cardiac surgery, OR 0.49 (95% CI 0.38–0.64) and higher rates of valvular disease, OR 1.60 (95% CI 1.07–2.39). Rates of ventricular dysfunction, 30-day and long-term all-cause mortality were similar. Conclusions Indigenous women had significantly different indications for angiography, lower rates of PCI or cardiac surgery and higher rates of clinically significant valvular disease despite presenting in gender ratios similar to the general population in FNQ. Funding Acknowledgement Type of funding source: None