Department of Medicine, Division of Cardiology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Department of Academic Family Medicine, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Can J Cardiol. 2024 Nov;40(11):2094-2101. doi: 10.1016/j.cjca.2024.04.025. Epub 2024 May 9.
In patients presenting with an acute coronary syndrome (ACS), the impact of efforts to bridge historical care gaps between Indigenous and non-Indigenous patients remains limited.
For consecutive ACS presentations (ST-segment elevation myocardial infarction [STEMI] and non-ST-segment elevation myocardial infarction [NSTEMI]/unstable angina [UA], respectively) at the Royal University Hospital, Saskatoon, we compared self-identified Indigenous and non-Indigenous patients' demographics, treatments, and all-cause mortality (in-hospital and within 3 years). We used propensity score inverse probability weighting to mitigate confounding and Cox regression models to estimate the adjusted hazard ratio (aHR) for all-cause mortality.
Of 3946 ACS patients, 37.2% (n = 1468) were STEMI, of whom 11.3% (n = 166) were Indigenous. Of the NSTEMI/UA (n = 2478), 12.6% (n = 311), were Indigenous. Overall, Indigenous compared with non-Indigenous patients were likely to be younger, female, have higher risk burden, and live more remotely; Indigenous STEMI patients triaged to primary percutaneous coronary intervention had longer times from first medical contact to device, and Indigenous NSTEMI/UA patients more likely to present with heart failure, cardiac arrest, and cardiogenic shock. No significant differences were noted for in-hospital mortality (STEMI 8.4% vs 5.7% [P = 0.16], NSTEMI/UA 1.9% vs 1.6% [P = 0.68]), although in follow-up, Indigenous STEMI patients were associated with a higher all-cause mortality risk (aHR 1.98, 95% CI 1.19-3.31; P = 0.009) with no between-group differences evident for NSTEMI/UA (aHR 1.03, 95% CI 0.63 1.69; P = 0.91).
Indigenous compared with non-Indigenous patients presenting with an ACS had higher cardiovascular risk profiles and consequent residual mortality risk. Improving primary care and intensifying secondary risk reduction, particularly for Indigenous patients, will substantially modify ACS outcomes in Saskatchewan.
在出现急性冠状动脉综合征(ACS)的患者中,弥合原住民和非原住民患者之间历史护理差距的努力所产生的影响仍然有限。
在萨斯卡通皇家大学医院连续收治的 ACS 患者(ST 段抬高型心肌梗死 [STEMI]和非 ST 段抬高型心肌梗死 [NSTEMI]/不稳定型心绞痛 [UA])中,我们比较了自我认定的原住民和非原住民患者的人口统计学、治疗方法和全因死亡率(住院内和 3 年内)。我们使用倾向评分逆概率加权来减轻混杂因素,并使用 Cox 回归模型来估计全因死亡率的调整后危险比(aHR)。
在 3946 例 ACS 患者中,37.2%(n=1468)为 STEMI,其中 11.3%(n=166)为原住民。在 NSTEMI/UA 患者中(n=2478),12.6%(n=311)为原住民。总体而言,与非原住民患者相比,原住民患者更年轻、女性、风险负担更高,居住地点更偏远;被分诊至直接经皮冠状动脉介入治疗的原住民 STEMI 患者从首次医疗接触到设备的时间更长,而原住民 NSTEMI/UA 患者更有可能出现心力衰竭、心脏骤停和心源性休克。住院死亡率没有显著差异(STEMI 为 8.4%比 5.7%[P=0.16],NSTEMI/UA 为 1.9%比 1.6%[P=0.68]),尽管在随访期间,原住民 STEMI 患者的全因死亡率风险更高(aHR 1.98,95%CI 1.19-3.31;P=0.009),而 NSTEMI/UA 患者之间则没有差异(aHR 1.03,95%CI 0.63-1.69;P=0.91)。
与出现 ACS 的非原住民患者相比,原住民患者具有更高的心血管风险特征和相应的残余死亡风险。改善初级保健并加强二级风险降低,特别是针对原住民患者,将大大改变萨斯喀彻温省的 ACS 结局。