Why the study?
To investigate how multivessel disease, incomplete revascularisation, and prescribing differences contribute to sex-based outcome disparities in STEMI, and whether cardiac death and MI differences persist long term.
Does female sex affect the risk of cardiac death and MI in patients with STEMI undergoing percutaneous coronary intervention?
Observational (n=2,083)
Does female sex affect the risk of cardiac death and MI in patients with STEMI undergoing percutaneous coronary intervention?
Hazard Ratio: 1.33 (95% CI 1.02–1.74)
Absolute Event Rate: 20.3% vs 13.2%
p-value: p=0.028
Women presenting with STEMI have a higher long-term risk of cardiac death and MI compared to men, which may be partly driven by lower rates of potent P2Y12 inhibitor prescription, particularly in those with multivessel disease.
Objective: To investigate the extent to which multivessel disease, incomplete revascularisation and prescribing differences contribute to sex-based outcome disparities in patients with ST-elevation MI (STEMI) and establish whether differences in cardiac death and MI (CDMI) rates persist at long-term follow-up. Methods and results: This observational study evaluates sex-based outcome differences (median follow-up 3.6 years; IQR [2.4–5.4]) in a consecutive cohort of patients (n=2,083) presenting with STEMI undergoing percutaneous coronary intervention). Of the studied patients 20.3% (423/2,083) were women and 38.3% (810/2,083) had multivessel disease (MVD). Incomplete revascularisation was common. The median residual SYNTAX score (rSS) was 5.0 (IQR [0–9]) in women and 5.0 (IQR [1–11]) in men (p=0.369), and in patients with MVD it was 9 (IQR [6–17]) in women and 10 (IQR [6–15]) in men (p=0.838). The primary endpoint CDMI occurred in 20.3% of women (86/423) and in 13.2% of men (219/1,660) (p=0.028). Differences persisted following multivariable risk adjustment: female sex was independently associated with CDMI (aHR 1.33; IQR [1.02–1.74]). Women with MVD had CDMI more often than all other groups (p<0.001 for all). Significant sex-based prescribing differences were evident: women were less likely to receive guideline-recommended potent P2Y12 inhibitors than men (31% versus 43%; p=0.012), and differences were particularly evident in patients with MVD (25% in women versus 45% in men, p=0.011). Conclusion: Sex-based differences in STEMI patient outcome persist at long-term follow-up. Poor outcomes were disproportionately found in women with MVD and those with rSS>8. Observed differences in P2Y12 prescribing practices may contribute to poor outcomes for women with MVD and incomplete revascularisation.
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Burgess et al. (2023) conducted an observational in ST-elevation MI (STEMI) (n=2,083). Female sex vs. Male sex was evaluated on Cardiac death and MI (CDMI) (aHR 1.33, 95% CI 1.02-1.74, p=0.028).
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