Sex Differences in Long-Term Cause-Specific Mortality After Percutaneous Coronary Intervention: Temporal Trends and

Claire E Raphael1, Mandeep Singh1, Malcolm Bell1

  • 1From the Department of Cardiovascular Diseases (C.E.R., M.S., M.B., A.L., A.P., C.S.R., B.J.G., R.G.) and Division of Biomedical Statistics and Informatics (D.C., R.J.L.), Mayo Clinic, Rochester, MN.

Insights

Women experience higher mortality after percutaneous coronary intervention due to noncardiac causes, not sex-specific factors. This increased risk is explained by older age and more comorbidities in women, impacting clinical care and trial design.

Area of Science:

  • Cardiology
  • Clinical Research
  • Sex Differences in Medicine

Background:

  • Women exhibit higher all-cause mortality rates post-percutaneous coronary intervention (PCI).
  • The reasons for this disparity, whether due to age, comorbidities, or sex-specific factors, remain unclear.

Purpose of the Study:

  • To investigate cause-specific long-term mortality after PCI in women versus men.
  • To determine if observed mortality differences are attributable to baseline characteristics or sex-specific risks.

Main Methods:

  • Retrospective analysis of 6,847 women and 16,280 men surviving index PCI hospitalization between 1991-2012.
  • Cause-specific mortality assessed using competing risks analyses, telephone interviews, medical records, and death certificates.
  • Analysis stratified across three time periods: 1991-1997, 1998-2005, and 2006-2012.

Main Results:

  • Women were older and had higher comorbidity burdens than men.
  • While both sexes showed declining cardiac deaths over time, women's excess mortality was driven by noncardiac causes.
  • Adjusted analyses revealed no evidence of sex-specific excess risk for cardiac or noncardiac mortality.

Conclusions:

  • Higher post-PCI mortality in women is primarily due to noncardiac causes.
  • This excess risk is accounted for by baseline age and comorbidities, not an independent sex-specific factor.
  • Findings necessitate consideration for sex-specific clinical care strategies and clinical trial designs.
Abstract

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