Association of baseline D-dimer with adverse outcomes after percutaneous coronary intervention in patients with

Huanlun Li1, Yun Liang, Zhichao Yuan

  • 1Department of Cardiovascular Medicine, Dongguan Dalong Hospital, Dongguan, Guangdong Province, China.

Medicine
|January 24, 2026
PubMed

Insights

High baseline D-dimers (DD) predict adverse outcomes in coronary heart disease (CHD) patients post-percutaneous coronary intervention (PCI). Elevated DD levels are linked to increased mortality and major adverse cardiovascular events (MACE).

Area of Science:

  • Cardiology
  • Biomarkers
  • Interventional Cardiology

Background:

  • Coronary heart disease (CHD) poses significant health risks.
  • Percutaneous coronary intervention (PCI) is a common treatment for CHD.
  • Predictive markers for adverse outcomes post-PCI are crucial for patient management.

Purpose of the Study:

  • To evaluate the association between baseline D-dimers (DD) and adverse clinical outcomes following PCI in CHD patients.
  • To synthesize evidence from multiple studies through meta-analysis.

Main Methods:

  • A comprehensive literature search was conducted across major databases (PubMed, Web of Science, Cochrane Library, Embase) up to November 2024.
  • Hazard ratios (HR) and 95% confidence intervals (CI) were pooled using fixed or random-effects models.
  • Analyzed outcomes included all-cause mortality, cardiovascular mortality, major adverse cardiovascular events (MACE), and revascularization.

Main Results:

  • Ten studies were included in this meta-analysis.
  • High baseline DD levels significantly correlated with increased risks of all-cause mortality (HR=2.35), cardiovascular mortality (HR=2.94), and MACE (HR=1.74).
  • No significant association was observed between baseline DD levels and revascularization risk (HR=1.02).

Conclusions:

  • Baseline D-dimer levels serve as a valuable predictor of adverse clinical outcomes in CHD patients undergoing PCI.
  • Elevated baseline DD levels are strongly associated with higher risks of mortality and MACE post-PCI.
Abstract

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