A study of intracoronary thrombolytic agents in high thrombus burden lesions during primary PCI

Venkata Rs Subrahmanya Sarma1, K Gopalakrishna1, K Purnachandra Rao1

  • 1Cardiology Department, Aayush Hospitals, Vijayawada, Andhra Pradesh, India.

Indian Heart Journal
|February 1, 2025
PubMed

Insights

Intracoronary thrombolysis in high thrombus burden patients undergoing primary percutaneous coronary intervention showed similar primary outcomes to stenting alone. However, event rates consistently rose in the stenting group over one year.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Clinical Trials

Background:

  • High thrombus burden in primary percutaneous coronary intervention is linked to adverse patient outcomes.
  • Current management strategies for these patients have limitations.

Purpose of the Study:

  • To evaluate the long-term results of primary percutaneous coronary intervention in patients with high thrombus burden.
  • To assess the effectiveness of intracoronary thrombolysis as an adjunctive therapy.

Main Methods:

  • A prospective observational study included 108 patients with high thrombus burden undergoing primary percutaneous coronary intervention.
  • Patients were divided into two groups: primary stenting versus primary stenting with adjunctive intracoronary thrombolysis.
  • Primary endpoint was Net Adverse Clinical Events; secondary endpoints included Major Adverse Cardiac Events.

Main Results:

  • The primary outcome occurred in 26% of the primary stent group (n=80) versus 6% in the intracoronary thrombolysis group (n=28).
  • No statistically significant difference was found in primary endpoints between the groups (p=0.042).
  • Kaplan-Meier curves indicated separated event-free survival curves at one year, with a consistent increase in events in the primary stent group.

Conclusions:

  • No significant difference in primary outcomes was observed between the two treatment strategies.
  • A trend towards increased adverse events was noted in the primary stent group over the one-year follow-up.
  • Larger randomized clinical trials are warranted to validate these findings and clarify treatment efficacy.
Abstract

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