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American Heart Association

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Final ID: Su4107

Comparison of 30-Day Outcomes of TAVR vs. SAVR in Patients with Prior CABG: A Meta-Analysis

Abstract Body (Do not enter title and authors here):
Introduction
Managing severe aortic stenosis in patients with a history of coronary artery bypass grafting (CABG) is challenging. Traditionally, surgical aortic valve replacement (SAVR) was the standard treatment, but transcatheter aortic valve replacement (TAVR) offers a less invasive alternative. This meta-analysis compares the 30-day outcomes of TAVR versus SAVR in patients with prior CABG.

Methods
A systematic review and meta-analysis were conducted according to PRISMA guidelines. Studies comparing TAVR and SAVR in patients with prior CABG were included. The primary outcomes were 30-day (cardiovascular) CV mortality, all-cause mortality, stroke, and myocardial infarction. Heterogeneity was assessed using the Chi-squared test and I-squared statistic. P value <0.05 was considered statistically significant.

Results
Nine studies with a total of 8,487 patients were included for the 30-day outcomes. The pooled odds ratio (OR) for 30-day CV mortality was 1.00 (95% CI: 0.48-2.06), with no significant difference between TAVR and SAVR (p=0.99). For 30-day all-cause mortality, the pooled OR was 0.75 (95% CI: 0.51-1.10), also showing no significant difference between TAVR and SAVR (p=0.14). The pooled OR for 30-day myocardial infarction was 0.34 (95% CI: 0.09-1.27), indicating no significant difference between TAVR and SAVR (p=0.11). However, the pooled OR for 30-day stroke was 0.67 (95% CI: 0.50-0.90), showing a significantly lower incidence with TAVR compared to SAVR (p=0.007). Detailed results in Figure 1.

Conclusion
In patients with a history of CABG, TAVR appears to have comparable 30-day outcomes to SAVR in terms of CV mortality, all-cause mortality, and myocardial infarction. However, TAVR is associated with a significantly lower incidence of 30-day stroke. These findings suggest that TAVR may be a safer option in the short term for this high-risk patient population. Further research is needed to confirm these results in larger, randomized controlled trials.
  • Qureshi, Muhammad Ahmad  ( Henry Ford Jackson Hospital , Jackson , Michigan , United States )
  • Munir, Shafia  ( Shifa College of Medicine , Rawalpindi , Pakistan )
  • Zulqarnain, Muhammad  ( King Edward Medical University , Lahore , Pakistan )
  • Qureshi, Ali Akram  ( King Edward Medical University , Lahore , Pakistan )
  • Haseeb, Shahan  ( Northwell health , Port Jefferson , New York , United States )
  • Bakht, Danyal  ( King Edward Medical University , Lahore , Pakistan )
  • Amir, Maaz  ( King Edward Medical University , Lahore , Pakistan )
  • Hussain, Muqaddas  ( King Edward Medical University , Lahore , Pakistan )
  • Ahmed, Omair  ( Henry Ford Jackson Hospital , Jackson , Michigan , United States )
  • Rehman, Aqeeb Ur  ( King Edward Medical University , Lahore , Pakistan )
  • Ahmed, Hafsa  ( Sheikh Zayed Medical College , Rahim Yar Khan , Pakistan )
  • Ansari, Umair  ( Newyork Presbyterian-Queens , Port Jefferson , New York , United States )
  • Author Disclosures:
    Muhammad Ahmad Qureshi: DO NOT have relevant financial relationships | Shafia Munir: DO NOT have relevant financial relationships | Muhammad Zulqarnain: DO NOT have relevant financial relationships | Ali Akram Qureshi: DO NOT have relevant financial relationships | Shahan Haseeb: DO NOT have relevant financial relationships | Danyal Bakht: DO NOT have relevant financial relationships | Maaz Amir: DO NOT have relevant financial relationships | Muqaddas Hussain: DO NOT have relevant financial relationships | Omair Ahmed: DO NOT have relevant financial relationships | Aqeeb Ur Rehman: DO NOT have relevant financial relationships | Hafsa Ahmed: DO NOT have relevant financial relationships | Umair Ansari: DO NOT have relevant financial relationships
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

TAVR Outcomes in Specific Subgroups

Sunday, 11/17/2024 , 03:15PM - 04:15PM

Abstract Poster Session

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