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Meta-Analysis of Physiology-Guided Complete or Culprit Lesion-Only Percutaneous Coronary Interventions in Myocardial Infarction.

Publication ,  Journal Article
Singh, S; Tantry, US; Bliden, K; Saad, M; Gurbel, PA; Abbott, JD; Garg, A
Published in: Am J Cardiol
December 1, 2024

Whether physiology-guided complete revascularization of nonculprit lesions is superior to culprit lesion-only percutaneous coronary intervention (PCI) in patients with myocardial infarction (MI) and multivessel disease remains debated. Online databases were searched for randomized controlled trials comparing physiology-guided complete revascularization and culprit lesion-only PCI in patients with MI. The outcomes of interest were all-cause death, cardiovascular (CV) death, repeat revascularization, MI, stent thrombosis, and contrast-associated nephropathy/acute kidney injury. Pooled odds ratios, along with 95% confidence intervals (CI) were calculated. A total of 4,849 patients (n = 2,288 physiology-guided complete revascularization, n = 2,561 culprit lesion-only PCI) were included. The mean age was 66 years and 76% were men. At a mean follow-up of 2.5 years, physiology-guided complete revascularization was associated with significant reductions in CV death (odds ratio 0.72, 95% CI 0.54 to 0.97, p = 0.03) and repeat revascularizations (0.50, 95% CI 0.38 to 0.66, p <0.00001) compared with culprit lesion-only PCI. There were no differences between the 2 approaches in all-cause death (0.91, 95% CI 0.69 to 1.19, p = 0.50), MI (0.85, 95% CI 0.59 to 1.21, p = 0.36), stent thrombosis (1.24, 95% CI 0.58 to 2.69, p = 0.58), and contrast-associated nephropathy/acute kidney injury (1.07, 95% CI 0.88 to 1.31, p = 0.50). In conclusion, among patients with MI and multivessel disease, physiology-guided complete revascularization was associated with significant reductions in CV death and revascularizations compared with culprit lesion-only PCI.

Duke Scholars

Published In

Am J Cardiol

DOI

EISSN

1879-1913

Publication Date

December 1, 2024

Volume

232

Start / End Page

49 / 56

Location

United States

Related Subject Headings

  • Percutaneous Coronary Intervention
  • Myocardial Infarction
  • Humans
  • Cardiovascular System & Hematology
  • 3201 Cardiovascular medicine and haematology
  • 1102 Cardiorespiratory Medicine and Haematology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Singh, S., Tantry, U. S., Bliden, K., Saad, M., Gurbel, P. A., Abbott, J. D., & Garg, A. (2024). Meta-Analysis of Physiology-Guided Complete or Culprit Lesion-Only Percutaneous Coronary Interventions in Myocardial Infarction. Am J Cardiol, 232, 49–56. https://doi.org/10.1016/j.amjcard.2024.09.013
Singh, Sahib, Udaya S. Tantry, Kevin Bliden, Marwan Saad, Paul A. Gurbel, J Dawn Abbott, and Aakash Garg. “Meta-Analysis of Physiology-Guided Complete or Culprit Lesion-Only Percutaneous Coronary Interventions in Myocardial Infarction.Am J Cardiol 232 (December 1, 2024): 49–56. https://doi.org/10.1016/j.amjcard.2024.09.013.
Singh S, Tantry US, Bliden K, Saad M, Gurbel PA, Abbott JD, et al. Meta-Analysis of Physiology-Guided Complete or Culprit Lesion-Only Percutaneous Coronary Interventions in Myocardial Infarction. Am J Cardiol. 2024 Dec 1;232:49–56.
Singh, Sahib, et al. “Meta-Analysis of Physiology-Guided Complete or Culprit Lesion-Only Percutaneous Coronary Interventions in Myocardial Infarction.Am J Cardiol, vol. 232, Dec. 2024, pp. 49–56. Pubmed, doi:10.1016/j.amjcard.2024.09.013.
Singh S, Tantry US, Bliden K, Saad M, Gurbel PA, Abbott JD, Garg A. Meta-Analysis of Physiology-Guided Complete or Culprit Lesion-Only Percutaneous Coronary Interventions in Myocardial Infarction. Am J Cardiol. 2024 Dec 1;232:49–56.
Journal cover image

Published In

Am J Cardiol

DOI

EISSN

1879-1913

Publication Date

December 1, 2024

Volume

232

Start / End Page

49 / 56

Location

United States

Related Subject Headings

  • Percutaneous Coronary Intervention
  • Myocardial Infarction
  • Humans
  • Cardiovascular System & Hematology
  • 3201 Cardiovascular medicine and haematology
  • 1102 Cardiorespiratory Medicine and Haematology