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Efficacy of revascularization in CTO patients based on hibernating myocardium therapy.

Authors :
Chen, Wenjie
Du, Zhiyong
Qin, Yanwen
Zheng, Ze
Liu, Jinghua
Shi, Yuchen
Source :
European Journal of Clinical Investigation. Sep2024, Vol. 54 Issue 9, p1-14. 14p.
Publication Year :
2024

Abstract

Background: The effectiveness of percutaneous coronary intervention (PCI) for chronic total occlusion (CTO) is still uncertain, especially for patients with ischemic left ventricular dysfunction. This study aimed to assess hibernating myocardium (HM), as determined by single‐photon emission computed tomography (SPECT) and 18F‐FDG positron emission tomography (PET), and to compare the benefits of PCI and optimal medical therapy (OMT). Methods: A retrospective study collected data from 332 patients with CTO and ischemic left ventricular dysfunction. The study compared patients who underwent PCI or OMT via propensity score matching (PSM) analysis which was performed with a 1:2 matching protocol using the nearest neighbour matching algorithm. The primary endpoint of the study was the occurrence of major adverse cardiac events (MACE), defined as a composite of cardiac death, readmission for worsening heart failure (WHF), revascularization and myocardial infarction (MI). Results: After PSM, there were a total of 246 individuals in the PCI and OMT groups. Following Cox regression, hibernating myocardium/total perfusion defect (HM/TPD) was identified as an independent risk factor (hazard ratio (HR): 1.03, 95% confidence interval (CI): 1.008–1.052, p =.007). The cut‐off value of HM/TPD was 38%. The results of the subgroup analysis suggest that for patients with HM/TPD >38%, the OMT group had a greater risk of MACE (p =.035). A sensitivity analysis restricting patients with single‐vessel CTO lesions, HM/TPD remained an independent predictor (HR 1.025, 95% CI 1.008–1.043, p =.005). Conclusion: HM/TPD is an independent predictor of MACE, and for patients with HM/TPD > 38%, CTO‐PCI had a lower risk of MACE compared with OMT. However, further validation is still needed through large‐scale studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00142972
Volume :
54
Issue :
9
Database :
Academic Search Index
Journal :
European Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
179169468
Full Text :
https://doi.org/10.1111/eci.14237