Key result
Transmural scar segments are linked to ~2.4-fold higher odds of LVEF non-improvement post-CABG.
Why the study?
Risk factors for LVEF improvement after CABG in ischemic cardiomyopathy were unclear, prompting development of a predictive model.
Cohort (n=106)
No
Odds Ratio: 2.398 (95% CI 1.607–3.579)
p-value: p=<0.001
A prediction model utilizing the number of transmural scar segments and LVESVI measured by preoperative CMR-LGE can accurately identify patients with ischemic cardiomyopathy who are unlikely to experience LVEF improvement after CABG.
CMR scar assessment may identify ischemic cardiomyopathy patients unlikely to recover LVEF post-CABG; hypothesis-generating and requires prospective validation before guiding decisions.
Background: To investigate the risk factors of left ventricular ejection fraction (LVEF) improvement in patients with ischemic cardiomyopathy (ICM) after coronary artery bypass grafting (CABG), and to construct a model that predicts LVEF improvement. Methods: A retrospective analysis was performed on 106 ICM patients who received CABG and underwent cardiac magnetic resonance (CMR) at Beijing Anzhen Hospital, Capital Medical University from January 2017 to June 2022. Patients were divided into two groups with improved LVEF and no improved LVEF based on the results of postoperative 6-month transthoracic echocardiography. To analyze the risk factors affecting the LVEF non-improvement after CABG and establish a prediction model. Results: There was LVEF non-improvement in 30.2% (32/106) of patients. Multivariate analysis showed that the number of transmural scar segments and left ventricular end-systolic volume index (LVESVI) were independent risk factors in LVEF non-improvement after CABG [odds ratio (OR) =2.398, 95% confidence interval (CI): 1.607–3.579, P<0.001; OR =1.036, 95% CI: 1.009–1.063, P=0.008]. The model is built and internally verified. ROC showed that the area under the curve (AUC) was 0.866 (95% CI: 0.792–0.940), calibration curve showed that the probability predicted by the model matched well with the clinical results, and decision curve analysis (DCA) showed that the model had good clinical applicability. During the mean follow-up time of 1.5 years, the incidence of major adverse cardiovascular and cerebrovascular events (MACCE) in the LVEF non-improvement group was higher (5.4% vs. 25.0%, P=0.009), and the NYHA grading was higher (P=0.016), when compared to the LVEF improvement group. Conclusions: The prediction model based on the number of transmural scar segments and LVESVI has good diagnostic efficacy. Our findings help to identify patients with improved LVEF and thus guide the selection of clinical treatment strategies.
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Zhang et al. (2023) conducted a cohort in Ischemic cardiomyopathy (n=106). Number of transmural scar segments was evaluated on LVEF non-improvement at 6 months after CABG (OR 2.398, 95% CI 1.607-3.579, p=<0.001). The number of transmural scar segments independently predicted LVEF non-improvement at 6 months post-CABG.
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