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Adding cardiac resynchronization therapy during CABG reduces heart failure readmission and all-cause mortalityAdding Cardiac Resynchronization Therapy During Surgery May Reduce Heart Failure Readmissions

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Key Takeaway
Note that adding CRT during CABG may reduce heart failure readmission and mortality, but results are hypothesis-generating.

This meta-analysis evaluates the impact of adding cardiac resynchronization therapy (CRT) during coronary artery bypass grafting (CABG) for patients with ischemic cardiomyopathy and electromechanical dyssynchrony. The analysis pooled data from 2 studies involving a total of 200 patients to assess outcomes related to heart failure management.

The meta-analysis found a significant reduction in the probability of heart failure readmission with the addition of CRT (RR = 0.25; 95% CI [0.13-0.49], P < 0.0001). Additionally, the study reported a lower probability of all-cause mortality for patients receiving CRT during CABG (RR = 0.44; 95% CI [0.25-0.78], p = 0.0048).

The authors note limitations including a small cumulative sample size and a limited number of included studies. Due to these factors, the results are considered hypothesis-generating. While the data suggest that perioperative epicardial CRT implantation may be associated with decreased heart failure rehospitalization and mortality, large-scale confirmatory randomized trials are warranted to establish definitive clinical evidence.

How this fits prior evidence

This meta-analysis addresses a gap in the management of patients with ischemic cardiomyopathy and electromechanical dyssynchrony. While prior coverage has addressed other heart failure management strategies, such as the use of IV albumin with furosemide to reduce worsening renal function to 25%, this study specifically evaluates the perioperative addition of CRT during CABG. The findings regarding reduced heart failure readmission and mortality are hypothesis-generating due to the small sample size of 200 patients across 2 studies.

Researchers looked at how adding cardiac resynchronization therapy (CRT) during coronary artery bypass grafting (CABG) affects patients with ischemic cardiomyopathy and electromechanical dyssynchrony. This analysis combined data from two studies involving 200 patients to see if the combined approach improved outcomes compared to surgery alone.

The results showed a lower probability of being readmitted to the hospital for heart failure. The data also showed a lower probability of all-cause mortality for those who received the combined treatment. These findings suggest that adding CRT during the surgery process may offer significant benefits for these specific heart conditions.

It is important to note that these results come from a small number of studies and a small total sample size. Because the evidence is limited, these findings are currently used to help form new ideas rather than change standard medical practice immediately. Patients should talk to their doctors to see if this approach is appropriate for their specific needs.

What this means for you:
Adding CRT during heart surgery may lower heart failure readmissions, but more large-scale studies are needed.

Common questions

What are the benefits of adding CRT during heart surgery?

Adding cardiac resynchronization therapy (CRT) during coronary artery bypass grafting may lower the probability of being readmitted to the hospital for heart failure. The data also showed a lower probability of all-cause mortality for patients with ischemic cardiomyopathy and electromechanical dyssynchrony who received this combined treatment.

Is this treatment safe for patients with heart failure?

The study did not report any specific adverse events, serious complications, or issues with how well the treatment was tolerated. However, because the study included a small number of patients and only two studies, more research is needed to confirm the safety and effectiveness of this approach.

How certain are these results for heart failure patients?

The results are currently considered hypothesis-generating because the total sample size was small (200 patients) and only two studies were included. While the data shows a link between the treatment and better outcomes, larger trials are needed to confirm these findings before they can change standard medical practices.

Study Details

Study typeMeta analysis
Sample sizen = 200
EvidenceLevel 1
PublishedNov 2026
View Original Abstract ↓
INTRODUCTION: Heart failure (HF) continues to be the leading cause of death and rehospitalization among cardiomyopathic patients undergoing coronary artery bypass grafting (CABG). OBJECTIVES: To systematically evaluate the effect of adding cardiac resynchronization therapy (CRT) to CABG versus CABG alone for patients with concomitant ischemic cardiomyopathy and electromechanical dyssynchrony. (PROSPERO ID: CRD420251006918) METHODS: A comprehensive literature search was conducted using PubMed, Web of Science, and Scopus to identify clinical trials and cohort studies evaluating the impact of inserting a CRT device during CABG surgery on survival and rehospitalization outcomes. A total of 3 studies involving 300 patients were included: 150 underwent CABG alone, and 150 received both CABG and CRT. RESULTS: The meta-analysis of two studies (n = 200) showed that adding CRT during CABG was associated with lowering the probability of HF readmission (RR = 0.25, 95% CI [0.13-0.49], P < 0.0001) and of all-cause mortality (RR = 0.44, 95% CI [0.25-0.78], p = 0.0048) in the targeted patient population. Analyses according to study design demonstrated consistent treatment effects across randomized and observational evidence, with no significant subgroup differences. CONCLUSION: In patients with ischemic cardiomyopathy and electromechanical dyssynchrony undergoing CABG, perioperative epicardial CRT implantation may be associated with decreased HF rehospitalization and all-cause mortality rates. However, given the limited number of included studies and small cumulative sample size, these findings should be considered hypothesis-generating, and large-scale confirmatory randomized trials are warranted. REGISTRATION: The study protocol was prospectively registered in PROSPERO. (CRID: CRD420251006918).
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