Clinical impacts of sacubitril/valsartan on patients eligible for cardiac resynchronization therapy
Hsin-Ti Huang1,2, Jin-Long Huang2,3,4, Po-Lin Lin5,6
1Division of Nephrology, Department of Internal Medicine and Medical Education, Taichung Veterans General Hospital, Taichung, Taiwan.
Insights
Sacubitril/valsartan (SAC/VAL) treatment shows less reverse cardiac remodelling in heart failure patients with wide QRS durations. Wide QRS durations negatively impact left ventricular improvement, suggesting further investigation for optimal intervention timing in CRT-eligible patients.
Area of Science:
- Cardiology
- Heart Failure Research
- Pharmacological Interventions
Background:
- Sacubitril/valsartan (SAC/VAL) is a key treatment for heart failure with reduced ejection fraction (HFrEF).
- Cardiac resynchronization therapy (CRT) benefits HFrEF patients with wide QRS durations.
- The impact of SAC/VAL on cardiac remodeling in relation to QRS duration and CRT eligibility is not fully understood.
Purpose of the Study:
- To evaluate the effects of SAC/VAL on reverse cardiac remodeling in HFrEF patients.
- To compare outcomes between CRT-eligible and CRT-ineligible HFrEF patients treated with SAC/VAL.
- To investigate the association between QRS duration and treatment response to SAC/VAL.
Main Methods:
- The TAROT-HF study, a multicenter observational study, analyzed 1168 HFrEF patients initiating SAC/VAL.
- Patients were categorized into CRT-eligible (wide QRS) and CRT-ineligible groups.
- Propensity score matching was used to adjust for confounders, with 1-year follow-up for LVEF and LVESVi.
Main Results:
- Patients in the CRT-ineligible group showed significantly greater improvements in LVEF (8.4% vs. 4.5%) and LVESVi (-14.4% vs. -9.6%) compared to the CRT-eligible group after 1 year.
- A higher proportion of CRT-ineligible patients achieved LVEF ≥50% (20.2% vs. 5.2%).
- Multivariate analyses indicated a negative association between wide QRS durations and reverse cardiac remodeling with SAC/VAL treatment.
Conclusions:
- Wide QRS durations are associated with diminished left ventricular improvement in HFrEF patients treated with SAC/VAL.
- The effectiveness of SAC/VAL may be less pronounced in patients with wider QRS durations.
- Further research is needed to determine optimal intervention timing for CRT-eligible patients receiving SAC/VAL.
Aims:
Sacubitril/valsartan (SAC/VAL) has been used in patients with heart failure and reduced ejection fraction (HFrEF), and cardiac resynchronization therapy (CRT) could benefit the HFrEF patients with wide QRS durations. This study aimed to evaluate the clinical impacts of SAC/VAL on reverse cardiac remodelling in CRT-eligible and CRT-ineligible HFrEF patients with different QRS durations.
Methods And Results:
The TAROT-HF study was a multicentre, observational study enrolling patients who initiated SAC/VAL from 10 hospitals since 2017. Patients with baseline left ventricular ejection fraction (LVEF) ≤ 35% were classified into two groups: (i) Group 1: CRT-eligible group, patients with left bundle branch block (LBBB) morphology plus QRS duration ≥130 ms or non-LBBB morphology plus QRS duration ≥150 ms; and (ii) Group 2: CRT-ineligible group. Propensity score matching was performed to adjust for confounders, and 1168 patients were analysed. Baseline characteristics were comparable between the two groups. The improvements in LVEF and left ventricular end-systolic volume index (LVESVi) were more significant in Group 2 than in Group 1 after 1 year SAC/VAL treatment (LVEF: 8.4% ± 11.3% vs. 4.5% ± 8.1%, P < 0.001; change percentages in LVESVi: -14.4% ± 25.9% vs. -9.6% ± 23.1%, P = 0.004). LVEF improving to ≥50% in Groups 1 and 2 constituted 5.2% and 20.2% after 1 year SAC/VAL treatment (P < 0.001). Multivariate analyses showed that wide QRS durations were negatively associated with the reverse cardiac remodelling in these HFrEF patients with SAC/VAL treatment.
Conclusion:
Despite SAC/VAL treatment, wide QRS durations are associated with lower degrees of left ventricular improvement than narrow ones in the HFrEF patients. Optimal intervention timing for the CRT-eligible patients requires further investigation.
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