# Evaluation of ivabradine plus beta-blocker versus beta-blocker alone in addition to standard care in reducing hospitalization and major adverse cardiovascular event in patients with chronic heart failure: a prospective observational study in tertiary care hospital in central India

**Authors:** Ramyaa Desingu, Shilpa Kaore, Gaurav Kandelwal, S. Balakrishnan

PMC · DOI: 10.1186/s43044-024-00500-7 · 2024-05-31

## TL;DR

This study compares ivabradine plus beta-blocker versus beta-blocker alone in heart failure patients, finding potential benefits in reducing hospitalization and cardiovascular events.

## Contribution

The study evaluates a drug combination's effect on heart failure outcomes in an Indian population, highlighting potential clinical benefits.

## Key findings

- Ivabradine plus beta-blocker significantly reduced heart rate compared to beta-blocker alone.
- The combination showed a trend toward fewer hospitalizations and delayed MACE events.
- No significant changes were observed in NYHA class or MLWHFQ scores.

## Abstract

In recent years, there has been an increase in cases of heart failure, ultimately leading to an increase in hospitalization for heart failure (HF) and cardiovascular mortality. The aim of our study was to evaluate ivabradine combined with beta-blocker versus beta-blocker alone in addition to standard care for chronic heart failure, followed for a period of 6 months for the rate of hospitalization and major adverse cardiovascular event (MACE) in patients with reduced left ventricular ejection fraction (LVEF < 35%).

A total of 64 patients were included in this observational study with 30 patients in the ivabradine + beta-blocker (IVA + BB) group and 34 in the beta-blocker (BB) group. The median (IQR) age of the study sample was 57 (50–62) and 58.5 (55–67) in IVA + BB and BB groups, respectively, with LVEF < 35%. The incidence of the primary endpoint of composite MACE (MI, stroke, death, worsening of HF) was 5 in both groups. The mean heart rate was significantly decreased (p < 0.001) at 3-month and 6-month follow-up from baseline in the ivabradine + beta-blocker group as compared to the beta-blocker group alone, while it significantly increased in the beta-blocker group at 3 months (p < 0.01) and also at sixth months (p < 0.05). Parameters such as the New York Heart Association (NYHA) class and the Minnesota Living with Heart Failure questionnaire (MLWHFQ) were also assessed but did not show significant change.

Overall, observations from the study results show that IVA + BB seems to be overall well tolerated in the study sample, with a somewhat smaller decrease in hospitalization and a delay in MACE events in the sample population enrolled in a tertiary care hospital in India. Further exploration in a larger sample is required concerning the Indian population.

## Linked entities

- **Chemicals:** ivabradine (PubChem CID 132999)
- **Diseases:** heart failure (MONDO:0005252), myocardial infarction (MONDO:0005068), stroke (MONDO:0005098)

## Full-text entities

- **Diseases:** death (MESH:D003643), MACE (MESH:D002318), stroke (MESH:D020521), HF (MESH:D006333)
- **Chemicals:** ivabradine (MESH:D000077550)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11143102/full.md

---
Source: https://tomesphere.com/paper/PMC11143102