# Effects of Levosimendan in Patients with Severe Mitral Insufficiency and Left Ventricular Dysfunction Undergoing Transcatheter Edge-to-Edge Repair: A Systematic Review and Meta-Analysis

**Authors:** Stephanie Gladys Kühne, Andrea Patrignani, Simon Wölbert, Eva Harmel, Damyan Penev, Sebastien Elvinger, Mauro Chiarito, Philip W. J. Raake, Dario Bongiovanni

PMC · DOI: 10.3390/jcdd13010040 · 2026-01-09

## TL;DR

This study reviews the effects of Levosimendan in patients with severe heart valve issues undergoing a specific repair procedure, finding no major benefits but some procedural advantages.

## Contribution

The study provides a systematic review and meta-analysis on the use of Levosimendan during TEER for severe mitral regurgitation.

## Key findings

- Levosimendan did not significantly improve postprocedural LV ejection fraction or systolic pulmonary artery pressure.
- Procedural success was higher and procedure duration shorter with Levosimendan.
- No significant hemodynamic benefits were observed from Levosimendan use.

## Abstract

Severe mitral regurgitation (MR) is one of the most common valvular heart diseases and is frequently associated with advanced left ventricular (LV) systolic dysfunction. Transcatheter edge-to-edge repair (TEER) offers effective symptom relief but may induce abrupt hemodynamic changes leading to afterload mismatch and acute LV failure. Levosimendan may help mitigate this complication by improving contractility, yet evidence supporting its use in this setting is scarce. Therefore, the aim of this study was to systematically evaluate the evidence on the effects of Levosimendan in patients with severe MR and LV dysfunction undergoing TEER. We performed a comprehensive search of PubMed, Embase, Scopus, and Google Scholar. Primary outcomes were postprocedural LV ejection fraction (LVEF) and systolic pulmonary artery pressure (sPAP). Secondary outcomes included procedural success, procedure duration, and in-hospital complications. Five studies comprising 315 patients (n = 141 Levosimendan, n = 174 controls) met the inclusion criteria. Pooled analysis showed no significant difference in postprocedural LVEF between Levosimendan-treated patients and controls (mean difference 0.45%, 95% CI [−1.46–2.35] p = 0.65) and no significant change from baseline. Similarly, postprocedural sPAP did not differ significantly. Procedural success was higher with Levosimendan, and procedure duration was shorter. These hypothesis-generating findings highlight the need for larger, prospective randomized trials to clarify the role of Levosimendan in this setting.

## Linked entities

- **Chemicals:** Levosimendan (PubChem CID 3033825)

## Full-text entities

- **Diseases:** MR (MESH:D008944), LV dysfunction (MESH:D018487), LV failure (MESH:D051437), valvular heart diseases (MESH:D006349)
- **Chemicals:** Levosimendan (MESH:D000077464)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12842285/full.md

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Source: https://tomesphere.com/paper/PMC12842285