Related Experiment Video
Updated: Jun 3, 2025

Testing the Efficacy of Pharmacological Agents in a Pericardial Target Delivery Model in the Swine
Published on: July 7, 2016
Destination Therapy Strategies of Advanced Heart Failure in Elderly Non-Heart Transplant Candidates: A Propensity
David Dobarro1, Sergio Raposeiras-Roubin1, Luis Almenar-Bonet2
1Hospital Álvaro Cunqueiro, Complexo Hospitalario Universitario de Vigo, IIS Galicia Sur, 36312 Vigo, Spain.
Insights
For advanced heart failure patients not eligible for heart transplantation, left ventricular assist devices (LVADs) offer better long-term survival than intermittent levosimendan. Levosimendan may be a reasonable alternative for those unsuitable for LVADs.
Area of Science:
- Cardiology
- Medical Devices
- Pharmacology
Background:
- Heart transplantation (HT) is the gold standard for advanced heart failure (ADHF), but many patients are ineligible.
- Left ventricular assist devices (LVADs) are an option for destination therapy in non-HT candidates.
- Alternative strategies are needed as most ADHF patients receive neither HT nor LVAD.
Purpose of the Study:
- To compare the efficacy of repetitive intermittent levosimendan versus LVAD as destination therapy in end-stage heart failure patients ineligible for HT.
- To evaluate long-term outcomes of these two therapeutic strategies in real-world patient cohorts.
Main Methods:
- Comparison of two multicenter cohorts from Spain: LEVO-D (intermittent levosimendan) and REGALAD (LVAD destination therapy).
- Analysis included 715 patients (403 from LEVO-D, 312 from REGALAD).
- Survival analysis was performed on both non-adjusted and matched cohorts.
Main Results:
- Non-adjusted median survival was shorter for the levosimendan group.
- LVAD therapy showed a survival advantage, primarily after the first year of treatment.
- This survival benefit was confirmed in the matched cohort analysis.
Conclusions:
- LVAD therapy provides significantly better long-term outcomes than intermittent levosimendan in elderly ADHF patients ineligible for HT.
- LVADs should be considered for carefully selected candidates.
- Intermittent levosimendan may be a viable alternative for patients unsuitable for LVADs or with high comorbidity, given similar 1-year outcomes.
Abstract:
Heart transplantation (HT) is the gold standard therapy for advanced heart failure (ADHF), and LVADs as destination therapy are an option in non-HT candidates. Most patients with ADHF never receive HT or an LVAD, so alternative strategies are needed. Intermittent levosimendan can reduce HF hospitalizations in ADHF patients in the short term. It is uncertain whether the results of the comparison of inotropes with older-generation LVADs would have the same outcomes in the current era of ADHF patients treated with levosimendan, who are less sick but older. In this paper, we compare the use of two therapeutic strategies for end-stage HF in patients who are not candidates for HT: repetitive intermittent levosimendan vs. LVAD as destination therapy. To do so, we compare two multicenter cohorts of real-life patients from Spain: the LEVO-D registry and the REGALAD registry. In total, 715 patients coming from the two registries were found: 403 from LEVO-D and 312 from REGALAD. Non-adjusted median survival was shorter for LEVO-D patients, with the benefit for the LVADs seen only after the first year of therapy. The survival advantage for the LVAD cohort was also true after analysis of the matched cohort but, as in the non-matched analysis, the survival benefit was mainly shown after one year of follow-up. We conclude that in elderly ADHF non-HT candidates, LVAD therapy offers significantly better long-term outcomes when compared to intermittent levosimendan; thus, it should be considered in carefully selected candidates. On the other hand, in poor LVAD candidates or highly comorbid patients, intermittent inotropic support with levosimendan could be a reasonable alternative to LVAD, as 1-year outcomes are similar.
Related Concept Videos
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Pathophysiology of Heart Failure
Heart Failure Drugs: β-Blockers
Heart Failure Drugs: Inotropic Agents

