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.

PubMed

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.

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