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Left Ventricular Assist Device as a Destination Therapy: Current Situation and the Importance of Patient Selection
María Melendo-Viu1,2,3, David Dobarro1,2, Sergio Raposeiras Roubin1,2
1Cardiology Department, University Hospital Álvaro Cunqueiro, 36213 Vigo, Spain.
Insights
Destination therapy left ventricular assist devices (DT-LVADs) offer improved prognosis for advanced heart failure patients due to donor heart shortages. This review covers device evolution and crucial patient selection criteria for optimal outcomes.
Area of Science:
- Cardiology
- Biomedical Engineering
- Medical Devices
Background:
- Advanced heart failure necessitates advanced treatment options, with cardiac transplantation being ideal but limited by donor availability.
- Left ventricular assist devices (LVADs) used as destination therapy (DT-LVAD) have emerged as a vital alternative, significantly improving mid-term prognosis and quality of life.
- Continuous flow centrifugal pumps represent the current standard for intracorporeal LVADs, with ongoing advancements since their initial approval in 2003.
Purpose of the Study:
- To review the technological advancements in LVADs, focusing on device improvements and updated clinical results.
- To emphasize the critical importance of comprehensive patient selection criteria for DT-LVAD candidacy.
- To provide an updated overview of current indications and the multiparametric evaluation required for potential recipients.
Main Methods:
- Literature review summarizing device evolution and clinical outcomes.
- Analysis of patient selection criteria, including frailty, comorbidities (renal/hepatic dysfunction), and medical history.
- Inclusion of clinical risk scores for assessing potential complications like right heart failure.
Main Results:
- LVAD technology has progressed, leading to smaller devices with enhanced survival and hemocompatibility.
- Current indications for DT-LVADs extend from INTERMACS class 2 to 4, requiring careful monitoring.
- Comprehensive multiparametric assessment is essential for candidacy, encompassing patient's basal condition and risk factors.
Conclusions:
- DT-LVADs are a crucial therapeutic option for advanced heart failure, offering significant benefits.
- Careful patient selection, considering a wide range of clinical factors and risk scores, is paramount for successful DT-LVAD implantation and management.
- Continued research and development in LVAD technology and patient selection strategies are vital for optimizing outcomes in this growing patient population.
Abstract:
Advanced heart failure is a growing problem for which the best treatment is cardiac transplantation. However, the shortage of donors' hearts made left ventricular assist devices as destination therapy (DT-LVAD) a highly recommended alternative: they improved mid-term prognosis as well as patients' quality of life. Current intracorporeal pumps with a centrifugal continuous flow evolved in the last few years. Since 2003, when first LVAD was approved for long-term support, smaller device sizes with better survival and hemocompatibility profile were reached. The most important difficulty lies in the moment of the implant. Recent indications range from INTERMACS class 2 to 4, with close monitoring in intermediate cases. Moreover, a large multiparametric study is needed for considering the candidacy: basal situation, with a special interest in frailty, comorbidities, including renal and hepatic dysfunction, and medical background, considering every prior cardiac condition, must be evaluated. In addition, some clinical risk scores can be helpful to measure the possibility of right heart failure or morbi-mortality. With this review, we sought to summarize all the device improvements, with their updated clinical results, as well as to focus on all the patient selection criteria.
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