Oxy-right Ventricular Assist Device for Bridging of Right Heart Failure to Lung Transplantation

2020 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Sung Kwang Lee ◽  
Do Hyung Kim ◽  
Woo Hyun Cho ◽  
Hye Ju Yeo
2021 ◽  
Author(s):  
Jae Guk Lee ◽  
Dong Kyu Oh ◽  
Ho Cheol Kim ◽  
Pil-Je Kang ◽  
Geun Dong Lee ◽  
...  

Abstract BackgroundRight ventricular heart failure (RVHF) is a critical complication in patients with respiratory failure particularly among those who transitioned to lung transplantation using veno-venous (V-V) extracorporeal membrane oxygenation (ECMO). In these patients, both cardiac and respiratory functions are supported using veno-arterial (V-A) or veno-arterial-venous (V-AV) ECMO. However, these modalities increase the risk of device-related complications, such as thromboembolism, bleeding, and limb ischemia, and they may disturb early rehabilitation. Due to these limitations, a right ventricular assist device with an oxygenator (Oxy-RVAD) using ECMO may be considered for patients with RVHF with V-V ECMO.MethodsThe study included patients who underwent Oxy-RVAD using ECMO due to RVHF while on V-V ECMO as a bridge to lung transplantation (BTT) due to severe respiratory failure. The patients were enrolled at a tertiary care, university hospital between 2018 and 2020.ResultsEight patients underwent Oxy-RVAD using ECMO due to RVHF for BTT. Seven patients were bridged successfully to lung transplantation. One patient died prior to transplantation from complications of interstitial lung disease. There were no major ECMO-related complications during the Oxy-RVAD using ECMO period in any patient. For those patients who were successfully bridged, the average duration of V-V ECMO was 10 days and Oxy-RVAD using ECMO was 12 days. All patients with BTT were discharged with a 30-day survival rate of 100% (7/7 patients). The 180-day survival rate was 85% (6/7 patients).ConclusionsThis study suggests that Oxy-RVAD using ECMO may be a viable option for bridging patients with RVHF to lung transplantation.


2020 ◽  
Vol 30 (4) ◽  
pp. 499-506
Author(s):  
Michael Salna ◽  
A Reshad Garan ◽  
Ajay J Kirtane ◽  
Dimitrios Karmpaliotis ◽  
Phil Green ◽  
...  

Abstract OBJECTIVES Right heart failure after left ventricular assist device (LVAD) implantation is associated with significant morbidity and mortality. A new generation of percutaneous right ventricular assist devices (RVADs) may mitigate the need for invasive surgical RVAD implantation. The purpose of this study was to evaluate the safety and efficacy of the Protek Duo (TandemLife, Pittsburgh, PA, USA) RVAD in patients who developed severe acute right heart failure in the intensive care unit after LVAD implantation. METHODS This was a retrospective cohort study of 27 patients who received a Protek Duo after LVAD implantation from January 2016 to March 2019 at our centre. The primary outcome of interest was survival to hospital discharge. Secondary outcomes included procedural success, device-related complications and conversion to a surgical RVAD. RESULTS The median age of patients was 63 years (interquartile range 58–71), 78% were men and 78% were Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) profile 1 or 2. Patients were on a median of 2 inotropes and 2 pressors prior to Protek Duo insertion. The device successfully implanted on the first attempt in all patients a median of 1 day (interquartile range 1–2) after LVAD implantation and the median duration of support was 11 days (interquartile range 7–16). Device weaning occurred in 86% of patients, with 15% in-hospital mortality. Major complications related to the device included new moderate-to-severe tricuspid regurgitation (36%), haemolysis (14%) and cannula migration (7%). Three patients (11%) required conversion to surgical RVAD. Overall survival to 1 year was 81%. CONCLUSIONS The use of the Protek Duo as a percutaneous RVAD is a safe and feasible treatment for patients who develop acute right heart failure after LVAD implantation.


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