Temporary right ventricular circulatory support following right ventricular infarction: results of a groin-free approach
Aims Acute right heart failure (RHF) is a severe complication of right ventricular infarction. The management of acute RHF poses a number of challenges, such as providing haemodynamic support. Temporary circulatory support (TCS) may be required upon failing medical therapy. The ProtekDuo® dual lumen...
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| Main Authors: | , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
5 August 2020
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| In: |
ESC heart failure
Year: 2020, Volume: 7, Issue: 5, Pages: 2853-2861 |
| ISSN: | 2055-5822 |
| DOI: | 10.1002/ehf2.12888 |
| Online Access: | Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ehf2.12888 Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ehf2.12888 
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| Author Notes: | Jamila Kremer, Mina Farag, Andreas Brcic, Alina Zubarevich, Joel Schamroth, Michael M. Kreusser, Matthias Karck, Arjang Ruhparwar and Bastian Schmack |
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| 245 | 1 | 0 | |a Temporary right ventricular circulatory support following right ventricular infarction |b results of a groin-free approach |c Jamila Kremer, Mina Farag, Andreas Brcic, Alina Zubarevich, Joel Schamroth, Michael M. Kreusser, Matthias Karck, Arjang Ruhparwar and Bastian Schmack |
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| 520 | |a Aims Acute right heart failure (RHF) is a severe complication of right ventricular infarction. The management of acute RHF poses a number of challenges, such as providing haemodynamic support. Temporary circulatory support (TCS) may be required upon failing medical therapy. The ProtekDuo® dual lumen cannula provides a minimally invasive option for (TCS) through a groin-free internal jugular vein approach. We present the largest patient series to date using the ProtekDuo® cannula as temporary right ventricular assist device (t-RVAD) in RHF after acute myocardial infarction (MI). Methods and results From July 2016 to November 2019, 10 patients underwent t-RVAD implantation for RHF following acute MI. Transthoracic and transoesophageal echocardiography were performed in all patients to assess cardiac function, with a particular focus on RV function. Cumulative 30-day survival was 60%. Mean TAPSE was 6.4 ± 3.1 mm, mean fractional area change was 12.1 ± 4.2%, and mean right ventricular end diastolic area was 19.8 ± 2.7 cm2. Mean implantation time was 32.8 ± 8.3 min. Mean interval after first cardiac intervention was 4.6 ± 5.8 days. Mean t-RVAD time was 10.0 ± 7.4 days with a significant reduction in central venous pressure 19.3 ± 2.7 vs. 8.2 ± 2.6 mmHg, P < 0.001 and a significant increase in central venous saturation 52.8 ± 15.6 vs. 80.0 ± 6.0%, P < 0.001. Mean intensive care unit stay was 18.6 ± 12.2 days. Four patients were weaned from TCS. Two patients were bridged to a long-term paracorporeal RVAD. There were no t-RVAD associated complications. Causes of death (n = 4) were multiorgan failure, electromechanical dissociation, and haemorrhagic stroke. Mean follow-up time was 96.0 ± 107.6 days. No independent predictors of mortality were identified in univariate analysis. Conclusions We show that groin-free, percutaneous implantation of the ProtekDuo® cannula is a feasible and safe tool for TCS in acute RHF post-MI. This approach provides the advantages of percutaneous implantation including complete mobilization and non-surgical bedside explantation, as well as the option for adding an oxygenator to the t-RVAD circuit. | ||
| 650 | 4 | |a Assist device | |
| 650 | 4 | |a Myocardial infarction | |
| 650 | 4 | |a Percutaneous implantation | |
| 650 | 4 | |a Temporary circulatory support | |
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