Outflow graft obstruction in patients with left ventricular assist devices: Stenting the kink
- PMID: 34851022
- DOI: 10.1002/ccd.29994
Outflow graft obstruction in patients with left ventricular assist devices: Stenting the kink
Comment on
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Outflow graft obstruction in patients with the HM 3 LVAD: A percutaneous approach.Catheter Cardiovasc Interv. 2021 Dec 1;98(7):1383-1390. doi: 10.1002/ccd.29785. Epub 2021 May 28. Catheter Cardiovasc Interv. 2021. PMID: 34047456
References
REFERENCES
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- Mehra MR, Uriel N, Naka Y, et al. A fully magnetically levitated left ventricular assist device-final report. N Engl J Med. 2019;380:1618-1627.
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- U. S. Food and Drug Administration. Medtronic stops distribution and sale of HeartWare HVAD system due to risk of neurological adverse events, mortality, and potential failure to restart. [Internet]. 2021. https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-sto....
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- Duero Posada JG, Moayedi Y, Alhussein M, et al. Outflow graft occlusion of the HeartMate 3 left ventricular assist device. Circ Heart Fail. 2017;10(9):e004275.
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- Milwidsky A, Villela MA, Wiley J, et al. Outflow graft obstruction in patients with the HM 3 LVAD: a percutaneous approach. Catheter Cardiovasc Interv. 2021;98:1383-1390.
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- U. S. Food and Drug Administration. Class 2 device recall VENOVO venous stent system. [Internet]. 2021. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=187686.
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