A Dual-Lumen Percutaneous Cannula for Managing Refractory Right Ventricular Failure
| Autor: | Nunzio Gaglianello, David L. Joyce, Michael T. Cain, Sakthi Sundararajan, B. Badu, David Ishizawar, Lucian A. Durham, Mitchell T. Saltzberg, Asim A. Mohammed, Lyle D. Joyce |
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| Rok vydání: | 2020 |
| Předmět: |
Adult
Male medicine.medical_specialty Percutaneous Ventricular Dysfunction Right Biomedical Engineering Biophysics Bioengineering 030204 cardiovascular system & hematology Prosthesis Implantation Biomaterials 03 medical and health sciences 0302 clinical medicine Cannula Humans Minimally Invasive Surgical Procedures Medicine Weaning Adverse effect Heart Failure business.industry Cardiogenic shock Mortality rate General Medicine Middle Aged medicine.disease Surgery Right Ventricular Assist Device Treatment Outcome 030228 respiratory system Respiratory failure Female Heart-Assist Devices business Vascular Surgical Procedures |
| Zdroj: | ASAIO Journal. 66:915-921 |
| ISSN: | 1058-2916 |
| Popis: | A right ventricular assist device (RVAD) using a dual-lumen percutaneous cannula inserted through the right internal jugular vein (IJV) might improve weaning in patients with refractory right ventricular (RV) failure. However, the reported experience with this cannula is limited. We reviewed the records of all patients receiving RVAD support with this new dual-lumen cannula at our institution between April 2017 and February 2019. We recorded data on weaning, mortality, and device-specific complications. We compared outcomes among three subgroups based on the indications for RVAD support (postcardiotomy, cardiogenic shock, and primary respiratory failure) and against similar results in the literature. Mean (standard deviation [SD]) age of the 40 patients (29 men) was 53 (15.5) years. Indications for implantation were postcardiotomy support in 18 patients, cardiogenic shock in 12, and respiratory failure in 10. In all, 17 (94%) patients in the postcardiotomy group were weaned from RVAD support, five (42%) in the cardiogenic shock group, and seven (70%) in the respiratory failure group, overall higher than those reported in the literature (49% to 59%) for surgically placed RVADs. Whereas published in-hospital mortality rates range from 42% to 50% for surgically placed RVADs and from 41% to 50% for RVADs with percutaneous cannulas implanted through the right IJV, mortality was 11%, 58%, and 40% in our subgroups, respectively. There were no major device-related complications. This percutaneous dual-lumen cannula appears to be safe and effective for managing refractory RV failure, with improved weaning and mortality profile, and with limited device-specific adverse events. |
| Databáze: | OpenAIRE |
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