1. Meta-Analysis of Usefulness of Percutaneous Left Ventricular Assist Devices for High-Risk Percutaneous Coronary Interventions.
- Author
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Briasoulis A, Telila T, Palla M, Mercado N, Kondur A, Grines C, and Schreiber T
- Subjects
- Blood Transfusion, Comorbidity, Coronary Artery Disease epidemiology, Humans, Mortality, Myocardial Infarction epidemiology, Postoperative Complications epidemiology, Postoperative Hemorrhage epidemiology, Postoperative Hemorrhage therapy, Treatment Outcome, Vascular System Injuries epidemiology, Ventricular Dysfunction, Left epidemiology, Assisted Circulation methods, Coronary Artery Disease surgery, Heart-Assist Devices, Percutaneous Coronary Intervention methods, Perioperative Care methods, Ventricular Dysfunction, Left therapy
- Abstract
High-risk percutaneous coronary intervention (PCI) is often offered to patients with extensive coronary artery disease, decreased left ventricular function, and co-morbid conditions that increase surgical risk. In these settings, percutaneous left ventricular assist devices (PVADs) can be used for hemodynamic support. To assess the effects of PVAD use on mortality, myocardial infarction, and complication rates in patients undergoing high-risk PCI, we systematically searched the electronic databases, MEDLINE, PUBMED, EMBASE, and Cochrane for prospective controlled trials and cohort studies of patients that received hemodynamic support with PVADs for high-risk PCI. The primary outcome measures were 30-day all-cause mortality, 30-day myocardial infarction rates, periprocedural major bleeding, and vascular complications. We included 12 studies with 1,346 participants who underwent Impella 2.5 L device placement and 8 cohort studies with 205 patients that received TandemHeart device for high-risk PCI. Short-term mortality rates were 3.5% and 8% and major bleeding rates were 7.1% and 3.6% with Impella and TandemHeart, respectively. Both devices are associated with comparable periprocedural outcomes in patients undergoing high-risk PCI., (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Published
- 2016
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