Single center first year experience and outcomes with Impella 5.5 left ventricular assist device.

ABSTRACT:

Background

The Impella 5.5® was approved by the FDA for use for mechanical circulatory support up to 14 days in late 2019 at limited centers in the United States. Our single center's experience with Impella 5.5® can expand the overall understanding for achieving successful patient outcomes as well as provide support for the expansion of its FDA-approved use.

Methods

This study is an IRB-approved single-center retrospective cohort analysis of hospitalized adult patient characteristics and outcomes in cases where the Impella 5.5® was utilized for mechanical circulatory support.

Results

A total of 26 implanted Impella 5.5® devices were identified in 24 hospitalized patients at our institution from January 2020 to January 2021. The overall survival rate during index hospi

SUBMITTER: Rock JR 

PROVIDER: S-EPMC9128113 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature