Patient Characteristics and Early Clinical Outcomes With Impella 5.5: A Systematic Review and Meta-Analysis

Author:

Kwon Jennie H.1ORCID,Bentley Dana2,Cevasco Marisa3,Blumer Vanessa4,Kanwar Manreet K.5,Silvestry Scott C.6,Daneshmand Mani A.7,Abraham Jacob8,Shorbaji Khaled1,Kilic Arman1

Affiliation:

1. Division of Cardiothoracic Surgery, Medical University of South Carolina, Charleston, South Carolina

2. Principle Scientific Affairs, Abiomed, Danvers, Massachusetts

3. Division of Cardiovascular Surgery, Hospital of University of Pennsylvania, Philadelphia, Pennsylvania

4. Department of Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland, Ohio

5. Cardiovascular Institute, Allegheny Health Network, Pittsburgh, Pennsylvania

6. Advent Health Transplant Institute, Orlando, Florida

7. Division of Cardiothoracic Surgery, Emory University, Atlanta, Georgia

8. Center for Cardiovascular Analytics, Research and Data Science, Providence Heart Institute, Providence Research Network, Portland, Oregon.

Abstract

Data regarding outcomes with Impella 5.5 are limited. The aim of this systematic review and meta-analysis was to summarize patient and treatment characteristics and early clinical outcomes among patients supported by Impella 5.5. A systematic literature search was conducted in PubMed, Scopus, and Cochrane databases from September 2019 to March 2023. Studies reporting outcomes in greater than or equal to 5 patients were included for review. Patient characteristics, treatment characteristics, and early clinical outcomes were extracted. Outcomes included adverse events, survival to hospital discharge, and 30 day survival. Random-effect models were used to estimate pooled effects for survival outcomes. Assessment for bias was performed using funnel plots and Egger’s tests. Fifteen studies were included for qualitative review, representing 707 patients. Mean duration of support was 9.9 ± 8.2 days. On meta-analysis of 13 studies reporting survival outcomes, survival to hospital discharge was 68% (95% confidence interval [CI], 58–78%), and 30 day survival was 65% (95% CI, 56–74%) among patients with Impella devices predominantly supported by Impella 5.5 (>60%). There was significant study heterogeneity for these outcomes. Among 294 patients with Impella 5.5 only, survival to discharge was 78% (95% CI, 72–82%) with no significant study heterogeneity. This data present early benchmarks for outcomes with Impella 5.5 as clinical experience with these devices accrues.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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