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Impella as a bridge-to-closure in post-infarction ventricular septal defect: a case series

Sandeep S. Jalli, K. Spinelli, E. Kirker, A. Venkataraman, Jacob Abraham

European Heart Journal: Case Reports, 2023

13 participants · 22 citations

Abstract

Abstract Background Post-infarction ventricular septal defect (PIVSD) is a rare, life-threatening complication of acute myocardial infarction (AMI). Few studies report the use of mechanical circulatory support (MCS) for the treatment of cardiogenic shock in this setting. We describe our experience using a microaxial, transvalvular device (Impella, Abiomed, Danvers, MA, USA) as a bridge-to-closure for PIVSD. Case summary We identified 13 patients from two centres with cardiogenic shock due to PIVSD who received an Impella device between January 2016 and February 2022. Nine patients were transferred from another hospital, three with MCS devices [two intra-aortic balloon pumps (IABP), 1 Impella CP]. Eight patients received Impella 5.0, three received Impella 5.5 (one escalated from Impella CP), and two received Impella CP. The median time from AMI to Impella insertion was 5 (3–6) days. Five patients died on Impella support without an attempt to close the ventricular septum (VSD). Seven patients underwent successful VSD closure: six had surgical and one had percutaneous closure. One patient died during attempted percutaneous closure. Time from Impella insertion to VSD closure was 10.5 (7.8–14.0) days. Time from AMI to Impella was 5.0 (2.0–5.3) days in the group that survived to closure, and 6.0 (4.0–7.0) days in those who did not. Thirty-day mortality was 46%. Discussion Support with Impella improved clinical stability in most patients, yet multi-system organ failure leading to…

How strong is the evidence?

Evidence Hub reads this as a case series, done in people. Its evidence level is 5 of 5 (Very low · case / narrative / animal / in vitro / in silico). Case reports, narrative reviews, and animal, cell or computer-model studies give the weakest evidence for human health. Reported size: 13 participants or records.

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