EMS, Left Ventricular Assist Device Management

Article Author:
Heesun Choi
Article Editor:
Stefan Merrill
Updated:
9/12/2018 5:56:39 PM
PubMed Link:
EMS, Left Ventricular Assist Device Management

Introduction

The incidence of heart failure has been increasing in the United States and worldwide, with estimates of 6 million and more than 30 million, respectively. This increasing prevalence of heart failure could be due to improved survival in patients with prior episodes of heart failure, and the overall aging of the population. The mortality rate for patients with advanced (stage D) heart failure is as high as 80% in 1 year of diagnosis. The only non-pharmacologic therapies approved in the United States for such heart failure patients are heart transplants and left ventricular assist devices (LVAD). In the past, LVADs were used as a bridge to transplant (BTT) for patients who were eligible for heart transplants. However, in January 2010, after the FDA approved a first-line intermediate-to-chronic left ventricular assist device for destination therapy, the number of patients who received LVAD implants increased significantly. As the population of patients with LVAD increases, it becomes important to have a standardized or universal LVAD management training system for prehospital emergency medical services. The goal of this article is to review a systematic approach to the management of LVAD patients in the pre-hospital setting. [1],[2],[3],[4],[5]

Issues of Concern

Ventricle assist devices are designed to supply cardiac output to perfuse vital organs for patients with a decreased left ventricular ejection fraction of less than 25%. This is achieved by removing preload from the ventricle and ejecting it into the proximal aorta. This can generate up to 8 to 10 L of blood flow to the system. The first generation of LVAD provided pulsatile blood flow to the systemic circulation, whereas second- and third-generation devices provided non-pulsatile and continuous blood flow. This continuous blood flow improves durability, decreases shear stress due to fewer moving parts, and allows for a smaller device with easier placement. The device is implanted in the thoracic cavity with the percutaneous driveline exposed over abdomen near the umbilicus. Patients with an LVAD usually carry a monitor, a controller, a spare controller, and 2 power sources with them at all times. They should also have an LVAD identification in the front pocket of an LVAD bag. It is important to identify all devices and transfer all pertinent equipment with the patient to the nearby hospital. [4],[6]

Clinical Significance

Management of an LVAD patient in a prehospital setting.