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The Annals of Thoracic Surgery, Vol 52, 506-513, Copyright © 1991 by The Society of Thoracic Surgeons
RK Wampler, OH Frazier, AM Lansing, RW Smalling, JM Nicklas, SJ Phillips, RA Guyton and LA Golding
A multiinstitutional study is in progress to evaluate the Hemopump in the
treatment of cardiogenic shock. Fifty-three patients with refractory
cardiogenic shock were selected for Hemopump assistance. The hemodynamic
definition of cardiogenic shock included (1) a cardiac index of less than
2.0 L.min-1.m-2, (2) pulmonary capillary wedge pressure of greater than 18
mm Hg, and (3) a systolic blood pressure of less than 90 mm Hg or a left
ventricular work index of less than 1,500 g-m.m-2.min-1. The Hemopump was
successfully inserted in 41 of 53 patients (77.3%). A significant
improvement in the hemodynamic status was seen during Hemopump assistance.
A minimal level of hemolysis was observed. No leg ischemia was observed.
The 30-day overall survival of the Hemopump group was 31.7%. Criteria
establishing indications for use and clinical utility are proposed. We
conclude that the Hemopump provides significant hemodynamic support of the
patient in cardiogenic shock allowing for recovery from ventricular
stunning in marginal ventricles, and that in select patients the Hemopump
may offer a major improvement in survival over conventional therapy.
ARTICLES
Treatment of cardiogenic shock with the Hemopump left ventricular assist device
Nimbus, Inc, Rancho Cordova, California.
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