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The Journal of Thoracic and Cardiovascular Surgery, Vol 86, 639-645, Copyright © 1983 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
DM Rose, SB Colvin, AT Culliford, OW Isom, JN Cunningham Jr, E Glassman and FC Spencer
Since July, 1978, we have inserted a roller pump type of left heart assist
device between the left atrium and ascending aorta in 35 patients. There
were no significant complications related to use of the device. Seventeen
patients recovered sufficiently to have the device removed. There were four
early deaths, 60 to 120 days following removal of the device. Three of
these patients died of septic complications and one patient died as a
result of a cardiac arrest. Of the 13 long-term survivors, seven are
working and six are retired. Five patients have mild to moderate cardiac
symptoms, whereas eight others are completely asymptomatic. In three
patients the ejection fraction was significantly lower than preoperatively;
however, in all other patients the ejection fraction either stayed the same
or improved postoperatively. We conclude that this type of left heart
assist device can provide adequate cardiac support in patients with
profound left ventricular dysfunction following cardiac operations.
Furthermore, surviving patients generally have satisfactory long-term
cardiac function and are leading productive lives.
ARTICLES
Late functional and hemodynamic status of surviving patients following insertion of the left heart assist device
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